Prokaryotic expression of a glycosyltransferase Med-ORF8 involved in an antitumor antibiotic medermycin biosynthesis aided by the molecular chaperone
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    Abstract:

    Glycosyltransferases play central roles in the glycosylation of biosynthetic pathways of many antibiotics. The prokaryotic expression and enzymatic features of Med-ORF8, a glycosyltransferase involved in the biosynthesis of medermycin with strong antitumor activity, still remains obscure. Here, firstly, we performed the computer modeling of the 3-D structure of Med-ORF8 to prove that the presence of 6*His-tag at the terminals of Med-ORF8 had no effect on its 3-D structure. Subsequently, we established two prokaryotic expression systems with pET vectors to express Med-ORF8, and found that pET-28a (+) could gain a higher yield of the target protein than pET-23a (+), but mostly in an insoluble form. Finally, we introduced a molecular chaperone gene into the system with pET-28a (+) and found that the co-expression of the molecular chaperone with Med-ORF8 could efficiently decrease the formation of the inclusion body and increase the accumulation of soluble Med-ORF8.

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    [1] 代焕琴, 王浩鑫, 沈月毛. 抗生素糖基转移酶研究进展[J]. 中国抗生素杂志, 2007, 32(5): 257?262.
    [2] Luzhetskyy A, Weiss H, Charge A, et al. A strategy for cloning glycosyltransferase genes involved in natural product biosynthesis[J]. Appl Microbiol Biotechnol, 2007, 75(6): 1367?1375.
    [3] 邓会群, 王惠利, 杨红, 等. 天然产物的C-糖基化研究进展[J]. 生物技术通报, 2009(5): 27?30.
    [4] Toral-Barza L, Zhang WG, Huang XY, et al. Discovery of lactoquinomycin and related pyranonaphthoquinones as potent and allosteric inhibitors of AKT/PKB: mechanistic involvement of AKT catalytic activation loop cysteines[ J]. Mol Cancer Ther, 2007, 6(11): 3028?3038.
    [5] Salaski EJ, Krishnamurthy G, Ding WD, et al. Pyranonaphthoquinone lactones:a new class of AKT selective kinase inhibitors alkylate a regulatory loop cysteine[J]. J Med Chem, 2009, 52(8): 2181?2184.
    [6] 蔡晓凤. 芳香聚酮抗生素美达霉素生物合成基因的研究[D]. 华中师范大学硕士学位论文, 2009.
    [7] Ichinose K, Ozawa M, Itou K, et al. Cloning,sequencing and heterologous expression of the medermycin biosynthetic gene cluster of Streptomyces sp. AM-7161: towards comparative analysis of the benzoisochromanequinone gene clusters[J]. Microbiology, 2003, 149(7): 1633?1645.
    [8] Mittler M, Bechthold A, Schulz GE. Structure and action of the C-C bond-forming glycosyltransferase UrdGT2 involved in the biosynthesis of the antibiotic urdamycin[J]. J Mol Biol, 2007, 372(1): 67?76.
    [9] Goodfellow M. Researching the unions[J]. Contemp Adm Long Term Care, 1984, 7(12): 40?42.
    [10] 刘庆坡, 冯英, 董辉. 20 个物种同义密码子偏性的比析[J]. 西北农林科技大学学报: 自然科学版, 2004, 32(7): 67?71.
    [11] 郑彬琼. 大肠杆菌同义密码子偏好性概述[J]. 硅谷, 2009(1): 3?4.
    [12] Spanjaard RA, Chen K, Walker JR, et al. Frameshift suppression at tandem AGA and AGG codons by cloned tRNA genes: assigning a codon to argU tRNA and T4 tRNAArg[J]. Nucl Acids Res, 1990, 18(17): 5031?5036.
    [13] Hoffmann F, van den Heuvel J, Zidek N, et al. Minimizing inclusion body formation during recombinant protein production in Escherichia coli at bench and pilot plant scale[J]. Enzyme Microbiol Technol, 2004, 34(1/2): 235?241.
    [14] Carrió MM, Villaverde A. Construction and deconstruction of bacterial inclusion bodies[J]. J Biotechnol, 2002, 96(1): 3?12.
    [15] 罗惠霞, 李敏, 王玉炯. 包涵体蛋白复性的几种方法[J]. 生物技术通报, 2007(5): 96?98.
    [16] Hartl FU, Hayer-Hartl M. Molecular chaperones in the cytosol: from nascent chain to folded protein[J]. Science, 2002, 295(5561): 1852?1858.
    [17] Crooke E, Wickner W. Trigger factor: a soluble protein that folds pro-OmpA into a membrane-assembly-competent form[J]. Proc Natl Acad Sci USA, 1987(84): 5216?5220.
    [18] Hesterkamp T, Hauser S, Lütcke H, et al. Escherichia coli trigger factor is a prolyl isomerase that associates with nascent polypeptide chains[J]. Proc Natl Acad Sci USA, 1996, 93(9): 4437?4441.
    [19] Valent QA, Kendall DA, High S, et al. Early events in preprotein recognition in E. coli: interaction of SRP and trigger factor with nascent polypeptides[J]. EMBO J, 1995, 14(22): 5494?5505.
    [20] Patzelt H, Rüdiger S, Brehmer D, et al. Binding specificity of Escherichia coli trigger factor[J]. Proc Natl Acad Sci USA, 2001, 98(25): 14244?14249.
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WAN Juan, DENG Hui-Qun, ZHANG Bi-Qian, WANG Wei, CAI Xiao-Feng, LI Ai-Ying. Prokaryotic expression of a glycosyltransferase Med-ORF8 involved in an antitumor antibiotic medermycin biosynthesis aided by the molecular chaperone[J]. Microbiology China, 2011, 38(2): 221-227

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History
  • Received:August 12,2010
  • Revised:November 30,2010
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