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哈维弧菌rbsB基因的克隆与表达 被引量:1

Cloning rbsB gene from Vibrio harveyi and its expression
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摘要 哈维弧菌(Vibrio harveyi)是海水鱼养殖中一种重要的病原菌。该研究根据已知rbs B(核糖体结合蛋白)基因序列设计引物,扩增得到哈维弧菌354(V.harveyi 354)rbs B基因的全序列(Gen Bank序列号MF797015),预测该序列可编码292个氨基酸,分子量为30.7 k D,理论等电点为5.05,亲水性系数为0.043,为疏水性蛋白。根据Rbs B氨基酸构建的系统进化树可以发现哈维弧菌Rbs B蛋白和欧文弧菌(V.owensii CAIM 1854)的关系最近。构建了p GEX-4t-1-rbs B重组质粒并转化至大肠埃希菌BL21(DE3)中,得到的重组蛋白的相对分子量约59 k D,在37℃、IPTG浓度为0.6 mmol·L–1诱导8 h时表达量最高。 Vibrio harveyi is one of the most important mariculture pathogens. We amplified the whole rbsB gene (GenBank ID MF797015) sequence of V.harveyi strain 354 which was predicted to encode 292 amino acid with molecular weight of 30.7 kD, isoelectric point of 5.05 and hydrophilic coefficient of 0.043. Thus, the Vh-RbsB may be a hydrophobic protein. Phylogenetic tree constructed based on RbsB amino acid sequence indicates that Vh-RbsB has the closest relationship with V.owensii CAIM 1854. A recombinant plasmid pGEX-4t-1-rbsB was constructed and transformed into Escherichia coli BL21 (DE3). The relative molecular weight of the recombinant protein was about 59 kD. The highest expression was observed at 37℃, 8 h, concentration of IPTG of 0.6 mmol·L-1.
作者 贝蕾 苏友禄 赵超 徐力文 刘广锋 王雨 郭志勋 冯娟 BEI Lei1,, SU Youlu1, ZHAO Chao1, XU Liwen1, LIU Guangfeng1, WANG Yu1, 3, GUO Zhixun1, FENG Juan1(1. Key Laboratory of South China Sea Fishery Resource Exploitation & Utilization, Ministry of Agriculture; South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510300, China; 2. College of Fisheries and Life Science, Shanghai Ocean University, Shanghai 201306, China; 3. Tropical Aquaculture Research and Development Center, South China Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Sanya 572018, Chin)
出处 《南方水产科学》 CAS CSCD 北大核心 2018年第2期75-82,共8页 South China Fisheries Science
基金 中国水产科学研究院中央级公益性科研院所基本科研业务费专项资金资助(2017HY-ZD1007) 海南省科技兴海项目(2015XH03) 广东省级鱼病防治专项资金项目(粤财农[2015]115) 广东省海洋渔业科技与产业发展专项资金(A201501814)
关键词 哈维弧菌 rbsB基因 全长克隆 原核表达 Vibrio harveyi rbsB gene gene clone prokaryotic expression
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