Haveman Shelley A, Greene E Anne, Stilwell Claire P, Voordouw Johanna K, Voordouw Gerrit
Department of Biological Sciences, University of Calgary, 2500 University Drive NW, Calgary, Alberta T2N 1N4, Canada.
J Bacteriol. 2004 Dec;186(23):7944-50. doi: 10.1128/JB.186.23.7944-7950.2004.
A Desulfovibrio vulgaris Hildenborough mutant lacking the nrfA gene for the catalytic subunit of periplasmic cytochrome c nitrite reductase (NrfHA) was constructed. In mid-log phase, growth of the wild type in medium containing lactate and sulfate was inhibited by 10 mM nitrite, whereas 0.6 mM nitrite inhibited the nrfA mutant. Lower concentrations (0.04 mM) inhibited the growth of both mutant and wild-type cells on plates. Macroarray hybridization indicated that nitrite upregulates the nrfHA genes and downregulates genes for sulfate reduction enzymes catalyzing steps preceding the reduction of sulfite to sulfide by dissimilatory sulfite reductase (DsrAB), for two membrane-bound electron transport complexes (qmoABC and dsrMKJOP) and for ATP synthase (atp). DsrAB is known to bind and slowly reduce nitrite. The data support a model in which nitrite inhibits DsrAB (apparent dissociation constant K(m) for nitrite = 0.03 mM), and in which NrfHA (K(m) for nitrite = 1.4 mM) limits nitrite entry by reducing it to ammonia when nitrite concentrations are at millimolar levels. The gene expression data and consideration of relative gene locations suggest that QmoABC and DsrMKJOP donate electrons to adenosine phosphosulfate reductase and DsrAB, respectively. Downregulation of atp genes, as well as the recorded cell death following addition of inhibitory nitrite concentrations, suggests that the proton gradient collapses when electrons are diverted from cytoplasmic sulfate to periplasmic nitrite reduction.
构建了一株缺失周质细胞色素c亚硝酸盐还原酶(NrfHA)催化亚基nrfA基因的希登伯勒脱硫弧菌突变体。在对数中期,野生型在含有乳酸盐和硫酸盐的培养基中生长受到10 mM亚硝酸盐的抑制,而0.6 mM亚硝酸盐抑制nrfA突变体的生长。较低浓度(0.04 mM)抑制突变体和野生型细胞在平板上的生长。宏阵列杂交表明,亚硝酸盐上调nrfHA基因,并下调催化亚硫酸盐通过异化亚硫酸盐还原酶(DsrAB)还原为硫化物之前步骤的硫酸盐还原酶基因、两个膜结合电子传递复合物(qmoABC和dsrMKJOP)以及ATP合酶(atp)的基因。已知DsrAB能结合并缓慢还原亚硝酸盐。这些数据支持一个模型,其中亚硝酸盐抑制DsrAB(亚硝酸盐的表观解离常数K(m)=0.03 mM),并且当亚硝酸盐浓度处于毫摩尔水平时,NrfHA(亚硝酸盐的K(m)=1.4 mM)通过将亚硝酸盐还原为氨来限制亚硝酸盐的进入。基因表达数据和对相对基因位置的考虑表明,QmoABC和DsrMKJOP分别向腺苷磷酸硫酸还原酶和DsrAB提供电子。atp基因的下调以及添加抑制性亚硝酸盐浓度后记录到的细胞死亡表明,当电子从细胞质硫酸盐转移到周质亚硝酸盐还原时,质子梯度会崩溃。