A new enzyme involved in the control of the stereochemistry in the decalin formation during equisetin biosynthesis.
Biochem Biophys Res Commun
; 460(2): 210-5, 2015 May 01.
Article
em En
| MEDLINE
| ID: mdl-25770422
Tetramic acid containing a decalin ring such as equisetin and phomasetin is one of the characteristic scaffolds found in fungal bioactive secondary metabolites. Polyketide (PKS)-nonribosomal peptide synthetase (NRPS) hybrid enzyme is responsible for the synthesis of the polyketide scaffold conjugated with an amino acid. PKS-NRPS hybrid complex programs to create structural diversity in the polyketide backbone have begun to be investigated, yet mechanism of control of the stereochemistry in a decalin formation via a Diels-Alder cycloaddition remains uncertain. Here, we demonstrate that fsa2, which showed no homology to genes encoding proteins of known function, in the fsa cluster responsible for equisetin and fusarisetin A biosynthesis in Fusarium sp. FN080326, is involved in the control of stereochemistry in decalin formation via a Diels-Alder reaction in the equisetin biosynthetic pathway.
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MEDLINE
Assunto principal:
Pirrolidinonas
/
Tetra-Hidronaftalenos
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Policetídeo Sintases
/
Naftalenos
Idioma:
En
Ano de publicação:
2015
Tipo de documento:
Article