中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Construction of shuttle, expression vector of human tumor necrosis factor alpha (hTNF-alpha) gene and its expression in a cyanobacterium, Anabaena sp. PCC 7120

文献类型:期刊论文

作者Liu, FL; Zhang, HB; Shi, DJ; Shang, ZD; Lin, C; Shao, N; Peng, GH; Zhang, XY; Zhang, HX; Wu, JY
刊名SCIENCE IN CHINA SERIES C-LIFE SCIENCES
出版日期1999-02-01
卷号42期号:1页码:25-33
关键词Human Tumor Necrosis Factor Alpha (htnf-Alpha) Anabaena Sp. Pcc 7120 Shuttle Expression Vector Triparental Conjugative Transfer Southern And Western Blottings Cytotoxicity
ISSN号1006-9305
文献子类Article
英文摘要The construction of the shuttle, expression vector of human tumor necrosis factor alpha (hTNF-alpha) gene and its expression in a cyanobacterium Anabaena sp. PCC 7120 was reported. The 700-bp hTNF cDNA fragments have been recovered from plasmid pRL-rhTNF, then inserted downstream of the promoter PpsbA in the plasmid pRL439. The resultant intermediary plasmid pRL-TC has further been combined with the shuttle vector pDC-8 to get the shuttle, expression vector pDC-TNF. The expression of the rhTNF gene in Escherichia coli has been analyzed by SDS-PAGE and thin-layer scanning, and the results show that the expressed TNF protein with these two vectors is 16.9 percent (pRL-TC) and 15.0 percent (pDC-TNF) of the total proteins in the cells, respectively, while the expression level of TNF gene in plasmid pRL-rhTNF is only 11.8 percent. Combined with the participation of the conjugal and helper plasmids, pDC-TNF has been introduced into Anabaena sg PCC 7120 by triparental conjugative transfer, and the stable transgenic strains have been obtained. The existence of the introduced plasmid pDC-TNF in recombinant cyanobacterial cells has been demonstrated by the results of the agarose electrophoresis with the extracted plasmid samples and Southern blotting with alpha-(32)p labeled hTNF cDNA probes, while the expression of the hTNF gene in Anabaena sp. PCC 7120 has been confirmed by the results of Western blotting with extracted protein samples and human TNF-alpha monoclonal antibodies. The cytotoxicity assays using the mouse cancer cell line L929 proved the cytotoxicity of the TNF in the crude extracts from the transgenic cyanobacterium Anabaena sp. PCC 7120.; The construction of the shuttle, expression vector of human tumor necrosis factor alpha (hTNF-alpha) gene and its expression in a cyanobacterium Anabaena sp. PCC 7120 was reported. The 700-bp hTNF cDNA fragments have been recovered from plasmid pRL-rhTNF, then inserted downstream of the promoter PpsbA in the plasmid pRL439. The resultant intermediary plasmid pRL-TC has further been combined with the shuttle vector pDC-8 to get the shuttle, expression vector pDC-TNF. The expression of the rhTNF gene in Escherichia coil has been analyzed by SDS-PAGE and thin-layer scanning, and the results show that the expressed TNF protein with these two vectors is 16.9 percent (pRL-TC) and 15.0 percent (pDC-TNF) of the total proteins in the cells, respectively, while the expression level of TNF gene in plasmid pRL-rhTNF is only 11.8 percent. Combined with the participation of the conjugal and helper plasmids, pDC-TNF has been introduced into Anabaena sg PCC 7120 by triparental conjugative transfer, and the stable transgenic strains have been obtained. The existence of the introduced plasmid pDC-TNF in recombinant cyanobacterial cells has been demonstrated by the results of the agarose electrophoresis with the extracted plasmid samples and Southern blotting with alpha-(32)p labeled hTNF cDNA probes, while the expression of the hTNF gene in Anabaena sp. PCC 7120 has been confirmed by the results of Western blotting with extracted protein samples and human TNF-alpha monoclonal antibodies. The cytotoxicity assays using the mouse cancer cell line L929 proved the cytotoxicity of the TNF in the crude extracts from the transgenic cyanobacterium Anabaena sp. PCC 7120.
学科主题Biology
语种英语
WOS记录号WOS:000078524100004
公开日期2010-12-22
源URL[http://ir.qdio.ac.cn/handle/337002/3357]  
专题海洋研究所_实验海洋生物学重点实验室
作者单位1.Chinese Acad Sci, Inst Bot, Lab Photosynth, Beijing 100093, Peoples R China
2.Guangzhou Gen Hosp, Guangzhou Mil Command, Guangzhou 510010, Peoples R China
3.Chinese Acad Med, Inst Oncol, State Key Lab Mol Oncol, Beijing 100021, Peoples R China
4.Chinese Acad Sci, Inst Oceanol, EMBL, Qingdao 266071, Peoples R China
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GB/T 7714
Liu, FL,Zhang, HB,Shi, DJ,et al. Construction of shuttle, expression vector of human tumor necrosis factor alpha (hTNF-alpha) gene and its expression in a cyanobacterium, Anabaena sp. PCC 7120[J]. SCIENCE IN CHINA SERIES C-LIFE SCIENCES,1999,42(1):25-33.
APA Liu, FL.,Zhang, HB.,Shi, DJ.,Shang, ZD.,Lin, C.,...&Zeng, CK.(1999).Construction of shuttle, expression vector of human tumor necrosis factor alpha (hTNF-alpha) gene and its expression in a cyanobacterium, Anabaena sp. PCC 7120.SCIENCE IN CHINA SERIES C-LIFE SCIENCES,42(1),25-33.
MLA Liu, FL,et al."Construction of shuttle, expression vector of human tumor necrosis factor alpha (hTNF-alpha) gene and its expression in a cyanobacterium, Anabaena sp. PCC 7120".SCIENCE IN CHINA SERIES C-LIFE SCIENCES 42.1(1999):25-33.

入库方式: OAI收割

来源:海洋研究所

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