No abstract

Malvasia (Vitis vinifera L.) grapes were harvested at 17.8% of soluble solids content (SSC) and placed inside an innovative dehydration room where temperature, relative humidity, and air flow were maintained, respectively, at 15 degrees C, 40%, and 1-1.5 m s(-1). Weight loss of bunches reached approximately 33% in 29 days. SSC increased inversely proportionally with the weight decrease, reaching at the end of experiment 23%. Abscisic acid (ABA) increased rapidly from around 29 to 80 microg g(-1) of dry weight at 11.7% of bunch weight loss and then declined gradually. Lipoxygenase (LOX) showed the same behavior as ABA, whereas alcohol dehydrogenase (ADH), read in the way of ethanol oxidation, increased continuously when the weight loss reached approximately 19.5%. In parallel with the activity of LOX, C6 compound [hexanal, hex-1-enol, (E)-hex-2-enal] concentrations reached a peak at 11.7% of weight loss, whereas ethanol and acetaldehyde increased with the increase of ADH and successively decrease and ethyl acetate increased. Proline increased initially as ABA and successively with the increase of ADH, 5.3-fold increase versus 4.2-fold increase of proteins. Postharvest dehydration of Malvasia grapes shows a biphasic pattern: a first metabolic stress response up to 11.7% of bunch weight loss and a second stress response beyond 19.5% of weight loss. The metabolic mechanism of these postharvest water stress responses is discussed.

Experiments were carried out using an innovative technology for dehydration based on the passage of air through a tunnel. It was possible to study the postharvest behaviour, at different rates of dehydration, of Malvasia, Trebbiano and Sangiovese grapes. Malvasia and Trebbiano grapes were picked with 17.5% SSC (soluble solids content), while Sangiovese grapes were harvested fully ripe with 26% SSC. All the grapes, in different experiments, were placed in the tunnel with an air speed of 1-1.5 m s −1 , 42% RH (relative humidity) and a temperature of 21 • C. After 18 days the weight loss was 50 and 34% respectively in tunnel-treated Malvasia and Trebbiano grapes, while it was only 13-14% in control grapes (outside the tunnel: RH around 65% and temperature about 20 • C without ventilation). The SSC rose to 35 and 27% respectively in tunnel-treated Malvasia and Trebbiano grapes compared with 23 and 21% respectively in control grapes. In the case of Sangiovese grapes, after 7 days (the end of treatment) the weight loss was 20.5% in tunnel-treated grapes and 10.5% in control grapes. The SSC rose to 32% and the acidity increased from 4.8 to 5.8 g l −1 in tunnel-treated grapes compared with 29% and 5 g l −1 respectively in control grapes. Total phenols and anthocyanins almost doubled in tunnel-treated Sangiovese berries. Volatile compound analysis revealed a higher ethanol concentration in all tunnel-treated grapes but a lower concentration of ethyl acetate and acetic acid.

No abstract

Clusters of Aleatico winegrape were picked at 18 degrees Brix and placed at 10, 20, or 30 degrees C, 45% relative humidity (RH) and 1.5 m/s of air flow to dehydrate the berries up to 40% of loss of initial fresh weight. Sampling was done at 0, 10, 20, 30, and 40% weight loss (wl). Selected polyphenols and sugar content (expressed as SSC = soluble solids content) both measured on dry weight basis, polyphenol oxidase (PPO), and phenylpropanoid pathway gene expression were analyzed. Phenolic acids increased significantly at 20% wl at 20 degrees C, while at 10 degrees C the increase was lower. Stilbenes (trans-resveratrol and trans-piceid) and catechins rose more than double to 100 mg/kg and more than 3-fold to 135 mg/kg at 20 degrees C and 10% wl. At 10 degrees C the increase of these compounds was less, but higher than initial values. At 30 degrees C, except for a significant rise at 10% wl for catechins and stilbenes, all the rest of the compounds diminished. Anthocyanins increased at 10 and 20 degrees C, but decreased at 30 degrees C. PPO rapidly increased at 20 and 30 degrees C at 10% wl and then declined, while at 10 degrees C the activity lasted longer. Relative gene expression of phenylalanine ammonia lyase (PAL), stilbene synthase (STS), chalcone isomerase (CHI), dihydroflavonol reductase (DFR) were upregulated at 10 degrees C more than at 20 degrees C, at 20% wl, while at 30 degrees C the gene expression was downregulated.