A new 3,6-dialkyl-α-pyrone produced by the heterologous expression of a PKS-NRPS hybrid enzyme derived from a Pestalotiopsis endophyte
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Ozaki, Taro
Sugawara, Akihiro
Morishita, Yohei
Tan, Yu Pei
Shivas, Roger G
Davis, Rohan A
Asai, Teigo
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Abstract
Genome mining of polyketide synthase (PKS)-nonribosomal peptide synthetase (NRPS) hybrid enzymes independent of trans-acting enoyl reductase using our in-house fungal draft genomic library led to the discovery of a unique PKS-NRPS hybrid enzyme, PbpsA, in a Pestalotiopsis fungus. Heterologously expressed PbpsA in Aspergillus oryzae provided a new 3,6-dialkyl-α-pyrone 1. This compound was fully characterized following the interpretation of NMR, UV, IR, and MS data. From the structure, we speculated that 1 was biosynthesized by the only PKS moiety of PbpsA, and that a 3-ethyl substitution was introduced by an endogenous enzyme from A. oryzae.
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Tetrahedron Letters
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134
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Biochemistry and cell biology
Medicinal and biomolecular chemistry
Organic chemistry
Science & Technology
Physical Sciences
Chemistry, Organic
Chemistry
Biosynthesis
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Shi, Y; Ozaki, T; Sugawara, A; Morishita, Y; Tan, YP; Shivas, RG; Davis, RA; Asai, T, A new 3,6-dialkyl-α-pyrone produced by the heterologous expression of a PKS-NRPS hybrid enzyme derived from a Pestalotiopsis endophyte, Tetrahedron Letters, 2024, 134, pp. 154865