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The Biosynthetic Gene Cluster of Mushroom‐Derived Antrocin Encodes Two Dual‐Functional Haloacid Dehalogenase‐like Terpene Cyclases

(−)‐Antrocin (1), produced by the medicinal mushroom Antrodia cinnamomea, is a potent antiproliferative compound. The biosynthetic gene cluster of 1 was identified, and the pathway was characterized by heterologous expression. We characterized a haloacid dehalogenase‐like terpene cyclase AncC that b...

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Published in:Angewandte Chemie International Edition 2023-02, Vol.62 (9), p.e202215566-n/a
Main Authors: Chen, Tzu‐Ho, Chen, Chien‐Ting, Lee, Chi‐Fang, Huang, Rou‐Jie, Chen, Kuan‐Lin, Lu, Yuan‐Chun, Liang, Suh‐Yuen, Pham, Mai‐Truc, Rao, Yerra Koteswara, Wu, Shih‐Hsiung, Chein, Rong‐Jie, Lin, Hsiao‐Ching
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cited_by cdi_FETCH-LOGICAL-c3736-94acd28edd3056374f3d9c18298ceb472220cc605d1f450a87c12cd49b1002233
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creator Chen, Tzu‐Ho
Chen, Chien‐Ting
Lee, Chi‐Fang
Huang, Rou‐Jie
Chen, Kuan‐Lin
Lu, Yuan‐Chun
Liang, Suh‐Yuen
Pham, Mai‐Truc
Rao, Yerra Koteswara
Wu, Shih‐Hsiung
Chein, Rong‐Jie
Lin, Hsiao‐Ching
description (−)‐Antrocin (1), produced by the medicinal mushroom Antrodia cinnamomea, is a potent antiproliferative compound. The biosynthetic gene cluster of 1 was identified, and the pathway was characterized by heterologous expression. We characterized a haloacid dehalogenase‐like terpene cyclase AncC that biosynthesizes the drimane‐type sesquiterpene (+)‐albicanol (2) from farnesyl pyrophosphate (FPP). Biochemical characterization of AncC, including kinetic studies and mutagenesis, demonstrated the functions of two domains: a terpene cyclase (TC) and a pyrophosphatase (PPase). The TC domain first cyclizes FPP to albicanyl pyrophosphate, and the PPase domain then removes the pyrophosphate to form 2. Intriguingly, AncA (94 % sequence identity to AncC), in the same gene cluster, converts FPP into (R)‐trans‐γ‐monocyclofarnesol instead of 2. Notably, Y283/F375 in the TC domain of AncA serve as a gatekeeper in controlling the formation of a cyclofarnesoid rather than a drimane‐type scaffold. We uncovered the biosynthesis of (−)‐antrocin, from the medicinal mushroom Antrodia cinnamomea, using genetic and biochemical approaches. Furthermore, two unusual dual‐functional haloacid dehalogenase‐like terpene cyclases, AncA and AncC, which generate cyclofarnesoid‐ and drimane‐type products, respectively, were characterized. These findings lay the foundation for the biotechnological production of antrocins independent of the Antrodia mushroom.
doi_str_mv 10.1002/anie.202215566
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The biosynthetic gene cluster of 1 was identified, and the pathway was characterized by heterologous expression. We characterized a haloacid dehalogenase‐like terpene cyclase AncC that biosynthesizes the drimane‐type sesquiterpene (+)‐albicanol (2) from farnesyl pyrophosphate (FPP). Biochemical characterization of AncC, including kinetic studies and mutagenesis, demonstrated the functions of two domains: a terpene cyclase (TC) and a pyrophosphatase (PPase). The TC domain first cyclizes FPP to albicanyl pyrophosphate, and the PPase domain then removes the pyrophosphate to form 2. Intriguingly, AncA (94 % sequence identity to AncC), in the same gene cluster, converts FPP into (R)‐trans‐γ‐monocyclofarnesol instead of 2. Notably, Y283/F375 in the TC domain of AncA serve as a gatekeeper in controlling the formation of a cyclofarnesoid rather than a drimane‐type scaffold. 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The biosynthetic gene cluster of 1 was identified, and the pathway was characterized by heterologous expression. We characterized a haloacid dehalogenase‐like terpene cyclase AncC that biosynthesizes the drimane‐type sesquiterpene (+)‐albicanol (2) from farnesyl pyrophosphate (FPP). Biochemical characterization of AncC, including kinetic studies and mutagenesis, demonstrated the functions of two domains: a terpene cyclase (TC) and a pyrophosphatase (PPase). The TC domain first cyclizes FPP to albicanyl pyrophosphate, and the PPase domain then removes the pyrophosphate to form 2. Intriguingly, AncA (94 % sequence identity to AncC), in the same gene cluster, converts FPP into (R)‐trans‐γ‐monocyclofarnesol instead of 2. Notably, Y283/F375 in the TC domain of AncA serve as a gatekeeper in controlling the formation of a cyclofarnesoid rather than a drimane‐type scaffold. We uncovered the biosynthesis of (−)‐antrocin, from the medicinal mushroom Antrodia cinnamomea, using genetic and biochemical approaches. Furthermore, two unusual dual‐functional haloacid dehalogenase‐like terpene cyclases, AncA and AncC, which generate cyclofarnesoid‐ and drimane‐type products, respectively, were characterized. These findings lay the foundation for the biotechnological production of antrocins independent of the Antrodia mushroom.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>36583947</pmid><doi>10.1002/anie.202215566</doi><tpages>8</tpages><edition>International ed. in English</edition><orcidid>https://orcid.org/0000-0001-8229-314X</orcidid></addata></record>
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subjects Agaricales - metabolism
Antibodies, Antineutrophil Cytoplasmic
Antineutrophil cytoplasmic antibodies
Biosynthesis
Diphosphates
Domains
Kinetics
Medicinal Mushrooms
Multigene Family
Mushrooms
Mutagenesis
Natural Products
Pyrophosphatase
Pyrophosphatases - metabolism
Sesquiterpenes - chemistry
Terpene Cyclases
Terpenes
Terpenes - metabolism
title The Biosynthetic Gene Cluster of Mushroom‐Derived Antrocin Encodes Two Dual‐Functional Haloacid Dehalogenase‐like Terpene Cyclases
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