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  • 1
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    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Ultramicroscopy 19 (1986), S. 408 
    ISSN: 0304-3991
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Electrical Engineering, Measurement and Control Technology , Natural Sciences in General , Physics
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  • 3
    ISSN: 0022-1910
    Keywords: Arthropod immunity ; Pacifastacus leniusculus ; degranulation ; haemocyte ; prophenoloxidase activating system
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 107 (1993), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract The cyanobacterium Nostoc sp. strain PCC 73102, cultured under nitrogen-fixing conditions, was investigated for the occurrence of ferrodoxins by SDS-PAGE/Western immunoblots using antisera directed against both a major plant-type and a bacterial-type ferredoxin purified from Anabaena variabilis. Immunocytological labelling and transmission electron microscopy were used to study the distribution of both types of ferredoxins in the Nostoc cells. SDS-PAGE/Western immunoblots revealed two proteins/polypeptides in the Nostoc strain, immunologically related to two soluble ferredoxins purified from Anabaena variabilis: the major plant-type ferredoxin (Fd I) and a bacterial-type ferredoxin (Fd III). Immunolocalization showed a uniform distribution of the plant-type and the bacterial-type ferredoxin in both the photosynthetic vegetative cells and in the nitrogen-fixing heterocysts, with no specific association with any subcellular inclusions. Using the particle analysis of an image processor, the labelling associated with the vegetative cells, expressed as number of gold particles per cell area, was found to be only slightly higher (1.2x) or almost twice as high (1.9x) compared to the heterocysts for the major plant-type and the bacterial-type ferredoxin, respectively.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Applied microbiology and biotechnology 50 (1998), S. 153-160 
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract In discussions about alternatives to our current fossil energy sources, basic and applied research leading to biological production of molecular hydrogen utilizing cyanobacteria deserves serious attention. In these oxygenic phototrophic bacteria, hydrogen can be produced by the activity of either nitrogenases or reversible/bidirectional hydrogenases. Knowledge of the physiological and molecular basis of some of the processes involved in hydrogen metabolism in these peculiar microorganisms has increased during the last decade. However, further efforts are required in basic as well as applied research in order to obtain a clear impression of these processes and their regulation. This information might then constitute the basis for optimizing the efficiency of hydrogen evolution by cyanobacteria. Progress might be achieved by screening more cyanobacterial strains for their ability to produce and evolve hydrogen, by genetically manipulating specific strains as well as by improving the conditions for cultivation in bioreactors.
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  • 6
    ISSN: 1432-2048
    Keywords: Anabaena ; Cyanobacteria ; Glutamine synthetase ; Immuno-gold localization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Localization of glutamine synthetase in thin sections of nitrogen-fixing Anabaena cylindrica was performed using immuno-gold/transmission electronmicroscopy. The enzyme was present in all of the three cell types possible; vegetative cells, heterocysts and akinetes. The specific gold label was always more pronounced in heterocysts compared with vegetative cells, and showed a uniform distribution in all three types. No specific label was associated with subcellular inclusions such as carboxysomes, cyanophycin granules and polyphosphate granules. When anti-glutamine synthetase antiserum was omitted, no label was observed.
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  • 7
    ISSN: 1432-2048
    Keywords: Carbon dioxide fixation ; Citrulline ; Coralloid roots ; Cycads (nitrogen fixation) ; Nitrogen fixation ; Nitrogen transport ; Nostoc
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Freshly detached coralloid roots of several cycad species were found to bleed spontaneously from xylem, permitting identification of products of nitrogen transfer from symbiotic organ to host. Structural features relevant to the export of fixed N were described for Macrozamia riedlei (Fisch. ex Gaud.) Gardn. the principal species studied. Citrulline (Cit), glutamine (Gln) and glutamic acid (Glu), the latter usually in a lesser amount, were the principal translocated solutes in Macrozamia (5 spp.), Encephalartos (4 spp.) and Lepidozamia (1 sp.), while Gln and a smaller amount of Glu, but no Cit were present in xylem sap of Bowenia (1 sp.),and Cycas (2 spp.). Time-course studies of 15N enrichment of the different tissue zones and the xylem sap of 15N2-pulse-fed coralloid roots of M. riedlei showed earlier 15N incorporation into Gln than into Cit, and a subsequent net decline in the 15N of Gln of the coralloid-root tissues, whereas Cit labeling continued to increase in inner cortex and stele and in the xylem sap. Hydrolysis of the 15N-labeled Cit and Gln consistently demonstrated much more intense labeling of the respective carbamyl and amide groups than of the other N-atoms. Coralloid roots of M. riedlei pulse-fed 14CO2 in darkness showed 14C labeling of aspartic acid (Asp) and Cit in all tissue zones and of Cit of xylem bleeding sap. Lateral roots and uninfected apogeotropic roots of M. riedlei and M. moorei also incorporated 14CO2 into Cit. The 14C of Cit was restricted to the carbamyl-C. Comparable 15N2 and CO2-feeding studies on corallid roots of Cycas revoluta showed Gln to be the dominant product of N2 fixation, with Asp and alanine as other major 14C-labeled amino compounds, but a total absence of Cit in labeled or unlabeled form.
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  • 8
    ISSN: 1432-2048
    Keywords: Cyanobacterium ; Cycad ; cyanobacterium symbiosis ; Cycas ; Glutamine synthetase ; Symbiosis ; Zamia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Nitrogen-fixing cyanobacteria inhabit the zone between the inner and outer cortex of cycad coralloid roots. In the growing tip of such roots the cyanobacterial heterocyst frequency, nitrogenase activity (C2H2-reduction) and glutamine synthetase activity (both transferase and biosynthetic) were comparable to those found in freeliving cyanobacteria. The relative level of glutamine synthetase protein and its pattern of cellular/subcellular localization in heterocysts and vegetative cells were also similar to those of free-living cyanobacteria. However, there was a progressive decline in nitrogenase activity along the coralloid root with maximum reduction occurring in the regions farthest from the growing tip. A similar but less pronounced pattern was observed for glutamine synthetase activity. Distribution of glutamine synthetase protein in cyanobacteria in the first 2–3 mm of the root tip indicated a slight decrease in the heterocysts and vegetative cells. However, the overall level of cyanobacterial glutamine synthetase protein did not change because of a drastic increase in the numbers of heterocysts, which contain a proportionally higher level of glutamine synthetase than the vegetative cells.
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  • 9
    ISSN: 1432-2048
    Keywords: Ammonium transport ; Anabaena ; Cycad-cyanobacterium symbiosis ; Cyanobacterium ; Cycas ; Methylammonium transport ; Symbiosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Using the ammonium analogue 14CH3NH 3 + , ammonium transport was studied in the cyanobiont cells freshly isolated from the root nodules of Cycas revoluta. An L-methionine-dl-sulphoximine (MSX)-insensitive ammonium-transport system, which was dependent on membrane potential (ΔΨ), was found in the cyanobiont. However, the cyanobiont was incapable of metabolizing exogenous 14CH3NH 3 + or NH 4 + because of the absence of another ammonium-transport system responsible for the uptake of ammonium for assimilation via glutamine synthetase (EC 6.3.1.2). Such a modification seems to be the result of symbiosis because the free-living cultured isolate, Anabaena cycadeae, has been shown to possess both the ammonium-transport systems.
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  • 10
    ISSN: 1615-6102
    Keywords: Carbamyl phosphate synthetase ; Immunogold localization ; Heterocyst ; Nostoc ; Vegetative cell
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Free-living nitrogen-fixingNostoc PCC 73102 cells, a filamentous heterocystous cyanobacterium originally isolated from the cycadMacrozamia, were grown without or with the addition of either citrulline or ornithine and examined for the presence of carbamyl phosphate synthetase (CPS) by SDS-PAGE and Western immunoblots. Transmission electron microscopy and immunocytochemical labelling were used to study the cellular and subcellular distribution of CPS in theNostoc cells. Western immunoblots revealed that a polypeptide with a molecular weight of approximately 130 kDa was immunologically related to CPS purified fromE. coli. Nitrogen-fixingNostoc 73102 cultures grown without or with the addition of either citrulline or ornithine showed no differences in their CPS-polypeptide levels, indicating no regulatory effect on the CPS-protein level by these two amino acids. Immunolocalization demonstrated that the CPS protein was located both in vegetative cells and heterocysts, subcellularly evenly distributed over the two cell-types. Using the particle analysis of an image processor and cells grown both without or with addition of either citrulline or ornithine, about 2.5 times more CPS-gold labelling per cell area were observed in the photosynthetic vegetative cells compared to the nitrogen-fixing heterocysts.
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