Thelen P, Tsuchiya T, Goldberg E B
Department of Molecular Biology and Microbiology, Tufts University Medical School, Boston, Massachusetts 02111.
J Bacteriol. 1991 Oct;173(20):6553-7. doi: 10.1128/jb.173.20.6553-6557.1991.
Using in vivo assays, we show that the Na+/H+ antiporter activity of the Escherichia coli mutant HIT-1 is reduced dramatically compared with activity in wild-type cells. An isogenic nhaA (formerly antA) deletion strain, however, is not significantly different from wild type in this respect. We call the locus affecting Na+/H+ antiporter activity of the HIT-1 mutant nhaB. The nhaB activity exhibits no pH dependence in the range between 7.0 and 8.5, whereas that of the nhaA gene increases considerably at pH levels above 8.0. Mutants with defects in nhaB grow normally on agar media containing 0.5 M NaCl, but nhaA mutants are sensitive to 0.5 M NaCl. We have mapped the nhaB mutation of HIT-1 to 25.6 min on the E. coli map. It is unlinked to the nhaA region, which is located at about 0.5 min. Since a cell with a mutation in nhaB alone is essentially Na+/H+ antiporter negative up to pH 8.0, we conclude that nhaB is required for the major Na+/H+ antiporter activity in the usual physiological pH range.
通过体内试验,我们发现大肠杆菌突变体HIT-1的Na⁺/H⁺逆向转运蛋白活性与野生型细胞相比显著降低。然而,在这方面,等基因的nhaA(以前称为antA)缺失菌株与野生型没有显著差异。我们将影响HIT-1突变体Na⁺/H⁺逆向转运蛋白活性的基因座称为nhaB。nhaB活性在7.0至8.5的范围内不表现出pH依赖性,而nhaA基因的活性在pH值高于8.0时显著增加。nhaB有缺陷的突变体在含有0.5 M NaCl的琼脂培养基上正常生长,但nhaA突变体对0.5 M NaCl敏感。我们已将HIT-1的nhaB突变定位到大肠杆菌染色体图谱上的25.6分钟处。它与位于约0.5分钟处的nhaA区域不连锁。由于仅nhaB发生突变的细胞在pH值达到8.0之前基本上是Na⁺/H⁺逆向转运蛋白阴性,我们得出结论,在通常的生理pH范围内,nhaB是主要的Na⁺/H⁺逆向转运蛋白活性所必需的。