1. Please check and comment entries here.
Table of Contents

    Topic review

    Phenolic Compounds

    View times: 35
    Submitted by: Leticia Goncalves


    Phenolic compounds are phytochemicals with functions in pigmentation, astringency, protection against ultraviolet rays and antioxidant activity, being widely found in natural sources such as fruits, teas, spices, wine and honey. These compounds have received much attention in recent decades due to evidence related to positive health effects, such as anti-inflammatory, antimicrobial, antithrombotic, vasodilatory and cardioprotective activity, contributing to the improvement in metabolic markers associated with diabetes, hypertension and obesity.

    1. Introduction

    Since antiquity, even without being aware of the proliferation of microorganisms, when observing the high perishability of meat and the need for its immediate consumption, man began to use techniques of physical and chemical changes capable of delaying spoilage and improving the flavor of this and other food classes, which allowed the significant extension of the availability period of certain foods. One of the oldest forms of meat processing is the manufacture of by-products from the processing of meat pieces, which started around 1500 BC in the Mediterranean region, whose climate was favorable for the maturation of products, when several procedures that resulted in the reduction in water activity and consequently the prolongation of their shelf life, such as desiccation, drying, curing, smoking, salting and/or mixture of aromatic herbs, were also applied [1][2].

    As they are nutritionally rich foods with a large amount of available water in their composition, meats become susceptible to contamination by pathogenic and spoiling microorganisms. In order to overcome this problem and offer safe meat products to consumers, it is necessary to adopt measures for their conservation, such as good manufacturing practices, use of low temperatures during storage, heat treatment and use of additives [3].

    Processing has the purpose of extending the shelf life of meat, adding value to deboning by-products, which are generally not marketed in the fresh form, in addition to generating a wide variety of differentiated products in terms of color, flavor, aroma and texture [4]. Due to the low cost and easy preparation, a considerable part of the population developed the habit of regularly consuming meat derivatives such as sausages, bologna and hamburgers, contributing to a significant expansion of the meat products market [5][6].

    The quality of meat derivatives is directly related to the origin of raw materials and ingredients and to the sanitary conditions of the manufacturing process. Products are classified according to the types of meat used, fat content, offal or edible by-products from slaughter, and may or may not be added with condiments and additives permitted by legislation [1]. In the meat production process, meat comminution increases the contact surface area, favoring microbial contamination and proliferation [7]. 272/2019, which regulates the use of food additives for each class of meat derivative, their conditions of use and maximum limits [8].

    For a long time, the food industry has incorporated various ingredients into formulations that do not have the function of nourishing, but rather have a technological purpose, while they can also make the food more attractive to consumers. These ingredients are called food additives and are classified according to their technological function [9]. The class of preservatives is one of them, the main purpose of which is to reduce the effect of spoilage caused by the multiplication of microorganisms or chemical reactions during the storage period [10][11]. Synthetic substances that have their use approved within an acceptable daily intake limit, such as nitrite and sodium nitrate, preservatives most commonly used in the production of meat derivatives, are also used, which in addition to their antimicrobial capacity, particularly for the control and prevention of the growth of anaerobic bacteria, especiallyClostridium botulinum, also promote a protective effect against lipid oxidation and act in the development and fixation of the pink color and flavor characteristics of cured meat products [2][9][11].

    The application of sodium nitrite in the production of cured meats allows obtaining differentiated products with regard to color and flavor, safe and stable during storage. However, a discussion that started around the 1970s showed the great risk to human health from the generation of a class of substances considered potentially carcinogenic, the nitrosamines, when high nitrite concentrations are exposed to high temperature conditions, as usually occurs in the manufacture of cured meat products, and since then, its use has been considered increasingly controversial [2][12].

    Although they are substances that significantly contribute to the conservation of products and have their use officially regulated, there are indications of negative health implications associated with the excessive consumption of these and other synthetic additives, such as carcinogenic effects and generation of toxic and mutagenic compounds, and, consequently, the maximum acceptable limits of their use have been gradually changed or prohibited in several countries [13][14].

    Diet is one of the important factors that affect the well-being and health of human beings, and today, there is great concern among consumers about the correlation between eating habits and health problems [15][16]. The reformulation of meat products through the substitution of ingredients, such as sodium nitrite, is an alternative to provide these products with a “cleaner label” in order to reduce the negative consumer perception about the excessive use of synthetic additives and their carcinogenic potential, decreasing the association between consumption of meat products and possible health problems [15][16]. For these reasons, many studies have been conducted in order to substitute synthetic antimicrobials for natural versions.

    2. Phenolic Compounds

    Phenolic compounds are phytochemicals with functions in pigmentation, astringency, protection against ultraviolet rays and antioxidant activity, being widely found in natural sources such as fruits, teas, spices, wine and honey [17]. These compounds have received much attention in recent decades due to evidence related to positive health effects, such as anti-inflammatory, antimicrobial, antithrombotic, vasodilatory and cardioprotective activity, contributing to the improvement in metabolic markers associated with diabetes, hypertension and obesity [18][19].

    Phenolic molecules are structurally characterized by the presence of at least one aromatic ring containing one or more hydroxyl radicals, the main groups being phenolic acids, flavonoids and polyphenols, whose main source is fruits [17]. In addition, recent studies have reported antioxidant and antimicrobial effects of phenolic compounds, indicating that their chemical nature, especially the presence of hydroxyl groups in the molecule, may be associated with inhibitory mechanisms through interaction with the cytoplasmic membrane, cell wall and nucleic acids of bacteria, impairing vital functions such as protein synthesis and DNA transport or replication [20][21].

    The generation of large amounts of waste from the processing of fruits and vegetables is one of the main challenges that the food industry has faced due to the need for large investment by companies to properly treat and dispose of this type of material in order to cause minimal negative impacts on the environment [13]. These agro-industrial waste products from fruits are rich in phenolic compounds and other bioactive substances that can add antioxidant and antimicrobial properties to foods and provide health benefits [22]. Thereby, the use of this raw material as a natural substitute for synthetic additives can be a great alternative, because in addition to providing compounds with functional properties, it reduces the environmental impact caused by the disposal of a significant part of the fruit, such as seeds and peels that are generally not used by the industry [23].

    Thus, this review searched the scientific literature for reports of extracts obtained from fruits or their agro-industrial waste rich in antimicrobial bioactive compounds and that have potential applications in meat products, being able to maintain microbiological stability and safety during storage. More specifically, this review focused on the natural extracts obtained from jabuticaba, grape and prickly pear.

    3. Fruit Extracts with Potential Application in Meat Products

    3.1. Jabuticaba (Myrciaria cauliflora)

    Jabuticaba (Myrciaria cauliflora), belonging to the Myrtaceae family, is a fruit tree native to Brazil, whose cultivation extends throughout the national territory, with greater productivity in the Southeastern region. From the nutritional point of view, jabuticaba varieties are considered excellent sources of dietary fibers, carbohydrates, vitamins and minerals such as iron, calcium and phosphorus, arousing great interest for its considerable amount of phenolic compounds with antioxidant and antimicrobial potential [24][25]. Among these compounds, anthocyanins and flavonoids are mainly concentrated in fruit peel, being the main components responsible for the development of its characteristic dark color. The anthocyanin content, of approximately 315 mg per 100 g of jabuticaba, is considered high compared to other fruits, demonstrating great potential as a substitute for synthetic dyes in several food classes, in addition to the benefits for the conservation of these products [26][27].
    The most attractive source for obtaining these natural pigments from jabuticaba, rich in antioxidant and antimicrobial bioactive compounds, is the use of residues from jelly- and liquor-processing industries, since peels and seeds represent approximately 50% of the fruit and are in general discarded by the industry [28][29].
    Baldin et al. [26] studied the application of microencapsulated jabuticaba extract in fresh sausage, evaluating the antimicrobial and antioxidant potential of this natural dye. Firstly, an in vitro experiment was carried out, which demonstrated an inhibitory effect on Gram-positive and Gram-negative bacteria, showing its antimicrobial potential. The minimum inhibitory concentration (MIC) results for the microencapsulated extract were 18.75 g/L (~2%) for both Staphylococcus aureus ATCC 25923 and Escherichia coli ATCC 25922. These results can be attributed to the high concentration of phenolic compounds (anthocyanins) in fruit peel, which are mainly responsible for the antimicrobial activity in this case [30].
    When applying microencapsulated jabuticaba extract in fresh sausage, Baldin et al. [26] observed a reduction in the counts of mesophilic bacteria and of thermotolerant coliforms in treatments with 2 and 4% extract on the first and fifteenth days of cold storage. For S. aureus, treatments with 2 and 4% microencapsulated extract also showed lower counts when compared to the control (without addition of extract or dye) and with the treatment with added cochineal carmine dye. The addition of 4% extract caused the elimination of S. aureus on the last day of storage (15 days). In the total count of aerobic psychrotrophic microorganisms, a reduction of 1 log cycle was observed at the end of the fourth day of storage of treatments with additions of 2 and 4% of jabuticaba extract; however, from the eighth day, all treatments tested exceeded the limit of 107 CFU/g recommended by the International Commission on Microbiological Specifications for Foods (ICMSF) [31], indicating spoilage that can lead to sensory loss in the attributes of odor, color and taste. The count of lactic bacteria increased from 4 log CFU/g at time zero (beginning of storage) to 6 log CFU/g at the end of storage in all treatments, not exceeding the limit of 107 CFU/g established by ICMSF [31]. Salmonella sp. tested negative in 25 g for all treatments, being in accordance with Brazilian legislation [32].
    Thus, the study recommended the addition of 2% of microencapsulated jabuticaba extract in fresh sausage, as it did not compromise the sensory attributes evaluated, except for the purplish color, which was slightly less accepted because it is not characteristic of the product. The aforementioned extract can be considered a good alternative for the production of cleaner label meat products as it satisfies the demand for the use of natural pigments with antimicrobial capacity and low cost, taking advantage of residues from the jabuticaba processing and with the appeal of health benefits.

    3.2. Grape (Vitis sp.)

    Grape (Vitis sp.) is one of the fruits most cultivated around the world, occupying an area of 7.5 million hectares of vineyards, with emphasis on the production of species Vitis vinifera in most countries [33][34]. In Brazil, the most commonly found cultivars are Vitis labrusca, Vitis bourquina, Vitis vinifera and several interspecific hybrids, occupying an area of 78 thousand hectares from the extreme south of the country to near the equator, showing characteristic poles of temperate, subtropical and tropical climates due to its expressive environmental diversity [35]. Brazilian grape production reached 1.5 million tons per year in 2018, with 50% destined for processing—wine making (42% table wines and 7% fine wines), juices (49%) and other derivatives (2%)—and the other half of the national volume marketed as grapes for fresh consumption [35].
    The generation of waste from the processing of this high volume of grapes is significant, and may correspond to 30% of the fruit when used for the production of wines, for example, consisting of by-products such as pomace, peels and seeds [33][36]. This waste is considered a source of phenolic compounds with antioxidant and antimicrobial effects, mainly catechins, epicatechins, gallic acid and procyanidins [36][37][38].
    Martin et al. [23] evaluated the in vitro antimicrobial capacity of ethanolic grape extracts from lyophilized seeds or agro-industrial waste. For the extract obtained from lyophilized pomace of “Pinot Noir” (Vitis vinifera) cultivar, the authors found MIC against Gram-positive S. aureus ATCC 25923 and Listeria monocytogenes ATCC 7644 pathogens of 6.25 and 12.5 g/L, respectively. “Petit Verdot” (Vitis vinifera) seeds ethanolic extract presented an MIC of 6.25 g/L for L. monocytogenes and 1.56 g/L for S. aureus (Table 1).
    Table 1. Minimum inhibitory concentration in vitro of grape extracts on bacteria.
    Strain Gram MIC Grape Cultivar Reference
    Staphylococcus aureus + 6.25 g/L Pinot Noir (V. vinifera) Martin et al. [23]
    1.56 g/L Petit Verdot (V. vinifera) Martin et al. [23]
    100.0 mL/L Tempranillo (V. vinifera) Adámez et al. [37]
    Listeria innocua + 100.0 mL/L Tempranillo (V. vinifera) Adámez et al. [37]
    Listeria monocytogenes + 12.5 g/L Pinot Noir (V. vinifera) Martin et al. [23]
    6.25 g/L Petit Verdot (V. vinifera) Martin et al. [23]
    MIC: minimal inhibitory concentration.
    Adámez et al. [37] estimated the in vitro antibacterial activity of aqueous grape seed extract (Vitis vinifera L.), Tempranillo cultivar, obtained after wine manufacture, and reported efficiency in inhibiting Gram-positive 976 S. aureus subsp. aureus and 910 Listeria innocuaI (Table 1). Similar results were obtained by Baydar et al. [34] in seeds from “Hasandede”, “Emir” and “Kalecik” cultivars (all Vitis vinifera L. species), which demonstrated a relationship between increased extract concentration and reduced growth of 15 bacterial strains, including the pathogens E. coli O157: H7 KUEN 1461, Aeromonas hydrophila ATCC 7965 and S. aureus Cowan 1. Additionally, extracts at concentrations of 0.5 and 1% showed a bacteriostatic effect on E. coli, while concentrations of 2.5 and 5% provided bactericidal activity.
    Despite the good in vitro results, data on the incorporation of this class of extract to guarantee microbiological stability in meat products were not found in thescientific literature. Carpes et al. [39] obtained lyophilized hydroethanolic (GPWL: grape pomace wine lyophilized) and microencapsulated (GPWM: grape pomace wine microencapsulated) extracts made with grape pomace from the processing of Vitis labrusca L. Bordeaux varieties and applied them to chicken pate in order to evaluate the effects of the addition of natural compounds on oxidative stability compared to negative control treatment (T1; no antioxidant added) and with the use of 300 ppm of the synthetic antioxidant sodium erythorbate (T2).
    The study reported satisfactory results for the inhibition of lipid oxidation in treatments with 3000 ppm of GPWL (T3) and GPWM (T4) extracts, analyzed by the index of substances reactive to 2-thiobarbituric acid (TBARs) during 42 days of cold storage (4 °C). At the end of the storage period, all treatments showed a significant difference from each other (p < 0.05) in relation to the TBARS assay, with the best results being observed for T3, followed by T4, T2 and T1, respectively. All treatments, except for T1, had results below 3 mg of malondialdehyde/kg of sample, a value considered the limit for the meat product to be considered adequate and safe for consumption according to some authors [40][41]. Both GPWL and GPWM demonstrated an effective reduction in lipid oxidation when compared to treatment elaborated with commercial synthetic antioxidant, an activity that can be attributed mainly to the presence of phenolic compounds such as gallic, caffeic, vanillic, ferulic and coumaric acids and trans-resveratrol [39].
    Thus, it appears that the extracts obtained from grape processing waste can be considered an interesting and innovative strategy for the incorporation of bioactive compounds in meat products with the substitution of synthetic preservatives for natural ones, since studies have shown their efficiency in inhibiting the growth of microorganisms related to outbreaks of foodborne diseases, such as Listeria, E. coli and S. aureus. However, studies on the in vivo influence on the sensory characteristics and antimicrobial action of meat products are necessary, since in general, studies have essentially evaluated the antioxidant activity.

    3.3. Prickly Pear (Opuntia ficus-indica)

    Opuntia ficus-indica, popularly known as prickly pear, is the fruit of a cactus species (Cactaceae family) native to tropical and subtropical regions of the Americas and currently also being cultivated in Europe, Africa and Australia, with approximately 300 known varieties [42]. The literature contains plenty of information about the chemical composition of its pulp, seeds and peel, as well as some properties of interest for the pharmaceutical and food industry, because it is a natural source of bioactive compounds.
    Brazil has the largest Opuntia ficus-indica cultivation system in South America, with a planting area of 500,000 hectares located mainly in the Northeastern region and recently extended to other regions. Cultivation is performed in general by small producers and a large part of the production is destined for animal fodder, when it is called forage palm or cattle palm [43]. In the region of Valinhos, state of São Paulo, production is destined for the generation of fruit for fresh consumption, aimed at export to Europe and the domestic market [44]. In 2017, around 18.01 tons of the fruit were sold at “Companhia de Entrepostos e Armazéns Gerais de São Paulo” (CEAGESP), ranking 326th among products sold by the company [45].
    In recent years, there has been a remarkable interest from the scientific community regarding the regular consumption of the genus Opuntia and its positive correlation with the treatment and prevention of chronic diseases related to oxidative stress [46][47]. Benefits such as reduction in triglycerides and total cholesterol in the bloodstream [48], antiulcerogenic activity [49], improved platelet aggregation [50] and reduced renal dysfunction [51][52] are some of the pieces of clinical and/or experimental evidence associated with the consumption of fig varieties. Other authors have found that extracts from the fruit and its peel and seeds have appreciable amounts of unsaturated fatty acids [53], with antioxidant activity [54][55], anticancer effects [56] and cardioprotective, antithrombotic, anti-inflammatory, antiarrhythmic, hypolipidemic and anti-hyperglycemic activities [57][58].
    Seo et al. [59] identified the antimicrobial effects of Opuntia ficus-indica extract on two important pathogens related to foodborne diseases, L. monocytogenes and E. coli O157: H7, suggesting that the extract can be used as a natural preservative in food products. Zito et al. [60] detected the presence of eleven substances with antimicrobial activities in peels, seeds and pulps of the yellow (Surfarina) and red (Sanguigna) fruit varieties. Of these, major components were carvacrol, limonene, squalene and hexadecanoic acid, which in addition to their antimicrobial capacity are also antioxidants.
    Parafati et al. [61] applied aqueous pulp extract of the purple and red Opuntia ficus-indica varieties in bovine hamburgers, testing the direct addition of the extract and the version encapsulated in sodium alginate. Microbiological analyses conducted after 8 days of cold storage (4 °C) showed the preservative effect in hamburgers with added prickly pear extract, which significantly reduced (p < 0.05) the count of mesophilic bacteria, Enterobacteriaceae and Pseudomonas sp., when compared to control sample with the addition of sterile distilled water. The authors concluded that the application of the extract, encapsulated or not, is an effective method for conservation of bovine hamburgers. However, studies are necessary to verify the influence of this component on the sensory and technological properties of products.
    The antibacterial activity of the hydroethanolic extract obtained from the whole Opuntia stricta fruit, another species of the genus Opuntia, was quantified by determining the MIC and the minimum bactericidal concentration (MBC) by Kharrat et al. [62]. The results in Table 2 show that the extract from the red variety of Opuntia stricta showed high antibacterial activity, with an MIC and MBC less than or equal to sodium nitrite, which is the synthetic preservative commonly used in meat products, demonstrating that the extract can be as or more effective than sodium nitrite. This finding is mainly due to the presence of the pigment betalain and other phenolic compounds in the fruit.
    Table 2. Minimum inhibitory concentration and minimum bactericidal concentration in vitro of Opuntia extract and sodium nitrite on bacteria.
    Strain Gram MIC (mg/L) MBC (mg/L)
    OE E250 OE E250
    Bacillus cereus + 62.5 125.0 500.0 500.0
    Staphylococcus aureus + 62.5 62.5 250.0 500.0
    Escherichia coli - 125.0 250.0 500.0 >1000.0
    Salmonella enteric - 125.0 500.0 1000.0 1000.0
    MIC: minimal inhibitory concentration; MBC: minimal bactericidal concentration; OE: Opuntia extract; E250: sodium nitrite. Adapted from Kharrat et al. [62].
    When incorporating 2.5% of Opuntia extract in salami, replacing sodium nitrite preservative and the cochineal carmine dye, Kharrat et al. [61] obtained an improvement in the microbiological stability of products and in the water retention capacity without causing sensory and texture changes. The microorganisms surveyed were mesophiles, molds and yeasts, S. aureus, Clostridium perfringens and Salmonella, and all counts were within limits established by the legislation for both the control treatment and salami with added natural extract, concluding that this is a good alternative for maintaining shelf life during cold storage of this type of meat product.
    Prickly pear and other Opuntia species, although showing an impressive profile of bioactive compounds, are not well valued in the country and in other parts of the world. Therefore, research on the antimicrobial capacity and the application of extracts from this fruit in meat products can be a good option for offering safe and cleaner label products.

    The entry is from 10.3390/foods10071469


    1. Ordoñez, J.A.; Rodriguez, M.I.C.; Sanz, M.L.G.; Minguillón, G.D.G.F.; Perales, L.H.; Cortecero, M.D.S. Tecnologia de Alimentos: Alimentos de Origem Animal; Artmed: Porto Alegre, Brazil, 2005; p. 279. ISBN 9788536304311.
    2. Sindelar, J.J.; Milkowski, A.L. Human safety controversies surrounding nitrate and nitrite in the diet. Nitric Oxide 2012, 26, 259–266.
    3. Terra, N.N. Apontamentos de Tecnologia de Carnes; Unisinos: São Leopoldo, Brazil, 1998; p. 216. ISBN 858558081X.
    4. Pardi, M.C.; dos Santos, I.F.; de Souza, E.R.; Pardi, H.S. Ciência, Higiene e Tecnologia Da Carne; UFG e Universidade Federal Fluminense (Eduff): Goiania, Brazil, 2006; ISBN 9788572741880.
    5. de Melo Filho, A.B.; Biscontini, T.M.B.; Andrade, S.A.C. Níveis de nitrito e nitrato em salsichas comercializadas na região metropolitana do recife. Ciência Tecnol. Aliment. 2004, 24, 390–392.
    6. Martins, L.L.; dos Santos, I.F.; Franco, R.M.; de Oliveira, L.A.T.; Bezz, J. Avaliação do perfil bacteriológico de salsicha tipo “Hot dog”comercializadas em embalagens a vácuo e a granel em supermercados dos municípios Rio de Janeiro e niterói, RJ/Brasil. Rev. Inst. Adolfo Lutz 2008, 67, 215–220.
    7. Malavota, L.C.M.; Conte-Junior, C.A.; Macedo, B.T.; Lopes, M.M.; de Souza, V.G.; Stussi, J.S.P.; Pardi, H.S.; Mano, S.B. Análise micológica de linguiça de frango embalada em atmosfera modificada. Rev. Bras. de Ciência Veterinária 2006, 13.
    8. Agência Nacional de Vigilância Sanitária. Resolução RDC No 272, de 14 de Março de 2019. Estabelece os aditivos alimentares autorizados para uso em carnes e produtos cárneos. Diário Of. União 2019, 52, 194. Available online: (accessed on 3 March 2020).
    9. Lamas, A.; Miranda, J.; Vázquez, B.; Cepeda, A.; Franco, C. An evaluation of alternatives to nitrites and sulfites to inhibit the growth of salmonella enterica and listeria monocytogenes in meat products. Foods 2016, 5, 74.
    10. Hasiak, R.J.; Chaves, J.; Sebranek, J.; Kraft, A.A. Effect of sodium nitrite and sodium erythorbate on the chemical, sensory and microbiological properties of water-added Turkey ham. Poult. Sci. 1984, 63, 1364–1371.
    11. Clemente, F.; Marinelli, P.S.; Otoboni, A.M.M.B.; Tanaka, A.Y.; da Oliveira, A.S.; Nicolau, C.C.T. Verificação do teor de nitrito e nitrato em salsichas tipo hot dog em função dos métodos de cocção. Rev. Anal. 2014, 1, 72–78.
    12. Cassens, R.G. Composition and safety of cured meats in the USA. Food Chem. 1997, 59, 561–566.
    13. Martínez, L.; Bastida, P.; Castillo, J.; Ros, G.; Nieto, G. Green alternatives to synthetic antioxidants, antimicrobials, nitrates, and nitrites in clean label Spanish chorizo. Antioxidants 2019, 8, 184.
    14. Verma, A.K.; Sharma, B.D.; Banerjee, R. Effect of sodium chloride replacement and apple pulp inclusion on the physico-chemical, textural and sensory properties of low fat chicken nuggets. LWT Food Sci. Technol. 2010, 43, 715–719.
    15. do Nascimento, R.; Campagnol, P.C.B.; Monteiro, E.S.; Pollonio, M.A.R. Substituição de cloreto de sódio por cloreto de potássio: Influência sobre as características físico-químicas e sensoriais de salsichas. Aliment. Nutr. Braz. J. Food Nutr. 2007, 18, 297–302.
    16. Pires, M.A.; Munekata, P.E.S.; Villanueva, N.D.M.; Tonin, F.G.; Baldin, J.C.; Rocha, Y.J.P.; Carvalho, L.T.; Rodrigues, I.; Trindade, M.A. The antioxidant capacity of rosemary and green tea extracts to replace the carcinogenic antioxidant (BHA) in chicken burgers. J. Food Qual. 2017, 2017, 1–6.
    17. Lima, M.C.; Paiva de Sousa, C.; Fernandez-Prada, C.; Harel, J.; Dubreuil, J.D.; de Souza, E.L. A review of the current evidence of fruit phenolic compounds as potential antimicrobials against pathogenic bacteria. Microb. Pathog. 2019, 130, 259–270.
    18. Rice-Evans, C.; Miller, N.; Paganga, G. Antioxidant properties of phenolic compounds. Trends Plant Sci. 1997, 2, 152–159.
    19. Balasundram, N.; Sundram, K.; Samman, S. Phenolic compounds in plants and agri-industrial by-products: Antioxidant activity, occurrence, and potential uses. Food Chem. 2006, 99, 191–203.
    20. Xie, Y.; Yang, W.; Tang, F.; Chen, X.; Ren, L. Antibacterial activities of flavonoids: Structure-activity relationship and mechanism. Curr. Med. Chem. 2015, 22, 132–149.
    21. Sanhueza, L.; Melo, R.; Montero, R.; Maisey, K.; Mendoza, L.; Wilkens, M. Synergistic interactions between phenolic compounds identified in grape pomace extract with antibiotics of different classes against staphylococcus aureus and escherichia coli. PLoS ONE 2017, 12, e0172273.
    22. Brewer, M.S. Natural antioxidants: Sources, compounds, mechanisms of action, and potential applications. Compr. Rev. Food Sci. Food Saf. 2011, 10.
    23. Martin, J.G.P.; Porto, E.; Corrêa, C.B.; de Alencar, S.M.; da Gloria, E.M.; Cabral, I.S.R.; de Aquino, L.M. Antimicrobial potential and chemical composition of agro-industrial wastes. J. Nat. Prod. 2012, 5, 27–36.
    24. Ascheri, D.P.R.; Ascheri, J.L.R.; Carvalho, C.W.P. De caracterização da farinha de bagaço de jabuticaba e propriedades funcionais dos extrusados. Ciência Tecnol. Aliment. 2006, 26, 897–905.
    25. Donadio, L.C. Jaboticaba (Myrciaria Cauliflora (Vell) Berg); Funep: Jaboticabal, Brazil, 2000.
    26. Baldin, J.C.; Michelin, E.C.; Polizer, Y.J.; Rodrigues, I.; de Godoy, S.H.S.; Fregonesi, R.P.; Pires, M.A.; Carvalho, L.T.; Fávaro-Trindade, C.S.; de Lima, C.G.; et al. Microencapsulated Jabuticaba (Myrciaria Cauliflora) extract added to fresh sausage as natural dye with antioxidant and antimicrobial activity. Meat Sci. 2016, 118, 15–21.
    27. Bordignon-Luiz, M.T.; Gauche, C.; Gris, E.F.; Falcão, L.D. Colour stability of anthocyanins from isabel grapes (Vitis Labrusca L.) in model systems. LWT Food Sci. Technol. 2007, 40, 594–599.
    28. de Oliveira, A.L.; Brunini, M.A.; Salandini, C.A.R.; Bazzo, F.R. Caracterização tecnológica de jabuticabas “sabará” provenientes de diferentes regiões de cultivo. Rev. Bras. Frutic. 2003, 25, 397–400.
    29. Pereira, M.C.T.; Salomão, L.C.C.; Mota, W.F.; Vieira, G. Atributos físicos e químicos de frutos de oito clones de jabuticabeiras. Rev. Bras. de Frutic. 2000, 22, 16–21.
    30. Caillet, S.; Côté, J.; Sylvain, J.F.; Lacroix, M. Antimicrobial effects of fractions from cranberry products on the growth of seven pathogenic bacteria. Food Control 2012, 23, 419–428.
    31. ICMSF (International Commission on Microbiological Specification for Foods). Microorganisms in Foods—Sampling for Microbiological Analysis: Principles and Specific Applications; University of Toronto Press: Toronto, ON, Canada, 1986; p. 193.
    32. Brazil. Ministério da Saúde/Agência Nacional de Vigilância Sanitária/Diretoria Colegiada. Resolução RDC No 331, de 23 de Dezembro de 2019. Dispõe Sobre Os Padrões Microbiológicos de Alimentos e Sua Aplicação. Available online: (accessed on 3 March 2020).
    33. FAO. Food and Agriculture Organization of the United Nations. Agribusiness Handbook: Grapes Wine; FAO Investment Centre Division: Rome, Italy, 2009; Available online: (accessed on 16 April 2020).
    34. Baydar, N.G.; Sagdic, O.; Ozkan, G.; Cetin, S. Determination of antibacterial effects and total phenolic contents of grape (Vitis Vinifera L.) seed extracts. Int. J. Food Sci. Technol. 2006, 41, 799–804.
    35. IBGE. Instituto Brasileiro de Geografia e Estatística. Inteligência e Mercado de Uva e Vinho: A Viticultura No Brasil. Available online: (accessed on 20 April 2020).
    36. Nardoia, M.; Ruiz-Capillas, C.; Casamassima, D.; Herrero, A.M.; Pintado, T.; Jiménez-Colmenero, F.; Chamorro, S.; Brenes, A. Effect of polyphenols dietary grape by-products on chicken patties. Eur. Food Res. Technol. 2018, 244, 367–377.
    37. Delgado Adámez, J.; Gamero Samino, E.; Valdés Sánchez, E.; González-Gómez, D. In Vitro Estimation of the Antibacterial Activity and Antioxidant Capacity of Aqueous Extracts from Grape-Seeds (Vitis Vinifera L.). Food Control 2012, 24, 136–141.
    38. Monagas, M.; Gómez-Cordovés, C.; Bartolomé, B.; Laureano, O.; Ricardo da Silva, J.M. Monomeric, oligomeric, and polymeric Flavan-3-Ol Composition of wines and grapes from Vitis Vinifera L. Cv. graciano, tempranillo, and cabernet sauvignon. J. Agric. Food Chem. 2003, 51, 6475–6481.
    39. Carpes, S.T.; Pereira, D.; de Moura, C.; dos Reis, A.S.; da Silva, L.D.; Oldoni, T.L.C.; Almeida, J.F.; Plata-Oviedo, M.V.S. Lyophilized and microencapsulated extracts of grape pomace from winemaking industry to prevent lipid oxidation in chicken pâté. Braz. J. Food Technol. 2020, 23, 1–13.
    40. Al-Kahtani, H.A.; Abu-Tarboush, H.M.; Bajaber, A.S.; Atia, M.; Abou-Arab, A.A.; El-Mojaddidi, M.A. Chemical changes after irradiation and post-irradiation storage in tilapia and Spanish mackerel. J. Food Sci. 1996, 61, 729–733.
    41. Selani, M.M.; Contreras-Castillo, C.J.; Shirahigue, L.D.; Gallo, C.R.; Plata-Oviedo, M.; Montes-Villanueva, N.D. Wine industry residues extracts as natural antioxidants in raw and cooked chicken meat during frozen storage. Meat Sci. 2011, 88, 397–403.
    42. Zakynthinos, G.; Varzakas, T. Lipid profile and antioxidant properties of selected pear cactus (Opuntia Ficus-Indica) ecotypes from southern greece. Curr. Res. Nutr. Food Sci. J. 2016, 4, 54–57.
    43. Taguchi, M.; Harinder Makkar, F.; Mounir Louhaichi, F.; Duffy, R.; Moretti, D.; Inglese, P.; Mondragon, C.; Nefzaoui, A.; Sáenz, C. Crop Ecology, Cultivation and Uses of Cactus Pear. Available online: (accessed on 16 April 2020).
    44. Maiorano, J.A. Figo Da Índia—Ficha Técnica. 2016. Available online: (accessed on 2 March 2020).
    45. CEAGESP. Companhia de Entrepostos e Armazéns Gerais de São Paulo. Guia CEAGESP: Figo Da Índia. 2018. Available online: (accessed on 2 March 2020).
    46. Osuna-Martínez, U.; Reyes-Esparza, J.; Rodríguez-Fragoso, L. Cactus (Opuntia Ficus-Indica): A review on its antioxidants properties and potential pharmacological use in chronic diseases. Nat. Prod. Chem. Res. 2014, 2, 1–8.
    47. Stintzing, F.C.; Herbach, K.M.; Mosshammer, M.R.; Carle, R.; Yi, W.; Sellappan, S.; Akoh, C.C.; Bunch, R.; Felker, P. Color, betalain pattern, and antioxidant properties of cactus pear (Opuntia spp.) clones. J. Agric. Food Chem. 2005, 53, 442–451.
    48. Palumbo, B.; Ethimiou, Y.; Stamatopoulos, J.; Oguogho, A.; Budinsky, A.; Palumbo, R.; Sinzinger, H. Prickly pear induces upregulation of liver LDL binding in familial heterozygous hypercholesterolemia. Nucl. Med. Rev. 2003, 6, 35–39.
    49. Galati, E.M.; Mondello, M.R.; Giuffrida, D.; Dugo, G.; Miceli, N.; Pergolizzi, S.; Taviano, M.F. Chemical characterization and biological effects of Sicilian Opuntia Ficus-Indica (L.) Mill. Fruit juice: Antioxidant and antiulcerogenic activity. J. Agric. Food Chem. 2003, 51, 4903–4908.
    50. Wolfram, R.; Budinsky, A.; Efthimiou, Y.; Stomatopoulos, J.; Oguogho, A.; Sinzinger, H. Daily prickly pear consumption improves platelet function. Prostaglandins Leukot. Essent. Fat. Acids 2003, 69, 61–66.
    51. Park, E.-H.; Kahng, J.-H.; Lee, S.H.; Shin, K.-H. An anti-inflammatory principle from cactus. Fitoterapia 2001, 72, 288–290.
    52. Sreekanth, D.; Arunasree, M.K.; Roy, K.R.; Chandramohan Reddy, T.; Reddy, G.V.; Reddanna, P. Betanin a betacyanin pigment purified from fruits of Opuntia Ficus-Indica induces apoptosis in human chronic myeloid leukemia cell line-K562. Phytomedicine 2007, 14, 739–746.
    53. Chougui, N.; Tamendjari, A.; Hamidj, W.; Hallal, S.; Barras, A.; Richard, T.; Larbat, R. Oil composition and characterisation of phenolic compounds of Opuntia Ficus-Indica Seeds. Food Chem. 2013, 139, 796–803.
    54. Liu, H.G.; Liang, Q.Y.; Meng, H.L.; Huang, H.X. Hypoglycemic effect of extracts of cactus pear fruit polysaccharide in rats. Zhong Yao Cai 2010, 33, 240–242.
    55. Matthäus, B.; Özcan, M.M. Habitat effects on yield, fatty acid composition and tocopherol contents of prickly pear (Opuntia Ficus-Indica L.) seed oils. Sci. Hortic. 2011, 131, 95–98.
    56. Abou-Elella, F.M.; Ali, R.F.M. Antioxidant and anticancer activities of different constituents extracted from Egyptian prickly pear cactus (Opuntia Ficus-Indica) Peel. Biochem. Anal. Biochem. 2014, 3, 1–9.
    57. Mobraten, K.; Haug, T.M.; Kleiveland, C.R.; Lea, T. Omega-3 and Omega-6 PUFAs induce the same GPR120-mediated signalling events, but with different kinetics and intensity in Caco-2 Cells. Lipids Health Dis. 2013, 12, 1–7.
    58. Berraaouan, A.; Ziyyat, A.; Mekhfi, H.; Legssyer, A.; Sindic, M.; Aziz, M.; Bnouham, M. Evaluation of antidiabetic properties of cactus pear seed oil in rats. Pharm. Biol. 2014, 52, 1286–1290.
    59. Seo, Y.H.; Han, C.H.; Lee, J.M.; Choi, S.M.; Moon, K.D. Effects of Opuntia Ficus-Indica extracts on inactivation of escherichia coli O157:H7 and listeria monocytogenes on fresh-cut apples. J. Korean Soc. Food Sci. Nutr. 2012, 41, 1009–1013.
    60. Zito, P.; Sajeva, M.; Bruno, M.; Rosselli, S.; Maggio, A.; Senatore, F. Essential Oils Composition of two Sicilian cultivars of Opuntia Ficus-Indica (L.) Mill. (Cactaceae) Fruits (Prickly Pear). Nat. Prod. Res. 2013, 27.
    61. Parafati, L.; Palmeri, R.; Trippa, D.; Restuccia, C.; Fallico, B. Quality Maintenance of Beef Burger Patties by Direct Addiction or Encapsulation of a Prickly Pear Fruit Extract. Front. Microbiol. 2019, 10.
    62. Kharrat, N.; Salem, H.; Mrabet, A.; Aloui, F.; Triki, S.; Fendri, A.; Gargouri, Y. Synergistic Effect of Polysaccharides, Betalain Pigment and Phenolic Compounds of Red Prickly Pear (Opuntia Stricta) in the Stabilization of Salami. Int. J. Biol. Macromol. 2018, 111, 561–568.