Unknown

Dataset Information

0

Genome mining and molecular characterization of the biosynthetic gene cluster of a diterpenic meroterpenoid, 15-deoxyoxalicine B, in Penicillium canescens.


ABSTRACT: Meroterpenoids are a class of secondary metabolites that are produced from polyketide and terpenoid precursors. 15-Deoxyoxalicine B (1) belongs to one structural group consisting of a unique pyridinyl-?-pyrone polyketide subunit and a diterpenoid subunit connected through a characteristic asymmetric spiro carbon atom. An understanding of the genes involved in the biosynthesis of this class of compounds should provide a means to facilitate engineering of second-generation molecules and increasing production of first-generation compounds. We found that the filamentous fungus Penicillium canescens produces 15-deoxyoxalicine B (1). Using targeted gene deletions, we have identified a cluster of 12 responsible contiguous genes. This gene cluster includes one polyketide synthase gene which we have designated olcA. Chemical analysis of wild-type and gene deletion mutant extracts enabled us to isolate and characterize 7 additional metabolites that are either intermediates or shunt products of the biosynthetic pathway. Two of the compounds identified have not been reported previously. Our data have allowed us to propose a biosynthetic pathway for 15-deoxyoxalicine B (1).

SUBMITTER: Yaegashi J 

PROVIDER: S-EPMC6054112 | biostudies-literature | 2015 Nov

REPOSITORIES: biostudies-literature

altmetric image

Publications

Genome mining and molecular characterization of the biosynthetic gene cluster of a diterpenic meroterpenoid, 15-deoxyoxalicine B, in <i>Penicillium canescens</i>.

Yaegashi Junko J   Romsdahl Jillian J   Chiang Yi-Ming YM   Wang Clay C C CCC  

Chemical science 20150806 11


Meroterpenoids are a class of secondary metabolites that are produced from polyketide and terpenoid precursors. 15-Deoxyoxalicine B (<b>1</b>) belongs to one structural group consisting of a unique pyridinyl-α-pyrone polyketide subunit and a diterpenoid subunit connected through a characteristic asymmetric spiro carbon atom. An understanding of the genes involved in the biosynthesis of this class of compounds should provide a means to facilitate engineering of second-generation molecules and inc  ...[more]

Similar Datasets

| S-EPMC6765103 | biostudies-literature
| S-EPMC4434069 | biostudies-literature
| S-EPMC3538129 | biostudies-literature
| S-EPMC3755882 | biostudies-literature
| S-EPMC5418334 | biostudies-literature
| S-EPMC5384830 | biostudies-literature
| S-EPMC7744662 | biostudies-literature
| S-EPMC7253712 | biostudies-literature
| S-EPMC3901203 | biostudies-literature
| PRJNA196381 | ENA