Literature DB >> 4208280

Cation reversal of inhibition of growth by valinomycin in Streptococcus pyogenes and Clostridium sporogenes.

D Seshachalam, D H Frahm, F M Ferraro.   

Abstract

Study of the antimicrobial spectrum of valinomycin revealed that, in addition to the gram-positive bacteria reported in literature, Streptococcus pyogenes and Clostridium sporogenes are also susceptible to this antibiotic. The minimal inhibitory concentrations (MIC) of the antibiotic for S. pyogenes grown aerobically and anaerobically did not differ markedly, negating the hypothesis that oxidative phosphorylation is involved in the mechanism of action of this antibiotic. This conclusion is further strengthened by the inhibition of growth of C. sporogenes, an obligate anaerobe. In a medium with a low K(+) concentration, the MIC for S. pyogenes was 0.02 mug/ml, the lowest ever recorded for this antibiotic. The inhibition of growth of S. pyogenes and C. sporogenes was readily reversed by addition of K(+) to the medium, indicating a compensation for net efflux of K(+) from the cells when the transmembrane potential reached equilibrium. In contrast to these bacteria, Bacillus subtilis was less susceptible to the antibiotic when the potassium concentration of the medium was low. The addition of potassium in the presence of valinomycin increased the inhibition of growth, which appears to result from dissipation of metabolic energy as in the mitochondrial system.

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Year:  1973        PMID: 4208280      PMCID: PMC444361          DOI: 10.1128/AAC.3.1.63

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  18 in total

1.  Proton-translocation phosphorylation in mitochondria, chloroplasts and bacteria: natural fuel cells and solar cells.

Authors:  P Mitchell
Journal:  Fed Proc       Date:  1967-09

2.  The structure-antimicrobial relation for valinomycin depsipeptides.

Authors:  M M Shemyakin; E I Vinogradova; M Y Feigina; N A Aldanova; N E Loginova; I D Ryabova; I A Pavlenko
Journal:  Experientia       Date:  1965-09-15

3.  The molecular structure and some transport properties of valinomycin.

Authors:  M Pinkerton; L K Steinrauf; P Dawkins
Journal:  Biochem Biophys Res Commun       Date:  1969-05-22       Impact factor: 3.575

4.  The direction of polarity of the mitochondrial trans-membrane potential.

Authors:  E J Harris; B C Pressman
Journal:  Biochim Biophys Acta       Date:  1969-01-14

5.  Ionophorous antibiotics as models for biological transport.

Authors:  B C Pressman
Journal:  Fed Proc       Date:  1968 Nov-Dec

6.  The action of certain antibiotics on mitochondrial, erythrocyte and artificial phospholipid membranes. The role of induced proton permeability.

Authors:  P J Henderson; J D McGivan; J B Chappell
Journal:  Biochem J       Date:  1969-02       Impact factor: 3.857

7.  Molar growth yields as evidence for oxidative phosphorylation in Streptococcus faecalis strain 10Cl.

Authors:  A J Smalley; P Jahrling; P J Van Demark
Journal:  J Bacteriol       Date:  1968-11       Impact factor: 3.490

8.  Effects of nigericin and monactin on cation permeability of Streptococcus faecalis and metabolic capacities of potassium-depleted cells.

Authors:  F M Harold; J R Baarda
Journal:  J Bacteriol       Date:  1968-03       Impact factor: 3.490

9.  Gramicidin, valinomycin, and cation permeability of Streptococcus faecalis.

Authors:  F M Harold; J R Baarda
Journal:  J Bacteriol       Date:  1967-07       Impact factor: 3.490

10.  Induced and spontaneous movements of potassium ions into mitochondria.

Authors:  E J Harris; R Cockrell; B C Pressman
Journal:  Biochem J       Date:  1966-04       Impact factor: 3.857

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  2 in total

1.  Comparative analysis of antimicrobial activities of valinomycin and cereulide, the Bacillus cereus emetic toxin.

Authors:  Marcel H Tempelaars; Susana Rodrigues; Tjakko Abee
Journal:  Appl Environ Microbiol       Date:  2011-02-25       Impact factor: 4.792

2.  Exploring the diversity and metabolic potential of actinomycetes from temperate marine sediments from Newfoundland, Canada.

Authors:  K R Duncan; B Haltli; K A Gill; H Correa; F Berrué; R G Kerr
Journal:  J Ind Microbiol Biotechnol       Date:  2014-11-05       Impact factor: 3.346

  2 in total

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