丹参SmJAZ1蛋白原核表达及条件优化  

Optimizing expression of recombinant jasmonate ZIM-domain protein from Salvia miltiorrhiza

作　　者：张利华[1] 吴文燕[2,3] 黄璐琦[2] 申业[2] 

机构地区：[1]首都医科大学中医药学院,北京100069 [2]中国中医科学院中药研究所,北京100070 [3]北京中医药大学中药学院,北京100029

出　　处：《中国中药杂志》2012年第24期3712-3716,共5页China Journal of Chinese Materia Medica

摘　　要：目的:在前期克隆丹参SmJAZ1基因的cDNA全长基础上,为研究丹参SmJAZ蛋白的功能,在大肠杆菌BL21(DE3)中诱导表达丹参SmJAZ1蛋白,并对其表达条件进行优化。方法:利用分子克隆的方法将丹参JAZ1基因构建到原核表达载体pET32a上,转化到大肠杆菌BL21(DE3)宿主菌中进行诱导表达。结果:对影响重组蛋白表达的4个因素,即诱导温度、诱导时间、IPTG浓度、及IPTG添加时间进行优化,确定丹参SmJAZ1重组蛋白最适表达条件。IPTG浓度对目的蛋白的表达量没有显著影响;随诱导时间和诱导温度增加,SmJAZ蛋白的表达量增加;而IPTG添加时间对蛋白的表达量有明显影响。结论:丹参JAZ1蛋白在30℃温度条件下,重组菌生长2 h(A600=0.9),加入0.1 mmol.L-1浓度的IPTG,诱导20 h后,表达条件最合适。Objective： Accumulation of tanshinton in Salvia miltiorrhiza are enhanced by exogenous application of jasmonates. The core JA signaling module COII/JAZ/MYC2 play a central role on control of downstream gene expression in the JA pathway. To ob- tained the antibody of SmJAZ, SmJAZ recombinant protein was expressed in Escherichia coli and optimal expression was performed. Method ： The full-length SmJAZ10RF was sub-cloned in a prokaryotic expression vector pET32a. The recombinant fusion protein had high expression level in BI21 （DE3） strain of E. coli, and SDS-PAGE analysis showed its molecular weight was about 24 kDa. Re- sult： The induction of E. coli [ pET32-JAZ1 ] in different temperature, induction time, IPTG concentrations and IPTG adding time of E. coli were performed. The induction time and the induction temperature are positively related trends with SmJAZ1 protein expression, and IPTG concentration had no significant impact in protein expression, whereas IPTG adding time had significant impact on protein expression. Conclusion： Shaking the culture at 30 ℃ until the A600 is approximately 0.9 （2 h in LB）, and add IPTG to a final concen- tration of 0. 1 mmol· L^- 1 , and then the optimal expression of SmJAZ1 recombinant protein were accumulated after the induction time of 20 h.

关 键 词：丹参 JAZ1 原核表达 条件优化 

分 类 号：R282[医药卫生—中药学]