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Betaine supplementation improved L-threonine fermentation of Escherichia coli THRD by upregulating zwf (glucose-6-phosphate dehydrogenase) expression
Li, Yanjun; Zhang, Dezhi; Cai, Ningyun; Han, Chao; Mao, Qiang; Wang, Ting; Zhou, Qian; Chen, Ning; Xie, Xixian.
  • Li, Yanjun; Tianjin University of Science and Technology. College of Biotechnology. Tianjin. CN
  • Zhang, Dezhi; Tianjin University of Science and Technology. College of Biotechnology. Tianjin. CN
  • Cai, Ningyun; Tianjin University of Science and Technology. College of Biotechnology. Tianjin. CN
  • Han, Chao; Tianjin University of Science and Technology. College of Biotechnology. Tianjin. CN
  • Mao, Qiang; Tianjin University of Science and Technology. College of Biotechnology. Tianjin. CN
  • Wang, Ting; Tianjin University of Science and Technology. College of Biotechnology. Tianjin. CN
  • Zhou, Qian; Tianjin University of Science and Technology. College of Biotechnology. Tianjin. CN
  • Chen, Ning; Tianjin University of Science and Technology. College of Biotechnology. Tianjin. CN
  • Xie, Xixian; Tianjin University of Science and Technology. College of Biotechnology. Tianjin. CN
Electron. j. biotechnol ; 39: 67-73, may. 2019. graf, tab
Article in English | LILACS | ID: biblio-1052039
ABSTRACT

BACKGROUND:

The supplementation of betaine, an osmoprotective compatible solute, in the cultivation media has been widely used to protect bacterial cells. To explore the effects of betaine addition on industrial fermentation, Escherichia coli THRD, an L-threonine producer, was used to examine the production of L-threonine with betaine supplementation and the underlying mechanism through which betaine functions was investigated.

RESULTS:

Betaine supplementation in the medium of E. coli THRD significantly improved L-threonine fermentation parameters. The transcription of zwf and corresponding enzyme activity of glucose-6-phosphate dehydrogenase were significantly promoted by betaine addition, which contributed to an enhanced expression of zwf that provided more nicotinamide adenine dinucleotide phosphate (NADPH) for L-threonine synthesis. In addition, as a result of the betaine addition, the betaine-stimulated expression of enhanced green fluorescent protein (eGFP) under the zwf promoter within a plasmid-based cassette proved to be a transcription-level response of zwf. Finally, the promoter of the phosphoenolpyruvate carboxylase gene ppc in THRD was replaced with that of zwf, while L-threonine fermentation of the new strain was promoted by betaine addition.

Conclusions:

We reveal a novel mode of betaine that facilitates the microbial production of useful compounds. Betaine supplementation upregulates the expression of zwf and increases the NADPH synthesis, which may be beneficial for the cell growth and thereby promote the production of L-threonine. This finding might be useful for the production of NADPH-dependent amino acids and derivatives in E. coli THRD or other E. coli strains.
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Full text: Available Index: LILACS (Americas) Main subject: Threonine / Betaine / Escherichia coli Language: English Journal: Electron. j. biotechnol Journal subject: Biotechnology Year: 2019 Type: Article Affiliation country: China Institution/Affiliation country: Tianjin University of Science and Technology/CN

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Full text: Available Index: LILACS (Americas) Main subject: Threonine / Betaine / Escherichia coli Language: English Journal: Electron. j. biotechnol Journal subject: Biotechnology Year: 2019 Type: Article Affiliation country: China Institution/Affiliation country: Tianjin University of Science and Technology/CN