Isolation and characterization of temperature-sensitive pantothenate kinase (coaA) mutants of Escherichia coli
Open Access
- 30 November 1987
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 169 (12) , 5795-5800
- https://doi.org/10.1128/jb.169.12.5795-5800.1987
Abstract
Escherichia coli mutants conditionally defective in the conversion of pantothenate to coenzyme A were isolated and characterized. The gene was designated coaA and localized between argEH and rpoB near min 90 of the chromosome. The coaA15(Ts) mutation caused a temperature-sensitive growth phenotype and temperature-dependent inactivation of pantothenate kinase activity assayed both in vivo and in vitro. At 30 degrees C, coaA15(Ts) extracts contained less than 20% of the wild-type pantothenate kinase activity; the kinase had near normal kinetic constants for the substrates ATP and pantothenate and was inhibited by coenzyme A to the same degree as the wild-type enzyme. These data define the coaA gene as the structural gene for pantothenate kinase.This publication has 33 references indexed in Scilit:
- ACETYLORNITHINASE OF ESCHERICHIA COLI: PARTIAL PURIFICATION AND SOME PROPERTIESPublished by Elsevier ,2021
- Preparation of high-specific-activity d-[3-3H]pantothenic acidAnalytical Biochemistry, 1986
- The properties and regulation of pantothenate kinase from rat heart.Journal of Biological Chemistry, 1985
- Regulation of pantothenate kinase from various tissues of the ratFEBS Letters, 1985
- Linkage map of Escherichia coli K-12, edition 7.1983
- Rate-limiting step and control of coenzyme A synthesis in cardiac muscle.Journal of Biological Chemistry, 1982
- Regulation of the Biosynthesis of CoA at the Level of Pantothenate KinaseEuropean Journal of Biochemistry, 1982
- Regulation of coenzyme A biosynthesis by glucagon and glucocorticoid in adult rat liver parenchymal cellsBiochemical Journal, 1980
- Purification and properties of d-pantothenate kinase from rat liverBiochimica et Biophysica Acta (BBA) - Enzymology, 1972
- The purification and properties of Neurospora malate dehydrogenaseArchives of Biochemistry and Biophysics, 1965