分子伴侣协助下抗肿瘤抗生素美达霉素生物合成中的糖基转移酶Med-ORF8的原核表达  

Prokaryotic expression of a glycosyltransferase Med-ORF8 involved in an antitumor antibiotic medermycin biosynthesis aided by the molecular chaperone

作　　者：万娟[1] 邓会群[1] 张碧乾[1] 王蔚[1] 蔡晓凤[1] 李爱英[1,2] 

机构地区：[1]华中师范大学生命科学学院,湖北武汉430079 [2]华中师范大学农药与化学生物学教育部重点实验室,湖北武汉430079

出　　处：《微生物学通报》2011年第2期221-227,共7页Microbiology China

基　　金：国家自然科学基金项目(No.30770036);教育部高等学校博士学科点专项科研基金项目(No.20070511004)

摘　　要：糖基转移酶在天然产物的糖基化修饰过程中起关键作用。目前链霉菌源抗肿瘤抗生素美达霉素(Medermycin)生物合成途径中的糖基转移酶Med-ORF8的原核表达及酶学性质还未有研究。首先通过结构模拟确定Med-ORF8的端部加上His-标签不会影响其三维结构的正确折叠,然后利用2种pET原核表达载体来进行Med-ORF8的原核表达,发现以pET-28a(+)为载体进行表达时,目的蛋白产量非常高,但是以不可溶的包涵体形式为主。当分子伴侣基因(编码大肠杆菌触发因子)与Med-ORF8的编码基因共表达时,在优化诱导条件的情况下,可以有效减少包涵体的形成,提高了Med-ORF8的可溶性表达效率,为Med-ORF8的酶学分析打下基础。Glycosyltransferases play central roles in the glycosylation of biosynthetic pathways of many antibiotics.The prokaryotic expression and enzymatic features of Med-ORF8,a glycosyltransferase involved in the biosynthesis of medermycin with strong antitumor activity,still remains obscure.Here,firstly,we performed the computer modeling of the 3-D structure of Med-ORF8 to prove that the presence of 6*His-tag at the terminals of Med-ORF8 had no effect on its 3-D structure.Subsequently,we established two prokaryotic expression systems with pET vectors to express Med-ORF8,and found that pET-28a(+) could gain a higher yield of the target protein than pET-23a(+),but mostly in an insoluble form.Finally,we introduced a molecular chaperone gene into the system with pET-28a(+) and found that the co-expression of the molecular chaperone with Med-ORF8 could efficiently decrease the formation of the inclusion body and increase the accumulation of soluble Med-ORF8.

关 键 词：糖基化 美达霉素 糖基转移酶 原核表达 分子伴侣 

分 类 号：Q78[生物学—分子生物学]