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The microbial biosynthesis of noncanonical terpenoids.

Authors :
Ma, Mengyu
Li, Mingkai
Wu, Zhenke
Liang, Xiqin
Zheng, Qiusheng
Li, Defang
Wang, Guoli
An, Tianyue
Source :
Applied Microbiology & Biotechnology. 2/21/2024, Vol. 108 Issue 1, p1-14. 14p.
Publication Year :
2024

Abstract

Terpenoids are a class of structurally complex, naturally occurring compounds found predominantly in plant, animal, and microorganism secondary metabolites. Classical terpenoids typically have carbon atoms in multiples of five and follow well-defined carbon skeletons, whereas noncanonical terpenoids deviate from these patterns. These noncanonical terpenoids often result from the methyltransferase-catalyzed methylation modification of substrate units, leading to irregular carbon skeletons. In this comprehensive review, various activities and applications of these noncanonical terpenes have been summarized. Importantly, the review delves into the biosynthetic pathways of noncanonical terpenes, including those with C6, C7, C11, C12, and C16 carbon skeletons, in bacteria and fungi host. It also covers noncanonical triterpenes synthesized from non-squalene substrates and nortriterpenes in Ganoderma lucidum, providing detailed examples to elucidate the intricate biosynthetic processes involved. Finally, the review outlines the potential future applications of noncanonical terpenoids. In conclusion, the insights gathered from this review provide a reference for understanding the biosynthesis of these noncanonical terpenes and pave the way for the discovery of additional unique and novel noncanonical terpenes. Key points: •The activities and applications of noncanonical terpenoids are introduced. •The noncanonical terpenoids with irregular carbon skeletons are presented. •The microbial biosynthesis of noncanonical terpenoids is summarized. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01757598
Volume :
108
Issue :
1
Database :
Academic Search Index
Journal :
Applied Microbiology & Biotechnology
Publication Type :
Academic Journal
Accession number :
177881524
Full Text :
https://doi.org/10.1007/s00253-024-13048-y