Kirner S, Krauss S, Sury G, Lam S T, Ligon J M, van Pée K H
Institut für Mikrobiologie, Universität Hohenheim, Stuttgart, Germany.
Microbiology (Reading). 1996 Aug;142 ( Pt 8):2129-35. doi: 10.1099/13500872-142-8-2129.
The non-haem chloroperoxidase gene (cpoF) from the pyrrolnitrin producer Pseudomonas fluorescens BL914 was cloned using an oligonucleotide derived from part of the N-terminal amino acid sequence of chloroperoxidase (CPO-P) from Pseudomonas pyrrocina as a probe. Based on the overexpression of cpoF in Escherichia coli and the stability of CPO-F against higher temperatures and proteases, the enzyme was purified to homogeneity. Partial characterization of the enzyme showed that it belongs to the class of bacterial non-haem CPOs. To investigate the role of CPO-F in pyrrolnitrin biosynthesis, the cpoF gene was inactivated by insertion of a kanamycin cassette. Exchange of the chromosomal cpoF gene against the disrupted copy had no influence on pyrrolnitrin production demonstrating that CPO-F was not involved in pyrrolnitrin biosynthesis.
利用源自吡咯菌素产生菌荧光假单胞菌BL914的非血红素氯过氧化物酶基因(cpoF)进行克隆,该克隆使用了一种寡核苷酸作为探针,该寡核苷酸来源于吡咯假单胞菌氯过氧化物酶(CPO-P)N端氨基酸序列的一部分。基于cpoF在大肠杆菌中的过表达以及CPO-F对高温和蛋白酶的稳定性,该酶被纯化至均一。对该酶的部分特性分析表明,它属于细菌非血红素CPO类别。为了研究CPO-F在吡咯菌素生物合成中的作用,通过插入卡那霉素盒使cpoF基因失活。用破坏的拷贝替换染色体上的cpoF基因对吡咯菌素的产生没有影响,这表明CPO-F不参与吡咯菌素的生物合成。