4.3 Article

Free and glycosylated green leaf volatiles, lipoxygenase and alcohol dehydrogenase in defoliated Nebbiolo grapes during postharvest dehydration

Journal

AUSTRALIAN JOURNAL OF GRAPE AND WINE RESEARCH
Volume 28, Issue 1, Pages 107-118

Publisher

WILEY
DOI: 10.1111/ajgw.12521

Keywords

alcohol dehydrogenase (ADH); defoliation; dehydration; glycosylated green leaf volatiles (GLVs); grape; lipoxygenase (LOX)

Funding

  1. Italian Ministry of University through the PRIN project 'Precision management of bunch microclimate during ripening and postharvest dehydration to improve aromatic and nutritional features of grape for wine production'
  2. MUVON project 'Innovazione tecnologica per la gestione della maturazione delle uve di vitigni autoctoni per la produzione di vini passiti, o speciali, di qualita-MUVON' by the Italian Ministry of Agriculture

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This research aimed to investigate the influence of fruit exposure to light and postharvest water loss on the concentration of green leaf volatiles (GLVs) and enzymes in Nebbiolo grapes. Defoliation affected the response of Nebbiolo grapes to dehydration temperature, inducing glycosylation of GLVs, alcohol formation, and membrane oxidation. Timing of defoliation and postharvest dehydration temperature are significant factors to mitigate the postharvest stress response of Nebbiolo grapes.
Background and Aims Nebbiolo grapes are used to produce Sfursat wine, following partial dehydration. This research aimed to clarify the influence of fruit exposure to light and postharvest water loss on the concentration of green leaf volatiles (GLVs) and lipoxygenase (LOX) and alcohol dehydrogenase (ADH) activity of grapes. Methods and Results Nebbiolo grapes from Control vines (no defoliation) (ND) and from vines defoliated at fruitset (DFS) or defoliated post-veraison (DPV) were harvested at about 23 degrees Brix and dehydrated at 10 and 20 degrees C, 60% RH and air flow of 1.5 m/s. Berries were sampled at 10 and 20% mass loss (ML). Significant differences in crop yield, bunch mass and berry mass were observed. As expected, the higher the dehydration temperature, the faster the dehydration process: 20% ML at 20 degrees C occurred between 18 and 25 days, the shortest time corresponding to ND and the longest to DFS; at 10 degrees C, the dehydration lasted between 27 and 32 days. At 10 degrees C, the ADH activity was almost double that at 20 degrees C, and in DFS was much higher than in other samples. At harvest, LOX did not show any difference among the samples, while at 10 degrees C and 10% ML, the enzyme activity increased significantly and then declined at 20% ML, especially in defoliated samples. At harvest, the total free GLVs associated with the metabolism of lipid oxidation were 9434, 7212 and 11 656 mu g/kg dry weight (DW) in ND, DFS and DPV samples, respectively; the total bound GLVs lipid-derived were 7599, 18 486 and 15 409 mu g/kg DW in ND, DFS and DPV samples, respectively. During dehydration at 10 degrees C, the ML induced ADH + LOX activity, especially in defoliated samples, but the bound GLVs, produced by defoliation, greatly decreased. Conclusions Defoliation affected the response of Nebbiolo grapes to dehydration temperature: postharvest cold stress (10 degrees C) and ML induced glycosylation of GLVs, alcohol formation (via ADH) and membrane oxidation (via LOX); a further stress effect was observed with leaf removal, regardless of the time of application. Significance of the Study The timing of defoliation and postharvest dehydration temperature are significant factors to mitigate the postharvest stress response of Nebbiolo grapes.

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