杂合抗菌肽Sα-Jp基因真核表达载体的构建  

Construction of Eukaryotic Expression Vector for Antibacterial Peptide Sα-Jp Gene

作　　者：陈晓平[1] 贾春兰[1] 马吉霞[2] 

机构地区：[1]吉林农业大学食品科学与工程学院,吉林长春30118 [2]通化农业学校,吉林通化134000

出　　处：《食品与发酵科技》2014年第2期9-12,26,共5页Food and Fermentation Science & Technology

基　　金：吉林省重点科技攻关项目(20060208)

摘　　要：为获取高效表达且具有抗菌活性的新型杂合抗菌抗菌肽。根据Spinigerinα、Japonicin II抗菌肽的氨基酸序列,结合蛋白质分子的结构和抗菌肽的抑菌机制,选用毕赤酵母偏爱密码子,设计合成杂合抗菌肽Sα-Jp基因,并将其定向克隆至真核表达载体pPICZαA上。经聚合酶链式反应,双酶切,序列分析等鉴定,所转化的宿主菌中含有插入Sα-Jp基因的重组表达载体pPICZαA-Sα-Jp。结果表明:已成功构建真核表达载体,可用于真核分泌表达。To obtain the new hybrid antibacterial peptide of high efficient expression and antimicrobial activity. According to the sequence of amino acids about Spinigerin α, Japonicin II antibacterial peptide, combined with the structure of the protein molecules and antibacterial mechanism of antibacterial peptides, choose pichia preference codon, design and synthesis hybrid antimicrobial peptide Sα-Jp gene, and directed cloning to eukaryotic expression vector pPICZαA. By polymerase chain reaction, the double enzyme digestion and the sequence analysis to identify the transformation of host insert is contained in the recombinant expression vector of pPICZαA-Sα-Jp. Results show that we have been successfully build a eukaryotic expression vector, and it can be used in the secretion of eukaryotic expression.

关 键 词：Sα-Jp杂合抗菌肽 基因的克隆 表达载体构建 

分 类 号：TS207.4[轻工技术与工程—食品科学]