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PMID: 6338477 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Amplification of ribonuclease II (rnb) activity in Escherichia coli K-12.

Nucleic acids research ·Vol. 11 ·No. 2 ·1983-01-25 ·Pages 265-75

Donovan WP, Kushner SR

Abstract

A 7.1 kb HindIII-XhoI fragment of E. coli DNA which contains the structural gene for ribonuclease II (rnb) has been cloned in the recombinant plasmid pDK24. At least two constitutively expressed genes are encoded on the fragment as shown by maxicell analysis. On denaturing polyacrylamide gels RNase II appears as a single 72,000 dalton species. The approximate site of transcription initiation of the rnb gene has been mapped. Although derivatives of E. coli harboring pDK24 contained 10-fold more RNase II activity that wild type strains without the plasmid, the degradation rate of mRNA was similar in all strains tested. Strains deficient in both RNase II and polynucleotide phosphorylase appear inviable.

MeSH Terms
Cloning, Molecular DNA, Recombinant/metabolism Escherichia coli/enzymology,genetics Exoribonucleases/genetics Gene Amplification Genes Genes, Bacterial Kinetics Molecular Weight Plasmids Transcription, Genetic
Chemicals
DNA, Recombinant Exoribonucleases exoribonuclease II
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Donovan W P
Kushner S R
References (27)
27 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1983-01-25
Pages
265-75
Language
English
Region
England
NLM ID
0411011
PMCID
PMC325713
Subset
IM
Grants
NIGMS NIH HHS · GM27994 · United States
NIGMS NIH HHS · GM28760 · United States
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