2012
DOI: 10.1016/j.jbiotec.2011.06.007
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Bioconversion of car-3-ene by a dioxygenase of Pleurotus sapidus

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Cited by 13 publications
(19 citation statements)
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“…(+)-Valencene, a sesquiterpene from orange oil, was converted to (+)-nootkatone and nootkatols [26]. Lyophilisates of P. sapidus catalyzed the oxyfunctionalization of R-(+)-limonene to carvone [40], of˛-pinene to verbenone/ol [41] and of (+)-car-3-en to car-3-ones/ols [42] as well as the transformation of various cycloalkenes to the corresponding enones [43]. This promiscuity calls for a biotechnological application to produce other bioactive or fragrant terpenoids.…”
Section: Resultsmentioning
confidence: 99%
“…(+)-Valencene, a sesquiterpene from orange oil, was converted to (+)-nootkatone and nootkatols [26]. Lyophilisates of P. sapidus catalyzed the oxyfunctionalization of R-(+)-limonene to carvone [40], of˛-pinene to verbenone/ol [41] and of (+)-car-3-en to car-3-ones/ols [42] as well as the transformation of various cycloalkenes to the corresponding enones [43]. This promiscuity calls for a biotechnological application to produce other bioactive or fragrant terpenoids.…”
Section: Resultsmentioning
confidence: 99%
“…Already in the 1960s, the aerobic metabolism of several monoterpenes (limonene and α -pinene) was described for soil pseudomonads and the fungus Aspergillus niger [4]. Pseudomonads also use the acyclic citronellol [5,6] and Pleurotus sapidus was found to transform the bicyclic Δ 3 -carene [7]. Limonene may be an intermediate in the metabolism of bicyclic [8] and acyclic monoterpenes [9].…”
Section: Introductionmentioning
confidence: 99%
“…Biotransformations of (A) heme-thiolate peroxygenases UPO’s [41,43,44] and (B) non-heme iron lipoxygenase-type dioxygenases (LOX) [60,61,79,80]. …”
Section: Figurementioning
confidence: 99%