Nisin dissipates the proton motive force of the obligate anaerobe Clostridium sporogenes PA 3679
The influence of nisin on the proton motive force generated by glucose-energized cells of the obligate putrefactive anaerobe Clostridium sporogenes PA 3679 was determined. The components of proton motive force, the transmembrane potential and the pH gradient were determined from the distributions of...
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Published in | Applied and Environmental Microbiology Vol. 58; no. 8; pp. 2463 - 2467 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
American Society for Microbiology
01.08.1992
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Subjects | |
Online Access | Get full text |
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Summary: | The influence of nisin on the proton motive force generated by glucose-energized cells of the obligate putrefactive anaerobe Clostridium sporogenes PA 3679 was determined. The components of proton motive force, the transmembrane potential and the pH gradient were determined from the distributions of the lipophilic cation [3H]TPP+ ([3H]tetraphenylphosphonium bromide) and [14C]salicylic acid, respectively. The cells maintained a constant proton motive force of -111 mV, consisting of a pH gradient of 0.4 to 1.0 pH units at an external pH of 5 to 7 and a transmembrane potential of -60 to -88 mV. Nisin, carbonyl cyanide m-chlorophenylhydrazone (CCCP), and N,N'-dicyclohexylcarbodiimide (DCCD) at pH 6.0 elicited the complete release of preaccumulated [3H]tetraphenylphosphonium bromide and [14C]salicylic acid, with a concomitant depletion of transmembrane potential and pH gradient. Nisin and DCCD caused rapid drops in intracellular ATP levels from 1.2 to 0.01 and 0.06 nmol/mg of cells (dry weight), respectively. Cells exposed to nisin and DCCD lost the ability to form colonies, thus suggesting that transmembrane potential and pH gradient are necessary for cell viability. The data suggest that depletion of proton motive force and exhaustion of cellular ATP reserves are the basis for nisin inhibition of C. sporogenes PA 3679. |
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Bibliography: | Q Q03 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0099-2240 1098-5336 |
DOI: | 10.1128/aem.58.8.2463-2467.1992 |