RT Journal Article SR Electronic(1) A1 Pelletier, Isabelle A1 Pfeifer, Otto A1 Altenbuchner, Josef A1 van Pée, Karl-HeinzYR 1994 T1 Cloning of a second non-haem bromoperoxidase gene from Streptomyces aureofaciens ATCC 10762: sequence analysis, expression in Streptomyces lividans and enzyme purification JF Microbiology, VO 140 IS 3 SP 509 OP 516 DO https://doi.org/10.1099/00221287-140-3-509 PB Microbiology Society, SN 1465-2080, AB The gene for BPO-A1, one of two non-haem bromoperoxidases in the tetracycline and 7-chlorotetracycline producer Streptomyces aureofaciens ATCC 10762, was cloned in the positive selection vector pIJ699 and expressed in Streptomyces lividans TK64. The cloned bromoperoxidase was over-produced up to 2800-fold by the S. lividans TK64 transformant. By taking advantage of the over-production of BPO-A1 and the heat stability of the enzyme, a new and simple purification procedure was developed. Subcloning into the vector pIJ487 and screening of recombinants by a newly developed histochemical assay located the bpoA1 gene on a 2•1 kb BamHI-HindIII fragment. The nucleotide sequence of the 2•1 kb fragment was determined; the bpoA1 gene was identified within the sequence on the basis of the biased codon usage of Streptomyces genes and the presence of a nucleotide sequence encoding the N-terminal amino acid sequence obtained from the purified BPO-A1. Comparison of the deduced primary structure of BPO-A1 with those deduced for the non-haem chloroperoxidase CPO-P from Pseudomonas pyrrocinia and the bromoperoxidase BPO-A2 from S. aureofaciens ATCC 10762 gave amino acid sequence identities of 49% and 40%, respectively., UL https://www.microbiologyresearch.org/content/journal/micro/10.1099/00221287-140-3-509