Next Article in Journal
First Nation-Wide Analysis of Food Safety and Acceptability Data in Lebanon
Previous Article in Journal
Effectiveness of Sprayed Bioactive Fruit Extracts in Counteracting Protein Oxidation in Lamb Cutlets Subjected to a High-Oxygen MAP
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

The Role of Fruit by-Products as Bioactive Compounds for Intestinal Health

by
Mohamed Aymen Chaouch
* and
Stefania Benvenuti
Department of Life Sciences, University of Modena and Reggio Emilia, Via G. Campi 103, 41125 Modena, Italy
*
Author to whom correspondence should be addressed.
Foods 2020, 9(11), 1716; https://doi.org/10.3390/foods9111716
Submission received: 21 October 2020 / Revised: 16 November 2020 / Accepted: 20 November 2020 / Published: 22 November 2020
(This article belongs to the Section Nutraceuticals, Functional Foods, and Novel Foods)

Abstract

:
The fruit processing industry generates large amounts of wastes (pomace, seeds, peels) that causes negative environmental impact with considerable treatment expenses. Nevertheless, various studies demonstrated that these by-products are still rich in bioactive compounds, especially dietary fibres and phenolic compounds, thus leading to significant chemical, physical and biological properties. These characteristics make fruits by-products a good source for new supplements in food products having important effect on intestinal function. Thus, the aim of this review is to evaluate the different bioactive compounds isolated from fruit by-products and to analyse their application in various formulations for the food and nutraceutical industries. In consideration of the biological properties of these compounds, their role in the functioning and action on intestine and gut flora was discussed.

Graphical Abstract

1. Introduction

The significant progress made in the field of chemistry, biology and agriculture has enabled better exploitation of agro-resources. Food is not seen as a simple nourishment, but its beneficial or harmful effects for the organism, and its role in the prevention of cardiovascular and metabolic pathologies are taken into consideration. No less important for the consumer is the impact on the environment of food production, both in terms of energy and human resources used, and of residues generated by agronomic practices, transformation and conservation. In this context the recovery of waste from agro-resource processing industries is considered of notable importance not only for economic matters but also for environmental sustainability, and offers new opportunities for economic development in many sectors. Thus, the economic burden of recycling waste becomes the production of high value-added co-products intended for resale to the biomedical, food, cosmetics, chemistry and design packaging materials industries [1,2]. The use of agro-resources and their co-products is motivated by their abundance, their renewable nature, their biodegradability and the added value which must justify any industrial development. Indeed, agro-resources could offer a new source of raw materials in many fields.
Even if the current globalization of the market ensures the availability of fresh fruit throughout the year, a large part is subjected to different transformation processes in order to obtain new products satisfying the different current demands of consumers. Thus, it has been reported that about a third of the edible portion of food intended for human consumption is lost or wasted along the food chain, from initial production to final consumption [3,4]. The large quantity of residues produced by the food industry, in addition to being a great loss of valuable materials, also raises serious management problems from an economic and ecological point of view. To address these economic and ecological problems, the recovery of residues represents a promising solution to absorb millions of tons of waste material. The valorization of by-products from the food industry gives a second life to co-products and limits the use of conventional energy sources [5].
Depending on the nature of the co-products to be recovered, several techniques have been developed. The transformation of co-products into biofuels and biosolvents represents a very promising economic and ecological recovery [6,7]. The integration of co-products into the animal feed market also means a promising recovery technique [4]. Fruit and vegetable co-products have been valued in the field of functional foods because of their health interests [8,9].

2. Bioactive Compounds from Fruit by-Products

Several researches have proven the presence of a wide range of bioactive compounds in various fruit industrial by-products which are essentially pomace, peels and seed fractions. These compounds consist mainly of carbohydrates (pectin, cellulose, hemicellulose…), secondary metabolites (phenolics, glycosides, alkaloids, gums, mucilage and volatile oils), lipids and proteins. Generally, seeds are rich in polyphenols and bioactive lipids whereas peels are considered as a rich source of dietary fibres [10,11]. Bioactive compounds are present in fruit by-products with various concentrations and combinations. These differences could be mainly related to the fruit variety, geographic location, maturation stage, as well as extraction parameters (solvent, extraction ratio, time and temperature) [9].
Several extraction techniques were carried out for the isolation of bioactive compounds from fruit by-products. For example, solid state fermentation (SSF) was applied for the extraction of polyphenolic antioxidants from grape skin [12] and bagasse [13] and for the isolation of ellagic acid from pomegranate Husks [14]. Citric acid was isolated from banana peel by SSF using Aspergillus niger [15], while pectin and limonene were extracted from orange peel through enzymatic and chemical hydrolysis [16]. Mango peels were subjected to autoclave treatment for the extraction of pectin and polyphenols [17]. The other processes that we can cite are ultrasound treatment (fatty acids and tocopherols from watermelon seeds) [18], microwave-assisted extraction (phenolic compounds from pitaya fruit peels) [19], steam explosion (limonene from orange peel) [20] and classic extraction with ethanol (phenolic antioxidants from avocado peel) [21] or n-hexane (antioxidant oils from melon seeds and carotenoids and anthocyanins from papaya peel) [22,23]. Another modern method for the isolation of bioactive compounds from fruit by-products is sub- and supercritical fluid extractions. This method was applied for the extraction of phenolic compounds, flavonoids, carotenoids, pectin, reducing sugars, lipids and proteins from several by-products such as citrus peels and pomace, pomegranate peels, apple pomace and seeds, grape pomace and seeds [24].
Plant bioactive metabolites exert pleiotropic effects by the modulation of multiple metabolic pathways through a variety of molecular targets. Previous studies revealed that dietary phenolic compounds displayed a pleiotropic behavior on key proteins, thus presenting beneficial effects in several chronic disorders which are related to oxidative stress, inflammation and aging. This is strongly related to the wide range of biological activities like antioxidant, antimicrobial, anti-inflammatory, anti-allergenic, anticancer and cardioprotective activities. Thus, it has been reported that natural phenolic compounds and their metabolites exerted significant effects on the main metabolic pathways involved in energy metabolism (the AMP-protein kinase AMPK and the mammalian target of rapamycin mTOR are the main regulators), as well as inflammatory response and aging (main regulators are the nuclear factor-erythroid 2 p45-related factor 2 (Nrf2) and sirtuins) [25,26]. For example, Marín-Aguila et al. (2013) described some nutraceutical compounds targeting AMPK pathways in cancer, cardiovascular disease, type 2 diabetes mellitus and neurodegenerative disease including phenolic acids, anthocyanins, stilbene, flavone, flavonol, alkaloids, lignan [26]. Thus, bioactive compounds isolated from fruit by-products showed a significant effect as bioingredients in functional foods as well as nutraceuticals in pharmaceutical and medicinal recipes. This was mainly due to their antioxidant, anti-inflammatory, antimicrobial, anti-allergenic, antithrombotic, anti-atherogenic, cardioprotective and vasodilatory capacities [11].

2.1. Phenolic Compounds

Various phenolic compounds were isolated such as hydroxybenzoic and hydroxycinnamic acids, flavonoids (flavonols, flavanones, flavones, flavanonols, isoflavones, flavanols, and anthocyanidins), lignans and stilbenes (Table 1). Many fruit wastes showed highest phenolic content, especially grape, pomegranate, apple and citrus varieties (orange, lemon).
Indeed, the interest accorded to these compounds was mainly related to their capacity to scavenge free radicals and to regulate the generation of free radicals in vivo, thus ensuring the prevention of oxidation reactions in food and cell damage. These characteristics allows them to replace synthetic preservatives [10].
For example, an important oxidative stability was found in the oil extracted from date seeds due to the higher phenolic content (about 19 mg GAE/g dry weight). This ensures the use of date seed oil as natural additive to other vegetable oils in order to improve its heat stability [27,28]. In addition, big amounts of seeds and peels residues are generated by the citrus industry. These residues constitute about 50% of the total fruit and are an important source of phenolic compounds. Also, it has been reported that the peels of many fruits, such as apples, peaches, pears, banana and pomegranate, have been found to contain highest content in phenolics than the edible portions [29].

2.2. Dietary Fibres (DFs)

Over the last decades, there has been an increasing trend to recover dietary fibre (DF) compounds from industrial by-products. These compounds refer essentially to the sum of non-starch polysaccharides and lignin. Thus, it has been reported that fruit by-products are mainly composed of cellulose, hemicellulose, pectin, gums and lignin [10].
Table 2 illustrates some DF compounds isolated from various fruit by-products.
DF compounds can be obtained from the by-products of various food processing industry, such as the beverage, canning and juice industries. This latter probably produces the most important amounts of by-products, composed mainly by pomace and peels [60].
From a general aspect, the interest given to DF is strongly associated to their significant role in decreasing many health disorders. Cellulose, hemicellulose and lignin are well-known for water absorption and intestinal regulation, whereas pectin and gums showed important effects in cholesterol reducing and glucose regulation [61].
The data reported refer to the dry weight, but the high amount of water in these by-products must be considered. The freeze-drying or spray-dry operations to remove water have to be considered because of their cost rather than preparing a concentrate with less energy consumption for the preparation.
Moreover, DFs showed widespread use in the food industry when they are incorporated into bakery products by enhancing the digestion, prolonging the freshness and retaining more water. They also improve the texture and provide a desirable resistance to melting of ice cream [61].

2.3. Proteins and Peptides

Proteins are important biomolecules for a good function of the human body, particularly to form muscles [29]. Thus, it has been reported that many health diseases are strongly related to protein deficiency such as Kwashiorkor, Marasmus (energy deficiency), mental disorders, organ failure, oedema and weakness immune system [69].
In more recent diets, especially aimed at athletes or for diseases related to diabetes and the cardiovascular system, increased protein intake plays an important role. It is also to be considered that a greater ecological awareness leads people more and more often to limit the consumption of meat, if not actually not to use it as is the case for vegan people.
The use of plants, fungi and their extracts as meat substitutes have become increasingly important in nutrition and satisfies the request for proteins and amino acids, essential for the regular human metabolism. Indeed, fruit by-products have been reported to be an important source of proteins and peptides (Table 3). These latter are generally obtained by the hydrolysis of proteins [10].
In comparison with vegetables, it has been reported that the oil isolated from hempseeds is mainly composed of polyunsaturated fatty acids, particularly linoleic (ω-6) and α-linolenic (ω-3) acids, whereas globulin (edestin) and albumin were found to be the major proteins [77]. The by-product resulted from canola oil extraction (Canola meal) is very rich in proteins (up to 50%), whereas canola seeds contain about 26% of protein. The protein content of canola meal, which consists mainly of napin and cruciferin, permits its use for human food and animal feed [78].
Marcet et al. reported that raw rice bran and raw soybean contained high amounts of peptides, 75% and 50% of the total protein content, respectively, whereas the amount of recovered amino acids from these two by-products was 5% of the total protein content. Peptides were also isolated from soy pulp with a percentage of 35% from the total dry matter [79].
Leuk leaves showed high crude protein content (19.4% on dry matter basis) with a total amino acid content of 14.1% (mainly Leu and Lys, 11.6 and 8.2 mg/g dry matter, respectively), while protein content in parsley was 17.0% from dry matter in which the percentage of essential amino acid was 40%. The most abundant ones were Leu and Lys, 12.4 and 8.3 mg/g dry matter, respectively [80].

2.4. Lipids

Lipids, water-insoluble molecules, are in essential components for the human organism. They play an important physiological and biochemical rolein the function of the human body, such as energy storage (fats and oils), structural components of biological membranes (phospholipids and sterols), electron carriers, enzyme cofactors, light-absorbing pigments, hydrophobic anchors for proteins and emulsifying agents in the digestive tract [81,82]. Besides their important nutritional role in the human diet, lipids are also exploited as food ingredients, thus improving texture, mouthfeel and flavour of new formulations [83]. Indeed, due the increasing demand for vegetable oils, the interest was oriented to the possibility of exploiting new oil sources with higher amount of polyunsaturated fatty acids. In this context, fruit by-products, particularly seeds, have been reported to be a potential alternative for lipids production. Several fatty acids were isolated from various fruit by-products such as linoleic acid, linolenic acid, palmitic acid, palmitoleic acid, oleic acid, lauric acid, myristic acid, stearic acid, lignoceric acid, arachidic acid, erucic acid [83].
Table 4 present the lipid content in various fruit by-products.
Apple seeds were reported to contain significant amount of lipids (277 g oil/kg apple seeds), in which unsaturated fatty acids were the predominant (89 g/100 g oil). These lipids are mainly linoleic acid (51.2 g/100 g oil), whereas others are palmitic (10.5 g/100 g oil), linolenic (5.6 g/100 g oil), stearic (4.3 g/100 g oil) and oleic acids (4.1 g/100 g oil) [89]. Wild and cultivated berries seeds are also an important source of lipids (14% to 18% of dry matter). Their rich composition in α-linoleic acid and their high content of α- and γ-tocopherols allows them to be beneficial for balancing diet fatty acid composition and skin regeneration [90,91]. Plum seeds are rich in sterol esters and n-3 PUFA (omega-3) [90], whereas the main lipids in passion fruit seeds are stearic acid, palmitic acid, oleic acid and linoleic acid [92].

3. Fruit by-Products and Intestinal Function

In the light of all above, we can assert that fruit by-products are a good source of bioactive compounds. In fact, from economic and environmental point of view, it is very important to proceed to the valorization of these wastes in many fields.
The most popular process for fruit by-products management is their incorporation into livestock feeds. In this context, numerous fruit by-products demonstrated the ability to be incorporated into animal feed because of their rich composition in proteins, digestible fiber, soluble sugars, vitamins and minerals. In addition, the majority of these by-products don’t present any adverse impacts on the productive and reproductive performance of animals. However, some by-products need some precautions when applying them in animal feed due to various factors such as limited shelf life (high moisture content), presence of pathogens agents or antinutrient metabolites [93]. Among the widely used fruit by-products for animal feed we can cite citrus pulp, [94] grape pomace [94], mango seeds [95], banana peels and leaves [96], apple waste [8,96], grape waste [96], pomegranate waste [96], banana peels [97], passion fruits peels [97] and bilberry pomace [8].
Beside their use as animal feed or to reduce methane production, the interest was oriented over the last decades to the application of fruit by-products in the food, cosmetic and pharmaceutical industries [48]. Thus, it has been reported that the incorporation of some fruit by-products into food products improves the quality of these products. This improvement was affirmed by the significant impact on the sensory evaluation (texture, taste, odor, color, overall acceptability…) of the new formulations (Table 5) [82].
Bioactive compounds from fruit by-products find several applications in the different fields of food processing industry. They could be considered as additives in food products, thus promoting the preservation and the enhancement of the quality, as well as the prevention of food oxidation and pathogenic microorganisms growth. In this context, pomegranate and grape seed extracts were reported to be good natural additives in foods and food packaging industry, due to their significant antioxidant and antimicrobial properties [98]. Another application of fruit by-products in the food processing industry is their use as packaging materials which is strongly related to the oxygen-impermeable properties. Various studies found promising results when incorporating fruit by-products into edible films that could be used as food packaging materials [99]. Other researches revealed also that fruit by-products can be also used as a reserve of wheat flour (example of berry pomace) [100], as a supplement in cakes and cookies (example of sour cherry pomace) [101] or in fermented beverages production (example of blueberry bagasse) [102]. Fruit by-products are now considered as value-added supplements for foods, due to their high content in bioactive compounds, especially dietary fiber. Indeed, their incorporation into foods leads to several beneficial effects such as the improvement of water and oil retention and the enhancement of oxidation stability and emulsification properties, as well as their consideration as non-caloric bulking agents [103].
According to the European Food Safety Agency (EFSA) and the European Commission (EC), some rules should be respected when talking about foods. For example, food additives are compounds which are added to a food product to achieve a specific technological aim, but they are not ingested as a food product. Indeed, according to EFSA, while accomplishing a specific technological goal (satisfaction of specific dietary requirement, Improvement of sensory quality, facility of production, packaging, transport and storage), a food additive should not present any safety trouble for consumers health and must attend specific purity criteria [104,105,106]. Thus, it has been reported that some additives, which are currently allowed by EC, are present in fruit by-products including anthocyanins (E163) (example of grape by-products) [107] and chlorophylls (E140) (principally in green leaves and mango peels) [108]. The different types of food additives and their functions as cited by European Food Safety Agency (EFSA) and European Commission (EC) were mentioned by Faustino et al. (2019) [109].
The gut microbiota plays an important role in the function of human gastrointestinal tract thought its interaction with food components and host cells. Thus, it has been reported that a balanced gut microbiota was strongly related to the adjustment of the immune system and antioxidant defense, while microbiota disorders leads to several health diseases such as rheumatoid arthritis, colorectal cancer, obesity, diabetes, irritable bowel disease, inflammatory bowel disease and cardiovascular disease [114,115].
Recently, gut microbiota has been investigated as a possible environmental factor influencing obesity through its role in fat storage. The intestinal microbiota contributes to the absorption by the host of carbohydrates and lipids and regulates the storage of fat [116]. In addition, it was observed that it occurs a change in the composition of the gut microbiota (dysbiosis) for people suffering from colorectal cancer or chronic inflammatory bowel disease [117,118]. Recent researches revealed that there is an accordance between autistic disorder and gastrointestinal disorders. Preliminary studies also showed that there is a form of dysbiosis in autistic children with a decrease in Akkermansia muciniphila and Bifidobacterium spp. in the stools of these patients [119,120].
Besides that, the microbiota plays an essential role in the maturation of the immune system and the development of its functions. This role is suggested by the many abnormalities observed in axenic mice: hypoplasia of Peyer’s patches, decreased number of intraepithelial lymphocytes, low production of serum immunoglobulins and cytokines. In addition, the spleen and lymph nodes of axenic mice show areas of atrophied lymphocytes. All of these abnormalities disappeared within a few weeks after inoculation of the microbiota of conventional mice into axenic mice [121].
Diet is a subject of very important interest in research programs because of its potential to modulate the intestinal microbiota of the host, whether beneficial or harmful. Eating habits have a significant impact on the composition of the intestinal microbiota, especially in the first years of life [122].
Dietary fiber intake can benefit people having a wide variety of metabolic syndromes and gastrointestinal disorders [123,124]. High fiber intake has been reported to be beneficial for patients with diabetes, high cholesterol, hypertriglyceridemia, obesity or hypertension [124,125]. It has also been reported that individuals with high fiber intake are less susceptible to the development of cardiovascular disease or colon cancer [126]. Likewise, diets with a high intake of fats and proteins, but with a low fiber content, are associated with a higher risk of developing colon cancer, unlike vegetarian or oriental diets with higher fiber intakes [127,128]. In addition, Japanese people who adopt a western diet are more likely to develop colon cancer [129].
DFs are the main source of carbon and energy for colonic microbes. The major components of DFs are non-starch polysaccharides (20–45% of the dry matter supplied to the colon), simple sugars (10%), oligosaccharides (10%) and starch and starch hydrolysis products (about 8% of dry matter) [122]. Furthermore, the proximal colon received daily about 5–10 g of lipid and 5–15 g of protein, mainly of dietary origin, in addition to some other minor components like polyphenols, lignin, tannins, catechins and micronutrients [122]. In the other hand, it has been also reported that the major part (about 90%) of 1 g/day of dietary polyphenols escapes absorption and digestion in the small intestine and persists in the colon. Then, by contact with the gut microbiota, they become like compounds for microbial production of small phenolic acids and SCFA or, thus having effect on species composition and their metabolic activity [130].
DFs were reported to have both preventative and therapeutic impact for various bowel intestine-related diseases such as obesity, type II diabetes and cardiovascular diseases [131]. They are fermented by the colonic microbiota to produce other metabolites like organic acids that supply energy for other bacteria, bowel epithelium and peripheral tissues [132]. DFs preserve bowel health by increasing digesta mass, which leads to the reduction of intracolonic pressure, dilution of toxins, and decrease of transit time, as well as an augmentation of defecation frequency. This increase was mainly due to the physical properties and the ability to adsorb water, especially of incompletely fermented fiber (insoluble non-starch polysaccharides, like cellulose) [132]. An increase in the fecal mass could be also made by DFs thought the enhancement of fermentation, thus conducting to bacterial proliferation and biomass increase [133].
Dietary polyphenols were also reported to be beneficial for the prevention of health from several diseases like cardiovascular disease and cancer due to their significant antioxidant or anti-inflammatory effects [122]. Generally, polyphenols are found in plant foods as a bound form (mostly as glycosides). The major part of them undergoes a metabolization process by gut microbiota, thus forming aglycones [134]. Flavonoid quercetin, flavonols, caffeic acid, (+)-catechin, (−)-epicatechin, resveratrol, ellagitannin and anthocyanins were reported to have significant impact on the modulation of the gut microecology [134].
Nowadays, it is well-known that obesity could be treated using diet with moderate amounts of protein, thus reducing health disorders associated with obesity. Moreover, dietary proteins also showed significant effects on gut health, particularly when combined with carbohydrates [122]. They are also the main source of nitrogen for colonic microbial growth [122]. Furthermore, fatty acid rich-diets showed positive effect on immune function, cholesterol and triglycerides levels, blood pressure and cardiovascular function [135,136].
Although cereal grains and their by-products are the most known source of DFs, it has been reported that fruit by-products could be an alternative source of DF because of their high content in DFs. Indeed, DFs are considered as important elements for the good function of human body, particularly for the improvement of the growth of beneficial of hind gut microbiota, the satiety and attenuation of constipation and the regulation of glucose and lipid levels, thus reducing the risk of coronary heart and cancer diseases [137].
The gastroprotective effect of several fruit by-products was studied, such as orange bagasse [138], passion fruit peels [138], grape pomace [139], grape peels [140], grape seed [141], pomegranate by-products [142,143,144], orange peels [145], apple peels [146], apple pomace [147,148] (Table 6).
In this context, Abboud et al. (2019) studied the gastroprotective effect of yellow passion fruit peel, which is an unexploited by-product from the juice industry in Brazil. Soluble dietary fibres (SDF) isolated from this by-product showed significant gastroprotective effects on animals following oral and intraperitoneal digestion. This effect was manifested by the decrease of gastric ulcer lesions induced by ethanol and the prevention of the exhaustion of gastric wall mucus and reduced glutathione (GSH) levels. Thus, oral pre-treatment with SDF reduced significantly the ethanol-induced gastric lesions in 72.25%, 79.23% and 87.17% by injection of 0.1, 1 and 10 mg/kg, respectively. The same doses were able to avoid the depletion of GSH levels in 52.20%, 41.91% and 50.33% and the gastric wall mucus in 26.32%, 25.03% and 31.00%. Moreover, the treatment by intraperitoneal route with SDF (1 mg/kg) reduced the gastric lesion area in 72.56% and prevented the depletion gastric wall mucus in 21.24% and the GSH levels in 40.81% [149].
Another research conducted by Athaydes et al. (2019) focused on the treatment of gastric disorder by avocado seeds, which is a by-product generally discarded as waste. The total indomethacin-induced gastric lesion area was significantly reduced after the treatment with avocado seeds (92% of protection). Results showed also that an injection of 75 mg/kg of ethyl acetate extract from avocado seeds increased mucus production by the stomach mucosal cells of about 2.38 ± 0.55 times compared to the control, which forms a mucoid layer, thus promoting tissue repair and accelerating epithelial recovery. The authors suggested that phenolic compounds present in this by-product are the main responsible on this significant effect [150].
Pomegranate peels extract has been reported to possess significant effects on stomach gastric mucosa (at a dose of 500 mg/kg), mainly manifested by the protective role against ethanol induced gastric ulcer in rats. This anti-ulcer impact was asserted by the high levels of TGFβ1 in serum and the decrease of ulcer lesion areas in the stomach layer. This significant antiulcer effect might be associated to existence of several bioactive compounds such as anthocyanins, anthocyanidins, punicic acid, ellagic acid, flavonoids and ellagitannins [152].
A significant anti-ulcer effect was also mentioned for the aqueous extract from orange (Citrus sinensis) peels. This effect was shown through the correction of the enhanced gastric lipid peroxidation and the reduction of TNF-α (tumor necrosis factor alpha) production, as well as the reduction of gastric DNA fragmentation and gastric COX-2 (cyclooxygenase-2) expression. Authors suggested that this beneficial effect was related to the capacity in chelating free iron and scavenging H2O2, thus leading to calcium homeostasis. In addition, the pre-treatment with Citrus sinensis extract ensure protection against the overload of cells of the gastric and duodenal mucosa caused by the sub-acute exposure of ethanol [153].
Polyphenol-rich extract from apple peels exhibited also an important inhibitory effect against Helicobacter pylori attachment, by avoiding of initial steps in the Helicobacter pylori colonization process and suppressing inflammation. Oral ingestion with doses of 150 and 300 mg/kg/day was reported to be good enough to avert the initial attachment of Helicobacter pylori to the antral mucosa which causes an inflammatory damage. The decrease in this damage by apple peel phenolic extract was essentially associated to its important antioxidant and anti-VacA (vacuolating bacterial toxin) properties. Thus, it has been reported that gastric Helicobacter pylori infection, which affects about half of the world’s population, is the main cause of various gastrointestinal disorders like gastric carcinoma and duodenal ulcer [154]. On the other hand, Mousa et al. (2012) asserted that apple pomace pectin could be a potential gastroprotective and hypolipidemic drug due to its significant content on citric and galacturonic acids. The gastroprotective effect against indomethacin induced ulcer was reported by preventing the formation of gastric mucosa lesions, lining the surface of the stomach and improving the resistance of the gastroduoden mucosa [147].
Grape by-products have been also studied for their effects on intestinal function. For example, Bhardwaj et al. (2018) investigated the impact of proanthocyanidins from grape seeds on different experimental models of gastric ulcers in rats. A 100 mg/kg dose of grape seed proanthocyanidin showed better treatment of gastric ulcers with fewer side effects. This effect was observed by the significant decrease in ulcer index and gastric acidity in pylorus ligation models, as well as the reduction in MDA (malondialdehyde) levels [141].
Sen et al. (2014) reported that pectin isolated by hot water-acid extraction from various fruit by-products (apple Malus domestica, lemon Citrus limon and orange Citrus sinensis) showed an important role in supporting the survival and the development of the probiotics in the gastrointestinal tract [157].
Fibers isolated from orange bagasse and passion fruit peels were reported to have significant impact on the modulation of the gut microbiota. They could be considered as an energy source for bacteria located in the distal colon. Thus, the negligible production of lactate and succinate permit the slow fermentation, which allows protection against colon cancer [138].
The effect of acerola by-product on the gut microbiota metabolism was also studied. The treatment with acerola by-product was found to have positive effect since a decrease of the NH4+ amount in the ascending colon was observed, as well as an increase in short-chain fatty acids (SCFAs) in the three regions of colon. This important effect was mainly due to high content in fibre and phenolic compounds in acerola by-product, which are responsible for the high antioxidant activity [155].
Another research conducted by Batista et al. revealed that by-products from acerola (Malpighia emarginata D.C.), cashew (Anacardium occidentale L.) and guava (Psidium guajava L.) fruits could be considered as protective compounds for intestinal health against the harmful effects induced by dyslipidaemic diet. Their role is the protection of colon and liver from tissue damage. This important role was experimentally assured manifested by several parameters such the decrease of faecal pH, serum lipid levels, liver fat and visceral fat, as well as the increase of faecal moisture and faecal fat excretion in dyslipidaemic female rats [156].
The consumption of insoluble dietary fiber from citrus by-products was strongly linked to intestinal motility by delaying the gastric emptying and extending the effective unstirred layer, which makes the absorption process in the small intestine slower thus giving an extended feeling of fullness. Several factors have been reported to assert the protective effect of fibers against gastrointestinal diseases including the decrease in intracolonic pressure and the transit time and the increase in stool weight. In the other hand, soluble dietary fibers from citrus by-products were considered as important compounds in reducing risks of coronary heart diseases by lowering triacylglycerol concentrations and enhancing insulin sensitivity. This was asserted through the delaying of the absorption process of macronutrients, especially carbohydrates and fat [158].

4. Conclusions

In conclusion, we can state that the large amounts of wastes generated by fruit processing industry represent a great origin of bioactive compounds having significant potential benefits for various applications in several industries. These by-products contain high contents of dietary fibres, polyphenols, lipids and proteins as described in this review, which makes them a considerable source of food additives. The latter could be integrated in several food industry sections like bakery products, dairy products, biscuits, cakes.
Nevertheless, several fruits by-products have been reported to exhibit potential good effect on the intestinal function. Treatment with dietary fibres, polyphenols or anthocyanins from several fruit by-products showed a significant effect on the improvement of gut health and the treatment of gastric disorders.

Author Contributions

All authors have contributed to conceptualization, data curation, writing, review and editing, equally. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by MonteRè, Cooperativa Modenese essiccazione frutta, S. Maria di Mugnano (Modena, Italy).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Gontard, N.; Sonesson, U.; Birkved, M.; Majone, M.; Bolzonella, D.; Celli, A.; Angellier-Coussy, H.; Jang, G.-W.; Verniquet, A.; Broeze, J. A research challenge vision regarding management of agricultural waste in a circular bio-based economy. Crit. Rev. Env. Sci. Tec. 2018, 48, 614–654. [Google Scholar] [CrossRef] [Green Version]
  2. Boccia, F.; Di Donato, P.; Covino, D.; Poli, A. Food waste and bio-economy: A scenario for the Italian tomato market. J. Clean. Prod. 2019, 227, 424–433. [Google Scholar] [CrossRef]
  3. FAO. Pertes et Gaspillages Alimentaires Dans le Monde–Ampleur, Causes et Prévention; FAO: Rome, Italy, 2012. [Google Scholar]
  4. Salami, S.A.; Luciano, G.; O’Grady, M.N.; Biondi, L.; Newbold, C.J.; Kerry, J.P.; Priolo, A. Sustainability of feeding plant by-products: A review of the implications for ruminant meat production. Anim. Feed Sci. Tech. 2019, 251, 37–55. [Google Scholar] [CrossRef]
  5. Lin, C.S.K.; Pfaltzgraff, L.A.; Herrero-Davila, L.; Mubofu, E.B.; Abderrahim, S.; Clark, J.H.; Koutinas, A.A.; Kopsahelis, N.; Stamatelatou, K.; Dickson, F. Food waste as a valuable resource for the production of chemicals, materials and fuels. Current situation and global perspective. Energ. Environ. Sci. 2013, 6, 426–464. [Google Scholar] [CrossRef]
  6. Kusch-Brandt, S.; Mumme, J.; Nashalian, O.; Girotto, F.; Lavagnolo, M.C.; Udenigwe, C. Valorization of Residues From Beverage Production. In Processing and Sustainability of Beverages; Elsevier: Woodhead Publishing: Cambridge, UK, 2019; pp. 451–494. [Google Scholar]
  7. Hossain, A.; Yusoff, W.M.W.; Veettil, V.N. Bioethanol Production from Fruit Biomass as Bio-antiseptic and Bio-antifermenter: Its Chemical and Biochemical Properties. J. Appl. Sci. 2019, 19, 311–318. [Google Scholar] [CrossRef] [Green Version]
  8. Majerska, J.; Michalska, A.; Figiel, A. A review of new directions in managing fruit and vegetable processing by-products. Trends Food Sci. Tech. 2019, 88, 207–219. [Google Scholar] [CrossRef]
  9. Trigo, J.P.; Alexandre, E.M.; Saraiva, J.A.; Pintado, M.E. High value-added compounds from fruit and vegetable by-products–Characterization, bioactivities, and application in the development of novel food products. Crit. Rev. Food Sci. Nutr. 2020, 60, 1388–1416. [Google Scholar] [CrossRef]
  10. Banerjee, J.; Singh, R.; Vijayaraghavan, R.; MacFarlane, D.; Patti, A.F.; Arora, A. Bioactives from fruit processing wastes: Green approaches to valuable chemicals. Food Chem. 2017, 225, 10–22. [Google Scholar] [CrossRef]
  11. Ran, X.-l.; Zhang, M.; Wang, Y.; Adhikari, B. Novel technologies applied for recovery and value addition of high value compounds from plant byproducts: A review. Crit. Rev. Food Sci. Nutr. 2019, 59, 450–461. [Google Scholar] [CrossRef]
  12. Martínez-Ávila, G.C.; Aguilera-Carbó, A.F.; Rodríguez-Herrera, R.; Aguilar, C.N. Fungal enhancement of the antioxidant properties of grape waste. Ann. Microbiol. 2012, 62, 923–930. [Google Scholar] [CrossRef]
  13. Larios-Cruz, R.; Buenrostro-Figueroa, J.; Prado-Barragán, A.; Rodríguez-Jasso, R.M.; Rodríguez-Herrera, R.; Montañez, J.C.; Aguilar, C.N. Valorization of Grapefruit By-Products as Solid Support for Solid-State Fermentation to Produce Antioxidant Bioactive Extracts. Waste Biomass Valorization 2019, 10, 763–769. [Google Scholar] [CrossRef]
  14. Sepúlveda, L.; Aguilera-Carbó, A.; Ascacio-Valdés, J.; Rodríguez-Herrera, R.; Martínez-Hernández, J.; Aguilar, C. Optimization of ellagic acid accumulation by Aspergillus niger GH1 in solid state culture using pomegranate shell powder as a support. Process Biochem. 2012, 47, 2199–2203. [Google Scholar] [CrossRef]
  15. Kareem, S.; Rahman, R. Utilization of banana peels for citric acid production by Aspergillus niger. Agric. Biol. J. N. Am. 2013, 4, 384–387. [Google Scholar] [CrossRef]
  16. John, I.; Muthukumar, K.; Arunagiri, A. A review on the potential of citrus waste for D-Limonene, pectin, and bioethanol production. Int. J. Green Energy 2017, 14, 599–612. [Google Scholar] [CrossRef]
  17. Rojas, R.; Alvarez-Pérez, O.B.; Contreras-Esquivel, J.C.; Vicente, A.; Flores, A.; Sandoval, J.; Aguilar, C.N. Valorisation of mango peels: Extraction of pectin and antioxidant and antifungal polyphenols. Waste Biomass Valorization 2020, 11, 89–98. [Google Scholar] [CrossRef] [Green Version]
  18. Górnaś, P.; Rudzińska, M. Seeds recovered from industry by-products of nine fruit species with a high potential utility as a source of unconventional oil for biodiesel and cosmetic and pharmaceutical sectors. Ind. Crop. Prod. 2016, 83, 329–338. [Google Scholar] [CrossRef]
  19. Ferreres, F.; Grosso, C.; Gil-Izquierdo, A.; Valentão, P.; Mota, A.T.; Andrade, P.B. Optimization of the recovery of high-value compounds from pitaya fruit by-products using microwave-assisted extraction. Food Chem. 2017, 230, 463–474. [Google Scholar] [CrossRef]
  20. Forgács, G.; Pourbafrani, M.; Niklasson, C.; Taherzadeh, M.J.; Hováth, I.S. Methane production from citrus wastes: Process development and cost estimation. J. Chem. Technol. Biotechnol. 2012, 87, 250–255. [Google Scholar] [CrossRef]
  21. Morais, D.R.; Rotta, E.M.; Sargi, S.C.; Schmidt, E.M.; Bonafe, E.G.; Eberlin, M.N.; Sawaya, A.C.; Visentainer, J.V. Antioxidant activity, phenolics and UPLC–ESI (–)–MS of extracts from different tropical fruits parts and processed peels. Food Res. Int. 2015, 77, 392–399. [Google Scholar] [CrossRef]
  22. Bonesi, M.; Saab, A.; Tenuta, M.; Leporini, M.; Saab, M.; Loizzo, M.; Tundis, R. Screening of traditional Lebanese medicinal plants as antioxidants and inhibitors of key enzymes linked to type 2 diabetes. Plant Biosyst. 2020, 154, 656–662. [Google Scholar] [CrossRef]
  23. Da Silva, L.M.R.; De Figueiredo, E.A.T.; Ricardo, N.M.P.S.; Vieira, I.G.P.; De Figueiredo, R.W.; Brasil, I.M.; Gomes, C.L. Quantification of bioactive compounds in pulps and by-products of tropical fruits from Brazil. Food Chem. 2014, 143, 398–404. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Gallego, R.; Bueno, M.; Herrero, M. Sub-and supercritical fluid extraction of bioactive compounds from plants, food-by-products, seaweeds and microalgae–An update. Trends. Analyt. Chem. 2019, 116, 198–213. [Google Scholar] [CrossRef]
  25. Villegas-Aguilar, M.d.C.; Fernández-Ochoa, Á.; Cádiz-Gurrea, M.d.l.L.; Pimentel-Moral, S.; Lozano-Sánchez, J.; Arráez-Román, D.; Segura-Carretero, A. Pleiotropic biological effects of dietary phenolic compounds and their metabolites on energy metabolism, inflammation and aging. Molecules 2020, 25, 596. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Marín-Aguilar, F.; Pavillard, L.E.; Giampieri, F.; Bullón, P.; Cordero, M.D. Adenosine monophosphate (AMP)-activated protein kinase: A new target for nutraceutical compounds. Int. J. Mol. Sci. 2017, 18, 288. [Google Scholar] [CrossRef] [Green Version]
  27. Golshan Tafti, A.; Panahi, B. Chemical composition of seed and seed oil from Iranian commercial date cultivars. J. Food Bioprocess Eng. 2019, 3, 1–8. [Google Scholar]
  28. Taha, E.; Abd-Elkarim, N.; Ahmed, Z. Date seed oil as a potential natural additive to improve oxidative stability of edible vegetable oils. Egypt. J. Food Sci. 2019, 47, 105–113. [Google Scholar] [CrossRef]
  29. Sagar, N.A.; Pareek, S.; Sharma, S.; Yahia, E.M.; Lobo, M.G. Fruit and vegetable waste: Bioactive compounds, their extraction, and possible utilization. Compr. Rev. Food Sci. Food Saf. 2018, 17, 512–531. [Google Scholar] [CrossRef] [Green Version]
  30. Smaoui, S.; Hlima, H.B.; Mtibaa, A.C.; Fourati, M.; Sellem, I.; Elhadef, K.; Ennouri, K.; Mellouli, L. Pomegranate peel as phenolic compounds source: Advanced analytical strategies and practical use in meat products. Meat Sci. 2019, 158, 107914. [Google Scholar] [CrossRef]
  31. Pal, J.; Raju, C.; Lakshmisha, I.; Pandey, G.; Raj, R.; Singh, R.R. Antioxidant activity of pomegranate peel extract and its effect on storage stability of cooked meat model system of indian mackerel (Rastrelliger Kanagurta) stored at 4±2 C. Biochem. Cell. Arch. 2017, 17, 183–187. [Google Scholar]
  32. Basiri, S.; Shekarforoush, S.S.; Aminlari, M.; Akbari, S. The effect of pomegranate peel extract (PPE) on the polyphenol oxidase (PPO) and quality of Pacific white shrimp (Litopenaeus vannamei) during refrigerated storage. LWT Food Sci. Technol. 2015, 60, 1025–1033. [Google Scholar] [CrossRef]
  33. Tavallali, H.; Bahmanzadegan, A.; Tavallali, V.; Rowshan, V. Phytochemical investigation of Punica granatum pomace: As source of bioactive and medicinal natural products. Adv. Med. Plant Res. 2020, 8, 1–13. [Google Scholar]
  34. Andrés, A.; Petrón, M.; Adámez, J.; López, M.; Timón, M. Food by-products as potential antioxidant and antimicrobial additives in chill stored raw lamb patties. Meat Sci. 2017, 129, 62–70. [Google Scholar] [CrossRef] [PubMed]
  35. Tańska, M.; Roszkowska, B.; Czaplicki, S.; Borowska, E.J.; Bojarska, J.; Dąbrowska, A. Effect of fruit pomace addition on shortbread cookies to improve their physical and nutritional values. Plant Food. Hum. Nutr. 2016, 71, 307–313. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Reißner, A.M.; Al-Hamimi, S.; Quiles, A.; Schmidt, C.; Struck, S.; Hernando, I.; Turner, C.; Rohm, H. Composition and physicochemical properties of dried berry pomace. J. Sci. Food Agr. 2019, 99, 1284–1293. [Google Scholar] [CrossRef] [PubMed]
  37. Li, W.; Yang, R.; Ying, D.; Yu, J.; Sanguansri, L.; Augustin, M.A. Analysis of polyphenols in apple pomace: A comparative study of different extraction and hydrolysis procedures. Ind. Crop. Prod. 2020, 147, 112250. [Google Scholar] [CrossRef]
  38. Du, G.; Zhu, Y.; Wang, X.; Zhang, J.; Tian, C.; Liu, L.; Meng, Y.; Guo, Y. Phenolic composition of apple products and by-products based on cold pressing technology. J. Food Sci. Tech. 2019, 56, 1389–1397. [Google Scholar] [CrossRef]
  39. Ahmad, I.; Khalique, A.; Shahid, M.Q.; Ahid Rashid, A.; Faiz, F.; Ikram, M.A.; Ahmed, S.; Imran, M.; Khan, M.A.; Nadeem, M. Studying the Influence of Apple Peel Polyphenol Extract Fortification on the Characteristics of Probiotic Yoghurt. Plants 2020, 9, 77. [Google Scholar] [CrossRef] [Green Version]
  40. Zhang, J.; Wang, J.; Wang, G.; Wang, C.; Huang, R. Extraction and characterization of phenolic compounds and dietary fibres from banana peel. Acta Aliment. 2019, 48, 525–537. [Google Scholar] [CrossRef]
  41. Jridi, M.; Souissi, N.; Salem, M.B.; Ayadi, M.; Nasri, M.; Azabou, S. Tunisian date (Phoenix dactylifera L.) by-products: Characterization and potential effects on sensory, textural and antioxidant properties of dairy desserts. Food Chem. 2015, 188, 8–15. [Google Scholar] [CrossRef]
  42. Abu-Reidah, I.M.; Gil-Izquierdo, Á.; Medina, S.; Ferreres, F. Phenolic composition profiling of different edible parts and by-products of date palm (Phoenix dactylifera L.) by using HPLC-DAD-ESI/MSn. Food Res. Int. 2017, 100, 494–500. [Google Scholar] [CrossRef]
  43. Kitrytė, V.; Laurinavičienė, A.; Syrpas, M.; Pukalskas, A.; Venskutonis, P.R. Modeling and optimization of supercritical carbon dioxide extraction for isolation of valuable lipophilic constituents from elderberry (Sambucus nigra L.) pomace. J. CO2 Util. 2020, 35, 225–235. [Google Scholar] [CrossRef]
  44. Waldbauer, K.; Seiringer, G.N.; Sykora, C.; Dirsch, V.M.; Zehl, M.; Kopp, B. Evaluation of Apricot, Bilberry, and Elderberry Pomace Constituents and Their Potential To Enhance the Endothelial Nitric Oxide Synthase (eNOS) Activity. ACS Omega 2018, 3, 10545–10553. [Google Scholar] [CrossRef] [PubMed]
  45. Vital, A.C.P.; Santos, N.W.; Matumoto-Pintro, P.T.; da Silva Scapim, M.R.; Madrona, G.S. Ice cream supplemented with grape juice residue as a source of antioxidants. Int. J. Dairy Technol. 2018, 71, 183–189. [Google Scholar] [CrossRef]
  46. Pezzini, V.; Agostini, F.; Smiderle, F.; Touguinha, L.; Salvador, M.; Moura, S. Grape juice by-products extracted by ultrasound and microwave-assisted with different solvents: A rich chemical composition. Food Sci. Biotechnol. 2019, 28, 691–699. [Google Scholar] [CrossRef] [PubMed]
  47. Mendoza, L.; Navarro, F.; Melo, R.; Báez, F.; Cotoras, M. Characterization of Polyphenol Profile of Extracts Obtained From Grape Pomace And Synergistic Effect of These Extracts And Fungicides Against Botrytis Cinerea. J. Chil. Chem. Soc. 2019, 64, 4607–4609. [Google Scholar] [CrossRef]
  48. Coman, V.; Teleky, B.-E.; Mitrea, L.; Martău, G.A.; Szabo, K.; Călinoiu, L.-F.; Vodnar, D.C. Bioactive potential of fruit and vegetable wastes. In Advances in Food and Nutrition Research; Elsevier Academic Press: Cambridge, MA, USA, 2020; Volume 91, pp. 157–225. [Google Scholar]
  49. Jana, K.; Mantana, B.; Josef, B.; Pavel, H.; Jan, T.; Naděžda, V. Juices enriched with phenolic extracts from grapes. Czech J. Food Sci. 2018, 36, 261–267. [Google Scholar]
  50. Tian, Y.; Wang, Y.; Ma, Y.; Zhu, P.; He, J.; Lei, J. Optimization of subcritical water extraction of resveratrol from grape seeds by response surface methodology. Appl. Sci. 2017, 7, 321. [Google Scholar] [CrossRef] [Green Version]
  51. Mutua, J.K.; Imathiu, S.; Owino, W. Evaluation of the proximate composition, antioxidant potential, and antimicrobial activity of mango seed kernel extracts. Food Sci. Nutr. 2017, 5, 349–357. [Google Scholar] [CrossRef]
  52. Casarotti, S.N.; Borgonovi, T.F.; Batista, C.L.; Penna, A.L.B. Guava, orange and passion fruit by-products: Characterization and its impacts on kinetics of acidification and properties of probiotic fermented products. LWT Food Sci. Technol. 2018, 98, 69–76. [Google Scholar] [CrossRef] [Green Version]
  53. Viuda-Martos, M.; Fernandez-Lopez, J.; Sayas-Barbera, E.; Sendra, E.; Perez-Alvarez, J.A. Physicochemical characterization of the orange juice waste water of a citrus by-product. J. Food Process. Pres. 2011, 35, 264–271. [Google Scholar] [CrossRef]
  54. Singh, B.; Singh, J.P.; Kaur, A.; Singh, N. Phenolic composition, antioxidant potential and health benefits of citrus peel. Food Res. Int. 2020, 132, 109114. [Google Scholar] [CrossRef] [PubMed]
  55. Xi, W.; Zhang, Y.; Sun, Y.; Shen, Y.; Ye, X.; Zhou, Z. Phenolic composition of Chinese wild mandarin (Citrus reticulata Balnco.) pulps and their antioxidant properties. Ind. Crop. Prod. 2014, 52, 466–474. [Google Scholar] [CrossRef]
  56. Sir Elkhatim, K.A.; Elagib, R.A.; Hassan, A.B. Content of phenolic compounds and vitamin C and antioxidant activity in wasted parts of Sudanese citrus fruits. Food Sci. Nutr. 2018, 6, 1214–1219. [Google Scholar] [CrossRef] [PubMed]
  57. Khalil, M.; El-Wahed, A.; Shalaby, H.S.; Gaballa, A. Production of Feta Like Cheese Fortified With Pomegranate and Lemon Peels Extract as Natural Antioxidants. Zagazig J. Agr. Res. 2019, 46, 710–720. [Google Scholar]
  58. Selani, M.M.; Bianchini, A.; Ratnayake, W.S.; Flores, R.A.; Massarioli, A.P.; de Alencar, S.M.; Brazaca, S.G.C. Physicochemical, functional and antioxidant properties of tropical fruits co-products. Plant Food. Hum. Nutr. 2016, 71, 137–144. [Google Scholar] [CrossRef]
  59. Yılmaz, F.M.; Görgüç, A.; Karaaslan, M.; Vardin, H.; Ersus Bilek, S.; Uygun, Ö.; Bircan, C. Sour cherry by-products: Compositions, functional properties and recovery potentials–a review. Crit. Rev. Food Sci. Nutr. 2019, 59, 3549–3563. [Google Scholar] [CrossRef] [PubMed]
  60. Garcia-Amezquita, L.E.; Tejada-Ortigoza, V.; Serna-Saldivar, S.O.; Welti-Chanes, J. Dietary fiber concentrates from fruit and vegetable by-products: Processing, modification, and application as functional ingredients. Food Bioprocess Tech. 2018, 11, 1439–1463. [Google Scholar] [CrossRef]
  61. Maurya, A.K.; Pandey, R.K.; Rai, D.; Porwal, P.; Rai, D.C. Waste product of fruits and vegetables processing as a source of dietary fibre: A review. Trends Biosci. 2015, 8, 5129–5140. [Google Scholar]
  62. Zlatanović, S.; Ostojić, S.; Micić, D.; Rankov, S.; Dodevska, M.; Vukosavljević, P.; Gorjanović, S. Thermal behaviour and degradation kinetics of apple pomace flours. Thermochim. Acta 2019, 673, 17–25. [Google Scholar] [CrossRef]
  63. Nakov, G.; Brandolini, A.; Hidalgo, A.; Ivanova, N.; Jukić, M.; Komlenić, D.K.; Lukinac, J. Influence of apple peel powder addition on the physico-chemical characteristics and nutritional quality of bread wheat cookies. Food Sci. Technol. Int. 2020, 26, 574–582. [Google Scholar] [CrossRef]
  64. Ayar, A.; Siçramaz, H.; Öztürk, S.; Öztürk Yilmaz, S. Probiotic properties of ice creams produced with dietary fibres from by-products of the food industry. Int. J. Dairy Technol. 2018, 71, 174–182. [Google Scholar] [CrossRef]
  65. Huang, Y.-L.; Ma, Y.-S.; Tsai, Y.-H.; Chang, S.K. In vitro hypoglycemic, cholesterol-lowering and fermentation capacities of fiber-rich orange pomace as affected by extrusion. Int. J. Biol. Macromol. 2019, 124, 796–801. [Google Scholar] [CrossRef] [PubMed]
  66. Garcia-Amezquita, L.E.; Tejada-Ortigoza, V.; Pérez-Carrillo, E.; Serna-Saldívar, S.O.; Campanella, O.H.; Welti-Chanes, J. Functional and compositional changes of orange peel fiber thermally-treated in a twin extruder. LWT Food Sci. Technol. 2019, 111, 673–681. [Google Scholar] [CrossRef]
  67. Mrabet, A.; Hammadi, H.; Rodríguez-Gutiérrez, G.; Jiménez-Araujo, A.; Sindic, M. Date Palm Fruits as a Potential Source of Functional Dietary Fiber: A Review. Food Sci. Technol. Res. 2019, 25, 1–10. [Google Scholar] [CrossRef]
  68. Essa, R.; Mohamed, E. Improvement of functional and technological characteristics of spaghetti by the integration of pomegranate peels powder. Am. J. Food Tech. 2018, 13, 1–7. [Google Scholar] [CrossRef]
  69. Khan, A.; Khan, S.; Jan, A. Health complication caused by protein deficiency. J. Food Sci. Nutr. 2017, 1, 645–647. [Google Scholar] [CrossRef]
  70. Ververi, M.; Goula, A.M. Pomegranate peel and orange juice by-product as new biosorbents of phenolic compounds from olive mill wastewaters. Chem. Eng. Process. Process Intensif. 2019, 138, 86–96. [Google Scholar] [CrossRef]
  71. Morales-Contreras, B.; Wicker, L.; Rosas-Flores, W.; Contreras-Esquivel, J.; Gallegos-Infante, J.; Reyes-Jaquez, D.; Morales-Castro, J. Apple pomace from variety “Blanca de Asturias” as sustainable source of pectin: Composition, rheological, and thermal properties. LWT Food Sci. Technol. 2020, 117, 108641. [Google Scholar] [CrossRef]
  72. Deng, Z.; Pan, Y.; Chen, W.; Chen, W.; Yun, Y.; Zhong, Q.; Zhang, W.; Chen, H. Effects of cultivar and growth region on the structural, emulsifying and rheological characteristic of mango peel pectin. Food Hydrocolloid. 2020, 103, 105707. [Google Scholar] [CrossRef]
  73. Gurumallesh, P.; Ramakrishnan, B.; Dhurai, B. A novel metalloprotease from banana peel and its biochemical characterization. Int. J. Biol. Macromol. 2019, 134, 527–535. [Google Scholar] [CrossRef]
  74. Kırbaş, Z.; Kumcuoglu, S.; Tavman, S. Effects of apple, orange and carrot pomace powders on gluten-free batter rheology and cake properties. J. Food Sci. Tech. 2019, 56, 914–926. [Google Scholar] [CrossRef] [PubMed]
  75. Lachos-Perez, D.; Baseggio, A.M.; Torres-Mayanga, P.C.; Ávila, P.F.; Tompsett, G.; Marostica, M.; Goldbeck, R.; Timko, M.T.; Rostagno, M.; Martinez, J. Sequential subcritical water process applied to orange peel for the recovery flavanones and sugars. J. Supercrit. Fluid. 2020, 160, 104789. [Google Scholar] [CrossRef]
  76. Iftikhar, M.; Wahab, S.; ul Haq, N.; Malik, S.N.; Amber, S.; Taran, N.U.; Rehman, S.U. 12. Utilization of citrus plant waste (peel) for the development of food product. Pure Appl. Biol. 2019, 8, 1991–1998. [Google Scholar] [CrossRef]
  77. Wang, Q.; Xiong, Y.L. Processing, nutrition, and functionality of hempseed protein: A review. Compr. Rev. Food Sci. Food Saf. 2019, 18, 936–952. [Google Scholar] [CrossRef] [Green Version]
  78. Dhillon, G.S. Protein Byproducts: Transformation from Environmental Burden Into Value-Added Products; Academic Press: Cambridge, MA, USA, 2016. [Google Scholar]
  79. Marcet, I.; Álvarez, C.; Paredes, B.; Díaz, M. The use of sub-critical water hydrolysis for the recovery of peptides and free amino acids from food processing wastes. Review of sources and main parameters. Waste Manag. 2016, 49, 364–371. [Google Scholar] [CrossRef] [PubMed]
  80. Prandi, B.; Faccini, A.; Lambertini, F.; Bencivenni, M.; Jorba, M.; Van Droogenbroek, B.; Bruggeman, G.; Schöber, J.; Petrusan, J.; Elst, K. Food wastes from agrifood industry as possible sources of proteins: A detailed molecular view on the composition of the nitrogen fraction, amino acid profile and racemisation degree of 39 food waste streams. Food Chem. 2019, 286, 567–575. [Google Scholar] [CrossRef]
  81. Baeza-Jiménez, R.; López-Martínez, L.X.; García-Varela, R.; García, H.S. Lipids in Fruits and Vegetables: Chemistry and Biological Activities. Fruit Vegetable Phytochem. Chem. Hum. Health 2017, 2, 423. [Google Scholar]
  82. Yahia, E.M. Postharvest physiology and biochemistry of fruits and vegetables. In Postharvest Physiology and Biochemistry of Fruits and Vegetables, 1st ed.; Yahia, E.M., Carrillo-López, A., Eds.; Woodhead Publishing: Duxford, UK, 2019; pp. 1–17. [Google Scholar]
  83. Raihana, A.N.; Marikkar, J.; Amin, I.; Shuhaimi, M. A review on food values of selected tropical fruits’ seeds. Int. J. Food Prop. 2015, 18, 2380–2392. [Google Scholar] [CrossRef]
  84. Natalello, A.; Priolo, A.; Valenti, B.; Codini, M.; Mattioli, S.; Pauselli, M.; Puccio, M.; Lanza, M.; Stergiadis, S.; Luciano, G. Dietary pomegranate by-product improves oxidative stability of lamb meat. Meat Sci. 2020, 162, 108037. [Google Scholar] [CrossRef]
  85. Lyu, F.; Luiz, S.F.; Azeredo, D.R.P.; Cruz, A.G.; Ajlouni, S.; Ranadheera, C.S. Apple pomace as a functional and healthy ingredient in food products: A Review. Processes 2020, 8, 319. [Google Scholar] [CrossRef] [Green Version]
  86. Bender, A.B.B.; Speroni, C.S.; Moro, K.I.B.; Morisso, F.D.P.; dos Santos, D.R.; da Silva, L.P.; Penna, N.G. Effects of micronization on dietary fiber composition, physicochemical properties, phenolic compounds, and antioxidant capacity of grape pomace and its dietary fiber concentrate. LWT Food Sci. Technol. 2020, 117, 108652. [Google Scholar] [CrossRef]
  87. Martínez-Trujillo, M.A.; Bautista-Rangel, K.; García-Rivero, M.; Martínez-Estrada, A.; Cruz-Díaz, M.R. Enzymatic saccharification of banana peel and sequential fermentation of the reducing sugars to produce lactic acid. Bioproc. Biosyst. Eng. 2020, 43, 413–427. [Google Scholar] [CrossRef] [PubMed]
  88. Ahmad, A.; Imtiaz, H. Chemical Composition of Date Pits: Potential to Extract and Characterize the Lipid Fraction. In Sustainable Agriculture Reviews; Naushad, M., Lichtfouse, E., Eds.; Springer: Cham, Germany, 2019; Volume 34, pp. 55–77. [Google Scholar]
  89. Yukui, R.; Wenya, W.; Rashid, F.; Qing, L. Fatty acids composition of apple and pear seed oils. Int. J. Food Prop. 2009, 12, 774–779. [Google Scholar] [CrossRef] [Green Version]
  90. Ben-Othman, S.; Jõudu, I.; Bhat, R. Bioactives from agri-food wastes: Present insights and future challenges. Molecules 2020, 25, 510. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  91. Mildner-Szkudlarz, S.; Różańska, M.; Siger, A.; Kowalczewski, P.Ł.; Rudzińska, M. Changes in chemical composition and oxidative stability of cold-pressed oils obtained from by-product roasted berry seeds. LWT Food Sci. Technol. 2019, 111, 541–547. [Google Scholar] [CrossRef]
  92. Regis, S.A.; Resende, E.D.d.; Antoniassi, R. Oil quality of passion fruit seeds subjected to a pulp-waste purification process. Cienc. Rural 2015, 45, 977–984. [Google Scholar] [CrossRef] [Green Version]
  93. Wadhwa, M.; Bakshi, M.P.S. Application of waste-derived proteins in the animal feed industry. In Protein Byproducts; Dhillon, G., Ed.; Academic Press: Oxford, UK, 2016; pp. 161–192. [Google Scholar]
  94. Tayengwa, T.; Chikwanha, O.C.; Dugan, M.E.; Mutsvangwa, T.; Mapiye, C. Influence of feeding fruit by-products as alternative dietary fibre sources to wheat bran on beef production and quality of Angus steers. Meat Sci. 2020, 161, 107969. [Google Scholar] [CrossRef] [PubMed]
  95. Yitbarek, M. Some Selected Vegetable and Fruit Wastes for Poultry Feed. J. Vet. Anim. Res. 2019, 1, 101. [Google Scholar]
  96. Azizi, M.; Seidavi, A.; Ragni, M.; Laudadio, V.; Tufarelli, V. Practical applications of agricultural wastes in poultry feeding in Mediterranean and Middle East regions. Part 1: Citrus, grape, pomegranate and apple wastes. World. Poultry Sci. J. 2018, 74, 489–498. [Google Scholar] [CrossRef]
  97. Caipang, C.M.A.; Mabuhay-Omar, J.; Gonzales-Plasus, M.M. Plant and fruit waste products as phytogenic feed additives in aquaculture. AACL Bioflux 2019, 12, 261–268. [Google Scholar]
  98. Andrade, M.A.; Lima, V.; Silva, A.S.; Vilarinho, F.; Castilho, M.C.; Khwaldia, K.; Ramos, F. Pomegranate and grape by-products and their active compounds: Are they a valuable source for food applications? Trends Food Sci. Tech. 2019, 86, 68–84. [Google Scholar] [CrossRef]
  99. Chiralt, A.; Menzel, C.; Hernandez-García, E.; Collazo, S.; Gonzalez-Martinez, C. Use of by-products in edible coatings and biodegradable packaging materials for food preservation. In Sustainability of the Food System; Betoret, N., Betoret, E., Eds.; Elsevier: Amsterdam, The Netherlands, 2020; pp. 101–127. [Google Scholar]
  100. Struck, S.; Straube, D.; Zahn, S.; Rohm, H. Interaction of wheat macromolecules and berry pomace in model dough: Rheology and microstructure. J. Food Eng. 2018, 223, 109–115. [Google Scholar] [CrossRef]
  101. Šaponjac, V.T.; Ćetković, G.; Čanadanović-Brunet, J.; Pajin, B.; Djilas, S.; Petrović, J.; Lončarević, I.; Stajčić, S.; Vulić, J. Sour cherry pomace extract encapsulated in whey and soy proteins: Incorporation in cookies. Food Chem. 2016, 207, 27–33. [Google Scholar] [CrossRef] [PubMed]
  102. Kowalska, H.; Czajkowska, K.; Cichowska, J.; Lenart, A. What’s new in biopotential of fruit and vegetable by-products applied in the food processing industry. Trends Food Sci. Tech. 2017, 67, 150–159. [Google Scholar] [CrossRef]
  103. Anal, A.K. Food Processing By-Products and Their Utilization; John Wiley & Sons: Hoboken, NJ, USA, 2017. [Google Scholar]
  104. EU. Regulation (EC) No 1333/2008 of the European Parliament and of the Council of 16 December 2008 on food additives (1). Off. J. Eur. Union 2009, 51, 16–33. [Google Scholar]
  105. EU. Commission Directive 2008/84/EC of 27 August 2008 laying down specific purity criteria on food additives other than colours and sweeteners (Codified version). Off. J. Eur. Union 2009, 1–175. [Google Scholar]
  106. Saltmarsh, M. Food Additive Regulations in Europe. In Saltmarsh’s Essential Guide to Food Additives; Royal Society of Chemistry: London, UK, 2020; pp. 40–51. [Google Scholar]
  107. Corrales, M.; Toepfl, S.; Butz, P.; Knorr, D.; Tauscher, B. Extraction of anthocyanins from grape by-products assisted by ultrasonics, high hydrostatic pressure or pulsed electric fields: A comparison. Innov. Food Sci. Emerg. Technol. 2008, 9, 85–91. [Google Scholar] [CrossRef]
  108. Ajila, C.; Naidu, K.; Bhat, S.; Rao, U.P. Bioactive compounds and antioxidant potential of mango peel extract. Food Chem. 2007, 105, 982–988. [Google Scholar] [CrossRef]
  109. Faustino, M.; Veiga, M.; Sousa, P.; Costa, E.M.; Silva, S.; Pintado, M. Agro-food byproducts as a new source of natural food additives. Molecules 2019, 24, 1056. [Google Scholar] [CrossRef] [Green Version]
  110. Bordiga, M.; Travaglia, F.; Locatelli, M. Valorisation of grape pomace: An approach that is increasingly reaching its maturity–A review. Int. J. Food Sci. Technol. 2019, 54, 933–942. [Google Scholar] [CrossRef]
  111. Martins, Z.; Pinho, O.; Ferreira, I. Food industry by-products used as functional ingredients of bakery products. Trends Food Sci. Tech. 2017, 67, 106–128. [Google Scholar] [CrossRef]
  112. Khoozani, A.A.; Birch, J.; Bekhit, A.E.-D.A. Production, application and health effects of banana pulp and peel flour in the food industry. J. Food Sci. Tech. 2019, 56, 548–559. [Google Scholar] [CrossRef] [PubMed]
  113. Mildner-Szkudlarz, S.; Bajerska, J.; Górnaś, P.; Segliņa, D.; Pilarska, A.; Jesionowski, T. Physical and bioactive properties of muffins enriched with raspberry and cranberry pomace powder: A promising application of fruit by-products rich in biocompounds. Plant Food. Hum. Nutr. 2016, 71, 165–173. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  114. Cuervo, A.; Valdés, L.; Salazar, N.; de los Reyes-Gavilán, C.G.; Ruas-Madiedo, P.; Gueimonde, M.; Gonzalez, S. Pilot study of diet and microbiota: Interactive associations of fibers and polyphenols with human intestinal bacteria. J. Agr. Food Chem. 2014, 62, 5330–5336. [Google Scholar] [CrossRef]
  115. Shreiner, A.B.; Kao, J.Y.; Young, V.B. The gut microbiome in health and in disease. Curr. Opin. Gastroen. 2015, 31, 69. [Google Scholar] [CrossRef]
  116. Turnbaugh, P.J.; Ley, R.E.; Mahowald, M.A.; Magrini, V.; Mardis, E.R.; Gordon, J.I. An obesity-associated gut microbiome with increased capacity for energy harvest. Nature 2006, 444, 1027. [Google Scholar] [CrossRef]
  117. Marchesi, J.R.; Dutilh, B.E.; Hall, N.; Peters, W.H.; Roelofs, R.; Boleij, A.; Tjalsma, H. Towards the human colorectal cancer microbiome. PLoS ONE 2011, 6, e20447. [Google Scholar] [CrossRef] [Green Version]
  118. Seksik, P. Gut microbiota and IBD. Gastroen. Clin. Biol. 2010, 34, S44–S51. [Google Scholar] [CrossRef]
  119. Wang, L.; Christophersen, C.T.; Sorich, M.J.; Gerber, J.P.; Angley, M.T.; Conlon, M.A. Low relative abundances of the mucolytic bacterium Akkermansia muciniphila and Bifidobacterium spp. in feces of children with autism. Appl. Environ. Microbiol. 2011, 77, 6718–6721. [Google Scholar] [CrossRef] [Green Version]
  120. Williams, B.L.; Hornig, M.; Parekh, T.; Lipkin, W.I. Application of novel PCR-based methods for detection, quantitation, and phylogenetic characterization of Sutterella species in intestinal biopsy samples from children with autism and gastrointestinal disturbances. MBio 2012, 3, e00261-11. [Google Scholar] [CrossRef] [Green Version]
  121. Barbut, F.; Joly, F. Le microbiote intestinal: Équilibre et dysbiose. Hépato-Gastro Oncol. Dig. 2010, 17, 511–520. [Google Scholar]
  122. Conlon, M.A.; Bird, A.R. The impact of diet and lifestyle on gut microbiota and human health. Nutrients 2015, 7, 17. [Google Scholar] [CrossRef] [PubMed]
  123. Holscher, H.D. Dietary fiber and prebiotics and the gastrointestinal microbiota. Gut Microbes 2017, 8, 172–184. [Google Scholar] [CrossRef] [PubMed]
  124. Chen, J.-P.; Chen, G.-C.; Wang, X.-P.; Qin, L.; Bai, Y. Dietary fiber and metabolic syndrome: A meta-analysis and review of related mechanisms. Nutrients 2018, 10, 24. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  125. Fujii, H.; Iwase, M.; Ohkuma, T.; Ogata-Kaizu, S.; Ide, H.; Kikuchi, Y.; Idewaki, Y.; Joudai, T.; Hirakawa, Y.; Uchida, K. Impact of dietary fiber intake on glycemic control, cardiovascular risk factors and chronic kidney disease in Japanese patients with type 2 diabetes mellitus: The Fukuoka Diabetes Registry. Nutr. J. 2013, 12, 159. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  126. O’Keefe, S.J. The association between dietary fibre deficiency and high-income lifestyle-associated diseases: Burkitt’s hypothesis revisited. Lancet Gastroenterol. Hepatol. 2019, 4, 984–996. [Google Scholar] [CrossRef]
  127. O’keefe, S.J. Diet, microorganisms and their metabolites, and colon cancer. Nat. Rev. Gastro. Hepat. 2016, 13, 691. [Google Scholar] [CrossRef]
  128. Yang, J.; Yu, J. The association of diet, gut microbiota and colorectal cancer: What we eat may imply what we get. Protein Cell 2018, 9, 474–487. [Google Scholar] [CrossRef] [Green Version]
  129. Shin, S.; Saito, E.; Sawada, N.; Ishihara, J.; Takachi, R.; Nanri, A.; Shimazu, T.; Yamaji, T.; Iwasaki, M.; Sasazuki, S. Dietary patterns and colorectal cancer risk in middle-aged adults: A large population-based prospective cohort study. Clin. Nutr. 2018, 37, 1019–1026. [Google Scholar] [CrossRef]
  130. Tuohy, K.M.; Conterno, L.; Gasperotti, M.; Viola, R. Up-regulating the human intestinal microbiome using whole plant foods, polyphenols, and/or fiber. J. Agr. Food Chem. 2012, 60, 8776–8782. [Google Scholar] [CrossRef]
  131. Bosaeus, I. Fibre effects on intestinal functions (diarrhoea, constipation and irritable bowel syndrome). Clin. Nutr. Suppl. 2004, 1, 33–38. [Google Scholar] [CrossRef]
  132. Seo, Y.S.; Lee, H.-B.; Kim, Y.; Park, H.-Y. Dietary Carbohydrate Constituents Related to Gut Dysbiosis and Health. Microorganisms 2020, 8, 427. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  133. Jha, R.; Fouhse, J.M.; Tiwari, U.P.; Li, L.; Willing, B.P. Dietary fiber and intestinal health of monogastric animals. Front. Vet. Sci. 2019, 6, 48. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  134. Laparra, J.M.; Sanz, Y. Interactions of gut microbiota with functional food components and nutraceuticals. Pharmacol. Res. 2010, 61, 219–225. [Google Scholar] [CrossRef] [Green Version]
  135. Saini, R.K.; Keum, Y.-S. Omega-3 and omega-6 polyunsaturated fatty acids: Dietary sources, metabolism, and significance—A review. Life Sci. 2018, 203, 255–267. [Google Scholar] [CrossRef]
  136. Wichansawakun, S.; Buttar, H.S. Antioxidant Diets and Functional Foods Promote Healthy Aging and Longevity Through Diverse Mechanisms of Action. In The Role of Functional Food Security in Global Health; Singh, R.B., Watson, R.R., Takahashi, T., Eds.; Academic Press: Cambridge, MA, USA, 2019; pp. 541–563. [Google Scholar]
  137. Tejada-Ortigoza, V.; Garcia-Amezquita, L.E.; Kazem, A.E.; Campanella, O.H.; Cano, M.P.; Hamaker, B.R.; Serna-Saldívar, S.O.; Welti-Chanes, J. In vitro fecal fermentation of high pressure-treated fruit peels used as dietary fiber sources. Molecules 2019, 24, 697. [Google Scholar] [CrossRef] [Green Version]
  138. De Souza, C.B.; Jonathan, M.; Saad, S.M.I.; Schols, H.A.; Venema, K. Degradation of fibres from fruit by-products allows selective modulation of the gut bacteria in an in vitro model of the proximal colon. J. Funct. Foods 2019, 57, 275–285. [Google Scholar] [CrossRef]
  139. Chedea, V.S.; Palade, L.M.; Marin, D.E.; Pelmus, R.S.; Habeanu, M.; Rotar, M.C.; Gras, M.A.; Pistol, G.C.; Taranu, I. Intestinal absorption and antioxidant activity of grape pomace polyphenols. Nutrients 2018, 10, 588. [Google Scholar] [CrossRef] [Green Version]
  140. Maurer, L.H.; Cazarin, C.B.B.; Quatrin, A.; Minuzzi, N.M.; Costa, E.L.; Morari, J.; Velloso, L.A.; Leal, R.F.; Rodrigues, E.; Bochi, V.C. Grape peel powder promotes intestinal barrier homeostasis in acute TNBS-colitis: A major role for dietary fiber and fiber-bound polyphenols. Food Res. Int. 2019, 123, 425–439. [Google Scholar] [CrossRef]
  141. Bhardwaj, V.; Bhardwaj, R.; Krishna, R.; Sharma, P. Investigation of Gastroprotective Potential of Grape Seed Proanthocyanidin Exract in Experimental Models of Gastric Ulcer, in Wistar Rats. J. Gastrointest. Dig. Syst. 2018, 8, 561. [Google Scholar] [CrossRef]
  142. Giuliani, C.; Marzorati, M.; Daghio, M.; Franzetti, A.; Innocenti, M.; Van de Wiele, T.; Mulinacci, N. Effects of Olive and Pomegranate By-Products on Human Microbiota: A Study Using the SHIME® In Vitro Simulator. Molecules 2019, 24, 3791. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  143. Zhao, R.; Long, X.; Yang, J.; Du, L.; Zhang, X.; Li, J.; Hou, C. Pomegranate peel polyphenols reduce chronic low-grade inflammatory responses by modulating gut microbiota and decreasing colonic tissue damage in rats fed a high-fat diet. Food Funct. 2019, 10, 8273–8285. [Google Scholar] [CrossRef] [PubMed]
  144. Mastrogiovanni, F.; Mukhopadhya, A.; Lacetera, N.; Ryan, M.T.; Romani, A.; Bernini, R.; Sweeney, T. Anti-inflammatory effects of pomegranate peel extracts on in vitro human intestinal caco-2 cells and ex vivo porcine colonic tissue explants. Nutrients 2019, 11, 548. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  145. Aboul Naser, A.; Younis, E.; El-Feky, A.; Elbatanony, M.; Hamed, M. Management of Citrus sinensis peels for protection and treatment against gastric ulcer induced by ethanol in rats. Biomarkers 2020, 25, 349–359. [Google Scholar] [CrossRef] [PubMed]
  146. Carrasco-Pozo, C.; Speisky, H.; Brunser, O.; Pastene, E.; Gotteland, M. Apple peel polyphenols protect against gastrointestinal mucosa alterations induced by indomethacin in rats. J. Agr. Food Chem. 2011, 59, 6459–6466. [Google Scholar] [CrossRef]
  147. Mousa, W.K.; Afifi, M.S.; Zaghloul, M.G.; El-Sharkawy, S.H. Apple Pomace; A source of Pharmaceuticals. J. Am. Sci. 2012, 8, 1114–1119. [Google Scholar]
  148. Waldbauer, K.; McKinnon, R.; Kopp, B. Apple pomace as potential source of natural active compounds. Planta Med. 2017, 83, 994–1010. [Google Scholar] [CrossRef] [Green Version]
  149. Abboud, K.Y.; da Luz, B.B.; Dallazen, J.L.; de Paula Werner, M.F.; Cazarin, C.B.B.; Junior, M.R.M.; Iacomini, M.; Cordeiro, L.M. Gastroprotective effect of soluble dietary fibres from yellow passion fruit (Passiflora edulis f. flavicarpa) peel against ethanol-induced ulcer in rats. J. Funct. Foods 2019, 54, 552–558. [Google Scholar] [CrossRef]
  150. Athaydes, B.R.; Alves, G.M.; de Assis, A.L.E.M.; Gomes, J.V.D.; Rodrigues, R.P.; Campagnaro, B.P.; Nogueira, B.V.; Silveira, D.; Kuster, R.M.; Pereira, T.M.C. Avocado seeds (Persea americana Mill.) prevents indomethacin-induced gastric ulcer in mice. Food Res. Int. 2019, 119, 751–760. [Google Scholar] [CrossRef]
  151. Oluwole, F.S.; Onasanwo, S.A.; Olaleye, S.B. Effects of aqueous and methanolic extracts of Persea americana leaf (Avocado pear) on gastric acid secretion in male albino rats. Eur. J. Scient. Res. 2011, 61, 474–481. [Google Scholar]
  152. Nuraddin, S.M.; Amin, Z.A.; Sofi, S.H.; Osman, S. Antibacterial and anti-ulcerogenic effects of Punicagranatum peel extract against ethanol-induced acute gastric lesion in rats. Zanco J. Med. Sci. 2019, 23, 308–314. [Google Scholar] [CrossRef]
  153. Selmi, S.; Rtibi, K.; Grami, D.; Sebai, H.; Marzouki, L. Protective effects of orange (Citrus sinensis L.) peel aqueous extract and hesperidin on oxidative stress and peptic ulcer induced by alcohol in rat. Lipids Health Dis. 2017, 16, 152. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  154. Pastene, E.; Speisky, H.; García, A.; Moreno, J.; Troncoso, M.; Figueroa, G. In vitro and in vivo effects of apple peel polyphenols against Helicobacter pylori. J. Agr. Food Chem. 2010, 58, 7172–7179. [Google Scholar] [CrossRef] [PubMed]
  155. Bianchi, F.; Lopes, N.P.; Adorno, M.A.T.; Sakamoto, I.K.; Genovese, M.I.; Saad, S.M.I.; Sivieri, K. Impact of combining acerola by-product with a probiotic strain on a gut microbiome model. Int. J. Food Sci. Nutr. 2019, 70, 182–194. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  156. Batista, K.S.; Alves, A.F.; dos Santos Lima, M.; da Silva, L.A.; Lins, P.P.; de Sousa Gomes, J.A.; Silva, A.S.; Toscano, L.T.; de Albuquerque Meireles, B.R.L.; de Magalhães Cordeiro, A.M.T. Beneficial effects of consumption of acerola, cashew or guava processing by-products on intestinal health and lipid metabolism in dyslipidaemic female Wistar rats. Br. J. Nutr. 2018, 119, 30–41. [Google Scholar] [CrossRef] [Green Version]
  157. Sen, A.; Manuel, S.; Kale, R. Fruit waste pectin in enhancing the establishment of probiotic bacteria. J. Nutr. Health Food Eng. 2014, 1, 124–126. [Google Scholar]
  158. Fernández-López, J.; Fernández-Ginés, J.; Aleson-Carbonell, L.; Sendra, E.; Sayas-Barberá, E.; Pérez-Alvarez, J. Application of functional citrus by-products to meat products. Trends Food Sci. Technol. 2004, 15, 176–185. [Google Scholar] [CrossRef]
Table 1. Content of phenolic compounds in some fruit by-products.
Table 1. Content of phenolic compounds in some fruit by-products.
Fruit by-ProductTPCPhenolic CompoundsReferences
Pomegranate peel139.4 *Punicalagin A, punicalagin B, catechin, gallic acid, ellagic acid[30,31,32]
420.6 ***
Pomegranate pomace134.8 **Gallic acid, catechin, ellagic acid, rosmarinic acid, hesperidin, p-coumaric acid, chlorogenic acid[33,34]
Rowanberry pomace167.4 ****Cyanidin, Chlorogenic acid, quercetin, kaempferol[35,36]
Apple pomace13.8 *Hydroxycinnamic acids, Hydroxycinnamates, phloretin glycosides, quercetin glycosides, catechins, procyanidins[37,38]
Apple peel34.3 *Gallic acid, caffeic acid, vanillic acid, catechin, epicatechin gallate, chlorogenic acids, phloridzin, rutin[38,39]
Banana peel29.2 *Epicatechin, rutin, hydroxybenzoic acid, myricetin, ferulic acid, chlorogenic acid, gallic acid[40]
Date by-products4.4 *Quercetin, luteolin, apigenin, chrysoeriol, kaempferol, isorhamnetin, malonyl derivatives[41,42]
Elderberry pomace4.7 * Cyanidin, rutin, oleanolic acid, ursolic acid, linoleic acid[43,44]
Grape juice by-product23.4 *Benzoic and hydroxycinnamic derivatives, catechins, flavanols, anthocyanins, tannins, proanthocyanidins[45,46]
Grape pomace142.1 *Phenolic acids (ferulic, p-coumaric, caffeic, gallic, vanillic, p-hydroxybenzoic), flavanols (proanthocyanidins), flavonols (kaempferol, quercetin, myricetin), stilbenes (resveratrol, piceid, astringin), anthocyanins[47,48]
Grape seed74.0 *Gallic acid, caftaric acid, catechin, epicatechin,
epicatechin gallate, procyanidins, resveratrol
[48,49,50]
Mango kernel72.1 *Gallates, gallotannins, gallic acid, ellagic acid and its derivatives[48,51]
Orange by-product4.21 *Caffeic acid, Ferulic acid, p-Coumaric acid, Eriocitrin, Narirutin, Hesperidin, Neohesperidin[52,53]
Orange peel65.7 *Caffeic acid, p-coumaric acid, naringin, kaempferol, neohesperidin, rutin[54]
Orange pulp22.3 *Flavonone (Eriocitrin, Narirutin, Hesperidin, Didymin…), Flavone (Quercitrin, Nobiletin…), Kaemperol, Benzoic acids, Cinnamic acids, Chlorogenic acid,[55]
Lemon peel49.8 *Caffeic acid, Coumaric acid, Ferulic acid, Sinapic acid[56,57]
Passion fruit by-products3.84 *p-coumaric acid, Epicatechin[52,58]
Guava by-product19.9 *Resveratrol, coumarin[23]
Cherry by-product91.3 *Flavonoids, anthocyanidins, stilbenes, resveratrol, quercetin, gallic acid[59]
* mg gallic acid eq./g extract DW; ** mg gallic acid eq./g liquid extract; *** mg tannic acid eq./g extract DW; **** mg catechin eq./g extract DW.
Table 2. Dietary fibre content in some fruit by-products.
Table 2. Dietary fibre content in some fruit by-products.
Fruit by-ProductTDF (g/100 DW)References
Apple Pomace45.0[62]
Apple Peel43.9[63]
Apple by product75.8[64]
Banana Peel49.6[40]
Orange Pomace63.8[65]
Orange Peel48.7[66]
Orange by-product58.2[52]
Passion fruit by-product64.2[52]
Guava by-product89.8[52]
Date seeds73.5[67]
Grape fruit by-product67.2[64]
Apricot by-product72.3[64]
Pomegranate Peel56.2[68]
Pomegranate pomace43.5[34]
Table 3. Protein content in some fruit by-products.
Table 3. Protein content in some fruit by-products.
Fruit by-ProductProtein (%)References
Orange by-product5.2[52]
Passion fruit by-product12.6[52]
Guava by-product2.1[52]
Date seeds6.0[67]
Pomegranate peels12.9[70]
Pomegranate pomace11.1[34]
Apple Pomace4.8[71]
Apple Peel3.2[63]
Mango peel4.3[72]
Banana Peel7.0[73]
Orange juice by-product18.9[70]
Orange Pomace9.8[74]
Orange Peel6.8[75]
Citrus peel4.5[76]
Grape fruit by-product5.8[13]
Table 4. Lipid content in some fruit by-products.
Table 4. Lipid content in some fruit by-products.
Fruit by-ProductLipid (%)References
Orange juice by-product8.4[70]
Pomegranate peel3.2[70]
Pomegranate by-product4.0[84]
Passion fruit by-product8.0[52]
Guava by-product1.2[52]
Apple Pomace4.2[85]
Apple Peel10.1[63]
Berry pomace20.2[36]
Grape fruit pomace8.5[86]
Banana Peel2.0[87]
Date seeds 8.8[88]
Table 5. Application of some fruit by-products into food products.
Table 5. Application of some fruit by-products into food products.
Fruit by-ProductFood ProductsEffectsReferences
Apple pomaceBakery products, cakes, cookies, meat products, yoghurt, jams, juice
-
Source of dietary fibre and polyphenols
-
Enhance nutritional value
-
Natural stabilizer and texturizer
[85]
Grape pomace and seedsBakery products, yoghurt, Meat product
-
Dietary fiber supplement
-
Modify the formulation and extend shelf life of meat
-
Reduction of meat lipid oxidation
[110]
Banana peelBakery products, Pasta, Confectionaries
-
High gluten bread
-
High ash, dietary fibre and total phenolic content
-
Increase of viscosity, volume, gumminess and odour acceptance
-
Increase in foaming stability and
-
overall acceptability
[111,112]
Mango by-productBakery products, biscuits
-
High content of dietary fiber and polyphenols
-
Increase of breaking strength, weight and density
-
Good sensory acceptability
[60,111]
Orange by-productBiscuits, sausage, Fermented milk, Ice cream, Pasta products
-
Wheat flour or starch substitute
-
Improve nutritional value
-
Reduce the caloric value
-
Good sensory acceptability
[60]
Peach by-productMuffins
-
Fat substitute
-
Enhance Nutritional value (dietary fiber)
-
Reduce the caloric value
-
Increase the hardness
-
Acceptable sensory evaluation
[60]
Raspberry and Cranberry by productsMuffins
-
Healthy nutritional profiles.
-
Improvement of viscoelastic properties and texture profile
[113]
Table 6. Effects of some fruit by-products on intestinal function.
Table 6. Effects of some fruit by-products on intestinal function.
by-ProductExtractExtraction TechniqueDoseEffectReferences
Yellow passion fruit (Passiflora edulis) peelSoluble dietary fibresEnzymatic-gravimetric method0.1, 1 and 10 mg/kg (oral pre-treatment)
-
Reduction of ethanol-induced gastric lesions in 72.25%, 79.23% and 87.17%
-
Avoiding depletion of GSH levels in 52.20%, 41.91% and 50.33%
-
Preventing gastric wall mucus in 26.32%, 25.03% and 31.00%
[149]
1 mg/kg (intraperitoneal route)
-
Reduction of gastric lesion area in 72.56%
-
Preventing depletion of gastric wall mucus in 21.24% and the GSH levels in 40.81%
Avocado (Persea americana Mill.) seedsEthyl acetate extract (SEAP)Hydroalcoholic extraction with 70% ethylic alcohol10, 35 and 75 mg/kg (oral gavage)
-
Significant ulcer index (UI) (2.89 ± 1.75, 2.4 ± 1.24 and 1.51 ± 0.72 for 10, 35 and 75 (UI) mg/kg, respectively) compared to lansoprazole which is a classic proton pump inhibitor (3.53 ± 1.50 UI)
-
Treatment with SEAP showed 92% of protection, while lansoprazole treatment showed 81% of protection
-
Increase of mucus production by the stomach mucosal cells of about 2.38 ± 0.55 times compared to the control
[150]
Avocado (Persea Americana) leavesAqueous and methanolic extracts
-
Water extraction (72 h)
-
Soxhlet (24 h/MeOH)
200 mg/kg (intraperitoneal injection)Significant inhibition of histamine-stimulated acid secretion through the action on H2-receptors[151]
Pomegranate (Punica granatum) peelsEthanol extractUltrasonic extraction with 99% ethanol500 mg/kg (Oral)
-
Significant protection of stomach mucosal layer from gastric ulcer induced by ethanol.
-
Stomach mucosal layer protection was improved by the increase in the dose.
[152]
Orange (Citrus sinensis L.) peelsFlavonoidsExtraction with 80% aqueous methanol100, 200
and 400 mg/kg
-
Correction of the enhanced gastric lipid peroxidation
-
Reduction of TNF-α (tumor necrosis factor alpha) production
-
Reduction of gastric DNA fragmentation and gastric COX-2 (cyclooxygenase-2) expression
[153]
Apple (Malus domestica cv.) peelsPolyphenol-rich extractRetention on absorber resin Sepabeads SP-850150 and 300 mg/kg/day (Oral ingestion)Avert the initial attachment of Helicobacter pylori to the antral mucosa and suppress inflammation[154]
Apple (Malus domestica) pomace PectinHot water-acid extraction25 mg/kg (oral)
-
Prevention of the formation of gastric mucosa lesions.
-
Lining the surface of the stomach
-
Improving the resistance of the gastroduoden mucosa
[147]
Grape seedsProanthocyanidinsCommercial product100 mg/kg
-
Significant decrease in ulcer index and TBARS level (dose dependent)
-
decrease in ulcer index and gastric acidity in pylorus ligation models
-
Reduction in MDA (malondialdehyde) levels
-
Decrease in the elevated levels of nitrite/nitrate, which are involved in the formation of intestinal inflammation
[141]
Orange bagasse and passion fruit peelsAlcohol insoluble solidsEnzymatic extraction/Extraction with 80% aqueous EtOH (4°/1 h)
-
Energy source for bacteria located in the distal colon
-
Could be considered as an agent for selective modulation of the gut microbiota
[138]
Acerola (Malpighia emarginata) by-product
(dried skin, seeds and pulp residues)
Polyphenol-rich extractExtraction with 70% aqueous methanol
-
Decrease in NH4+ amount in the ascending colon.
-
Increase in short-chain fatty acids (SCFAs) in the colon three regions
-
Positive effect on the gut microbiota metabolism for the probiotic strain Bifidobacterium longum BB-46 when combined with acerola by-product
[155]
By-products of acerola (Malpighia emarginata D.C.),
cashew (Anacardium occidentale L.) and guava (Psidium guajava L.) fruits
Phenolic compounds and dietary fibresFreezing in liquid N2 and freeze-drying400 mg/kg body weight (orogastric administration)
-
Reduction of body weight (3.42%, 3.08% and 5.20%) in dyslipidaemic female rats
-
Decrease in faecal pH, liver fat, visceral fat and serum lipid levels
-
Increase in faecal moisture, faecal fat excretion, amounts of organic acids in faeces and faecal Bifidobacterium spp. and Lactobacillus spp. counts.
-
Protection of colon and liver from tissue damage (e.g., destruction of liver and colon cells and increased fat deposition in hepatocytes) induced by dyslipidaemic diet.
[156]
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Chaouch, M.A.; Benvenuti, S. The Role of Fruit by-Products as Bioactive Compounds for Intestinal Health. Foods 2020, 9, 1716. https://doi.org/10.3390/foods9111716

AMA Style

Chaouch MA, Benvenuti S. The Role of Fruit by-Products as Bioactive Compounds for Intestinal Health. Foods. 2020; 9(11):1716. https://doi.org/10.3390/foods9111716

Chicago/Turabian Style

Chaouch, Mohamed Aymen, and Stefania Benvenuti. 2020. "The Role of Fruit by-Products as Bioactive Compounds for Intestinal Health" Foods 9, no. 11: 1716. https://doi.org/10.3390/foods9111716

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop