Xu Xixi, Jiao Lingxia, Feng Xin, Ran Junjian, Liang Xinhong, Zhao Ruixiang
School of Food Science, Henan Institute of Science and Technology, Hualan Road, Xinxiang City, 453003, Henan Province, China.
AMB Express. 2017 Dec;7(1):36. doi: 10.1186/s13568-017-0337-x. Epub 2017 Feb 13.
Alicyclobacillus acidoterrestris, an acidophilic and thermophilic bacteria, is an important microbial resource for stress resistance genes screening. In this study, DnaK gene from A. acidoterrestris was subcloned to construct the recombinant plasmid pET28a-DnaK. The successful construction of the plasmid was verified by double-enzyme digestion and sequencing analysis. The recombinant plasmid was transformed into Escherichia coli BL21 and isopropy-β-D-thiogalactoside (IPTG) was used to induce recombinant E. coli to express DnaK gene. A 70 kD fusion protein was identified by SDS-PAGE, which suggested that DnaK gene from A. acidoterrestris was successfully expressed. The recombinant and wild BL21 were treated with high temperatures of 54, 56 and 58 °C at pH values of 5.0-7.0 to compare the effects of heterogeneous expression of the DnaK gene from A. acidoterrestris on the stress resistance. The experimental results showed that survival rate of recombinant BL21-DnaK has been improved considerably under heat and acid stresses in contrast with the wild BL21, and D-values of recombinant BL21 were 14.7-72% higher than that of wild BL21, which demonstrated that heterogeneous expression of DnaK gene from A. acidoterrestris could significantly enhance the resistance of host bacteria E. coli against heat and acid stresses.
嗜酸耐热栖热放线菌是一种嗜酸嗜热细菌,是筛选抗逆基因的重要微生物资源。本研究中,嗜酸耐热栖热放线菌的DnaK基因被亚克隆以构建重组质粒pET28a-DnaK。通过双酶切和测序分析验证了质粒的成功构建。将重组质粒转化到大肠杆菌BL21中,并用异丙基-β-D-硫代半乳糖苷(IPTG)诱导重组大肠杆菌表达DnaK基因。通过SDS-PAGE鉴定出一个70 kD的融合蛋白,这表明嗜酸耐热栖热放线菌的DnaK基因成功表达。将重组菌和野生型BL21在pH值为5.0 - 7.0的条件下分别用54、56和58 °C的高温处理,以比较嗜酸耐热栖热放线菌DnaK基因异源表达对其抗逆性的影响。实验结果表明,与野生型BL21相比,重组BL21-DnaK在热胁迫和酸胁迫下的存活率有显著提高,重组BL21的D值比野生型BL21高14.7 - 72%,这表明嗜酸耐热栖热放线菌DnaK基因的异源表达可显著增强宿主菌大肠杆菌对热胁迫和酸胁迫的抗性。