Hotter G S, Wilson T, Collins D M
AgResearch, Wallaceville Animal Research Centre, P.O. Box 40063, Upper Hutt, New Zealand.
FEMS Microbiol Lett. 2001 Jun 25;200(2):151-5. doi: 10.1111/j.1574-6968.2001.tb10707.x.
A 17-kDa protein (CadI) was induced by cadmium in Mycobacterium bovis and Mycobacterium tuberculosis. Comparison of the N-terminal sequence from M. bovis CadI with the annotated M. tuberculosis genome database identified Rv2641 as the encoding gene. Long and short promoter fragments from M. bovis cadI were fused to the lacZ reporter gene in pYUB76. Only the long fragment directed cadmium-inducible activity when electroporated into M. bovis. The cadI promoter has potential for both constitutive and inducible expression studies in M. bovis and M. tuberculosis.
一种17千道尔顿的蛋白质(CadI)在牛分枝杆菌和结核分枝杆菌中由镉诱导产生。将牛分枝杆菌CadI的N端序列与注释的结核分枝杆菌基因组数据库进行比较,确定Rv2641为编码基因。来自牛分枝杆菌cadI的长启动子片段和短启动子片段与pYUB76中的lacZ报告基因融合。当电穿孔导入牛分枝杆菌时,只有长片段具有镉诱导活性。cadI启动子在牛分枝杆菌和结核分枝杆菌的组成型和诱导型表达研究中均具有潜力。