Enhanced production of plasmid DNA by engineered Escherichia coli strains

被引:13
作者
Pablos, Tania E. [1 ]
Soto, Rene [2 ]
Meza Mora, Eugenio [3 ]
Le Borgne, Sylvie [1 ]
Ramirez, Octavio T. [2 ]
Gosset, Guillermo [3 ]
Lara, Alvaro R. [1 ]
机构
[1] Univ Autonoma Metropolitana Cuajimalpa, Dept Proc & Tecnol, Mexico City 01120, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Med Mol & Bioproc, Cuernavaca 62210, Morelos, Mexico
[3] Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Ingn Celular & Biocatalisis, Cuernavaca 62210, Morelos, Mexico
关键词
Plasmid DNA; Escherichia coli; PTS; pykA; pDNA vaccines; Acetate; SYSTEM; PERFORMANCE; METABOLISM; ACETATE; GLUCOSE; GROWTH;
D O I
10.1016/j.jbiotec.2011.04.015
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Escherichia coli strains VH33 (PTS- GalP(+) strain displaying a strongly reduced overflow metabolism) and VH34 (additionally lacking the pyruvate kinase A) were evaluated for the production of a plasmid DNA (pDNA) vaccine. The parent (W3110) and mutant strains were cultured using 10 g of glucose/L. While the specific growth rates of the three strains were similar, they presented differences in the accumulation of acetate. W3110 accumulated up to 4 g/L of acetate, VH33 produced 1.4 g/L, and VH34 only 0.78 g/L. VH33 and VH34 produced 76% and 300% more pDNA than W3110. Moreover, VH34 demanded 33% less oxygen than VH33 and W3110, which can be advantageous for large-scale applications. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:211 / 214
页数:4
相关论文
共 50 条
  • [41] Production of mevalonate by a metabolically-engineered Escherichia coli
    Kazuhiko Tabata
    Shin-Ichi Hashimoto
    Biotechnology Letters, 2004, 26 : 1487 - 1491
  • [42] L-Fucose production by engineered Escherichia coli
    Liu, Jing-Jing
    Lee, Jae Won
    Yun, Eun Ju
    Jung, Sang-Min
    Seo, Jin-Ho
    Jin, Yong-Su
    BIOTECHNOLOGY AND BIOENGINEERING, 2019, 116 (04) : 904 - 911
  • [43] Production of mevalonate by a metabolically-engineered Escherichia coli
    Tabata, K
    Hashimoto, SI
    BIOTECHNOLOGY LETTERS, 2004, 26 (19) : 1487 - 1491
  • [44] Biotin-independent strains of Escherichia coli for enhanced streptavidin production
    Jeschek, Markus
    Bahls, Maximilian O.
    Schneider, Veronika
    Marliere, Philippe
    Ward, Thomas R.
    Panke, Sven
    METABOLIC ENGINEERING, 2017, 40 : 33 - 40
  • [45] Engineering of bacterial strains and vectors for the production of plasmid DNA
    Bower, Diana M.
    Prather, Kristala L. J.
    APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2009, 82 (05) : 805 - 813
  • [46] Efficient glutathione production in metabolically engineered Escherichia coli strains using constitutive promoters
    Cui, Xiangwei
    Wan, Junxian
    Zhang, Xing
    Wu, Hui
    Li, Zhimin
    Ye, Qin
    JOURNAL OF BIOTECHNOLOGY, 2019, 289 : 39 - 45
  • [47] Enhanced production of nonanedioic acid from nonanoic acid by engineered Escherichia coli
    Lee, Yongjoo
    Sathesh-Prabu, Chandran
    Kwak, Geun Hwa
    Bang, Ina
    Jung, Hyun Wook
    Kim, Donghyuk
    Lee, Sung Kuk
    BIOTECHNOLOGY JOURNAL, 2022, 17 (03)
  • [48] Optimization of Culture Conditions for Enhanced Lysine Production Using Engineered Escherichia coli
    Ying, Hanxiao
    He, Xun
    Li, Yan
    Chen, Kequan
    Ouyang, Pingkai
    APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 2014, 172 (08) : 3835 - 3843
  • [49] Strategies for efficient repetitive production of succinate using metabolically engineered Escherichia coli
    Ma, Jiang-feng
    Jiang, Min
    Chen, Ke-quan
    Xu, Bing
    Liu, Shu-wen
    Wei, Ping
    Ying, Han-jie
    Chang, Ho-Nam
    Ouyang, Ping-kai
    BIOPROCESS AND BIOSYSTEMS ENGINEERING, 2011, 34 (04) : 411 - 418
  • [50] Eliminating acetate formation improves citramalate production by metabolically engineered Escherichia coli
    Naga Sirisha Parimi
    Ian A. Durie
    Xianghao Wu
    Afaq M. M. Niyas
    Mark A. Eiteman
    Microbial Cell Factories, 16