首页 | 本学科首页   官方微博 | 高级检索  
   检索      

透明颤菌血红蛋白的DNA改组研究
引用本文:袁宁,胡又佳,朱春宝,朱宝泉.透明颤菌血红蛋白的DNA改组研究[J].中国生物工程杂志,2006,26(11):14-19.
作者姓名:袁宁  胡又佳  朱春宝  朱宝泉
作者单位:上海医药工业研究院 上海医药工业研究院 上海医药工业研究院 上海医药工业研究院
基金项目:国家高技术研究发展计划(863计划)
摘    要:为提高透明颤菌血红蛋白在限氧条件下促进宿主细胞生长的能力,首先通过易错PCR向透明颤菌血红蛋白基因中引入突变,再结合DNA改组对其进行改造。将改组基因置于透明颤菌血红蛋白天然启动子下游,转化大肠杆菌DH5α,构建改组文库。以限氧培养条件下菌体沉淀的颜色为指标进行试管初筛,再以限氧和极端限氧条件下菌体湿重为指标进行摇瓶复筛,最终得到一个高活性突变蛋白VHb'042506。该蛋白使宿主的菌体湿重在限氧和极端限氧条件下较原基因转化子分别提高了31.25%和58.75%。经测序和比对,该基因与原基因相比发生了11处碱基点突变,致氨基酸4处错义突变。CO差光谱实验显示该蛋白具有更强的特征吸收。

关 键 词:透明颤菌血红蛋白  DNA改组  易错PCR  
收稿时间:2006-08-25
修稿时间:2006-10-17

DNA shuffling of Vitreoscilla Hemoglobin
YUAN Ning,HU You-jia,ZHU Chun-bao,ZHU Bao-quan.DNA shuffling of Vitreoscilla Hemoglobin[J].China Biotechnology,2006,26(11):14-19.
Authors:YUAN Ning  HU You-jia  ZHU Chun-bao  ZHU Bao-quan
Institution:Shanghai Institute of Pharmaceutical Industry, Shanghai 200437, China
Abstract:To improve the growth enhancement activity of Vitreoscilla hemoglobin(VHb), Vitreoscilla hemoglobin gene(vgb) was mutated by error-prone PCR and then reconstituted by DNA shuffling. The shuffling library was constructed by inserting the shuffled genes into downstream of the vgb natural promoter and transforming them into E.coli DH5α. Mutated active VHb proteins were first screened in test tubes according to host cell pellets color and then in shake flasks according to host pellets wet weight .One active mutant protein, VHb'042506, was obtained after second screening. It can increased the host wet weight by 31.25% and 58.75% than that of the control which bearing natural VHb under microaerobic and extremely microaerobic conditions, respectively. Sequencing and alignment results showed that 11 nucleotides were mutated, thus resulted in 4 amino acids changes occurred in this mutant protein. CO difference spectrum test also indicated that it had higher specific absorption.
Keywords:Vitreoscilla hemoglobin(VHb) Error-prone PCR DNA shuffling
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《中国生物工程杂志》浏览原始摘要信息
点击此处可从《中国生物工程杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号