Ito M, Guffanti A A, Zemsky J, Ivey D M, Krulwich T A
Department of Biochemistry, Mount Sinai School of Medicine of the City University of New York, New York 10029, USA.
J Bacteriol. 1997 Jun;179(12):3851-7. doi: 10.1128/jb.179.12.3851-3857.1997.
Application of protoplast transformation and single- and double-crossover mutagenesis protocols to alkaliphilic Bacillus firmus OF4811M (an auxotrophic strain of B. firmus OF4) facilitated the extension of the sequence of the previously cloned nhaC gene, which encodes an Na+/H+ antiporter, and the surrounding region. The nhaC gene is part of a likely 2-gene operon encompassing nhaC and a small gene that was designated nhaS; the operon is preceded by novel direct repeats. The predicted alkaliphile NhaC, based on the extended sequence analysis, would be a membrane protein with 462 amino acid residues and 12 transmembrane segments that is highly homologous to the deduced products of homologous genes of unknown function from Bacillus subtilis and Haemophilus influenzae. The full-length version of nhaC complemented the Na+-sensitive phenotype of an antiporter-deficient mutant strain of Escherichia coli but not the alkali-sensitive growth phenotypes of Na+/H+-deficient mutants of either alkaliphilic B. firmus OF4811M or B. subtilis. Indeed, NhaC has no required role in alkaliphily, inasmuch as the nhaC deletion strain of B. firmus OF4811M, N13, grew well at pH 10.5 at Na+ concentrations equal to or greater than 10 mM. Even at lower Na+ concentrations, N13 exhibited only a modest growth defect at pH 10.5. This was accompanied by a reduced capacity to acidify the cytoplasm relative to the medium compared to the wild-type strain or to N13 complemented by cloned nhaC. The most notable deficiency observed in N13 was its poor growth at pH 7.5 and Na+ concentrations up to 25 mM. During growth at pH 7.5, NhaC is apparently a major component of the relatively high affinity Na+/H+ antiport activity available to extrude the Na+ and to confer some initial protection in the face of a sudden upshift in external pH, i.e., before full induction of additional antiporters. Consistent with the inference that NhaC is a relatively high affinity, electrogenic Na+/H+ antiporter, N13 exhibited a defect in diffusion potential-energized efflux of 22Na+ from right-side-out membrane vesicles from cells that were preloaded with 2 mM Na+ and energized at pH 7.5. When the experiment was conducted with vesicles loaded with 25 mM Na+, comparable efflux was observed in preparations from all the strains.
将原生质体转化以及单交换和双交换诱变方案应用于嗜碱芽孢杆菌OF4811M(嗜碱芽孢杆菌OF4的营养缺陷型菌株),有助于扩展先前克隆的编码Na⁺/H⁺反向转运蛋白的nhaC基因及其周边区域的序列。nhaC基因是一个可能由nhaC和一个名为nhaS的小基因组成的双基因操纵子的一部分;该操纵子之前有新的直接重复序列。基于扩展序列分析预测的嗜碱菌NhaC将是一种具有462个氨基酸残基和12个跨膜区段的膜蛋白,与枯草芽孢杆菌和流感嗜血杆菌中功能未知的同源基因推导产物高度同源。nhaC的全长版本补充了大肠杆菌反向转运蛋白缺陷突变株的Na⁺敏感表型,但不能补充嗜碱芽孢杆菌OF4811M或枯草芽孢杆菌的Na⁺/H⁺缺陷突变株的碱敏感生长表型。实际上,NhaC在嗜碱性方面没有必需作用,因为嗜碱芽孢杆菌OF4811M的nhaC缺失菌株N13在Na⁺浓度等于或大于10 mM时于pH 10.5下生长良好。即使在较低的Na⁺浓度下,N13在pH 10.5时也仅表现出适度的生长缺陷。与野生型菌株或由克隆的nhaC互补的N13相比,这伴随着相对于培养基酸化细胞质的能力降低。在N13中观察到的最显著缺陷是其在pH 7.5和高达25 mM的Na⁺浓度下生长不良。在pH 7.5生长期间,NhaC显然是相对高亲和力的Na⁺/H⁺反向转运活性的主要成分,可用于排出Na⁺并在外部pH突然升高时提供一些初始保护,即在额外反向转运蛋白完全诱导之前。与NhaC是相对高亲和力的电生性Na⁺/H⁺反向转运蛋白的推断一致,N13在从预先加载2 mM Na⁺并在pH 7.5下供能的细胞的外翻膜囊泡中22Na⁺的扩散电位驱动外排方面表现出缺陷。当用加载25 mM Na⁺的囊泡进行实验时,在所有菌株的制剂中观察到了相当的外排。