Clade III Synthases Add Cyclic And Linear Terpenoids To The Psilocybe Metabolome.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
ChemBioChem Pub Date : 2025-05-03 DOI:10.1002/cbic.202500167
Nick Zschoche, Sebastian Schober, Karl Walther, Andrew R Chadeayne, Markus Gressler, Stefan Bartram, Sarah E O'Connor, Dirk Hoffmeister
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引用次数: 0

Abstract

Psilocybe "magic mushrooms" are best known for their indolethylamine psilocybin, yet they encode enzymes for a much more diverse arsenal of small and potentially bioactive molecules. Here, we report on four Psilocybe cubensis clade III sesquiterpene synthases, CubB-CubE, whose genes are differently expressed in fruiting bodies compared to vegetative mycelium. CubB-CubE were functionally characterized in vitro by product formation assays with heterologously produced enzymes and in vivo by transgene expression in Aspergillus niger, followed by extensive GC-MS analyses. CubB was identified as a single product (3R,6E)-(-)-nerolidol synthase. CubC is a multi-product enzyme producing β-caryophyllene, β-elemene, α-humulene, and β-farnesene. CubD and CubE catalyzed (near-)exclusively sterpurene formation. P. cubensis young fruiting bodies and vegetative mycelium were analyzed for sesquiterpenes which verified the presence of the CubB product α-(3R,6E)-(-)-nerolidol. As various Psilocybe species encode highly similar enzymes, this study contributes generally to the as yet little understood secondary metabolome of the genus.

Clade III合酶在裸盖菇代谢组中添加环状和线性萜类。
裸盖菇“神奇蘑菇”以其吲哚乙胺裸盖菇素而闻名,但它们为更多样化的小分子和潜在的生物活性分子编码酶。在这里,我们报道了四种裸盖菇分支III倍半萜合成酶CubB-CubE,它们的基因在子实体中的表达与营养菌丝的表达不同。通过异种酶的体外产物形成实验和在黑曲霉中的转基因表达,以及广泛的气相色谱-质谱分析,对CubB-CubE进行了功能表征。CubB被鉴定为单一产物(3R,6E)-(-)-神经醇合成酶。CubC是一种多产物酶,可产生β-石竹烯、β-榄香烯、α-葎草烯和β-法尼烯。cud和CubE催化(近)纯sterpurene生成。对幼子实体和营养菌丝体进行了倍半萜素分析,证实了CubB产物α-(3R,6E)-(-)-神经醇的存在。由于各种裸盖菇物种编码高度相似的酶,本研究一般有助于尚不清楚的次生代谢组属。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ChemBioChem
ChemBioChem 生物-生化与分子生物学
CiteScore
6.10
自引率
3.10%
发文量
407
审稿时长
1 months
期刊介绍: ChemBioChem (Impact Factor 2018: 2.641) publishes important breakthroughs across all areas at the interface of chemistry and biology, including the fields of chemical biology, bioorganic chemistry, bioinorganic chemistry, synthetic biology, biocatalysis, bionanotechnology, and biomaterials. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and supported by the Asian Chemical Editorial Society (ACES).
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