2015
DOI: 10.1007/s12275-015-5081-9
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Biotransformation of (-)-α-pinene and geraniol to α-terpineol and p-menthane-3,8-diol by the white rot fungus, Polyporus brumalis

Abstract: In this study, the monoterpenes, α-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 α-terpineol was synthesized from α-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., α-terpineol and PMD, are known to be bioactiv… Show more

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Cited by 20 publications
(10 citation statements)
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“…Regarding the terpenoids, α-terpineol was detected in the grape samples, but was absent in the respective wines. Several studies are present in the literature [44][45][46] focused on terpenoid conversions, which require the presence of various microorganisms. The absence of α-terpineol in wine could therefore be linked to a biotransformation of this terpenoid during the wine making process.…”
Section: Volatile Aroma In Winementioning
confidence: 99%
“…Regarding the terpenoids, α-terpineol was detected in the grape samples, but was absent in the respective wines. Several studies are present in the literature [44][45][46] focused on terpenoid conversions, which require the presence of various microorganisms. The absence of α-terpineol in wine could therefore be linked to a biotransformation of this terpenoid during the wine making process.…”
Section: Volatile Aroma In Winementioning
confidence: 99%
“…This white rot fungus produced α-terpineol (24 mg L −1 ), fenchol (3.71 mg L −1 ) and borneol (5.75 mg L −1 ) after 5 days when cultivated in SM medium (1% glucose, 0.02% ammonium tartrate, 0.01% monopotassium phosphate, 0.05% magnesium sulfate, and 0.01% calcium chloride) in shaken flasks at 26°C and 80 rpm. Lee et al (2015) β-Pinene as substrate Aspergillus sp. Aspergillus sp.…”
Section: Polyporus Brumalismentioning
confidence: 99%
“…This reaction is catalyzed by P. brumalis resulted in the formation of α-terpineol (35.85% − 39.05%), with minor products also identi ed, such as borneol (CAS 507-70-0) (8.59%) and fenchol (CAS 1632-73-1) (5.54%), after ve days of reaction (Fig. 5, route f) (Lee et al 2015b).…”
Section: Fungal Biotransformation Of Pinene For Production Of Aroma Compoundsmentioning
confidence: 97%