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Construction of shuttle, expression vector of human tumor necrosis factor alpha (hTNF-alpha) gene and its expression in a cyanobacterium, Anabaena sp. PCC 7120
Liu, FL; Zhang, HB; Shi, DJ; Shang, ZD; Lin, C; Shao, N; Peng, GH; Zhang, XY; Zhang, HX; Wu, JY; Wang, J; Xu, XD; Jiang, YH; Zhong, ZP; Zhao, SJ; Wu, M; Zeng, CK
1999-02-01
发表期刊SCIENCE IN CHINA SERIES C-LIFE SCIENCES
ISSN1006-9305
卷号42期号:1页码:25-33
文章类型Article
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.
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
学科领域Biology
收录类别SCI
语种英语
WOS记录号WOS:000078524100004
引用统计
被引频次:11[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.qdio.ac.cn/handle/337002/3356
专题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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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.
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