Ashish Sachan1,2*, Shashwati Ghosh1,2and Adinpunya Mitra1
The aim of this paper was to study the catabolic product(s) of p-coumaric acid by a white rot fungus, Schizophyllum commune. TLC and HPLC chromatogram showed that p-hydroxybenzoic acid was formed as a major degradation product of p-coumaric acid. The purity of p-hydroxybenzoic acid was further confirmed by mass spectrometry. A maximum amount 2.5 mg/l of p-hydroxybenzoic acid was detected in the culture medium on 12 th day of incubation using 5.0 mM p-coumaric acid as sole source of carbon. It was assumed that during the process of p-coumaric acid degradation, phydroxybenzaldehyde was produced as an unstable intermediate, which was rapidly converted into phydroxybenzoic acid and accumulated in the media. An indication of a very slow reverse conversion, that is, p-hydroxybenzoic acid into p-hydroxybenzaldehyde was also traced.
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