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Applications of protein engineering in the microbial synthesis of plant triterpenoids

  • Yan Luo
  • , Yaozhu Jiang
  • , Linhao Chen
  • , Chun Li
  • , Ying Wang*
  • *Corresponding author for this work
  • Beijing Institute of Technology
  • Tsinghua University

Research output: Contribution to journalReview articlepeer-review

Abstract

Triterpenoids are a class of natural products widely used in fields related to medicine and health due to their biological activities such as hepatoprotection, anti-inflammation, anti-viral, and anti-tumor. With the advancement in biotechnology, microorganisms have been used as cell factories to produce diverse natural products. Despite the significant progress that has been made in the construction of microbial cell factories for the heterogeneous biosynthesis of triterpenoids, the industrial production of triterpenoids employing microorganisms has been stymied due to the shortage of efficient enzymes as well as the low expression and low catalytic activity of heterologous proteins in microbes. Protein engineering has been demonstrated as an effective way for improving the specificity, catalytic activity, and stability of the enzyme, which can be employed to overcome these challenges. This review summarizes the current progress in the studies of Oxidosqualene cyclases (OSCs), cytochrome P450s (P450s), and UDP-glycosyltransferases (UGTs), the key enzymes in the triterpenoids synthetic pathway. The main obstacles restricting the efficient catalysis of these key enzymes are analyzed, the applications of protein engineering for the three key enzymes in the microbial synthesis of triterpenoids are systematically reviewed, and the challenges and prospects of protein engineering are also discussed.

Original languageEnglish
Pages (from-to)20-32
Number of pages13
JournalSynthetic and Systems Biotechnology
Volume8
Issue number1
DOIs
Publication statusPublished - Mar 2023
Externally publishedYes

Keywords

  • Cytochrome P450
  • Oxidosqualene cyclase
  • Protein engineering
  • Triterpenoids
  • UDP-Glycosyltransferase

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