Literature DB >> 33350420

Sesterterpenoids: chemistry, biology, and biosynthesis.

Keke Li1, Kirk R Gustafson.   

Abstract

Covering: July 2012 to December 2019Over the last seven years, expanding research efforts focused on sesterterpenoids has led to the isolation, identification, and characterization of numerous structurally novel and biologically active sesterterpenoids. These newly reported sesterterpenoids provide diverse structures that often incorporate unprecedented ring systems and new carbon skeletons, as well as unusual functional group arrays. Biological activities of potential biomedical importance including suppression of cancer cell growth, inhibition of enzymatic activity, and modulation of receptor signaling, as well as ecologically important functions such as antimicrobial effects and deterrence of herbivorous insects have been associated with a variety of sesterterpenoids. There has also been a rapid growth in our knowledge of the genomics, enzymology, and specific pathways associated with sesterterpene biosynthesis. This has opened up new opportunities for future sesterterpene discovery and diversification through the expression of new cryptic metabolites and the engineered manipulation of associated biosynthetic machinery and processes. In this paper we reviewed 498 new sesterterpenoids, including their structures, source organisms, country of origin, relevant bioactivities, and biosynthesis.

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Year:  2020        PMID: 33350420     DOI: 10.1039/d0np00070a

Source DB:  PubMed          Journal:  Nat Prod Rep        ISSN: 0265-0568            Impact factor:   13.423


  6 in total

1.  Schultriene and nigtetraene: two sesterterpenes characterized from pathogenetic fungi via genome mining approach.

Authors:  Lan Jiang; Huanting Yang; Xue Zhang; Xiaoying Li; Kangjie Lv; Weiyan Zhang; Guoliang Zhu; Chengwei Liu; Yongheng Wang; Tom Hsiang; Lixin Zhang; Xueting Liu
Journal:  Appl Microbiol Biotechnol       Date:  2022-08-30       Impact factor: 5.560

Review 2.  Occurrence and biosynthesis of plant sesterterpenes (C25), a new addition to terpene diversity.

Authors:  Qingwen Chen; Jianxu Li; Yihua Ma; Weiliang Yuan; Peng Zhang; Guodong Wang
Journal:  Plant Commun       Date:  2021-03-30

3.  An extremely promiscuous terpenoid synthase from the Lamiaceae plant Colquhounia coccinea var. mollis catalyzes the formation of sester-/di-/sesqui-/mono-terpenoids.

Authors:  De-Sen Li; Juan Hua; Shi-Hong Luo; Yan-Chun Liu; Yue-Gui Chen; Yi Ling; Kai Guo; Yan Liu; Sheng-Hong Li
Journal:  Plant Commun       Date:  2021-08-12

4.  An Alternative Approach towards C-12 Functionalized Scalaranic Sesterterpenoids Synthesis of 17-Oxo-20-norscalaran-12α,19-O-lactone.

Authors:  Olga Morarescu; Marina Grinco; Veaceslav Kulciţki; Sergiu Shova; Nicon Ungur
Journal:  Mar Drugs       Date:  2021-11-12       Impact factor: 5.118

5.  Discovery of Ircinianin Lactones B and C-Two New Cyclic Sesterterpenes from the Marine Sponge Ircinia wistarii.

Authors:  Thomas Majer; Keshab Bhattarai; Jan Straetener; Justus Pohlmann; Patrick Cahill; Markus O Zimmermann; Marc P Hübner; Marcel Kaiser; Johan Svenson; Michael Schindler; Heike Brötz-Oesterhelt; Frank M Boeckler; Harald Gross
Journal:  Mar Drugs       Date:  2022-08-19       Impact factor: 6.085

6.  Norditerpenoids biosynthesized by variediene synthase-associated P450 machinery along with modifications by the host cell Aspergillus oryzae.

Authors:  Lan Jiang; Kangjie Lv; Guoliang Zhu; Zhi Lin; Xue Zhang; Cuiping Xing; Huanting Yang; Weiyan Zhang; Zhixin Wang; Chengwei Liu; Xudong Qu; Tom Hsiang; Lixin Zhang; Xueting Liu
Journal:  Synth Syst Biotechnol       Date:  2022-08-23
  6 in total

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