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作 者:刘晓华[1] 李慧美[1] 柯颖笑 张凯强[1] 李响敏[1] 李欣[1] 付金衡[1] 李海星[1] LIU Xiaohua;LI Huimei;KE Yingxiao;ZHANG Kaiqiang;LI Xiangmin;LI Xin;FU Jinheng;LI Haixing(State Key Laboratory of Food Science and Technology, Sino-German Joint Research Institute,Nanchang University, Nanchang 330047, China)
机构地区:[1]南昌大学中德联合研究院,食品科学与技术国家重点实验室,江西南昌330047
出 处:《食品科学》2017年第6期1-5,共5页Food Science
基 金:国家自然科学基金地区科学基金项目(31260373);江西省重点研发计划项目(20161BBF60094)
摘 要:以从黄牛瘤胃中分离到的一株具有将亚油酸转化为c9,t11-共轭亚油酸(conjugated linoleic acid,CLA)的干酪乳杆菌(Lactobacillus casei)Fx为出发菌株,提取其基因组DNA,聚合酶链式反应(polymerase chain reaction,PCR)扩增得到1 700 bp大小的亚油酸异构酶(linoleic acid isomerase,LAI)基因片段,将该基因片段纯化后进行TA克隆,得到重组质粒p UCm-T-LAI,将重组质粒p UCm-T-LAI和表达质粒p ET-Dsb A同时进行双酶切,连接得到重组表达载体p ET-Dsb A-LAI,经PCR鉴定和酶切后,将重组表达载体转化到大肠杆菌BL21中,得到具有LAI活性的重组菌株,能将亚油酸转化为c9,t11-CLA,表明从Lactobacillus casei Fx成功克隆LAI,该研究将有助于深入了解不同瘤胃细菌特异性合成不同CLA异构体的LAI基因差异。Lactobacillus casei Fx was isolated from cattle rumen for its ability to transform linoleic acid into c9,t11-conjugated linoleic acid(CLA).Genomic DNA was extracted and a1700-bp linoleic acid isomerase(LAI)gene fragmentwas amplified from the strain by PCR.The gene fragment was purified and cloned into the plasmid pUCm-T-LAI to obtainrecombinant plasmid pUCm-T-LAI by TA cloning.The recombinant plasmid and the expression plasmid pET-DsbA weresubjected to double enzyme digestion and ligated to the recombinant expression vector pET-DsbA-LAI.After identificationby PCR and enzymatic digestion,the recombinant expression vector was transformed into E.coli BL21.The recombinantstrain,having LAI activity,possessed the ability to specifically transform linoleic acid into c9,t11-CLA isomer.The resultsshowed that the LAI gene from L.casei Fx was successfully cloned.This work makes it possible to understand the differenceamong the LAI genes in different rumen bacteria.
关 键 词:共轭亚油酸 亚油酸异构酶 干酪乳杆菌 克隆 表达
分 类 号:TS201.2[轻工技术与工程—食品科学]
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