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中国可可盐湖钠离子/氢离子反向转运蛋白基因的宏基因组克隆及功能分析。

Metagenome cloning and functional analysis of Na⁺/H⁺ antiporter genes from Keke Salt Lake in China.

机构信息

State Key Laboratory of Agrobiotechnology, China Agricultural University, Beijing, 100193, People's Republic of China.

出版信息

Curr Microbiol. 2012 Feb;64(2):179-84. doi: 10.1007/s00284-011-0053-8. Epub 2011 Nov 19.

Abstract

Na⁺/H⁺ antiporters are ubiquitous membrane proteins and play a central role in cell homeostasis including pH regulation, osmoregulation, and Na⁺/Li⁺ tolerance in bacteria. The microbial communities in extremely hypersaline soil are an important resource for isolating Na⁺/H⁺ antiporter genes. A metagenomic library containing 35,700 clones was constructed by using genomic DNA obtained from the hypersaline soil samples of Keke Salt Lake in Northwest of China. Two Na⁺/H⁺ antiporters, K1-NhaD, and K2-NhaD belonging to NhaD family, were screened and cloned from this metagenome by complementing the triple mutant Escherichia coli strain KNabc (nhaA⁻, nhaB⁻, chaA⁻) in medium containing 0.2 M NaCl. K1-NhaD and K2-NhaD have 75.5% identity at the predicted amino acid sequence. K1-NhaD has 78% identity with Na⁺/H⁺ antiporter NhaD from Halomonas elongate at the predicted amino acid sequence. The predicted K1-NhaD is a 53.5 kDa protein (487 amino acids) with 13 transmembrane helices. K2-NhaD has 73% identity with Alkalimonas amylolytica NhaD. The predicted K2-NhaD is a 55 kDa protein (495 amino acids) with 12 transmembrane helices. Both K1-NhaD and K2-NhaD could make the triple mutant E. coli KNabc (nhaA⁻, nhaB⁻, chaA⁻) grow in the LBK medium containing 0.2-0.6 M Na⁺ or with 0.05-0.4 M Li⁺. Everted membrane vesicles prepared from E. coli KNabc cells carrying K1-NhaD or K2-NhaD exhibited Na⁺/H⁺ and Li⁺/H⁺ antiporter activities which were pH-dependent with the highest activity at pH 9.5. Little K⁺/H⁺ antiporter activity was also detected in vesicles form E. coli KNabc carrying K1-NhaD or K2-NhaD.

摘要

钠离子/氢离子反向转运蛋白是普遍存在的膜蛋白,在细胞内稳态中发挥着核心作用,包括 pH 调节、渗透调节以及细菌中钠离子/锂离子的耐受。极度高盐土壤中的微生物群落是分离钠离子/氢离子反向转运蛋白基因的重要资源。使用来自中国西北部可可盐湖高盐土壤样本的基因组 DNA 构建了一个包含 35700 个克隆的宏基因组文库。通过在含有 0.2 M NaCl 的培养基中补充三重突变体大肠杆菌 KNabc(nhaA-,nhaB-,chaA-),从该宏基因组中筛选并克隆了两种属于 NhaD 家族的钠离子/氢离子反向转运蛋白,K1-NhaD 和 K2-NhaD。K1-NhaD 和 K2-NhaD 在预测的氨基酸序列上具有 75.5%的同一性。K1-NhaD 在预测的氨基酸序列上与伸长盐单胞菌的 Na+/H+反向转运蛋白 NhaD 具有 78%的同一性。预测的 K1-NhaD 是一种 53.5 kDa 的蛋白质(487 个氨基酸),具有 13 个跨膜螺旋。K2-NhaD 与嗜碱盐单胞菌 NhaD 具有 73%的同一性。预测的 K2-NhaD 是一种 55 kDa 的蛋白质(495 个氨基酸),具有 12 个跨膜螺旋。K1-NhaD 和 K2-NhaD 都可以使三重突变体大肠杆菌 KNabc(nhaA-,nhaB-,chaA-)在含有 0.2-0.6 M Na+或 0.05-0.4 M Li+的 LBK 培养基中生长。从携带 K1-NhaD 或 K2-NhaD 的大肠杆菌 KNabc 细胞制备的外翻膜囊泡表现出 Na+/H+和 Li+/H+反向转运蛋白活性,该活性在 pH9.5 时具有最高活性。在携带 K1-NhaD 或 K2-NhaD 的大肠杆菌 KNabc 囊泡中也检测到少量的 K+/H+反向转运蛋白活性。

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