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Springer (part of Springer Nature), Biotechnology Letters, 11(29), p. 1771-1774

DOI: 10.1007/s10529-007-9440-4

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Chemoenzymatic synthesis of feruloyl D-arabinose as a potential anti-mycobacterial agent

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

The feruloyl esterase (StFaeC) produced by Sporotrichum thermophile transfered the feruloyl group to d-arabinose using a mixture of n-hexane, t-butanol and water. About 45% conversion of d-arabinose to the feruloylated derivative was achieved. The compound had an MIC value against Mycobacterium bovis BCG of 25 μg/ml.