Crosses between monokaryons of Pleurotus sapidus or Pleurotus florida show an improved biotransformation of (+)-valencene to (+)-nootkatone
[Display omitted] •Classical genetics approach improved the biotransformation ability of Pleurotus.•Some of the mono- and new dikaryotic strains gave higher yields of (+)-nootkatone.•A slow growth rate of monokaryons seemed to correlate with enhanced yield.•Productive dikaryons were not strictly rel...
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Veröffentlicht in: | Bioresource technology 2014-11, Vol.171, p.113-119 |
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Sprache: | eng |
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•Classical genetics approach improved the biotransformation ability of Pleurotus.•Some of the mono- and new dikaryotic strains gave higher yields of (+)-nootkatone.•A slow growth rate of monokaryons seemed to correlate with enhanced yield.•Productive dikaryons were not strictly related to productive parent monokaryons.•LOX activity of some mono- and new dikaryons was higher than of the parental dikaryon.
Several hundred monokaryotic and new dikaryotic strains derived thereof were established from (+)-valencene tolerant Pleurotus species. When grouped according to their growth rate on agar plates and compared to the parental of Pleurotus sapidus 69, the slowly growing monokaryons converted (+)-valencene more efficiently to the grapefruit flavour compound (+)-nootkatone. The fast growing monokaryons and the slow×slow and the fast×fast dikaryotic crosses showed similar or inferior yields. Some slow×fast dikaryons, however, exceeded the biotransformation capability of the parental dikaryon significantly. The activity of the responsible enzyme, lipoxygenase, showed a weak correlation with the yields of (+)-nootkatone indicating that the determination of enzyme activity using the primary substrate linoleic acid may be misleading in predicting the biotransformation efficiency. This exploratory study indicated that a classical genetics approach resulted in altered and partly improved terpene transformation capability (plus 60%) and lipoxygenase activity of the strains. |
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ISSN: | 0960-8524 1873-2976 |
DOI: | 10.1016/j.biortech.2014.08.061 |