Nies D H
Institut für Pflanzenphysiologie und Mikrobiologie, Freie Universität Berlin, Germany.
J Bacteriol. 1992 Dec;174(24):8102-10. doi: 10.1128/jb.174.24.8102-8110.1992.
The czcR gene, one of the two control genes responsible for induction of resistance to Co2+, Zn2+, and Cd2+ (czc system) in the Alcaligenes eutrophus plasmid pMOL30, was cloned and characterized. The 1,376-bp sequence upstream of the czcCBAD structural genes encodes a 41.4-kDa protein, the czcR gene product, transcribed in the opposite direction of that of the czcCBAD genes. The putative CzcR polypeptide (355 amino acid residues) contains 11 cysteine and 14 histidine residues which might form metal cation-binding sites. A czcC::lacZ reporter gene translational fusion was constructed, inserted into plasmid pMOL30 in A. eutrophus, and expressed under the control of CzcR. Zn2+, Co2+, and Cd2+, as well as Ni2+, Cu2+, Hg2+, and Mn2+ and even Al3+, served as inducers of beta-galactosidase activity. Besides the CzcR protein, the membrane-bound CzcD protein was essential for induction of czc. The CzcR and CzcD proteins display no sequence similarity to two-component regulatory systems of a sensor and a response activator type; however, CzcD has 34% identity with the ZRC-1 protein, which mediates zinc resistance in Saccharomyces cerevisiae (A. Kamizomo, M. Nishizawa, Y. Teranishi, K. Murata, and A. Kimura, Mol. Gen. Genet. 219:161-167, 1989).
嗜碱假单胞菌质粒pMOL30中负责诱导对Co2+、Zn2+和Cd2+产生抗性(czc系统)的两个控制基因之一的czcR基因被克隆并进行了表征。czcCBAD结构基因上游1376 bp的序列编码一个41.4 kDa的蛋白质,即czcR基因产物,其转录方向与czcCBAD基因相反。推测的CzcR多肽(355个氨基酸残基)含有11个半胱氨酸和14个组氨酸残基,它们可能形成金属阳离子结合位点。构建了一个czcC::lacZ报告基因翻译融合体,将其插入嗜碱假单胞菌的质粒pMOL30中,并在CzcR的控制下表达。Zn2+、Co2+、Cd2+以及Ni2+、Cu2+、Hg2+、Mn2+甚至Al3+均可作为β-半乳糖苷酶活性的诱导剂。除CzcR蛋白外,膜结合的CzcD蛋白对于czc的诱导也是必不可少的。CzcR和CzcD蛋白与传感器和反应激活剂类型的双组分调节系统没有序列相似性;然而,CzcD与酿酒酵母中介导锌抗性的ZRC-1蛋白有34%的同一性(A. Kamizomo、M. Nishizawa、Y. Teranishi、K. Murata和A. Kimura,《分子与普通遗传学》219:161-167,1989)。