TY - JOUR
T1 - ydfD encodes a novel lytic protein in Escherichia coli
AU - Masuda, Hisako
AU - Awano, Naoki
AU - Inouye, Masayori
N1 - Funding Information:
The authors are grateful to Dr Peter Tupa and Dr Marcia Gillette for critical reading of the manuscript. The work was supported by the Indiana Academy of Science senior grant (2015-12) and by Grants in Aid from Indiana University Kokomo. HM was supported by NRSA Individual Postdoctoral Fellowship (F32) from National Institute of Health (GM095200). The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Publisher Copyright:
© FEMS 2016.
PY - 2016/3/8
Y1 - 2016/3/8
N2 - 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).
AB - 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).
KW - Escherichia coli
KW - Lysis
KW - Prophage
KW - Ydfd
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U2 - 10.1093/femsle/fnw039
DO - 10.1093/femsle/fnw039
M3 - Article
C2 - 26887840
AN - SCOPUS:84963752043
SN - 0378-1097
VL - 363
JO - FEMS Microbiology Letters
JF - FEMS Microbiology Letters
IS - 6
M1 - fnw039
ER -