Abstract
Certain mutations in the C-terminal region of the Escherichia coli division inhibitor protein MinC cause loss of function of the division inhibitor by making MinC more sensitive to degradation by Lon protease, implying a possible role for the C-terminal region in regulating the stability and cellular concentration of MinC.
MeSH Terms
ATP-Dependent Proteases
Bacterial Proteins/analysis,chemistry,genetics
Cell Division
Escherichia coli/cytology,genetics
Escherichia coli Proteins
Heat-Shock Proteins/metabolism
Mutation
Phenotype
Protease La
Serine Endopeptidases/metabolism
Chemicals
Bacterial Proteins
Escherichia coli Proteins
Heat-Shock Proteins
MinC protein, Bacteria
ATP-Dependent Proteases
Serine Endopeptidases
Lon protein, E coli
Protease La
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Sen M
Department of Microbiology, University of Connecticut Health Center, Farmington 06032, USA.
Rothfield L I
References (6)
6 references, click to expand
-
Roles of MinC and MinD in the site-specific septation block mediated by the MinCDE system of Escherichia coli.
J Bacteriol. 1992 Jan;174(1):63-70
PMID: 1729224
-
Isolation and properties of minB, a complex genetic locus involved in correct placement of the division site in Escherichia coli.
J Bacteriol. 1988 May;170(5):2106-12
PMID: 2834323
-
Cell division inhibition gene dicB is regulated by a locus similar to lambdoid bacteriophage immunity loci.
Mol Gen Genet. 1988 Apr;212(1):11-9
PMID: 2836697
-
A division inhibitor and a topological specificity factor coded for by the minicell locus determine proper placement of the division septum in E. coli.
Cell. 1989 Feb 24;56(4):641-9
PMID: 2645057
-
Central role for the Escherichia coli minC gene product in two different cell division-inhibition systems.
Proc Natl Acad Sci U S A. 1990 Feb;87(3):1129-33
PMID: 2137246
-
New minC mutations suggest different interactions of the same region of division inhibitor MinC with proteins specific for minD and dicB coinhibition pathways.
J Bacteriol. 1992 Jan;174(1):35-9
PMID: 1729222