| 修江帆、魏川川、尚小丽、国果、吴沁怡、吴建伟.家蝇（Musca domestica）羧肽酶基因克隆及原核表达[J].广东农业科学,2014,41(10):152-154 |
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家蝇（Musca domestica）羧肽酶基因克隆及原核表达 |
| Cloning and prokaryotic expression of Muscadomestica carboxypeptidase gene |
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| DOI： |
| 中文关键词: 家蝇 羧肽酶 克隆 原核表达 |
| 英文关键词: Musca domestic carboxypeptidase cloning prokaryotic expression |
| 基金项目:国家科技支撑计划项目（2011BAC06B12）；国家
自然科学基金（81360254、81160204）；国家教育部博士点专项基
金（2008-220、20105215120001) |
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| 摘要点击次数: 1574 |
| 全文下载次数: 651 |
| 中文摘要: |
| 从构建的家蝇幼虫cDNA 质粒文库中筛选到羧肽酶（Carboxypeptidase、CP）基因、以该基因的cDNA 文库
质粒为模板、通过PCR 扩增、获得CP 基因完整编码序列（登录号；KF939629.1）。运用生物信息学方法对该基因及其
编码蛋白的基本理化性质尧信号肽和亚细胞定位等进行预测和分析。构建PEASY-E1-CP 重组质粒、转化到大肠杆菌
OrigamiB (DE3)中进行诱导表达。研究结果表明、CP 基因ORF 全长1 284 bp、编码428 个氨基酸、理论分子量47.8
ku、等电点为6.10、具有CP 家族的蛋白保守结构域；重组原核质粒pEASY-E1-CP 经IPTG 诱导、蛋白在大肠杆菌中
获得表达。 |
| 英文摘要: |
| The complete coding sequence (registration number: KF939629.1) of carboxypeptidase (CP) gene screened
from cDNA library plasmid of Musca domestica was obtained by PCR conducted with the CP cNA library plasmid as
template. The basic physical and chemical properties of the gene and its coding protein, signal peptide and subcellular
localization were predicted and analyzed by the bioinformatics methods. Recombinant plasmid PEASY -E1 -CP was
constructed and induced expression in E. coli OrigamiB(DE3). The results showed that the CP-ORF was 1 284 bp in length
encoding 428 amino acids with a predicted molecular mass of 47.8 ku, pI of 6.10 and conserved domain of
carboxypeptidase family. The recombinant plasmid PEASY-E1-CP was induced by IPTG and the protein expressed in E.
coli |
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