Literature DB >> 4142029

Effect of uncoupling agents and respiratory inhibitors on the growth of Streptococcus agalactiae.

M N Mickelson.   

Abstract

2,4-Dinitrophenol, dicoumarol, carbonylcyanide, m-chlorophenyl-hydrazone and pentachlorophenol all depressed aerobic molar growth yields of Streptococcus agalactiae to values equal to, or less than, those supported by substrate level phosphorylation. When the only source of energy was from substrate phosphorylation (anaerobic growth conditions), there was also a severe depression of the molar growth yield by the same four uncoupling agents. These results indicate that the effect of these agents is to uncouple both substrate and oxidative phosphorylation in S. agalactiae. Amytal inhibited glucose utilization, reduced the amount of O(2) used per mole of substrate and reduced the molar cell yield to that supported by substrate phosphorylation. Atebrin inhibited the respiration rate, but final O(2) consumed per mole of substrate was unchanged, and the respiration was coupled to biosynthesis. Rotenone had no effect on respiration, substrate utilization, or on molar growth yields.

Entities:  

Mesh:

Substances:

Year:  1974        PMID: 4142029      PMCID: PMC245833          DOI: 10.1128/jb.120.2.733-740.1974

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  17 in total

1.  Coupling of phosphorylation to electron and hydrogen transfer by a chemi-osmotic type of mechanism.

Authors:  P MITCHELL
Journal:  Nature       Date:  1961-07-08       Impact factor: 49.962

2.  Electron transport and coupled energy generation in Pseudomonas saccharophila.

Authors:  M Ishaque; A Donawa; M I Aleem
Journal:  Can J Biochem       Date:  1971-11

3.  A suggested mechanism of uncoupling of respiratory-chain phosphorylation.

Authors:  K van Dam; E C Slater
Journal:  Proc Natl Acad Sci U S A       Date:  1967-11       Impact factor: 11.205

4.  Interference of uncoupling agents with cellular energy-requiring processes in anaerobic conditions.

Authors:  T Galeotti; L Kovác; B Hess
Journal:  Nature       Date:  1968-04-13       Impact factor: 49.962

5.  Effect of uncoupling agents and azide on the synthesis of beta-galactosidase in aerobically and anaerobically grown Escherichia coli.

Authors:  L Kovác; S Kuzela
Journal:  Biochim Biophys Acta       Date:  1966-10-31

6.  Oxidative phosphorylation in yeast. V. Phosphorylation efficiencies in growing cells determined from molar growth yields.

Authors:  V Kormancíkov'A; L Kovác; M Vidová
Journal:  Biochim Biophys Acta       Date:  1969-05

7.  The effect of 2,4-dinitrophenol on the electrical resistance of phospholipid bilayer membranes.

Authors:  J Bielawski; T E Thompson; A L Lehninger
Journal:  Biochem Biophys Res Commun       Date:  1966-09-22       Impact factor: 3.575

8.  2,4-Dinitrophenol and azide as inhibitors of protein and ribonucleic acid synthesis in anaerobic yeast.

Authors:  L Jarett; R W Hendler
Journal:  Biochemistry       Date:  1967-06       Impact factor: 3.162

9.  Glucose degradation, molar growth yields, and evidence for oxidative phosphorylation in Streptococcus agalactiae.

Authors:  M N Mickelson
Journal:  J Bacteriol       Date:  1972-01       Impact factor: 3.490

10.  Phosphorylation and the reduced nicotinamide adenine dinucleotide oxidase reaction in Streptococcus agalactiae.

Authors:  M N Mickelson
Journal:  J Bacteriol       Date:  1969-11       Impact factor: 3.490

View more
  3 in total

1.  Ammonium uptake and metabolism by mitrogen fixing bacteria. II. Klebsiella pneumoniae.

Authors:  D Kleiner
Journal:  Arch Microbiol       Date:  1976-12-01       Impact factor: 2.552

Review 2.  The Emerging Role of Glucose Metabolism in Cartilage Development.

Authors:  Judith M Hollander; Li Zeng
Journal:  Curr Osteoporos Rep       Date:  2019-04       Impact factor: 5.096

3.  Branched-chain amino acid transport in Streptococcus agalactiae.

Authors:  J W Moran
Journal:  Appl Environ Microbiol       Date:  1980-07       Impact factor: 4.792

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.