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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 123 (1994), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Strains of Escherichia coli lacking serine transacetylase or a positive regulator (Cys B protein) of the assimilatory sulfate reduction (ASR) pathway were unable to assimilate sulfonate-S, wihle single mutants in O-acetyl-L-serine sulfhydrylase (either ‘A’ or ‘B’) were able to do so. Mutants unable to reduce sulfate to sulfite were nonetheless able to form and accumulate sulfide and then cysteine from sulfonates, while strains lacking sulfite reductase were not. Thus terminal portions of the ASR pathway are involved in reduction of sulfonate-S to that of cysteine. E. coli K-12 formed cysteine more slowly, and accumulated lesser amounts of it with sulfonate-sulfur than it did from either sulfate or sulfite. These observations are consistent with our earlier report that sulfate is the preferred sulfur source when present simultaneously with a sulfonate.
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  • 2
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The organosulfur compound taurine (2-aminoethanesulfonate), but no other sulfonates tested, served as the sole carbon, sulfur and energy source for the growth of eight Rhodococcus strains examined, taurine's nitrogen was utilized as well. Several sulfonates that were not used as sole sources of carbon, sulfur and energy were nevertheless able to serve as the sole sulfur source for growth when succinate or acetate were carbon and energy sources. Taurine consumption resulted in release of sulfite and ammonium ion into growth medium. Taurine utilization appeared to be an inducible trait. The sulfonate utilization ability appears to be a heretofore unrecognized trait of rhodococci.
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    FEMS microbiology letters 114 (1993), S. 0 
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract Three sulfonates were tested for their ability to serve as nutrients for Hansenula wingei, Rhodotorula glutinis, Trigonopsis variabilis and Saccharomyces cerevisiae. Cysteate, taurine and isethionate, under aerobic conditions, could be utilized as sources of sulfur, although in some instances final cell yields were less than those obtained with an equimolar amount of sulfate-sulfur. Sulfonate assimilation by S. cerevisiae resembled that of bacteria (reported earlier by us) in several aspects: first, sulfate-S was used in preference to that of sulfonate, when both were present; second, mutants unable to use a source of sulfur because of deficiencies in ATP sulfurylase, adenylylsulfate kinase (APS kinase) or PAPS reductase were able to utilize sulfonates; and third, mutants deficient in sulfite reductase were unable to utilize sulfonates.
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 324 (1986), S. 367-369 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Cultures (A650 = 0.8) mutagenized with N-methyl-N'-nitro-Af-nitrosoguanidine (0.3 mg ml"1) for 60 min were diluted and plated on LTY agar (Fig. 2 legend); 48 spreading-deficient clones were selected on the basis of colony morphology. The colonies formed by gliding cells expand rapidly, are thin and ...
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 30 (1958), S. 91-118 
    ISSN: 1432-072X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 152 (1989), S. 387-392 
    ISSN: 1432-072X
    Keywords: Sulfate assimilation ; Regulation of sulfate assimilation ; Sulfonolipids ; Gliding bacteria ; Cytophaga johnsonae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We have studied the regulation of sulfate assimilation by the gliding bacterium Cytophaga johnsonae in which 20% of the total sulfur is in the sulfornate moiety of sulfonolipid. Added cystine inhibited sulfate uptake and growth with cystine as sulfur source resulted in a repression of sulfate uptake. However, low concentrations of cystine preferentially repressed the terminal reactions of sulfate assimilation responsible for cysteine synthesis while allowing the transport and activation of sulfate for sulfonolipid synthesis. The significance of this novel pattern of regulation in bacteria is discussed.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 160 (1993), S. 121-125 
    ISSN: 1432-072X
    Keywords: Gliding motility ; Colony spreading ; Raft formation ; Inhibitory sugar ; Bead movement ; Cytophoga johnsonae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract It is a common observation that gliding bacteria form raised, smooth-edged colonies on nutrient-rich media, and typical thin, spreading, uneven-edged colonies on nutrient-poor media. An earlier study of the effect of different sugars on colony spreading by Cytophaga johnsonae was expanded to include the effects of several sugars and other organic compounds on the motility of groups of cells (“rafts”), and latex bead movement on cells' surfaces. When the structures of those sugars that did, or did not, affect raft formation and colony spreading were compared, it was noted that those sugars that inhibited these two manifestations of gliding motility all possessed a common sub-structure, that found in the portion of glucopyranose comprising carbons 3, 4, 5, and 6. If these structural features were altered chemically or stereochemically, the resulting molecule had little to no effect on motility. The differential effects of some compounds on raft formation, colony spreading, and bead movement are noted. A regulatory mechanism that would turn off motility in the presence of an inhibitory sugar is implicated, and the relevance of such a system to the life of the organism is discussed. We report, as well, additional compounds that will serve as carbon and energy sources for C. johnsonae.
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  • 8
    ISSN: 1432-072X
    Keywords: Sulfonate utilization ; Assimilatory sulfate reduction ; Sulfonate-sulfur assimilation ; Escherichia coli K-12
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Selected biochemical features of sulfonate assimilation in Escherichia coli K-12 were studied in detail. Competition between sulfonate-sulfur and sulfur sources with different oxidation states, such as cysteine, sulfite and sulfate, was examined. The ability of the enzyme sulfite reductase to attack the C-S linkage of sulfonates was directly examined. Intact cells formed sulfite from sulfonate-sulfur. In cysteine-grown cells, when cysteine was present with either cysteate or sulfate, assimilation of both of the more oxidized sulfur sources was substantially inhibited. In contrast, none of three sulfonates had a competitive effect on sulfate assimilation. In studies of competition between different sulfonates, the presence of taurine resulted in a decrease in cysteate uptake by one-half, while in the presence of isethionate, cysteate uptake was almost completely inhibited. In sulfite-grown cells, sulfonates had no competitive effect on sulfite utilization. An E. coli mutant lacking sulfite reductase and unable to utilize isethionate as the sole source of sulfur formed significant amounts of sulfite from isethionate. In cell extracts, sulfite reductase itself did not utilize sulfonate-sulfur as an electron acceptor. These findings indicate that sulfonate utilization may share some intermediates (e.g. sulfite) and regulatory features (repression by cysteine) of the assimilatory sulfate reductive pathway, but sulfonates do not exert regulatory effects on sulfate utilization. Other results suggest that unrecognized aspects of sulfonate metabolism, such as specific transport mechanisms for sulfonates and different regulatory features, may exist.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 159 (1993), S. 440-444 
    ISSN: 1432-072X
    Keywords: Sulfonate ; Sulfur assimilation ; Sulfur cycle ; Comamonas acidovorans
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Bacteria able to use cysteate, taurine or isethionate as sole source of carbon and energy were isolated from the soil. Tests of sulfur assimilation showed that sulfonate sulfur and sulfate sulfur supported comparable cell yields. Methanesulfonate, 1-dodecanesulfonate and p-toluenesulfonate also served as sole source of sulfur for strain I91, identified as Comamonas (Pseudomonas) acidovorans. Competition studies with strain I91 showed that the presence of sulfate inhibits cysteate, isethionate or taurine incorporation. Pseudomonas aeruginosa PAO1, Comamonas acidovorans 14 and 105, and Acidovorax (Pseudomonas) facilis 332 used cysteate, isethionate, or taurine as sole source of sulfur while P. aeruginosa PAO716 and PAO718 used only taurine.
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  • 10
    ISSN: 1432-072X
    Keywords: Gliding motility ; Peptidoglycan ; Cytophaga ; Surface growth
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The peptidoglycan sacculi of surface-grown Cytophaga johnsonae had associated with them a large amoutn of protein (the major species is 50 kDa) whereas sacculi from liquid-grown cells had little or no attached protein. The 50 kDa protein was localized in the outer membrane of liquid-grown cells. A portion of this membrane-derived 50 kDa protein was attached to the peptidoglycan only when the cells made contact with the substratum. Protein synthesis did not appear to be required for attachment as the process was not inhibited by chloramphenicol. Association of the 50 kDa protein with the peptidoglycan in response to cell contact with the substratum is suggested.
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