| Literature DB >> 6302075 |
Abstract
The DNA coding for RNase H from a mutant strain of Escherichia coli (FB2) was cloned into plasmid pBR322. DNA sequence analysis and the exchange of a portion of the mutant and wild-type genes revealed that a single-base alteration (C-->T) in the coding region of the structural gene for RNase H is responsible for the difference in RNase H activity of the wild-type and mutant cells.Entities:
Mesh:
Substances:
Year: 1983 PMID: 6302075 PMCID: PMC217564 DOI: 10.1128/jb.154.2.1021-1026.1983
Source DB: PubMed Journal: J Bacteriol ISSN: 0021-9193 Impact factor: 3.490