Ohyama T, Igarashi K, Kobayashi H
Faculty of Pharmaceutical Sciences, Chiba University, Japan.
J Bacteriol. 1994 Jul;176(14):4311-5. doi: 10.1128/jb.176.14.4311-4315.1994.
Ohyama et al. previously isolated Escherichia coli mutant RS1, which had a negligible activity for sodium ion extrusion at alkaline pH (T. Ohyama, R. Imaizumi, K. Igarashi, and H. Kobayashi, J. Bacteriol. 174:7743-7749, 1992). Our present study showed that the mutation of RS1 was compensated for by a cloned chaA gene. It has been proposed that sodium ion extrusion by ChaA is prevented under physiological conditions (D. M. Ivey, A. A. Guffanti, J. Zemsky, E. Pinner, R. Karpel, E. Padan, S. Schuldiner, and T. A. Krulwich, J. Biol. Chem. 268:11296-11303, 1993). In order to clarify the physiological role of chaA in sodium ion circulation at alkaline pH, we constructed a delta chaA mutant. The resultant mutant, TO112, deficient in both nhaA and chaA, was unable to grow at pH 8.5 in medium containing 0.1 M sodium chloride and had negligible sodium ion extrusion activity. However, TO112 grew at pH 7.0 in medium containing 0.4 M sodium chloride. Sodium ions were extruded from TO112 cells at neutral pH. The extrusion activity at pH 7.5 was greatly reduced by the deletion of nhaB. These data demonstrate that the activity of nhaB is low at high pH and that ChaA extrudes sodium ions at alkaline pH. The uptake of calcium ions by everted membrane vesicles prepared from the delta chaA mutant TO110 was 60% of the activity observed in the vesicles of the wild-type strain at pH 8.5, but the activity at neutral pH was not reduced by the deletion of chaA. Therefore, it was also suggested that ChaA plays a role in calcium ion circulation at alkaline pH.
小山等人先前分离出大肠杆菌突变体RS1,该突变体在碱性pH条件下钠离子外排活性可忽略不计(T. 小山、R. 今泉、K. 五十岚和H. 小林,《细菌学杂志》174:7743 - 7749,1992年)。我们目前的研究表明,RS1的突变可通过克隆的chaA基因得到补偿。有人提出,在生理条件下ChaA介导的钠离子外排受到抑制(D.M. 艾维、A.A. 古凡蒂、J. 泽姆斯基、E. 平纳、R. 卡佩尔、E. 帕丹、S. 舒尔迪纳和T.A. 克鲁利奇,《生物化学杂志》268:11296 - 11303,1993年)。为了阐明chaA在碱性pH条件下钠离子循环中的生理作用,我们构建了一个∆chaA突变体。所得突变体TO112同时缺乏nhaA和chaA,在含有0.1 M氯化钠的培养基中pH 8.5时无法生长,且钠离子外排活性可忽略不计。然而,TO112在含有0.4 M氯化钠的培养基中pH 7.0时能够生长。在中性pH条件下,钠离子从TO112细胞中被外排。nhaB的缺失极大地降低了pH 7.5时的外排活性。这些数据表明,nhaB在高pH时活性较低,且ChaA在碱性pH条件下可外排钠离子。从∆chaA突变体TO110制备的外翻膜囊泡在pH 8.5时对钙离子的摄取活性是野生型菌株囊泡中观察到活性的60%,但在中性pH条件下,chaA的缺失并未降低其活性。因此,也有人提出ChaA在碱性pH条件下的钙离子循环中发挥作用。