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Knockout of the Aldehyde Dehydrogenase Gene in Fusarium oxysporum for Enhanced Ethanol Yield

Author

Listed:
  • Jinxia Fan

    (College of Engineering, Northeast Agricultural University, Harbin 150030, China
    Key Laboratory of Swine Facilities Engineering, Ministry of Agriculture and Rural Affairs, Harbin 150030, China)

  • Xiaomei Huang

    (Department of Bioengineering, Heilongjiang Vocational College of Agricultural Technology, Jiamusi 154007, China)

  • Guoxiang Zheng

    (College of Engineering, Northeast Agricultural University, Harbin 150030, China
    Key Laboratory of Swine Facilities Engineering, Ministry of Agriculture and Rural Affairs, Harbin 150030, China)

  • Changyu Liu

    (College of Engineering, Northeast Agricultural University, Harbin 150030, China
    Key Laboratory of Swine Facilities Engineering, Ministry of Agriculture and Rural Affairs, Harbin 150030, China)

  • Ming Wang

    (College of Engineering, Northeast Agricultural University, Harbin 150030, China
    Key Laboratory of Swine Facilities Engineering, Ministry of Agriculture and Rural Affairs, Harbin 150030, China)

  • Yong Sun

    (College of Engineering, Northeast Agricultural University, Harbin 150030, China
    Key Laboratory of Swine Facilities Engineering, Ministry of Agriculture and Rural Affairs, Harbin 150030, China)

  • Qian Yang

    (Department of Life Science and Engineering, Harbin Institute of Technology, Harbin 150001, China)

Abstract

Acetic acid is the primary by-product generated from ethanol production by Fusarium oxysporum using glucose or xylose as a substrate. Aldehyde dehydrogenase (ALDH) is the critical enzyme in acetic acid metabolism. To decrease acetic acid yield in ethanol production, the 1509 bp DNA of aldh , encoding a 502 amino acid protein with a calculated molecular mass of 54.33 kDa and an isoelectric point of 6.21, was cloned from F. oxysporum . Sequence analysis confirmed that the screened proteins belonged to the ALDH family. A knockout vector, ∆ aldh , containing positive (hygromycin resistance gene) and negative (thymidine kinase gene from the herpes simplex virus) selectable markers, was constructed. Ethanol production by the mutant (cs28pCAM-Pstal-∆ aldh ) in glucose- and xylose-containing media was 0.46 and 0.39 g/g, respectively, and these yields were 16.93% and 34.63% higher than those by the wild-type strain (0.393 and 0.289 g/g). Furthermore, the acetic acid yield of the mutant was 3.50 and 3.01 g/L, respectively, showing a 23.10% and 39.55% decrease compared with the wild-type strain (4.308 and 4.196 g/L). The biomass of the mutant (4.05 and 4.52 g/L) was lower than that of the wild-type strain (4.71 and 5.97 g/L). These results demonstrated the potential use of the genetically stable mutant for industrial bioethanol production.

Suggested Citation

  • Jinxia Fan & Xiaomei Huang & Guoxiang Zheng & Changyu Liu & Ming Wang & Yong Sun & Qian Yang, 2022. "Knockout of the Aldehyde Dehydrogenase Gene in Fusarium oxysporum for Enhanced Ethanol Yield," Energies, MDPI, vol. 16(1), pages 1-12, December.
  • Handle: RePEc:gam:jeners:v:16:y:2022:i:1:p:427-:d:1020007
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