期刊文献+

东方拟无枝酸菌中基因AORI_2943的敲除对ECO-0501合成的影响

Effect of gene disruption of AORI_2943 on ECO-0501 production in Amycolatopsis orientalis
下载PDF
导出
摘要 目的对位于ECO-0501生物合成基因簇内AORI_2943基因进行功能鉴定,进一步解析东方拟无枝酸菌中ECO-0501的生物合成途径。方法通过同源重组和定点整合的方式构建AORI_2943缺失、回补及过表达突变株。高效液相及质谱分析突变株发酵产物的变化,分析AORI_2943在ECO-0501合成中的作用。结果 AORI_2943缺失突变株不产ECO-0501和去甲基ECO-0501,只产生结构上缺失了C5N单位(2-氨基-3-羟基环戊-2-烯酮)的前体物质a和b,发酵液中未检测出C5N单位。对缺失突变株回补后,有少量ECO-0501及去甲基ECO-0501产生,同时仍然有大量前体化合物a和b的积累。在野生菌的基础上过表达AORI_2943,并未明显提高ECO-0501的产量。结论 AORI_2943是ECO-0501合成的关键基因,主要参与了ECO-0501前体化合物C5N单位的合成。 Objective To determine the function of the AORI_2943 gene located in the biosynthesis gene cluster of ECO-0501 from Amycolatopsis orientalis.Methods The disruption, complementation and overexpression of AORI_2943 were conducted by homologous recombination and site-specified integration. The metabolites in the fermentation broth of the resulted mutants were analyzed by high performance liquid chromatography and mass spectrometry.Results Disruption of AORI_2943 in Amycolatopsis orientalis resulted in the disappearance of ECO-0501 and demethyl-ECO-0501 and the appearance of two new compounds a and b in the fermentation broth of the mutant. The two new compounds a and b, lacking the 2-amino-3-hydroxy-cyclopent-2-enone moiety (C5N) in ECO-0501, were determined as the precursors of ECO-0501 and demethyl-ECO-0501, respectively. Complementation of the disrupted mutant with intact AORI_2943 restored the ECO-0501 production. However, overexpression of A ORI_2943 did not improve the production of ECO-0501.Conclusion AORI_ 2943 is crucial for ECO-0501, specifically the C5N unit biosynthesis. To improve the production of ECO-0501, overexpression of AORI-2943 alone is not enough.
出处 《中国医药生物技术》 2015年第4期330-334,共5页 Chinese Medicinal Biotechnology
基金 国家自然科学基金(81202440)
关键词 东方拟无枝酸菌 ECO-0501 AORI_2943 Amycolatopsis orientalis ECO-0501 AORI_ 2943
  • 相关文献

参考文献11

  • 1Banskota AH, Mcalpine JB, Sorensen D, et al. Genomic analyses lead to novel secondary metabolites. Part 3. ECO-0501, a novel antibacterial of a new class. J Antibiot (Tokyo), 2006, 59(9):533-542.
  • 2郦伟翔,阮林高,盛下放,戈梅,陈代杰.ECO-0501产生菌的发酵条件优化[J].中国医药工业杂志,2008,39(10):736-738. 被引量:4
  • 3Alarco A, Dimitriadou V, McAlpine J, et al. ECO-0501, a novel anti-gram positive compound defining a new antibacterial structural class: preclinical evaluations. In: Proceedings of the 44th Annual ICAAC conference. Washington DC, 2004: Poster F-719. http://www. the freelibrary.com/Ecopia+Present s+Three+Posters+on+its+Antibacterial+Agent+ECO-0501+at...-a0123845408.
  • 4申洋,黄鹤,朱丽,杨晟,戈梅,陈代杰.东方拟无枝酸菌中ECO-0501生物合成基因簇的筛选及其相关调控基因的初步分析[J].中国抗生素杂志,2013,38(5):327-331. 被引量:2
  • 5Shen Y, Huang H, Zhu L, et al. Type II thioesterase gene (ECO-orf27) from Amycolatopsis orientalis influences production of the polyketide antibiotic, ECO-0501 (LW01). Biotechnol Lett, 2012, 34(11):2087- 2091.
  • 6Shen Y, Huang H, Zhu L, et al. A regulatory gene (ECO-orf4) required for ECO-0501 biosynthesis in Amycolatopsis orientalis. J Basic Microbiol, 2014, 54(2): 104-110.
  • 7申洋,朱丽,阮林高,陈代杰.产N-demethyl ECO-0501工程菌的构建[J].中国抗生素杂志,2013,38(4):251-254. 被引量:1
  • 8盖忆青,朱丽,陈代杰,张怡轩.东方拟无枝酸菌HCCB10007内attB位点的人工构建[J].中国抗生素杂志,2014,39(3):193-197. 被引量:4
  • 9Stegmann E, Pelzer S, Wilken K, et al. Development of three different gene cloning systems for genetic investigation of the new species Amycolatopsis japonicum MG417-CF 17, the ethylacid producer. J Biotechnol, 2001, 92(2): 195-204.
  • 10Sambrook J, Russell DW. Molecular cloning: a laboratory manual. 3rd Ed. New York: Cold Spring Harbor Laboratory Press, 2001.

二级参考文献38

  • 1张桂敏,周秀芬,邓子新,庄永红.将透明颤菌血红蛋白基因(vgb)转移到链霉菌染色体整合载体的构建[J].华中农业大学学报,2004,23(6):602-605. 被引量:4
  • 2Sambrook J,Russell D,著.黄培堂,王嘉玺,朱厚础,等,译.分子克隆实验指南[M].第三版.北京:科学出版社,2002.99-102.
  • 3Banskota AH, Mcalpine JB, Sorensen D, et al, Genomic analyses lead to novel secondary metabolites. Part 3. ECO-0501, a novel antiba'cterial of a new class [J]. J Antibiot; 2006, 59 (9) : 533-542.
  • 4Leeds JA, Schmitt EK, Krastel P. Recent developments in antibacterial drug discovery: microbe-derived natural products-from collection to the clinic [J]. Expert Opin Investig Drugs, 2006, 15 (3) : 211-226.
  • 5Butler MS, Buss AD. Natural products-the future scaffolds for novel antibiotics [J]. Biochem Pharmacol, 2006, 71 (7) : 919-929.
  • 6Mcalpine JB, Farnet CM, Zazopoulos E, et al. Polyene polyketides and methods of production: WO, 2005024025 [P]. 2005-03-17. (CA2005, 142: 313100)
  • 7Banskota A H, McAlpine J B, Sorensen D, et al. Genomic analyses lead to novel secondary metabolites[J]. J Antibiot, 2006, 59(9): 533-542.
  • 8Butler M S, Buss A D. Natural products-The future scaffolds for novel antibiotics[J]? Biochem Pharmacol 2006, 71(7): 919-929.
  • 9Mcalpine. Polyene polyketides and methods of production:WO, 2005/024025A1 [P]. 2005-03-17.
  • 10Kieser T, Bibb M J, Buttner M J, et al. Practical Streptomyces genetics. Norwich: The John Innes Foundation, 2000.

共引文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部