Discovery and Biosynthesis of a Novel Acorane-Type Sesquiterpene from Rhynchosporium agropyri

Abstract Acoranes represent an important family of sesquiterpenes featuring a unique spiro[4.5]decane skeleton with remarkable structural diversity and extensive biological activities. In this study, genome mining of the plant pathogenic fungus Rhynchosporium agropyri enabled the identification of a small biosynthetic gene cluster (rhy) encoding sesquiterpene synthase RhyA and cytochrome P450 RhyB, which together catalyze the formation of a novel acorane-type sesquiterpene, rhyagracorone (1). Furthermore, by elucidating the biosynthetic pathway of 1, we confirmed that RhyA acts as an acora-3(4),7(8)-diene (2) synthase and further explored the critical residues for RhyA’s catalytic activity through site-directed mutagenesis. Finally, bioactivity assays revealed that compound 1 exhibited inhibitory activity against the crop pathogenic fungus Cochliobolus heterostrophus with an EC50 of 91.6 μg/mL. These findings lay an important foundation for the further discovery of acorane-type sesquiterpenes and provide a potential lead compound for the research and development of agricultural antifungal agents.

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Journal
Journal of Agricultural and Food Chemistry
Published
2026-09-18
DOI
https://doi.org/10.1021/acs.jafc.6c09526
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Discovery and Biosynthesis of a Novel Acorane-Type Sesquiterpene from Rhynchosporium agropyri

L. Nagaprasada Rao, Haichun Zeng, Jiatong Zeng, Beilin Meng et al.
Journal of Agricultural and Food Chemistry
Microbial Natural Products and Biosynthesis
article

Discovery and Biosynthesis of a Novel Acorane-Type Sesquiterpene from Rhynchosporium agropyri

L. Nagaprasada Rao, Haichun Zeng, Jiatong Zeng, Beilin Meng, Yuxin Zhou
article en

Abstract

Abstract Acoranes represent an important family of sesquiterpenes featuring a unique spiro[4.5]decane skeleton with remarkable structural diversity and extensive biological activities. In this study, genome mining of the plant pathogenic fungus Rhynchosporium agropyri enabled the identification of a small biosynthetic gene cluster (rhy) encoding sesquiterpene synthase RhyA and cytochrome P450 RhyB, which together catalyze the formation of a novel acorane-type sesquiterpene, rhyagracorone (1). Furthermore, by elucidating the biosynthetic pathway of 1, we confirmed that RhyA acts as an acora-3(4),7(8)-diene (2) synthase and further explored the critical residues for RhyA’s catalytic activity through site-directed mutagenesis. Finally, bioactivity assays revealed that compound 1 exhibited inhibitory activity against the crop pathogenic fungus Cochliobolus heterostrophus with an EC50 of 91.6 μg/mL. These findings lay an important foundation for the further discovery of acorane-type sesquiterpenes and provide a potential lead compound for the research and development of agricultural antifungal agents.

Journal of Agricultural and Food Chemistry
Chongqing University of Science and Technology (CN), Chongqing Medical and Pharmaceutical College (CN)
National Natural Science Foundation of China, Chongqing Municipal Education Commission
Zero hunger
Openalex Percentile: Top 12%
Microbial Natural Products and Biosynthesis
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Discovery and Biosynthesis of a Novel Acorane-Type Sesquiterpene from Rhynchosporium agropyri — L. Nagaprasada Rao, Haichun Zeng, et al. · Journal of Agricultural and Food Chemistry (2026) | TGRS Research Map | TGRS