Intermediates in the barnol biosynthesis in Penicillium baarnense

Acta Chem Scand B. 1977;31(5):391-4. doi: 10.3891/acta.chem.scand.31b-0391.

Abstract

By using appropriate 14C-labelled phenolic substances as precursors in feeding experiments the following steps in barnol biosynthesis have been established: acetate + malonate leads to 2,4-dihydroxy-6-ethyl-5-methylbenzaldehyde leads to 1,3-dihydroxy-4,6-dimethyl-2-ethylbenzene leads to barnol. P. baarnense can also reduce orcylaldehyde and 2,4-dihydroxy-5,6-dimethylbenzaldehyde to dimethylresorcinol and trimethylresorcinol, respecitively.

MeSH terms

  • Chemical Phenomena
  • Chemistry
  • Culture Media
  • Penicillium / growth & development
  • Penicillium / metabolism*
  • Xylenes / biosynthesis*

Substances

  • Culture Media
  • Xylenes