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Title: Transcriptional and translational analyzes of recA mutant alleles in Pseudomonas aeruginosa

Journal Article · · J. Bacteriol.; (United States)
OSTI ID:6998615

Recombinant plasmids containing the recA gene from Pseudomonas aeruginosa were used in complementation, transcriptional, and translational studies to examine the nature of rec-102 and rec-2, mutations which confer a recA-like mutant phenotype on P. aeruginosa PAO strains. For comparison, recA7::Tn501 mutants of strain PAO were constructed by gene replacement. The rec-2 and rec-102 alleles were shown to be recA alleles; plasmids containing the recA gene complemented the three rec mutants strains for defects associated with recA mutation. A minicell analysis showed that a plasmid expressing both of the recA gene transcripts or one that expressed only the smaller transcript both produced the same 42-kilodalton recA protein. A chloramphenicol acetyl-transferase gene fusion in the 3' end of the recA transcript showed that the recA gene of P. aeruginosa was induced following treatment with a DNA-damaging agent (methyl methanesulfonate). The rec-2 allele of recA was normal with respect to induction of mRNA, but these transcripts were defective in either translation or synthesis of a stable protein. The rec-102 mutant also produced a detectable transcript and no recA protein following induction. The recA defect in this mutant is apparently in the interaction between recA and a lexA-like repressor.

Research Organization:
Univ. of California, Berkeley (USA)
OSTI ID:
6998615
Journal Information:
J. Bacteriol.; (United States), Vol. 170:4
Country of Publication:
United States
Language:
English