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通育粳1号水稻乙醇脱氢酶基因克隆与原核表达
引用本文:梁燕,严建萍,谭湘陵.通育粳1号水稻乙醇脱氢酶基因克隆与原核表达[J].生物技术通报,2011(3).
作者姓名:梁燕  严建萍  谭湘陵
作者单位:1. 南通高等师范学校,南通,226001
2. 南通大学生物工程研究所,南通,226019
摘    要:克隆通育粳1号水稻乙醇脱氢酶(alcohol dehydrogenase,ADH)基因,并在原核系统中进行体外表达。取通育粳1号水稻幼根,提取总RNA,RT-PCR法扩增ADH基因开放阅读框架片段,双酶切后连接至pGEX-4T-1表达质粒中。将质粒转化至BL21(DE3)宿主菌中,平皿培养,挑取阳性菌落培养,提取重组质粒,酶切、电泳鉴定插入片段并测定其序列。pGEX-4T-1-ADH/BL21进行常规LB扩大培养,IPTG(1 mmol/L)作用2、3和4 h诱导表达,SDS-PAGE检测表达产物。结果显示,插入质粒中的ADH片段序列和方向正确无误,表达蛋白分子量符合预期值42 kD,表达至最大值的诱导时间为3 h。因此,该基因的成功克隆和表达为进一步研究水稻中ADH的作用和应用生物工程法大量获得ADH奠定基础。

关 键 词:ADH  水稻  克隆  原核表达  

Cloning and Prokaryotic Expression of ADH in E.coli from Rice of No.1 Tongyujing
Liang Yan,Yan Jianping,Tan Xiangling.Cloning and Prokaryotic Expression of ADH in E.coli from Rice of No.1 Tongyujing[J].Biotechnology Bulletin,2011(3).
Authors:Liang Yan  Yan Jianping  Tan Xiangling
Institution:Liang Yan1 Yan Jianping1 Tan Xiangling2(1Nantong Higher Normal Institute,Nantong 226001,2Institute of Bioengineering,Nantong University,Nantong 226019)
Abstract:It was to clone of alcohol dehydrogenase(ADH) and expression in E.coli from rice of No.1 Tongyujing.Total RNA was extracted from young root of rice,and ORF fragment of ADH was amplified using RT-PCR.The fragment was connected to expression plasmid pGEX-4T-1 after double cutting using restriction enzyme,and then transformed into E.coli of BL21(DE3),and was cultured at plate medium.Positive colony of E.coli was selected and cultured,and plasmid was extracted.Insert fragment was confirmed by cutting plasmid us...
Keywords:ADH Rice Cloning Prokaryotic expression  
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