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作 者:王秀青[1] 朱明星[2] 张爱君[1] 丁淑琴[1] 风琴
机构地区:[1]宁夏医科大学检验学院,银川750004 [2]宁夏医科大学实验动物中心,银川750004
出 处:《东北农业大学学报》2009年第11期95-98,共4页Journal of Northeast Agricultural University
基 金:宁夏医科大学启动项目(XT200712)
摘 要:根据天蚕素类抗菌肽作用机制假说,设计引物对前期构建成功的载体天蚕素类杂合肽cecropinA-magainin进行定点突变,使其生成杂合肽的衍生物,测序正确后转化Pichia pastoris受体菌SMD1168,在醇氧化酶(AOX)启动子调控下,分子质量约119ku的cecA-mag杂合抗菌肽突变体获得表达,并通过琼脂扩散试验对表达产物的抑菌活性与cecA-mag进行了比较。结果表明,突变体对金黄色葡萄球菌抑菌活性比cecA-mag提高了1.2倍。According to the partiality codon of Pichia pastoris, hybrid antimicrobial peptide cecA-mag gene was synthesized and cloned into pPICZα-A to construct the recombinant expression vector pPICZ α- A-CA. The recombinant antibacterial peptide cecA-mag was mutanted by the recombinant PCR. In this way, the mutant was gained. The Sac Ⅰ -linearized plasmid pPICZA-A-CA-mu was transformed into P. pastoris SMD1168 by electroporation. Under the control of the promoter AOXp(alcoholoxidasep), an approximately 119 ku cecA-mag-mu protein was expressed. According to agarose diffusion assay, antibacterial activity of cecA-mag-mu was 1.2 times than that of cecA-mag.
关 键 词:杂合抗菌肽cecA—mag 突变体 毕赤酵母 分泌表达 抑菌活性
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