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. 2018 Aug 24;8(1):137.
doi: 10.1186/s13568-018-0666-4.

Biotransformation of vanillin into vanillyl alcohol by a novel strain of Cystobasidium laryngis isolated from decaying wood

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Biotransformation of vanillin into vanillyl alcohol by a novel strain of Cystobasidium laryngis isolated from decaying wood

Jonas Rönnander et al. AMB Express. .

Abstract

Vanillin is an aromatic aldehyde found as a component of lignocellulosic material, and in the cured pods of orchidaceae plants. Like other phenolic substances, vanillin has antimicrobial activity and can be extracted from lignin either by a thermo-chemical process or through microbial degradation. Vanillin, can serve as a model monomer in biodegradation studies of lignin. In the present study, a yeast isolated from decaying wood on the Faroe Islands, was identified as Cystobasidium laryngis strain FMYD002, based on internal transcribed spacer sequence analysis. It demonstrated the ability to convert vanillin to vanillyl alcohol, as detected by ultra-high performance liquid chromatography-quadrupole-time-of-flight. Structural analysis of vanillyl alcohol was carried out by using gas chromatography-mass spectrometry and 1H NMR spectroscopy, and further verified by synthesis. The reduction of vanillin to vanillyl alcohol has been documented for only a few species of fungi. However, to our knowledge, this biotransformation has not yet been reported for basidiomycetous yeast species, nor for any representative of the subphylum Pucciniomycotina. The biotransformation capability of the present strain might prove useful in the industrial utilisation of lignocellulosic residues.

Keywords: Bioconversion; Biodegradation; Cystobasidiomycetes; Cystobasidium; Rhodotorula; Vanillin.

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Figures

Fig. 1
Fig. 1
LC–QTOF–MS run of 0 h and 48 h cultures in triplicate, showing vanillin and the first biodegradation peak detected in a MeOH:H2O gradient elutant system comprising 7 min. No peak was detected in the negative control
Fig. 2
Fig. 2
GC–MS runs of the crude synthate of vanillyl alcohol (lower chromatogram), as well as of the collected fraction from preparatory LC (upper chromatogram) are shown

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