Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1982 Oct;152(1):26-34.
doi: 10.1128/jb.152.1.26-34.1982.

Induction and control of the autolytic system of Escherichia coli

Induction and control of the autolytic system of Escherichia coli

M Leduc et al. J Bacteriol. 1982 Oct.

Abstract

Various methods of inducing autolysis of Escherichia coli cells were investigated, some being described here for the first time. For the autolysis of growing cells only induction methods interfering with the biosynthesis of peptidoglycan were taken into consideration, whereas with harvested cells autolysis was induced by rapid osmotic or EDTA shock treatments. The highest rates of autolysis were observed after induction by moenomycin, EDTA, or cephaloridine. The different autolyses examined shared certain common properties. In particular, regardless of the induction method used, more or less extensive peptidoglycan degradation was observed, and 10(-2) M Mg2+ efficiently inhibited the autolytic process. However, for other properties a distinction was made between methods used for growing cells and those used for harvested cells. Autolysis of growing cells required RNA, protein, and fatty acid synthesis. No such requirements were observed with shock-induced autolysis performed with harvested cells. Thus, the effects of Mg2+, rifampicin, chloramphenicol, and cerulenin clearly suggest that distinct factors are involved in the control of the autolytic system of E. Coli. Uncoupling agents such as sodium azide, 2,4-dinitrophenol, and carbonyl-cyanide-m-chlorophenyl hydrazone used at their usual inhibiting concentration had no effect on the cephaloridine or shock-induced autolysis.

PubMed Disclaimer

References

    1. Annu Rev Microbiol. 1979;33:113-37 - PubMed
    1. J Bacteriol. 1981 Apr;146(1):331-6 - PubMed
    1. Biotechnol Bioeng. 1971 May;13(3):399-407 - PubMed
    1. Antimicrob Agents Chemother. 1979 Dec;16(6):858-61 - PubMed
    1. Bacteriol Rev. 1972 Jun;36(2):172-230 - PubMed

Publication types

LinkOut - more resources