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极端嗜碱菌的钠离子循环:一种次级钠离子/氢离子反向转运蛋白和钠离子/溶质同向转运蛋白。

The Na+ cycle of extreme alkalophiles: a secondary Na+/H+ antiporter and Na+/solute symporters.

作者信息

Krulwich T A, Guffanti A A

机构信息

Department of Biochemistry, Mount Sinai School of Medicine of the City University of New York, New York 10029.

出版信息

J Bioenerg Biomembr. 1989 Dec;21(6):663-77. doi: 10.1007/BF00762685.

Abstract

Extremely alkalophilic bacteria that grow optimally at pH 10.5 and above are generally aerobic bacilli that grow at mesophilic temperatures and moderate salt levels. The adaptations to alkalophily in these organisms may be distinguished from responses to combined challenges of high pH together with other stresses such as salinity or anaerobiosis. These alkalophiles all possess a simple and physiologically crucial Na+ cycle that accomplishes the key task of pH homeostasis. An electrogenic, secondary Na+/H+ antiporter is energized by the electrochemical proton gradient formed by the proton-pumping respiratory chain. The antiporter facilitates maintenance of a pHin that is two or more pH units lower than pHout at optimal pH values for growth. It also largely converts the initial electrochemical proton gradient formed by respiration into an electrochemical sodium gradient that energizes motility as well as a plethora of Na+ solute symporters. These symporters catalyze solute accumulation and, importantly, reentry of Na+. The extreme nonmarine alkalophiles exhibit no primary sodium pumping dependent upon either respiration or ATP. ATP synthesis is not part of their Na+ cycle. Rather, the specific details of oxidative phosphorylation in these organisms are an interesting analogue of the same process in mitochondria, and may utilize some common features to optimize energy transduction.

摘要

在pH 10.5及以上环境中生长最佳的极端嗜碱菌通常是嗜温需氧芽孢杆菌,能在中等盐浓度下生长。这些生物体对嗜碱性的适应可能与对高pH值与其他胁迫(如盐度或厌氧环境)共同挑战的反应有所不同。这些嗜碱菌都拥有一个简单且生理上至关重要的Na⁺循环,该循环完成了pH值稳态的关键任务。一种生电的次级Na⁺/H⁺反向转运蛋白由质子泵呼吸链形成的电化学质子梯度提供能量。在生长的最佳pH值下,该反向转运蛋白有助于维持胞内pH值比胞外pH值低两个或更多pH单位。它还在很大程度上将呼吸作用形成的初始电化学质子梯度转化为电化学钠梯度,为运动性以及大量的Na⁺溶质同向转运体提供能量。这些同向转运体催化溶质积累,重要的是,促进Na⁺的重新进入。极端非海洋嗜碱菌没有依赖呼吸作用或ATP的初级钠泵。ATP合成不是它们Na⁺循环的一部分。相反,这些生物体中氧化磷酸化的具体细节是线粒体中相同过程的有趣类似物,并且可能利用一些共同特征来优化能量转导。

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