The 3-ketoacyl-CoA thiolase: an engineered enzyme for carbon chain elongation of chemical compounds

Appl Microbiol Biotechnol. 2020 Oct;104(19):8117-8129. doi: 10.1007/s00253-020-10848-w. Epub 2020 Aug 24.

Abstract

Because of their function of catalyzing the rearrangement of the carbon chains, thiolases have attracted increasing attentions over the past decades. The 3-ketoacyl-CoA thiolase (KAT) is a member of the thiolase, which is capable of catalyzing the Claisen condensation reaction between the two acyl-CoAs, thereby achieving carbon chain elongation. In this way, diverse value-added compounds might be synthesized starting from simple small CoA thioesters. However, most KATs are hampered by low stability and poor substrate specificity, which has hindered the development of large-scale biosynthesis. In this review, the common characteristics in the three-dimensional structure of KATs from different sources are summarized. Moreover, structure-guided rational engineering is discussed as a strategy for enhancing the performance of KATs. Finally, we reviewed the metabolic engineering applications of KATs for producing various energy-storage molecules, such as n-butanol, fatty acids, dicarboxylic acids, and polyhydroxyalkanoates. KEY POINTS: • Summarize the structural characteristics and catalyzation mechanisms of KATs. • Review on the rational engineering to enhance the performance of KATs. • Discuss the applications of KATs for producing energy-storage molecules.

Keywords: Claisen condensation; Metabolic engineering; Reverse β-oxidation; Thiolase.

Publication types

  • Review

MeSH terms

  • Acetyl-CoA C-Acetyltransferase / genetics
  • Acetyl-CoA C-Acyltransferase* / genetics
  • Acyl Coenzyme A
  • Carbon*
  • Metabolic Engineering

Substances

  • Acyl Coenzyme A
  • Carbon
  • Acetyl-CoA C-Acyltransferase
  • Acetyl-CoA C-Acetyltransferase