| Literature DB >> 6356186 |
Abstract
By cloning a 3.6-kb EcoRI fragment of the Escherichia coli chromosome with pBR322 we located more precisely recF relative to dnaN. By deletion mapping we localized functional recF to a 1.65-kb region of the cloned fragment and allowed rough mapping of the C terminus of dnaN. Cloned recF+, separated from functional flanking genes dnaN and gyrB, complemented chromosomal recF mutations presumably by coding for a cytodiffusible product. The protein encoded by dnaN was observed as a band on a polyacrylamide gel from minicells. Identification of a recF protein was not made.Entities:
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Year: 1983 PMID: 6356186 DOI: 10.1016/0147-619x(83)90062-8
Source DB: PubMed Journal: Plasmid ISSN: 0147-619X Impact factor: 3.466