Key Laboratory of Food Biotechnology of Sichuan, College of Bioengineering, Xihua University, Sichuan, China.
FEMS Microbiol Lett. 2010 May;306(1):22-9. doi: 10.1111/j.1574-6968.2010.01929.x. Epub 2010 Feb 15.
Metagenomic DNA libraries constructed from the Dagong Ancient Brine Well were screened for genes with Na(+)/H(+) antiporter activity on the antiporter-deficient Escherichia coli KNabc strain. One clone with a stable Na(+)-resistant phenotype was obtained and its Na(+)/H(+) antiporter gene was sequenced and designated as m-nha. The deduced amino acid sequence of M-Nha protein consists of 523 residues with a calculated molecular weight of 58 147 Da and a pI of 5.50, which is homologous with NhaH from Halobacillus dabanensis D-8(T) (92%) and Halobacillus aidingensis AD-6(T) (86%), and with Nhe2 from Bacillus sp. NRRL B-14911 (64%). It had a hydropathy profile with 10 putative transmembrane domains and a long carboxyl terminal hydrophilic tail of 140 amino acid residues, similar to Nhap from Synechocystis sp. and Aphanothece halophytica, as well as NhaG from Bacillus subtilis. The m-nha gene in the antiporter-negative mutant E. coli KNabc conferred resistance to Na(+) and the ability to grow under alkaline conditions. The difference in amino acid sequence and the putative secondary structure suggested that the m-nha isolated from the Dagong Ancient Brine Well in this study was a novel Na(+)/H(+) antiporter gene.
从大龚古盐井构建的宏基因组 DNA 文库中,筛选了在缺乏 Na(+)/H(+)反向转运蛋白的大肠杆菌 KNabc 菌株上具有 Na(+)/H(+)反向转运活性的基因。获得了一个具有稳定 Na(+)抗性表型的克隆,并对其 Na(+)/H(+)反向转运蛋白基因进行了测序,并命名为 m-nha。M-Nha 蛋白的推导氨基酸序列由 523 个残基组成,计算分子量为 58147Da,等电点为 5.50,与来自 D-8(T)的 Halobacillus dabanensis NhaH(92%)和来自 AD-6(T)的 Halobacillus aidingensis NhaH(86%)同源,与来自 Bacillus sp. NRRL B-14911 的 Nhe2(64%)同源。它具有 10 个假定跨膜结构域和 140 个氨基酸残基的长羧基末端亲水尾巴的疏水性图谱,与来自 Synechocystis sp.和 Aphanothece halophytica 的 Nhap 以及来自 Bacillus subtilis 的 NhaG 相似。在反向转运蛋白阴性突变大肠杆菌 KNabc 中,m-nha 基因赋予了对 Na(+)的抗性和在碱性条件下生长的能力。氨基酸序列和假定二级结构的差异表明,本研究从大龚古盐井中分离出的 m-nha 是一种新型的 Na(+)/H(+)反向转运蛋白基因。