Kaur P
Department of Biology, Georgia State University, Atlanta 30303, USA.
J Bacteriol. 1997 Feb;179(3):569-75. doi: 10.1128/jb.179.3.569-575.1997.
Streptomyces peucetius, a microorganism that produces the anticancer drugs doxorubicin and daunorubicin, is itself resistant to the action of these drugs. The genes conferring resistance to doxorubicin and daunorubicin in S. peucetius have been sequenced (P. G. Guilfoile and R. Hutchinson, Proc. Natl. Acad. Sci. USA 88:8553-8557, 1991). Two open reading frames, drrA and drrB, were proposed to encode for an ABC (ATP-binding cassette) type of permease that carries out export of the antibiotics in an ATP-dependent manner. This article reports subcloning of the drrA and drrB genes into Escherichia coli expression vectors and characterization of their gene products. Upon induction from the lac promoter, a 36-kDa DrrA protein could be identified on Coomassie blue-stained gels. The DrrB protein was identified by use of a polyclonal antiserum generated against a synthetic peptide corresponding to a portion of the DrrB protein. Together, the DrrA and DrrB proteins conferred resistance to doxorubicin in E. coli. The DrrB protein was localized to the cell membrane. The DrrA protein bound ATP or GTP in a Mg2+-dependent fashion. ATP binding was enhanced on addition of doxorubicin or daunorubicin.
佩西链霉菌是一种能产生抗癌药物阿霉素和柔红霉素的微生物,它自身对这些药物具有抗性。已对佩西链霉菌中赋予对阿霉素和柔红霉素抗性的基因进行了测序(P.G. 吉尔福伊尔和R. 哈钦森,《美国国家科学院院刊》88:8553 - 8557, 1991)。有人提出两个开放阅读框drrA和drrB编码一种ABC(ATP结合盒)型通透酶,该通透酶以ATP依赖的方式进行抗生素的输出。本文报道了将drrA和drrB基因亚克隆到大肠杆菌表达载体中并对其基因产物进行表征。从lac启动子诱导后,在考马斯亮蓝染色的凝胶上可鉴定出一种36 kDa的DrrA蛋白。通过使用针对与DrrB蛋白一部分相对应的合成肽产生的多克隆抗血清来鉴定DrrB蛋白。DrrA和DrrB蛋白共同赋予大肠杆菌对阿霉素的抗性。DrrB蛋白定位于细胞膜。DrrA蛋白以Mg2 +依赖的方式结合ATP或GTP。加入阿霉素或柔红霉素后,ATP结合增强。