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  • 11
    ISSN: 1432-1432
    Keywords: Symbiosis ; Plant mitochondria ; 5S RNA ; Evolution ; Purple bacteria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The complete nucleotide sequences of 5S ribosomal RNAs fromRhodocyclus gelatinosa, Rhodobacter sphaeroides, andPseudomonas cepacia were determined. Comparisons of these 5S RNA sequences show that rather than being phylogenetically related to one another, the two photosynthetic bacterial 5S RNAs share more sequence and signature homology with the RNAs of two nonphotosynthetic strains.Rhodobacter sphaeroides is specifically related toParacoccus denitrificans andRc. gelatinosa is related toPs. cepacia.These results support earlier 16S ribosomal RNA studies and add two important groups to the 5S RNA data base. Unique 5S RNA structural features previously found inP. denitrificans are present also in the 5S RNA ofRb. sphaeroides; these provide the basis for subdivisional signatures. The immediate consequence of our obtaining these new sequences is that we are able to clarify the phylogenetic origins of the plant mitochondrion. In particular, we find a close phylogenetic relationship between the plant mitochondria and members of the alpha subdivision of the purple photosynthetic bacteria, namely,Rb. sphaeroides, P. denitrificans, andRhodospirillum rubrum.
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 95 (1987), S. 131-142 
    ISSN: 1432-1424
    Keywords: Synechococcus ; permeability ; ammonia ; methylamine ; ammonium transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Permeabilities of ammonia (NH3), methylamine (CH3NH2) and ethylamine (CH3CH2NH2) in the cyanobacterium (cyanophyte)Synechococcus R-2 (Anacystis nidulans) have been measured. Based on net uptake rates of DCMU (dichlorophenyldimethylurea) treated cells, the permeability of ammonia was 6.44±1.22 μm sec−1 (n=13). The permeabilities of methylamine and ethylamine, based on steady-state14C labeling were more than ten times that of ammonia (P methylamine=84.6±9.47 μm sec−1 (76),P ethylamine=109±11 μm sec−1 (55)). The apparent permeabilities based on net uptake rates of methylamine and ethylamine uptake were significantly lower, but this effect was partially reversible by ammonia, suggesting that net amine fluxes are rate limited by proton fluxes to an upper limit of about 700 nmol m−2 sec−1. Increasing concentrations of amines in alkaline conditions partially dissipated the pH gradient across the cell membrane, and this property could be used to calculate the relative permeabilities of different amines. The ratio of ethylamine to methylamine permeabilities was not significantly different from that calculated from the direct measurements of permeabilities; ammonia was much less effective in dissipating the pH gradient across the cell membrane than methylamine or ethylamine. An apparent permeability of ammonia of 5.7±0.9 μm sec−1 could be calculated from the permeability ratio of ammonia to methylamine and the experimentally measured permeability of methylamine. The permeability properties of ammonia and methylamine are very different; this poses problems in the interpretation of experiments where14C-methylamine is used as an ammonia analogue.
    Type of Medium: Electronic Resource
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  • 13
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    Detroit, Mich. : Periodicals Archive Online (PAO)
    Technology and Culture. 32:2 (1991:Apr.) 414 
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  • 14
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    Unknown
    Detroit, Mich. : Periodicals Archive Online (PAO)
    Technology and Culture. 34:3 (1993:July) 682 
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  • 15
    Electronic Resource
    Electronic Resource
    Springer
    Archives of environmental contamination and toxicology 15 (1986), S. 519-523 
    ISSN: 1432-0703
    Source: Springer Online Journal Archives 1860-2000
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Medicine
    Notes: Abstract The toxicity and possible accumulation of ruthenium nitrosyl complexes by marine bacteria and test organisms have been studied, A range of these complexes show no toxic effects towardsEscherichia coli K12 at concentrations of mM and below. Yeasts are more sensitive, showing effects on growth at 10 ΜM. The ruthenium nitrosyl complexes tested are unable to permeate the cytoplasmic membrane ofE. coli. This may account for their lack of toxicity. However, these compounds did not have significant inhibitory effects on Mg2+-ATPase activity in cell-extracts, I50 values lying in the range 2 to 125 Μmol(mg protein)−1. Marine bacteria are capable of taking up ruthenium complexes from simulated effluent, but this cannot be demonstrated in the presence of sediment which competes effectively for binding of complexes. There is minimal likelihood of concentration of ruthenium compounds from effluents by marine bacteria.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 91 (1973), S. 255-272 
    ISSN: 1432-072X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. Chromatium was unable to use any amino acids as carbon source, and only glutamate, glutamine and aspartate as nitrogen sources. 2. Addition of individual amino acids to otherwise adequate medium at concentrations of 5 mM did not inhibit growth. 3. Radioactive leucine and valine were incorporated only into cell protein during growth. Only leucine was labelled following growth in radioactive leucine but both valine and leucine were labelled following growth in valine. 4. After labelled alanine incorporation, radioactivity was found in the lipid and nucleic acid fractions as well as in protein, but over 70% of the counts recovered in the protein fraction were in alanine. 5. Growth and short-term uptake experiments showed reduction of leucine uptake in the presence of valine or isoleucine. Uptake of leucine and alanine was light-stimulated and reduced by chloramphenicol. 6. No evidence of induction of amino acid uptake systems was found, and amino acid converting enzymes, as well as some key biosyntehtic activities, were not affected by growth in amino-acid-containing media. 7. It is suggested that the limited use made of amino acids by Chromatium is due to absence of high-affinity transport systems, to limited product inhibition of key biosynthetic enzymes, and to restricted capacity for metabolic conversion of exogenous compounds.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 59 (1967), S. 104-112 
    ISSN: 1432-072X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary 1. The substrate-dependent oxygen uptake of Chromatium D has been measured. Although the rates observed were only of the order of 1 μmole/hour x mg dry weight, they are comparable with the rates found for other photosynthetic bacteria. 2. Light inhibits the rate of O2 consumption of suspensions equilibrated with excess substrate, but may stimulate the rates in previously starved suspensions. 3. Prolonged aeration of suspensions of Chromatium with thiosulfate leads to accumulation of sulfur globules in the cells, and does not lead to a rapid loss of viability. 4. Measurements of ATP content of suspensions after exposure to air indicate a limited capacity for oxidative phosphorylation in Chromatium. The failure of aerobic growth in Chromatium is probably due to a combination of factors such as low Q O 2 and low phosphorylation efficiency.
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 130 (1981), S. 175-179 
    ISSN: 1432-072X
    Keywords: Acetate ; pH gradients ; Membrane permeability ; Cyanobacteria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Mutants of Synechococcus and of Aphanocapsa which were unable to activate acetate have been used to demonstrate that acetate entered the cells rapidly in darkness, and to a greater extent in light. Total internal concentrations under different conditions can be explained if acetic acid equilibrates rapidly across the cell membrane while acetate ion is strongly hindered. Acetate as well as other weak acids such as 5,5-dimethyl-2,4-oxazolidenedione can therefore be used as a probe of internal pH in these mutants. The intracellular pH was maintained at about 7.1 in darkness and 7.6 in light when external pH was varied from 6.8–8.0 No carrier involved in acetic acid equilibration could be demonstrated. Of other organic acids investigated, only propionate distributed in accordance with pH differences between the cells and surrounding fluid. The low uptake rates of glycolate, pyruvate and leucine appeared limited by slow movement of molecules into the cells.
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 102 (1975), S. 23-28 
    ISSN: 1432-072X
    Keywords: Anacystis nidulans ; Phosphate Limitation ; Photosynthetic Pigments ; Alkaline Phosphatase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Anacystis nidulans (Synechococcus) was maintained in a medium of low phosphate concentration (0.1 mM) and grew with a normal doubling time of 5 hrs at 30°C. Such cultures ahd a normal pigment composition and alkaline phosphatase was detectable at low specific activities only. The onset of phosphate-limited growth occurred when the phosphate concentration in the medium fell to a value below 4 μM (the limit of accurate determination by the assay method used) and resulted in increases in alkaline phosphatase activity, reaching a final 10 to 15 fold increase in specific activity after a period of several hours. Marked changes in the overall pigment composition occurred in this period of growth restriction. The addition of phosphate to such cultures resulted in a halt in synthesis of the enzyme and the restoration of normal pigmentation before growth resumed at the normal rate. Several organic phosphate esters could replace inorganic phosphate for growth and were also hydrolyzed by the partially purified enzyme, but growth rates were characteristically lower and the specific activity only 3 to 4 fold higher than in cultures grown in phosphate excess. Studies with the partially purified enzyme suggested that it differed in some of its properties from other alkaline phosphatases described in the literature.
    Type of Medium: Electronic Resource
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  • 20
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 164 (1995), S. 337-345 
    ISSN: 1432-072X
    Keywords: Key wordsRhodopseudomonas palustris ; Aryl-CoA ligase ; Thioesterase ; Anaerobic degradation of aromatic compounds ; Cyclohexane carboxylate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Cyclohexane carboxylate supported relatively rapid growth (doubling times 7–8 h) of Rhodopseudomonas palustris under oxic or photosynthetic conditions, but did not serve as a substrate for either of the known aromatic CoA ligases. A CoA ligase that thioesterifies cyclohexane carboxylate was partially purified and did not cross react immunologically with the two CoA ligases purified previously from this bacterium. Crude extracts of R. palustris cells grown with a range of aromatic or alicyclic acids contained a dehydrogenase that reacted with cyclohexane carboxyl-CoA or cyclohex-1-ene carboxyl-CoA, using 2,6-dichlorophenolindophenol or ferricenium ion as electron carrier. This activity was not detected in extracts of adipate-, glutamate-, or succinate-grown cells. No oxidation or reduction of nonesterified cyclohexane carboxylate or cyclohexene carbocylate was detected in extracts of cells grown with aromatic or aliphatic substrates, neither aerobically nor anaerobically. A constitutively expressed thioesterase that hydrolyzed cyclohexane carboxyl-CoA and also some alicyclic and aliphatic CoA derivatives was purified and characterized. The enzyme had little or no activity on benzoyl-CoA or 4-hydroxybenzoyl-CoA. The presence of a thioesterase that effectively hydrolyzes cyclohexane carboxyl-CoA suggests that transient production of cyclohexane carboxylate is a physiological response to temporary excess of reductant during metabolism of aromatic compounds.
    Type of Medium: Electronic Resource
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