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嗜碱芽孢杆菌C-125菌株Na+/H+逆向转运蛋白系统相关基因的特性分析

Characterization of a gene responsible for the Na+/H+ antiporter system of alkalophilic Bacillus species strain C-125.

作者信息

Hamamoto T, Hashimoto M, Hino M, Kitada M, Seto Y, Kudo T, Horikoshi K

机构信息

Institute of Physical and Chemical Research (RIKEN), Saitama, Japan.

出版信息

Mol Microbiol. 1994 Dec;14(5):939-46. doi: 10.1111/j.1365-2958.1994.tb01329.x.

Abstract

An alkali-sensitive mutant, 38154, of the alkalophilic Bacillus sp. strain C-125 could not grow at an alkaline pH. The nucleotide sequence of a 3.7 kb parental DNA fragment that recovers the growth of 38154 at alkaline pH has four open reading frames (ORF1-4). By subcloning the fragment, we demonstrated that a 0.25 kb DNA region is responsible for the recovery. Direct sequencing of the mutant's corresponding region revealed a G to A substitution. The mutation resulted in an amino acid substitution from Gly-393 to Arg of the putative ORF1 product, which was deduced to be an 804-amino-acid polypeptide with a molecular weight of 89,070. The N-terminal part of the putative ORF1 product showed amino acid similarity to those of the chain-5 products of eukaryotic NADH quinone oxidoreductases. Membrane vesicles prepared from 38154 did not show membrane potential (delta psi)-driven Na+/H+ antiporter activity. Antiporter activity was resumed by introducing a parental DNA fragment which recovered the mutant's alkalophily. These results indicate that the mutation in 38154 affects, either directly or indirectly, the electrogenic Na+/H+ antiporter activity. This is the first report which shows that a gene responsible for the Na+/H+ antiporter system is important in the alkalophily of alkalophilic microorganisms.

摘要

嗜碱芽孢杆菌C-125的碱敏感突变体38154在碱性pH条件下无法生长。一个能使38154在碱性pH条件下恢复生长的3.7 kb亲本DNA片段的核苷酸序列含有四个开放阅读框(ORF1 - 4)。通过对该片段进行亚克隆,我们证明一个0.25 kb的DNA区域负责这种恢复作用。对突变体相应区域的直接测序显示有一个G到A的替换。该突变导致推定的ORF1产物从第393位的甘氨酸被替换为精氨酸,该产物被推导为一个804个氨基酸的多肽,分子量为89,070。推定的ORF1产物的N端部分与真核生物NADH醌氧化还原酶的链5产物的氨基酸具有相似性。从38154制备的膜囊泡未显示出膜电位(Δψ)驱动的Na⁺/H⁺反向转运活性。通过导入能恢复突变体嗜碱性的亲本DNA片段,反向转运活性得以恢复。这些结果表明,38154中的突变直接或间接影响了生电Na⁺/H⁺反向转运活性。这是首次报道表明负责Na⁺/H⁺反向转运系统的基因在嗜碱微生物的嗜碱性中起重要作用。

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