Functional expression of RuBisCO reduces CO2 emission during fermentation by engineered Saccharomyces cerevisiae

  • Sujeong Park
  • , Bo Ram Park
  • , Deokyeol Jeong
  • , Jongbeom Park
  • , Ja Kyong Ko
  • , Soo Jung Kim
  • , Jeong Sun Kim
  • , Yong Su Jin
  • , Soo Rin Kim

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Industrial biotechnology based on yeast fermentation is a promising strategy that can alleviate global warming and climate change. However, Saccharomyces cerevisiae, widely used in bioprocesses, releases a large amount of carbon dioxide (CO2) during fermentation. This study developed a mixotrophic CO2-fixing S. cerevisiae to achieve carbon neutrality and sustainability in bioprocess. A CO2-fixation pathway was constructed in a xylose-utilizing S. cerevisiae by heterologous expression of ribulose-1,5-bisphosphate carboxylase-oxygenase (RuBisCO) and phosphoribulokinase (PRK). Furthermore, a delta-integration strategy was utilized, and the RuBisCO gene copy number was increased to 10 copies to improve the efficiency of CO2-fixation. An additional Cas9-based genome editing was performed to overexpress other CO2-fixation related genes. The resulting CO2-fixing yeast, SJ03, exhibited the highest RuBisCO activity. During anaerobic xylose fermentation, ethanol concentration was increased by 17% and ethanol yield was increased by 16% compared to the control strain. In addition, CO2 emissions decreased by 7%. These results suggest that overexpression of the CO2-fixation pathway coupled with xylose utilization in S. cerevisiae might reduce CO2 emission in bioprocesses.

Original languageEnglish
Pages (from-to)286-293
Number of pages8
JournalProcess Biochemistry
Volume134
DOIs
StatePublished - Nov 2023

Keywords

  • 5-bisphosphate carboxylase/oxygenase
  • CRISPR/Cas9
  • Carbon dioxide fixation
  • Delta-integration strategy
  • Ribulose-1
  • Saccharomyces cerevisiae

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