CLONING, SEQUENCING AND COMPLEMENTATION ANALYSIS OF THE RECA GENE FROM PREVOTELLA-RUMINICOLA (VOL 144, PG 53, 1996)

Citation
Ri. Aminov et al., CLONING, SEQUENCING AND COMPLEMENTATION ANALYSIS OF THE RECA GENE FROM PREVOTELLA-RUMINICOLA (VOL 144, PG 53, 1996), FEMS microbiology letters, 145(3), 1996, pp. 473-473
Citations number
1
Categorie Soggetti
Microbiology
Journal title
ISSN journal
03781097
Volume
145
Issue
3
Year of publication
1996
Pages
473 - 473
Database
ISI
SICI code
0378-1097(1996)145:3<473:CSACAO>2.0.ZU;2-J
Abstract
Degenerate PCR primers based on conserved RecA protein regions were us ed to amplify a portion of recA from Prevotella ruminicola strain 23, which was used as a probe to isolate the full-length recA gene from th e P. ruminicola genomic library. The P. ruminicola recA gene encoded a protein of 340 amino acids with a molecular mass of 36.81 kDa. P. rum inicola RecA was highly similar to other RecA proteins and most closel y resembled that of Bacteroides fragilis (75% identity). It alleviated the methyl methanesulfonate and mitomycin C sensitivities of Escheric hia coli recA mutants, but did not restore the resistance to UV-light irradiation. Mitomycin C treatment of otherwise isogenic E. coli strai ns showed a higher level of prophage induction in a recA harboring lys ogen.