Evidence for two recA genes mediating DNA repair in Bacillus megaterium

Nahrstedt H, Schroder C, Meinhardt F

Research article (journal) | Peer reviewed

Abstract

Isolation and subsequent knockout of a recA-homologous gene in Bacillus megaterium DSM 319 resulted in a mutant displaying increased sensitivity to mitomycin C. However, this mutant did not exhibit UV hypersensitivity, a finding which eventually led to identification of a second functional recA gene. Evidence for recA duplicates was also obtained for two other B. megaterium strains. In agreement with potential DinR boxes located within their promoter regions, expression of both genes (recA 1 and recA2) was found to be damage-inducible. Transcription from the recA2 promoter was significantly higher than that of recA1. Since a recA2 knockout could not be achieved, functional complementation studies were performed in Escherichia coli. Heterologous expression in a RecA null mutant resulted in increased survival after UV irradiation and mitomycin C treatment, proving both recA gene products to be functional in DNA repair. Thus, there is evidence for an SOS-like pathway in B. megaterium that differs from that of Bacillus subtilis.

Details about the publication

JournalMicrobiology
Volume151
Page range775-787
StatusPublished
Release year2005 (31/03/2005)
Language in which the publication is writtenEnglish
Keywordscompetence transcription factor gram-positive bacteria uv-sensitive mutants escherichia-coli binding-site myxococcus-xanthus subtilis cloning protein expression

Authors from the University of Münster

Meinhardt, Friedhelm

Projects the publication originates from

Duration: 26/11/2008 - 31/05/2012
Funded by: Wirtschaft
Type of project: Individual project