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梅氏杯形菌萜类化合物组的表征

Characterization of the Cubamyces Menziesii Terpenome.

作者信息

Leydet Létitia, Couillaud Julie, Amouric Agnès, Courvoisier-Dezord Elise, Avesque Carole, Giardina Thierry, Attolini Mireille, Rousselot-Pailley Pierre, Duquesne Katia, Rosso Marie-Noelle, Iacazio Gilles

机构信息

CNRS, Centrale Med, ISM2, Aix Marseille Univ, Marseille, France.

Materials Synthetic Biology, INM - Leibniz-Institut für Neue Materialien gGmbH, Campus D2, 66123, Saarbrücken, Germany.

出版信息

Chembiochem. 2025 Aug 22;26(15):e202401083. doi: 10.1002/cbic.202401083. Epub 2025 Apr 30.

Abstract

Long-lasting polypore fungi are significant producers of terpene cyclases of high interest for medicinal or biotechnological applications. Following the 1000 Fungal Genomes initiative launched by the Joint Genome Institute, the genome of Cubamyces (C.) menziesii and identified 18 genes encoding sesquiterpene cyclases (STCs) is explored. In a search for robust catalysts suitable for practical applications, the 18 codon-optimized open reading frames are cloned and overproduced the C. menziesii STCs in Escherichia coli. In ten cases, the catalytically active enzyme is purified and tested with three chemically synthesized linear diphosphates: geranyl diphosphate, farnesyl diphosphate (FDP), and geranylgeranyl diphosphate. Only FDP proved to be a substrate for these 10 enzymes. The product specificity of all these enzymes is determined by (GC-MS) gas chromatography mass spectrometry and (NMR) nuclear magnetic resonance analysis. Among the 10 enzymes, four produced a predominant compound, four yielded two main compounds, and the remaining two acted as a multiproduct catalysts. This work sheds light on the potential sesquiterpenes involved in the chemical ecology of the polypore C. menziesii and provides evidence for the potential of Polyporales fungi in the identification of new sesquiterpene cyclase activities.

摘要

持久多孔菌是萜烯环化酶的重要生产者,这些酶在医学或生物技术应用中具有很高的研究价值。继联合基因组研究所发起的1000种真菌基因组计划之后,对孟氏立方多孔菌(Cubamyces menziesii)的基因组进行了探索,并鉴定出18个编码倍半萜环化酶(STCs)的基因。为了寻找适合实际应用的强大催化剂,克隆了18个密码子优化的开放阅读框,并在大肠杆菌中过量表达了孟氏立方多孔菌的STCs。在10种情况下,纯化了具有催化活性的酶,并用三种化学合成的线性二磷酸酯进行了测试:香叶基二磷酸、法尼基二磷酸(FDP)和香叶基香叶基二磷酸。结果表明,只有FDP是这10种酶的底物。通过气相色谱-质谱联用(GC-MS)和核磁共振(NMR)分析确定了所有这些酶的产物特异性。在这10种酶中,有4种产生了一种主要化合物,4种产生了两种主要化合物,其余两种则作为多产物催化剂。这项工作揭示了参与孟氏立方多孔菌化学生态学的潜在倍半萜,并为多孔菌目真菌在鉴定新的倍半萜环化酶活性方面的潜力提供了证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d61/12376244/6defa5908b68/CBIC-26-e202401083-g003.jpg

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