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  • Articles  (1,958)
  • Springer  (1,251)
  • Wiley  (707)
  • Cambridge University Press
  • 1980-1984  (1,958)
  • 1975-1979
  • 1984  (1,958)
  • Process Engineering, Biotechnology, Nutrition Technology  (1,958)
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  • Articles  (1,958)
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Years
  • 1980-1984  (1,958)
  • 1975-1979
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  • 1
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    Springer
    Applied microbiology and biotechnology 19 (1984), S. 5-12 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Periplasmic-leaky (lky) Hfr mutant strains of Escherichia coli K12, grown in low-phosphate Tris medium, excreted alkaline phosphatase (AP) into the extracellular fluid. The lky207 mutation, which proved to induce the highest AP excretion rate, was transferred to an F- host, carrying a phoS, T mutation allowing constitutive AP biosynthesis. Use of high-phosphate LB-rich medium for growing this F- lky strain improved cell biomass, extracellular AP activity and excretion specificity in favour of the enzyme. Physiological studies helped us to develop a new culture medium (LB 8.3) giving higher enzyme and excretion yields. LB 8.3 medium also increased cell viability of lky mutants stored at 4° C. Using optimized culture conditions, the highest extracellular enzyme activity produced by lky mutant 706 was reached in the late stationary growth phase and was equal to 1,400 U/ml of culture medium (i.e., 6 times the intracellular AP content of wild-type strain, Ga15, developed in derepressed conditions); AP released into the extracellular fluid corresponded to 34% of total excreted proteins and was equivalent to a purified enzyme preparation.
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  • 2
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The adaptation of Lodderomyces elongisporus cells to n-alkane utilization was found to be connected with several alterations in the enzyme pattern of the whole cell and the microsomal fraction in particular. A strong induction was found for the microsomal localized cytochrome P-450 alkane hydroxylase system and other enzymes which are directly involved in the terminal degradation pathway of n-alkanes (long-chain alcohol and aldehyde dehydrogenases, catalase). The decrease of the pO2 in the medium enhances the concentration of the constituents of the alkane hydroxylase system as well as that of several other haemoproteins (catalase, cytochrome oxidase), while the long-chain alcohol and aldehyde dehydrogenase enzymes are probably unaffected.
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  • 3
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    Applied microbiology and biotechnology 19 (1984), S. 58-60 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A mixture of commercially available chitinase and cellulase released mycelial protoplasts of Coprinus macrorhizus in yields exceeding 108/ml plasts from C. macrorhizus FisC regenerated hyphae and developed into normal fruiting bodies at frequencies of 20%–50%. The same method also released good yields of protoplasts from several other edible mushroom species.
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  • 4
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    Applied microbiology and biotechnology 19 (1984), S. 75-78 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary From continuous culture studies it has been shown that the protein concentrations of strains of Z. mobilis (62–68%) were appreciably higher than for the yeast S.uvarum (45–50%). The DNA and RNA contents were similar for the two species. Comparison of the essential amino acids indicated that Z.mobilis did not exhibit the deficiency in methionine which was apparent in the yeast. Such a study of the macromolecular composition of cells of Z.mobilis is important in assessing its by-product nutritional value for animal feed supplementation.
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  • 5
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    Applied microbiology and biotechnology 19 (1984), S. 114-119 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A new gram-positive filamentous bacterium with coccoid cells has been isolated from bulking sludge from five sewage treatment plants in West-Germany. The characteristics of five strains are described. Their fatty acids and cell wall composition are similar to the Streptococcaceae and they mainly degrade monomeric and dimeric carbon sources. They are classified as a new genus and species of the family Streptococcaceae: Trichococcus flocculiformis gen. nov. sp. nov.
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  • 6
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    Applied microbiology and biotechnology 19 (1984), S. 125-130 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The effect of monensin and 2-bromoethanesulfonic acid (BESA) on methane production from cattle manure and on volatile fatty acids metabolism was tested. At 10 days retention time 0.81 biogas per liter cattle manure and day were produced. Methanogenesis was inhibited 20% by 3 mM BESA per liter and 45% by 2–5 mg monensin per liter. When the digestion was inhibited with either of the both drugs, the acetate pool increased drastically. Like in untreated fermentations the propionate pool increased in BESA-inhibited fermentations for several hours after substrate addition. After 24 h however it did not decrease to the low level reached in non-inhibited fermentations. When monensin was the inhibitor, the propionate pool did not change for 15 h, but then decreased with the same rate as in the control experiment. Adaptation processes or detoxification may be responsible for the delayed degradation. The degradation of low concentrations of buty-rate to acetate and the turn over rates of the butyrate pool are almost identical in cattle manure containing BESA, monensin, or no inhibitor. The turn over of 14C-acetate from butyrate degradation is delayed in BESA and monensin inhibited fermentations. From the data presented it can be concluded, that BESA mainly inhibits the methanogens, while monensin seems to inhibit both, methanogenic and nonmethanogenic organisms. However, a fast adaptation to or detoxification of the antibiotic seems to occur.
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  • 7
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Myxovirescin A is a new antibiotic from Myxococcus virescens. Conditions of growth on peptone media result in the antibiotic being secreted during the transition to the stationary phase. When growth is exponential, no detectable production occurs. In an attempt to improve production of the antibiotic, peptone was fed to the peptone-limited culture at differing feed rates. Product formation was found to be dependent on the peptone supply, and the product concentration could be improved from 0.04 to 2 mg/l myxovirescin A.
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  • 8
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary An alcohol electrode was constructed which consisted of an oxygen probe onto which alcohol oxidase was immobilized. This enzyme electrode was used, in combination with a reference oxygen electrode, to study the short-term kinetics of alcoholic fermentation by aerobic yeast suspensions after pulsing with glucose. The results demonstrate that this device is an excellent tool in obtaining quantitative data on the short-term expression of the Crabtree effect in yeasts. Samples from aerobic glucose-limited chemostat cultures of Saccharomyces cerevisiae not producing ethanol, immediately (within 2 min) exhibited aerobic alcoholic fermentation after being pulsed with excess glucose. With chemostat-grown Candida utilis, however, ethanol production was not detectable even at high sugar concentrations. The Crabtree effect in S. cerevisiae was studied in more detail with commercial baker's yeast. Ethanol formation occurred only at initial glucose concentrations exceeding 150 mg·l-1, and the rate of alcoholic fermentation increased with increasing glucose concentrations up to 1,000 mg·l-1 glucose. Similar experiments with batch cultures of certain ‘non-fermentative’ yeasts revealed that these organisms are capable of alcoholic fermentation. Thus, even under fully aerobic conditions, Hansenula nonfermentans and Candida buffonii produced ethanol after being pulsed with glucose. In C. buffonii ethanol formation was already apparent at very low glucose concentrations (10 mg·l-1) and alcoholic fermentation even proceeded at a higher rate than in S. cerevisiae. With Rhodotorula rubra, however, the rate of ethanol formation was below the detection limit, i.e., less than 0.1 mmol·g cells-1·h-1.
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  • 9
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    Applied microbiology and biotechnology 19 (1984), S. 203-206 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary For batch fermentations by Clostridium beyerinckii LMD 27.7 (formerly known as Clostridium butylicum) whey ultrafiltrate, glucose, lactose, and galactose were used as substrates. The aims of the experiments were to find the conditions for butanol production from whey ultrafiltrate and to compare the results with those of other substrates. The conditions necessary for butanol production were established. The mean solvent productivity found on whey ultrafiltrate fermentation was two to three times lower than that found on glucose; the overall solvent yields were comparable. Butanol production from galactose and mixtures of glucose and galactose was also possible.
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  • 10
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    Applied microbiology and biotechnology 19 (1984), S. 237-240 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A synthetic medium for continuous cultivation of Zymomonas mobilis was developed using the chemostat pulse technique in appropriate experimental designs. Yeast extract could be replaced by a mixture of six mineral salts, Ca-pantothenate, l-as-partate, and l-serine. Kinetic data from continuous cultivations of strains ATCC 10988 and ZM4 are presented and compared with published data.
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  • 11
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    Applied microbiology and biotechnology 19 (1984), S. 224-228 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Organic waste is converted in a two-stage process to methane and carbon dioxide by mixed cultures of microorganisms. Acetate, a product of acidogenic and acetogenic bacteria and the main substrate for methanogenic bacteria, is an important intermediate of the anaerobic degradation process, which results in the generation of methane. It was shown by labelling experiments using (U-14C) acetate that as much as 65%–96% of the total methane produced came from the acetate. The first order utilization rate for acetate in the methanogenic stages of a two-stage digestion process was between 0.17 h-1 and 0.5 h-1. The kinetics as well as the mass flow and yields of acetate and the methyl group of acetate were determined by pulse-labelling experiments with (U-14C) acetate and (2-14C) acetate without a significant rise of the total concentrations. Up to 58% of the acetate carbon was transformed to methane, and about 30% to carbon dioxide; only 4%–15% was incorporated into the biomass. There are at least two parallel degradation mechanisms in the metabolic transformation of acetate to methane: acetate is cleaved either to form methane and carbon dioxide or to form hydrogen and carbon dioxide, which can be transformed by an additional reaction to methane. Labelling experiments with (2-14C) acetate show that both mechanisms took place at similar order.
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  • 12
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The kinetics and enzymology of d-xylose utilization were studied in aerobic and anaerobic batch cultures of the facultatively fermentative yeasts Candida utilis, Pachysolen tannophilus, and Pichia stipitis. These yeasts did not produce ethanol under aerobic conditions. When shifted to anaerobiosis cultures of C. utilis did not show fermentation of xylose; in Pa. tannophilus a very low rate of ethanol formation was apparent, whereas with Pi. stipitis rapid fermentation of xylose occurred. The different behaviour of these yeasts ist most probably explained by differences in the nature of the initial steps of xylose metabolism: in C. utilis xylose is metabolized via an NADPH-dependent xylose reductase and an NAD+-linked xylitol dehydrogenase. As a consequence, conversion of xylose to ethanol by C. utilis leads to an overproduction of NADH which blocks metabolic activity in the absence of oxygen. In Pa. tannophilus and Pi. stipitis, however, apart from an NADPH-linked xylose reductase also an NADH-linked xylose reductase was present. Apparently xylose metabolism via the NADH-dependent reductase circumvents the imbalance of the NAD+/NADH redox system, thus allowing fermentation of xylose to ethanol under anaerobic conditions. The finding that the rate of xylose fermentation in Pa. tannophilus and Pi. stipitis corresponds with the activity of the NADH-linked xylose reductase activity is in line with this hypothesis. Furthermore, a comparative study with various xylose-assimilating yeasts showed that significant alcoholic fermentation of xylose only occurred in those organisms which possessed NADH-linked aldose reductase.
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  • 13
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    Applied microbiology and biotechnology 20 (1984), S. 10-15 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Sedimentation and fluidization of yeast flocs were found to be non-synonymous processes. The analysis of Richardson and Zaki (1954) was found not to hold when applied to yeast flocs in both regimes. Partial support and channelling were implicated in the deviations from idela behaviour. Other factors responsible for the behaviour of yeast flocs in these regimes are discussed.
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  • 14
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    Applied microbiology and biotechnology 20 (1984), S. 33-39 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Alfalfa residual juice (ARJ) supported good growth of the yeast Phaffia rhodozyma but formation of astaxanthin was inhibited. Supplementary nutrients did not reverse the inhibition, indicating that the the juice probably contained some inhibitor of astaxanthin biosynthesis. Six strains of P. rhodozyma were tested and found to be susceptible to the inhibitory effects of the juice. Concentrations of ARJ above 1.25% (v/v) were inhibitory to pigmentation of the yeast. Above approximately 3.7%, total inhibition of astaxanthin formation was observed but some chromogenic components of the juice were adsorbed on Phaffia cells and appeared as artefacts in astaxanthin analyses. Phaffia biomass produced in ARJ showed greater susceptibility to autolysis than that produced in a peptone-glucose-salts medium. Supplementation of ARJ with glucose enhanced yield of cell mass and minimised the autolytic phenomenon, and is potentially useful for producing Phaffia biomass for use as a source of single cell protein. Unsupplemented brewer's malt wort and molasses, separately and in a suitable combination, were compared with ARJ and were found suitable for growth and pigmentation of P. rhodozyma.
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  • 15
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    Applied microbiology and biotechnology 20 (1984), S. 66-71 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The pathway for uptake of acids during the solvent formation phase of an acetone-butanol fermentation by Clostridium acetobutylicum ATCC 824 was studied. 13C NMR investigations on actively metabolizing cells showed that butyrate can be taken up from the medium and quantitatively converted to butanol without accumulation of intermediates. The activities of acetate phosphotransacetylase, acetate kinase and phosphate butyryltransferase rapidly decreased to very low levels when the organism began to form solvents. This indicates that the uptake of acids does not occur via a reversal of these acid forming enzymes. No short-chain acyl-CoA synthetase activity or butyryl phosphate reducing activity could be detected. Based on our results and a critical analysis of literature data on acetone-butanol fermentations, it is suggested that an acetoacetyl-CoA: acetate (butyrate) CoA-transferase is solely responsible for uptake and activation of acetate and butyrate in C. acetobutylicum. The transferase exhibits a broad carboxylic acid specificity. The key enzyme in the uptake is acetoacetate decarboxylase, which is induced late in the fermentation and pulls the transferase reaction towards formation of acetoacetate. The major implication is that it is not feasible to obtain a batch-wise butanol fermentation without acetone formation and retention of a good yield of butanol.
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  • 16
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The enzymatic hydrolysis of cellobiose and cellulose by the cell-free culture filtrate of Trichoderma reesei QM 9414 was investigated. The concentrations of cellobiose and glucose were measured as a function of time for different initial concentrations of cellobiose. It was not possible to describe these concentration variations by a model which considers only the cellobiase hydrolysis with competitive and noncompetitive substrate and product inhibition; it is necessary that the endo-β-1.4-glucanase with competitive product inhibition is also taken into account. The enzymatic hydrolysis of cellulose (Avicel) was described with a mathematical model by using the results of the decomposition of cellobiose by the same enzyme mixture. the identified model parameters are presented. A sensitivity analysis of the parameter was carried out also.
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  • 17
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    Applied microbiology and biotechnology 20 (1984), S. 207-212 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Extracellular proteins from Streptomyces sp. ATCC 11238 grown on fungal mycelia and chitin as C- and N-sources were concentrated by ultrafiltration and acetone precipitation. The crude preparation containing chitin and laminarin degrading enzymes was fractionated by repeated gel filtrations. Three different types of β-1,3-glucanases were found. Besides oligomeric breakdown products laminaritriose is the main product of laminarin hydrolysis by one endo-β-1,3-glucanase. A second laminarin degrading (exo-splitting) enzyme yields predominantly laminaribiose. Another exo-β-1,3-glucanase liberates glucose but no, oligosaccharides from the nonreducing end of laminarin.
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  • 18
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    Applied microbiology and biotechnology 20 (1984), S. 129-132 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The effect of the herbicides MCPA, MCPB, mecoprop, dichlorprop, 2,4-D, 2,4-DB, and 2,4,5-T on l-lysine fermentation was investigated using a lysine-producing mutant of Corynebacterium glutamicum. Stimulation of l-lysine production by 6% to 36% was observed in shaken flask experiments when the test herbicides were added at a concentration of 5 · 10-4 M to growing cultures after 24 h of cultivation. The most effective stimulators were MCPA, mecoprop and dichlorprop. Detailed studies of the effect of MCPA (5 · 10-6 M to 5 · 10-3 M) showed that the degree of stimulation depended on medium composition and aeration. In the synthetic medium, maximum production of 50 g · l-1 lys · HCl occurred at 5 · 10-4 M MCPA and an oxygen transfer rate (OTR) of 1.97 g O2 · l-1 · h-1, while 61.7 g · l-1 of lys · HCL was formed at 5 · 10-3 M MCPA and an OTR of 3.75 g O2 · l-1 · h-1. In the amino-nitrogen rich medium, maximum production of 42 g · l-1 lys · HCl was observed at 5 · 10-6 M MCPA and an oxygen transfer rate of 1.5 g O2 · l-1 · h-1. Results from batch l-lysine fermentation in a fermenter showed similar stimulatory effects, with an optimal concentration of MCPA for l-lysine production of 5 · 10-5 M. Without herbicide addition, the test strain produced 16.25 g · l-1 of product and with addition of 5 · 10-5 M MCPA, the same strain produced 52.1 g · l-1 lys · HCl after 72 h of fermentation.
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  • 19
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    Applied microbiology and biotechnology 20 (1984), S. 233-237 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Whole cells of Saccharomyces cerevisiae were entrapped in polymers of 2-hydroxyethylmetha-crylate and sucrose hydrolysis catalysed by its invertase was investigated. Analysis of the experimental results confirmed that diffusional resistance to mass transfer of reactant and product was not induced by immobilization. For the yeast cells in the hydrogel, invertase activity obeyed a Michaelis-Menten kinetic and the value of Km (40 mM) was the same as that for yeast cells in bulk phase. The recovery of biocatalyst activity ranged between 17% and 23%, depending on immobilization temperature; the optimum pH range was found to be slightly wider. Storage stability at refrigerator temperature was quite satisfactory; invertase half-life was 267 days. Operational stability of immobilized cells at 45°C (half-life 110 days) was almost twice that of free cells. Finally, cell distribution in the polymer, observed with a scanning electron microscope, was found to be uniform.
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  • 20
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary We have used a chimerical plasmid containing the long terminal repeat of Moloney sarcoma virus to direct the expression of the human fibroblast interferon gene in mouse L cells. Constitutive secretion in cell culture supernatants was achieved at a level higher than 2.103 U/ml/72 h. The antiviral activity was indistinguishable from that of authentic human fibroblast interfereon by both immunological and physical criteria. Northern blotting analysis showed unambiguously that the expression was under the control of the putative transcriptional regulatory sequences previously described in the long terminal repeat of Moloney murine sarcoma virus (Dhar et al. 1980).
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  • 21
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    Applied microbiology and biotechnology 20 (1984), S. 281-283 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Final biomass yields of Chlorella vulgaris cultured heterotrophically in bristol medium amended with 0.1% (w/v) yeast extract (Difco) or 0.5% glucose (w/v) were 26 and 58 times higher, respectively, than yields obtained for autotrophically grown cells in the light. Similarly, final biomass increases were 35 and 138 fold for these organic substrates in the dark. The mixture of 0.1% yeast extract and 0.5% glucose was optimal and produced increases in final biomass of 70 and 140 times in the light and dark, respectively.
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  • 22
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    Applied microbiology and biotechnology 20 (1984), S. 303-309 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Enzymic conversion of glucose to fructose was carried out in a packed bed and in a fluidized bed reactor. The flow dynamics of these two flow systems, loaded with two different types of immobilized loaded with two different types of immobilized glucose isomerase particles, were studied. The theoretical RTD curve calculated from the axial dispersed plug flow model equation was matched to the experimental RTD curve by an optimization technique. The effect of fluid velocity on the extent of liquid dispersion was established. Theoretical predictions on the conversion of glucose to fructose were calculated using three mathematical models, namely, a plug flow model, a continuous stirred tank reactor (CSTR) model and an axial dispersed plug flow model. The experimental results showed that the axial dispersed plug flow model was superior in predicting the performance of both the packed bed and fluidized bed reactor.
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  • 23
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    Applied microbiology and biotechnology 20 (1984), S. 318-325 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Streptomyces clavuligerus produced simultaneously cephamycin C and clavulanic acid in defined medium in long-term fermentations and in resting-cell cultures. Biosynthesis of cephamycin by phosphate-limited resting cells was dissociated from clavulanic acid formation by removing either glycerol or sulphate from the culture medium. In absence of glycerol no clavulanic acid was formed but cephamycin production occurred, whereas in absence of sulphate no cephamycin was synthesized but clavulanic biosynthesis took place. Sulphate, sulphite and thiosulphate were excellent sulphur sources for cephamycin biosynthesis while l-methionine and l-cysteine were poor precursors of this antibiotic. Increasing concentrations of sulphate also stimulated clavulanic acid formation. The biosynthesis of clavulanic acid was much more sensitive to phosphate (10–100 mM) regulation than that of cephamycin. Therefore, the formation of both metabolites was pertially dissociated at 25 mM phosphate. By contrast, nitrogen regulation by ammonium salts or glutamic acid strongly reduced the biosynthesis of both cephamycin and clavulanic acid.
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  • 24
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    Source: Springer Online Journal Archives 1860-2000
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    Notes: Summary Bacteria able to secrete proteins efficiently into the growth medium occur relatively rarely amongst Gram-negative species. However, the increasing technological interest in protein secretion has focused attention on this process. We have demonstrated that Myxococcus xanthus actively secretes protein. The number of proteins secreted is quite large, but the total amount is strictly regulated and remains constant under conditions that change the specific activities of some of the secreted enzymes. Tn5-insertion mutants were obtained which were impaired in what seems to be the control system for protein secretion. Two of the mutants displayed increased levels of extracellular protein.
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  • 25
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
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    Notes: Summary Molecular hydrogen in the effluent gas from an E. coli- cultivation was detected on line by means of a palladium metal-oxide-semiconductor based (Pd-MOS) hydrogen gas sensor. Under conditions of oxygen limitation there was a sharply defined evolution of hydrogen gas which was reversible with respect to an increase in aeration. It is suggested that this sensor could be used for characterization of inhomogeneity of mixing in scale-up studies of bioreactors.
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  • 26
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    Applied microbiology and biotechnology 20 (1984), S. 285-290 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A Pseudomonas sp. which was isolated from phenol-containing soil was immobilized in alginate and polyacrylamide-hydrazide (PAAH) and cultivated in a special airlift fermenter. The immobilized Pseudomonas sp. was able to degrade phenol at initial concentrations up to 2 g/l in less than 2 days, although the free cells did not grow at this concentration. The immobilization materials act as a protective cover against phenol, PAAH being more effective than alginate. The degradation activity as well as the outgrowth of bacteria can be manipulated by the concentration of the immobilization material, the temperature and the nitrogen content in the medium. The cells grew predominantly in microcolonies in the outer area of the beads when nitrogen was available as 1.0g NH4NO3/l and 0.5g (NH4)2SO4/l.
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  • 27
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    Applied microbiology and biotechnology 20 (1984), S. 310-312 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Bioconversion of new methylcyclohexene derivatives with bulky side chains ending in aromatic or heteroaromatic rings by Streptomyces natalensis and Mycobacterium smegmatis results in monohydroxylation of the cyclohexene ring. Further oxidation of the hydroxyl group into a keto group is effected only with M. smegmatis. The synthesis of the substrates and proof of the structure of the products is given in detail.
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  • 28
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Analysis of a large number of experimental data from the cultivation of Bacillus subtilis formed the basis for a kinetic model of the process explaining the effect of composition of the culture medium and of the growth rate on the rate of enzyme production. The resulting rate of formation of α-amylase (EC 3.2.1.1) reflects the sum of the rate of enzyme production and the rate of its degradation as affected by the environment. The kinetic dependence confirms the previously described mechanism of regulation of enzyme biosynthesis. The mathematical model of the process served here to determine the optimal conditions for enzyme biosynthesis which were then verified in a fed-batch cultivation. The production of the enzyme in fed-batch culture was found to be twice that found in a batch cultivation.
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  • 29
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    Notes: Summary β-Isopropylmalate (IPM) dehydrogenase gene of Citrobacter freundii was cloned in both Escherichia coli and Bacillus subtilis. Plasmid pCBL 1 containing C. freundii β-IPM dehydrogenase gene was isolated using E. coli (leuB) as a host, pBR 322 as a vector and Hind III as an enzyme. The molecular weight (mol.wt.) of pCBL 1 was 7.7 megadalton (Md) and the plasmid was restricted at two sites by Hind III or Sal I, at three sites by BamH I and at four sites by Pst I. The second hybrid plasmid pCBL 2 containing β-IPM dehydrogenase gene was reconstructed from 2.1 Md Pst I fragment of pCBL 1 and pBR 322. β-IPM dehydrogenase activities of E. coli transformants with pCBL 1 or pCBL 2 were 2–7-fold higher than those of the present strains. The β-IPM dehydrogenase gene was transferred from pBR 322 to pLS 353, a shuttle vector between E. coli and B. subtilis. The third plasmid, pCBL 3 (mol.wt. 5.6Md), was cloned in B. subtilis (leuC) and expressed the enzyme activity which complemented the Leucharacter. The enzyme activities of B. subtilis transformants with pCBL 3 were about 5-fold higher than those of present strains. Thus, the C. freundii gene was effectively expressed in both E. coli and B. subtilis.
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    Applied microbiology and biotechnology 20 (1984), S. 393-399 
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    Notes: Summary In addition to the excretion of soluble acidic polysaccharides many fast-growing rhizobia deposit insoluble neutral capsular polysaccharide (CPS), which is composed of d-mannose, d-galactose, and d-glucose in the ratios 1:4:1. CPS was found to occur in all strains of Rhizobium leguminosarum and R. trifolii. Synthesis takes place in the stationary phase of growth, but the extent of synthesis differs widely for individual strains. CPS was not found in the species R. phaseoli and R. meliloti. CPS can be extracted from the cell pellet with N NAOH and the so obtained material is notable for its gelling character. It is insoluble in cold water and dissolves in hot water to a clear solution. On cooling to room temperature the solution solidifies to a resilient gel at a setting point of 40–45° C, and remelts on heating at 50–55° C. Gel strength of CPS in 500 g/cm2 for a 1% suspension.
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    Applied microbiology and biotechnology 20 (1984), S. 406-412 
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    Notes: Summary Effect of the cloned gene of Bacillus licheniformis on the extracellular proteolytic activities of B. subtilis was investigated. The gene was cloned onto the vector plasmid pUB110 (3.0 Md), and the introduction of the hybrid plasmid [pAN2 (5.4 Md)] into the cells of B. subtilis resulted in a marked increase of activities of the extracellular alkaline and neutral proteases, which had optimal pHs at 10.5 and 7.2, respectively. On DEAE-Sephadex column chromatography, the extracellular activity of B. subtilis with pAN2 was separated into two active fractions (a1 and b1). The activity in a1 was specifically inactivated by diisopropyl phosphorofluoridate (DFP) and tosyl fluoride (TSF), potent inhibitors of alkaline proteases, while, the activitiy in b1 was inhibited by ethylenediaminetetraacetate (EDTA), an inhibitor of neutral protease, but not by DEP or TSF. Sub-cloning with genes shortened to about 0.85 Md (pAN2-1) and 0.25 Md (pAN2-2) increased the activities of both alkaline and neutral proteases. The extracellular α-amylase and ribonuclease production was also increased when the host strain was transformed with these hybrid plasmids (pAN2, pAN2-1, pAN2-2). The increase in activity of proteases by the cloning was discussed in relation to regulation of the production and/or secretion of the enzyme.
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    Applied microbiology and biotechnology 19 (1984), S. 1-4 
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    Notes: Summary Methanotrophic bacteria have been shown to oxidize gaseous alkenes to the corresponding epoxides utilizing an NADH2-dependent methane monooxygenase. A cell paste of methane-grown methylotrophs was coated on porous glass beads. The production of propylene oxide from propylene was performed in a gas-solid bioreactor to ensure continuous production and removal of product epoxide from the microenvironment of the biocatalyst. The amount of propylene oxide produced before cofactor regeneration was between 120–145 μmoles/20 mg cells in about 10 h depending on the microbial strains used. The conversion rate for propylene was 2.7%. Regeneration of cofactor NADH2 was performed in the bioreactor with the vapor of a cosubstrate, methanol.
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    Applied microbiology and biotechnology 19 (1984), S. 85-90 
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    Notes: Summary In order to improve L-malic acid productivity by Brevibacterium flavum immobilized with ϰ-carrageenan, addition of Chinese gallotannin to the immobilization medium was investigated. As the results show, the optimal concentration of Chinese gallotannin was 0.1% (w/v). Fumarase activity and the stability of this improved preparation were higher than in one with only ϰ-carrageenan. Addition of Chinese gallotannin was more advantageous to stability towards ethanol than addition of polyethyleneimine. The L-malic acid productivity of the immobilized cells at 37°C was 42.2 kg/h per 1,000 l column, and increased threefold compared with that of B. flavum immobilized with only ϰ-carrageenan, and was 25 times that of B. ammoniagenes immobilized with polyacrylamide. Persimmon tannin also increased the stability of fumarase.
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    Applied microbiology and biotechnology 19 (1984), S. 110-113 
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    Notes: Summary The degradation of hexadecane and tetradecane by Acetobacter rancens CCM 1774 was investigated. It was found that this strain is able to grow to a limited extent on hexadecane as a carbon source. The occurrence of n-alkanoic acids and alcohols among the reaction products of growing as well as resting cells indicates a monoterminal degradation of long-chain alkanes. Both alkane-grown and glucose-grown resting cells exhibited alkane oxidizing activities which were not influenced by chloramphenicol. This suggested a constitutive nature of the appropriate enzymes.
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    Applied microbiology and biotechnology 19 (1984), S. 139-139 
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    Applied microbiology and biotechnology 19 (1984), S. 146-152 
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    Notes: Summary The antibiotic nikkomycin can be produced by calcium alginate immobilized mycelium of Streptomyces tendae Tü 901 in batch and continuous culture. Scanning electron micrographs show the porous structure of the matrix and the distribution of the cells in the gel. Some physiological properties of free and immobilized mycelia were compared. Immobilization does not change the relative amounts of nikkomycin compounds in the culture broth. DNA and protein content were the same in free and immobilized cells. The specific activity of fructosediphosphate aldolase dropped during fermentation and was lower for entrapped than for free cells. The specific activity of mannitol dehydrogenase increased up to the end of the fermentation and was the same for free and immobilized mycelium. In continuous culture the relative amount of mannitol consumed decreased with increasing flow rate. When the medium was supplemented with amino acids mannitol consumption increased significantly.
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    Applied microbiology and biotechnology 19 (1984), S. 177-180 
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    Notes: Summary Derivative spectrophotometry has been used to study the culture of Pseudomonas fluorescens NCIB 11615 grown in complex medium containing acetanilide. By using fourth derivative spectra it has proved possible to determine both acetanilide (substrate) and aniline (product) concentration in culture samples. The method has been found to possess several advantages over other techniques. It allows simultaneous determination of more than one species, requires a minimum volume of culture, needs no sample pretreatment and yields results within two to three minutes of sampling.
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    Applied microbiology and biotechnology 19 (1984), S. 186-190 
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    Notes: Summary Lipoperoxidation appears to play a role in inducing aflatoxin biosynthesis. In vitro, synthetic lipoperoxides greatly stimulate aflatoxin production when added to cultures of toxigenic strains of Aspergillus parasiticus or A. flavus. In vivo, the amount of toxin formed in sunflower seeds of different ages inoculated with A. parasiticus is directly related to the peroxide number of their oil content: the higher the peroxide number, the higher the aflatoxin production. In cultures of A. parasiticus carbon tetrachloride (CCl4) greatly stimulates aflatoxin biosynthesis. This effect might be due to the peroxidation of lipids of the endoplasmic reticulum of Aspergillus by the highly reactive CCl . 3 radicals formed by interaction with the NADPH-cytochrome P-450 system.
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    Applied microbiology and biotechnology 19 (1984), S. 207-216 
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    Notes: Summary A two-stage fermentation process has been developed for continuous ethanol production by immobilized cells of Zymomonas mobilis. About 90–92 kg/m3 ethanol was produced after 4 h of residence time. Entrapped cells of Zymomonas mobilis have a capability to convert glucose to ethanol at 93% of the theoretical yield. The immobilized cell system has functioned for several weeks, and experience indicates that the carrageenan gel apparently facilitates easy diffusion of glucose and ethanol. The simplicity and the high productivity of the plug-flow reactor employing immobilized cells makes it economically attrative. An evaluation of process economics of an immobilized cell system indicates that at least 4 c/l of ethanol can be saved using the immobilized cell system rather than the conventional batch system. The high productivity achieved in the immobilized cell reactor results in the requirement for only small reactor vessels indicating low capital cost. Consequently, by switching from batch to immobilized processing, the fixed capital investment is substantially reduced, thus increasing the profitability of ethanol production by fermentation.
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    Applied microbiology and biotechnology 19 (1984), S. 217-223 
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    Notes: Summary The immobilization in polyacrylamide gel (PAAG) of the Aspergillus niger mycelium, which has the activity of hydroxylating indolyl-3-acetic acid (IAA) at 4-, 5-, and 6-positions of the indole nucleus, was studied. To preserve the hydroxylating activity, the immobilization should be performed at 5°C–10°C for 5–10 min. The hydroxylating activity of the A. niger mycelium entrapped in PAAG attained 70%–80% of that of free cells. The IAA transformation in the presence of sodium desoxycholate, polyethylene-glycol-400 (PEG-400), Span-60 or preincubation of granules entrapping mycelia in the presence of Tween-80 or PEG-400 not only double the hydroxylation rate but stabilize the activity as well. Gels entrapping mycelia may be used five or six times without altering activity. Incubation of gels with mycelium in the nutrient medium also increases and stabilizes the hydroxylating activity. In aerated columns, it is possible to obtain continuous hydroxylation of IAA, at a concentration of 0.5 g/l, by the immobilized mycelium of A. niger. The yield of hydroxy derivatives reached 70%, the activity remaining unaltered during 15 days' operation of the column.
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    Applied microbiology and biotechnology 19 (1984), S. 241-246 
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    Notes: Summary Cells of the yeast Lodderomyces elongisporus, precultured on glycerol, were incubated with long-chain n-alkanes. The results whow that monoterminal alkane oxidation is the main pathway of alkane degradation in the investigated yeast. The amount of diterminal activity is negligible, while subterminal degradation did not occur at all. Fatty acids were the first detectable intermediates. Using different n-alkanes, in every case the fatty acids with substrate chain length predominated in the cells. The formation of radioactive fatty acids from (1-14C)-hexadecane was time-dependent and indicated that desaturation elongation and β-oxidation occurred. Extracellularly, the fatty acid pattern was similar, except for the additional presence of fatty acid methyl esters and the prevalence of octadecenoic acid after growth of cells on n-hexadecane.
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    Applied microbiology and biotechnology 19 (1984), S. 261-266 
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    Notes: Summary The ability of a Candida shehatae and a Pachysolen tannophilus strain to ferment D-xylose to ethanol was evaluated in defined and complex media under different levels of aeration. Aeration enhanced the ethanol productivity of both yeasts considerably. C. shehatae maintained a higher fermentation rate and ethanol yield than P. tannophilus over a wide range of aeration levels. Ethanol production by C. shehatae commenced during the early stage of the fermentation, whereas with P. tannophilus there was a considerable lag between the initiation of growth and ethanol production. Both yeasts produced appreciable quantities of xylitol late in the fermentation. P. tannophilus failed to grow under anoxic conditions, producing a maximum of only 0.5 g · l-1 ethanol. In comparison, C. shehatae exhibited limited growth in anoxic cultures, and produced ethanol much more rapidly. Under the condition of aeration where C. shehatae exhibited the highest ethanol productivity, the fermentation parameters were: maximum specific growth rate, 0.15 h-1; maximum volumetric and specific rates of ethanol production, 0.7 g (l · h)-1 and 0.34 g ethanol (g cells · h)-1 respectively; ethanol yield, 0.36 g (g xylose)-1. The best values obtained with P. tannophilus were: maximum specific growth rate, 0.14 h-1; maximum volumetric and specific rates of ethanol production, 0.22 g (l · h)-1 and 0.07 h-1 respectively; ethanol yield coefficient, 0.28. Because of its higher ethanol productivity at various levels of aeration, C. shehatae has a greater potential for ethanol production from xylose than P. tannophilus.
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    Applied microbiology and biotechnology 19 (1984), S. 281-287 
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    Notes: Summary Microcalorimetry was used to study the energetic aerobic growth of Cellulomonas sp. 21399 on glucose, cellobiose and amorphous and crystalline cellulose. The thermochemical aspect of growth on glucose was established with regard to the anabolic contribution. The results obtained allowed the use of glucose as a reference substrate for cellulose degradation. The experimental enthalpy change and the maximum catabolic activity, calculated from the maximum power evolved by the culture, were, respectively,-1079 kJ/mol and 0.85 mmol glucose per hour per dry weight of cells. The growth response on amorphous cellulose was equivalent to that demonstrated on glucose. However, on crystalline cellulose media, Cellulomonas sp. 21399 exhibited eight times less power and the quantity of heat evolved during growth showed that 50% of the cellulose was degraded. Quantitative results and the shape of power-time curves achieved indicate that the structural features of cellulose strongly influence its microbial degradability.
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  • 44
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    Notes: Summary A commercial preparation of cellulase was immobilized on CNBr-sepharose, ConA-sepharose, and CNBr-glass beads. When filter paper was used as the substrate, the specific activity of the enzyme immobilized on ConA-sepharose was more than twice that of the soluble enzyme, while the activity of the enzymes immobilized on the other two substrates was either very slightly (CNBr-sepharose) or slightly (CNBr-glass beads) reduced. The immobilized enzymes showed alterations both in the Km and V max values: these were generally either slightly increased (Km) or reduced (V max). In addition, the immobilized enzymes were more resistant to inhibition both by glucose and cellobiose, they were all more stable than the soluble enzyme and solubilized three different natural lignocellulosic materials (alfa-alfa, wheat straw, and pine needles) to a much greater or significantly greater extext than the soluble enzyme: the ConA-sepharose cellulase was the most efficient. The possibility of reusing the immobilized enzyme was also tested. It was found that the ConA-sepharose cellulase could be reused five times with a final loss of activity that ranged between 30% and 50%.
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    Applied microbiology and biotechnology 19 (1984), S. 326-334 
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    Notes: Summary Thermoanaerobium brockii was grown in batch and continuous culture at supraoptimal temperatures (〉65° C). Specific growth rates were lower in batch (μmax〉1.0 h-1) than in continuous cultures (μmax1.2–1.4 h-1). Acetone addition to the medium did not increase critical dilution rate significantly. The media used contained significantly less organic material and sulfide than previously reported media; however, yeast extract requirements were shown to be exceptionally high (60% of the glucose concentration used). Organic substrates inhibited growth and product formation in chemostat cultures whereas the slow formation of acetic acid was observed in batch cultures, but also with virtually no growth. The inhibiting concentration was found to be approximately 15 g organic carbon·l-1. The maintenance requirements of T. brockii were in the same range as expected of aerobic extreme thermophiles (ms∼0.5 g·g-1·h-1) and could be met only by glucose and not by yeast extract. Maintenance was obviously not independent of specific growth rate. Production of the stereospecific alcohol-aldehyde/ketone oxidore-ductase was strictly growth associated and its formation was not affected by acetone added to medium.
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    Applied microbiology and biotechnology 19 (1984), S. 335-340 
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    Notes: Summary Four strains (W1, W2, W3, and W4) of alkalophilic thermophilic bacteria which produced xylanase were isolated from soils. They were aerobic, spore-forming, Gram-positive, and rod-shaped bacteria and hence identified as the genus Bacillus. The optimal temperatures for growth of the four strains were between 45° C and 50° C and pH optima were between 9.0 and 10.0. No growth occurred below pH 7.0 or above 55° C. The four strains produced xylanases in medium containing xylan or xylose under these conditions. The optimal pH and temperature for activities of the four xylanases ranged from 6.0 to 7.0 and from 65° C to 70° C, respectively. The four xylanases were stable in the wide pH range from 4.5 to 10.5 at 45° C for 1 h. All xylanases split xylan to yield xylose and xylobiose.
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    Applied microbiology and biotechnology 19 (1984), S. 382-383 
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    Notes: Summary Encapsulation of Bacillus thuringiensis var. israelensis Serotype H-14 (B.t.i.) in polyethylene strongly increased its persistence against second stage Aedes aegypti larvae in laboratory conditions simulating natural field conditions. B.t.i. encapsulated in palmitic acid was less persistent. The reasons for the enhanced efficacy of encapsulated B.t.i. are discussed.
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    Notes: Summary Stability studies of photosynthetic activity under continuous saturating illumination are presented. Chloroplast membranes (thylakoids) are isolated in a classical Hepes/sorbitol buffer or in high salt concentration buffers (citrate or sulphate) and then immobilized in a co-crosslinking serum albumin-glutaraldehyde matrix. The activities of these immobilized systems tested in a batch reactor are greatly increased by high concentrations of salts (223 and 277 μmol ferrocyanide/mg of chlorophyll per hour for citrate; 243 and 267 μmol ferrocyanide/mg of chlorophyll per hour for sulphate, compared with 141 μmol ferrocyanide/mg of chlorophyll per hour for sorbitol). In continuous stirred-tank reactors, the conversion rates increase when high concentrations of salts are present in the buffer (approximately 36% for citrate and 34% for sulphate compared with 18% for sorbitol). The functional stability of these immobilized systems during continuous illuminations is higher in citrate (7.5 h) than in sulphate (5.5 h) or sorbitol (3.5 h). These experiments performed in batch or in continuous stirred-tank reactors underline the importance of salt ions in the reaction media.
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    Applied microbiology and biotechnology 19 (1984), S. 414-421 
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    Notes: Summary Using α-amylase as an example, extremely thermophilic Bacilli isolated from heat-treated sewage sludge are shown to be a source for enzymes stable and active at high temperatures. The isolates which are classified as subspecies of Bacillus stearothermophilus differ from each other in protein composition indicating the heterogeneiety of that subspecies. Media are evaluated for good growth and high enzyme productivity. Best media are those composed of three or four different complex components like combinations of peptone, soy grist, and malt extract, α-amylase production on simple carbon sources is negligible. From the cultivation supernatants crude α-amylase extracts are prepared and their behaviour at high temperatures is described. The optimal temperature of all tested enzymes is 80°C. They are stable at suboptimal temperatures for over 20 h and at 95° C 50% of their activity is lost within 2 h. The activity at 95° C is however preserved for over 3 h in presence of starch. The products of the starch digestion are maltotriose, maltose, and some glucose. The amylases can therefore compete in activity and stability with commercially available α-amylases from Bacillus licheniformis.
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    Applied microbiology and biotechnology 19 (1984), S. 430-434 
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    Notes: Summary By using batch-culture enrichment techniques a mixed culture of two bacterial spe cies identified as Cellulomonas flavigena and Xanthomonas sp was isolated. The capacity of both bacteria to grow as pure cultures in a min eral medium with alkaline pretreated sugar cane bagasse or cellobiose was tested. C. flavigena as pure culture was able to grow on both substrates only when yeast extract or biotin and thiamine were added to the culture medium, while Xanthomonas sp. could not grow on sugar cane ba gasse, but assimilated cellobiose if yeast extract was supplied. However, both bacteria in mixed culture grew very well on both substrates and did not require any growth factor. It was concluded that the interaction was favourable to both species. The mixed culture had the capacity to degrade a number of different agricul tural wastes and to use them as the sole carbon and energy source for the production mainly of biomass. More than 80% of pineapple bagasse, without chemical pretreatment, was used up by the microbial system.
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    Notes: Summary Acetolactate decarboxylase activity has been detected among three genera, nine species and 263 strains of lactic acid bacteria tested in the course of a screening for acetolactate decarboxylases amenable for use in brewing as maturation aid. Streptococcus diacetylactis strain FD-64-D was found to generate a decarboxylase exhibiting a satisfactory activity and an excellent stability at the pH prevailing in beer and wort. This decarboxylase could not be solubilized but enzymatically active, freeze-dried cells were effective for satisfactory flavour maturation of beer although difficulties were encountered during attempts to remove the applied cell material by filtration of the beer. Lactobacillus casei DSM 2547 was likewise found to produce a decarboxylase exhibiting a satisfactory activity and stability at the low pH of beer and which, in addition, was readily solubilized. A method has been developed for pilot scale production of preparations of this decarboxylase suitable for use in brewing.
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    Applied microbiology and biotechnology 20 (1984), S. 54-58 
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    Notes: Summary the effect of N-methyl-1-deoxy-nojirimycin (NMDN; 1,5-dideoxy-1,5-imino-N-methyl-D-glucit) was studied with crude extracts, growing cells, and permeabilized cells from batch cultures of Cellulomonas cartalyticum (DSM 20106) grown on cellobiose. The following results were obtained: 1. β-Glucosidase (cellobiase, β-d-glucoside glucohydrolase EC 3.2.1.21) is competitively inhibited and the following apparent kinetic constants were determined: K M app(with cellobiose)= 45.5 mM, i i app with cellobiose = 5.6 mM; K M app (with ONP-Gluc) = 2.67 mM, K i app (with ONP-Gluc) = 7.5 mM. 2. Growth of C. cartalycium with cellobiose as a sole source of energy and carbon as well as oxygen consumption was not inhibited in the presence of different ratios of cellobiose and NMDN. 3. Cellobiose hydrolysis by permeabilized cells of C. cartalyticum was competitively inhibited and the following apparent kinetic constants were observed with cellobiose as substrate: K M app = 41.7 mM, K i app = 3.65 mM.
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    Applied microbiology and biotechnology 20 (1984), S. 100-104 
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    Notes: Summary A new approach for continuous production of ethanol was developed using a Hollow fiber fermentor (HFF). Saccharomyces cerevisiae cells were packed into the shell-side of a hollow fiber module. Using 100 g/l glucose in the feed gave an optimum ethanol productivity, based on total HFF volume, of 40 g ethanol/l/h at a dilution rate of 3.0 h-1. Under these conditions, glucose utilization was 30%. However, at 85% glucose utilization the productivity was 10 g ethanol/l/h. This compares to batch fermentor productivity of 2.1 g ethanol/l/h at 100% glucose utilization.
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    Applied microbiology and biotechnology 20 (1984), S. 118-123 
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    Notes: Summary Sorbitol is formed as the major by-product in ethanol fermentations by Zymomonas mobilis when both glucose and fructose are present in the fermentation medium. The amount of sorbitol produced was equivalent to as much as 11% of the original carbon source, decreasing the ethanol yield correspondingly. Only minor amounts of sorbitol were formed from glucose or fructose alone. The formation of sorbitol is apparently a consequence of the inhibition of fructokinase by glucose.
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    Applied microbiology and biotechnology 20 (1984), S. 139-145 
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    Notes: Summary Following growth on n-alkanes, undecanoic acid in high concentrations completely inhibits the acylation of fatty acids formed during the terminal oxidation so that the intracellular fatty acid pattern is composed exclusively of components from the de novo synthesis. An inhibitory effect of undecanoic acid stems presumably from the effect it has on the long-chain acyl-coenzyme A synthetase I, whereas the corresponding long-chain acyl-coenzyme A synthetase II, which is bound to specific cell organelles remains untouched by this inhibition. The strongly reduced growth, even following glucose oxidation, probably comes from the effect of C11-acid on specific intramitochondrial situated enzymes.
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    Applied microbiology and biotechnology 20 (1984), S. 251-255 
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    Notes: Summary Mutants sensitive to far ultraviolet light (UV) and 4-nitroquinoline-1-oxide (4NQO) have been isolated from Penicillium chrysogenum NRRL 1951. Two strains HP500 and HP508 are examined in detail. Their cross sensitivity to and altered mutation by UV and 4NQO suggests that damage caused by both agents is repaired through similar pathways in Penicillium chrysogenum. Strain HP500 is refractive to UV and 4NQO mutagenesis and is likely to be defective in an error-prone mechanism of repair. Mutation by N-methyl-N′-nitro-N-nitrosoguanidine (MNNG) in HP500 is also reduced, indicating involvement of an error-prone UV repair process in MNNG mutagenesis in Penicillium chrysogenum. Strain HP508 shows an increase of forward mutation rate up to 4.5 times over that of the wild-type, when compared at similar surviving fractions and is also hypermutable by 4NQO. The repair defect present in strain HP508 has been demonstrated by its inability to remove DNA sites sensitive to single strand specific nuclease during post-irradiation incubation of protoplasts.
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    Applied microbiology and biotechnology 20 (1984), S. 384-388 
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    Notes: Summary The fungus Aspergillus niger, an unidentified filamentous fungus (strain no. PDDCC8239) and the yeast Candida tropicalis were grown in continuous culture in stirred tank reactors at dilution retes varying between 0.02–0.1 h-1 on a bark extract medium made by dilute acid hydrolysis of Pinus radiata bark. Maximum yields were 5.1, 18.7, and 61.5 mg biomass·g-1 bark for the unidentified fungus, A. niger and C. tropicalis respectively. Culturing in a tower fermenter under otherwise identical environmental conditions increased the yield of A. niger to 27.3 mg biomass·g-1 bark. The yield of C. tropicalis represents a productivity of 0.26g biomass·l-1·h-1 which exceeds other reported values of bark fermentations. Analysis of the medium and spent broth revealed significant breakdown of tannin material by C. tropicalis during growth. This ability may be of value in the treatment of tannin-based industrial effluents.
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    Applied microbiology and biotechnology 20 (1984), S. 378-383 
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    Notes: Summary A phthalate ester hydrolyzing enzyme has been purified from the culture broth of Nocardia erythropolis, a Gram-positive bacterium capable of degrading phthalate esters rapidly. The purified enzyme appeared homogeneous on polyacrylamide gel disc-electrophoresis, and its molecular weight was estimated to be about 15,000. The optimal pH and temperature were pH 8.6 and 42°C, respectively. The enzyme was stable in a pH range from 7.0 to 8.0 and below 30°C. The enzyme activity was stimulated by Ca2+ and taurocholate, but inhibited by several metals such as Hg2+. Most of the phthalate esters tested were hydrolyzed to phthalate and alcohols regardless of the type of side-chain. In addition, the enzyme rapidly hydrolyzed olive oil and tributyrin. This enzyme from N. erythropolis may be a novel type of lipase with broad substrate specificity.
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    Applied microbiology and biotechnology 20 (1984), S. 413-415 
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    Applied microbiology and biotechnology 19 (1984), S. 18-22 
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    Notes: Summary An enzyme sensor for hypoxanthine (Hx) and inosine (HxR), consisting of an enzyme membrane and an oxygen electrode, was constructed, Xanthine oxidase (XO) and nucleoside phosphorylase (NP) were both immobilized on a membrane prepared from cellulose triacetate, 1,8-diamino-4-aminomethyloctane and glutaraldehyde. The enzyme sensor responded to Hx and HxR in the presence of phosphate, while it responded only to Hx in the absence of phosphate. A linear correlation was observed between current decrease and the concentrations of Hx and HxR in the range 0.5–2.0 mM respectively. Correlation coefficients between the present enzyme sensor and a conventional enzymatic method were 0.98 and 0.94 for Hx and HxR respectively. The standard deviation was +-1.5 μM and 0.75 μM for Hx and HxR respectively in 100 experiments. A simple and rapid determination of Hx and HxR in fish meat was possible within 3 min with the enzyme sensor.
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    Applied microbiology and biotechnology 19 (1984), S. 70-74 
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    Notes: Summary The kinetics of anaerobic fermentation of rice straw to methane were studied. Rice straw was the only carbon source at influent volatile solid concentrations of 18.9 and 37.8 g/l. Semicontinous runs were carried out at 37°C in laboratory scale perfectly mixed reactors. The Contois' kinetic model constants were calculated from the experimental data. Arefrac tory coefficient was measured (R=0.374) to account for the nonbiodegradable portion of the organic matter of rice straw and incorporated into the kinetic equations. The predicted values of effluent substrate concentration, volumetric methane yield, volumetric methane production rate, and biodegradable conversion efficiency fit well with those measured experi mentally. Percent destruction values of feed constituents were measured.
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    Applied microbiology and biotechnology 19 (1984), S. 100-105 
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    Notes: Summary Bacteria with the ability to form L-phenylalanine from acetamidocinnamic acid were isolated from several soils. Among them, strain no. S-7 and strain no. N-7 were identified as Alcaligenus faecalis S-7 and Bacillus sphaericus N-7, respectively. The L-phenylalanine-forming enzyme systems in both bacteria were found to be inducible and intracellular. With intact cells of both bacteria and 40 mg/ml as wet base, 10 mg/ml acetamidocinnamic acid was utilized, and 7.7 mg/ml L-phenylalanine in a molar yield of 94% was produced after 72h incubation. The pathway of L-phenylalanine formation is considered to take the following course: acetamidocinnamic acid is deacetylated to α-amino cinnamic acid; this is spontaneously changed to phenylpyruvic acid, and L-phenylalanine is formed by transamination.
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    Applied microbiology and biotechnology 19 (1984), S. 91-99 
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    Notes: Summary In previous papers it was shown that the bacterium Zymomonas mobilis might be an interesting alternative for industrial alcohol production from sugar, compared to Saccharomyces bayanus. Factors that might increase the glucose to ethanol conversion efficiency and which are in favour of the bacterium, are the production of less biomass and less by-products such as glycerol, succinic acid, butanediol, acetoin, and acetic acid. In order to reduce the synthesis of biomass three metabolic inhibitors were now studied: dinitrophenol, azide and arsenate. Their effects on the alcoholic fermentation in batch and in immobilized cell system were investigated, using three yeasts: Saccharomyces bayanus, Schizosacharomyces pombe, and Saccharomyces diastaticus. It was found that dinitrophenol in 0.1 mM concentration was effective in increasing the conversion of glucose to ethanol especially with Saccharomyces bayanus while azide in 0.1 mM concentration was better with Schizosaccharomyces pombe. In immobilized systems high steady state ethanol production from 15% glucose media was obtained by inclusion into the media of dinitrophenol or azide. Arsenate had less effect at the concentration used. Arsenate had less effect at the concentrations used. As a result ethanol productivity in g·l-1·h-1 was increased from around 70 in the absence of inhibitor to around 74 in the presence of dinitrophenol with Saccharomyces bayanus. With Schizosaccharomyces pombe the productivity was increased from around 65 in the absence of inhibitor to around 74 in the presence of azide. The specific ethanol productivity expressed as g ethanol formed per hour and per g viable cells was increased from 0.87 to 1.37 for Schizosaccharomyces pombe and from 1.02 to 1.66 for Saccharomyces bayanus.
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    Applied microbiology and biotechnology 19 (1984), S. 120-124 
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    Notes: Summary Filament-forming bacilli were isolated from bulking sludge. They were physiologically very similar. However, they developed into rhizoid or non-rhizoid colonies. According to their morphological, physiological, and genetical properties the isolates were identified as Bacillus mycoides and Bacillus cereus.
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    Applied microbiology and biotechnology 19 (1984), S. 134-138 
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    Notes: Summary The cellulolytic enzyme complex was studied during the diauxic growth of Cellulomonas sp.IIbc on alkali-pretreated sugar cane bagasse pith. In the first growth phase only a low cell-bound aryl-β-glucosidase activity was detected. Formation of extracellular and bound (cell-, bagasse-) CM- and FP-cellulases occurred later, i.e. at the beginning and during the second growth phase. The levels of all cellulolytic enzymes, mainly bound ones, increased with the growth of cells. At the end of the linear growth phase almost all bound cellulolytic enzymes, except for cell-bound aryl-β-glucosidase, are released to the medium as an extracellular complex. A considerable level of the intracellular aryl-β-glucosidase activity is still present at the end of the fermentation.
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    Applied microbiology and biotechnology 19 (1984), S. 153-156 
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    Notes: Summary A mathematical model simulating the behaviour or Streptomyces aureofaciens in batch culture under conditions when tetracyclines are synthesized in excessive amounts has been formulated. The response of the mathematical model to the experimental conditions applied corresponds with data obtained in the experiments. The mathematical model demonstrated that the level of tetracycline production is determined during the period of culture growth beginning with exhaustion of inorganic phosphate from the medium and ending with inhibition of the synthesis of enzymes caused by the synthesized tetracyclines. Further tetracycline synthesis is then proportional to the amount of enzymes synthesized in this interval.
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    Applied microbiology and biotechnology 19 (1984), S. 167-176 
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    Notes: Summary A new dehydrogenase from Lactobacillus confusus has been purified. The following reactions are catalyzed by this enzyme: $$\vec F_\alpha$$ Various 2-ketocarboxylic acids are stereospecifically reduced to the corresponding l-2-hydroxycarboxylic acids. In the reverse reaction the NAD dependent dehydrogenation of l-2-hydroxycarboxylic acids is observed. l-2-hydroxyisocaproate seems to be the best substrate for this enzyme which we therefore call l-2-hydroxyisocaproate dehydrogenase (l-HicDH). The enzyme requires NAD(H) as a cofactor, which cannot be replaced by NADP(H). The large scale purification of the enzyme is described starting with 24 kg wet cells, it involved homogenization using a continuously operating high speed bead mill, liquid-liquid extraction with aqueous two-phase systems and diafiltration followed by ion-exchange chromatography on DEAE-cellulose. At this stage the enzyme was purified 177-fold resulting in a specific activity of 30 U/mg. This technical catalyst can be used for the continuous production of l-2-hydroxycarboxylic acids in an enzyme membrane reactor. Further purification up to 450–480 U/mg can be carried out by interfacial salting out chromatography or affinity chromatography, respectively. Properties of the purified enzyme were investigated in detail especially the parameters which are important for an industrial application.
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    Applied microbiology and biotechnology 19 (1984), S. 199-202 
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    Notes: Summary Anaerobically digested cow dung was separated by centrifugation into solid residue and liquid supernatant fractions. Clarified supernatant fraction, rich in volatile fatty acids, supported the growth of photosynthetic bacteria. Single cell protein from different photosynthetic bacteria, grown on clarified supernatant, was found to be rich in essential and sulphur amino acids. Rhodopseudomonas capsulata produced the best single cell protein.
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    Applied microbiology and biotechnology 19 (1984), S. 247-251 
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    Notes: Summary Selected microorganisms were screened for their ability to N-dealkylate drug molecules. The compounds studied enabled the investigation of N-alkyl groups in different chemical environments, including alkylaminoalkyl chains, saturated cyclic structures and in amide functions. Transformation products were extracted from the transformation mixtures, derivatised and analysed by gas liquid chromatography (GLC). For the purposes of screening, important transformation products were identified by comparison of their GLC retention data with similar derivatives of authentic standards. N-demethylation was effected by all test strains of the fungus Cunninghamella, except C. elegans, and also by three of the Streptomyces species tested. The Cunninghamella demonstrated the widest spectrum of transformation activity, N-demethylating the alkylaminoalkyl side chains of amitriptyline and chlorpromazine, the N-methylpiperidine function of codeine, and the cyclic amide function of diazepam. The N-demethylation of the latter substrate, which is only slightly water soluble, occurred in surprisingly high yield. There was no evidence that bulky groups such as N-dimethylallyl were celaved and selectivity for N-demethylation rather than O-demethylation was demonstrated when both N-and O-methyl functions were present in the same molecule. Comparisons are made with the mammalian metabolic pathways of the drug compounds studied.
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    Applied microbiology and biotechnology 19 (1984), S. 267-271 
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    Notes: Summary Candida utilis var. major NRRL-Y-1084 was grown in a defined medium without a phosphorous (P) source. During the exponential phase, cells divided according to a specific growth rate of 0.32 h-1, which is lower than the usual rate for a balanced medium (0.4–0.6 h-1). The relative P content of the biomass decreased from 2.70% to 0.75% over a period of 6 h, including 2 h of cell division arrest. At the end of this period there was another interruption of cell division. After that, multiplication restarted at a considerably lower rate and it deviated slightly from the exponential pattern. The stationary phase began when biomass P content reached 0.4%–0.5%, slowly decreasing afterwards to 0.25–0.20%. Biomass synthesis was less affected than cell division by the relative decrease of endogenous P, the two processes differing partially in their kinetics. Cell lysis started shortly before the stationary phase and affected about 20% of the population by the end of the assay. RNA and P content of the resulting biomass were 2.4% and 0.25% respecitvely, P being mainly incorporated to RNA. The relationship of biomass production to glucose uptake was very low, probably because the marked P deficiency called for an increase in energy consumption for growth and specially for maintenance. Compared with yeasts grown in a balanced medium, 40% increase in glycogen was observed, whereas no mean changes in the content of cell wall carbohydrates (glucan and mannan) and that of “true protein” were found.
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    Applied microbiology and biotechnology 19 (1984), S. 296-299 
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    Notes: Summary Interaction of Escherichia coli spheroplasts with Neurospora crassa slime cells was examined by transmission electron microscopy after treatment with polyvinyl alcohol followed by dilution with the high pH-high Ca buffer. Bacterial spheroplasts were found either adhering to the flat surface, associating with the invaginating surface, or residing within the intracellular vesicle of fungal protoplasts. In addition, bacterial spheroplasts free of the surrounding vesicles and those in the course of breakdown were observed in the fungal cytoplasm. It was concluded that Escherichia coli spheroplasts are taken up by Neurospora crassa protoplasts almost exclusively via endocytosis. This is the first cytological evidence for the endocytic activity of fungal cells.
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    Applied microbiology and biotechnology 19 (1984), S. 301-305 
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    Notes: Summary The concentration and productivity of α-amylase increased remarkably, 15- and 11-fold respectively, in a continuous culture of Bacillus caldolyticus DSM 405 compared with batch culture, provided starch was used as the sugar source in a casitone medium. In the casitone medium with or without glucose hardly any improvement of enzyme production was observed in continuous culture. The addition of a small amount of starch to the glucose-casitone medium had a marked effect in stimulating amylase formation in continuous culture but no effect in batch culture. It was suggested that the higher production of α-amylase in the continuous culture using starch as the inducer was partly related to the predominance of some conditional non-sporulating variants with a higher amylase forming activity and to derepression of the enzyme at a low glucose concentration.
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    Applied microbiology and biotechnology 19 (1984), S. 312-315 
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    Notes: Summary Radioactive penicillin G production from l-[1-14C]-valine (1.75 GBq · mmol-1) by native and by calcium alginate gel immobilized mycelium of Penicillium chrysogenum PQ-96 in a medium for antibiotic production as well as by vesicles isolated from the protoplasts of the same strain in a well-defined reaction mixture was investigated. Specific radioactivity of the penicillin G produced by the native vesicles was 1.45 GBq · mmol-1 and that of the antibiotic synthesized by the calcium alginate gel immobilized vesicles was 1.48 GBq · mmol-1. By comparison, the specific radioactivity of penicillin G produced by native mycelium was 0.42 GBq · mmol-1 and of that synthesized by the immobilized mycelium was 0.96 GBq · mmol-1. Production of radioactive penicillin G by native and immobilized vesicles in repeated use was also investigated. At the beginning of the production phase, the radioactive penicillin G synthesized by the immobilized vesicles was 25 nmol · mg protein-1 · h-1 and decreased after 8 days to a level of 11 nmol · mg protein-1 · h-1. The half-life of the immobilized vesicles was 7 days. The native vesicles showed a rapid decrease in radioactive antibiotic production. In comparison, the penicillin G production in a repeated use of immobilized vesicles decreased during 40 days from 140 nmol · mg protein-1 · h-1 to 60 nmol · mg protein-1 · h-1. The half-life of the immobilized vesicles was 35 days. The native vesicles showed after 4 days a lack of activity of penicillin G production. The stability of immobilized mycelium or vesicles in the process of radioactive penicillin G production is discussed.
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    Applied microbiology and biotechnology 19 (1984), S. 347-352 
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    Notes: Summary This paper describes the characteristics of the structural and functional organization of cellular membranes rehydrated after dehydration of the yeast Saccharomyces cerevisiae. It was noted that dehydration and subsequent rehydration of yeast cells causes a considerable increase of cytoplasmic membrane permeability. Addition of CaCl2, glucose and polyethyleneglycol to the rehydration medium caused a decrease in cell permeability, assessed as the losses of potassium ions, nucleotides, as well as the total losses of intracellular compounds. KCl had a positive effect only at concentrations above 10%. Yeast cells, dried to residual moisture lower than 20%, showed a decrease in membrane permeability as temperatures of the rehydration medium increased up to 38°–43°C. Upon reactivation of viable dehydrated cells in a nutrient medium, a reparation of the structural damages of various intracellular membranes takes place. It was established that at cell dehydration to residual moistures of 8%–12% all the free and a part of bound water is evaporated from cells.
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    Applied microbiology and biotechnology 19 (1984), S. 365-372 
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    Notes: Summary Hemicellulose-rich fractions from several agricultural residues were converted to 2,3-butanediol by a combined enzymatic hydrolysis and fermentation process. Culture filtrates from Trichoderma harzianum E58 were used to hydrolyze the substrates while Klebsiella pneumoniae fermented the liberated sugars to 2,3-butanediol. Approximately 50–60% of a 5% (w/v) xylan preparation could be hydrolyzed and quantitatively converted to 2,3-butanediol using this procedure. Although enzymatic hydrolysis was optimal at pH 5.0 and 50° C, the combined hydrolysis and fermentation was most efficient at pH 6.5 and 30° C. Combined hydrolysis and fermentation resulted in butanediol levels that were 20–40% higher than could be obtained with a separate hydrolysis and fermentation process. The hemicellulose-rich water-soluble fractions obtained from a variety of steam-exploded agricultural residues could be readily used by the combined hydrolysis and fermentation approach resulting in butanediol yields of 0.4–0.5 g/g of reducing sugar utilized.
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    Applied microbiology and biotechnology 19 (1984), S. 384-386 
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    Notes: Summary Laboratory experiments using small raceway ponds have shown that Spirulina maxima can be adapted easily to grow in sea-water supplemented with nitrate, phosphate, bicarbonate, and Fe-EDTA. To prevent precipitate formation, phosphate was supplied by diffusion through a dialysis membrane; the amount of Na-bicarbonate added was low (100 ppm) and the pH was kept in the range 8.6–8.8 by bubbling CO2 into the culture. No significant differences have been noticed in productivity or in the chemical composition of the biomass between cultures in sea-water and in the standard bicarbonate medium. Cultures subjected to light/dark cycles of 12/12 h showed a higher respiration rate in sea-water than in the bicarbonate medium. The higher weight loss in the sea-water medium in the dark was counterbalanced by an increased synthesis of carbohydrates during the light period.
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    Notes: Summary The kinetics of growth and acid and solvent production are examined in batch fermentation of Clostridium acetobutylicum at pH between 4.5 and 6.0. At the lower pH, growth occurs in two consecutive phases and solvents are the main excreted metabolites. At the higher pH, there is a single growth phase with only acid formation. The influence of the pH can be correlated with a critical role of the concentration of undissociated butyric acid in the medium: cellular growth is inhibited above 0.5 g/l and solvent production starts at an undissociated acid level of 1.5 g/l. Reducing the intracellular acid dissociation by lowering the intracellular pH also favours the production of acetone and butanol.
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    Applied microbiology and biotechnology 19 (1984), S. 437-438 
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    Notes: Summary A Rhodotorula sp., isolated from soil, which showed a versttile capacity to degrade various aromatic and aliphatic hydrocarbons, was used to treat oil sludge. As a result of treatment, there was significant cecrease in BOD, COD and contents of various petroleum fractions. The susceptibility to degradation was in the following order: saturate fraction〉aromatic fraction〉asphaltic fraction.
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    Applied microbiology and biotechnology 20 (1984), S. 1-1 
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    Applied microbiology and biotechnology 20 (1984), S. 3-5 
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    Notes: Summary Chorismate, one of the key intermediates of aromatic amino acid biosynthesis, is excreted by the mutant Enterobacter aerogenes 62–1. It is shown that the bacteria immobilized in polyacrylamide gel accumulate chorismic acid in amounts comparable to those obtained by free cells. The accumulation was performed by batch processing, and the immobilized cells could be used for several sequential processes. However, the yield of excreted chorismate was reduced by about 50% subsequent to the initial cycle. Reactivation of the cells was attempted with precursors of chorismate and with DMSO as membran permeabilizing agent. In all cases it was not possible to increase the level of activity of the cells after they had been used.
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    Applied microbiology and biotechnology 20 (1984), S. 29-32 
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    Notes: Summary Succinic acid can just as well be replaced by citric acid in submerged fermentation of lysergic acid derivatives by a strain of Claviceps paspali. The highest alkaloid yields were obtained with a 1% citric acid concentration in the medium at a constant pH of 5.2. When the optimal pH was not maintained, growth was inhibited and all aspects of metabolic activity of the fungus were depressed.
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    Applied microbiology and biotechnology 20 (1984), S. 46-53 
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    Notes: Summary The cellulases produced under pH controlled fermentation conditions with 5% Solka Floc and cornsteep liquor as substrates by Trichoderma reesei wild type QM6a and two mutants, Rut-C30 and RL-P37, have been separated by isoelectric focusing in polyacrylamide gels. The total complement of secreted proteins of the two mutants was distinct from the parent. However, the number and isoelectric points of the various enzymes in the cellulase complex were unchanged in the mutants. All secreted proteins stained with Schiff's reagent which indicated they were glycoproteins. One mutant, Rut-C30, exhibited a dramatic shift in the CBH I proteins during the course of the fermentation. RL-P37 showed a two-fold increase in the specific activity of both the total cellulase complex and endoglucanase. In addition a productivity on the order of 100 IU/l/h was achieved. Co-produced with the cellulases were at least two acid proteases with differential activity towards azocoll and azocasein.
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    Applied microbiology and biotechnology 20 (1984), S. 72-76 
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    Notes: Summary Three strains of Cryptococcus terricolus have been examined for their ability to accumulate intra-cellular lipid. Of those only C. terricolus IFO 1322 was capable of accumulating substantial amounts (35–40% w/w) when cultivated in batch culture. The pattern of lipid accumulation was unusual in that the maximum rate of lipid synthesis was observed to occur during the exponential phase of growth when exogenous nitrogen was still available. Thus these results confirmed the earlier observations of Pedersen (1961; 1962a, b, c) that lipid levels in this organism were constitutively high. A preliminary biochemical analysis has failed to indicate why this unusual pattern of lipid accumulation occurs. The potential value of C. terricolus IFO 1322 for use in the production of single cell oil is discussed.
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  • 84
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    Applied microbiology and biotechnology 20 (1984), S. 77-82 
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    Notes: Summary The degradation of dimeric phenylpropanoid lignin model compounds using mixed bacterial cultures was studied. The six model compounds contained the most common linkages of lignin: β-O-4, β-β, β-5, and β-1. The results indicate that it is possible to enrich bacteria which are able to degrade all these compounds. Bacteria were also able to use these dimers as the sole source of carbon for growth. In view of these results it seems probable that bacterial inability to degrade polymeric lignin is due to the physical properties such as the molecular size of lignin.
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    Applied microbiology and biotechnology 20 (1984), S. 94-99 
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    Notes: Summary Thiobacillus ferrooxidans was immobilized by entrapment into calcium alginate matrix. The immobilized bacteria were used in packed-bed column reactors for the continuous oxidation of ferrous ion at pH 1.5. The presence of mineral salts resulted in a shorter lag period before a steady-state of about 95% iron oxidation was achieved. Parallel shake flask experiments were used to evaluate pH, mineral salts, and alginate toxicity as factors influencing biological iron oxidation. Manometric experiments indicated that the previous growth history of T. ferrooxidans was important in determining the rate of iron oxidation. Scanning electron microscopy and energy dispersive analysis of X-rays were used to characterize bacteria entrapped in calcium alginate and the enrichment of iron in the matrix.
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  • 86
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    Applied microbiology and biotechnology 20 (1984), S. 124-128 
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    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The production of α-amylase activity in the yeast Schwanniomyces castellii strain 1402 is repressed in the presence of the non-metabolizable glucose analogue, 2-deoxy-glucose. Selection for resistance to 2-deoxy-glucose after treatment with ethyl methane sulphonate (EMS) or UV light has yielded mutants displaing increased α-amylase activities. One such mutant, S. castellii strain 1436, was found to exhibit constitutive α-amylase activity in glucose-containing medium. This constitutive enzyme activity was also observed under pilot scale fermentation conditions when the pH was maintained constant at 5.5±0.1. The disaccharide maltose served as a stronger inducer of α-amylase activity than the natural substrate starch in both the wild type (1402) and mutant (1436) strains.
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  • 87
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    Applied microbiology and biotechnology 20 (1984), S. 146-149 
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    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The effect of yeast metabolism on the dispersion characteristics of a fluidised bed fermentor containing flocs of the yeast Saccharomyces carlsbergensis was investigated. Dispersion in the metabolizing fluidised yeast floc system was compared with the dispersion in an inert yeast floc system and in a glass bead system. Breakdown in plug-flow was found to occur in the metabolically active yeast bed when the flow rate was increased over a relatively narrow operating range (up to a dilution rate of 0.08 h-1). The superficial liquid velocity at which perfect mixing was approximated was some 18 times greater in the inert yeast floc system than in the metabolizing yeast floc system.
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  • 88
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    Applied microbiology and biotechnology 20 (1984), S. 150-154 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary During growth of Pleurotus on cotton straw both the straw in general and the lignin in particular were degraded. After 4 days of fungal growth, activity of laccase, catechol oxidase, peroxidase, and cellulase were detected. This activity, however, declined rapidly after 8–10 days of growth. Lignin degradation began after 10 days and reached a maximum after 21 days. It would seem that the preliminary action of laccase is a prerequisite for lignin degradation. The Pleurotus ostreatus strain ‘P3’ had no detectable laccase activity and showed very poor ability to degrade cotton straw and lignin. Water extract of cotton straw was found to be a potent inducer of laccase in liquid medium and had an effect much stronger than several small phenolic compounds. The degradation of washed cotton straw and lignin from this straw was lower than native straw, so was laccase activity on this medium. High carbon dioxide concentrations encouraged straw degradation by P. ostreatus ‘florida’ but severly limited lignin degradation. Other fungi including the known lignin degrader Phanarochaete chrysosporium were able to degrade up to 40% of cotton straw dry weight within 21 days of fungal growth. The percentage degradation of lignin, however, was very low (only 10% in 21 days). Pleurotus ostreatus ‘florida’ was able to degrade up to 56% of the lignin within this time. After treatment with P. ostreatus ‘florida’ almost four times as much glucose was released when the straw was treated with commercial cellulases, showing increased availability of cellulose. It is suggested that treatment with P. ostreatus ‘florida’ may be used to enrich low value food materials for ruminant animals.
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  • 89
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    Applied microbiology and biotechnology 20 (1984), S. 183-188 
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    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Test systems were set up in order to evaluate the ability of biomass from a continuous culture to form biofilms. A film-forming strain of Pseudomonas putida was used as the test organism. The adsorption of resting cells onto glass surfaces was measured in specially designed chambers containing 1 ml of cell suspension. Both the quantity and the physiological activity of the adsorbed cells, in terms of optical density after detachment and pH change of a substrate exposed to the adsorbed cells, were measured. The analysis of biomass from continuous cultures of Pseudomonas putida verified the suitability of the methods. Furthermore, other properties of importance to biofilm formation such as hydrophobicity and flocculation capacity of the cells were investigated. It was shown for samples deriving from different dilution rates that the cell adsorption rate drastically increased at dilution rates higher than the μmax of the culture. Simultaneously, higher values of hydrophobicity and flocculation capacity were observed. It was also shown that the age and thickness of the biofilm subsequently produced in the continuous culture influenced the metabolic activity per unit of biomass attached to the surface. The methods described in this investigation may facilitate the study of parameters important to biofilm formation as well as the metabolic activity of the attached biomass.
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  • 90
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    Applied microbiology and biotechnology 20 (1984), S. 213-217 
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    Notes: Summary The resting cells of methanogen strain HU could be used as biocatalyser for converting exoge nous NADP+ into NADPH, using either formate or hydrogen as electron donor. To enhance the conversion efficiency of NADPH from NADP+, several inhibitors of methylcoenzyme M reductase were used in order to avoid further oxidation of NADPH to CH4. When methyl viologen (7.5 μmol ml-1) was added to the reaction mixture (17 mg of dry cells, 2 mg Triton X-100, 294 μmol of Na-formate and 12 μmol of NADP+ per ml reaction mixture), 9.6 μmol ml-1 NADPH (80% yield) could be produced in a 2-h reaction, compared with 7.2 μmol ml-1 NADPH (60% yield) in a 6-h reaction in the absence of methyl viologen. Molecular hydrogen istead of formate also served as electron donor to convert NADP+ into NADPH. A gas mixture of H2/N2 (75/25) yielded 9.8 μmol ml-1 NADPH (82% yield) in a 3-h reaction in the absence of formate, suggesting that H2 might be a promising, inexpensive electron donor for this reaction system.
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  • 91
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    Applied microbiology and biotechnology 20 (1984), S. 161-165 
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    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The influence of the concentration of oxygen on lipase production by the fungus Rhizopus delemar was studied in different fermenters. The effect of oxygen limitation (≤ 47 μmol/l) on lipase production by R. delemar is large as could be demonstrated in pellet and filamentous cultures. A model is proposed to describe the extent of oxygen limitation in pellet cultures. Model estimates indicate that oxygen is the limiting substrate in shake flask cultures and that an optimal inoculum size for oxygen-dependent processes can occur. Low oxygen concentrations greatly negatively affect the metabolism of R. delemar, which could be shown by cultivation in continuous cultures in filamentous growth form (Doptimal=0.086 h-1). Continuous cultivations of R. delemar at constant, low-oxygen concentrations are a useful tool to scale down fermentation processes in cases where a transient or local oxygen limitation occurs.
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  • 92
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    Applied microbiology and biotechnology 20 (1984), S. 256-261 
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    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A minimal medium was used to investigate the triggers regulating the initiation of solvent production and differentiation in Clostridium acetobutylicum P262. The accumulation of acid end-products caused the inhibition of cell division and the initiation of solvent production and cell differentiation. Initiation only occurred with a narrow pH range. Glucose or ammonium limited cultures failed to achieve the necessary threshold of acid end-products and solvent production and differentiation were not initiated. The addition of acid end-products or ammonium to cultures containing suboptimal levels of glucose or nitrogen respectively, enhanced solvent production. Resuspension of cells in media containing the threshold level of acid end-products and residual glucose induced endospore formation. Glucose or ammonium limitation did not induce sporulation and there was a requirement for glucose and ammonium during solventogenesis and endospore formation. Initiation of solvent production and clostridial stage formation were essential for sporulation. The induction of endospore formation in C. acetobutylicum P262 differs from that in the aerobic endospore forming bacteria where sporulation is initiated by nutrient starvation.
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  • 93
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    Applied microbiology and biotechnology 20 (1984), S. 275-277 
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    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A fungus, Robillarda, sp. Y-20, which produces mainly, β-1,4-glucan glucanohydrolase (Cx-enzyme) in the culture filtrate, was isolated from soil. The specific activity of the Cx-enzyme was up to 4.9 times higher than that of Trichoderma reesei QM 9414.
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    Applied microbiology and biotechnology 20 (1984), S. 291-295 
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    Notes: Summary In our laboratory, EAPc-7 a strain having higher aspartase activity was derived from Escherichia coli ATCC 11303. For the improvement of l-aspartic acid productivity using EAPc-7 cells immobilized in χ-carrageenan, it was necessary to eliminate the fumarase activity which converts fumaric acid to l-malic acid. Several treatments for specifically eliminating fumarase activity from EAPc-7 cells were tested and it was found that when EAPc-7 cells were treated in a culture broth (pH 4.9) containing 50 mM l-aspartic acid at 45° C for 1 h, fumarase activity was almost completely eliminated without inactivation of the aspartase. The treated cells, immobilized in χ-carrageenan, were used for continuous production of l-aspartic acid from ammonium fumarate. The formation of l-malic acid was negligible and the half-life of the immobilized preparation was 126 days. Productivity of immobilized preparation of treated EAPc-7 cells in l-aspartic acid production was six times of that of the parent cell preparation.
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    Applied microbiology and biotechnology 20 (1984), S. 313-317 
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    Notes: Summary The steroid-hydroxylating activity during spore swelling prior to germination (I), during germ tube formation (II) and during branching of the growth hyphae (III) is two to five times that of the mycelium (IV) and control spores. The increased steroid-transforming activity is not correlated with the overall degradation of free amino acid pools but only with that of alanine, glutamate, arginine and proline. A higher ratio NADPH:(NADP++NADPH) was observed in development phases I, II, and III, which indicates a possible role of alanine, glutamate and other amino acids decomposed via glutamate, in NADPH generation and steroid-hydroxylase activation.
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  • 96
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    Notes: Summary Previous publications have revealed that a pretreatment of lignocellulosic wastes is necessary if they are to be employed as the hydrocarbon source of single cell protein production. A hot alkaline treatment is the most common. We have treated sugar cane bagasse pith with 1% NaOH solution at room temperature, at a NaOH/pith ratio of 10%. Different contact times were used in the experiments. The shortest contact period required for maximum protein production was 24 h at 25° C. A mixed culture of Cellulomonas sp. and Bacillus subtilis was used in the experiments. The values obtained for hemicellulose and cellulose in the treated pith did not differ greatly from those of untreated pith, in contrast the amount of lignin was 33% lower in the treated pith. The effect of reutilization of the alkaline liquor used for the pretreatment of pith upon protein production was also investigated. With four recyclings, there was a NaOH saving of 34.4 kg per 100 kg produced protein as compared to when the liquor was only used once. The quality of the resulting effluents, as measured by the chemical oxygen demand (COD), proved to be very similar for both types of treatment.
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    Applied microbiology and biotechnology 20 (1984), S. 356-359 
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    Notes: Summary The sporulation of the fungus Claviceps purpurea is connected with the change in its respiration rate which is effected by deficiency of dissolved oxygen tension. It stops the vegetative growth of the fungus and induces the formation of conidiophores with conidia production until glucose is exhausted. With exhaustion of glucose the conidiophores continue to produce conidia by transforming vegetative cell material into conidia. Therefore final conidial concentration in batch fermentation depends on these two processes which can be regulated by oxygen input.
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  • 98
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    Notes: Summary Continuing the investigation into possible yeast influence on ferment degradation of residual pesticides, two dicarboxymide antibotrytic fungicides (Iprodione and Procymidone), three acylanilide antiperonosporic fungicides (Benalaxyl, Furalaxyl and Ofurace) and two pyrethroid insecticides (Permethrin and Fenvalerate) were tested. Only the pyrethroids were degraded completely during fermentation.
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    Applied microbiology and biotechnology 20 (1984), S. 400-405 
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    Notes: Summary When G. oxydans ATCC 621-H was grown in batch culture in a complex medium with glucose, ketogluconates were produced when the pH in the culture was maintained at 5.5. Without pH control gluconate was the only product of glucose oxidation, but at pH 5.5 the gluconate so produced was further oxidized to ketogluconates. Production of ketogluconates started when glucose was almost completely exhausted. It was shown that the actual glucose and gluconate concentrations in the culture do not determine the onset of ketogluconate formation during growth. Both 2 and 5 ketogluconate were produced. Addition of CaCO3 to the medium favored the production of 5 ketogluconate. However, under these conditions minor quantities of 2 ketogluconate were also formed. The sequential production of gluconate and ketogluconates from glucose was not only restricted to G. oxydans ATCC 621-H. A number of G. oxydans strains when grown under standard conditions in a pH controlled batch culture, all produced ketogluconates from glucose via an intermediate accumulation of gluconate. Although the ratios of the ketogluconates produced varied from strain to strain, all strains produced both 2 and 5 ketogluconate.
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    Applied microbiology and biotechnology 20 (1984), S. 427-429 
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    Notes: Summary The highest production of extracellular cellulases (Filter paper activity, Carboxymethyl cellulase and β-glucosidase) by Trichoderma harzianum was achieved on delignified wheat straw. Glycerol at a concentration of one per cent strongly repressed the formation of all the cellulolytic components. Addition of cyclic AMP did not relieve the repression caused by glycerol but lowered the level of existing cellulase enzymes.
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