Immobilization of a Cutinase from Fusarium oxysporum and Application in Pineapple Flavor Synthesis

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[1] Nikolaivits, Efstratios
[2] Makris, Georgios
[3] Topakas, Evangelos
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Topakas, Evangelos (vtopakas@chemeng.ntua.gr) | 1600年 / American Chemical Society卷 / 65期
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Enzyme immobilization - Aggregates - Reusability - Fungi;
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In the present study, the immobilization of a cutinase from Fusarium oxysporum was carried out as cross-linked enzyme aggregates. Under optimal immobilization conditions, acetonitrile was selected as precipitant, utilizing 9.4 mg protein/mL and 10 mM glutaraldehyde as cross-linker. The immobilized cutinase (imFocut5a) was tested in isooctane for the synthesis of short-chain butyrate esters, displaying enhanced thermostability compared to the free enzyme. Pineapple flavor (butyl butyrate) synthesis was optimized, leading to a conversion yield of >99% after 6 h, with an initial reaction rate of 18.2 mmol/L/h. Optimal reaction conditions were found to be 50 °C, a vinyl butyrate/butanol molar ratio of 3:1, vinyl butyrate concentration of 100 mM, and enzyme loading of 11 U. Reusability studies of imFocut5a showed that after four consecutive runs, the reaction yield reaches 54% of the maximum. The efficient bioconversion offers a sustainable and environmentally friendly process for the production of natural aroma compounds essential for the food industry. © 2017 American Chemical Society.
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