Premium
UV‐LYSOGENIC INDUCTION OF Λ PHAGE IN lexA 1 MUTANTS OF Escherichia coli : KINETICS OF THE PROCESS
Author(s) -
Carvalho R. E. S.,
Leitāo A. C.
Publication year - 1984
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/j.1751-1097.1984.tb03900.x
Subject(s) - repressor lexa , prophage , lysogenic cycle , sos response , mutant , biology , escherichia coli , repressor , lysogen , microbiology and biotechnology , bacteriophage , genetics , gene , gene expression
— Although the lex gene has been described until recently as being required for lysogenic induction, both our work and the work of others have reported Λ prophage induction in some lexA mutants. However, the characteristics of the process were not defined. We describe UV induction of prophage in a lexA1 mutant at a slightly lower level and requiring 2 times longer than the wild type. As demonstrated in some work, in cells treated with low levels of rifampicin (RIF) no new synthesis of RecA protein is needed for the prophage induction although the onset of lysis is delayed. We suggest that the lysogenic induction in lexA cells is due to the same mechanism that induces prophage in the wild type cells treated with RIF. That is, the induction is due to the cleavage of Λ represser by the basal RecA protease in the DNA‐single‐strand gap, since RecA protease and monomer represser both have high affinity for this type of DNA. So, LexA protein need not be cleaved for the prophage induction. No Weigle‐reactivation (WR) was detected in the lex mutant even after a long post‐irradiation incubation, suggesting that unlike prophage induction, WR requires LexA protein cleavage.