Egan S M, Stewart V
Section of Microbiology, Cornell University, Ithaca, New York 14853-8101.
J Bacteriol. 1991 Jul;173(14):4424-32. doi: 10.1128/jb.173.14.4424-4432.1991.
The narL gene product, NarL, is the nitrate-responsive regulator of anaerobic respiratory gene expression. We used genetic analysis of narL mutants to better understand the mechanism of NarL-mediated gene regulation. We selected and analyzed seven nitrate-independent narL mutants. Each of three independent, strongly constitutive mutants had changes of Val-88 to Ala. The other four mutants were weakly constitutive. The narL505(V88A) allele was largely dominant to narL+, while narX+ had a negative influence on its constitutive phenotype, suggesting that NarX may play a negative role in nitrate regulation. We also constructed two narL mutations that are analogous to previously characterized constitutive degU alleles. The first, narL503(H15L), was a recessive null allele. The second, narL504(D110K), functioned essentially as wild type but was dependent on narX+ for full activity. We changed Asp-59 of NarL, which corresponds to the site of phosphorylation of other response regulators, to Asn. This change, narL502(D59N), was a recessive null allele, which is consistent with the hypothesis that NarL requires phosphorylation for activation. Finally, we tested the requirement for molybdate on regulation in a narL505(V88A) strain. Although narL505(V88A) conferred some nitrate-independent expression of fdnGHI (encoding formate dehydrogenase-N) in limiting molybdate, it required excess molybdate for full induction both in the absence and in the presence of nitrate. This finding suggests that narL505(V88A) did not confer molybdate-independent expression of fdnGHI.
narL基因产物NarL是厌氧呼吸基因表达的硝酸盐响应调节因子。我们利用narL突变体的遗传分析来更好地理解NarL介导的基因调控机制。我们挑选并分析了7个硝酸盐非依赖型narL突变体。三个独立的强组成型突变体中的每一个都有Val-88突变为Ala。其他四个突变体为弱组成型。narL505(V88A)等位基因对narL+在很大程度上呈显性,而narX+对其组成型表型有负面影响,这表明NarX在硝酸盐调节中可能起负作用。我们还构建了两个与先前鉴定的组成型degU等位基因类似的narL突变。第一个是narL503(H15L),是一个隐性无效等位基因。第二个是narL504(D110K),其功能基本与野生型相同,但完全活性依赖于narX+。我们将NarL的Asp-59(对应于其他应答调节因子的磷酸化位点)突变为Asn。这种变化,narL502(D59N),是一个隐性无效等位基因,这与NarL需要磷酸化来激活的假设一致。最后,我们在narL505(V88A)菌株中测试了钼酸盐对调节的需求。尽管narL505(V88A)在钼酸盐有限的情况下赋予了fdnGHI(编码甲酸脱氢酶-N)一些硝酸盐非依赖型表达,但无论在有无硝酸盐的情况下,它都需要过量的钼酸盐来实现完全诱导。这一发现表明narL505(V88A)并未赋予fdnGHI钼酸盐非依赖型表达。