Escherichia coli and Saccharomyces cerevisiae acetylornithine aminotransferase: evolutionary relationship with ornithine aminotransferase

Gene. 1990 May 31;90(1):69-78. doi: 10.1016/0378-1119(90)90440-3.

Abstract

Genes argD and ARG8, encoding the acetylornithine aminotransferase (ACOAT) subunit in Escherichia coli and Saccharomyces cerevisiae, respectively, have been cloned and sequenced. The deduced amino acid sequences show substantial similarity. Moreover, they resemble ornithine aminotransferase (OAT) sequences (i.e., those from yeast, rat and man); the observed similarities are statistically significant, indicating that the enzymes are homologous. However, in contrast to OATs, which appear to be substrate (i.e., ornithine)-specific, S. cerevisiae ACOAT transaminates ornithine about as efficiently as E. coli does. The evolutionary relationship between ACOATs and OATs is discussed in terms of substrate ambiguity.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Arginine / metabolism
  • Base Sequence
  • Biological Evolution
  • Escherichia coli / genetics*
  • Genes, Bacterial*
  • Genes, Fungal*
  • Molecular Sequence Data
  • Pyridoxal Phosphate / metabolism
  • Saccharomyces cerevisiae / genetics*
  • Substrate Specificity
  • Transaminases / genetics*
  • Transaminases / metabolism

Substances

  • Pyridoxal Phosphate
  • Arginine
  • Transaminases
  • acetylornithine transaminase

Associated data

  • GENBANK/M32795
  • GENBANK/M32796