半滑舌鳎生长因子midkine的定点改造及原核表达
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青岛市海洋与渔业局,国家海洋局北海环境监测中心,中国海洋大学海洋生命学院,中国海洋大学海洋生命学院,中国海洋大学海洋生命学院,中国海洋大学海洋生命学院,中国海洋大学海洋生命学院

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国家高技术研究发展计划(2012AA100802, 2012AA100801)


The site-directed mutagenesis and prokaryotic expression of midkine gene in Cynoglossus semilaevis
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Ocean and Fishery Bureau of Qingdao,North China Sea Environment Monitoring Center, SOA,College of Marine Life Science,Ocean University of China,Key Laboratory of Marine Genetics and Breeding,Ministry of Education,College of Marine Life Science,Ocean University of China,Key Laboratory of Marine Genetics and Breeding,Ministry of Education,College of Marine Life Science,Ocean University of China,Key Laboratory of Marine Genetics and Breeding,Ministry of Education,College of Marine Life Science,Ocean University of China,Key Laboratory of Marine Genetics and Breeding,Ministry of Education,College of Marine Life Science,Ocean University of China,Key Laboratory of Marine Genetics and Breeding,Ministry of Education

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Project supported by the National High Technology Research and Development Program of China (2012AA100802, 2012AA100801)

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    摘要:

    为进一步的研究半滑舌鳎(Cynoglossu semilaevis)MK成熟肽活性与功能,对半滑舌鳎生长因子midkine成熟肽进行定点改造及原核表达。根据大肠杆菌偏爱密码子的特点,实验利用SOEing PCR法对半滑舌鳎MK成熟肽进行定点突变。将改造后的半滑舌鳎成熟肽MK克隆到载体质粒pET32a( ),构建原核表达载体pET32a( )-MK,并转化大肠杆菌BL21(DE3)pLysS菌株中。SDS-PAGE结果显示,与对照组相比,经IPTG诱导表达后半滑舌鳎重组蛋白MK存在于大肠杆菌上清中,产物相对分子质量约为33 kD。研究表明,本实验对半滑舌鳎生长因子midkine成功进行了定点改造,原核表达质粒成功构建并在大肠杆菌中高效表达,且主要以可溶形式存在。

    Abstract:

    Midkine is a kind of heparin-binding cytokine, and it promotes growth, survival, migration and other activities of target cells. The expression of fusion protein MK will facilitate further studies for its biological functions in half-smooth tongue sole (Cynoglossus semilaevis). Based on the plasmid containing full length of half-smooth tongue sole MK cDNA sequence, the site-directed mutagenesis of predicted mature MK sequence was successfully obtained by SOEing PCR method according to the E. coli codon bias. After being confirmed by sequencing, the resulting gene was cloned to the vector pET32a ( ) to yield an identified recombinant plasmid pET32a( )-MK, which was then transformed into E. coli host strain BL21(DE3)pLysS. SDS-PAGE analysis revealed that high level of fusion protein MK was induced by 1mmol/L IPTG at 37℃ and was mainly detected in sonicated supernatant. The yielded fusion protein MK was approximately 33 kD which was in accordance with the theoretical molecular weight. This research establish the bases for further study for its detailed functions in half-smooth tongue sole.

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王亚楠,刘旭东,穆琳琳,刘志鹏,李春梅,于海洋,张全启.半滑舌鳎生长因子midkine的定点改造及原核表达[J].水产学报,2013,37(3):330~336

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  • 收稿日期:2012-02-08
  • 最后修改日期:2012-12-23
  • 录用日期:2013-03-12
  • 在线发布日期: 2013-03-20
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