MOLECULAR CHARACTERIZATION OF PMBA, AN ESCHERICHIA-COLI CHROMOSOMAL GENE REQUIRED FOR THE PRODUCTION OF THE ANTIBIOTIC PEPTIDE MCCB17

Microcin B17 (MccB17) is a peptide antibiotic produced by Escherichia coli strains harbouring plasmid pMccB17. We have isolated two mutations that strongly reduce the production of MccB17. These mutations, which map at 96 min on the E. coli chromosome, define a new gene that we have caiied pmbA. A chromosomal DNA fragment of about 13kb, including the wild‐type pmbA allele, was cloned into a mini‐Mu piasmid vector. pmbA was located within the cloned DNA fragment by insertional mutagenesis and deletion analysis. The nucleotide sequence of a 1.7 kb DNA region containing the gene was determined. pmbA encodes a hydrophilic protein of 450‐amino‐acid residues with a predicted molecular size of 48375 D, which was visualized in polyacrylamide gels. Protein profiles of cellular envelope and soluble fractions from cells with plasmids overproducing PmbA indicated that it is cytoplasmic. Physiological experiments suggested that pmbA mutants synthesize a molecule (pro‐MccB17) able to inhibit DNA replication but unable to the released from cells. We propose that PmbA facilitates the secretion of the antibiotic by completing its maturation. Copyright © 1990, Wiley Blackwell. All rights reserved