Liew Chong Wai, Illias Rosli Md, Mahadi Nor Muhammad, Najimudin Nazalan
Department of Bioprocess Engineering, Faculty of Chemical and Natural Resources Engineering, Universiti Teknologi Malaysia, Skudai, Johor, Malaysia.
FEMS Microbiol Lett. 2007 Nov;276(1):114-22. doi: 10.1111/j.1574-6968.2007.00925.x.
A Na(+)/H(+) antiporter gene was isolated from alkaliphilic Bacillus sp. G1. The full-length sequence of the Na(+)/H(+) antiporter gene was obtained using a genome walking method, and designated as g1-nhaC. An ORF preceded by a promoter-like sequence and a Shine-Dalgarno sequence, and followed by a terminator-like sequence was identified. The deduced amino acid sequence consists of 535 amino acids, and a calculated molecular mass of 57 776 Da. g1-nhaC was subsequently cloned into pET22b(+) and expressed in Escherichia coli BL21 (DE3). Recombinant E. coli harboring the g1-nhaC gene was able to grow in modified L medium at various concentrations of NaCl (0.2-2.0 M) at different pH values. The recombinant bacteria grew well in the medium with concentrations of NaCl as high as 1.75 M at pH 8.0-9.0. Minimal growth was observed at 2.0 M NaCl, pH 8.0-9.0. At pH 10, the recombinant bacteria grew well in a medium with a low concentration of NaCl (0.2 M). These results suggested that the g1-NhaC antiporter from Bacillus sp. G1 plays a role in Na(+) extrusion at lower pH values and in pH homeostasis at pH 10 under Na(+)-limiting conditions.
从嗜碱芽孢杆菌G1中分离出一个Na(+)/H(+)反向转运蛋白基因。利用基因组步移法获得了Na(+)/H(+)反向转运蛋白基因的全长序列,并将其命名为g1-nhaC。鉴定出一个开放阅读框,其前面有一个类似启动子的序列和一个Shine-Dalgarno序列,后面跟着一个类似终止子的序列。推导的氨基酸序列由535个氨基酸组成,计算分子量为57 776 Da。随后将g1-nhaC克隆到pET22b(+)中并在大肠杆菌BL21(DE3)中表达。携带g1-nhaC基因的重组大肠杆菌能够在不同pH值下的各种NaCl浓度(0.2 - 2.0 M)的改良L培养基中生长。在pH 8.0 - 9.0时,重组细菌在NaCl浓度高达1.75 M的培养基中生长良好。在2.0 M NaCl、pH 8.0 - 9.0时观察到最小生长。在pH 10时,重组细菌在低浓度NaCl(0.2 M)的培养基中生长良好。这些结果表明,芽孢杆菌G1的g1-NhaC反向转运蛋白在较低pH值下的Na(+)外排以及在Na(+)限制条件下pH 10时的pH稳态中发挥作用。