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利用家蚕生产慈姑蛋白酶抑制剂
引用本文:季平,张志芳,何家禄,宓怡德,吴祥甫.利用家蚕生产慈姑蛋白酶抑制剂[J].蚕业科学,1995,21(4):223-227.
作者姓名:季平  张志芳  何家禄  宓怡德  吴祥甫
作者单位:中国农业科学院蚕业研究所,中国科学院上海生物化学研究所
摘    要:将慈姑蛋白酶抑制剂B(ArrowheadProteinaseInhibitor,B,AIB)基因插入转移载体pUBM—4中,得到重组转移载体pUBM(AIB);与Bm—NPVDNA共转染家蚕细胞,经空斑纯化,得到不含多角体的重组病毒BmNPV(AIB);感染家蚕幼虫,利用家蚕高效表达了AIB,其表达量为1.0×105U/mL血淋巴,比活为3.29×103U/mg。

关 键 词:慈姑蛋白酶抑制剂B,cDNA序列,家蚕核型多角体病毒,空斑纯化,基因表达

PRODUCTION OF THE ARROWHEAD PROTEINASE INHIBITOR IN THE SILKWORM LARVAE
Ji Ping Zhang ZHifang He Jialu.PRODUCTION OF THE ARROWHEAD PROTEINASE INHIBITOR IN THE SILKWORM LARVAE[J].Acta Sericologica Sinica,1995,21(4):223-227.
Authors:Ji Ping Zhang ZHifang He Jialu
Abstract:Arrowhead proteinase inhibitor B sequence was cloned into transfer vector pUBM 4 to form the recombinant transfer vector pUBM(AIB).Then ,pUBM(AIB)and BmNPV DNA were co-transfected into the BmN with lipofectin entrapment. After that,the recombinant virus of BmNPV(AIB)Ⅰ Ⅲ were isolated and purified by plaque assay.AIB was expressed in the silkworm larvae at high level. The product exhibited bilogical activity.
Keywords:Arrowhead proteinase inhibitor B cDNA sequence BmNPV Plaque assay Gene expression
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