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中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2010, Vol. 30 Issue (01): 35-40    
技术与方法     
人粒细胞-巨噬细胞集落刺激因子的克隆及在毕赤酵母中的表达
李俏俏1,王清路1**,张玉军1,张锐2,徐寿增1
1.山东万杰医学院 淄博 255213
2.中国农业科学院生物技术研究所 北京 100081
Cloning and Expression in Pichia pastoris of Human Granulocyte-macrophage Colony Stimulating Factor
LI Qiao-qiao1,WANG Qing-lu1,ZHANG Yu-jun1,ZHANG Rui2,XU Shou-zeng1
1.Shandong Wanjie Medical College, Zibo 255213,China
2.Institute of Biotechnology, Chinese Academy of Agricultural Sciences,Beijing 100081,China
 全文: PDF(555 KB)   HTML
摘要:

采用加长引物5'端的方法克隆了hGM-CSF的编码基因,克隆过程中对该基因的局部做了密码子优化。然后克隆进毕赤酵母分泌型表达载体pPIC9K,电击转化毕赤酵母。PCR、SDS-PAGE与Western blotting证实hGM-CSF已整合进酵母基因组,摇瓶水平粗蛋白表达量达389mg/L,动物实验证实蛋白产物活性正常,SDS-PAGE与N-糖苷酶F去糖基化分析发现hGM-CSF被糖基化。

关键词: 粒细胞-巨噬细胞集落刺激因子毕赤酵母引物5'端加长法糖基化    
Abstract:

Code gene being cloned from the human genome by the primer5′extension, as the same time that code had been optimized partly to gene in the cloned procession. It was integrated into the gene secreted Pichia pastoris expression vector pPIC9K and translated yeast Pichia pastoris. PCR, SDS-PAGE and Western blotting confirmed hGM-CSF gene was integrated into the yeast genome and expression was successful. The expressed hGM-CSF was secreted into medium at the level of 389mg/L. Experiments in vivo showed that activity of hGM-CSF was normal. SDS-PAGE electrophoresis revealed that the hGM-CSF expression had occurred in glycosylation, N-glycosidase F to glycosylation also confirmed this point.

Key words: human granulocyte-macrophage colony stimulating factor    primer-5 '-extension    Pichia pastorion    glycosylation
收稿日期: 2009-09-21 出版日期: 2010-01-27
基金资助:

山东省教育厅科研项目(J06L77)资助项目

通讯作者: 王清路     E-mail: wql_zcq@126.com
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引用本文:

李俏俏 王清路 张玉军 张锐 徐寿增. 人粒细胞-巨噬细胞集落刺激因子的克隆及在毕赤酵母中的表达[J]. 中国生物工程杂志, 2010, 30(01): 35-40.

LI Qiao-Qiao, WANG Qing-Lu, ZHANG Yu-Jun, ZHANG Dui, XU Shou-Ceng. Cloning and Expression in Pichia pastoris of Human Granulocyte-macrophage Colony Stimulating Factor. China Biotechnology, 2010, 30(01): 35-40.

链接本文:

https://manu60.magtech.com.cn/biotech/CN/        https://manu60.magtech.com.cn/biotech/CN/Y2010/V30/I01/35

[1] 陈建魁,尹秀云,刘晓晴,等.集落刺激因子的分子生物学基础及其对血细胞分析的影响.中华临床医学杂志,2004, 5(3):5355. Chen J K,Yin X Y,Liu X Q,et al.Chiese Journal of Clinical Practical Medicine,2004,5(3):5355. 
[2] 肖振宇,郭葆玉.粒/巨噬细胞集落刺激因子.见:郭葆玉.基因工程药学.上海:第二军医大学出版社,2000.199208. Xiao Z Y, Guo B Y.Granulocytemacrophage colony stimulating factor.In:Guo B Y.Genetic Engineering Pharmacy.Shanghai:Second Military Medical University Press,2000.199208. 
[3] 范海荣,夏永静,孙福成,等.四种全血基因组DNA提取方法的比较.中国动脉硬化杂志,2002,10(6):535536. Fan H R, Xia Y J, Sun F C,et al. Chinese Journal of Arteriosclerosis,2002,10(6):535536. 
[4] Wong G G, Witek J S, Temple P A, et al. Human GMCSF: molecular cloning of the complementary DNA and purification of the natural and recombinant proteins. Science, 1985, 228(4701): 810815. 
[5] Armitage J O.Emerging application of recombinant human granulocytemacrophage colony stimulating factor.Blood, 1998,9(12):44914508. 
[6] Kaushansky K, O′Hara P J, Hart C E, et al.Role of carbohydrate in the function of human granulocytemacrophage colony stimulating factor.Biochemistry, 1987,26(15):48614867.
[7] Metcalf D.The granulocyte macrophage colony stimulating factors.Science, 1985,229(4708):1622.
[8] Wolf M, Klausmann M, Havemann K.rhGMCSF in the treatment of small cell lung canner.Semin Oncol, 1994,21(6):5165.
[9] Vanz A L S, Renard G, Palma M S, et al. Human granulocyte colony stimulating factor (hGCSF): cloning,overexpression, purification and characterization. Microbial Cell Factories, 2008, 7(13):12. 
[10] Schwanke R C, Renard G, Chies J M, et al. Molecular cloning, expression in Escherichia coli and production of bioactive homogeneous recombinant human granulocyte and macrophage colony stimulating factor. International Journal of Biological Macromolecules, 2009,45(2):97102. 
[11] 段淑敏, 李福胜.大肠杆菌表达的rhGMCSF发酵纯化工艺研究.中国生物制品学杂志, 1996,9(3):124128. Duan S M, Li F S. Chinese Journal of Biologicals,1996,9(3):124128.
[12] Guise A D, West S M, Chaudhuri J B.Protein folding in vivo and renatureation of recombinant proteins from inclusion bodies. Mol Biotechmol, 1996,6(1):5364.
[13] Cheland J L, Builder S E, Swartz J R, et al.Polyethylene glycol enhanced protein refolding. Biotechnology, 1992(10):10131019.
[14] Zardeneta G, Horowitz P M.Detergent, liposome and micelleassisted protein refolding.Anal Biochem, 1994,223(1):16.

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