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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 155 (1990), S. 89-93 
    ISSN: 1432-072X
    Keywords: Pelobacter acetylenicus ; Acetobacterium woodii ; Methanobacterium bryantii ; Desulfovibrio desulfuricans ; Growth yield ; Maintenance coefficient ; Gibbs free energy ; YATP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The ethanol-oxidizing, proton-reducing Pelobacter acetylenicus was grown in chemostat cocultures with either Acetobacterium woodii, Methanobacterium bryantii, or Desulfovibrio desulfuricans. Ymax and me were determined from the total molar growth yields determined at growth (dilution) rates between 0.02 and 0.14 h-1. The individual growth yields of the partner organisms were determined from their numbers and cellular mass in the chemostat cocultures. The Gibbs free energy (ΔG=-16.3 kJ/mol ethanol) available to P. acetylenicus as well as its Ymax (1.7–2.2 g/mol ethanol) were almost constant in the different cocultures. P. acetylenicus shared 44–67% of the total biomass produced, whereas it shared only 19, 23, and 37% of the total Gibbs free energy (ΔG) available from ethanol oxidation coupled to sulfate reduction, methanogenesis, and homoacetogenesis, respectively. The residual 63–81% of the total available ΔG were shared by the H2 oxidizers which exhibited Ymax values being highest for A. woodii (6.6 g/mol acetate) 〉 D. desulfuricans (3.8 g/mol sulfide) 〉 M. bryantii (2.2 g/mol CH4). The results are discussed with respect to ATP generation and coupling of catabolism with cell production.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 155 (1990), S. 82-88 
    ISSN: 1432-072X
    Keywords: Homoacetogenesis ; Methanogenesis ; Sulfate reduction ; Caffeate reduction ; Nitrate reduction ; Interspecies H2 transfer ; Affinity ; H2 threshold ; “Critical” Gibbs free energy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The ethanol-oxidizing, proton-reducing Pelobacter acetylenicus was grown in chemostat cocultures with either Acetobacterium woodii, Methanobacterium bryantii, or Desulfovibrio desulfuricans. Stable steady state conditions with tightly coupled growth were reached at various dilution rates between 0.02 and 0.14 h-1. Both ethanol and H2 steady state concentrations increased with growth rate and were lower in cocultures with the sulfate reducer 〈 methanogen 〈 homoacetogen. Due to the higher affinity for H2, D. desulfuricans outcompeted M. bryantii, and this one A. woodii when inoculated in cocultures with P. acetylenicus. Cocultures with A. woodii had lower H2 steady state concentrations when bicarbonate reduction was replaced by the energetically more favourable caffeate reduction. Similarly, cocultures with D. desulfuricans had lower H2 concentrations with nitrate than with sulfate as electron acceptor. The Gibbs free energy (ΔG) available to the H2-producing P. acetylenicus was independent of growth rate and the H2-utilizing partner, whereas the ΔG available to the latter increased with growth rate and the energy yielding potential of the H2 oxidation reaction. The “critical” Gibbs free energy (ΔGc), i.e. the minimum energy required for H2 production and H2 oxidation, was-5.5 to-8.0 kJ mol-1 H2 for P. acetylenicus,-5.1 to-6.3 kJ mol-1 H2 for A. woodii,-7.5 to-9.1 kJ mol-1 H2 for M. bryantii, and-10.3 to-12.3 kJ mol-1 H2 for D. desulfuricans. Obviously, the potentially available energy was used more efficiently by homoacetogens 〉 methanogens 〉 sulfate reducers.
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 71 (1990), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Pelobacter acetylenicus accumulated only small amounts of H2 (〈 3.5 kPa) during fermentation of acetoin or acetylene to acetate and ethanol. Formate was also produced in small amounts (〈 0.5 mM). Growth on acetoin was retarded by addition of ethanol, but not by addition of H2 or formate. However, addition of H2 and/or formate resulted in increased production of 2,3-butanediol, whereas addition of H2-scavenging Methanospirillum hungatei resulted in production of acetate plus H2 (as CH4) instead of acetate plus ethanol. Growth yields were consistent with acetate kinase as the sole ATP-generating reaction. The results are discussed with respect to thermodynamics and ATP synthesis during substrate conversion.
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : American Institute of Physics (AIP)
    Review of Scientific Instruments 61 (1990), S. 1044-1054 
    ISSN: 1089-7623
    Source: AIP Digital Archive
    Topics: Physics , Electrical Engineering, Measurement and Control Technology
    Notes: A voltage detector and its connected focusing system for voltage measurements on integrated circuits by laser induced photoemission are presented. The capabilities of the system are analyzed theoretically and verified experimentally. Application to metal lines of submicrometer width and spacing is possible, combined with picosecond time resolution and a voltage sensitivity far exceeding that of electron beam probing. An excellent insensitivity to static crosstalk perturbations is demonstrated. Voltage contrast measurements and measurements of photoemission spectra have also been performed with this system.
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  • 5
    ISSN: 1432-203X
    Keywords: Solanum tuberosum ; anthocyanins ; gamma-irradiation ; protoplasts ; protoclones
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Callus cell lines of potato (Solanum tuberosum L. cv. Zarevo) were obtained from seedlings germinated from gamma-irradiated seeds (200 Gy). Some of these cell lines produce red-violet pigments which were identified as acylated anthocyanins. The major anthocyanin was determined to be peonidin 3-O-[6-O-(4-O-E-p-coumaroyl-rhamnosyl)-glucoside]-5-O-glucoside (“peonanin”). Single cell-derived protoclones from non-pigmented protoplasts sometimes also gave rise to pigmented cell clusters thus indicating that the changes in the expression of the anthocyanin pathway can also occur after the stage of initial callus induction.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Empirical economics 16 (1991), S. 233-252 
    ISSN: 1435-8921
    Source: Springer Online Journal Archives 1860-2000
    Topics: Economics
    Notes: Abstract The present paper examines the role of inventories for the short run adjustment behavior of firms. A theoretical model of a monopolistic firm carrying inventories that includes costs of adjusting output is examined. The model is tested empirically by using business survey data collected by the IFO-Institute, Munich. It is shown, that if data on individual firms are used and econometric estimation techniques are applied that properly take this into account, the estimates derived are fully compatible with the appealing idea of production smoothing by inventories.
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  • 7
    ISSN: 1573-5044
    Keywords: acylated anthocyanins ; cinnamic acids ; daucus carota (wild carrot) ; flavonoid intermediates ; HPLC separations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Anthocyanins isolated and characterized from the wild carrot suspension cultures used here were 3-O-β-D-glucopyranosyl-(1→6)-[β-D-xylopyranosyl-(1→2)-]β-D〈-galactopyranosylcyanidin (1), 3-O-[β-D- xylopyranosyl-(1→2)-β-D-galactopyranosyl]cyanidin (2), 3-O-(6-O-sinapoyl)-β-D-glucopyranosyl-(1→6)-[β-D- xylopyranosyl-(1→2)-]β-D-galactopyranos ylcyanidin (3), 3-O-(6-O-feruoyl)-β-D-glucopyranosyl-(1→6)-[β- D-xylopyranosyl-(1→2)-]β-D-galactopyranosylcyanidin (4), 3-O-(6-O-coumaroyl)-β-D-glucopyranosyl-(1→6)- [β-D-xylopyranosyl-(1→2)-]β-D-galactopyrano sylcyanidin (5), 3-O-[6-O-(3,4,5-trimethoxycinnamoyl)]-β- D-glucopyranosyl-(1→6)-[β-D-xylopyranosyl-(1→2)-]β-D-galactopyranosylcyanidin (6), 3-O-[6-O-(3,4-dime- thoxycinnamoyl)]-β-D-glucopyranosyl-(1→6)-[β-D-xylopyranosyl-(1→2)-]β-D-galactopyranosylcyanidin (7), 3-O-[(6-O-sinapoyl)-β-D-glucopyranosyl-(1→6)-β-D-galactopyranosyl]cyanidin (8), and 3-O-(β-D-galactopyranosyl)cyanidin (9). Except when cinnamic acids were provided in the culture medium, the major anthocyanin present in the two clones examined was 2. When the naturally occurring and some non-naturally occurring cinnamic acids were provided individually in the medium, 1 and 2 were minor components and the anthocyanin acylated with the supplied cinnamic acid, namely 3, 4, 5, 6, or 7 was the major anthocyanin present in the tissue. When caffeic acid was provided the major anthocyanin in the tissue was 4, thereby suggesting that the caffeic acid was methylated before its use in anthocyanin biosynthesis. Other cinnamic acids supplied had limited effects on the anthocyanins accumulated and appeared not to result in the accumulation of new anthocyanins by the tissue. Thus the tissue can use some but not all analogues of sinapic acid to acylate anthocyanins. Additional anthocyanins were detected in extracts of the wild carrot tissue cultures using mass spectrometry (both MS/MS and HPLC/MS). The additional compounds detected have also been found in cultures of black carrot, an Afghan cultivar of Daucus carota ssp. sativa and the flowers of wild carrot giving no evidence for qualitative differences in the anthocyanins synthesized by subspecies, cell cultures from subspecies, or clones from cell cultures. There are major differences in the amounts of individual anthocyanins found in cultures from different subspecies and in different clones from cell cultures. Here anthocyanins without acyl groups were usually found in the tissues and their accumulation is discussed. On the basis of the structures of the isolated anthocyanins, a likely pathway from cyanidin to the accumulated anthocyanins is proposed and discussed.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Parasitology research 78 (1992), S. 56-59 
    ISSN: 1432-1955
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Experimental simultaneous infections ofAnopheles stephensi (Diptera: Culicidae) withNosema algerae (Microsporida: Nosematidae) andPlasmodium yoelli nigeriensis under standardized laboratory conditions showed partial suppression of the malaria parasite. At 9 days after an infective bloodmeal, the oocysts in the midgut were counted; 12.1%–66.6% of the double-infected mosquitoes exhibited no oocysts, whereas only 4.5%–12% of the control group showed no oocysts. The mean reduction in oocyst numbers under the influence ofNosema was 84.68%. At 14 days after infection withPlasmodium, the amount of sporozoites was examined; their mean reduction in eight experiments was 70%.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Parasitology research 78 (1992), S. 168-171 
    ISSN: 1432-1955
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract To quantify the effect ofNosema algerae (Microsporida, Nosematidae) on the development ofPlasmodium falciparum inAnopheles stephensi (Diptera, Culicidae), we carried out infection experiments under standardized laboratory conditions. Apart from a mean reduction of 69% in oocyst development, smaller numbers of oocysts and fewer sporozoites were found in theNosema-infected mosquitoes. In addition, nosematosis resulted in higher mortality. The potential role ofNosema algerae as a biological control agent is discussed.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Parasitology research 79 (1993), S. 378-384 
    ISSN: 1432-1955
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Several components were tested for their ability to replace human serum in cultures ofPlasmodium falciparum set up for the development of gametocytes. Besides a serum-free medium, A*I*M*V (Gibco BRL), RPMI medium supplemented with commercially available serum substitutes was used to culture gametocytes. The following substances served as serum replacements: Basal Medium Supplement (Biochrom), Ultroser G (Gibco BRL) and Nutridoma-SR (Boehringer Mannheim). All serum-free additives supported some parasite growth, but only in RPMI supplemented with Nutridoma-SR were morphologically mature gametocytes obtained. The asexual forms developed almost as well as in RPMI with human serum added.
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