Hackett C S, MacGregor C H
J Bacteriol. 1981 Apr;146(1):352-9. doi: 10.1128/jb.146.1.352-359.1981.
The biosynthesis, insertion, and in vivo stability of nitrate reductase were examined by following the amount of labeled enzyme present in both membranes and cytoplasm at varying times after a short pulse of radioactive sulfate. Nitrate reductase levels were measured by autoradiography of immunoprecipitated material after fractionation on sodium dodecyl sulfate-polyacrylamide gels. These experiments demonstrated that subunits A and B were synthesized in the cytoplasm and subsequently inserted into membranes. The insertion of these subunits was dependent upon the synthesis of another protein, and the rate of synthesis of this protein determined the rate of insertion of subunits A and B. The nitrate reductase produced by the chlA mutant was inserted into membranes in the normal fashion, whereas the nitrate reductase produced by the chlC and chlE mutants was poorly incorporated. The nitrate reductase in the wild type was completely stable in vivo under inducing or noninducing conditions, whereas in the chlC and chlE mutants nitrate reductase was degraded extensively in both the cytoplasm and membranes, even under inducing conditions. Under similar conditions, nitrate reductase was stable in the chlA mutant.
通过在短时间脉冲放射性硫酸盐后不同时间跟踪膜和细胞质中标记酶的含量,研究了硝酸还原酶的生物合成、插入及体内稳定性。在十二烷基硫酸钠-聚丙烯酰胺凝胶上分级分离后,通过对免疫沉淀物质进行放射自显影来测量硝酸还原酶水平。这些实验表明,亚基A和B在细胞质中合成,随后插入膜中。这些亚基的插入依赖于另一种蛋白质的合成,并且这种蛋白质的合成速率决定了亚基A和B的插入速率。chlA突变体产生的硝酸还原酶以正常方式插入膜中,而chlC和chlE突变体产生的硝酸还原酶整合较差。野生型中的硝酸还原酶在诱导或非诱导条件下在体内完全稳定,而在chlC和chlE突变体中,即使在诱导条件下,硝酸还原酶在细胞质和膜中都被大量降解。在类似条件下,硝酸还原酶在chlA突变体中是稳定的。