Sugimoto Shinya, Nakayama Jiro, Fukuda Daisuke, Sonezaki Shino, Watanabe Maki, Tosukhowong Amonlaya, Sonomoto Kenji
Laboratory of Microbial Technology, Division of Microbial Science and Technology, Department of Bioscience and Biotechnology, Faculty of Agriculture, Graduate School, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan.
J Biosci Bioeng. 2003;96(2):129-33. doi: 10.1016/s1389-1723(03)90114-9.
Molecular chaperone DnaK of halophilic Tetragenococcus halophilus JCM5888 was characterized under salinity conditions both in vitro and in vivo. The dnaK gene was cloned into an expression vector and transformed into Escherichia coli. The DnaK protein obtained from the recombinant E. coli showed a significantly higher refolding activity of denatured lactate dehydrogenase than that from non-halophilic Lactococcus lactis under NaCl concentrations higher than 1 M. E. coli without the overexpression of DnaK exhibited a growth profile with a prolonged lag phase and suppressed maximum cell density in Luria-Bertani medium containing 5% (0.86 M) NaCl. On the contrary, the overexpression of T. halophilus DnaK greatly shortened this prolonged lag phase with no effect on maximum growth, while that of L. lactis DnaK decreased maximum growth. The amount of protein aggregates was increased by salt stress in the E. coli cells, while this aggregation was greatly suppressed by the overexpression of T, halophilus DnaK. These results suggest that heterologous overexpression of T. halophilus DnaK, via its chaperone activity, promotes salinity adaptation of E. coli.
嗜盐嗜盐四联球菌JCM5888的分子伴侣DnaK在体外和体内盐度条件下进行了表征。将dnaK基因克隆到表达载体中并转化到大肠杆菌中。在高于1 M的NaCl浓度下,从重组大肠杆菌中获得的DnaK蛋白对变性乳酸脱氢酶的重折叠活性明显高于非嗜盐乳酸乳球菌。在含有5%(0.86 M)NaCl的Luria-Bertani培养基中,未过表达DnaK的大肠杆菌呈现出延迟期延长和最大细胞密度受抑制的生长曲线。相反,嗜盐嗜盐四联球菌DnaK的过表达极大地缩短了这个延长的延迟期,对最大生长没有影响,而乳酸乳球菌DnaK的过表达则降低了最大生长。盐胁迫会增加大肠杆菌细胞中蛋白质聚集体的数量,而嗜盐嗜盐四联球菌DnaK的过表达则极大地抑制了这种聚集。这些结果表明,嗜盐嗜盐四联球菌DnaK的异源过表达通过其伴侣活性促进了大肠杆菌对盐度的适应。