| 易道生，魏晓东，缪永建，陈燕飞.鸡β- 防御素7 的克隆及表达[J].广东农业科学,2018,45(2):130-134 |
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鸡β- 防御素7 的克隆及表达 |
| Cloning and expression of avian beta defensin 7 gene from chicken |
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| DOI：10.16768/j.issn.1004-874X.2018.02.021 |
| 中文关键词: β- 防御素 克隆 原核表达 基因重组 |
| 英文关键词: beta defensin 7 cloning expression gene recombinant |
| 基金项目:韶关市科技计划项目（405-99000313）；国家大学生创新创业项目（201410576007）；韶关学院校级
课题（314-140642） |
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| 摘要点击次数: 1912 |
| 全文下载次数: 870 |
| 中文摘要: |
| 以NCBI 已登录的鸡β- 防御素7（登录号：NM_001001194）为模板，设计特异性引物，扩增
鸡β- 防御素7 基因，目的基因与pET32a 载体相连，构建表达质粒并导入大肠杆菌BL21，经IPTG 诱导表
达和抗菌试验。结果表明，PCR 扩增的目的片段，经测序证明与鸡β- 防御素7 基因NM_001001194 序列
同源性达99%，经IPTG 诱导表达的重组蛋白与预期大小相符。平板抑菌试验结果表明，该重组多肽对金黄
色葡萄球菌有较强的抗菌活性。 |
| 英文摘要: |
| A pairs of primers used in polymerase chain reaction (PCR) was designed following the
NM_001001194 from GenBank to amplify the beta defensin 7 gene of chicken. The total RNA was isolated from
spinal cord cells of chicken，and the first cDNA strand was obtained by approach of reverse transcription PCR.
The products of PCR were linked with T plasmid vectors，and then transformed into Escherichia coli（E. Coli）
DH5α strain cells subsequently. Expressional plasmid vector，pET32a-gal7，was reconstructed with restriction
endonuclease Hind Ⅲ and BamH I. Recombinant plasmid vector，pET32a-gal7，was induced with Isopropyl-
β-D-Thiogalacto Pyranoside (IPTG) in E. Coli DE3 strain cells to produce recombinant Gal7 protein. The results
showed that the cloned cDNA sequence of beta defensin 7 gene of chicken was comprised of 132 nucleotide acid
residues，and encoded the beta defensin 7 with 44 amino acids and predicted molecular weight 4923.81Da.
The identity to NM_001001194 is 99%. The recombinant peptides had strong antibacterial activity against
staphylococcus aureus in vitro. |
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