Kakinuma Y, Igarashi K
Faculty of Pharmaceutical Sciences, Chiba University, Japan.
J Bacteriol. 1990 Apr;172(4):1732-5. doi: 10.1128/jb.172.4.1732-1735.1990.
Alkali-sensitive mutants which grow at pH 7.5 but not at pH 9.5 in Na(+)-rich media were isolated from Streptococcus faecalis ATCC 9790. One of the mutants, designated Nak1, lacked activities of both Na(+)-stimulated ATPase and KtrII (active K+ uptake by sodium ATPase). These activities were restored in a spontaneous revertant designated Nak1R. Active sodium extrusion from Nak1 was observed at pH 7.0, which allows the cells to generate a proton potential, but not at pH 9.5, which reverses the proton potential, making it positive. Sodium extrusion at pH 7.0 was inhibited by addition of dicyclohexylcarbodiimide and protonophores. Even at pH 9.5, Nak1 did grow well in Na(+)-poor media. In Na(+)-rich media at pH 7.5, growth of Nak1 but not that of 9790 was severely inhibited by a protonophore. These results indicate that mutant Nak1 lacks sodium ATPase but contains a sodium/proton antiporter and that sodium ATPase is essential for the growth of this organism at high pH in Na(+)-rich conditions.
从粪肠球菌ATCC 9790中分离出在富含Na⁺的培养基中于pH 7.5生长但在pH 9.5不生长的碱敏感突变体。其中一个突变体,命名为Nak1,缺乏Na⁺刺激的ATP酶和KtrII(由钠ATP酶介导的活性K⁺摄取)的活性。这些活性在一个自发回复突变体Nak1R中得以恢复。在pH 7.0时观察到Nak1有活性钠外流,此时细胞能够产生质子电位,但在pH 9.5时没有,pH 9.5会使质子电位反转并变为正值。pH 7.0时的钠外流受到二环己基碳二亚胺和质子载体的抑制。即使在pH 9.5时,Nak1在低Na⁺培养基中也生长良好。在pH 7.5的富含Na⁺的培养基中,质子载体严重抑制了Nak1的生长,但对9790没有影响。这些结果表明,突变体Nak1缺乏钠ATP酶,但含有钠/质子反向转运体,并且钠ATP酶对于该生物体在富含Na⁺的条件下于高pH时的生长至关重要。