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乳酸乳球菌苹果酸-乳酸酶基因的克隆
引用本文:董华,刘天明,吴克学.乳酸乳球菌苹果酸-乳酸酶基因的克隆[J].生物技术通报,2006(5):94-96.
作者姓名:董华  刘天明  吴克学
作者单位:1. 山东轻工业学院,济南,250100
2. 长春金赛药业,长春,130012
摘    要:用酚抽提的方法提取乳酸乳球菌的基因组DNA,利用PCR方法从乳酸菌的基因组DNA中扩增出含有苹果酸-乳酸酶基因(malolactic enzyme gene,mle)的约1.6kb的DNA片断,用1%的琼脂糖凝胶分离扩增的片断,用试剂盒回收目的基因。将回收的目的基因与pGEM-T载体连接构建mle-T载体并转化大肠杆菌DH5a,挑取阳性克隆(白色菌落),酶切鉴定并测序。SalI酶切mle-T,回收mle DNA片断,与表达载体pET-28a载体连接,构建细菌Escherichia coli表达载体。

关 键 词:苹果酸-乳酸酶基因(mle)  克隆  PCR  测序
收稿时间:2006-02-28
修稿时间:2006年2月28日

Malolactic Enzyme Gene(mle) Cloning from Lactococcus Lactis. Lactis
Dong Hua,Liu Tianming,Wu Kexue.Malolactic Enzyme Gene(mle) Cloning from Lactococcus Lactis. Lactis[J].Biotechnology Bulletin,2006(5):94-96.
Authors:Dong Hua  Liu Tianming  Wu Kexue
Institution:1.Shandong Institute of Light Industry, Jinan 250100; 2.Changchtm GeneScience Pharmacenticals Co., Ltd, Changchtm 130012
Abstract:The genomic DNA from Lactococcus lactis.lactis was extracted with the method of phenol.1.6kb malolactic enzyme gene(mle) was amplicated by PCR from the enomic DNA PCR production was purified by means of electrophoresis of 1% agrose gel and DNA reagent kit,then was linked to pGEM-T vector by T4-DNA ligase,and then transformed into E.coli DH5a,finally screening the recombinant depending on Blue-White clony.
Keywords:Mle Cloneing PCR Sequence
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