Smith_1990_EMBO.J_9_2743

Reference

Title : The multifunctional peptide synthetase performing the first step of penicillin biosynthesis in Penicillium chrysogenum is a 421,073 dalton protein similar to Bacillus brevis peptide antibiotic synthetases - Smith_1990_EMBO.J_9_2743
Author(s) : Smith DJ , Earl AJ , Turner G
Ref : EMBO Journal , 9 :2743 , 1990
Abstract :

The nucleotide sequence of the Penicillium chrysogenum Oli13 acvA gene encoding delta-(L-alpha-aminoadipyl)-L-cysteinyl-D-valine synthetase, which performs the first step in penicillin biosynthesis, has been determined. The acvA gene contains an open reading frame of 11,238 bp encoding a protein of 3746 amino acids with a predicted mol. wt of 421,073 dalton. Three domains within the protein of approximately 570 amino acids have between 38% and 43% identity with each other and share similarity with two antibiotic peptide synthetases from Bacillus brevis as well as two other enzymes capable of performing ATP-pyrophosphate exchange reactions. The acvA gene is located close to the pcbC gene encoding isopenicillin N synthetase, the enzyme for the second step of beta-lactam biosynthesis, and is transcribed in the opposite orientation to it. The intergenic region of 1107 bp from which the acvA and pcbC genes are divergently transcribed has also been sequenced.

PubMedSearch : Smith_1990_EMBO.J_9_2743
PubMedID: 2118102
Gene_locus related to this paper: pench-acvt

Related information

Gene_locus pench-acvt

Citations formats

Smith DJ, Earl AJ, Turner G (1990)
The multifunctional peptide synthetase performing the first step of penicillin biosynthesis in Penicillium chrysogenum is a 421,073 dalton protein similar to Bacillus brevis peptide antibiotic synthetases
EMBO Journal 9 :2743

Smith DJ, Earl AJ, Turner G (1990)
EMBO Journal 9 :2743