Effect of packaging conditions on quality and shelf-life of fresh-cut pineapple (Ananas comosus)

Influence of packaging conditions on fresh-cut ‘Gold’ pineapple shelf-life were studied during 20 d of storage at 5 °C. Fresh-cut fruit pieces were packed in polypropylene trays (PP) and wrapped with 64 μm polypropylene film under active (high 40% or low oxygen, 11.4%) or passive modified atmospheres (air or cut fruit coated with 1%, w/v alginate). Changes in headspace composition, titratable acidity, pH, soluble solids content, juice leakage, color, texture, and microbial growth were evaluated over time. For all packaging conditions, oxygen concentration continuously decreased below its initial concentration over 20 d storage, but never reached levels below 2% O₂. Meanwhile, CO₂ concentration inside all packages continuously increased over time up to 10.6–11.7% from the initial conditions. Ethylene concentrations were always less than 0.4 μl L⁻¹ while ethanol was detected only after 13 d of storage. Color parameters L^* and b^* significantly decreased over time in all packaging conditions and were directly attributed to the translucency phenomenon in the fruit flesh. When alginate coating was used, juice leakage was significantly reduced in contrast with the substantial juice accumulation observed in the rest of the packaging conditions. Texture profile analysis (TPA) parameters, did not significantly change over time, suggesting that structural characteristics of fresh-cut pineapple pieces were preserved throughout storage. From the microbial point of view, the shelf-life of ‘Gold’ fresh-cut pineapple was limited to 14 d by mesophilic bacterial growth. Further studies are needed to evaluate the sensory aspects, as well as to characterize the flesh translucency phenomenon and reduce juice leakage of fresh-cut pineapple.     

Effect of 1-methylcyclopropene (1-MCP) on reducing postharvest decay in tomatoes (Solanum lycopersicum L.)

1-Methylcyclopropene (1-MCP as SmartFresh™ technology), an ethylene antagonist, was evaluated for affecting postharvest decay caused by Alternaria alternata, Botrytis cinerea, and Fusarium spp. on ‘Quality 23’ and ‘Seminis 35’ tomatoes at green or pink stages. Fruit with natural or artificial infection were subjected to 1-MCP at 0.0 μL L⁻¹, 0.6 μL L⁻¹ for 12 h, and 1.0 μL L⁻¹ for 6 h. After 31-42 d storage, disease incidence and severity of individual diseases in 1-MCP treated fruit was significantly reduced compared with that of the untreated controls, except in one inoculated test for ‘Quality 23’ where severity of Alternaria rot in 1.0 μL L⁻¹ treated fruit were significantly higher than that of the untreated control. Fruit treated with 1-MCP at 1.0 L⁻¹ for 6 h also had significantly higher incidence of Alternaria rot in the inoculated ‘Quality 23’ and in the non-inoculated ‘Seminis 35’ compared with the fruit treated with 1-MCP at 0.6 μL L⁻¹ for 12 h. The results of this study indicate that 1-MCP can reduce postharvest decay within a certain storage period.     

Influence of aqueous 1-methylcyclopropene concentration, immersion duration, and solution longevity on the postharvest ripening of breaker-turning tomato (Solanum lycopersicum L.) fruit

The influence of aqueous 1-methylcyclopropene (1-MCP) concentration, immersion duration, and solution longevity on the ripening of early ripening-stage tomato (Solanum lycopersicum L.) has been investigated. Tomato fruit at the breaker-turning stage were fully immersed in aqueous 1-MCP at 50, 200, 400 and 600 μg L⁻¹ for 1 min, quickly dried, and then stored at 20 °C. Ethylene production, respiration, surface color development, and rate of accumulation of lycopene and polygalacturonase (PG) activity were suppressed and/or delayed in fruit exposed to aqueous 1-MCP. Suppression of ripening was concentration dependent, with maximum inhibition in response to 1 min immersion occurring at concentrations of 400 and 600 μg L⁻¹. Climacteric ethylene peaks were delayed approximately 6, 7, and 9 d and respiration was strongly suppressed in fruit treated with aqueous 1-MCP at 200, 400, and 600 μg L⁻¹, respectively, compared with control fruit. Fruit firmness, lycopene content, PG activity, and surface hue of fruit treated at the three higher levels remained strongly suppressed compared with control. Skin hue values and pericarp lycopene content in response to treatment at the subthreshold 50 μg L⁻¹ provided evidence for differential ripening suppression in external versus internal tissues. Maximum delay of softening and surface color development in response to 50 μg L⁻¹ aqueous 1-MCP occurred following immersion periods of between 6 and 12 min. Factors affecting fruit penetration by aqueous 1-MCP and mechanisms contributing to recovery from 1-MCP-induced ripening inhibition are discussed.