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机构地区:[1]中国科学院海洋生物资源可持续利用重点实验室,中国科学院海洋微生物研究中心,广东省海洋药物重点实验室,中国科学院南海海洋研究所,广州510301 [2]中国科学院大学,北京100049
出 处:《微生物学报》2013年第11期1179-1188,共10页Acta Microbiologica Sinica
基 金:国家自然科学基金(21172231);国家"973项目"(2010CB833805)~~
摘 要:【目的】鉴定sgvS是绿灰霉素生物合成起始结构单元3-羟基吡啶甲酸的必需基因;测定绿灰霉素起始结构单元3-羟基吡啶甲酸的活化特异性。【方法】构建sgvS的基因失活突变株和反式回补菌株,对其发酵产物进行HPLC分析。并在突变菌株sgvS的发酵液中分别添加3-羟基吡啶甲酸,吡啶-2-甲酸,3-氯-吡啶-2-甲酸,4-氯-吡啶-2-甲酸,3,5-二氯-吡啶-2-甲酸,烟酸,2-氟-烟酸,2-氯-烟酸,5-氟-烟酸,6-氟-烟酸和环哌啶-2-甲酸,用HPLC分析其代谢产物的变化。【结果】突变菌株sgvS丧失了绿灰霉素的生产能力,sgvS基因反式回补突变株恢复了绿灰霉素的生产能力。向突变菌株sgvS中添加3-羟基吡啶甲酸也能恢复绿灰霉素的生产,但添加其它上述衍生物均无法恢复绿灰霉素的生产或介导产生新的结构类似物。【结论】sgvS是绿灰霉素及其骨架起始单元3-羟基吡啶甲酸生物合成的必需基因,SgvD1对3-羟基吡啶甲酸结构单元的激活存在着严格的底物选择特异性。[ Objective] To explore the role of sgvS in the biosynthesis of 3-hydroxypicolinic acid moiety ofviridogrsein, and to analyze the substrate specificity of 3-hydroxypicolinic acid moiety in the viridogrsein biosynthetic pathway. [ Methods] Through gene insertion inactivation and in trans complementation strategies, we obtained the gene inactivation mutant sgvS andits complementation mutant AsgvS::sgvS. Meanwhile, we fed 3-hydroxypicolinic acid, picolinic acid, 2- piperidinecarboxylic acid, 3-chloropyridinecarboxylie acid, 4-cbloropyridinecarboxylic acid, 3,5-chloropyridinecarboxylic acid, nicotinic acid, 2-chloronicotinic acid, 2-fluoronicotinic acid acid, 5-fluoronicotinic acid and 6-fluoronicotinic acid to the sgvSmutant, respectively. Thefermentation extracts were analyzed by HPLC. [ Resultsl sgvS mutant abolished the viridogrsein production; viridogrsein production was restored through in trans complementation of sgvS mutant or by feeding 3-hydroxypicolinic acid to the sgvS mutant. No new viridogrsein analogues were observed by feeding other above mentioned 3-hydroxypicolinic acid analogues totbe AsgvS mutant. [ Conclusion ] sgvS is necessary for the biosynthesis of 3- hydroxypicolinic acid moiety. The biosynthetic protein, SgvD1 ,activates 3-hydroxypicolinie acid, showing strict substrate specificity en route to the viridogrsein biosynthesis.
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