Poly-beta-hydroxybutyrate (PHB) biosynthesis in Alcaligenes eutrophus H16. Identification and characterization of the PHB polymerase gene (phbC)

J Biol Chem. 1989 Sep 15;264(26):15298-303.

Abstract

The phbC gene encoding the third enzyme of the poly-beta-hydroxybutyrate biosynthetic pathway, poly-beta-hydroxybutyrate polymerase, in Alcaligenes eutrophus H16 has been identified by the complementation of poly-beta-hydroxybutyrate negative mutants of A. eutrophus H16. These results demonstrate that the three enzymes of the poly-beta-hydroxybutyrate biosynthetic pathway are organized phbC-phbA-phbB. Expression of all three genes in Escherichia coli results in a significant level (50% dry cell weight) of poly-beta-hydroxybutyrate production. phbC encodes a polypeptide of Mr = 63,900 which has a hydropathy profile distinct from typical membrane proteins indicating that poly-beta-hydroxybutyrate biosynthesis probably does not involve a membrane complex.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Alcaligenes / enzymology
  • Alcaligenes / genetics*
  • Amino Acid Sequence
  • Base Sequence
  • Chromosome Deletion
  • Cloning, Molecular
  • Escherichia coli / genetics
  • Gene Amplification
  • Genes*
  • Genes, Bacterial*
  • Hydroxybutyrates / metabolism*
  • Molecular Sequence Data
  • Mutation
  • Plasmids
  • Polyesters / metabolism*
  • Restriction Mapping

Substances

  • Hydroxybutyrates
  • Polyesters
  • poly-beta-hydroxybutyrate

Associated data

  • GENBANK/J05003