层理鞭枝藻藻红蓝蛋白操纵子F基因的克隆和表达

郑敏, 答亮, 邓明刚, 秦艺旻, 周明, 赵开弘

郑敏, 答亮, 邓明刚, 秦艺旻, 周明, 赵开弘. 层理鞭枝藻藻红蓝蛋白操纵子F基因的克隆和表达[J]. 水生生物学报, 2002, 26(2): 168-174.
引用本文: 郑敏, 答亮, 邓明刚, 秦艺旻, 周明, 赵开弘. 层理鞭枝藻藻红蓝蛋白操纵子F基因的克隆和表达[J]. 水生生物学报, 2002, 26(2): 168-174.
ZHENG Min, DA Liang, DENG Ming gang, QING Yi min, ZHOU Ming, ZHAO Kai hong. CLONING AND OVEREXPRESSING OF PHYCOERYTHROCYANIN OPERON F-GENE OF MASTIGOCLADUS LAMINOSUS IN ESCHERICHIA COLI[J]. ACTA HYDROBIOLOGICA SINICA, 2002, 26(2): 168-174.
Citation: ZHENG Min, DA Liang, DENG Ming gang, QING Yi min, ZHOU Ming, ZHAO Kai hong. CLONING AND OVEREXPRESSING OF PHYCOERYTHROCYANIN OPERON F-GENE OF MASTIGOCLADUS LAMINOSUS IN ESCHERICHIA COLI[J]. ACTA HYDROBIOLOGICA SINICA, 2002, 26(2): 168-174.

层理鞭枝藻藻红蓝蛋白操纵子F基因的克隆和表达

基金项目: 

国家自然科学基金(编号:39770175)资助项目

武汉市晨光计划(编号:965001037-21)资助项目

CLONING AND OVEREXPRESSING OF PHYCOERYTHROCYANIN OPERON F-GENE OF MASTIGOCLADUS LAMINOSUS IN ESCHERICHIA COLI

  • 摘要: 以层理鞭枝藻总DNA为模板,用PCR技术扩增得到藻红蓝蛋白操纵子F基因(pecF),然后克隆于质粒pBluescript sk(+).将pecF基因亚克隆于表达载体pGEMD,所形成重组质粒pGEMD-pecF在E.coli BL21(DE3)中获得10%外源表达蛋白并形成包涵体.这个表达产物的分子量为22.5kDa,与按DNA序列预测的蛋白分子量一致.经藻红蓝蛋白α-亚基的重组实验证明,该pecF基因编码的表达产物PecF与藻红蓝蛋白操纵子E基因(pecE)的表达产物PecE共同存在时,具有藻红蓝蛋白裂合酶活性.
    Abstract: By PCR method, apo phycoerythrocyanin operon F gene(pecF)of Mastigocladus laninosus was amplified from its genomic DNA,and then cloned in pBluescript The pecF gene was subcloned into the expression vector pGEMD,and then transformed into E.coli BL21(DE3)After induction, a new protein of molecular weight 22 5kDa existing in inclusion body was overexpressed The expression product was confirmed to possess phycoerythrocyanin lyase activity
  • [1]

    Glazer A N.Light harvesting by phycobilisomes,Ann.Rev[J].Biophys.Biophys. Chem.,1985,14:47[2] Zuber H.Molecular Biology of the Photosynthetic Apparatus(Stemhack K E.Ed)[M].New York: Cold Spring Harbor Laboratory press.1985,233[3] Fairchild C D,Zhao J,Zhou J J,et al.Phycocyanin α-subunit phycocyanobilin layse Proc[J].Natl. Acad. Sci. USA.,1992,89:7017[4] Zhao K H,Scheer H. Type Ⅰ and type Ⅱ reversible photochemistry of phycoerythrocyanin α-subunit from Mastigocladus Laminosus both involve Z,E isomerization of phycoviolobilin chromophore and are controlled by sulfhydryls in apoprotein [J].Biochimica et Biophysica Acta. 1995,1228:244[5] Zhao K H.Rainer Haessner, Edmund Cmiel, Hugo Scheer, Type I reversible photochemistry of phycoerythrocyanin involves Z/E-isomerization of α-84 phycoviolobilin chromophore[J].Biochemica et Biophysica Acta.1995,1228:235[6] Sambrook J, Fritsch E F,Maniatis T.Molecular Cloning A laboratory manual(second. ed.)[M].New York:Cold Spring Harbor Laboratory Press,1989[7] Studier F W,Moffatt P A. Analysis of bacteriophage T7 early RNAs and proteins on slab gels [J].J.Mol. Biol.,1986,189:113[8] O′Carra, P. and O′hEocha, C. Bilins released from algae and bilinproteins by methanolic extraction.[J].Phytochemistry 5,1966,993[9] Ebelein M, Kufer W.Genes encoding both subunits of phycoerythrocyanin, a light-harvesting biliprotein from the cyanobacterium Mastigocladus laminosus[J].Gene,1990,94:133

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出版历程
  • 收稿日期:  2000-07-03
  • 修回日期:  2001-08-29
  • 发布日期:  2002-03-24

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