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Aroma Release in Wine Using Co-Immobilized Enzyme Aggregates
Katherine Ahumada1, Ana Martínez-Gil2, Yerko Moreno-Simunovic3
1School of Biochemical Engineering, Pontificia Universidad Católica de Valparaíso, Valparaíso 2362803, Chile. elisabet.ahumada@gmail.com.
Molecules (Basel, Switzerland)
|November 12, 2016
Summary
Immobilized β-glycosidases (combi-CLEAs) enhance wine aroma by increasing terpene concentration. These stable, reusable enzymes offer a cost-effective solution for aroma liberation in winemaking.
Area of Science:
- Enology
- Biotechnology
- Food Science
Background:
- Wine aroma is crucial for quality and consumer preference.
- Aromatic compounds often exist as glycosidic precursors.
- Soluble enzymes require precipitating agents and are single-use.
Purpose of the Study:
- Evaluate co-immobilized β-glycosidases crosslinked enzyme aggregates (combi-CLEAs) for wine aroma enhancement.
- Assess enzyme stability and impact on wine volatile composition.
- Compare combi-CLEAs with soluble enzymes and a control.
Main Methods:
- Co-immobilization of β-glycosidases (α-l-arabinofuranosidase and β-d-glucopyranosidase) using crosslinked enzyme aggregates (CLEAs).
- Stability assessment of soluble and immobilized enzymes in wine conditions over 60 days.
- Analysis of wine volatile composition using Solid Phase Extraction-Gas Chromatography-Mass Spectrometry (SPE-GC-MS).
Main Results:
- Combi-CLEAs exhibited significantly higher stability (80% activity after 60 days) compared to soluble enzymes (20% activity after 20 days).
- Wine treated with combi-CLEAs showed increased total terpenes (18%) and key aroma compounds: linalool (20%), nerol (20%), and geraniol (100%).
- Co-immobilized enzymes proved reusable, reducing winemaking costs.
Conclusions:
- Co-immobilized β-glycosidases (combi-CLEAs) are highly stable and effective for aroma liberation in winemaking.
- This technology enhances key aroma compounds, improving Muscat wine typicity.
- Immobilized enzymes offer a reusable and cost-effective alternative to soluble enzymes.
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