Extending ripening of hard cheeses well beyond the traditional ripening period is becoming increasingly popular, although little is known about the actual evolution of their characteristics. The present work aimed at investigating selected traits of Parmigiano Reggiano cheese ripened for 12, 18, 24, 30, 40 and 50 months. Two cheeses per each ripening period were sampled. Although moisture constantly decreased and was close to 25% in 50-month cheeses, with a parallel increase in cheese hardness, several biochemical changes occurred involving the activity of both native and microbial enzymes. Capillary electrophoresis demonstrated degradation of αs1- and β-casein, indicating residual activity of both chymosin and plasmin. Similarly, continuous release of free amino acids supported the activity of peptidases deriving from lysed bacterial cells. Volatile flavor compounds, such as short-chain fatty acids and some derived ketones, alcohols and esters, evaluated by gas chromatography with solid-phase micro-extraction, accumulated as well. Cheese microstructure was characterized by free fat trapped in irregularly shaped areas within a protein network, with native fat globules being no longer visible. This study showed for the first time that numerous biochemical and structural variations still occur in a hard cheese at up to 50 months of aging, proving that the ripening extension deserves to be highlighted to the consumer and may justify a premium price.

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15Mechanical properties of dried apples rings were studied through two different rapid compression tests. A

Modern durum wheat cultivars are more prone to ozone stress because of their high photosynthetic efficiency and leaf gas exchanges that cause a greater pollutant uptake. This, in turn, generates an increased reactive oxygen species (ROS) production that is a challenge to control by the antioxidant system of the plant, therefore affecting final yield, with a reduction up to 25%. With the aim of mitigating oxidative stress in wheat, we used chitosan nanoparticles (CHT-NPs) either unloaded or loaded with the antioxidant compound N-acetyl cysteine (NAC), on plants grown either in a greenhouse or in an open field. NAC-loaded NPs were prepared by adding 0.5 mg/mL NAC to the CHT solution before ionotropic gelation with tripolyphosphate (TTP). Greenhouse experiments evidenced that CHT-NPs and CHT-NPs-NAC were able to increase the level of the leaf antioxidant pool, particularly ascorbic acid (AsA) content. However, the results of field trials, while confirming the increase in the AsA level, at least in the first phenological stages, were less conclusive. The presence of NAC did not appear to significantly affect the leaf antioxidant pool, although the grain yield was slightly higher in NAC-treated parcels. Furthermore, both NAC-loaded and -unloaded CHT-NPs partially reduced the symptom severity and increased the weight of 1000 seeds, thus showing a moderate mitigation of ozone injury.

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The aim of this work was to investigate the feasibility of near infrared (NIR) spectroscopy both in quantifying the residual water content of osmo-air dehydrated apple rings and in differentiating them on the basis of the sugar solution used in the osmotic pretreatment so identifying the osmotic syrup used. In order to achieve this, a set of products obtained by different processing conditions was created. Apple rings were dipped for different lengths of time (30, 60 and 90 min) in three different sugar solutions at the same water activity (aw = 0.90): sucrose (59% wt / wt), maltose (62% wt / wt) and a mixture (53% wt / wt) of fructose, glucose and sucrose having the same composition as apple. Air drying was then performed at different temperatures (70°, 80°, 90°C) and the obtained osmo-air dehydrated apple rings were packed in polypropylene film under vacuum in order to avoid water absorption phenomena. NIR spectra, in the range 10,000-4000 cm-1 , were recorded directly on packed apple rings using a FT-NIR spectrometer equipped with fiber optic probe. In calibrating the residual water content the coefficient of determination (R 2) was 0.93, the RPD value was 3.33 and RER value was 13.79, which could be considered, for our purposes, suitable for controlling the dehydration process. Moreover, applying a classification statistic method on NIR data, such as PLS discrimination analysis, it was also possible to identify correctly which sugar solution was used in the osmotic pre-treatment independently of the conditions used. Two-dimensional correlation analysis was also carried out, in order to investigate how the ratios between the main constituents, sugars and water, involved in the osmo-air dehydration varied as a function of the process variable used.

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