Abstract
Adsorption of cloacin DF13 onto sensitive cells induces a leakage of potassium ions after a lag of 15–20 min. The rate of the potassium efflux is proportional to the bacteriocin concentration used. The extent of the potassium loss depends on the concentrations of bacteriocin and of extracellular potassium. Leakage of potassium ions is accompanied by an uptake of sodium ions. Cloacin DF13 does not affect the transport of magnesium ions, phosphate ions or amino acids. About 10 min after addition of the bacteriocin the ATP content of the cells begins to decrease gradually to about 25% of the original level. Anaerobiosis, lack of energy source and inhibition of oxidative phosphorylation may protect the cells if applied within 10 min after addition of the bacteriocin. The results suggest that the action of cloacin DF13 proceeds through at least two distinct phases. Phase I is a period after bacteriocin adsorption which is reversible and in some way depends on oxidative phosphorylation. This phase does not cause any cellular damage. Phase II is irreversible and results in a disturbance of several cellular functions.
Similar content being viewed by others
References
Boon, T. 1971. Inactivation of ribosomesin vitro by colicin E3. — Proc. Nat. Acad. Sci.68: 2421–2425.
Bowman, C. M., Sidikaro, J. andNomura, M. 1971. Specific inactivation of ribosomes by colicin E3in vitro and mechanism of immunity in colicinogenic cells. — Nature New Biology234: 133–137.
Feingold, D. S. 1970. The mechanism of colicin E1 action. — J. Membrane Biol.3: 372–386.
de Graaf, F. K., Spanjaerdt Speckman, E. A. andStouthamer, A. H. 1969. Mode of action of a bacteriocin produced byEnterobacter cloacae DF13. — Antonie van Leeuwenhoek35: 287–306.
de Graaf, F. K., Goedvolk-de Groot, L. E. andStouthamer, A. H. 1970. Purification of a bacteriocin produced byEnterobacter cloacae DF13. — Biochim. Biophys. Acta221: 566–575.
de Graaf, F. K., Planta, R. J. andStouthamer, A. H. 1971. Effect of a bacteriocin produced byEnterobacter cloacae on protein biosynthesis. — Biochim. Biophys. Acta240: 122–136.
Hirata, H., Fukui, S. andIshikawa, S. 1969. Initial events caused by colicin K infection. Cation movement and depletion of ATP pool. — J. Biochem. (Tokyo)65: 843–847.
Konisky, J. andNomura, M. 1967. Interaction of colicins with bacterial cells. II. Specific alteration ofEscherichia coli ribosomes induced by colicin E3in vivo. — J. Mol. Biol.26: 181–195.
Luria, S. E. 1964. On the mechanisms of action of colicins. — Ann. Inst. Pasteur107: suppl. 5, 67–73.
Nomura, M. andMaeda, A. 1965. Mechanism of action of colicines. — Zentr. Bakteriol. Parasitenk., 1. Abt. Orig.196: 216–239.
Roberton, A. M. andWolfe, R. S. 1970. Adenosine triphosphate pools inMethanobacterium. — J. Bacteriol.102: 43–51.
Senior, B. W., Kwasniak, J. andHolland, I. B. 1970. Colicin E3-directed changes in ribosome function and polyribosome metabolism inEscherichia coli K12. — J. Mol. Biol.53: 205–220.
Wendt, L. 1970. Mechanism of colicin action: early events. — J. Bacteriol.104: 1236–1241.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
de Graaf, F.K. Effects of cloacin DF13 on the functioning of the cytoplasmic membrane. Antonie van Leeuwenhoek 39, 109–119 (1973). https://doi.org/10.1007/BF02578846
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF02578846