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真菌独特的里氏木霉菌合酶样倍半萜合酶的基因组挖掘

Genome Mining of Fungal Unique Trichodiene Synthase-like Sesquiterpene Synthases.

作者信息

Cong Zhanren, Yin Qiang, Tian Kunhong, Mukoma Njeru Joe, Ouyang Liming, Hsiang Tom, Zhang Lixin, Jiang Lan, Liu Xueting

机构信息

State Key Laboratory of Bioreactor Engineering, East China University of Science of Technology, Shanghai 200237, China.

School of Environmental Sciences, University of Guelph, 50 Stone Road East, Guelph, ON N1G 2W1, Canada.

出版信息

J Fungi (Basel). 2024 May 13;10(5):350. doi: 10.3390/jof10050350.

Abstract

Sesquiterpenoids served as an important source for natural product drug discovery. Although genome mining approaches have revealed numerous novel sesquiterpenoids and biosynthetic enzymes, the comprehensive landscape of fungal sesquiterpene synthases (STSs) remains elusive. In this study, 123 previously reported fungal STSs were subjected to phylogenetic analysis, resulting in the identification of a fungi-specific STS family known as trichodiene synthase-like sesquiterpene synthases (TDTSs). Subsequently, the application of hidden Markov models allowed the discovery of 517 TDTSs from our in-house fungi genome library of over 400 sequenced genomes, and these TDTSs were defined into 79 families based on a sequence similarity network. Based on the novelty of protein sequences and the completeness of their biosynthetic gene clusters, 23 genes were selected for heterologous expression in . In total, 10 TDTSs were active and collectively produced 12 mono- and sesquiterpenes, resulting in the identification of the first chamipinene synthase, as well as the first fungi-derived cedrene, sabinene, and camphene synthases. Additionally, with the guidance of functionally characterized TDTSs, we found that TDTSs in Family 1 could produce bridged-cyclic sesquiterpenes, while those in Family 2 could synthesize spiro- and bridged-cyclic sesquiterpenes. Our research presents a new avenue for the genome mining of fungal sesquiterpenoids.

摘要

倍半萜类化合物是天然产物药物发现的重要来源。尽管基因组挖掘方法已经揭示了许多新型倍半萜类化合物和生物合成酶,但真菌倍半萜合酶(STSs)的全貌仍不清楚。在本研究中,对123个先前报道的真菌STSs进行了系统发育分析,从而鉴定出一个真菌特异性的STSs家族,即类trichodiene合酶倍半萜合酶(TDTSs)。随后,应用隐马尔可夫模型从我们拥有的400多个已测序基因组的真菌基因组文库中发现了517个TDTSs,并根据序列相似性网络将这些TDTSs分为79个家族。基于蛋白质序列的新颖性及其生物合成基因簇的完整性,选择了23个基因在[具体宿主]中进行异源表达。总共10个TDTSs具有活性,共同产生了12种单萜和倍半萜,从而鉴定出了首个chamipinene合酶,以及首个真菌来源的雪松烯、桧烯和莰烯合酶。此外,在功能表征的TDTSs的指导下,我们发现第1家族的TDTSs可以产生桥环倍半萜,而第2家族的TDTSs可以合成螺环和桥环倍半萜。我们的研究为真菌倍半萜类化合物的基因组挖掘提供了一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/250a/11122449/83576ab0bd43/jof-10-00350-g001.jpg

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