ydfDencodes a novel lytic protein inEscherichia coli
Author(s) -
Hisako Masuda,
Naoki Awano,
Masayori Inouye
Publication year - 2016
Publication title -
fems microbiology letters
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 151
eISSN - 1574-6968
pISSN - 0378-1097
DOI - 10.1093/femsle/fnw039
Subject(s) - lytic cycle , prophage , lysis , escherichia coli , cell division , biology , microbiology and biotechnology , cytoplasm , gene , cell , cytolysis , biochemistry , genetics , bacteriophage , cytotoxicity , virus , in vitro
Bacteria carry a number of genes that cause cell growth arrest or cell lysis upon expression. Notably, defective prophages retain many lysis proteins. Here, we identified a novel lytic gene, ydfD, on the Qin prophage segment of the Escherichia coli genome. YdfD lyses 99.9% of cells within 2 h of its induction. The co-expression of the upstream gene, dicB, encoding a cell division inhibitor, as well as sulA, encoding another cell division inhibitor, abolished YdfD-induced cell lysis. These results imply that YdfD-induced lysis is a cell division-dependent event. We further found that by deleting the hydrophobic 22-residue N-terminal domain, the resulting 42-residue C-terminal domain was still toxic to cause cell lysis. We propose that YdfD, associated with the cytoplasmic membrane, inhibits an essential cellular process(s).
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