Literature DB >> 12113939

Identification and characterization of the Escherichia coli envC gene encoding a periplasmic coiled-coil protein with putative peptidase activity.

Hiroshi Hara1, Setsuko Narita, Doris Karibian, James T Park, Yoshihiro Yamamoto, Yukinobu Nishimura.   

Abstract

PM61 is a chain-forming envC strain of Escherichia coli with a leaky outer membrane. It was found to have an oversized penicillin-binding protein 3, which was the result of an IS4 insertion in the prc gene. The other properties of PM61 were caused by the envC mutation. We cloned the envC (yibP) gene and identified the mutation site, causing a single residue substitution, H366Y, in the PM61 envC allele. The gene product was predicted to be a periplasmic protein having coiled-coil structure in the N-terminal region and homology to lysostaphin in the C-terminal region. Overexpression of envC inhibited cell growth, and overexpression of the PM61 mutant allele caused cell lysis. Disruption of the chromosomal envC caused the same defects as the envC point mutation, indicating the gene is dispensable for growth but important for normal septation/separation and cell envelope integrity.

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Year:  2002        PMID: 12113939     DOI: 10.1111/j.1574-6968.2002.tb11271.x

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  16 in total

1.  An ATP-binding cassette transporter-like complex governs cell-wall hydrolysis at the bacterial cytokinetic ring.

Authors:  Desirée C Yang; Nick T Peters; Katherine R Parzych; Tsuyoshi Uehara; Monica Markovski; Thomas G Bernhardt
Journal:  Proc Natl Acad Sci U S A       Date:  2011-10-17       Impact factor: 11.205

2.  Daughter cell separation is controlled by cytokinetic ring-activated cell wall hydrolysis.

Authors:  Tsuyoshi Uehara; Katherine R Parzych; Thuy Dinh; Thomas G Bernhardt
Journal:  EMBO J       Date:  2010-03-18       Impact factor: 11.598

3.  A fail-safe mechanism in the septal ring assembly pathway generated by the sequential recruitment of cell separation amidases and their activators.

Authors:  Nick T Peters; Thuy Dinh; Thomas G Bernhardt
Journal:  J Bacteriol       Date:  2011-07-15       Impact factor: 3.490

4.  The cell wall amidase AmiB is essential for Pseudomonas aeruginosa cell division, drug resistance and viability.

Authors:  Anastasiya A Yakhnina; Heather R McManus; Thomas G Bernhardt
Journal:  Mol Microbiol       Date:  2015-07-14       Impact factor: 3.501

Review 5.  Peptidoglycan hydrolases of Escherichia coli.

Authors:  Jean van Heijenoort
Journal:  Microbiol Mol Biol Rev       Date:  2011-12       Impact factor: 11.056

6.  Structure-function analysis of the LytM domain of EnvC, an activator of cell wall remodelling at the Escherichia coli division site.

Authors:  Nick T Peters; Cécile Morlot; Desirée C Yang; Tsuyoshi Uehara; Thierry Vernet; Thomas G Bernhardt
Journal:  Mol Microbiol       Date:  2013-07-23       Impact factor: 3.501

7.  Cell division defects in Escherichia coli deficient in the multidrug efflux transporter AcrEF-TolC.

Authors:  Sze Yi Lau; Helen I Zgurskaya
Journal:  J Bacteriol       Date:  2005-11       Impact factor: 3.490

8.  A protein critical for cell constriction in the Gram-negative bacterium Caulobacter crescentus localizes at the division site through its peptidoglycan-binding LysM domains.

Authors:  Sebastian Poggio; Constantin N Takacs; Waldemar Vollmer; Christine Jacobs-Wagner
Journal:  Mol Microbiol       Date:  2010-05-24       Impact factor: 3.501

9.  DipM links peptidoglycan remodelling to outer membrane organization in Caulobacter.

Authors:  Erin D Goley; Luis R Comolli; Katherine E Fero; Kenneth H Downing; Lucy Shapiro
Journal:  Mol Microbiol       Date:  2010-05-24       Impact factor: 3.501

10.  LytM-domain factors are required for daughter cell separation and rapid ampicillin-induced lysis in Escherichia coli.

Authors:  Tsuyoshi Uehara; Thuy Dinh; Thomas G Bernhardt
Journal:  J Bacteriol       Date:  2009-06-12       Impact factor: 3.490

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