KMID : 0880220150530070462
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Journal of Microbiology 2015 Volume.53 No. 7 p.462 ~ p.467
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Biotransformation of (-)-¥á-pinene and geraniol to ¥á-terpineol and p-menthane-3,8-diol by the white rot fungus, Polyporus brumalis
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Lee Su-Yeon
Kim Seon-Hong Hong Chang-Young Park Se-Yeong Choi In-Gyu
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Abstract
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In this study, the monoterpenes, ¥á-pinene and geraniol, were biotransformed to synthesize monoterpene alcohol compounds. Polyporus brumalis which is classified as a white rot fungus was used as a biocatalyst. Consequently ¥á-terpineol was synthesized from ¥á-pinene by P. brumalis mycelium, after three days. Moreover, another substrate, the acyclic monoterpenoids geraniol was transformed into the cyclic compound, p-menthane-3, 8-diol (PMD). The main metabolites, i.e., ¥á-terpineol and PMD, are known to be bioactive monoterpene alcohol compounds. This study highlights the potential of fungal biocatalysts for monoterpene transformation.
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KEYWORD
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biotransformation, monoterpene, ¥á-pinene, geraniol, Polyporus brumalis
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