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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Planta 153 (1981), S. 279-285 
    ISSN: 1432-2048
    Keywords: Carboxysomes ; Chlorogloeopsis ; Cyanobacteria ; Polyhedral bodies ; Ribulose bisphosphate carboxylase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Ribulose 1,5-bisphosphate (RuBP) carboxylase (EC 4.1.1.39) activity was approximately equally distributed between supernatant and pellet fractions produced by differential centrifugation of disrupted cells of Chlorogloeopsis fritschii. Low ionic strength buffer favoured the recovery of particulate RuBP carboxylase. Density gradient centrifugation of resuspended cell-free particulate material produced a single band of RuBP carboxylase activity, which was associated with the polyhedral body fraction, rather than with the thylakoids or other observable particles. Isolated polyhedral body stability was improved by density gradient centrifugation through gradients of Percoll plus sucrose in buffer, which yielded apparently intact polyhedral bodies. These were 100 to 150 nm in diameter and contained ring-shaped, 12 nm diameter particles. It is inferred that the C. fritschii polyhedral bodies are carboxysomes. Sodium dodecyl sulphate (SDS) polyacrylamide gel electrophoresis of SDS-dissociated polyhedral bodies revealed 8 major polypeptides. The most abundant, with molecular weights of 52,000 and 13,000, correspond with the large and small subunits, respectively, of RuBP carboxylase.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Planta 153 (1981), S. 312-316 
    ISSN: 1432-2048
    Keywords: Anabaena ; Cyanobacteria ; Hydrogen evolution ; Photobleaching ; Photolysis ; Reversible hydrogenase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We have studied the evolution of hydrogen by photobleached filaments of the heterocystous bluegreen alga Anabaena cylindrica. The photobleached cells became orange-yellow due to the heavy accumulation of carotenoids. We found that the yellow filaments produced much larger amounts of hydrogen than the normal, green ones, while the nitrogenase activity responsible for hydrogen evolution increased to a lesser extent. We suggest that a reversible hydrogenase activity induced in photobleached filaments is responsible for the excess amount of hydrogen. 3-(3′,4′-dichlorophenyl)-1,1-dimethyl urea (DCMU) inhibits the hydrogen evolution of the yellow filaments which produce much more oxygen and fix less CO2 than the green filaments. Therefore we consider the water to be a possible electron source for this hydrogenase. The low efficiency of light energy conversion (0.3%) in nitrogenase-catalyzed H2 evolution (Laczkó, 1980 Z. Pflanzenphysiol. 100, 241–245) is increased to 1.5–2% by the appearance of the reversible hydrogenase activity.
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  • 3
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    Springer
    Planta 156 (1982), S. 70-77 
    ISSN: 1432-2048
    Keywords: Cyanelles ; Cyanobacteria ; Cyanophora ; Endosymbiosis ; Nitrate assimilation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The taxonomic affinity of Cyanophora paradoxa and its endosymbiotically living cyanelles has not yet been resolved. In the present communication, the enzymes of assimilatory nitrate reduction are investigated in cell-free preparations from the cyanelles and from the eukaryotic host. Nitrate reductase of Cyanophora is a NADH-dependent, soluble enzyme, occurring only in the protoplasm of the eukaryotic host. In contrast, nitrite reductase is ferredoxin-dependent and bound to the thylakoids of cyanelles. Glutamine synthetase and ferredoxin-dependent glutamate synthase (GOGAT) are present both in cyanelles and the eukaryote. Activity levels of alanine dehydrogenase and glutamic acid dehydrogenase are marginal in Cyanopnora, indicating that ammonia is suggest assimilated by the glutamine synthetase GOGAT pathway. The data also that NH 4 + leaves the cyanelles to meet the nitrogen requirements of the eukaryote. It is concluded that the pathway of assimilatory nitrate reduction is similar in Cyanophora and photosynthetic eukaryotic cells and is different from that in byanobacteria.
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  • 4
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    Planta 156 (1982), S. 78-83 
    ISSN: 1432-2048
    Keywords: Cyanelles ; Cyanobacteria ; Cyanophora ; Endosymbiosis ; Photosynthesis (Cyanophora) ; Respiration (Cyanophora)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Isolated cyanelles of Cyanophora paradoxa perform photosystem I and II dependent Hill reactions. The photosynthetic electron transport of the cyanelles does not show special features uncommon in cyanobacteria or chloroplasts of red algae. A preparation of cyanelles performs photosynthetic O2-evolution with approximately 1/3 of the rate of intact Cyanophora, in only, however, the first three minutes of the experiment. All attempts to stabilize the CO2-fixation activity of isolated cyanelles failed. Isolated cyanelles do not perform KCN-sensitive O2-uptake, indicating that respiratory cytochrome oxidase is lacking in cyanelles. O2-consumption by crude extracts from Cyanophora is inhibited by KCN when N-tetramethyl-p-phenylenediamine/ascorbate or NADH but not NADPH are supplied as the electron donors in contrast to the situation in cyanobacteria. These findings suggest that cyanelles do not respire. It is concluded that cyanelles are not so much related to cyanobacteria as formerly believed, but share many properties with chloroplasts of eukaryotic cells.
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  • 5
    ISSN: 1432-2048
    Keywords: Ammonium ; Cyanobacteria ; Lichen ; Nitrate ; Nitrogenase ; Photosynthesis (lichens)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Uptake of NH 4 + and NO 3 - by the N2-fixing lichens Peltigera praetextata (two-component lichen) and P. aphthosa (three-component lichen) was studied. In addition, the effects of these ions, separately and in combination, on C2H2 reduction and CO2 exchange were examined. Both NH 4 + and NO 3 - were utilized by the lichens. NH4NO3 caused an increased liberation of NO 3 - from the lichens as compared to the release observed in untreated lichen thalli. NH 4 + and NO 3 - led to reduced C2H2 reduction by P. praetextata, which, however, was less pronounced than when the two ions were given in combination. In P. aphthosa the C2H2 reduction was inhibited by NH 4 + and NH4NO3, but not by NO 3 - alone. NH 4 + and NO 3 - had no effect on the net photosynthesis of P. praetextata, while, in combination, they led to inhibition, although only at a concentration higher than that inhibitory to the C2H2 reduction of P. aphthosa. The photsynthesis was inhibited by all salts, but only initially, probably a “salt effect”. Effects of NH 4 + on the membrane potential of the cyanobiont are suggested as an important factor causing the depression of net photosynthesis.
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  • 6
    ISSN: 1432-2048
    Keywords: Cyanobacteria ; Cyanocyta ; Cyanophora ; Endosymbiosis ; Regulation (development)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The prokaryote Cyanocyta korschikoffiana was isolated from the eukaryote Cyanophora paradoxa. The synthesis of several thylakoid proteins in these cyanelles is influenced by light and darkness and is sensitive to cycloheximide, the inhibitor of the eukaryotic host's translation. The possibility of a direct coordination between the translations of the host and of the cyanelles is discussed.
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  • 7
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    Planta 151 (1981), S. 256-264 
    ISSN: 1432-2048
    Keywords: Cyanobacteria ; (dark) CO2 fixation ; Lichens ; Nitrogenase ; Pettigera
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The lichen Peltigera aphthosa consists of a fungus and green alga (Coccomyxa) in the main thallus and of a Nostoc located in superficial packets, intermixed with fungus, called cephalodia. Dark nitrogenase activity (acetylene reduction) of lichen discs (of alga, fungus and Nostoc) and of excised cephalodia was sustained at higher rates and for longer than was the dark nitrogenase activity of the isolated Nostoc growing exponentially. Dark nitrogenase activity of the symbiotic Nostoc was supported by the catabolism of polyglucose accumulated in the ligh and which in darkness served to supply ATP and reductant. The decrease in glucose content of the cephalodia paralleled the decline in dark nitrogenase activity in the presence of CO2; in the absence of CO2 dark nitrogenase activity declined faster although the rate of glucose loss was similar in the presence and absence of CO2. Dark CO2 fixation, which after 30 min in darkness represented 17 and 20% of the light rates of discs and cephalodia, respectively, also facilitated dark nitrogenase activity. The isolated Nostoc, the Coccomyxa and the excised fungus all fixed CO2 in the dark; in the lichen most dark CO2 fixation was probably due to the fungus. Kinetic studies using discs or cephalodia showed highest initial incorporation of 14CO2 in the dark in to oxaloacetate, aspartate, malate and fumarate; incorporation in to alanine and citrulline was low; incorporation in to sugar phosphates, phosphoglyceric acid and sugar alcohols was not significant. Substantial activities of the enzymes phosphoenolpyruvate (PEP) carboxylase (EC 4.1.1.31) and carbamoyl-phosphate synthase (EC 2.7.2.5 and 2.7.2.9) were detected but the activities of PEP carboxykinase (EC 4.1.1.49) and PEP carboxyphosphotransferase (EC 4.1.1.38) were negligible. In the dark nitrogenase activity by the cephalodia, but not by the free-living Nostoc, declined more rapidly in the absence than in the presence of CO2 in the gas phase. Exogenous NH 4 + inhibited nitrogenase activity by cephalodia in the dark especially in the absence of CO2 but had no effect in the light. The overall data suggest that in the lichen dark CO2 fixation by the fungus may provide carbon skeletons which accept NH 4 + released by the cyanobacterium and that in the absence of CO2, NH 4 + directly, or indirectly via a mechanism which involves glutamine synthetase, inhibits nitrogenase activity.
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  • 8
    ISSN: 1432-2048
    Keywords: Anabaena ; C2H2 reduction ; CO2 fixation ; Cyanobacteria ; Glyoxylate ; Nitrogenase Photorespiration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Raising the pO2 reduced nitrogenase activity (C2H2 reduction) of Anabaena cylindrica for both glyoxylate-treated (5 mM) and untreated cells. The stimulation caused by glyoxylate, however, increased with increases of pO2 from 2 to 99 kPa. As the pO2 increased the net CO2 fixation was lowered (Warburg effect) while the CO2 compensation point increased. Glyoxylate partly relieved this sensitivity of net photosynthesis to oxygen and reduced the compensation point considerably. The cells used were preincubated in the dark to exhaust photosynthetic pools. A more pronounced reduction in sensitivity of nitrogenase to oxygen for glyoxylate-treated cells was evident when a preincubation in air with reduced pCO2 (13 μl l-1) was used. This was, however, not evident until after a 10-h incubation in air. Before this point 2 kPa O2 sustained the highest nitrogenase activity. Addition of 0.5 and 5 mM of HCO 3 - to Anabaena cultures preincubated at low CO2 levels (29 μl l-1) abolished the stimulatory effect of glyoxylate on the nitrogenase. Thus, the results sustain the suggestion that glyoxylate may act as an inhibitor of photorespiratory activities in cyanobacteria and can be used as a means of increasing their nitrogen and CO2 fixation capacities.
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  • 9
    ISSN: 1432-2048
    Keywords: Cyanobacteria ; Mastigocladus ; Phycobiliproteins ; Phycobilisomes ; Phycoerythrocyanin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A method for the effective isolation of functionally intact phycobilisomes from the thermophilic cyanobacterium M. laminosus is presented, using an unconventional high buffer molarity for stabilizing the aggregates and introducing a DNAse treatment of the disrupted cells to obtain sharp banding of the phycobilisomes in the linear sucrose density gradients. The structural integrity of the isolated phycobilisomes is demonstrated by a fluorescence emission maximum at 673 nm of aggregated allophycocyanin and by electron microscopy. Besides C-phycocyanin and allophycocyanin, phycoerythrocyanin is a constituent pigment of the phycobilisomes. These pigments indicated in the absorption spectrum of phycobilisomes with a maximum at 610 nm and two shoulders at 650 and 580 nm, respectively, were characterized by spectral data and isoelectric points.
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  • 10
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    Planta 152 (1981), S. 101-104 
    ISSN: 1432-2048
    Keywords: Cyanobacteria ; Fructose-bisphosphatase ; Synechococcus ; Thioredoxin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Fructose-1,6-bisphosphatase was isolated from the cyanobacterium Synechococcus 6301 by acid precipitation, ammonium-sulfate fractionation, and Sephadex gel chromatography. The purified enzyme needed thiols and MgCl2 for activity. The following Km-values were obtained: a) for fructose-1,6-bisphosphate: 1.7 mM; b) for MgCl2: 12.5 mM; c) for dithiocrythritol: 0,56 mM; d) for glutathione: 14 mM; e) for mercaptoethanol: 22 mM; f) for cysteine: 50 mM. Thioredoxin B isolated from this organism will activate this fructose-1,6-bisphosphatase. The Km of thioredoxin B for this fructose-1,6-bisphosphatase was determined to be 1.7 μM, endicotiy that thioredoxin might activate the fructose-1,6-bisphosphatase in Synechococcus in vivo.
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  • 11
    ISSN: 1432-2048
    Keywords: Ammonium assimilation ; Anthoceros ; Bryophyta ; Cyanobacteria ; Glutamine and glutamate formation ; Nostoc ; Symbiosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The pathways of assimilation of ammonium by pure cultures of symbiont-free Anthoceros punctatus L. and the reconstituted Anthoceros-Nostoc symbiotic association were determined from time-course (5–300 s) and inhibitor experiments using 13NH 4 + . The major product of assimilation after all incubation times was glutamine, whether the tissues were cultured with excess ammonium or no combined nitrogen. The 13N in glutamine was predominantly in the amide-nitrogen position. Formation of glutamine and glutamate by Anthoceros-Nostoc was strongly inhibited by either 1mM methionine sulfoximine (MSX) or 1 mM exogenous ammonium. These data are consistent with the assimilation of 13NH 4 + and formation of glutamate by the glutamine synthetase (EC 6.3.1.2)-glutamate synthase (EC 1.4.7.1) pathway in dinitrogen-grown Anthoceros-Nostoc. However, in symbiont-free Anthoceros, grown with 2.5 mM ammonium, formation of glutamine, but not glutamate, was decreased by either MSX or exogenous ammonium. These results indicate that during short incubation times ammonium is assimilated in nitrogenreplete Anthoceros by the activities of both glutamine synthetase and glutamate dehydrogenase (EC 1.4.1.2). In-vitro activities of glutamine synthetase were similar in nitrogen-replete Anthoceros and Anthoceros-Nostoc, indicating that the differences in the routes of glutamate formation were not based upon regulation of synthesis of the initial enzyme of the glutamine synthetase-glutamate synthase pathway. When symbiont-free Anthoceros was cultured for 2 d in the absence of combined nitrogen, total 13NH 4 + assimilation, and glutamine and glutamate formation in the presence of inhibitors, were similar to dinitrogen-grown Anthoceros-Nostoc. The routes of immediate (within 2 min) glutamate formation and ammonium assimilation in Anthoceros were apparently determined by the intracellular levels of ammonium; at low levels the glutamine synthetase-glutamate synthase pathway was predominant, while at high levels independent activities of both glutamine synthetase and glutamate dehydrogenase were expressed.
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  • 12
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    Planta 158 (1983), S. 451-457 
    ISSN: 1432-2048
    Keywords: Cyanobacteria ; Mastigocladus (cyanobacterium) ; Photosystem II (freeze fracture) ; Phycobilisome ; Thylakoid (freeze fracture)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The thylakoids of the thermophilic cyanobacterium Mastigocladus laminosus were examined by freeze-fracture analysis. The expolasmatic (EF)-freeze-fracture particles are organized in rows, separated by 45 nm or more with a 12-nm center-tocenter spacing of neighboring particles. Phycobilisomes, associated to the outer thylakoid surfaces show a similar spacing pattern. Fractures exposing simultaneously phycobilisomes and EF-freeze-fracture particles on the same thylakoid show a direct alignment of both systems. Consequently the phycobilisomes are concluded to be associated peripherally on top of the EF-freeze-fracture particles in a 1:1 assembly pattern. The periodicity of the EF-freeze-fracture particles determines the arrangement of the phycobilisomes in the rows. The planar phycobilisome model of Mörschel et al. (1977) easily allows a successive arrangement of the phycobilisomes in a row, whereas with the staggered model developed by Bryant et al. (1979), only a cogged arrangement of neighboring phycobilisomes is possible.
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  • 13
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    Planta 152 (1981), S. 408-414 
    ISSN: 1432-2048
    Keywords: Anacystis ; Cyanobacteria ; Cyanophage infection ; Oxido-reductive enzyme modulation ; Phosphatase, acid and alkaline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Ascorbic acid (AA) increased the phosphatase activity (pH 6.8) in 10,000 g supernatants from Anacystis nidulans. The enzyme activated by AA was deactivated by dehydroascorbic acid (DHAA). The modulation by AA/DHAA of phosphatase activity in Anacystis appears to be specific; a number of other redox compounds, known to modulate other enzymes, had no effect on the Anacystis phosphatase. A purified phosphatase preparation from Anacystis was also deactivated by DHAA. In contrast, the purified enzyme was not activated by AA, suggesting that a factor mediating the effect of AA was lost during purification. Another factor was found to protect the purified phosphatase against deactivation by DHAA. The enzyme was characterized as a phosphatase with a broad substrate specificity, an apparent molecular weight of 19,000, and a pH optimum of 6.0–7.0. Dialysis of the enzyme preparation against EDTA abolished the phosphatase activity which could be restored by Zn2+ ions and partially restored by Co2+ ions. Crude extracts also contained a latent enzyme, the phosphatase activity of which could be detected in the presence of Co2+ ions only. Zn2+ ions did not activate this enzymatically inactive protein. The Co2+-dependent phosphatase had an apparent mol. wt. of 40,000, a broad substrate specificity, and an alkaline pH-optimum. Infection of Anacystis cultures by cyanophage AS-1 resulted in a decrease in phosphatase activity. The enzyme present in 10,000 g supernatants from infected cells could not be modulated by the AA/DHAA system.
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  • 14
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Anabaena cylindrica ; Canavanine ; Akinete differentiation ; Akinete pattern
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Addition of the arginine analogue, canavanine, to cultures of nitrogen-fixing Anabaena cylindrica at the onset of akinete formation, resulted in the development of akinetes randomly distributed within the filament, in addition to those adjacent to heterocysts. The total frequency of akinetes increased up to five-fold. A feature of akinetes is their increased content of cyanophycin granules (an arginine-aspartic acid polymer) and addition of canavanine to cultures at an earlier stage resulted in entire filaments becoming agranular and containing agranular akinetes. The effects on akinete pattern appeared to be specific for canavanine since other amino acid analogues, although increasing the frequency of akinetes (approximately two-fold), had no effect on their position relative to heterocysts. In ammonia-grown, stationary phase cultures of A. cylindrica, akinetes were observed adjacent to proheterocysts and in positions more than 20 cells from any heterocyst. These observations indicate that nitrogen fixation and heterocysts are not essential for akinete formation in A. cylindrica, although the availability of a source of fixed nitrogen does appear to be a requirement. These results suggest that during exponential growth some aspect of the physiology of vegetative cells suppresses their development into akinetes and that the role of the heterocyst may not be one of direct stimulation of adjacent vegetative cells to form akinetes, but the removal or negation of the inhibition within them. A model for akinete formation and the involvement of canavanine is given.
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  • 15
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    Archives of microbiology 128 (1980), S. 137-144 
    ISSN: 1432-072X
    Keywords: Anacystis nidulans ; Anabaena ; Nostoc ; Blue-green algae ; Cyanobacteria ; Nitrate assimilation ; Ammonium inhibition ; Ammonium assimilation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Ammonium at low concentrations caused a rapid and effective inhibition of nitrate utilization in the light by the cyanobacterium Anacystis nidulans without affecting the cellular level of nitrate reductase activity. The inhibition was reversible, and the ability of the cells to utilize nitrate was restored immediately after ammonium had been exhausted. The inhibitory effect was dependent on consumption by the cells of the added ammonium which was rapidly incorporated into amino acids. In the presence of L-methionine-d,l-sulfoximine (MSX) or azaserine, inhibitors of the glutamine synthetase-glutamate synthase pathway, ammonium did not exhibit any inhibitory effect on nitrate utilization. Ammonium assimilation, rather than ammonium itself, seems to regulate nitrate utilization in A. nidulans. Short-term inhibition by ammonium of nitrate utilization and its prevention by MSX were also demonstrated in the filamentous cyanobacteria Anabaena and Nostoc.
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  • 16
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    Archives of microbiology 128 (1980), S. 242-247 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Taxonomy ; Endonucleases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Three nucleotide sequence-specific deoxyribonucleases present in extracts of Anabaena subcylindrica have been purified and characterized. Endo R·AsuI recognizes and cleaves the nucleotide sequence G↓GNCC (Hughes et al., 1980) while Endo R·AsuII and III split the sequences TT·CGAA and GPu↓CGPyC, respectively (this paper). An Anabaena strain “Waterbury” converging genetically at the 30–35% level with both A. subcylindrica and A. cylindrica (as judged by DNA-DNA hybridization, in vitro) was shown to possess the endonuclease pattern typical for A. cylindrica (de Waard et al., 1978). The usefulness of these specific endonucleases as taxonomic markers for the classification of cyanobacteria is discussed.
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  • 17
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    Archives of microbiology 124 (1980), S. 39-47 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Synechococcus ; Phycobilisomes ; Phycobiliproteins ; Phycocyanin ; Turnover ; Nitrogen starvation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In exponentially growing cells of Synechococcus sp. 6301, over 95% of the phycobiliproteins are located in phycobilisomes, and the remainder is present in the form of low molecular weight aggregates. In addition to the subunits of the phycobiliproteins (C-phycocyanin, allophycocyanin, allophycocyanin B), the phycobilisomes of this unicellular cyanobacterium contain five non-pigmented polypeptides. During the initial phase of starvation (24 h after removal of combined nitrogen from the growth medium), the phycobiliproteins in the low molecular weight fraction largely disappeared. Phycocyanin was lost more rapidly from this fraction than allophycocyanin. Simultaneous changes in the phycobilisome were (1) a decrease in sedimentation coefficient, (2) a decrease in phycocyanin: allophycocyanin ratio, (3) a shift in the fluorescence emission maximum from 673 to 676 nm, and (4) a selective complete loss of a 30,000 dalton non-pigmented polypeptide. Upon extensive nitrogen starvation (72 h), the intracellular level of phycocyanin decreased by over 30-fold. These results indicate that in the early stage of nitrogen starvation, the free phycobiliproteins of the cell are degraded, as well as a significant proportion of the phycocyanin from the periphery of the phycobilisome. However, the structures partially depleted of phycocyanin still function efficiently in energy transfer. On extended starvation, total degradation of residual phycobilisomes takes place, possibly in conjunction with the detachment of these structures from the thylakoids. None of the effects of the absence of combined nitrogen were seen when cells were starved in the presence of chloramphenicol, or in a methionine auxotroph starved for methionine.
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  • 18
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    Archives of microbiology 124 (1980), S. 155-160 
    ISSN: 1432-072X
    Keywords: Photosynthesis ; Thylakoid membranes ; Electron transport ; Photophosphorylation ; Thermophily ; Proton uptake ; Cyanobacteria ; Matigocladus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Photosynthetically active membranes have been prepared from the thermophilic cyanobacterium Mastigogladus laminosus by treatment with lysozyme. The membranes were active in electron transport through photosystem I and II as well as in photophosphorylation and proton uptake. Cells were grown at 40°, 45° and 55°C respectively. The temperature optimum of oxygen evolution of whole cells was about 10°C higher than the growth temperature. In isolated membranes the temperature optimum for cyclic photophosphorylation was identical to the growth temperature of the cells whereas the optimum for photosystem II electron transport never exceeded 40°C. Photophosphorylation was inhibited by N, N′-dicyclohexyl carbodiimide (DCCD), carbonyl-cyanide-m-chlorophenylhydrazone and NH4Cl, whereas proton uptake was enhanced by DCCD. Electron transport was slightly inhibited by these treatments. The membranes could be stored for several weeks at-20°C in 50% glycerol without any loss in the activities.
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  • 19
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    Archives of microbiology 128 (1981), S. 336-340 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Anabaena variabilis ; Electron flow ; Photosynthesis ; Respiration ; Cytochrome oxidase ; Cytochrome c-553 ; Plastocyanin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The cytochrome oxidase activity (oxygen uptake in the dark) of a membrane preparation from Anabaena variabilis was found to be stimulated by cytochrome c-553 and plastocyanin obtained from this alga. Cytochrome c from horse heart was as active as cytochrome c-553, whereas little or no stimulation of oxygen uptake was obtained with cytochromes c 2 from two Rhodospirillaceae, the plastidic cytochrome c-552 from Euglena, and plastocyanin from spinach. Cytochrome c-553 (A. variabilis) stimulated photosystem 1 activity in the same preparation much more than cytochrome c (horse heart). The results indicate that cytochrome c-553 and plastocyanin, besides their established function as electron donors of photosystem 1, participate in respiratory electron transport as reductants of a terminal oxidase. Photooxidation and dark oxidation show a different donor specificity.
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  • 20
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    Archives of microbiology 133 (1982), S. 11-19 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Ultrastructure ; Mastigocladus laminosus ; Fischerella ; True branching
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The morphology and ultrastructure of the thermophilic cyanobacteriumMastigocladus laminosus were examined by scanning and transmission electron microscopy. Mature cultures consisted of relatively old, wide filaments that branched frequently to form younger, thinner filaments. The cells of the younger filaments had a consistently cylindrical morphology, while those of older filaments were rounded and pleomorphic. The internal ultrastructure of the cells depended somewhat on their age. As young cells became larger and wider, their thylakoids underwent slight rearrangement and spread out toward the center of the cytoplasm. Polyphosphate bodies, carboxysomes (polyhedral bodies), and lipid-body-like structures increased in number as the cells aged, but ribosomes and cyanophycin granules were depleted. Cell division involved septum formation followed by ingrowth of the outer membrane and sheath. Cells in older filaments were separated from each other by a complete layer of sheath material. Septum formation in older cells was also seen to occur parallel to the long axis of the filament, thereby confirming that true branching took place.
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  • 21
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    Archives of microbiology 134 (1983), S. 73-79 
    ISSN: 1432-072X
    Keywords: Isocitrate dehydrogenase ; Cyanobacteria ; Heterocysts ; Vegetative cells ; Thioredoxin ; Anabaena cylindrica ; Nostoc muscorum ; Anacystis nidulans
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The present communication describes the properties of isocitrate dehydrogenase in crude extracts from the unicellular Anacystis nidulans and from heterocysts and vegetative cells of Nostoc muscorum and Anabaena cylindrica. The activity levels of this enzyme are much higher in heterocysts than in vegetative cells of N. muscorum and A. cylindrica. Isocitrate dehydrogenase is virtually inactive in vegetative cells of A. cylindrica. The enzyme is negatively regulated by the reduction charge and scarcely affected by oxoglutarate in the three cyanobacteria. The inhibition by ATP and ADP is competitive with respect to isocitrate and NADP+ in A. cylindrica and N. muscorum and noncompetitive in A. nidulans. Isocitrate dehydrogenase from the three cyanobacteria seems to be a hysteretic enzyme. All the experimental data suggest that the major physiological role of isocitrate and the isocitrate dehydrogenase in heterocysts is not to generate reducing equivalents for N2-fixation. Oxoglutarate formed by the enzyme reaction is likely required for the biosynthesis of glutamate inside the heterocysts. Thioredoxin preparations from spinach chloroplasts or from A. cylindrica activate isocitrate dehydrogenase from either heterocysts or vegetative cells of A. cylindrica. Activation is completed within seconds and requires dithiothreitol besides thioredoxin. The thioredoxin preparation which activates isocitrate dehydrogenase also activates NADP+-dependent malate dehydrogenase from spinach chloroplasts or heterocysts of A. cylindrica. Isocitrate dehydrogenase from A. cylindrica is deactivated by oxidized glutathione. It is speculated that isocitrate dehydrogenase and thioredoxin play a role in the differentiation of vegetative cells to heterocysts.
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  • 22
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    Archives of microbiology 135 (1983), S. 287-292 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Respiration ; Nitrogen fixation ; Heterocysts ; K m for O2 ; Anabaena variabilis
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    Topics: Biology
    Notes: Abstract Simultaneous measurements of acetylene reduction by Anabaena variabilis and the concentration of dissolved oxygen in the suspension were made using a specially designed vessel which allowed measurements under steady-state conditions. The rate of acetylene reduction in the dark increased with increasing oxygen concentrations until a maximum value was reached at 300 μM O2 (corresponding to 30% O2 in the gas phase at 35°C). This presumably results from a requirement for energy provided by respiration. Measurements of the dependence of respiration rate on dissolved oxygen concentration were made under comparable conditions using an open system to allow conditions close to steady-state to be obtained. The respiration rate of diazotrophically grown Anabaena variabilis had a dependence on oxygen concentration corresponding to the sum of two activities. These had K m values of 1.0 μM and 69 μM and values of V max of similar magnitude. Only the high affinity activity was observed in nitrate-grown cyanobacteria lacking heterocysts, and this presumably represent activity in the vegetative cells. The oxygen concentration dependence of the low affinity activity resembled that for the stimulation of acetylene reduction. We interpret this as the result of oxygen uptake by the heterocysts. The results are consistent with the idea that in intact filaments of cyanobacteria O2 enters heterocysts much more slowly than it enters the vegetative cells.
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  • 23
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Synechococcus ; Synechocystis ; Thermophily ; Temperature effects ; Glucose-6-phosphate dehydrogenase ; 6-Phosphogluconate dehydrogenase ; Enzyme kinetics ; Enzyme regulation
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    Notes: Abstract The activities and kinetics of the enzymes G6PDH (glucose-6-phosphate dehydrogenase) and 6PGDH (6-phosphogluconate dehydrogenase) from the mesophilic cyanobacterium Synechococcus 6307 and the thermophilic cyanobacterium Synechococcus 6716 are studied in relation to temperature. In Synechococcus 6307 the apparent K m's are for G6PDH: 80μM (substrate) and 20μM (NADP+); for 6PGDH: 90μM (substrate) and 25μM (NADP+). In Synechococcus 6716 the apparent K m's are for G6PDH: 550μM (substrate) and 30μM (NADP+); for 6PGDH: 40μM (substrate) and 10μM (NADP+). None of the K m's is influenced by the growth temperature and only the K m's of G6PDH for G6P are influenced by the assay temperature in both organisms. The idea that, in general, thermophilic enzymes possess a lower affinity for their substrates and co-enzymes than mesophilic enzymes is challenged. Although ATP, ribulose-1,5-bisphosphate, NADPH and pH can all influence the activities of G6PDH and 6PGDH to a certain extent (without any difference between the mesophilic and the thermophilic strain), they cannot be responsible for the total deactivation of the enzyme activities observed in the light, thus blocking the pentose phosphate pathway.
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  • 24
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    Archives of microbiology 137 (1984), S. 220-225 
    ISSN: 1432-072X
    Keywords: Biological control ; Colony ; Cyanobacteria ; Entrapment ; Lysis ; Myxococcus ; Phormidium ; Predatory ; Prey ; Spherule
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Two strains of Myxococcus xanthus, and a strain of Myxococcus fulvus were compared with respect to their ability to entrap and lyse trichomes of the cyanobacterium Phormidium luridum var. olivaceae. All of these isolates form colonial aggregates and spherules in either axenic culture with a tryptone-salts medium or in a mixed culture with viable cyanobacterial cells as the sole source of nutrients. Light microscopy showed evidence of swarming activity on the surface of all three myxococci with the accompanying formation of fruiting structures. Extended incubation of mixed cultures showed the myxococci to be capable of long-term control of the cyanobacterial population with predator-prey population cycling occurring on average every 9 days. Serial transfer of mixed cultures into either fresh autotrophic medium or cyanobacterial cultures of 107 per ml showed the persistence of predatory activity. Myxococcal densities were shown to return repeatedly to initial virulent levels. Predator inoculum levels could be reduced to 50 cells per 100 ml in a cyanobacterial culture of 107 per ml. These in vitro data enhance the potential of the myxococcus predatory colony as a biological control agent for in situ cyanobacteria.
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  • 25
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    Archives of microbiology 138 (1984), S. 299-305 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Oscillatoria ; Anoxygenic photosynthesis ; Sulfide ; Photosystem II ; Photoreduction
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    Topics: Biology
    Notes: Abstract Oscillatoria amphigranulata is a fast-growing (3 doublings/day) cyanobacterium isolated from sulfide hot springs in New Zealand. Photosynthesis, as measured by incorporation of [14C]-HCO 3 - , was initially inhibited by 0.3–1.5 mM sulfide at pH 7.9–8.1. However, conversion to sulfide-dependent anoxygenic photosynthesis occurred in about 2 h or less under light intensities of 3–14 klx. Under the stimulation of higher light intensity (8–14 klx) a partial recovery of oxygenic photosynthesis also occurred. It was concluded that oxygenic photosynthesis was responsible for 21–42% of the total incorporation at sulfide concentrations of 1.0–0.3 mM, respectively. This contribution was suppressed at 1.5 mM sulfide and not elicited under lower light intensities (3–7 klx). As judged by the inhibitory effect of 10 μg/ml chloramphenicol protein synthesis was required for attainment of both anoxygenic photosynthesis and photosystem II recovery. Sulfide could not be replaced by thiosulfate, elemental sulfur or dithionite as electron donors in photosynthesis, but elemental sulfur could serve as the sole assimilatory source of sulfur. Oxygenic photosynthesis was inhibited by DCMU [3-(3,4-dichlorophenyl)-1,1-dimethylurea] or DBMIB (2,5-dibromo-3-methyl-6-isopropyl-p-benzoquinone), but sulfide relieved the effect of either inhibitor in adapted cells, indicating that electrons derived from sulfide enter the photosynthetic electron transport chain at a point beyond plastoquinone.
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  • 26
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    Archives of microbiology 130 (1981), S. 175-179 
    ISSN: 1432-072X
    Keywords: Acetate ; pH gradients ; Membrane permeability ; Cyanobacteria
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    Notes: Abstract Mutants of Synechococcus and of Aphanocapsa which were unable to activate acetate have been used to demonstrate that acetate entered the cells rapidly in darkness, and to a greater extent in light. Total internal concentrations under different conditions can be explained if acetic acid equilibrates rapidly across the cell membrane while acetate ion is strongly hindered. Acetate as well as other weak acids such as 5,5-dimethyl-2,4-oxazolidenedione can therefore be used as a probe of internal pH in these mutants. The intracellular pH was maintained at about 7.1 in darkness and 7.6 in light when external pH was varied from 6.8–8.0 No carrier involved in acetic acid equilibration could be demonstrated. Of other organic acids investigated, only propionate distributed in accordance with pH differences between the cells and surrounding fluid. The low uptake rates of glycolate, pyruvate and leucine appeared limited by slow movement of molecules into the cells.
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  • 27
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    Archives of microbiology 130 (1981), S. 204-212 
    ISSN: 1432-072X
    Keywords: Agmenellum quadruplicatum ; Nitrogen starvation ; Ultrastructure ; PATO poststain ; Cyanobacteria
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    Notes: Abstract The effects of nitrogen limitation on the ultrastructure of the unicellular cyanobacterium, Agmenellum quadruplicatum, were studied by thin sectioning transmission electron microscopy. Nitrogen became limiting for growth 14–15 h after transfer to nitrogen-limiting medium, but cultures retained full viability for at least 45 h. The c-phycocyanin: chlorophyll a ratio and cellular nitrogen content of the culture dropped rapidly after 14–15 h, as a progressive deterioration of major cell structures took place. Phycobilisomes were degraded first, followed by ribosomes and, then, thylakoid membranes. These structures were virtually depleted from the cells within 26 h. Intracellular polysaccharide accumulated in place of the normal cell structures throughout this period. Nitrogen limitation did not affect polyphosphate bodies, carboxysomes, lipid granules, the cell envelope, or the extra-cellular glycocalyx. All of the ultrastructural changes resulting from nitrogen limitation were reversed upon addition of nitrate to a starved culture. Most cell structures were restored within 3 h, and restoration was complete within 9 h.
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  • 28
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    Archives of microbiology 138 (1984), S. 306-309 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Oscillatoria ; Anoxygenic photosynthesis ; Sulfide intolerance
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    Notes: Abstract A spontaneous variant incapable of anoxygenic photosynthesis was derived from a fully competent strain of Oscillatoria amphigramulata which was originally isolated from a high sulfide-containing hot spring of New Zealand. Although the variant (Oa-2) acquired a slight ability to photosynthesize in the presence of 0.3–0.4 mM sulfide, this was only after a 24 h exposure to sulfide and represented oxygenic photosynthesis only. Unlike the parent strain, the incompetent variant never grew in the presence of sulfide 〉0.05 mM, nor was there any relief of the inhibition by DCMU [3-(3,4-dichlorophenyl)-1,1-dimethylurea] of CO2 photoincorporation when sulfide was present. The variant strain has retained all of these characteristics over a 4 year period with monthyl transfers in non-sulfide medium. The wild type, under identical conditions, has retained all of its competence with respect to sulfide.
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  • 29
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    Archives of microbiology 140 (1984), S. 120-125 
    ISSN: 1432-072X
    Keywords: Photosynthesis ; Glycogen ; Fructose ; Reductant supply ; Nitrogenase ; Oxygen protection ; Cyanobacteria
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    Notes: Abstract Nitrogenase (=acetylene-reducing activity) was followed during photoautotrophic growth of Anabaena variabilis (ATCC 29413). When cell density increased during growth, (1) inhibition of light-dependent activity by DCMU, an inhibitor of photosynthesis, increased, and (2) nitrogenase activity in the dark decreased. Addition of fructose stabilized dark activity and alleviated the DCMU effect in cultures of high cell density. The resistance of nitrogenase towards oxygen inactivation decreased after transfer of autotrophically grown cells into the dark at subsequent stages of increasing culture density. The inactivation was prevented by addition of fructose. Recovery of acetylene-reducing activity in the light, and in the dark with fructose present, was suppressed by ammonia or chloramphenicol. In the light, also DCMU abolished recovery. To prove whether the observed effects were related to a lack of photosynthetic storage products, glycogen of filaments was extracted and assayed enzymatically. The glycogen content of cells was highest 10 h after inoculation, while light-dependent nitrogenase activity was at its maximum about 24 h after inoculation. Glycogen decreased markedly as growth proceeded and dropped sharply when the cells were transferred to darkness. Thus, when C-supply (by photosynthesis or added fructose) was not effective, the glycogen content of filaments determined the activity of nitrogenase and its stability against oxygen. In cells lacking glycogen, nitrogenase activity recovered only when carbohydrates were supplied by exogenously added fructose or by photosynthesis.
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  • 30
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    Archives of microbiology 139 (1984), S. 196-201 
    ISSN: 1432-072X
    Keywords: Anabaena cylindrica ; Cyanobacteria ; Heterocyst ; Akinete ; Cell division ; Differentiation
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    Notes: Abstract Neo-peptone B119 (Difco) was found to have a significant effect on differentiation of heterocysts and akinetes in Anabaena cylindrica. On adding neopeptone (0.4 g/l) to exponential phase culture of A. cylindrica, the following effects were observed (i) increased heterocyst frequency with altered heterocyst spacing and presence of double and multiple heterocysts after 24 h in cultures grown on N-free medium, (ii) induction of regular pattern of heterocysts after 48 h, in culture grown on medium supplemented with NH4Cl, (iii) induction of pro-akinetes after 48 h in both N-free and ammonium-grown cultures. The higher concentrations of neo-peptone were lytic to A. cylindrica, and, its lytic and inductive effects could be decreased by acid hydrolysis or supplementation of NH4Cl. Gel-filtration of neo-peptone showed that the inductive as well as the lytic effect was associated with some active factor(s) with molecular weight between 10,000–20,000. The retention of the inductive effect on autoclavation but its loss on trypsin digestion suggested that active factor(s) may be heat stable polypeptide(s). The heterocyst induction by active factor(s) decreased and akinete induction increased with increasing culture age. The pro-akinetes induced during exponential phase divided before maturation, while those induced during late exponential phase, could achieve full maturity. Growth and nitrogenase activity was unaffected while there was an increase in mean cell length on treatment of A. cylindrica with active factor(s) from neo-peptone, indicating that the effect may be mediated through cell division process(es).
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  • 31
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    Archives of microbiology 124 (1980), S. 143-148 
    ISSN: 1432-072X
    Keywords: Anacystis ; Blue-green algae ; Cyanobacteria ; Mutation ; Pigments ; Red light ; Synecaococcus
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    Notes: Abstract Under far-red (〉650 nm) illumination Anacystis nidulans grows poorly and develops a low chlorophyll content. During continued culture over many generations there are increases in growth rate and in the chlorophyll/phycocyanin ratio, usually occurring in concomitant and stepwise fashion. From such selection cultures six clones have been established which differ from the parent in pigment content and show improved growth rate in far-red light. From the evidence at hand the six clones are presumed to be spontaneous mutants selected under the photosynthetically restrictive condition of far-red illumination.
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  • 32
    ISSN: 1432-072X
    Keywords: Anacystis nidulans ; Auxotroph ; Cyanobacteria ; Mutant isolation ; Synechococcus PCC 6301 ; Ethyl methanesulphonate
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    Notes: Abstract Previous attempts to isolate auxotrophic mutants of Anacystis nidulans produced only a limited range of phenotypes. The frequency of recovery of auxotrophic mutants has been quantified following different mutagenic and selective treatments, and their yield has been improved by using (1) a complete medium, (2) additional mutagens, (3) multiple cycles of penicillin enrichment and (4) altered pre-enrichment starvation conditions. These modified induction and selection conditions permitted the isolation of mutants defective in nitrate reductase, nitrite reductase or malate dehydrogenase, unable to reduce sulphate, or deficient in the synthesis of biotin, thiamine, paminobenzoate, serine, glutamate, adenine or uracil.
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  • 33
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    Archives of microbiology 129 (1981), S. 181-189 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Gloeobacter violaceus ; Synechocystis ; Freeze-etching ; Membranes ; Phycobilisomes
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    Notes: Abstract The fine structure of the atypical cyanobacterium Gloeobacter violaceus has been studied on frozen-etched replicas and compared to that of a typical unicellular strain: Synechocystis 6701. The complementary fracture faces of G. violaceus cytoplasmic membrane contain particles less numerous and more heterogenous in size than either the cytoplasmic membrane or the thylakoid membranes of Synechocystis. The most frequently observed particles of the exoplasmic fracture (EF) face of the G. violaceus cytoplasmic membrane are 11 nm in diameter and occasionally form short alignments. This particle class is similar in appearance to the numerous, aligned EF particles of Synechocystis thylakoid membranes. In replicas of cross-fractured G. violaceus, a layer 50–70 nm thick, composed of rod-like elements, underlies the inner surface of the cytoplasmic membrane. The rods, 12–14 nm in diameter, are oriented perpendicularly to the cytoplasmic membrane and show a 6 nm repeat along their length. Isolated phycobilisomes of G. violaceus appear, after fixation and negative staining, as bundles of 6 parallel rodshaped elements connected to an ill-defined basal structure. The bundles are 40–45 nm wide and 75–90 nm long. The rods are 10–12 nm in width; their length varies between 50 and 70 nm. These rods are morphologically similar to those observed at the periphery of hemidiscoidal phycobilisomes of other cyanobacteria, with a strong repeat at 6 nm intervals and a weaker one at 3 nm intervals along their length. The calculated molar ratio of phycobiliproteins in isolated G. violaceus phycobilisomes corresponds to 1:3.9:2.9 for allophycocyanin, phycocyanin and phycoerythrin respectively. When excited at 500 nm, isolated phycobilisomes exhibit a major fluorescence emission band centered at 663 nm.
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  • 34
    ISSN: 1432-072X
    Keywords: Biological control ; Cyanobacteria ; Electron microscopy ; Entrapment ; lysis ; Myxococcus ; Phormidium ; Spherule
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    Notes: Abstract A Myxococcus xanthus isolate from a farm drainage ditch, designated strain PCO2, is capable of rapidly inducing lysis of both agar and liquid-grown cultures of the cyanobacterium, Phormidium luridum, var. olivacea. Microscopic studies of the predator-prey interaction demonstrate that lysis of the cyanobacterium occurs within clumps and spherules formed by the cells of M. xanthus PCO2. In the earliest stage, one sees the formation of irregular microclumps of bacteria and cyanobacterial filaments. As these clumps mature, colonies 1 to 6 mm in diameter develops. The center of these densely green colonies contains cyanohacteria in various stages of degradation, while the periphery is almost exclusively a tightly woven mass of myxobacterial cells. Electron microscopy shows that long extrusions from the outer membrane of the M. xanthus PCO2 cells are involved in the formation both of initial clumps and of mature colonial spherules. These extrusions appear to efficiently entangle the cyanobacterial filaments in the culture environment. Predator-to-prey ratios of 1/10, 1/100 and 1/1,000 have resulted in cyanobacterial lysis. Because the entrapment and lysis of P. luridum filaments by M. xanthus PCO2 appears to be independent of any other heterotrophic nutritional requirement, as well as of environmental agitation, this system has potential as a biological control technique for undesirable aquatic cyanobacteria.
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  • 35
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    Keywords: Cyanobacteria ; Microplasmodesmata ; Intercellular communication ; Hetorocysts ; Freezefracture ; Plasma membrane
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    Notes: Abstract Structures which may establish cytoplasmic continuity between adjacent cells of filamentous cyanobacteria have been observed by freeze-fracture electron microscopy. They are visible in the septum region of the plasma membrane as pits on the E-face (EF) and corresponding protrusions on the P-face (PF). Between 100 and 250 of these structures, termed microplasmodesmata, were present between adjacent vegetative cells in all four strains of heterocyst-forming filamentous cyanobacteria, Anabaena cylindrica Lemm, A. variabilis (IUCC B377), A. variabilis Kütz. (ATCC 29413) and Nostoc muscorum, examined. Only 30–40 microplasmodesmata were observed between adjacent cells in two species, Phormidium luridum and Plectonema boryanum, that do not form heterocysts. The results suggest that in species that form heterocysts a greater degree of cytoplasmic continuity is established, presumably to facilitate the exchange of metabolites. In species capable of forming heterocysts, the number of microplasmodesmata per septum between two adjacent vegetative cells remained constant whether the filaments were grown in the presence of NH4 and lacked heteroxysts or under N2-fixing conditions and contained heterocysts. When a vegetative cell differentiates into a heterocyst, about 80% of the existing microplasmodesmata are destroyed as the poles of the cell become constricted into narrow necks leaving smaller areas of contact with the adjacent vegetative cells.
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  • 36
    ISSN: 1432-072X
    Keywords: Chlorogloea fritschii ; Cyanobacteria ; Bluegreen algae ; Chrotenoids ; Cell morphology ; Photosystems ; β-Carotene ; Myxoxanthophyll
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    Notes: Abstract The cell morphology and carotenoid composition of the Cyanobacterium Clorogloea fritschii are known to depend on growth conditions. The presence of sucrose in the medium resulted in an increase in the amount of the carotenoid glycoside myxoxanthophyll and an increased proportion of aseriate cells. The same carotenoids were present in light and dark-grown cultures, but light was needed for these carotenoids to be fixed into photosynthetic membranes. Photosystem 1 and 2 preparations both contained carotenoids; PS1 was enriched in β-carotene, PS2 in myxoxanthophyll. Both photosystems were depleted in echinenone; the location of this in the cell has not been identified.
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  • 37
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    Archives of microbiology 137 (1984), S. 21-25 
    ISSN: 1432-072X
    Keywords: Anabaena ; Cyanobacteria ; Ammonium release ; Photorespiration ; Glycollate pathway
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    Notes: Abstract A release of ammonium by non-nitrogen-fixing Anabaena cylindrica (grown on NH4Cl) in the presence of MSX (methionine sulfoximine) and absence of any external nitrogen source was found. In the light the release was maximal at 0.2 mM MSX, a concentration which did not affect net CO2 fixation nor the glycollate excretion, but inhibited the glutamine synthetase activity and the reassimilation of ammonium. It is suggested that the major source of the ammonium released is the photorespiratory conversion of glycine to serine as (1) the release was stimulated by increase in light intensity, (2) high CO2 (3%) lowered the release, if not given as a longer pretreatment (as CO2 or HCO 3 - ) when a stimulation was observed, (3) glyoxylate and glutamate stimulated the release, the latter compound particularly under nitrogen-deficient conditions and (4) isonicotinic acid hydrazide caused a reduced release of ammonium. Furthermore, a substantial part of the ammonium released by N2-fixing A. cylindrica in presence of MSX may thus originate from the glycollate pathway. The data show that in the light the glycine to serine conversion is active in cyanobacteria with a concomitant production of ammonium which is assimilated by glutamine synthetase.
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  • 38
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    Archives of microbiology 137 (1984), S. 194-199 
    ISSN: 1432-072X
    Keywords: Heterocysts ; Immunoferritin labelling ; Cyanobacteria ; Anabaena ; Nitrogenase
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    Notes: Abstract The question of whether the vegetative cells of Anabaena cylindrica synthesize nitrogenase under anaerobic conditions was studied by immunoferritin labelling of the Fe-Mo protein (Component I). Differentiating cultures, incubated under an argon atmosphere, were treated with DCMU 12 h following initiation of induction. DCMU inhibited photosynthetic O2 production, thus insuring strict anaerobic conditions, but had no effect on nitrogenase induction. Fe-Mo protein levels, as determined by rocket immunoelectrophoresis, increased 5-fold within 24h of DCMU treatment. Immunoferritin labelling of aldehyde fixed, ultrathin cryosections of anaerobically induced filaments showed that the Fe-Mo protein was restricted to the heterocyst. Ferritin labelling was shown to be specific by the following criteria: (a) substituting preimmune goat serum for the anti-Fe-Mo protein IgG prevented ferritin labelling; (b) ferritin-conjugated, non-homologous rabbit anti-goat IgG did not bind; (c) incubation of anti-Fe-Mo protein IgG treated sections with rabbit anti-goat IgG prior to the treatment with the ferritin label also prevented labelling. The results provide direct immunochemical evidence that nitrogenase is restricted to the heterocysts even under strictly anaerobic conditions.
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  • 39
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    Archives of microbiology 138 (1984), S. 119-123 
    ISSN: 1432-072X
    Keywords: Cyanophycin granule polypeptide ; Multi-L-arginyl-poly (L-aspartic acid) ; Proteolytic enzyme ; Protease ; Cyanobacteria ; Blue-green algae
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    Notes: Abstract An assay was developed to measure the proteolysis of cyanophycin granule polypeptide in crude extracts of a unicellular cyanobacterium. The substrate was radioactively labeled cyanophycin granule polypeptide formed by an unicellular cyanobacterium grown in the presence of chloramphenicol. Substrate polypeptide displayed identical chemical properties with polypeptide isolated from non-chloramphenicol-treated cells. Solubilization of radioactivity as arginine indicated hydrolysis of polypeptide. Radioactively labeled aspartate and arginine from hydrolyzed polypeptide was related to nmol amino acid using a combination of paper chromatography, liquid scintillation analysis, and ninhydrin quantitation. Protease activity was found in extracts of nitrogen-limited cells harvested 16–24 h after a nitrogen source was added back. Optimal pH for protease activity was 8.0 and optimum temperature was 35°C. Protease activity in crude extracts followed Michaelis-Menten kinetics with a V max of 92 nmol arginine per 15 min/mg protein and a K m of 2.1×103 nmol arginine. Protease activity was inhibited by arginine and by high concentrations of aspartate.
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  • 40
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    Archives of microbiology 138 (1984), S. 273-277 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Secondary metabolite ; Allelopathy ; Photosynthesis ; Electron transport ; Thylakoids ; Herbicides ; Electron microscopy
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    Notes: Abstract Cyanobacterin is a secondary metabolite produced by the cyanobacterium, Scytonema hofmanni. Highly purified cyanobacterin was found to inhibit the growth of many cyanobacteria at a minimum effective dose of 2 μg/ml (4.6 μM). The antibiotic had no effect on eubacteria including the photosynthetic Rhodospirillum rubrum. The site of action of cyanobacterin was further investigated in the unicellular cyanobacterium, Synechococcus sp. Electron micrographs of antibiotic-treated Synechococcus cells indicated that cyanobacterin affects thylakoid membrane structure. The antibiotic also inhibited light-dependent oxygen evolution in Synechococcus cells and in spheroplasts. These data support our conclusion that cyanobacterin specifically inhibits photosynthetic electron transport. This activity is similar to herbicides such as 3-(3,4-dichlorophenyl)-1,1-dimethyl urea (DCMU). The anhydro analog of cyanobacterin had no biological activity.
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  • 41
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    Archives of microbiology 130 (1981), S. 272-275 
    ISSN: 1432-072X
    Keywords: Aniline ; Cyanobacteria ; Biotransformation ; Toxicity ; N-Formylation ; N-Acetylation ; Ring hydroxylation
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    Topics: Biology
    Notes: Abstract Agmenellum quadruplicatum strain PR-6 and Oscillatoria sp. strain JCM grown photoautotrophically in the presence of aniline metabolized the aromatic amine to formanilide, acetanilide and p-aminophenol. The metabolites were isolated by either thin-layer, gas-liquid or high pressure liquid chromatography and identified by comparison of their chromatographic, ultraviolet absorbance and mass spectral properties with those of authentic compounds. The toxicity of aniline derivatives towards Agmenellum quadruplicatum strain PR-6 indicated that the cyanobacterium was extremely sensitive to o-, m- and p-aminophenols, and phenylhydroxylamine.
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  • 42
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    Archives of microbiology 131 (1982), S. 91-94 
    ISSN: 1432-072X
    Keywords: Anacystis nidulans ; Blue-green algae ; Cyanobacteria ; Ammonium production ; Amino acid catabolism ; Amino acid oxidase ; BasicL-amino acids
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    Topics: Biology
    Notes: Abstract The incubation of the cyanobacteriumAnacystis nidulans withL-Arg,L-Lys orL-Orn, but neither with the correspondingD-isomers nor with other twentyL-amino acids, resulted in the production of large amounts of ammonium which accumulated in the outer medium. Relevant properties of thisin vivo ammonium production activity have been studied in cell suspensions treated with the glutamine synthetase inactivatorL-methionine-D,l-sulfoximine (MSX) to prevent assimilation by the cells of the resulting ammonium. In addition to its specificity for the basicL-amino acids, the system exhibited a set of properties (K m value for substrates, requirement of oxygen which is taken up stoichiometrically with the production of ammonium, inhibition by o-phenanthroline and divalent cations) all of which are shared by a peculiarL-amino acid oxidase recently isolated fromA. nidulans. The data strongly suggest the participation of this enzyme in the production of ammonium from basic amino acids byA. nidulans, an activity that could account for the ability of this cyanobacterium to use arginine as a nitrogen source.
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  • 43
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    Archives of microbiology 131 (1982), S. 107-111 
    ISSN: 1432-072X
    Keywords: Cyanophyta ; Cyanobacteria ; Oscillatoria rubescens ; Photosynthetic pathways ; Photosynthetic enzymes ; Ecology
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    Topics: Biology
    Notes: Abstract Short term14C labelling experiments and enzymatic activities related to primary pathways of photosynthesis have been studied in the cyanophytaOscillatoria rubescens D.C. from axenic cyclostat cultures. Responses of samples from cultures with different amounts of nitrogen are presented and compared. Variations in photosynthetic pigments are used to quantify the degree of nitrogen starvation at different levels. PEPcarboxylase activity remains low and is not affected by nitrogen starvation. RuBPcarboxylase activity is lowered to nearly two thirds of its normal metabolic rate by starvation but PEPcarboxykinase and aspartate aminotransferase activities are significantly higher in this case. Malate dehydrogenase is slightly altered and malic enzyme is never active. Starved algae replaced in fresh complete media fix rapidly14C in nitrogen compounds such as amino acids. Results are discussed in regard to both physiological and ecological characteristics ofO. rubescens. PEPcarboxykinase can play a role in making efficient use of HCO 3 - .
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  • 44
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Cytochrome oxidase ; Cytochrome aa 3 ; Horse heart cytochrome c ; Respiration ; Inhibitors
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    Notes: Abstract The cytochrome content of membranes isolated from seven species of cyanobacteria was investigated in terms of conventional difference spectra, carbon monoxide difference spectra, photoaction spectra and photodissociation spectra, and by extraction of acid-labile heme followed by spectral identification. In addition, the effect of various inhibitors and activators on the oxidation of horse heart cytochrome c by the membrane was studied. Both the spectral features and the properties of the cytochrome oxidase reaction catalysed by the membranes suggested the presence of a terminal oxidase strikingly similar to mitochondrial ferrocytochrome c: oxygen oxidoreductase (EC. 1.9.3.1).
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  • 45
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    Archives of microbiology 131 (1982), S. 302-307 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Deoxyribonuclease
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    Notes: Abstract Six out of 158 axenic strains of heterocyst-forming cyanobacteria consistently failed to produce circles of clearing in agar medium containing DNA-methyl green. When tested with [3H]DNA and coliphage λDNA, supernatant fluids from cultures of two of these strains [University of Texas Culture Collection (UTEX) strain 2014 and 19-6C-C] showed no detectable deoxyribonuclease activity, and such fluids from another two of the six, and four others, showed low but detectable deoxyribonuclease activity. Covalently closed circular (plasmid) DNA was not detectably degraded by supernatant fluids from UTEX 2014 and 19-6C-C and from four of the other strains. When λ DNA was incubated with whole cells of certain strains, a sereis of fragments of discrete size was produced, perhaps by cell-bound, periplasmic, restriction endonucleases. Inclusion of one-tenth strength saline sodium citrate (SSC) in an eight-fold dilution of the medium of Allen and Arnon had little effect on growth of Anabaena variabilis American Type Culture Collection (ATCC) strain 29413 yet prevented all but slight degradation of plasmid pBR322 or of λ DNA.
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  • 46
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Anabaena variabilis ; Heterocysts ; Nitrogenase-electron donors ; Glycolysis ; Ferredoxin: NADP oxidoreductase ; Photosystem-I electron transport ; Inhibitors ; NADPH/NADP ratio
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    Notes: Abstract A cell-free preparation of heterocysts from Anabaena variabilis showed high nitrogenase activities with several physiological electron donors, dependent on addition of an ATP-generating system. Light-induced acetylene reduction with the artificial electron donor to photosystem I, diaminodurol, exhibited the same light saturation as with hydrogen as donor. Inhibitors of electron flow through plastoquinone affected light-induced, hydrogen- or NADH-dependent nitrogenase activity in a similar way. Several uncoupling agents were without effect, indicating that energized membranes are not a prerequisite for nitrogen fixation. We conclude that NADH or hydrogen deliver electrons to nitrogenase via photosystem I and ferredoxin, feeding in at the plastoquinone site. In the light, addition of NADP induced a lag in H2- or NADH-supported acetylene reduction apparently by competing with nitrogenase for electrons at the reducing side of photosystem I. Time reversal of this inibition reflects a regulation of photosystem I-dependent nitrogenase activity by the NADPH/NADP ratio in the cell. This was directly demonstrated by differently adjusted NADPH/NADP ratios. NADPH donates electrons to nitrogenase in the dark and in the light, the light reaction being DBMIB-sensitive. NADPH-supported acetylene reduction was inhibited by NADP. This inhibition was not reversed with time, pointing to an involvement of ferredoxin: NADP oxidoreductase (EC 1.18.1.2) in this pathway. Apparently, in the dark, this enzyme is able to directly reduce ferredoxin, whereas in the light electrons from NADPH first have to pass through photosystem I before reducing ferredoxin, hence nitrogenase. Intermediates of glycolysis, like glucose-6-phosphate, fructose-1,6-bisphosphate, and dihydroxyacetone phosphate supported nitrogenase activity in the dark, each with catalytic amounts of both NAD and NADP as equally effective cofactors. We conclude that in heterocysts electrons for nitrogen fixation are essentially supplied by dark reactions, mainly by glycolysis. NADH (and hydrogen) contribute electrons via photosystem I in the light, whereas the NADPH/NADP ratio regulates linear and cyclic electron flow at the reducing side of photosystem I to provide a ratio of ATP/electrons most effective for nitrogenase.
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  • 47
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Heterocysts ; Utrastructure ; Cytology ; Akinetes ; Mastigocladus laminosus
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    Topics: Biology
    Notes: Abstract The morphological and ultrastructural characteristics of the cyanobacterium Mastigocladus laminosus growing under N2-fixing conditions were examined with light and electron microscopy. Vegetative cells in narrow filaments contained randomly arranged segments of thylakoid membrane, centrally located carboxysomes (polyhedral bodies), peripherally located lipid bodies, and large numbers of polysaccharide granules in addition to nuclear material and ribosomes. The ultrastructural characteristics of cells in wide filaments were similar, except for increased numbers of carboxysomes and lipid bodies. Heterocytes and proheterocysts developed at a variety of locations in narrow filaments, wide filaments, and the lateral branches off of wide filaments. Akinetes were not observed in any of the filaments. The morphological characteristics of heterocysts and proheterocysts were variable and depended on those of the vegative cells from which the heterocysts and proheterocysts developed. Mature M. laminosus heterocysts were somewhat similar to those formed in other cyanobacterial genera, but they possessed a number of distinct and unique ultrastructural characteristics, including (i) the absence of a fibrous and, possibly, a laminated wall layer, (ii) the presence many closely packed membranes throughout most of the cytoplasm, and (iii) the presence of unidentified, spherical inclusion bodies of variable electron density.
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  • 48
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    Archives of microbiology 137 (1984), S. 241-246 
    ISSN: 1432-072X
    Keywords: Ammonium transport ; Anabaena azollae ; Anabaena variabilis ; Cyanobacteria ; Methylammonium transport ; Symbiosis
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    Topics: Biology
    Notes: Abstract The free-living cyanobacterium Anabaena variabilis showed a biphasic pattern of 14CH3NH 3 + uptake. Initial accumulation (up to 60 s) was independent of CH3NH 3 + metabolism, but long-term uptake was dependent on its metabolism via glutamine synthetase (GS). The CH3NH 3 + was converted into methylglutamine which was not further metabolised. The addition of l-methionine-dl-sulphoximine (MSX), to inhibit GS, inhibited CH3NH 3 + metabolism, but did not affect the CH3NH 3 + transport system. NH 4 + , when added after the addition of 14CH3NH 3 + , caused the efflux of free CH3NH 3 + ; when added before 14CH3NH 3 + , NH 4 + inhibited its uptake indicating that both NH 4 + and CH3NH 3 + share a common transport system. Carbonylcyanide m-chlorophenylhydrazone and triphenyl-methylphosphonium both inhibited CH3NH 3 + accumulation indicating that the transport system was Δψ-dependent. At pH 7 and at an external CH3NH 3 + concentration of 30 μmol dm-3, A. variabilis showed a 40-fold intracellular accumulation of CH3NH 3 + (internal concentration 1.4 mmol dm-3). Packets of the symbiotic cyanobacterium Anabaena azollae, directly isolated from the water fern Azolla caroliniana, also showed a Δψ-dependent NH 4 + transport system suggesting that the reduced inhibitory effect of NH 4 + on nitrogenase cannot be attributed to the absence of an NH 4 + transport system but is probably related to the reduced GS activity of the cyanobiont.
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  • 49
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    Archives of microbiology 125 (1980), S. 123-131 
    ISSN: 1432-072X
    Keywords: Respiration ; Electron transport ; Oxyhydrogen reaction ; Inhibitors ; Anacystis ; Cyanobacteria
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    Topics: Biology
    Notes: Abstract Respiratory particles from hydrogen-grown Anacystis nidulans were found to oxidize H2, NADPH, NADH, succinate and ascorbate plus N,N,N′,N′-tetramethyl-p-phenylenediamine at rates corresponding to 28, 15, 6, 2.5, and 70 nmol O2 taken up x mg protein−1xmin−1, respectively. The particles were isolated by brief sonication of lysozyme-pretreated cells. Respiratory activities were studied in terms of both substrate oxidation and O2 uptake. The stoichiometry between oxidation of H2, NADPH, NADH or succinate, and consumption of O2 was calculated to be 1.95+-0.1 with each substrate. Inhibitors of flavoproteins did not affect the oxyhydrogen reaction while 2-n-heptyl-8-hydroxyquinoline-N-oxide as well as compounds known to block the terminal oxidase impaired the oxidation of both H2 and of NAD(P)H or succinate in a parallel fashion. No additivity of O2 uptake was observed when NADPH, NADH or succinate was present in addition to H2. Instead, H2 uptake was depressed under such conditions, and also the oxidation of NAD(P)H or succinate was increasingly lowered by increasing H2 tensions. The results suggest that in Anacystis molecular hydrogen is oxidized through the same type of respiratory chain as are NAD(P)H and succinate. Moreover, the cyanide-resistant branch of respiratory O2 uptake will be discussed, and a few results obtained with particles prepared from thylakoid-free Anacystis will also be presented.
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  • 50
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    Archives of microbiology 128 (1980), S. 8-11 
    ISSN: 1432-072X
    Keywords: Agmenellum quadruplicatum ; Glycocalyx ; Cyanobacteria
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    Notes: Abstract The marine cyanobacterium Agmenellum quadruplicatum was shown to possess an extracellular glycocalyx similar in structure to those surrounding other bacteria from a variety of natural environments. Thin sections of cells stained with ruthenium red and frozen-etched preparations of unfixed cells indicated the glycocalyx was a network of small fibrils. The glycocalyx was present during all phases of growth, and was not degraded during nutrient limitation.
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  • 51
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    Archives of microbiology 132 (1982), S. 163-167 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Nostoc muscorum ; Cell envelope ; Thylakoids ; Heterocysts ; Salt adaptation
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    Notes: Abstract The physiological and biochemical changes during the adaptation of Nostoc muscorum to salt are accompanied by specific structural changes. Cells of Nostoc muscorum exposed to saline medium vary in size and envelope organization. There are also drastic changes in the intracellular organization of the thylakoidal assembly. The heterocysts exhibit a preferential tolerance to NaCl rather than mannitol. These findings suggest that Nostoc muscorum is equipped with a specific physiological capacity for NaCl tolerance.
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  • 52
    ISSN: 1432-072X
    Keywords: Proton transport ; 9-aminoacridine fluorescence changes ; Cyanobacteria ; Thylakoids ; Cytoplasmic membrane ; Plectonema boryanum
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    Notes: Abstract Light-induced fluorescence changes of 9-aminoacridine, an indicator of proton gradient in energy-transducing membranes, were studied in Plectonema boryanum and other cyanobacteria. The fluorescence changes observed in cell suspensions resulted from a superposition of fluorescence quenching and enhancement as the analysis of the kinetic data shows. Both components of the fluorescence changes are abolished by 3-(3,4-dichlorophenyl)-1,1-dimethyl urea (DCMU) and m-chlorocarbonylcyanide phenylhydrazone. The inhibitory effect of DCMU is removed by 2,3,5,6- or N,N,N′,N′-tetramethyl-p-phenylenediamine. The fluorescence quenching sensitive to substrates and uncouplers of the photophosphorylation is only observed in membrane vesicles obtained by osmotic shock of P. boryanum spheroplasts. Presumably, light-induced quenching of the dye fluorescence in the cells of cyanobacteria is due to the proton transport from the cytoplasm in the inner space of thylakoids while fluorescence enhancement is due to the proton efflux from the cytoplasm into the incubation medium.
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  • 53
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Akinete ; Germination ; Respiration ; Photosynthesis
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    Notes: Abstract Although akinetes ofNostoc PCC 7524 lost little of their main photosynthetic pigments, phycocyanin and chlorophyll, with increasing age after the onset of sporulation, they lost at least 90% of their photosynthetic and respiratory capacities. Germination needed the supply of light throughout the process, though previous dark metabolism accelerated the following light process. In standard conditions, both respiratory and photosynthetic capacities increased markedly during the first 9–10 h, a time sufficient for the first doublets to appear, but when pigment contents had not yet changed. However, while respiratory capacity could be reacquired without de nove metabolism, resumption of photosynthetic capacity needed RNA and protein synthesis. The energetic requirement for germination was not efficiently fulfilled by cyclic photosynthesis on PSI alone or respiration alone. In the presence of both PSI and respiratory activities only 21% of the akinetes germinated, their endogenous carbon reserves thus being inadequate to support the process to completion. The addition of sucrose to such cultures permitted all of the akinetes to germinate, but at a very slow rate. Rapid and complete germination was only observed when both photosystem operated.
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  • 54
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    Archives of microbiology 129 (1981), S. 325-330 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Anacystis ; Chloride transport ; Membrane potential ; ATP level
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    Notes: Abstract Chloride uptake by the cyanobacterium Anacystis nidulans at 38°C is energy dependent showing maximum rate (around 5.10-7 mol Cl-xml cell water-1xmin-1) and accumulation (up to 160 fold) in light and air. The respective values in air and darkness were 40–70% lower. In the dark under N2 no uptake was found. Chloride transport had an optimum at pH 6.7 and a K M of 2.10-5 M which was pH-independent. It was inhibited by carbonyl cyanide m-chlorophenylhydrazone and N,N′-dicyclohexylcarbodiimide in the light and in the dark, and also to a lesser extent by valinomycin. 3-(3,4-dichlorophenyl)-1,1-dimethylurea in the light caused a moderate stimulation. To obtain information about the energy source of active chloride transport the action of the four inhibitors on membrane potential (determined through the distribution of triphenylmethylphosphonium) and ATP level (determined by the firefly method) was examined. It was found that a high negative membrane potential was unfavorable for chloride accumulation probably by stimulating passive efflux. On the other hand a good correlation between ATP level and chloride transport activity was obtained. Attempts to induce chloride uptake by sudden acidification of the external medium in presence of N,N′-dicyclohexyl-carbodiimide or during anaerobiosis were not successful. Two mechanisms of chloride uptake are discussed: a) primary active transport by an ATP-dependent pump, and b) “chemiosmotic” secondary active transport linked to a proton gradient, the present data favoring mechanism a.
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  • 55
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    Archives of microbiology 136 (1983), S. 81-83 
    ISSN: 1432-072X
    Keywords: Ammonia production ; Anabaena ; Cyanobacteria ; Nitrate reductase ; Nitrogen fixation
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    Topics: Biology
    Notes: Abstract In the filamentous heterocystous cyanobacterium Anabaena sp. strain ATCC 33047 dinitrogen fixation and nitrate reduction are mutually exclusive processes. Nitrate promotes nitrate reductase synthesis and represses nitrogenase formation. Inhibition of ammonium assimilation by l-methionine-d,l-sulfoximine (MSX) alleviates the repressive effect of nitrate on nitrogenase synthesis, thus indicating that the nitrate effect is indirect through metabolites generated from the ammonium derived from nitrate reduction. In MSX-treated cells both nitrate reduction and dinitrogen fixation take place simultaneously, although at different sites of the filament, without any apparent competition for the required reducing power. The MSX-treated Anabaena cells generate ammonium from both nitrate and dinitrogen, simultaneously.
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  • 56
    ISSN: 1432-072X
    Keywords: Biotransformation ; Toxicity ; 1-Methylnaphthalene ; 2-Methylnaphthalene ; 1-Hydroxymethylnaphthalene ; 2-Hydroxymethylnaphthalene ; Cyanobacteria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Agmenellum quadruplicatum strain PR-6, Oscillatoria sp. strain JCM and Anabaena sp., strain CA grown photoautotrophically in the presence of either 1- or 2-methylnaphthalene oxidized both compounds at the methyl group to form 1-hydroxymethylnaphthalene and 2-hydroxymethylnaphthalene, respectively. Ring hydroxylated metabolites were not detected. The metabolites were isolated by thin-layer, high performance liquid and gas chromatography and identified by comparison of chromatographic and mass spectral properties with those of authentic compounds. The extent of 1- and 2-methylnaphthalene metabolism to ethyl acetate soluble metabolites ranged from 0.7 to 3.2%. Incubation of Agmenellum quadruplicatum strain PR-6 with 2-methylnaphthalene and molecular oxygen-18 led to the isolation of 2-hydroxymethylnaphthalene that contained oxygen-18. The toxicity of naphthalene, 1- and 2-methylnaphthalene and their derivatives on the growth of Agmenellum quadruplicatum strain PR-6 was investigated using the algal lawn technique. Phenol and quinone derivatives of naphthalene, 1- and 2-methylnaphthalene were most inhibitory. Alkyl side chain hydroxylation products, such as the hydroxymethyl derivatives of 1- and 2-methylnaphthalene were more toxic than the parent methylnaphthalenes. 1- and 2-Naphthoic were not toxic to the cyanobacterium.
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  • 57
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    Archives of microbiology 130 (1981), S. 267-271 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Chroococcidiopsis ; Chroococcus ; Water stress ; Photosynthesis ; Endolithic ; Matric ; Osmotic ; Taxonomy
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    Notes: Abstract Four strains of Chroococcidiopsis and one Chroococcus, all isolated from extreme arid desert rocks, and one marine Chroococcus, were subjected to water stress using both matric and osmotic control methods. For all Chroococcidiopsis strains, photosynthetic rates decreased with decreasing water potential. After 24h preincubation the decrease was linear but after 72h there was a sharp drop below-3400 kPa (a w≏0.976). In contrast, the two Chroococcus strains showed optimum photosynthesis between-3000 and-4000 KPa. It appears, therefore, that Chroococcidiopsis in deserts may have a different survival strategy in response to aridity than Chroococcus (rare in deserts). Absolute rates of 14CO2 uptake were higher in matric than in osmotic control systems. It is suggested that, in a matric experimental system, the water status is more representative of the natural conditions in arid environments. The consistent differences between different strains in their response to water stress suggest that this character in Cyanobacteria may be of taxonomic significance.
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  • 58
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    Archives of microbiology 138 (1984), S. 333-337 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Osmotic adjustment ; Osmoregulation ; Quaternary ammonium compounds ; Glycine betaine ; Halotolerance
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    Notes: Abstract The intracellular concentrations of the monovalent inorganic cations K+ and Na+, low molecular weight carbohydrates and quaternary ammonium compounds have been determined for 4 strains of cyanobacteria (Aphanothece halophytica, Coccochloris elabens, Dactylococcopsis salina and Synechocystis DUN52) originally isolated from hypersaline habitats (i.e. habitats with a salinity greater than that of seawater) over a range of external salt concentration (from 50% to 400% seawater). Intracellular cation levels (Na+ and K+) were determined to be within the range 80–320 mmol · dm-3 (cell volume), showing only minor changes in response to salinity. Intracellular carbohydrates were found to comprise a negligible component of the intracellular osmotic potential [at 2–19 mmol · dm-3 (cell volume)], throughout the salinity range. Quaternary ammonium compounds, however, were recorded in osmotically significant quantities [up to 1,640 mmol · dm-3 (cell volume)] in these strains, showing major variation in response to salinity. Thus Synechocystis DUN 52 showed an increase in quaternary ammonium compounds in the oder of 1,200 mmol · dm-3 between 50% and 400% seawater medium, accounting for a significant proportion of the change in external osmotic potential. Examination of intact cells and cell extracts using 13C and 1H nuclear magnetic resonance (NMR) spectroscopy confirmed the presence of the quaternary ammonium compound glycine betaine as the major osmoticum in the 4 strains; no other compounds were detected during NMR assays. These results suggest a common mechanism of osmotic adjustment, involving quaternary ammonium compounds, in cyanobacteria from hypersaline environments.
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  • 59
    ISSN: 1432-072X
    Keywords: Ribulose bisphosphate carboxylase ; Quaternary structure ; Molecular weight ; Electron microscopy ; Cyanobacteria ; Synechococcus
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    Notes: Abstract Ribulose bisphosphate (RuP2) carboxylase from the marme cyanobacterium, Synechococcus sp., comprised both large (57,000 dalton) and small (12,000 dalton) subunits. The undissociated, purified enzyme was considerably smaller than the spinach enzyme when compared by pore-gradient electrophoresis, gel filtration and density-gradient centrifugation. This suggested that the cyanobacterial enzyme might have a hexameric (L6S6) subunit structure, unlike the enzymes from spinach and many other organisms which are octamers (L8S8). However, the molecular weight of the Synechococcus enzyme was measured by equilibrium sedimentation and found to be 530,000, which is within the range observed for L8S8-type enzymes. Furthermore, electron microscopic studies of negatively stained preparations of both the native enzyme, and a preparation depleted of 87% of its small subunits by repeated mild-acid precipitation, revealed four-fold symmetry characteristic of an octameric, cubical structure. Synechococcus RuP2 carboxylase therefore must be an L8S8 octamer and its anomalous pore-penetration behaviour may be due to an asymmetric shape. Some support for the latter possibility was provided by electron miscoscopic observations of two different types of images which may be different views of the molecule in two planes.
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  • 60
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    Archives of microbiology 140 (1984), S. 215-217 
    ISSN: 1432-072X
    Keywords: Glutathione reductase ; Cyanobacteria ; Nostoc muscorum ; O2 protection ; Glutathione ; Nitrogen fixation
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    Notes: Abstract Glutathione reductase activity was detected and characterized in heterocysts and vegetative cells of the cyanobacterium Nostoc muscorum. The activity of the enzyme varied between 50 and 150 nmol reduced glutathione· min-1·mg protein-1, and the apparent Km for NADPH was 0.125 and 0.200 mM for heterocysts and vegetative cells, respectively. The enzyme was found to be sensitive to Zn+2 ions, however, preincubation with oxidized glutathione rendered its resistance to Zn+2 inhibition. Nostoc muscorum filaments were found to contain 0.6–0.7mM glutathione, and it is suggested that glutathione reductase can regenerate reduced glutathione in both cell types. The combined activity of glutathione reductase and isocitrate dehydrogenase in heterocysts was as high as 18 nmol reduced glutathione·min-1·mg protein-1. A relatively high superoxide dismutase activity was found in the two cell types; 34.2 and 64.3 enzyme units·min-1·mg protein-1 in heterocysts and vegetative cells, respectively. We suggest that glutathione reductase plays a role in the protection mechanism which removes oxygen radicals in the N2-fixing cyanobacterium Nostoc muscorum.
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  • 61
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Fluorescence induction ; Oxygen evolution ; Photosystem II ; DCMU-sensitivity ; Electron transport ; Oscillatoria chalybea
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The filamentous cyanobacterium Oscillatoria chalybea grows phototrophically on a mineral medium in the presence of either nitrate or ammonium ions as nitrogen source at similar growth rates. In the absence of any combined nitrogen source in the medium the cyanobacterium also grows, although at a reduced growth rate. The steady state rate of oxygen evolution by filaments from these three culture conditions is approximately constant if compared on an equal chlorophyll basis. Qualitative differences, however, emerge, if transient phenomena, e.g. the oxygen gush, are investigated. Only nitrate-and nitrogen-free-grown cultures show an oxygen gush, whereas ammonium sulfate-grown cultures do not show this phenomenon. Fluorescence induction in O. chalybea shows a fast monophasic rise, comparable to the fluorescence rise curves of higher plant chloroplasts in the presence of dithionite. The steady state level of fluorescence in ammonium sulfate-grown cells is up to seven times higher than in nitrate-grown cells when compared on an equal chlorophyll basis. In ammonium sulfate-grown cells, DCMU (N,N′-3,4-Dichlorophenyl dimethylurea) causes a further increase in fluorescence level. In nitrate-grown cyanobacteria, however, the effect of DCMU consists of a decrease of the steady state level of fluorescence. In context with earlier research on Anabaena cylindrica, another filamentous cyanobacterium, it appears that the type of the nitrogen source used for growth determines the main location of the DCMU-block in this organism. It thus appears that in O. chalybea the site of DCMU inhibition lies on the oxygen-evolving side of photosystem II, if the organism is grown on nitrate. If grown on ammonium sulfate, no substantial difference of the location of the inhibition site when compared to algae or higher plant chloroplasts is found. Thylakoid preparations of O. chalybea perform the usual Hill reactions with ferricyanide, p-benzoquinone or silicomolybdate as electron acceptors. In each case it is seen that with thylakoids of nitrate-grown cells the steady-state level of fluorescence is lowered by DCMU in the presence of these acceptors, which should be the case, if DCMU inhibits electron transfer on the donor side of photosystem II. According to the literature silicomolybdate accepts electrons mainly before the DCMU-block in higher plant chloroplasts. Hence, in higher plants this reaction is mainly DCMU-insensitive. In thylakoids of O. chalybea, however, the Hill reaction with silicomolybdate is DCMU-sensitive which provides further evidence that the DCMU-block is on the oxygen-evolving side of photosystem II in O. chalybea provided the cells have been grown on nitrate.
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  • 62
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    Archives of microbiology 128 (1980), S. 1-7 
    ISSN: 1432-072X
    Keywords: Nitrogen limitation ; Nitrogen recovery ; Cyanobacteria ; Aphanocapsa 6308 ; Multi-l-arginine-poly (l-aspartic acid) ; Cyanophycin granule polypeptide ; Phycocyanin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The effects of nitrogen limitation and recovery on nitrogen-containing macromolecules were followed in the cyanobacterium Aphanocapsa 6308. Removal of nitrogen from growth media triggers the degradation of the endogenous nitrogen reserves phycocyanin and cyanophycin granule polypeptide in the cyanobacterium Aphanocapsa 6308. Nitrogen recovery involves immediate synthesis of cyanophycin granule polypeptide with peak levels of 5–12% of cell dry weight found 8–12 h after a utilizable nitrogen source is added. A rapid decrease in cyanophycin granule polypeptide level then occurs and the level remains low even in light-limited stationary growth with all nitrogen sources tested except nitrate and ammonia. Protein and phycocyanin recoveries began 3 h after a utilizable nitrogen source was added. Data suggest continuous activity of the enzyme system synthesizing cyanophycin granule polypeptide in nitrogen-limited cells, but synthesis of a degrading system only after nitrogen recovery begins.
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  • 63
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    Archives of microbiology 132 (1982), S. 168-172 
    ISSN: 1432-072X
    Keywords: Nostoc muscorum ; Cyanobacteria ; Osmoregulation ; Salt-adaptation photosynthesis ; N2-fixation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Adaptation to salt in the cyanobacterium Nostocmuscorum, is composed of a few mechanisms which together lead to the generation of a salt-tolerant cell. The initial mechanism combines a stimulation of photosynthetic activity with the accumulation of sucrose as an osmoregulator. The secondary mechanism involves the adaptation of N2 fixation activity and protein biosynthesis. The adaptation is most efficient in response to NaCl-induced stress and functions only partially under stress induced by either KCl or a nonionic osmoticum such as mannitol.
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  • 64
    ISSN: 1432-072X
    Keywords: Prochloron ; Cyanobacteria ; Didemnid ascidians ; Phylogeny ; Taxonomy ; 16S ribosomal RNA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The relationship of Prochloron sp. isolated from four different didemnid ascidian hosts, namely Lissoclinum patella, Lissoclinum voeltzkowi, Diplosoma virensand Trididemnum cyclops was elucidated by comparative analysis of their 16S ribosomal ribonucleic acid (RNA). The oligonucleotide catalogues of the 16S rRNA obtained are almost identical, indicating a very close relationship among the prochlorophytes investigated. Phylogenetically Prochloron is a member of Cyanobacteriales.
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  • 65
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    Archives of microbiology 133 (1982), S. 97-99 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Thylakoid centers ; Photosynthetic membranes/thylakoids ; Membranes ; Membrane biogenesis ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An ultrastructural study of four cyanobacteria (Anabaena cylindrica, Dermocarpa violaceae, Gleocapsa alpicola, Pleurocapsa minor) indicates the presence of previously undescribed thylakoid centers from which photosynthetic membranes (thylakoids) radiate. These peripherally located thylakoid centers are cylinders 30 nm wide by 320 nm long, consisting of globular subunits oriented in nonparallel stacked arrays. Thylakoids are attached to the outer surface of the cylinder along its longitudinal axis. Thylakoid centers appear to be functionally significant due to their structure, location and thylakoid association.
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  • 66
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Ultrastructure ; Nitrogen fixation ; Water stress ; Taxonomy ; DNA ; Plasmids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Two strains of desiccation-tolerant coccoid cyanobacteria, Chroococcus S24, a marine form, and Chroococcus N41, a cryptoendolith isolated from a hot-desert rock, have been characterized. The mol % DNA base compositions of the strains are 47.1 and 48.9% respectively. Plasmid DNA was not detected in either strain. The pigment contents and nutritional characteristics of the strains are identical. Both lack phycoerythrinoid pigments and, in culture, behave as slow-growing halotolerant marine forms with elevated requirements for Na+, Cl−, Mg2+ and Ca2+. Sucrose was the only carbon source of those tested that supported photoheterotrophic growth. Each strain synthesizes nitrogenase under anaerobic conditions but not in air. Morphologically the two strains are indistinguishable. They are considered to be independent isolates of the same cyanobacterial species. Chroococcus N41 was studied in detail with the electron microscope. When brought to equilibrium at matric water potentials of-168 MPa and lower (to-673 MPa=c0.12a w) the protoplast shrinks, but the cells maintain the same size and diameter as those at-2,156 kPa (MN medium; control); the sheath expands and remains attached to the cell wall outer membrane by fibrils. The cell wall, cell membrane, thylakoid membranes, cyanophycin granules and carboxysomes appeared intact in desiccated cells.
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  • 67
    ISSN: 1432-072X
    Keywords: Biliprotein complexes ; Allophycocyanin core ; Phycoerythrocyanin ; Phycobilisome ; Mastigocladus laminosus ; Cyanobacteria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The dissociation products of isolated phycobilisomes of Mastigocladus laminosus were separated and analyzed by ultracentrifugation and, in part, by isoelectric focusing. With the exception of the allophycocyanin core, the sedimentation constants of peripheral phycocyanin- and phycoerythrocyanin-phycocyanin complexes lay in the range of 6 to 17S. The latter was represented by a 17S aggregate of two hexameric phycocyanins (dodecamer, dipartite unit). A complex with an absorption maximum at 610 nm (phycocyanin) and a shoulder at 580 nm (phycoerythrocyanin), a fluorescence emission maximum at 645 nm and a sedimentation constant of 11 S is described as a heterogeneously composed hexamer of (αβ)3-phycoerythrocyanin-(αβ)3-phycocyanin. It was stable under extended dissociation in the cold and under isoelectric focusing. An aggregate of 14 S with an absorption maximum at 576 nm and a shoulder in the fluorescence emission spectrum at 625 nm (phycoerythrocyanin) in addition to the maximum at 645 nm (phycocyanin) is interpreted as a polar phycoerythrocyanin/ phycoerythrocyanin-phycocyanin complex. Combining these complexes with phycocyanin dodecamers creates peripheral rods of the phycobilisome. A proposal of the phycobiliprotein distribution within the phycobilisome of M. laminosus is presented.
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  • 68
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    Archives of microbiology 130 (1981), S. 23-30 
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Phycobilisome assembly ; Phycocyanin ; Linker polypeptides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Phycobilisomes of the cyanobacterium Synechococcus 6301 contain the phycobiliproteins phycocyanin, allophycocyanin, and allophycocyanin B, and four major non pigmented polypeptides of 75, 33, 30, and 27 kdaltons. The molar ratio of phycocyanin to allophycocyanin in wild type phycobilisomes can be varied over about a two-fold range by alterations in culture conditions with parallel changes in the amounts of the 33 and 30 kdalton polypeptides whereas the levels of the 27 and 75 kdalton polypeptides do not vary. Two nitrosoguanidine-induced mutants, AN112 and AN135, produce abnormally small phycobilisomes, containing only 35 and 50% of the wild type level of phycocyanin. AN135 phycobilisomes contain less 33 kdalton polypeptide than wild type and the 30 kdalton polypeptide is only detected in phycobilisomes from cultures grown under conditions favoring high levels of phycocyanin. AN112 lacks both the 30 and 33 kdalton polypeptides and produces phycobilisomes of constant size and composition, independent of growth conditions. Both mutant phycobilisomes have wild type levels of 27 and 75 kdalton polypeptides relative to allophycocyanin and have normal energy transfer properties. These results indicate that modulation of phycobilisome size involves concurrent regulation of the levels of phycocyanin and of both the 30 and 33 kdalton polypeptides with no change in the composition of the allophycocyanin-containing core.
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  • 69
    ISSN: 1432-072X
    Keywords: O2 evolution ; Lag-phase ; Membrane surface charge ; Transmembrane H+ electrochemical potential difference ; 9-Aminoacridine fluorescence changes ; Ionophore antibiotics ; Cyanobacteria ; Anabaena variabilis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The establishment of the steady-state rate of photosynthetic O2 evolution by cells of Anabaena variabilis and other cyanobacteria was found to be preceded by a lag-phase the duration of which depended on the time of cell preincubation in the dark. Electron acceptors (benzoquinone, N,N,N′,N′-tetramethyl-p-phenylenediamine, 2,3,5,6-tetramethyl-p-phenylenediamine or 2,6-dichlorophenolindophenol) abolished the lag-phase as well as the inhibitory effect of cyanide on electron transfer. Mono-, di-and trivalent cations added to the cell suspension markedly reduced the lag-phase. As cation concentrations were increased, acceleration and subsequent deceleration of the O2 evolution rate were observed. The efficient concentrations of cations decreased as their valency increased. The lag-phase and the rate of photosynthetic O2 evolution by the blue-green algae are suggested to depend on the value of the membrane surface charge governing the electrostatic interaction between unidentified membrane-bound redox components. The combination of valinomycin and nigericin as well as gramicidin D enhanced the duration of the lagphase by deenergization of thylakoid membrane.
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  • 70
    ISSN: 1432-072X
    Keywords: Cyanobacteria ; Synechocystis 6701 ; Phycobilisomes ; Ultra-violet ; Mutagenesis ; Assembly ; Chromatic ; Adaptation ; Rods ; Cores
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Mutations affecting pigmentation of the cyanobacterium Synechocystis sp. 6701 were induced with ultraviolet light. Two mutants with phycobilisome structural changes were selected for structural studies. One mutant, UV08, was defective in chromatic adaptation and incorporated phycoerythrin into phycobilisomes in white or red light at a level typical of growth in green light. The other mutant, UV16, was defective in phycobilisome assembly: little phycocyanin was made and none was attached to the phycobilisome cores. The cores were completely free of any rod substructures and contained the major core peptides plus the 27,000 Mr linker peptide that attaches rods to the core. Micrographs of the core particles established their structural details. Phycoerythrin in UV 16 was assembled into rod structures that were not associated with core material or phycocyanin. The 30,500 Mr and 31,500 Mr linker peptides were present in the phycoerythrin rods with the 30,500 Mr protein as the major component. Phycobilisome assembly in vivo is discussed in light of this unusual mutant.
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  • 71
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    Planta 157 (1983), S. 561-566 
    ISSN: 1432-2048
    Keywords: Carbon-dioxide fixation ; Cyanobacteria ; Microcystis ; Photoinhibition ; Photosynthesis (electron transport)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We have examined characteristics of the photoinhibition of photosynthesis which occur in the unicellular cyanobacterium Microcystis aeruginosa, following exposure to photon fluence rates in excess of those required for growth. Photoinhibition occurs following exposure of cells to a photon fluence rate of 1,000 μmol m-2 s-1, which is manifested as a decrease in either light-limited CO2 fixation or light-saturated CO2-dependent O2 evolution. The extent and rapidity of this photoinhibition is greatly enhanced under CO2-depleted conditions. Experiments in which cultures were sparged with different gases indicate that photoinhibition is not an obvious consequence of elevated O2 tensions, unlike the photooxidative bleaching of photosynthetic pigments. Comparative studies on the photoinactivation of CO2-dependent O2 evolution and of the methyl viologen-dependent Mehler reaction, in whole cells, indicate that a primary site of light damage is within the photosynthetic electron-transport reactions and that carbon fixation is initially unaffected.
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  • 72
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    Planta 154 (1982), S. 251-258 
    ISSN: 1432-2048
    Keywords: Biliproteins ; Cyanobacteria ; Phycobilisomes ; Rhodophyceae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Phycobilisomes of red algae and cyanobacteria contain small amounts of nonpigmented polypeptides in addition to the major constituent biliprotein pigments. The localization of these polypeptides is analyzed by gel electrophoresis of phycobilisome fragments obtained by selective dissociation and subsequent separation. Five groups of biliprotein aggregates are determined, belonging to the 6, 11, 16, 18 and 23 S categories. Accessory nonpigmented high molecular weight proteins (80,000 MW) are exclusively bound to phycobilisome core fractions and thylakoids, thus apparently serving as links between the phycobilisomes and the photosynthetic units of the thylakoids. In contrast, smaller nonpigmented accessory polypeptides of 20,000 to 60,000 MW are preferably found in the peripheral biliprotein stacks. They may either form a compatible link between the phycobilisome core and periphery or bind and co-polymerize with hexameric biliproteins in the peripheral stacks to enhance or effect binding of the aggregates. Furthermore, they may determine the arrangement and composition of the phycobilisomes during development and chromatic adaptation.
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  • 73
    ISSN: 1432-2048
    Keywords: Carboxysome ; Chlorogloeopsis ; Cyanobacteria ; Polyhedral bodies ; Ribulose 1,5-bisphosphate carboxylase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Ribulose 1,5-bisphosphate (RuBP) carboxylase is present in the cytoplasm and carboxysomes (polyhedral bodies) of the cyanobacterium Chlorogloeopsis fritschii. In vitro enzyme activities have been measured throughout photoautotrophic batch culture, together with RuBP carboxylase protein concentrations, determined by rocket immunoelectrophoresis. Enzyme activities and protein levels in the cytoplasmic and carboxysomal fractions varied in an apparently inverse manner during growth. The RuBP carboxylase activities per unit enzyme protein were maximal in late lag phase/early exponential phase for both cellular enzyme pools. Both rates per unit enzyme protein declined during exponential phase, cytoplasmic enzyme activity remaining consistently higher than that of the carboxysomal enzyme. Activities per unit cytoplasmic and carboxysomal enzyme protein showed very low, similar rates in late stationary phase and death phase. Dialysis experiments indicated that such changes were not due to interference in activity assays by soluble endogenous effectors. Major shifts in the subcellular distribution of RuBP carboxylase protein were found versus culture age, enzyme protein levels being predominantly carboxysomal in lag phase, mainly soluble in exponential phase and then mainly carboxysomal again in stationary/death phase. The data are discussed in terms of carboxysome function and the question of control of RuBP carboxylase synthesis in cyanobacteria.
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  • 74
    ISSN: 1432-2048
    Keywords: Cyanobacteria ; Fluorescence induction (chlorophyll) ; Microcystis ; Photoinhibition ; Photosynthesis (electron transport) ; Photosystem II
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Sites of photoinhibition and photo-oxidative damage to the photosynthetic electrontransport system of the unicellular cyanobacterium Microcystis aeruginosa were identified by studies of the kinetics of chlorophyll fluorescence induction by whole cells at room temperature and from partial photosynthetic electron-transport reactions in vitro in thylakoid preparations. Chlorophyll fluorescence intensity decreased following photoinhibitory light treatment. This was attributed to decreases both in the activity of photosystem II and in electron flow through the primary electron acceptor, Q. This inhibition was only partially reversed over a 50-min dark recovery period. Partial photosynthetic electron-transport experiments in vitro demonstrated that photosystem I was not affected by the photoinhibitory treatment. Light damage was associated exclusively with the light reactions, of photosystem II, at a site close to the reaction centre, between the site where diphenylcarbazide can donate electrons and the site where silicomolybdate can accept electrons. This damage presumably reduced production of ATP by noncyclic photophosphorylation and production of NADPH by photosystem I, decreasing the availability of these co-factors for reducing CO2 in the ‘dark’ reactions of photosynthesis. The importance of these findings is discussed.
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  • 75
    ISSN: 1615-6102
    Keywords: Alkaline phosphatase ; Cyanobacteria ; Enzym localization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Histochemical techniques applied at the ultrastructural level have established the periplasmic space as the site of cell bound alkaline phosphatase activity inAnabaena cylindrica andCoccochloris peniocytis. For localization of activity unfixed cells were reacted with calcium nitrate, which acts as the initial capture reagent. After this deposition, the cells were suspended in 2% lead nitrate to convert the calcium phosphate to more electron dense lead phosphate. The majority of cell bound activity appeared to be associated with layer 3 of the cell wall. InA. cylindrica a secondary site of cell bound activity appeared to be in the sheath. Placement in a phosphate free medium caused a substantial increase in the enzyme activity ofA. cylindrica while the activity present in log phase cells ofC. peniocytis was similar to that found in phosphate starved cells.C. peniocytis also secretes the enzyme into the surrounding medium.
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  • 76
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    Protoplasma 123 (1984), S. 104-115 
    ISSN: 1615-6102
    Keywords: Constrictive binary fission ; Cyanobacteria ; Development ; Multiple fission ; Septate binary fission ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary An ultrastructural examination of cell division in two baeocyte producing cyanobacteria,Pleurocapsa minor andDermocarpa violaceae, reveals two distinct patterns of binary (transverse) fission. Septate binary fission, inPleurocapsa minor, involves centripetal synthesis and deposition of the mucopolymer cell wall layer (L 2). The ingrowth of the cytoplasmic membrane and L 1 cell wall layer, along with the synthesis of the L 2 cell wall layer, results in the formation of a prominent septum. Partitioning of the cell occurs by the constriction of the outer cell wall layers (L 3 and L 4) through the septum. InDermocarpa violaceae, constrictive binary fission occurs by the simultaneous ingrowth or constriction of the cytoplasmic membrane and all cell wall layers (L1, L2, L3, L4). Septate and constrictive binary fission may proceed symmetrically (medially) or asymmetrically (nonmedially). Multiple fission occurs regularly inDermocarpa violaceae and provides for a rapid means of reproduction when compared to binary fission. Successive radial and tangential divisions of the protoplast result in formation of many small daughter cells (baeocytes). The process of multiple fission is similar to septate binary fission with reduced septa being formed. However, constriction of the outer cell wall layers, through the septa, proceeds concurrently with septum formation.
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  • 77
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    Journal of bioenergetics and biomembranes 15 (1983), S. 111-119 
    ISSN: 1573-6881
    Keywords: Cyanobacteria ; mitochondrial cristae ; membrane microheterogeneity ; proton gradient ; membrane potential
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Physics
    Notes: Abstract The possibility is analyzed that the pH of the water space localized inside the invagination of a membrane can differ from the pH of the external bulk buffer outside the invagination. The proton flow responsible for decreased pH values inside mitochondrial cristae and membrane invaginations of cyanobacteria has been calculated. If Δψ (electric potential difference) inside and outside the invaginations is the same, there may exist a lateral microheterogeneity of transmembrane ΔpH, and hence $$\Delta \overline \mu _{H^ + }$$ . It seems that the invagination is a kind of buffer for accumulating $$\Delta \overline \mu _{H^ + }$$ in membrane systems. In eutrified waters (pH〉9) and also under the conditions of a sudden decrease or increase of light, or of a respiratory substrate of O2, ATP synthesis should proceed in the invaginated rather than in the flat regions of a membrane.
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