Literature DB >> 7814316

Two Lactococcus lactis genes, including lacX, cooperate to trigger an SOS response in a recA-negative background.

X F Huang1, D C Huang, G Novel, M Novel.   

Abstract

A 4.3-kb EcoRI fragment from a Lactococcus lactis genomic library alleviates the methyl methanesulfonate, mitomycin C, and UV sensitivities of an Escherichia coli recA mutant (M. Novel, X. F. Huang, and G. Novel, FEMS Microbiol. Lett. 72:309-314, 1990). It complements recA1 and delta recA mutations but not recA13. Three proteins (with molecular masses of 20, 35, and 23 kDa) were produced from this fragment in a T7-directed system, and three corresponding genes were detected by DNA sequencing, namely, ISS1CH;lacX, which is the distal gene of the lac operon; and a third open reading frame, named lacN, which encodes 211 amino acids. Mutations produced in either lacX or in lacN resulted in the loss of the resistance to DNA-damaging agents. Thus, these two genes appeared to be involved in this activity. Introduction of pUCB214 carrying the 4.3-kb fragment into a lexA+ delta recA306 sfiA::lacZ strain resulted in UV-inducible synthesis of beta-galactosidase. A uvrA strain or a lexA (Ind-) strain containing pUCB214 did not support any DNA repair. However, a lexA (Def-) strain carrying pUCB214 could partly repair UV damage. We discuss possible targets for LacX and LacN products, and we speculate that LacX and LacN may constitute a two-component regulatory system that is able to respond to SOS signals, and then to act in the SOS response, bypassing the RecA-activated function.

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Year:  1995        PMID: 7814316      PMCID: PMC176589          DOI: 10.1128/jb.177.2.283-289.1995

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  43 in total

1.  Role of uracil-DNA glycosylase in mutation avoidance by Streptococcus pneumoniae.

Authors:  J D Chen; S A Lacks
Journal:  J Bacteriol       Date:  1991-01       Impact factor: 3.490

2.  Identification of a new insertion element, similar to gram-negative IS26, on the lactose plasmid of Streptococcus lactis ML3.

Authors:  K M Polzin; M Shimizu-Kadota
Journal:  J Bacteriol       Date:  1987-12       Impact factor: 3.490

3.  Effect of tsl (thermosensitive suppressor of lex) mutation on postreplication repair in Escherichia coli K-12.

Authors:  A K Ganesan; P C Seawell; D W Mount
Journal:  J Bacteriol       Date:  1978-09       Impact factor: 3.490

4.  Cloning and characterization of Bacillus subtilis iep, which has positive and negative effects on production of extracellular proteases.

Authors:  T Tanaka; M Kawata
Journal:  J Bacteriol       Date:  1988-08       Impact factor: 3.490

5.  Cloning and expression of the Escherichia coli recA gene in Bacillus subtilis.

Authors:  W M de Vos; S C de Vries; G Venema
Journal:  Gene       Date:  1983-11       Impact factor: 3.688

6.  Cloning and characterization of DNA damage-inducible promoter regions from Bacillus subtilis.

Authors:  D L Cheo; K W Bayles; R E Yasbin
Journal:  J Bacteriol       Date:  1991-03       Impact factor: 3.490

7.  Molecular cloning and characterization of a genetic region from Serratia marcescens involved in DNA repair.

Authors:  K E Murphy; H D Braymer
Journal:  Mol Microbiol       Date:  1989-02       Impact factor: 3.501

8.  Nucleotide and deduced amino acid sequences of the lacR, lacABCD, and lacFE genes encoding the repressor, tagatose 6-phosphate gene cluster, and sugar-specific phosphotransferase system components of the lactose operon of Streptococcus mutans.

Authors:  E L Rosey; G C Stewart
Journal:  J Bacteriol       Date:  1992-10       Impact factor: 3.490

9.  Isolation and structural analysis of the phospho-beta-galactosidase gene from Streptococcus lactis Z268.

Authors:  B Boizet; D Villeval; P Slos; M Novel; G Novel; A Mercenier
Journal:  Gene       Date:  1988       Impact factor: 3.688

10.  Characterization of the Lactococcus lactis lactose operon promoter: contribution of flanking sequences and LacR repressor to promoter activity.

Authors:  R J van Rooijen; M J Gasson; W M de Vos
Journal:  J Bacteriol       Date:  1992-04       Impact factor: 3.490

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