期刊文献+

产丁二酸谷氨酸棒状杆菌基因缺失代谢工程菌株的构建 被引量:8

Construction a metabolic engineering strain to produce succinic acid from Corynebacterium glutamicum by gene deletion mutation
原文传递
导出
摘要 【目的】提高谷氨酸棒状杆菌(Corynebacterium glutamicum)ATCC13032厌氧条件下的丁二酸产量,并降低发酵产物中副产物的含量。【方法】以谷氨酸棒状杆菌(Corynebacterium glutamicum)ATCC13032为出发菌,首先敲除乳酸形成的关键酶乳酸脱氢酶基因(ldh),构建ldh缺失株谷氨酸棒状杆菌ATCC13032Δldh;然后以缺失株谷氨酸棒状杆菌ATCC13032Δldh为出发菌,敲除该菌的丙酮酸脱氢酶系的E1p酶基因(aceE),构建一株双缺失突变菌株谷氨酸棒状杆菌ATCC13032ΔldhΔaceE。【结果】与供试菌比较,谷氨酸棒状杆菌ATCC13032Δldh的丁二酸产量和转化率分别提高了94.9%和32%,并且主要的副产物乳酸产量由出发菌产量的63.5 g/L降低到很微量的程度。丙酮酸脱氢酶的失活并不能完全消除副产物乙酸的形成,但乙酸的产量较ATCC13032Δldh降低了37.9%,丁二酸的产量略有提高。【结论】该重组菌具有较强的丁二酸生产工业化潜力,并且该研究方法为微生物代谢育种提供参考。 [Objective] In order to improve the production of succinic acid and decrease the accumulation of by-products under the oxygen deprivation by Corynebacterium glutamicum 13032. [Methods] From the C. glutamicum ATCC13032, firstly, the gene of lactic dehydrogenase (ldh) was knocked-out and the single deletion mutation strain C. glutamicum ATCC13032Δldh was constructed. Secondly, we interrupted the pathway of pyruvic acid flux to acetic acid by marker-free deletion the E1p gene (aceE) which encode the essential part of the pyruvate dehydrogenase complex (PDHC). [Results] The production and yield of succinic acid of recombination strain improved 94.9% and 32%, respectively, compared to the parent strain C. glutamicum ATCC13032 and what’s more, the main by-product lactic acid was eliminated to none from 63.5 g/L. The inactive of the pyruvate dehydrogenase complex could not prevent the formation of acetic acid absolutely, but the production of acetic acid decreased 37.9%, compared to C. glutamicum ATCC13032Δldh and the production of succinic acid improved a little. [Conclusion] This recombination bacteria has a potential in industrial applications, and this study methods could provide reference for microbial metabolism breeding.
出处 《微生物学通报》 CAS CSCD 北大核心 2013年第5期739-748,共10页 Microbiology China
关键词 谷氨酸棒状杆菌 丁二酸 基因敲除 厌氧转化 Corynebacterium glutamicum, Succinic acid, Gene deletion, Anaerobic conversion
  • 相关文献

参考文献19

  • 1Fukui K, Koseki C, Yamamoto Y, et al.Identification of succinate exporter inCorynebacterium glutamicum and its physiologicalroles under anaerobic conditions[J]. Journal ofBiotechnology, 2011, 154(1): 25-34.
  • 2Mckinlay JB, Vieille C, Zeikus JG. Prospects for abio-based succinate industry[J]. AppliedMicrobiology and Biotechnology, 2007,76(4):727—740.
  • 3Song H, Lee SY. Production of succinic acid bybacterial fermentation[J]. Enzyme and MicrobialTechnology, 2006,39(3): 352-361.
  • 4Inui M, Murakami S, Okino S, et al. Metabolic analysisof Corynebacterium glutamicum during lactate andsuccinate productions under oxygen deprivationconditions [J]. Journal of Molecular Microbiology andBiotechnology, 2004, 7(4): 182-196.
  • 5Inui M,Kawaguchi H, Murakami S,et al.Metabolic engineering of Corynebacteriumglutamicum for fuel ethanol production underoxygen-deprivation conditions[J]. Journal ofMolecular Microbiology and Biotechnology, 2004,8(4): 243-254.
  • 6Becker J,Klopprogge C,Wittmann C. Metabolicresponses to pyruvate kinase deletion in lysineproducing Corynebacterium glutam icum [J].Microbial Cell Factories, 2008,7: 8.
  • 7Hou X, Chen X,Zhang Y, et al. (L)-Valineproduction with minimization of by-products’synthesis in corynebacterium glutamicum andbrevibacterium flavum[J]. Amino Acids, 2012,43(6): 2301-2311.
  • 8Schafer A, Tauch A, Jager W, et al. Smallmobilizable multi-purpose cloning vectors derivedfrom the Escherichia coli plasmids Pkl8 and Pkl9:selection of defined deletions in the chromosome ofCorynebacterium glutamicum[J]. Gene, 1994,145(1): 69-73.
  • 9黄培堂,王嘉玺,朱厚照,等(译).2002.分子克隆实验指南[M].第3版.北京:科学出版社:224-233
  • 10Eggeling L, Bott M. Handbook of Corynebacteriumglutamicum[M]. CRC, Boca Raton, 2005: 535-545.

二级参考文献79

共引文献106

同被引文献86

引证文献8

二级引证文献15

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