Production of 1,4-butanediol through Clostridia C4 pathways

Mingwei Zha, Jiangxin Gu, Jian Chen, Huifang Zhang, Mengting Li, Yong Chen, Huanqing Niu, Chenjie Zhu, Ting Guo, Zhenyu Wang, Dong Liu, Hanjie Ying

Research output: Contribution to journalArticlepeer-review

Abstract

1,4-butanediol (1,4-BDO) is an important building block in the chemical industry that has been mainly produced from fossil fuels, but now biosynthesis of 1,4-BDO has received more and more attention due to environmental issues. The Clostridia C4 pathway produces an intermediate crotonyl-CoA which could be diverted to 1,4-BDO by 4-hydroxybutyryl-CoA dehydratase (4HBD). Here, we compared this pathway with other 1,4-BDO biosynthesis pathways and illustrated its potential advantages regarding cellular energy conservation and theoretical yield. Then, the feasibility of 1,4-BDO production in this way was tested by introducing a single 4HBD in Clostridium acetobutylicum that natively produced the C4 intermediate and a variety of aldehyde/alcohol dehydrogenases (AdhE). Five different 4HBD genes were screened and the Cbei-2100 gene from Clostridium beijerinckii was the most effective, producing 0.066 mg/mL of 1,4-BDO. To block the metabolic flux towards the main product butanol, disruption of butyryl-CoA dehydrogenase (Bcd) was tried but failed, while inactivation of its homologue (FAD/FMN-containing dehydrogenase, Fcd) obtained little effect. Alternatively, the electron-transferring flavoprotein EtfA coupled with Bcd was inactivated, and 1,4-BDO production was greatly increased to 0.182 mg/mL. In conclusion, this study demonstrated the feasibility of 1,4-BDO production through the Clostridia C4 pathway. Further blocking of the competing flux towards butanol would be effective to improve the production of in the future.

Original languageEnglish
Article number2415039
JournalBiotechnology and Biotechnological Equipment
Volume38
Issue number1
DOIs
StatePublished - 2024

Keywords

  • 1,4-butanediol
  • 4-hydroxybutyryl-CoA dehydratase
  • Clostridium acetobutylicum
  • reverse β-oxidation

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