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小链霉菌HCCB10043敲除硫酯酶基因的工程菌株构建及其代谢产物的研究
引用本文:尹芳,饶敏,魏维,陈玲玲,陈代杰. 小链霉菌HCCB10043敲除硫酯酶基因的工程菌株构建及其代谢产物的研究[J]. 上海师范大学学报(自然科学版), 2013, 42(4): 392-397
作者姓名:尹芳  饶敏  魏维  陈玲玲  陈代杰
作者单位:[1]上海来益生物药物研发中心生物Ⅱ实验室,上海200240 [2]上海交通大学药学院,上海200240
基金项目:国家自然科学基金(81102354)
摘    要:小链霉菌(Streptomyces parvus)HCCB10043的主要代谢产物为脂肽类化合物A21978C,其基因组序列中包括了非核糖体肽合成酶(NRPS non ribosomal peptide synthetase)、聚酮合酶(PKS polyketide synthases)以及NRPS-PKS混合的多酶体系基因簇,它们的共同特点是在代谢产物生物合成簇中连接有一个硫酯酶域,即TE(thioesterase)domain.硫酯酶可以使已经合成的化合物链的合成过程终止,并且具有水解释放成熟脂肽以及环化线性脂肽链的功能.通过对联二吡啶类代谢产物合成簇中TE基因的敲除构得工程菌株,工程菌发酵结果表明联二吡啶类代谢产物产量减少.

关 键 词:基因敲除  工程菌株  硫酯酶  代谢产物
收稿时间:2013-06-05

Construction of an engineering strain which knocked out the gene of thioesterase for Streptomyces parvus HCCB10043 and the reach of metabolites
YIN Fang,RAO Min,WEI Wei,CHEN Lingling and CHEN Daijie. Construction of an engineering strain which knocked out the gene of thioesterase for Streptomyces parvus HCCB10043 and the reach of metabolites[J]. Journal of Shanghai Normal University(Natural Sciences), 2013, 42(4): 392-397
Authors:YIN Fang  RAO Min  WEI Wei  CHEN Lingling  CHEN Daijie
Affiliation:2. ( 1. Shanghai Laiyi biopharmaceutical R&D center Biological Laboratory 11 , Shanghai 200240, China; 2. College of pharmacy, Shanghai jiaotong university, Shanghai 200240, China)
Abstract:The major metabolites of Streptomyces parvus HCCB10043 is lipopeptide compounds A21978C,its genome sequence includes the non ribosomal peptide synthetase(NRPS),polyketide synthases(PKS) and hybrid NRPS-PKS multi-enzyme system gene clusters,they do have a their common feature in the metabolite biosynthetic cluster,which is called TE domain as well.Thioesterase can synthesized the synthesis of compounds of the chain termination,and with functions to release mature lipopeptide hydrolysis and cyclized peptide chain aliphatic linear.This study,we knockout the TE domain of a gene cluster,which guide the biosynthesis of bipyridine,to obtain engineered bacteria.The fermentation results demonstrates reduced yields for metabolites 2,2′-Bipyridine (2,2′-BP).
Keywords:gene knockout  engineering strain  thioesterase  metabolites
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