Literature DB >> 25027724

Microbial transformations of halolactones with p-menthane system.

Marcelina Mazur1, Aleksandra Grudniewska2, Czesław Wawrzeńczyk3.   

Abstract

Biologically active piperitone-derived racemic iodo-, bromo- and chlorolactones (1-3) were transformed with the use of microbial enzymatic systems. Four strains of filamentous fungi Absidia glauca AM254, Absidia cylindrospora AM336, Mortierella vinaceae AM149 and Nigrospora oryzae AM8 transformed halolactones (1-3) to four new halohydroxylactones (4-7). In all biotransformations the hydroxy group was incorporated in inactivated methine carbon atom at isopropyl substituent. In N. oryzae AM8 culture the bromolactone with additional hydroxy group in α-position, relative to CO bond in γ-lactone ring, was also formed as a product. The structures of new compounds were established on the basis of spectral data.
Copyright © 2014 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Fungal transformation; Halolactones; Microbial hydroxylation; Piperytone derivatives; Terpenoid lactones

Mesh:

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Year:  2014        PMID: 25027724     DOI: 10.1016/j.jbiosc.2014.06.007

Source DB:  PubMed          Journal:  J Biosci Bioeng        ISSN: 1347-4421            Impact factor:   2.894


  1 in total

1.  Regio- and enantioselective microbial hydroxylation and evaluation of cytotoxic activity of β-cyclocitral-derived halolactones.

Authors:  Marcelina Mazur; Witold Gładkowski; Višnja Gaurina Srček; Kristina Radošević; Gabriela Maciejewska; Czesław Wawrzeńczyk
Journal:  PLoS One       Date:  2017-08-24       Impact factor: 3.240

  1 in total

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