Incubation of spirolaxine 1a with the fungus Absidia cuneospora afforded 5 beta-glucosyl-spirolaxine 2b; the structure of the biotransformed product was deduced on the basis of MS. NMR data and chemical semi-synthesis. When using Trametes hirsuta as a bioagent 1a afforded 5 beta-xylosyl-spirolaxine 3a; the identification of the sugar moiety came from acidic hydrolysis of the new metabolite. (c) 2012 Elsevier B.V. All rights reserved.

Biotransformation of spirolaxine by Absidia cuneospora and Trametes hirsuta: Formation of beta-glycosyl and beta-xylosyl derivatives

Fronza Giovanni
2012

Abstract

Incubation of spirolaxine 1a with the fungus Absidia cuneospora afforded 5 beta-glucosyl-spirolaxine 2b; the structure of the biotransformed product was deduced on the basis of MS. NMR data and chemical semi-synthesis. When using Trametes hirsuta as a bioagent 1a afforded 5 beta-xylosyl-spirolaxine 3a; the identification of the sugar moiety came from acidic hydrolysis of the new metabolite. (c) 2012 Elsevier B.V. All rights reserved.
2012
Istituto di Chimica del Riconoscimento Molecolare - ICRM - Sede Milano
Fungal metabolites
Spirolaxine
Biotransformation
Glycosyl and xylosyl derivative
Semi-synthesis
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/234664
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