Abstract
Wild-type strains of Escherichia coli K-12 cannot grow in media with gamma-aminobutyrate (GABA) as the sole source of carbon or nitrogen. Mutants were isolated which could utilize GABA as the sole source of nitrogen. These mutants were found to have six- to ninefold higher activities of gamma-aminobutyrate-alpha-ketoglutarate transaminase (EC 2.6.1.19) and succinate semialdehyde dehydrogenase (EC 1.2.1.16) than those of the wild-type parent strains. Secondary mutants derived from these GABA-nitrogen-utilizing strains were able to grow on GABA as the sole source of carbon and nitrogen. They also grew faster on a variety of other carbon and nitrogen sources, and their growth was more strongly inhibited by different metabolic inhibitors than was that of the parent strains. The nature of the two mutations and the possible genes involved are discussed. A scheme of the pathway for GABA breakdown in E. coli K-12 is presented.
MeSH Terms
Acetates/pharmacology
Aminobutyrates/metabolism
Aspartate Aminotransferases/metabolism
Aspartic Acid
Carbon/metabolism
Carbon Isotopes
Cell-Free System
Chloramphenicol/pharmacology
Culture Media
Dimethyl Sulfoxide/pharmacology
Escherichia coli/drug effects,enzymology,growth & development,metabolism
Genetics, Microbial
Glutamate Dehydrogenase/metabolism
Glutamates/pharmacology
Lyases/metabolism
Models, Chemical
Mutation
Nitrogen/metabolism
Oxidoreductases/metabolism
Puromycin/pharmacology
Transaminases/metabolism
Chemicals
Acetates
Aminobutyrates
Carbon Isotopes
Culture Media
Glutamates
Aspartic Acid
Puromycin
Chloramphenicol
Carbon
Oxidoreductases
Glutamate Dehydrogenase
Transaminases
Aspartate Aminotransferases
Lyases
Nitrogen
Dimethyl Sulfoxide
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Dover S
Halpern Y S
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