Wolfframm C, van Pée K H, Lingens F
Institut für Mikrobiologie, Universität Hohenheim, Stuttgart, FRG.
FEBS Lett. 1988 Oct 10;238(2):325-8. doi: 10.1016/0014-5793(88)80505-2.
A chloroperoxidase gene from Pseudomonas pyrrocinia was cloned into Escherichia coli using the cosmid vector pJB8. The gene coding for the chloroperoxidase could be localized to a 1.5 kb fragment of DNA which was subcloned into the high-copy-number plasmid pUC18. In one subclone increased halogenating activity could be found which was 570-fold greater than in P. pyrrocinia. The halogenating enzyme was identified as the chloroperoxidase by SDS-polyacrylamide gel electrophoresis.
利用黏粒载体pJB8将来自吡咯菌素假单胞菌的氯过氧化物酶基因克隆到大肠杆菌中。编码氯过氧化物酶的基因可定位到一段1.5 kb的DNA片段上,该片段被亚克隆到高拷贝数质粒pUC18中。在一个亚克隆中发现卤化活性增加,比吡咯菌素假单胞菌中的卤化活性高570倍。通过SDS-聚丙烯酰胺凝胶电泳将卤化酶鉴定为氯过氧化物酶。