Sweet cherry (Prunus avium) fibers extracted from microwave- and steam-blanched recovered fruits: Photo-antioxidant activity in milk proteins
Introduction
Sweet cherry (Prunus avium L.) is a highly valued fruit crop of temperate regions. Although countries of the southern hemisphere (mainly Chile, South Africa, Australia and Argentina) contribute with only 5% of the world's production of sweet cherry, this crop is economically important for local development and has counter-seasonal marketing advantages (San Martino, Manavella, Garcia, & Salato, 2008; Coriolis Report, 2018).
For the fresh market, sweet cherries are hand-harvested, often mechanically sorted and frequently in transit for several weeks to distant markets. The growers' ability to competitively sell fresh cherries may be restricted by over-production and an excess in the market. In addition, since market intermediaries indicate a willingness to pay producers more per pound for fruit greater than 2.5 cm in diameter, firmness above 300 g/mm, and solid soluble contents above 18°Brix (Piaskowski et al., 2018), cherries without these features are usually discarded (Jara-Rojas, Guerra, Adasme-Berrios, Engler, & Valdés, 2015). However, these discarded cherries can be upgraded to powders highly enriched in dietary fiber and valuable natural antioxidants, which can be useful as additives and/or ingredients for food preservation during storage. This possibility is based on the fact that antioxidants are co-extracted with the cell wall biopolymers (fibers) from fruits and vegetables rich in phenolic compounds (Basanta et al., 2016; Renard, Watrelot, & Le Bourvellec, 2015), carotenoids and tocopherols (Idrovo Encalada et al., 2019). This adds an important functionality to the healthy effects of fibers within the gastrointestinal tract (Saura-Calixto, 2011) and their rheological effects (gelling, thickening, water absorption) (Idrovo Encalada, Basanta, Fissore, De’Nobili, & Rojas, 2016; Idrovo Encalada et al., 2019).
Before processing for fiber extraction, discarded fruits and vegetables need to be immediately stabilized by blanching (May 1990), a process that consists of heating the fruit for a short time prior to cooling and subsequent freezing. Blanching allows stabilizing the color, texture, flavor and nutritional quality of fruits by inactivating peroxidase (POX) and polyphenoloxidase (PPO), which are enzymes that catalyze the degradation of phenolic compounds and thus lead to subsequent browning. Blanching can extend the shelf life of the extracted fiber powders during their storage and use as additives or ingredients in foods of high water activity. Blanching also shows associated side benefits (Reyes de Corcuera, Cavalieri, & Powers, 2004; Sezer & Demirdöven, 2015), including its contribution to pathogen inactivation (Burke, 2019).
The usefulness of cherry fibers as functional food antioxidant preservatives can be determined not only through the 2,2-diphenyl-1-picrylhydrazyl radical (DPPH) scavenging and ferric antioxidant power (FRAP) assays but also by evaluation of their antioxidant capacity in real food systems. Although the study of food oxidation has mostly been focused on lipid oxidation (Li, Wang, Zhang, Shao, & Guo, 2019), during the past few years, protein oxidation has also been studied. Protein oxidation is due to the off flavor caused by the oxidation of specific amino acids, with simultaneous changes in functionality, and a decrease in digestibility and nutritional quality (Fernández, Ganan, Guerra, & Hierro, 2014). The effects of protein oxidation on essential enzymatic pathways involved in processes such as fermentations and cheese ripening are also of high relevance for the food industry (Dalsgaard, Otzen, Nielsen, & Larsen, 2007). The most harmful light-induced oxidation reactions in dairy products, meat and meat products, frozen fish, vegetable oils, beer and other alcoholic beverages are photo-oxidation and photoisomerization, which are due to the presence of photosensitizers such as myoglobin, riboflavin, bilirubin, and chlorophylls (Gordon, 2001; Lund, 2010).
Based on the above, the aim of the present work was to upgrade sweet cherries discarded at harvesting as antioxidant fibers for natural food preservation. We also aimed to analyze whether blanching affected the chemical composition of fibers and phenolic compounds, or the functionality and performance of cherry fibers as antioxidants to preserve milk proteins from photo-oxidation under UV-C radiation (200–280 nm).
Section snippets
Chemicals
All chemical reagents were of analytical grade from Sigma-Aldrich (St. Louis, USA) and Merck (Argentina). Deionized water (Milli-Q™, Millipore, USA) was used.
Plant material
Misshapen and small-sized sweet cherries (Prunus avium L.) discarded during harvesting in the Alto Valle del Río Negro, Argentine Patagonia (39° 01′ 32″ S, 67° 44′ 22″ W, 242 m above sea level) in November 2018, were carefully washed with deionized water.
Blanching of cherry fruits
To analyze whether blanching affected the fibers, the blanching conditions (time and
Blanching of cherry fruits
As described above, before the extraction of fibers, cherry fruits were blanched to inactivate PPO and POX. This was done because blanching can prevent enzyme re-activation when fiber powders are used as additives or ingredients in processed foods with high water activity. Microwave blanching was used to compare with the traditional blanching process with saturated water vapor at normal pressure. Microwave blanching was performed with simultaneous immersion of fruits in water (2 g/1 mL) to
Conclusions
Blanching of sweet cherry fruits by saturated water vapor or microwaves to inactivate the enzymes responsible for phenolic oxidation and browning allowed obtaining water insoluble fiber products constituted by the cell wall biopolymers and relevant amounts of co-extracted phenolic compounds, predominantly proanthocyanidins (≈600 mg/100 g fiber) of ≈4 and 3.5 DP and lower amounts of extractable phenolics like cyanidin-3-(6′-p-coumaroyl) glucoside, an anthocyanin responsible for the dark violet
Author contributions
Agostina Aramburu: Collected the data; Contributed data or analysis tools; Performed analysis.
Evelyn L. Bonifazi: Contributed data or analysis tools; Performed analysis.
Lia N. Gerschenson: Contributed data or analysis tools; Other contribution.
Ana M. Rojas: Conceived and desingned the analysis; Contributed data or analysis tools; Performed analysis; Wrote the paper; Other contribution.
Maria F. Basanta: Conceived and designed the analysis; Collected the data; Contributed data or analysis tools;
Declaration of competing interest
The authors whose names are listed immediately below certify that they have NO affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers’ bureaus; membership, employment, consultancies, stock ownership, or other equity interest; and expert testimony or patent-licensing arrangements), or non-financial interest (such as personal or professional relationships, affiliations, knowledge or beliefs) in
Acknowledgements
We thank the financial support from University of Buenos Aires [UBACyT 2018–2021 20020170100229BA] and ANPCyT [PICT 2015–2109; PICT 2017-1146]. We also thank CONICET.
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