首页> 外文期刊>The journal of microbiology >Cloning and characterization of a Na+/H+ antiporter gene of the moderately halophilic bacterium Halobacillus aidingensis AD-6T
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Cloning and characterization of a Na+/H+ antiporter gene of the moderately halophilic bacterium Halobacillus aidingensis AD-6T

机译:中度嗜盐菌爱德华氏嗜盐杆菌AD-6T Na + / H +反转运蛋白基因的克隆与鉴定

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摘要

A gene encoding a Na+/H+ antiporter was obtained from the genome of Halobacillus aidingensis AD-6T, which was sequenced and designated as nhaH. The deduced amino acid sequence of the gene was 91% identical to the NhaH of H. dabanensis, and shared 54% identity with the NhaG of Bacillus subtilis. The cloned gene enable the Escherichia coli KNabc cell, which lack all of the major Na+/H+ antiporters, to grow in medium containing 0.2 M NaCl or 10 mM LiCl. The nhaH gene was predicted to encode a 43.5 kDa protein (403 amino acid residues) with 11 putative transmembrane regions. Everted membrane vesicles prepared from E. coli KNabc cells carrying NhaH exhibited Na+/H+ as well as Li+/H+ antiporter activity, which was pH-dependent with the highest activity at pH 8.0, and no K+/H+ antiporter activity was detected. The deletion of hydrophilic C-terminal amino acid residues showed that the short C-terminal tail was vital for Na+/H+ antiporter activity.
机译:从爱丁氏嗜盐杆菌AD-6T的基因组中获得了编码Na + / H +反转运蛋白的基因,该基因被测序并命名为nhaH。该基因推导的氨基酸序列与达巴木霉的NhaH具有91%的同一性,与枯草芽孢杆菌的NhaG具有54%的同一性。克隆的基因能够使缺少所有主要Na + / H +反转运蛋白的大肠杆菌KNabc细胞在含有0.2 M NaCl或10 mM LiCl的培养基中生长。预测nhaH基因编码43.5 kDa蛋白(403个氨基酸残基),具有11个假定的跨膜区域。由携带NhaH的大肠杆菌KNabc细胞制备的外翻膜囊泡表现出Na + / H +以及Li + / H +反转运蛋白活性,这是pH依赖性的,在pH 8.0时具有最高活性,并且未检测到K + / H +反转运蛋白活性。亲水的C末端氨基酸残基的删除表明,短的C末端尾巴对Na + / H +反转运蛋白活性至关重要。

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