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类鼻疽伯克霍尔德菌BPSS0180基因的克隆、原核表达及生物信息学分析

张振兴 李亚颖 王凤阳 杜丽 聂鑫 杨小健 曹瑞勇 李宝宝 黄海峰 朱姝 李国华 彭冬梅

中国畜牧兽医2017,Vol.44Issue(11):3313-3319,7.
中国畜牧兽医2017,Vol.44Issue(11):3313-3319,7.DOI:10.16431/j.cnki.1671-7236.2017.11.029

类鼻疽伯克霍尔德菌BPSS0180基因的克隆、原核表达及生物信息学分析

Cloning, Prokaryotic Expression and Bioinformatics Analysis of BPSS0180 Gene of Burkholderia pseudomallei

张振兴 1李亚颖 1王凤阳 1杜丽 1聂鑫 1杨小健 1曹瑞勇 1李宝宝 1黄海峰 1朱姝 1李国华 1彭冬梅1

作者信息

  • 1. 海南大学热带农林学院动物科技学院,海南省热带动物繁育与疫病研究重点实验室,海口市动物基因工程重点实验室,海口 570228
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摘要

Abstract

This study was aimed to clone and express the BPSS0180 gene of Burkholderia pseudomallei (B.pseudomallea),and perform bioinformatics analysis of its protein.A pair of primers was designed according to the BPSS0180 gene sequence information of B.pseudomallea K96243 strain in GenBank.BPSS0180 gene fragment was obtained by PCR amplification of B.pseudomallea hn-1 strain.The BPSS0180 gene fragment was ligated into the pET-28a(+) vector to construct the pET-28a(+)-BPSS0180 recombinant plasmid.The recombinant plasmid pET-28a (+)-BPSS0180 was transformed into E.coli DH5α competent cells,and the plasmids were identified by restriction enzyme digestion.Then,the recombinant plasmid pET-28a(+)-BPSS0180 was transformed into E.coli BL21 (DE3) competent cells.The expression was induced by IPTG.The expressed product was analyzed by SDS-PAGE and Western blotting.Bioinformatics analysis of BPSS0180 gene sequence was carried out using DNAMAN,ProtParam,SOPMA and Protscale.The results showed that the length of BPSS0180 gene was 1146 bp;The expressed His-BPSS0180 fusion protein was about 45 ku,and was predominantly in the form of inclusion bodies;The molecular weight of the BPSS0180 protein was 40.6 ku (C1779 H2809 N545 O536 S7);The extinction coefficient was 40 575;The hydrophobic index was 85.43;The instability coefficient was 46.52,which belonged to unstable protein;The theoretical isoelectric point (pI) was 5.54 and was acidic protein;The total average hydrophobicity (GRAVY) was-0.261,as hydrophilic protein;The secondary structure of the protein were mainly α-helix (58.79 %) and random curl (32.02 %),and its half-life of reticulocytes in mammals was predicted to be 30 h.This study provided a theoretical basis for further exploring the fuction of BPSS0180 gene of B.pseudomallei.

关键词

类鼻疽伯克霍尔德菌/BPSS0180基因/克隆/原核表达/生物信息学分析

Key words

Burkholderia pseudomallei/BPSS0180 gene/cloning/prokaryotic expression/bioinformatics analysis

分类

医药卫生

引用本文复制引用

张振兴,李亚颖,王凤阳,杜丽,聂鑫,杨小健,曹瑞勇,李宝宝,黄海峰,朱姝,李国华,彭冬梅..类鼻疽伯克霍尔德菌BPSS0180基因的克隆、原核表达及生物信息学分析[J].中国畜牧兽医,2017,44(11):3313-3319,7.

基金项目

海南省重大科技计划项目(ZDKJ2016017-01) (ZDKJ2016017-01)

中国畜牧兽医

OA北大核心CSTPCD

1671-7236

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