TY - JOUR
T1 - Latent potentials of the white-rot basidiomycete Phanerochaete chrysosporium responsible for sesquiterpene metabolism
T2 - CYP5158A1 and CYP5144C8 decorate (E)-α-bisabolene
AU - Ichinose, Hirofumi
AU - Ukeba, Shota
AU - Kitaoka, Takuya
N1 - Funding Information:
This research was supported in part by a Grant-in-Aid for Scientific Research B [No. 20H03045 to HI] and for Scientific Research on Innovative Areas [No. 19H04660 to HI] from the Japan Society for the Promotion of Science, Institute for Fermentation Osaka (IFO) research grant (to HI) and a Kato Memorial Bioscience Foundation research grant (to HI). NMR analysis was carried out at the Center for Advanced Instrumental and Educational Support, Faculty of Agriculture Kyushu University, Japan. The authors thank Edanz (https://jp.edanz.com/ac) for editing a draft of this manuscript.
Funding Information:
This research was supported in part by a Grant-in-Aid for Scientific Research B [No. 20H03045 to HI] and for Scientific Research on Innovative Areas [No. 19H04660 to HI] from the Japan Society for the Promotion of Science, Institute for Fermentation Osaka (IFO) research grant (to HI) and a Kato Memorial Bioscience Foundation research grant (to HI). NMR analysis was carried out at the Center for Advanced Instrumental and Educational Support, Faculty of Agriculture Kyushu University, Japan. The authors thank Edanz (https://jp.edanz.com/ac) for editing a draft of this manuscript.
Publisher Copyright:
© 2022 Elsevier Inc.
PY - 2022/8
Y1 - 2022/8
N2 - Basidiomycetes produce various sesquiterpenoids and their relevance for pharmaceutical and agricultural applications and understanding their biosynthetic machinery to produce these secondary metabolites have attracted significant interest. Because sesquiterpene synthases (STSs) and cytochrome P450 monooxygenases (P450s) play pivotal roles in the production of sesquiterpenoids, functional characterization of these enzymes is fundamentally essential. In this study, we found 11 possible STSs from the white-rot basidiomycete Phanerochaete chrysosporium (PcSTSs) and isolated nine of these as full-length cDNAs encoding a mature open reading frame. Using the isolated cDNAs, we performed heterologous expression of PcSTSs in Saccharomyces cerevisiae. Metabolic studies revealed that seven of the PcSTSs produce a series of sesquiterpene scaffolds, including (E)-α-bisabolene. Furthermore, we constructed a co-expression system of (E)-α-bisabolene synthase and P450 from P. chrysosporium (PcCYP). Semi-comprehensive screening using 120 isoforms of PcCYPs resulted in the identification of CYP5158A1 and CYP5144C8, two P450s capable of decorating (E)-α-bisabolene.
AB - Basidiomycetes produce various sesquiterpenoids and their relevance for pharmaceutical and agricultural applications and understanding their biosynthetic machinery to produce these secondary metabolites have attracted significant interest. Because sesquiterpene synthases (STSs) and cytochrome P450 monooxygenases (P450s) play pivotal roles in the production of sesquiterpenoids, functional characterization of these enzymes is fundamentally essential. In this study, we found 11 possible STSs from the white-rot basidiomycete Phanerochaete chrysosporium (PcSTSs) and isolated nine of these as full-length cDNAs encoding a mature open reading frame. Using the isolated cDNAs, we performed heterologous expression of PcSTSs in Saccharomyces cerevisiae. Metabolic studies revealed that seven of the PcSTSs produce a series of sesquiterpene scaffolds, including (E)-α-bisabolene. Furthermore, we constructed a co-expression system of (E)-α-bisabolene synthase and P450 from P. chrysosporium (PcCYP). Semi-comprehensive screening using 120 isoforms of PcCYPs resulted in the identification of CYP5158A1 and CYP5144C8, two P450s capable of decorating (E)-α-bisabolene.
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U2 - 10.1016/j.enzmictec.2022.110037
DO - 10.1016/j.enzmictec.2022.110037
M3 - Article
C2 - 35378352
AN - SCOPUS:85127320905
SN - 0141-0229
VL - 158
JO - Enzyme and Microbial Technology
JF - Enzyme and Microbial Technology
M1 - 110037
ER -