Literature DB >> 7765685

The microbiological transformation of two ent-16 beta,17-epoxykaurane derivatives by Gibberella fujikuroi.

B M Fraga1, P González, R Guillermo, J R Hanson, M G Hernández, J A Takahashi.   

Abstract

The biotransformation of ent-16beta-17-epoxy-7 alpha-hydroxykaurane by Gibberella fujikuroi affords ent-7 alpha,11 alpha,16 beta,17-tetrahydroxykaurane and ent-7 alpha, 9 alpha, 16 beta, 17-tetrahydroxykaurane. These results indicated that the presence of the 16 alpha, 17-diol group, into which the 16 alpha, 17-epoxy is transformed in the medium, inhibits oxidation at C-19 and favours hydroxylation at C-11(beta). Incubation of ent-16 beta, 17-epoxykauran-19-oic acid, via the 16 alpha, 17-diol, gave the 7-aldehyde of 16 alpha, 17-dihydroxy-GA12.

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Year:  1994        PMID: 7765685     DOI: 10.1016/s0031-9422(00)90345-5

Source DB:  PubMed          Journal:  Phytochemistry        ISSN: 0031-9422            Impact factor:   4.072


  2 in total

Review 1.  Occurrence, biological activities and synthesis of kaurane diterpenes and their glycosides.

Authors:  Pablo Anselmo García; Alaíde Braga de Oliveira; Ronan Batista
Journal:  Molecules       Date:  2007-03-13       Impact factor: 4.411

2.  Selective activity of Mucor plumbeus reductase towards (-)-camphorquinone.

Authors:  Giovanni Gontijo de Souza; Cleber Paulo Andrada Anconi; Sjef Cornelissen; Wagner Batista De Almeida; Hélio Ferreira Dos Santos; Isabel Cristina Pereira Fortes; Jacqueline Aparecida Takahashi
Journal:  J Ind Microbiol Biotechnol       Date:  2009-05-13       Impact factor: 3.346

  2 in total

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