Bañuelos M A, Rodríguez-Navarro A
Departamento de Biotecnología, Escuela Técnica Superior de Ingenieros Agrónomos, Universidad Politécnica de Madrid, Spain.
J Biol Chem. 1998 Jan 16;273(3):1640-6. doi: 10.1074/jbc.273.3.1640.
Two genes isolated from Schwanniomyces occidentalis, ENA1 and ENA2, encode P-type ATPases highly homologous to the Na-ATPases of Saccharomyces cerevisiae and complement the Na+ sensitivity of an S. cerevisiae mutant strain lacking its own Na-ATPases. The expression of both ENA1 and ENA2 was highly dependent on a high external pH, but whereas a high pH was sufficient for the expression of ENA2, the expression of ENA1 required a high pH and the presence of Na+. Disruption of ENA1 rendered the cells less tolerant to Na+ than the wild-type strain and decreased their capacity for Na+ extrusion. Disruption of ENA2 did not affect Na+ tolerance, but decreased both the growth at high pH and K+ efflux. We discuss these results and propose that fungal Na-ATPases should be considered alkali cation ATPases. By sequence comparison, we found that fungal Na-ATPases form a homogeneous group that can be distinguished from other cation-pumping P-type ATPases, except from the cta3 Ca-ATPase of Schizosaccharomyces pombe.
从西方许旺酵母中分离出的两个基因ENA1和ENA2,编码与酿酒酵母的钠ATP酶高度同源的P型ATP酶,并能弥补缺乏自身钠ATP酶的酿酒酵母突变株对钠的敏感性。ENA1和ENA2的表达都高度依赖于高外部pH值,但虽然高pH值足以使ENA2表达,但ENA1的表达需要高pH值和钠离子的存在。ENA1的破坏使细胞对钠的耐受性低于野生型菌株,并降低了它们的钠外排能力。ENA2的破坏不影响对钠的耐受性,但降低了在高pH值下的生长和钾外流。我们讨论了这些结果,并提出真菌钠ATP酶应被视为碱金属阳离子ATP酶。通过序列比较,我们发现真菌钠ATP酶形成了一个同质的群体,除了粟酒裂殖酵母的cta3钙ATP酶外,它可以与其他阳离子泵P型ATP酶区分开来。