Bryant C, Hubbard L, McElroy W D
Department of Chemistry, University of California, San Diego, La Jolla 92093.
J Biol Chem. 1991 Mar 5;266(7):4126-30.
The "classical" nitroreductases of enteric bacteria are flavoproteins which catalyze the reduction of a variety of nitroaromatic compounds to metabolites which are highly toxic, mutagenic, or carcinogenic. The gene for the nitroreductase Enterobacter cloacae has now been cloned using an antibody specific to this protein. The nucleotide sequence of the structural gene and flanking regions are reported. Sequence analysis indicates that this gene belongs to a gene family of flavoproteins which have not been previously described. Analysis of the 5'-untranslated region reveals the presence of putative regulatory elements which may be involved in the modulation of the expression of this enzyme. The cloned gene was placed under the control of a T7 promoter for overexpression of the protein in Escherichia coli. The expressed recombinant protein was purified to homogeneity and exhibited physical, spectral, and catalytic properties identical to the protein isolated from E. cloacae.
肠道细菌的“经典”硝基还原酶是黄素蛋白,可催化多种硝基芳香化合物还原为具有高毒性、致突变性或致癌性的代谢产物。现在已使用针对该蛋白的特异性抗体克隆了阴沟肠杆菌硝基还原酶的基因。报告了结构基因及其侧翼区域的核苷酸序列。序列分析表明,该基因属于一个以前未描述过的黄素蛋白基因家族。对5'非翻译区的分析揭示了可能参与调节该酶表达的假定调控元件的存在。将克隆的基因置于T7启动子的控制下,以便在大肠杆菌中过量表达该蛋白。表达的重组蛋白被纯化至同质,并表现出与从阴沟肠杆菌分离的蛋白相同的物理、光谱和催化特性。