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作 者:王相生[1] 孙亚宁 阮崇美[1] 张全伟[3] 张勇[1] 胡骁飞[2]
机构地区:[1]甘肃农业大学动物医学院,兰州730070 [2]河南省农业科学院,农业部动物免疫学重点实验室,郑州450002 [3]甘肃农业大学生命科学技术学院,兰州730070
出 处:《动物营养学报》2017年第11期4019-4025,共7页CHINESE JOURNAL OF ANIMAL NUTRITION
基 金:“十二五”国家科技支撑计划“畜禽产品安全监控和检测技术研究与示范”(2014BAD13B05)
摘 要:本试验旨在建立玉米赤霉烯酮(ZEN)降解酶基因ZEN-jjm在枯草芽孢杆菌中的表达体系,确定其产物的生物降解活性及对母猪繁殖性能的作用。克隆ZEN-jjm基因,经EcoRⅠ和NotⅠ双酶切后连接至p HT01表达载体中,构建重组质粒;转化枯草芽孢杆菌,通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)分析ZEN-jjm蛋白表达水平。高效液相色谱法(HPLC)检测表达的ZEN-jjm蛋白降解ZEN的活性。通过对母猪的繁殖性能的评价,确定ZEN降解酶降解ZEN对母猪繁殖性能的影响。双酶切和测序结果表明:ZEN-jjm成功插入p HT01中,SDSPAGE表明获得1株高效表达目的蛋白的重组枯草芽孢杆菌,其大小约为29 ku。HPLC结果表明表达的ZEN-jjm蛋白能有效地降解ZEN;表达的ZEN-jjm蛋白能显著缓解ZEN对繁殖母猪的毒害作用(P<0.05)。综上:1)本研究成功构建了表达ZEN-jjm在枯草芽孢杆菌中的表达载体,并在枯草芽孢杆菌中得到了表达。2)表达的ZEN-jjm蛋白具有降解ZEN的生物活性。3)在饲粮中添加ZEN-jjm蛋白能显著降低ZEN对母猪能繁殖性能的危害。The purpose of this study w as to establish an expressing system of zearalenone( ZEN) degrading enzyme gene( ZEN-jjm) in Bacillus subtilis,and to determine the biodegradation activity and effect of its expression product on reproductive performance of sow s. The ZEN-jjm gene w as cloned and the recombinant expression plasmid w as constructed by ligation cloned ZEN-jjm and p HT01 vector digested w ith EcoRⅠand NotⅠ enzymes,and then transformed into Bacillus subilis. Expression of ZEN-jjm protein in Bacillus subilis was analyzed by dodecyl sulfate polyacrylamide gel electrophoresis( SDS-PAGE). And the degrading activity of ZEN-jjm protein w as determined by high performance liquid chromatography( HPLC). The effects of ZEN degrading enzyme on reproductive performance of sow s w ere evaluated. The results of double enzyme digestion and DNA sequencing demonstrated that ZEN-jjm w as inserted into p H T01. The SDS-PAGE show ed that one Bacillus subilis strain w ith high-level expression w as obtained,and the size of the expressed protein w as about29 ku. The HPLC result illustrated that the expressed ZEN-jjm protein could effectively degrade ZEN. The evaluation results of reproductive performance of sow s indicated that the expressed ZEN-jjm protein could significantly relieve the toxicity for sow s caused by ZEN( P〈0.05). In conclusion: 1) the ZEN-jjm expression vector is successfully constructed and the ZEN-jjm protein is expressed in Bacillus subtilis in this study. 2) The expressed ZEN-jjm protein has the biological activity of degrading ZEN. 3) ZEN-jjm protein can significantly reduce the harm of ZEN on reproductive performance of sow s w hen it is added in the feed.
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