TY - JOUR
T1 - Insight into metabolic diversity of the brown-rot basidiomycete Postia placenta responsible for sesquiterpene biosynthesis
T2 - semi-comprehensive screening of cytochrome P450 monooxygenase involved in protoilludene metabolism
AU - Ichinose, Hirofumi
AU - Kitaoka, Takuya
N1 - Funding Information:
Received 29 May, 2018; accepted 19 July, 2018. *For correspondence. E-mail ichinose@agr.kyushu-u.ac.jp; Tel./Fax +81-92-642-2994. Microbial Biotechnology (2018) 11(5), 952–965 doi:10.1111/1751-7915.13304 Funding Information This research was supported in part by an Institute for Fermentation, Osaka (IFO) research grant (to HI), a Kato Memorial Bioscience Foundation research grant (to HI) and a Grant-in-Aid for Scientific Research B (No. 16H04955 to HI) from the Japan Society for the Promotion of Science.
Funding Information:
This research was supported in part by an Institute for Fermentation, Osaka (IFO) research grant (to HI), a Kato Memorial Bioscience Foundation research grant (to HI) and a Grant-in-Aid for Scientific Research B (No. 16H04955 to HI) from the Japan Society for the Promotion of Science. The authors thank the Edanz Group (www.edanzediting.com/ac) for editing a draft of this manuscript.
Publisher Copyright:
© 2018 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology.
PY - 2018/9
Y1 - 2018/9
N2 - A wide variety of sesquiterpenoids have been isolated from basidiomycetes, and their bioactive properties have attracted significant attention in an effort to understand biosynthetic machineries. As both sesquiterpene synthases and cytochrome P450 monooxygenases play key roles in the diversification of sesquiterpenoids, it is important to widely and mutually understand their biochemical properties. In this study, we performed genome-wide annotation and functional characterization of sesquiterpene synthases from the brown-rot basidiomycete Postia placenta. Using RT-PCR, we isolated 16 sesquiterpene synthases genes as full-length cDNAs. Heterologous expression revealed that the sesquiterpene synthases could produce a series of sesquiterpene scaffolds with distinct metabolic profiles. Based on metabolic studies, we identified 25 sesquiterpene scaffolds including Δ6-protoilludene produced by the sesquiterpene synthases. In particular, a protoilludene synthase from the brown-rot basidiomycete was characterized for the first time. Furthermore, we conducted a semi-comprehensive functional screening of cytochrome P450 monooxygenases from P. placenta to elucidate biosynthetic machineries involved in metabolisms of Δ6-protoilludene. Coexpression of protoilludene synthase and 184 isoforms of cytochrome P450 monooxygenases enabled the identification of CYP5344B1, CYP5348E1 and CYP5348J3, which catalysed the hydroxylation reaction of Δ6-protoilludene to produce Δ6-protoilludene-8-ol and Δ6-protoilludene-5-ol. Furthermore, structural isomers of Δ7-protoilludene-6-ol were obtained from incubation of Δ6-protoilludene-8-ol in acidic culture medium.
AB - A wide variety of sesquiterpenoids have been isolated from basidiomycetes, and their bioactive properties have attracted significant attention in an effort to understand biosynthetic machineries. As both sesquiterpene synthases and cytochrome P450 monooxygenases play key roles in the diversification of sesquiterpenoids, it is important to widely and mutually understand their biochemical properties. In this study, we performed genome-wide annotation and functional characterization of sesquiterpene synthases from the brown-rot basidiomycete Postia placenta. Using RT-PCR, we isolated 16 sesquiterpene synthases genes as full-length cDNAs. Heterologous expression revealed that the sesquiterpene synthases could produce a series of sesquiterpene scaffolds with distinct metabolic profiles. Based on metabolic studies, we identified 25 sesquiterpene scaffolds including Δ6-protoilludene produced by the sesquiterpene synthases. In particular, a protoilludene synthase from the brown-rot basidiomycete was characterized for the first time. Furthermore, we conducted a semi-comprehensive functional screening of cytochrome P450 monooxygenases from P. placenta to elucidate biosynthetic machineries involved in metabolisms of Δ6-protoilludene. Coexpression of protoilludene synthase and 184 isoforms of cytochrome P450 monooxygenases enabled the identification of CYP5344B1, CYP5348E1 and CYP5348J3, which catalysed the hydroxylation reaction of Δ6-protoilludene to produce Δ6-protoilludene-8-ol and Δ6-protoilludene-5-ol. Furthermore, structural isomers of Δ7-protoilludene-6-ol were obtained from incubation of Δ6-protoilludene-8-ol in acidic culture medium.
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U2 - 10.1111/1751-7915.13304
DO - 10.1111/1751-7915.13304
M3 - Article
C2 - 30105900
AN - SCOPUS:85052104325
SN - 1751-7907
VL - 11
SP - 952
EP - 965
JO - Microbial Biotechnology
JF - Microbial Biotechnology
IS - 5
ER -