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U.S. Department of Energy
Office of Scientific and Technical Information

Inducible error-prone repair in B. subtilis. Progress report, September 1, 1981-April 30, 1983

Technical Report ·
OSTI ID:6602790
Considerable progress has been made on determining the mechanisms of mutagenesis in B. subtilis and on elucidating the interactions between DNA repair systems and mutagenesis in this bacterium. Specifically, the B. subtilis W-reactivation system has been shown to involve a damage-specific (pyrimidine dimer) repair mechanism which may or may not be error-free. On the other hand, error-prone repair (as defined by the ability of cells to be mutated by low doses of uv) has been definitively established in this bacterium. The investigation of the genes controlling the error-prone repair system has revealed that uv mutagenesis is significantly decreased in cells carrying the recG13 mutation. In addition, cells lacking a functional excision repair system are hypermutable to EMS, although these cells are not hypersensitive to the killing activity of EMS. Both EMS and uv generate the same spectrum of mutants (reversions vs suppressors); however, cells lacking a functional excision repair system apparently generate more suppressor mutations when exposed to uv as compared to the other strains tested. A genomic library for B. subtilis has been established. This library will be specifically used to isolate a cloned fragment of DNA which codes for the major subunit of the Bacillus DNA polymerase III. However, this bank can also be used to isolate Bacillus genes which control most of the repair functions. Furthermore, we have begun the process of cloning the E. coli phr/sup +/ gene in to B. subtilis.
Research Organization:
Rochester Univ., NY (USA). Dept. of Microbiology
DOE Contract Number:
AC02-81ER60017
OSTI ID:
6602790
Report Number(s):
DOE/ER/60017-1; ON: DE83004521
Country of Publication:
United States
Language:
English