Evidence map›Paper›PMID 42866665›Full record

ReviewSynthetic and systems biotechnology2027

Diverse oxidosqualene cyclases for triterpenoid biosynthesis.

Qiannan Hao, Shengli Wang, Lei Zhang, Lin Yuan, Guangrong Zhao, Jianjun Qiao, Weiguo Li, Qinggele Caiyin

Abstract readReview
In one paragraph

Review in Synthetic and systems biotechnology, 2027. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Qiannan HaoState Key Laboratory of Synthetic Biology, Tianjin University, Tianjin, 300072, China.
Shengli WangState Key Laboratory of Synthetic Biology, Tianjin University, Tianjin, 300072, China.
Lei ZhangState Key Laboratory of Synthetic Biology, Tianjin University, Tianjin, 300072, China.
Lin YuanTianjin Agricultural University, Tianjin, 300072, China.
Guangrong ZhaoState Key Laboratory of Synthetic Biology, Tianjin University, Tianjin, 300072, China.
Jianjun QiaoState Key Laboratory of Synthetic Biology, Tianjin University, Tianjin, 300072, China.
Weiguo LiZhejiang Institute of Tianjin University (Shaoxing), Shaoxing, 312300, China.
Qinggele CaiyinState Key Laboratory of Synthetic Biology, Tianjin University, Tianjin, 300072, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Triterpenoids, a significant group of secondary metabolites, possess diverse skeletons and excellent pharmacological activities and are widely applied in cosmetics, medicine, and biopesticides. Traditional plant extraction and chemical synthesis cannot meet the needs of commercial production, and heterologous biosynthesis of triterpenoids has become a promising strategy. Oxidosqualene cyclases (OSCs) are the key enzymes that determine triterpenoid biosynthesis. However, most OSCs exhibit low heterologous expression, low catalytic activity, and promiscuous catalytic products, which impedes the heterologous biosynthesis of triterpenoids. In this study, we constructed a dataset of 348 OSCs with known functions, which is the largest centralized resource of characterized OSCs to date. The 88 triterpenoid skeletons produced by these OSCs are classified based on their structural features, 49 of which have been experimentally characterized as the main products of OSCs, and the formation mechanisms of the common skeletons are summarized. Phylogenetic analysis and motif analysis elucidated the relationships among the sequences, structures, and products of plant-derived OSCs. Phylogenetic analysis showed that plant-derived OSCs were divided into two major clades, which corresponded to the biosynthetic mechanisms of the "protosteryl/dammarenyl" dichotomy. Motif analysis showed that 5 motifs are present in plant-derived OSCs, including 3 related to the catalytic activity of the OSCs and 2 related to product specificity. Finally, we summarized the common strategies for mining OSCs to provide directions for the discovery of novel OSCs and new triterpenoid skeletons. Our study will help discover or design OSCs with specific product profiles as functional elements for applications in synthetic biology.

Indexed as

BiosynthesisCatalytic mechanismEnzyme discoveryOxidosqualene cyclasesTriterpenoids

Identifiers

PMID42866665
PMCPMC13657253

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.