期刊文献+

利用三阶段葡萄糖添加策略减少乙酸合成并促进重组大肠杆菌生产L-苯丙氨酸 被引量:2

Decreased acetic acid synthesis and enhanced L-phenylalanine production by E.coli WSH-Z06(pAP-B03) using three stage glucose feeding strategy
下载PDF
导出
摘要 为了降低副产物乙酸的积累和提高L-苯丙氨酸的产量,分别优化了L-苯丙氨酸发酵的初始葡萄糖浓度和葡萄糖的指数流加策略。结果表明,20 g/L的初始葡萄糖浓度可以控制细胞的比生长速率低于临界值0.3 h-1,显著地降低了乙酸的积累,提高了L-苯丙氨酸的产量。采用预设比生长速率μ3 *=0.4(h-1)进行葡萄糖的指数流加取得了实际最大比生长速率0.29 h-1,使细胞的比生长速率低于临界值,促进了L-苯丙氨酸的合成,最终获得L-苯丙氨酸的产量达48.45g/L,比本实验室原有水平提高了37%。 In order to minimize the accumulation of acetic acid and enhance the production of L-phenylalanine, the initial glucose concentration and the exponential feeding strategy were optimized. The results indicate that initial glucose concentration of 20 g/L could control the cell specific growth acetic acid accumulation and promoting L-Phe production not only benefit cell growth , but also control cell specific rate below the critical value of 0.3 h-1 , greatly lowering the The exponential feeding strategy with μ3'=0.4(h-1) could rate within critical value, yielding L-Phe titer of 48.45 g/L, exhibiting 37% increase compared to the previously reported value in our lab.
出处 《工业微生物》 CAS CSCD 2013年第1期6-10,共5页 Industrial Microbiology
基金 863项目(2007CB02Z229) 973前期研究专项(2010CB535014) 973前期研究专项(2007CB714306) 国家杰出青年基金项目(31000054) 国家自然科学基金重点项目(20836003) 江南大学自主科研计划资助(JUSRP10917)
关键词 L-苯丙氨酸 重组大肠杆菌 指数流加 乙酸 L-phenylalanine recombinant E. coli exponential feeding strategy acetic acid
  • 相关文献

参考文献1

二级参考文献5

  • 1Shih-Kuang Hsu,Long-Liu Lin,Hsueh-Hsia Lo,Wen-Hwei Hsu.Mutational analysis of feedback inhibition and catalytic sites of prephenate dehydratase from Corynebacterium glutamicum[J].Archives of Microbiology.2004(3)
  • 2M. E. van der Rest,C. Lange,D. Molenaar.A heat shock following electroporation induces highly efficient transformation of Corynebacterium glutamicum with xenogeneic plasmid DNA[J].Applied Microbiology and Biotechnology.1999(4)
  • 3R. Fitzpatrick,M. O’Donohue,J. Joy,D. M. Heery,L. K. Dunican.Construction and characterization of recA mutant strains of Corynebacterium glutamicum and Brevibacterium lactofermentum[J].Applied Microbiology and Biotechnology.1994(4)
  • 4Masato Ikeda,Akio Ozaki,Ryoichi Katsumata.Phenylalanine production by metabolically engineered Corynebacterium glutamicum with the pheA gene of Escherichia coli[J].Applied Microbiology and Biotechnology.1993(3)
  • 5Akio Ozaki,Ryoichi Katsumata,Tetsuo Oka,Akira Furuya.Functional expression of the genes of Escherichia coli in gram-positive Corynebacterium glutamicum[J].MGG Molecular & General Genetics.1984(1)

共引文献5

同被引文献21

  • 1史悦,于慧敏,田卓玲,沈忠耀.产腈水合酶重组大肠杆菌的质粒稳定性研究[J].中国生物工程杂志,2005,25(8):70-75. 被引量:12
  • 2张彩,王郡甫,刘金生,许晓群,张建华,张捷,冯进波,田志刚.重组人白细胞介素15工程菌高密度发酵条件探讨[J].中国生化药物杂志,2007,28(1):1-3. 被引量:8
  • 3OPPERMANN U, FILLING C, HULT M, et al. Short-chain dehydroge- nases/reductases (SDR): the 2002 update[J]. Chem Biol Interact, 2003, 143-144: 247-253.
  • 4SONG C E, LEE J K, LEE S H, et al. New Method for the Preparation of R-Camitine[M]. Tetrahedron: Asymmetry, 1995.
  • 5WHITE S W, ZHENG J, ZHANG Y M, et al. The structural biology of type II fatty acid biosynthesis[J]. Annu Rev Biochem, 2005, 74:791-831.
  • 6CAMPBELL J W, CRONAN J E JR. Bacterial fatty acid biosynthesis:tar- gets for antibacterial drug discovery[J]. Annu Rev Mierobiol, 2001, 55: 305-332.
  • 7WARNES A, STEPHENSON J R, FOOKS A R, et al. Expression of re- combinant protein A from the lac promoter in Escherichia coil JM83 is not subject to catabolite repression when grown under specific condi- tions of continuous culture[J]. Bioteehnol Bioeng, 1991, 38(9): 1050- 1058.
  • 8WANG H, CHENG H, WEI D, et al. Comparison of methods for mea- suring viable E. coli cells during cultivation: great differences in the ear- ly and late exponential growth phases[J]. J Mierobiol Methods, 2011, 84(1): 140-143.
  • 9HOFFMANN F, RINAS U. On-line estimation of the metabolic burden resulting from the synthesis of plasmid-encoded and heat-shock proteins by monitoring respiratory energy generation [J]. Biotechnol Bioeng, 2001, 76(4): 333-340.
  • 10VEIT A, POLEN T, WENDISCH V. Global gene expression analysis of glucose overflow metabolism in Escherichia coil and reduction of aero- bic acetate formation[J]. Appl Mierobiol Biotechnol, 2007, 74(2): 406- 421.

引证文献2

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