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PMID: 387765 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

RNase E, an RNA processing enzyme from Escherichia coli.

The Journal of biological chemistry ·Vol. 254 ·No. 21 ·1979-11-10 ·Pages 11154-9

Misra TK, Apirion D

Abstract

An activity, RNase E, was purified about 100-fold from Escherichia coli cells, it can process p5 rRNA from a 9 S RNA molecule which accumulates in a mutant of E. coli defective in the maturation of 5 S rRNA. The enzyme requires Na+, K+, or NH4+, and Mg2+ or Mn2+. The molecular weight of the enzyme is about 70,000 and its pH optimum is 7.6 to 8.0. Its temperature optimum is around 30 degrees C, and it can be irreversibly inactivated at 50 degrees C. It has a very high degree of specificity but the reaction can be inhibited by nonspecific RNAs. We interpret its mode of action in producing p5 RNA as being accomplished in two steps, 9 S RNA is first processed to 7 S and 4 S, and subsequently 7 S is further processed to p5.

MeSH Terms
Ammonia/pharmacology Endoribonucleases Escherichia coli/enzymology Kinetics Magnesium/pharmacology Manganese/pharmacology Molecular Weight Mutation Potassium/pharmacology Ribonucleases/isolation & purification,metabolism Sodium/pharmacology Substrate Specificity
Chemicals
Manganese Ammonia Sodium Endoribonucleases Ribonucleases ribonuclease E Magnesium Potassium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Misra T K
Apirion D
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1979-11-10
Pages
11154-9
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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