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DNA克隆载体的"三片段克隆法"改造策略
引用本文:谢锋,朱蕾,尚广东.DNA克隆载体的"三片段克隆法"改造策略[J].南京师大学报,2007,30(4):80-83.
作者姓名:谢锋  朱蕾  尚广东
作者单位:江苏省生物多样性和生物技术重点实验室,江苏南京210046
基金项目:国家高技术研究发展计划(863计划)
摘    要:

关 键 词:重组工程  三片段克隆法  结合转移载体  克隆载体  片段克隆  改造策略  Modification  Vector  Direct  Method  放线菌  大肠杆菌  转移载体  问题  碱基突变  回收  凝胶  紫外线  暴露  长片段  限制性内切酶  克隆策略  快速
文章编号:1001-4616(2007)04-0080-04
收稿时间:2007-06-05
修稿时间:2007-06-20

A General Method for Direct DNA Vector Modification
Xie Feng,Zhu Lei,Shang Guangdong.A General Method for Direct DNA Vector Modification[J].Journal of Nanjing Normal University(Natural Science Edition),2007,30(4):80-83.
Authors:Xie Feng  Zhu Lei  Shang Guangdong
Abstract:Cloning one or more DNA fragments into a vector is the one of most commonly used techniques in molecular biology. Classic cloning strategy, when dealt with complicated cloning steps, like multiple fragments insertion, selective marker exchange, are often troubled by the choice of restriction enzymes, the base mutations caused by long fragment PCR, UV exposure and gel purification. We made use of the Red/ET technology to clone two fragments into the vector while remove the unnecessary vector part in a single step. This three pieces cloning manipulation is straightforward and convenient, with the potential to be a general cloning strategy for vector engineering.
Keywords:recombineering  three pieces cloning  conjugal transfer vector
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