Preprint
Review

This version is not peer-reviewed.

Importance of Crops in Arid Zones of Mexico with Food Development Potential: An Alternative in Low-Water Requirement Crops and Food Production

A peer-reviewed article of this preprint also exists.

Submitted:

08 November 2024

Posted:

11 November 2024

You are already at the latest version

Abstract
(1) Background: Climate change has several consequences; one of them is increasing the severity of droughts. This leads to an opportunity to study arid zone plants as food sources that have potential biological activities and improve consumer´s health; (2) Methods: In this work we review recent research focused on the traditional use and importance of arid zone plants, their nutritional contribution, and the beneficial effects on health when consumed; these effects are primarily because of the antioxidant activity that inhibits free radicals and contributes to improved nutrition that benefits consumer’s health; (3) Results: Several plant-based functional foods studies have shown that the consumption of bioactive compounds is a complement to drugs for preventing some chronic-degenerative diseases such as gastrointestinal diseases, diabetes, and obesity; (4) Conclusions: With all the previously mentioned, plants from arid and semi-arid zone are potential sources for developing foodstuffs in the current climate change situation.
Keywords: 
;  ;  ;  

1. Introduction

Global warming and desertification have been the most important reasons for exploiting crops with low water requirements [1]. Arid areas occupy 46% of the planet’s surface [2], receives less than 400 mm of annual precipitation, and is supported by more than 20% of the world’s population [3]. Arid zone is expected to expand further, leading to an increase in the severity of droughts and food security [4,5]. Consequently, it is proposed to select crops from semi-arid and arid regions, which are undervalued by the general public, as a viable solution [6]. The use of Arid Zone Plants (AZP) has the potential to improve the sustainability of the agricultural sector in a context of climate change, thus contributing to ensure food security [7].
AZP have evolved distinct genotypic, biochemical, and physiological traits to adapt to harsh environmental conditions. The predominant physiological attributes exhibited by these plants include the existence of an extensive root system, stomatal pits, smaller leaves, leaf hairs, and waxy cuticles, which allow them greater adaptability to extreme ecosystems. In addition, they employ efficient photosynthetic pathways that allow them to optimize carbon assimilation while minimizing water transpiration [8,9,10]. Because of this, AZP could play a vital role in feeding in the coming years with low maintenance and low investment [11].
AZP are of great interest for their nutritional contribution, mainly fiber and amino acids [12]. Some of these plants or fruits are considered a nutritionally complete food due to their varied contribution of vitamins and minerals, besides being a potential source of bioactive compounds, mainly phenolic compounds with an important antioxidant activity useful for the prevention of diseases such as diabetes, hypercholesterolemia, obesity and hypertension, offering a better quality of life since they eliminate free radicals generated in our organism by environmental and other factors [13,14].
The objective of this review is to highlight the importance of Mexican AZP with low water requirements and food potential, their traditional consumption and their nutritional or beneficial effect on health.

2. Arid Zone Plants in Mexico

Mexico has a substantial variety of AZP that have functional food potential, primarily in the northern states (Figure 1). Whereas arid zones represent about 56.92 million hectares out of the 138 million hectares of forest in the country, the largest population of flora is found in semi-arid areas. Other plants have adapted to dry sub-humid areas, because of their adaptability and water availability, which have led to higher economic development [15]. Within the Mexican national territory there is a substantial biodiversity of species from arid zones that have nutritional and medicinal properties; some of these species have the potential to be exploited by the food, pharmaceutical, and chemical, allowing the development of new products that allow their use and provide health benefits.
Agave spp. is a plant endemic to the American continent that has been used as a food source for more than 10,000 years, it is commonly known as maguey (Mexcalli from the Nahuatl language) [16]. There are more than 310 reported species, of which 272 are endemic to Mexico [17]. Agaves have great economic importance, they grow in arid and semi-arid areas and are characterized by three main parts: the leaves, which can be wide or narrow with or without thorns; a stem (heart or “pineapple”), this is found in the center of the plant surrounded by the leaves and is rich in fermentable sugars to obtain alcohols; and at the end of the plant’s life (8-10 years and some species, such as A. salmiana, present a ramified inflorescence with flowers (“quiote”) [18].
Yucca spp. belongs to the Agavoideae family of the genus Asparagaceae. Yucca spp. is endemic to North America, and it is one of the most representative succulents in Mexico, with nearly 50 species used in traditional medicine by Native Americans [19,20]. It is one of the plants with the lowest water requirements, consuming about 0.015 m3/day. It does not need much work to be cultivated and tolerates drought conditions in the arid and semi-arid zones, where it thrives [21].
Opuntia spp it is a cactus native to Mexico with exploitation in a substantial number of industries. It has been used as human and livestock food, in pharmaceutical development, wastewater treatment, pigment production, and soil erosion control [22]. Opuntia Opuntia is a perennial shrub or tree species with a trunk and crown of 3-5 m in height, characterized by segments called “cladodes” similar in appearance to a flat, fleshy, oval-shaped leaf; most species are found in Mexico, although cultivars have spread to some areas of Europe, Africa and Asia [23,24,25].
Opuntia spp. fruits, commonly called “tuna”, have a spherical shape with cylindrical tendencies with different yellow, green, red and purple colorations due to their bioactive compounds. The fruits are small, between 7-9 cm long by 5-6 cm wide, while their weight varies between 86 to 146 g. Inside, the pulp contains seeds rich in linoleic acid, which has potential to be exploited in nutritional supplements, cosmetics and pharmaceuticals. While its peel whose main function is to protect the fruit, has a thickness of 0.65 mm and a coloration similar to that of its pulp, with small thorns of 3 to 10 mm and an umbilical zone. The peel comprises 40% of the fresh fruit weight and has potential for the extraction of starches, pectin, and fiber [26,27].
Hylocereus spp., also known as “pitayaha” or dragon fruit, are optional epiphytes that initially grow in the soil and then become epiphytes. The pitahaya is endemic to Mexico, Martinique, Guatemala, Costa Rica, Salvador, and Colombia. Although it is cultivated in many countries it is most cultivated countries with in arid, semi-arid or water-scarce regions. They grow in warm climates (38 to 40 °C) and thrive in rainy regions, but can adapt to different types of well-drained soils [28]. Depending on the variety, the flesh of the fruit is juicy and white, dark red or yellow, depending on the variety, and the pulp contains small black seeds. Its skin is bright red with green scales and represents 33% of the weight of the fruit, due to the appearance the fruit is decorative [29,30].
Stenocereus spp. Belongs to the Cactaceae family, which is composed of 24 species, some of which are mainly cultivated for their economic value such as S. pruinosus, S. stellatus, and S. queretaroensis, S. thurberi, S. griseus, S. laevigatus, S. longispinus, and S. huastecorum; they have been categorized as endemic to Mexico. The genus Stenocereus grows as a columnar cactus in arid and semi-arid areas, and it has low water and nutrient requirements; their reproductive season takes place between April and September. They bloom pink flowers, which can lead to a small, slightly oval, or spherical fruit with deciduous thorns in its skin. The fruit’s pulp can be of different intense colors due to the presence of betalains (white, yellow, pink, orange, red or purple), it has small edible seeds, low acidity, and a sweet flavour [31,32].
Being plants with low water requirements and that thrive in drought conditions, they can be considered an alternative for developing food additives or used directly as foodstuff. The nutritional value of some of these species has not been studied enough to be considered as food ingredients with some beneficial functionality to health, so it is important to raise awareness among the population of their use for greater utilization and in encourage the population to use them for better utilization and in response to the availability of low-maintenance food.
As these plants have low water requirements and thrive in drought conditions, they can be considered as an alternative to develop food additives or be used directly as food. The nutritional value of some of these species has not been studied enough to be considered as food ingredients with some beneficial functionality to health, however, it is important to encourage the population to use them for better utilization and in response to the availability of low-maintenance food.

3. Nutritional Benefits and Importance of Arid Zone Plants

Several studies have evaluated the nutritional composition of plants from arid and semi-arid areas. These studies have determined the content of moisture, proteins, carbohydrates, fiber and lipids, most of these plants are characterized by their high moisture and carbohydrate content (Table 1), however, in some cases the amount of lipids and proteins is important.
Agave spp. Its main use has been for the production of distilled and non-distilled alcoholic beverages thanks to its high reserve sugar content [39]. Agaves contain mostly carbohydrates such as sucrose, fructose, glucose and fructans [40]. Fructans are fructose polymers derived from sucrose with β (2→1) and/or β (2→6) bonds that can have terminal or intermediate glucose, nutritionally they have been of interest due to their prebiotic benefits such as soluble dietary fiber helping improve intestinal health, as well as the improvement of technological functions in foods such as stabilizers and sweeteners [41,42,43].
Yucca spp.’s flowers have been the primary interest of Yucca spp. because of their antioxidant compound content and their effect on chronic-degenerative diseases [44].
Opuntia spp.’s nutritional profiles vary according to the species, the post-harvest treatment, the environmental conditions, and the age of the plant. One of the greatest nutritional compounds of interest is its natural fiber, in which the soluble fiber is in the form of a mucilage [24,45,46]. Opuntia fruits are 57 % of the edible fraction; most of the edible fraction is composed of water, whereas the rest are different nutrients: primarily carbohydrates, fiber, and proteins. In addition, it has a high content of minerals including potassium, magnesium, and calcium and a high content of vitamins, namely, vitamin C and niacin [23].
Hylocereus pulp represent 45 % of the fruit; water content in the pulp ranges from 87 to 88 %. It is a fruit with acceptable nutritional value because of its high content of carbohydrate, fiber, protein, and vitamins (B1, B2, B3, and C), providing some minerals such as a potassium, sodium, phosphorus, iron, and calcium [37,47].
Stenocereus or pitaya fruits contain nutrients very similar to the fruit of Hylocereus, but with different concentrations. They have an acidic pH of 3.7 to 4.46 and presence of carbohydrates, proteins, fiber, and fats [38,48].

4. Importance and Traditional Use of Arid Zone Plants

The use of most of the Mexican endemic plants is focused on medicine in accordance to the belief of the native indigenous people that some plants were able to alleviate the discomforts of the body through their consumption. Recent research has helped to understand these beliefs. However, a substantial number of the AZP have been consumed as part of the diet or for specific purposes. Many of these plants have strong culinary importance within traditional gastronomy as well as new food applications. Some of these uses can be seen in Figure 2.
Agaves, in Mexican culture, have been used as a source of food for man and livestock, medicine, drinks, preparation of some dishes, honey, syrups, construction material, fibers, vinegar and ornaments. Currently, greater importance has been given to the production of alcoholic beverages [39,49]. Alcoholic beverages obtained from agaves have different names depending on their process and their designation of origin [50]. Some of the distillates are Tequila, Mezcal, Bacanora, and Raicilla, obtained from different species of agaves and their name is given by the state where the species are grown [18,51]. While in fermented drinks, pulque is found with probiotic properties and is obtained through the fermentation of aguamiel, a sweet liquid obtained from the center of species such as A. salmiana. A bread called “Pan de Pulque” is also produced from pulque [18,52].
Yucca spp. is mostly used for its flowers, which receive different names depending on the geographical area (“flor de izote”, “chochas” or “flor de palma”). It is common to see them freshly cut in local markets. The flowers are incorporated into various dishes of Mexican cuisine: salads, side dishes, and stews with various vegetables, meats, and peppers. To prepare them, the stem and pistil are removed, then they are cooked with water and salt. One of its principal characteristics is its bitter taste, and its consumption is limited to the traditional use of indigenous cultures [44].
Traditional dishes with the cladodes of Opuntia spp. have been used in traditional folk medicine for its beneficial effects to treat chronic diseases, but also as a food source because of its nutritional properties and biological activities. Its consumption is distributed worldwide due to its low cost, and in gastronomy there is a great diversity of dishes made with this plant [53]. In some places the plant is used as livestock food, to build fences, and for ornamental purposes [54].
Opuntia spp.´s fruit or “tuna” is used in traditional folk medicine for treating stomach-related diseases, diabetes, and obesity [55]. In ancient times it was used to make wine, however, recently it is used to produce cheese, jam, and juices, in addition to various compounds of interest to the food industry. Fruit residues are also used as fodder for animal in dry seasons [56].
In the pre-Hispanic Mexican population, pitaya and pitahaya fruits have been an important source of food because of their water and nutrient content, but also parts of the plant such as the stem have been used for gastritis problems. Because of their flavor, the fruits have been consumed as fresh fruit or in processed products such as dried fruits and licors [48]. The pulp of Hylocereus has nutritional and healing properties, its consumption can help reduce blood sugar levels, improve nutrient absorption, reduce blood cholesterol, while the leaves have antibacterial properties that have been used in the treatment of infectious diseases and the stems have helped to improve the health of some people, due to its traditional consumption there are some theories that indicate that the fruit of Hylocereus prevents colon cancer and improves the functioning of the brain, kidneys and visual acuity [37].

5. Arid Zone Plants’ Bioactive Compounds and Their Foodstuff Usage

Bioactive compounds are relevant in foodstuffs because they can improve health through the different functional activities involved in their metabolism. AZP contain several bioactive compounds that have been evaluated for human consumption, and several have been found to improve health. Table 2 lists the bioactive compounds found in AZP and briefly describes their functional activities.

5.1. Agave Leaves

Agave leaves, which are considered an agro-industrial waste, are of interest because they contain bioactive compounds with substantial biological activities (López-Romero et al. 2017; Puente-Garza, García-Lara, et al. 2017). Saponins, flavonoids, homoisoflavonoids, phenolic acids, and fatty acids have been identified in different cultivars of Agaves. Saponins and homoisoflavonoids have shown anti-inflammatory and ulceroprotective activities in rats treated with extracts from A. pygmaea (81 and 85 % protection) and A. angustifolia var. Marginata (84 % and 91 % protection). These results compared to the 96.875 % protection offered by ranitidine suggests that these extracts could be an alternative to a drug treatment for ulcers (El-Hawary et al. 2020). The crude extracts of A. americana have shown the presence of alkaloids, saponins, tannins, polyphenols, and flavonoids. The antibacterial activity of these extracts has been evaluated in the crude and the solvent fractions; the results showed an efficient bactericidal effect with an inhibition of 17 to 40 mm, comparable to gentamicin, in pathogenic bacteria commonly present in food as S. typhi, S. aureus and E. coli. The bactericidal effect obtained is mostly due to the saponins, however, other compounds could also interfere with the antimicrobial activity as alkaloids, flavonoids, tannins, and phenolic compounds (Shegute and Wasihun 2020). Although agave leaves have been mostly used for developing biopolymers, recent research suggests the use of bioactive compounds in the pharmaceutical industry. Nevertheless, the application of agave leaves in the food industry is of primary relevance.

5.2. Pulque and Agave Syrup

Pulque, a beverage of traditional relevance, has been used for prevention and treatment of gastrointestinal diseases; the Lactobacillus it contains exert and anti-inflammatory effect whereas its exopolysaccharides reduce cholesterol [85]. Fructooligosaccharides in agave syrup help activating the immune system; consequently, increasing resistance to infections [86]. Recent research suggests that consumption of agave fructans can help treat obesity, metabolic syndrome, type II diabetes, and gastrointestinal diseases such as Crohn’s disease, ulcerative colitis, and irritable bowel syndrome [60,87]. The most important component of mead and pulque is the substantial diversity of microorganisms that confer a probiotic effect. Researchers have identified yeasts of the Candida, Kluyveromyces, Saccharomyces, and Clavispora genus and bacteria of Lactobacillus, Leuconostoc, and Acetobacter genus in mead and pulque [88]. In addition, the fructan content can lead to a prebiotic effect, which means that these beverages can have a symbiotic effect in the gastrointestinal microbiota. The symbiotic effect improves health by producing short-chain fatty acids such as acetate, propionate, and butyrate [89]. Kammogenins, manogenin, gentrogenin, and hecogenin derived saponins have been identified in mead; the saponin content heavily relies on the maturity of the agave used to produce the mead. These saponins have several biological properties such as anticancer, antibacterial, and antifungal activities. In addition, their antioxidant effect has been reported equivalent to 904.8 μM of gallic acid, which means they can also provide antioxidant-associated health benefits [90].

5.3. Yucca Leaves and Fruits

Yucca spp. have a high saponin content that have surfactant and detergent properties. The plant is rich in polyphenols with antioxidant, antimicrobial, and anti-inflammatory properties and they are used to improve intestinal health [65,66]. Additionally, there are several other compounds that have shown antimicrobial activity towards relevant bacteria in food safety, namely, Escherichia coli, Salmonella typhimurium, and Staphylococcus aureus. These compounds are saponins (Spirostan-3-ol, spirostanol-3-ol-dihexose, di-glucoside, and hecogenin), organic and phenolic acids (maleic acid, citraconic acid, muconic acid, and caffeic acid) and other compounds such as flavones, flavonoids, and some glycosides.
One of the negative effects of food infections by bacteria is intestinal inflammation, it has been shown that the compounds present in yucca reduce inflammation by the effect of antioxidant activity capable of eliminating free radicals, a study demonstrated through a model of acute inflammation in mice the reduction of edema in paw using 200 mg / kg of Yucca gigantea extract in which a reduction was obtained from 0. 3703 mm to 0.01 mm after four hours of study, so the antimicrobial effect of this plant promises the ability to help reduce or prevent intestinal inflammation caused by pathogens and in turn could prevent cancer when incorporated into functional foods, nutraceuticals, or natural drugs [91]. Morales-Figueroa and colleagues determined the antimicrobial activity of the phenolic compounds and saponins found in Y. baccata against gram-negative bacteria with relevance in the pharmaceutical and food industry as an Escherichia coli, Pseudomonas aeruginosa, and Salmonella typhi. Values of 100 mg mL-1 and 120 mg mL-1 of minimum inhibitory concentration were estimated for pathogenic bacteria; the inhibitory effect was higher for large negative bacteria due to the presence of phenolic compounds and saponins [92]. Similarly, the oil of Y. aloifolia Linn fruits were characterized, and the results showed the presence of fatty acids, namely, linoleic acid (73.38 %), oleic acid (13.52 %), and palmitic acid (8. 18 %), and a total of 204 mg/100 g of vitamin E. All these compounds provide potential for antioxidant, anticarcinogenic, neuro and cardio protective effects, in addition to cholesterol-lowering properties. In vivo and clinical studies should be conducted to determine it, but this could lead to consider Y. aloifolia fruit oil a functional oil with beneficial effects to human health that could be used for disease prevention [93].

5.4. Opuntia Cladodes and Fruits

Several studies working with Opuntia plants have shown in vitro and in vivo that their biological activities are beneficial to health [23,53]. Cladodes and fruits are rich in phenolic compounds and terpenoids [67,68,69,70]. Consuming Opuntia cladodes and fruits regulates weight, control diabetes, and reduce cholesterol levels; also, they are a good source of potassium [24,45,46]. When Opuntia fruits are consumed raw, their bioactive compounds show antimicrobial, antiproliferative, hypolipidemic, glycemic control and positive effects on colonic health [27].
Fermenting the juice from O. humifusa cladodes with lactic acid bacteria (LAB) and the own plant’s enzymes has shown to improve its functional properties. The fermentation increases polyphenol content during the first 24 hours; after fermenting the juice with LAB for 60 h, the final amount of polyphenols was in the range of 723 to 785 μg GAE mL-1. Testing Lactobacillus plantarum, Streptococcus salivarius, and Weissella confuse, and a mixture of the three bacteria by adding an enzyme to all treatments, a treatment with the enzyme alone was used, which showed a lower antioxidant activity. Therefore, this helped to determine that the interaction of LAB in the presence of an enzyme works to increase the phenolic content of the treatments. Two of the identified compounds responsible for the antioxidant activity were quercetin and isorhamnetin, which are flavonoid aglycones with strong antioxidant power. However, the isorhamnetin-3-O-glucoside content decreased to undetectable levels after fermentation, which might lead to believe the highest antioxidant activity relies on quercetin. This study demonstrates that fermentation with certain bacteria may be suitable to enhance the beneficial effects of the compounds found in these plants and have a greater effect on consumer’s health [94].
O. littoralis cladodes and fruits have already been characterized. Kaempferol was quantitated at 503.96 mg g-1 in cladodes and 428.96 mg g-1 in fruits. Terpenes were quantitated at 16.75 mg g-1 in cladodes and 15.69 mg g-1 in fruits. Additionally, the total content of betalains in fruits were determined to 59.5 mg g-1, of which, 23 mg g-1 are betaxanthins and 36.7 mg g-1 to betacyanins. Similarly, Opuntia fruits have a significant antidiabetic activity due to the α-glucosidase inhibitor. A microplate study showed an anti-diabetic activity due to the α-glucosidase inhibitor of IC50 57.7 % compared to the control drug (Acarbose) with an inhibition of IC50 30.57 %. This effect is given by the compounds present in the fruit such as Kaempferol and ferulic acid which help in blood glucose lowering. This could lead to Opuntia fruits being able to be considered for the prevention, treatment or both of glycemia and type 2 diabetes mellitus [95].
Opuntia fruits are rich in organic acids including, phenolic compounds, betalains, and carotenoids [72,73,74,75]. Its fiber content causes significant reductions in total cholesterol in hyperlipidemic populations; however, the effects are lower in patients that consumed the fruits and cladodes [46]. The fruit’s antioxidant, hypoglycemic, anti-ulcerogenic, and anti-inflammatory activity has also been documented [26].
The antioxidant and antimicrobial compounds of O. microdasys’ and O. macrorhiza’s fruits were quantitated. The fruits’ peels have phenolic compounds, with a content of 0.58 mg g-1 for O. microdasys’ peel and 1.55 mg g-1 for O. macrorhiza’s peel, and betacyanins with a content of 3.6 for O. microdasys’ skin and 131 mg g-1 O. macrorhiza’s skin. The same study demonstrated the antifungal and antimicrobial potential that the fruit peel has; the fruit’s peel showed inhibition of microorganisms and leads to think that the fruit’s peel has an important food application [96].
A comparative study of the betalain content between of O. ficus-indica’s fruits from Mexican and Spanish cultivars showed that both cultivars have potential to be used as functional ingredients. Betalain content was quantitated to 2422.5 μg g-1 for the Mexican cultivar and 1650.6 μg g-1 for the Spanish cultivar in purple dry whole fruit. In dry red whole fruit, it was determined to 582.6 μg g-1 for the Mexican cultivar and to 819.8 μg g-1 for the Spanish cultivar. Finally, for yellow dry whole fruit the betalain content was quantitated to 587.9 μg g-1 for the Mexican cultivar and 156.2 μg g-1 for the Spanish cultivar. Additionally, the psidic acid content was determined to be 43882.7 μg g-1 in dry peel of the purple Spanish cultivar. A betalain content of 2422.5 and 1650.6 μg g-1 dry base of the whole fruit (purple), 582.6 and 819.8 μg g-1 dry base of the whole fruit (red) 587.9 and 156.2 μg g-1 respectively in dry base of the whole fruit (yellow) and an important content of phenolic compounds such as piscidic acid with a value of 43882.7 μg g-1 dry base in the peel of the purple Spanish cultivar were identified. These results indicate that the content of betalains and phenols in these cultivars is important for their use in the development of foods and nutraceuticals, as well as in the investigation of their biological activities [97].

5.5. Pitahaya and Pitaya Fruits

Hylocereus’ (pitahaya) fruits, also known as dragon fruits, contain several phenolic compounds that exert antioxidant and antimicrobial activities [47,80,81]. Its main component is betalains [31]. Dragon fruits’ pulp also contain oligosaccharides of different molecular weights that can provide prebiotic effects against beneficial strains, including Lactobacillus and Bifidobacterium. Its consistent consumption regulates cholesterol metabolism and ameliorates weight control and diabetes [47].
The seeds are a source of antioxidants and essential fatty acids such as linoleic acid, and they may be a new source of essential oils because they are in higher amounts than in canola, flaxseed, or sesame seeds [47]. Bioactive compounds in the fruit have shown to aid in obesity control, non-alcoholic fatty liver disease, type II diabetes, and they prevent colon and intestines inflammation [98].
Stenocereus (pitaya) fruits are distinctive by their betalains content [84], which is responsible for the color of the fruit, and by their water-soluble phenolic compounds that confer the fruits their antioxidant activity. The presence of both betalains and phenolic compounds makes the pitaya fruits a better alternative to other natural pigments [31,99].

6. Use of Traditional Crops for the Development of Functional Foods

Currently, the area of functional foods has focused on using raw foodstuffs, with bioactive activities, to can help improve consumer’s health, many of these foods have been associated with a lower incidence related to health problems. The primary objective of functional food and nutrition research is to ameliorate health problems that society faces including bioactive compounds such as fiber, antioxidants, phytochemicals, and others, these have the capacity to improve health, generate well-being, and are useful to prevent the risk of suffering diseases nowadays like gastrointestinal diseases, diabetes, obesity, cancer, and diseases related with free radicals in the human body. Incorporating bioactive compounds into foodstuffs leads to several changes; these include modifying the physical characteristics of a product, decreasing the caloric intake of the food, and improving absorption the bioactive compounds and nutrients during digestion. Ultimately, these bioactive compounds are a healthier option than chemical additives have a better stability and bioavailability of their benefits, representing a better option for the use of food ingredients [100,101,102].
Every passing day consumers are more involved in their nutrition and the health benefits proper nutrition offers [103]. There is a direct relationship between food and health, however, factors such as urbanization, economic development and changes in lifestyle can negatively affect eating habits [104]. Therefore, improving nutrition with foods, plants, and fruits with a functional effect to reduce the health issues is of great importance.
Recent research shows us an alternative to new products that could be marketed within the functional food market. However, two of the greatest challenges are determining the effectiveness in human health of this type of food and achieving consumer acceptance. Therefore, it of great importance to continue working to obtain foods that guarantee health benefits and at the same time have the sensory characteristics that the customer demands.
The different foods developed with AZP are mainly characterized by their antioxidant content. Unfortunately, no study has been able to guarantee the effectiveness of the bioactive potential directly in humans in a clinical setting. However, tests carried out at laboratory level show a strong response to biological activities, namely, antioxidant, antimicrobial, hypoglycemic, anti-inflammatory, probiotic, and prebiotic activities. These could be able to contribute to prevent health problems in addition to proper nutrition and physical activity. Table 3 summarizes work done using AZP in different foodstuffs.

7. Conclusions

In recent years, growing concern has focused on food shortage and climate change; crops or plants that thrive with low water requirements have become an alternative in human diet due to their accessibility, low cost, and nutritional contributions.
AZP contain various bioactive compounds that possess different biological activities, primarily antioxidant activity. However, studies to verify their effectiveness in a clinical setting are limited; it would be ideal to study the effects directly on humans to evaluate the beneficial potential of a compound, plant, or food. It should be expected in the future that clinical research will be done to continue innovating with nutritious, safe, and functional products that help improve consumer’s health, while also contributing to food security.

Author Contributions

Conceptualization, M.I.M.R. and R.B.; methodology, M.I.M.R., P.A.Z.; validation, A.A.N.V., M.C.; formal analysis, M.I.M.R.; investigation, M.I.M.R., M.C. and R.B.; resources, M.C., R.B., A.A.N.V.; writing—original draft preparation, M.I.M.R.; writing—review and editing, R.B., M.C.; visualization, S.N.R.B.; supervision, M.C., S.N.R.B.; project administration, R.B.; funding acquisition, M.C., R.B. All authors have read and agreed to the published version of the manuscript.

Funding

The authors acknowledge the National Council for Humanities, Science and Technology (CONAHCYT, Mexico) for financial support through the postgraduate scholarship (1007539). Fund to promote the development of science and technology in the state of Coahuila (FONCYT) under the scope of the strategic funding of COAH-2019-C13-C110.

Data Availability Statement

Not applicable.

Acknowledgments

M.I.M.R would like to thank every mentor and colleague at Autonomous University of Coahuila and the Functional Food & Nutrition Group.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Morte, A.; Kagan-Zur, V.; Navarro-Ródenas, A.; Sitrit, Y. Cultivation of Desert Truffles—A Crop Suitable for Arid and Semi-Arid Zones. Agronomy 2021, 11, 1–13. [CrossRef]
  2. Gaur, M.K.; Squires, V.R. Climate Variability Impacts on Land Use and Livelihoods in Drylands. In Climate Variability Impacts on Land Use and Livelihoods in Drylands; 2017; pp. 1–20 ISBN 9783319566818.
  3. Ruiz-Nieto, J.E.; Hernández-Ruiz, J.; Hernández-Marín, J.; Mendoza-Carrillo, J.; Abraham-Juárez, M.; Isiordia-Lachica, P.M.; Mireles-Arriaga, A.I. Mesquite (Prosopis Spp.) Tree as a Feed Resource for Animal Growth. Agrofor. Syst. 2020, 94, 1139–1149. [CrossRef]
  4. Tan, M.; Zheng, L. Increase in Economic Efficiency of Water Use Caused by Crop Structure Adjustment in Arid Areas. J. Environ. Manage. 2019, 230, 386–391. [CrossRef]
  5. Jiang, L.; Hu, D.; Wang, H.; Lv, G. Discriminating Ecological Processes Affecting Different Dimensions of α- and β-Diversity in Desert Plant Communities. Ecol. Evol. 2022, 12, 1–13. [CrossRef]
  6. Mizrahi, Y. Do We Need New Crops for Arid Regions? A Review of Fruit Species Domestication in Israel. Agronomy 2020, 10. [CrossRef]
  7. Muluneh, M.G. Impact of Climate Change on Biodiversity and Food Security: A Global Perspective—a Review Article. Agric. Food Secur. 2021, 10, 1–25. [CrossRef]
  8. Marasco, R.; Mosqueira, M.J.; Cherif, A.; Daffonchio, D. Diversity and Plant Growth-Promoting Properties of Microbiomes Associated with Plants in Desert Soils BT - Microbiology of Hot Deserts. In; Ramond, J.-B., Cowan, D.A., Eds.; Springer International Publishing: Cham, 2022; pp. 205–233 ISBN 978-3-030-98415-1.
  9. Mohanta, T.K.; Mohanta, Y.K.; Kaushik, P.; Kumar, J. Physiology, Genomics, and Evolutionary Aspects of Desert Plants. J. Adv. Res. 2023. [CrossRef]
  10. Yang, X.D.; Wu, N.C.; Gong, X.W. Plant Adaptation to Extreme Environments in Drylands. Forests 2023, 14, 2–4. [CrossRef]
  11. Arba, M. The Potential of Cactus Pear (Opuntia Ficus-Indica (L.) Mill.) as Food and Forage Crop. In Emerging research in Alternative Crops; Hirich, A., Choukr-Allah, R., Ragab, R., Eds.; Cham, Switzerland, 2020; Vol. 58, pp. 335–357 ISBN 978-3-319-90471-9.
  12. Daniloski, D.; D’Cunha, N.M.; Speer, H.; McKune, A.J.; Alexopoulos, N.; Panagiotakos, D.B.; Petkoska, A.T.; Naumovski, N. Recent Developments on Opuntia Spp., Their Bioactive Composition, Nutritional Values, and Health Effects. Food Biosci. 2022, 47, 101665. [CrossRef]
  13. Aldughaylibi, F.S.; Raza, M.A.; Naeem, S.; Rafi, H.; Alam, M.W.; Souayeh, B.; Farhan, M.; Aamir, M.; Zaidi, N.; Mir, T.A. Extraction of Bioactive Compounds for Antioxidant, Antimicrobial, and Antidiabetic Applications. Molecules 2022, 27, 1–16. [CrossRef]
  14. Rodrigues, C.; Paula, C.D. de; Lahbouki, S.; Meddich, A.; Outzourhit, A.; Rashad, M.; Pari, L.; Coelhoso, I.; Fernando, A.L.; Souza, V.G.L. Opuntia Spp.: An Overview of the Bioactive Profile and Food Applications of This Versatile Crop Adapted to Arid Lands. Foods 2023, 12, 1–31. [CrossRef]
  15. CONAFOR Las Zonas Áridas Son Más Que Desierto Available online: https://www.gob.mx/conafor/es/articulos/las-zonas-aridas-son-mas-que-desierto?idiom=es.
  16. Álvarez-Chávez, J.; Santos-Zea, L.; Ramírez-Jiménez, A.K.; Kleinschek, K.S. Agave By-Products: An Overview of Their Nutraceutical Value, Current Applications, and Processing Methods. Polysaccharides 2021, Vol. 2, Pages 720-743 2021, 2, 720–743. [CrossRef]
  17. Martínez, Y.; Iser, M.; Valdivié, M.; Rosales, M.; Albarrán, E.; Sánchez, D. Dietary Supplementation with Agave Tequilana (Weber Var. Blue) Stem Powder Improves the Performance and Intestinal Integrity of Broiler Rabbits. Anim. 2022, Vol. 12, Page 1117 2022, 12, 1117. [CrossRef]
  18. Pérez-Zavala, M. de L.; Hernández-Arzaba, J.C.; Bideshi, D.K.; Barboza-Corona, J.E. Agave: A Natural Renewable Resource with Multiple Applications. J. Sci. Food Agric. 2020, 100, 5324–5333. [CrossRef]
  19. Jiménez, G.G.; Durán, A.G.; Macías, F.A.; Simonet, A.M. Structure, Bioactivity and Analytical Methods for the Determination of Yucca Saponins. Molecules 2021, 26, 1–30. [CrossRef]
  20. López-Ramírez, Y.; Cabañas-García, E.; Areche, C.; Trejo-Tapia, G.; Pérez-Molphe-Balch, E.; Gómez-Aguirre, Y.A. Callus Induction and Phytochemical Profiling of Yucca Carnerosana (Trel.) McKelvey Obtained from in Vitro Cultures. Rev. Mex. Ing. Quim. 2021, 20, 823–837. [CrossRef]
  21. Al-Sulbi, A.O.; Alghanem, A.A. Synchronous Management of Public Green Spaces: The Case of Imam Abdulrahman Bin Faisal University’s Eastern Campus – Dammam, Saudi Arabia. Ain Shams Eng. J. 2022, 13, 1–10. [CrossRef]
  22. Krümpel, J.; George, T.; Gasston, B.; Francis, G.; Lemmer, A. Suitability of Opuntia Ficus-Indica (L) Mill. and Euphorbia Tirucalli L. as Energy Crops for Anaerobic Digestion. J. Arid Environ. 2020, 174, 1–8. [CrossRef]
  23. Eleojo, C.; Amoo, S.O.; Kudanga, T. Opuntia (Cactaceae) Plant Compounds, Biological Activities and Prospects – A Comprehensive Review. Food Res. Int. 2018, 112, 328–344. [CrossRef]
  24. du Toit, A.; de Wit, M.; Osthoff, G.; Hugo, A. Antioxidant Properties of Fresh and Processed Cactus Pear Cladodes from Selected Opuntia Ficus-Indica and O. Robusta Cultivars. South African J. Bot. 2018, 118, 44–51. [CrossRef]
  25. Besné-Eseverri, I.; Trepiana, J.; Gómez-Zorita, S.; Antunes-Ricardo, M.; Cano, M.P.; Portillo, M.P. Beneficial Effects of Opuntia Spp. on Liver Health. Antioxidants 2023, 12, 1–20. [CrossRef]
  26. Regalado-Rentería, E.; Aguirre-Rivera, J.R.; González-Chávez, M.M.; Sánchez-Sánchez, R.; Martínez-Gutiérrez, F.; Juárez-Flores, B.I. Assessment of Extraction Methods and Biological Value of Seed Oil from Eight Variants of Prickly Pear Fruit (Opuntia Spp.). Waste and Biomass Valorization 2018, 11, 1181–1189. [CrossRef]
  27. Manzur-Valdespino, S.; Arias-Rico, J.; Ramírez-Moreno, E.; Sánchez-Mata, M. de C.; Jaramillo-Morales, O.A.; Angel-García, J.; Zafra-Rojas, Q.Y.; Barrera-Gálvez, R.; Cruz-Cansino, N.D.S. Applications and Pharmacological Properties of Cactus Pear (Opuntia Spp.) Peel: A Review. Life 2022, 12. [CrossRef]
  28. Balendres, M.A.; Bengoa, J.C. Diseases of Dragon Fruit (Hylocereus Species): Etiology and Current Management Options. Crop Prot. 2019, 126, 1–7. [CrossRef]
  29. Attar, S.H.; Urün, I.; Kafkas, S.; Kafkas, N.E.; Ercisli, S.; Ge, C.; Mlcek, J.; Adamkova, A. Nutritional Analysis of Red-Purple and White-Fleshed Pitaya ( Hylocereus ) Species. 2022.
  30. Tang, W.; Li, W.; Yang, Y.; Lin, X.; Wang, L.; Li, C.; Yang, R. Phenolic Compounds Profile and Antioxidant Capacity Of. Foods 2021, 10, 1183.
  31. García-Cruz, L.; Dueñas, M.; Santos-Buelgas, C.; Valle-Guadarrama, S.; Salinas-Moreno, Y. Betalains and Phenolic Compounds Profiling and Antioxidant Capacity of Pitaya (Stenocereus Spp.) Fruit from Two Species (S. Pruinosus and S. Stellatus). Food Chem. 2017, 234, 111–118. [CrossRef]
  32. García Ordoñez, T.E.; Díaz Castro, F.; Castellanos Suárez, J.A.; Sedano Castro, G.; Almeraya Quintero, S.X. Characterization of the Pitaya Crop Stenocereus Pruinosus in the Community of Dolores Hidalgo, Huitziltepec, Puebla. Rev. Científica y Académica 2024, 5, 632–648. [CrossRef]
  33. Escobedo-García, S.; Salas-Tovar, J.A.; Flores-Gallegos, A.C.; Contreras-Esquivel, J.C.; González-Montemayor, Á.M.; López, M.G.; Rodríguez-Herrera, R. Functionality of Agave Bagasse as Supplement for the Development of Prebiotics-Enriched Foods. Plant Foods Hum. Nutr. 2019 751 2019, 75, 96–102. [CrossRef]
  34. Juárez-Trujillo, N.; Monribot-Villanueva, J.L.; Jiménez-Fernández, V.M.; Suárez-Montaño, R.; Aguilar-Colorado, Á.S.; Guerrero-Analco, J.A.; Jiménez, M. Phytochemical Characterization of Izote (Yucca Elephantipes) Flowers. J. Appl. Bot. Food Qual. 2018, 91, 202–210. [CrossRef]
  35. Rezende, F.M.; Véras, A.S.C.; Siqueira, M.C.B.; Conceição, M.G.; Lima, C.L.; Almeida, M.P.; Mora-Luna, R.E.; Neves, M.L.M.W.; Monteiro, C.C.F.; Ferreira, M.A. Nutritional Effects of Using Cactus Cladodes (Opuntia Stricta Haw Haw) to Replace Sorghum Silage in Sheep Diet. Trop. Anim. Health Prod. 2020. [CrossRef]
  36. Pulido-Hornedo, N.A.; Ventura-Juárez, J.; Guevara-Lara, F.; González-Ponce, H.A.; Sánchez-Alemán, E.; Buist-Homan, M.; Moshage, H.; Martínez-Saldaña, M.C. Hepatoprotective Effect of Opuntia Robusta Fruit Biocomponents in a Rat Model of Thioacetamide-Induced Liver Fibrosis. Plants 2022, 11. [CrossRef]
  37. Rathi, K.M.; Singh, S.L.; Gigi, G.G.; Shekade, S.V. Nutrition and Therapeutic Potential of the Dragon Fruit: A Qualitative Approach. Pharmacognosy Res. 2023, 16, 1–9. [CrossRef]
  38. Corzo-Rios, L.J.; Bautista-Ramírez, M.E.; Gómez y Gómez, Y. de la M.; Torres-Bustillos, L.G. Frutas de Cactáceas: Compuestos Bioactivos y Sus Propiedades Nutracéuticas. Propiedades Funcionales hoy 2017, 35–66. [CrossRef]
  39. Arellano-Plaza, M.; Paez-Lerma, J.B.; Soto-Cruz, N.O.; Kirchmayr, M.R.; Gschaedler Mathis, A. Mezcal Production in Mexico: Between Tradition and Commercial Exploitation. Front. Sustain. Food Syst. 2022, 6, 46. [CrossRef]
  40. de la Rosa, O.; Flores-Gallegos, A.C.; Muñíz-Márquez, D.; Contreras-Esquivel, J.C.; Teixeira, J.A.; Nobre, C.; Aguilar, C.N. Successive Fermentation of Aguamiel and Molasses by Aspergillus Oryzae and Saccharomyces Cerevisiae to Obtain High Purity Fructooligosaccharides. Foods 2022, 11, 1–15. [CrossRef]
  41. Aldrete-Herrera, P.I.; López, M.G.; Medina-Torres, L.; Ragazzo-Sánchez, J.A.; Calderón-Santoyo, M.; González-Ávila, M.; Ortiz-Basurto, R.I. Physicochemical Composition and Apparent Degree of Polymerization of Fructans in Five Wild Agave Varieties: Potential Industrial Use. Foods 2019, Vol. 8, Page 404 2019, 8, 404. [CrossRef]
  42. Vázquez-Vuelvas, O.F.; Chávez-Camacho, F.A.; Meza-Velázquez, J.A.; Mendez-Merino, E.; Ríos-Licea, M.M.; Contreras-Esquivel, J.C. A Comparative FTIR Study for Supplemented Agavin as Functional Food. Food Hydrocoll. 2020, 103, 1–10. [CrossRef]
  43. Martinez Gamiño, D.; Garcia Soto, M.J.; Gonzalez Acevedo, O.; Godinez Hernandez, C.; Juarez Flores, B.; Ortiz Basurto, R.I.; Rodriguez Aguilar, M.; Flores Ramirez, R.; Martinez Martinez, M.; Ratering, S.; et al. Prebiotic Effect of Fructans from Agave Salmiana on Probiotic Lactic Acid Bacteria and in Children as a Supplement for Malnutrition. Food Funct. 2022, 13, 4184–4193. [CrossRef]
  44. Mulík, S.; Ozuna, C. Mexican Edible Flowers: Cultural Background, Traditional Culinary Uses, and Potential Health Benefits. Int. J. Gastron. Food Sci. 2020, 21, 1–14. [CrossRef]
  45. Attanzio, A.; Diana, P.; Barraja, P.; Carbone, A.; Spanò, V.; Parrino, B.; Cascioferro, S.M.; Allegra, M.; Cirrincione, G.; Tesoriere, L.; et al. Quality, Functional and Sensory Evaluation of Pasta Fortified with Extracts from Opuntia Ficus-Indica Cladodes. J. Sci. Food Agric. 2019, 99, 4242–4247. [CrossRef]
  46. Gouws, C.; Mortazavi, R.; Mellor, D.; McKune, A.; Naumovski, N. The Effects of Prickly Pear Fruit and Cladode (Opuntia Spp.) Consumption on Blood Lipids: A Systematic Review. Complement. Ther. Med. 2020, 50, 102384. [CrossRef]
  47. Ibrahim, S.R.M.; Mohamed, G.A.; Khedr, A.I.M.; Zayed, M.F.; El-Kholy, A.A.E.S. Genus Hylocereus: Beneficial Phytochemicals, Nutritional Importance, and Biological Relevance-A Review. J. Food Biochem. 2018, 42, 1–29. [CrossRef]
  48. Rivera, G.; Bocanegra-García, V.; Monge, A. Traditional Plants as Source of Functional Foods: A Review. CYTA - J. Food 2010, 8, 159–167. [CrossRef]
  49. García-Morales, S.; Corzo-Jiménez, I.J.; Silva-Córdova, N.F.; Soto-Cordero, A.M.; Rodríguez-Mejía, D.I.; Pardo-Núñez, J.; León-Morales, J.M. Comparative Study of Steroidal Sapogenins Content in Leaves of Five Agave Species. J. Sci. Food Agric. 2022, 102, 5653–5659. [CrossRef]
  50. González-Llanes, M.D.; Hernández-Calderón, O.M.; Rios-Iribe, E.Y.; Alarid-García, C.; Castro Montoya, A.J.; Escamilla-Silva, E.M. Fermentable Sugars Production by Enzymatic Processing of Agave Leaf Juice. Can. J. Chem. Eng. 2018, 96, 639–650. [CrossRef]
  51. López-Romero, J.C.; Ayala-Zavala, J.F.; González-Aguilar, G.A.; Peña- Ramos, E.A.; González-Rios, H. Biological Activities of Agave-by-Products and Their Possible Applications in Food and Pharmaceuticals. J. Sci. Food Agric. 2017, 98, 2461–2474. [CrossRef]
  52. Vernon-Carter, E.J.; Garcia-Diaz, S.; Reyes, I.; Carrillo-Navas, H.; Alvarez-Ramirez, J. Rheological and Thermal Properties of Dough and Textural and Microstructural Characteristics of Bread with Pulque as Leavening Agent. Int. J. Gastron. Food Sci. 2017, 9, 39–48. [CrossRef]
  53. Aruwa, C.E.; Amoo, S.O.; Kudanga, T. Extractable and Macromolecular Antioxidants of Opuntia Ficus-Indica Cladodes: Phytochemical Profiling, Antioxidant and Antibacterial Activities. South African J. Bot. 2019, 125, 402–410. [CrossRef]
  54. Khaled, S.; Dahmoune, F.; Madani, K.; Urieta, J.S.; Mainar, A.M. Supercritical Fractionation of Antioxidants from Algerian Opuntia Ficus-indica (L.) Mill. Seeds. J. Food Process. Preserv. 2019, 44, 1–12. [CrossRef]
  55. Bakar, B.; Çakmak, M.; Ibrahim, M.S.; Özer, D.; Saydam, S.; Karatas, F. Investigation of Amounts of Vitamins, Lycopene, and Elements in the Fruits of Opuntia Ficus-Indica Subjected to Different Pretreatments. Biol. Trace Elem. Res. 2020. [CrossRef]
  56. Diboune, N.; Nancib, A.; Nancib, N.; Aníbal, J.; Boudrant, J. Utilization of Prickly Pear Waste for Baker’s Yeast Production. Biotechnol. Appl. Biochem. 2019, 66, 744–755. [CrossRef]
  57. Puente-Garza, C.A.; García-Lara, S.; Gutiérrez-Uribe, J.A. Enhancement of Saponins and Flavonols by Micropropagation of Agave Salmiana. Ind. Crops Prod. 2017, 105, 225–230. [CrossRef]
  58. Puente-Garza, C.A.; Meza-Miranda, C.; Ochoa-Martínez, D.; García-Lara, S. Effect of in Vitro Drought Stress on Phenolic Acids, Flavonols, Saponins, and Antioxidant Activity in Agave Salmiana. Plant Physiol. Biochem. 2017, 115, 400–407. [CrossRef]
  59. Santiago-García, P.A.; Mellado-Mojica, E.; León-Martínez, F.M.; López, M.G. Evaluation of Agave Angustifolia Fructans as Fat Replacer in the Cookies Manufacture. LWT - Food Sci. Technol. 2017, 77, 100–109. [CrossRef]
  60. Martinez-Gutierrez, F.; Ratering, S.; Juárez-Flores, B.; Godinez-Hernandez, C.; Geissler-Plaum, R.; Prell, F.; Zorn, H.; Czermak, P.; Schnell, S. Potential Use of Agave Salmiana as a Prebiotic That Stimulates the Growth of Probiotic Bacteria. Lwt 2017, 84, 151–159. [CrossRef]
  61. Palatnik, D.R.; Aldrete Herrera, P.; Rinaldoni, A.N.; Ortiz Basurto, R.I.; Campderrós, M.E. Development of Reduced-Fat Cheeses with the Addition of Agave Fructans. Int. J. Dairy Technol. 2017, 70, 212–219. [CrossRef]
  62. Pintor-Jardines, A.; Arjona-Román, J.L.; Totosaus-Sánchez, A.; Severiano-Pérez, P.; González-González, L.R.; Escalona-Buendia, H.B. The Influence of Agave Fructans on Thermal Properties of Low-Fat, and Low-Fat and Sugar Ice Cream. Lwt 2018, 93, 679–685. [CrossRef]
  63. Andrade, A.I.C.; Bautista, C.R.; Cabrera, M.A.R.; Guerra, R.E.S.; Chávez, E.G.; Ahumada, C.F.; Lagunes, A.G. Agave Salmiana Fructans as Gut Health Promoters: Prebiotic Activity and Inflammatory Response in Wistar Healthy Rats. Int. J. Biol. Macromol. 2019, 136, 785–795. [CrossRef]
  64. González-Herrera, S.M.; Rocha-Guzmán, N.E.; Simental-Mendía, L.E.; Rodríguez-Herrera, R.; Aguilar, C.N.; Rutiaga-Quiñones, O.M.; López, M.G.; Gamboa-Gómez, C.I. Dehydrated Apple-Based Snack Supplemented with Agave Fructans Exerts Prebiotic Effect Regulating the Production of Short-Chain Fatty Acid in Mice. J. Food Process. Preserv. 2019, 43, 1–8. [CrossRef]
  65. Bafundo, K.W.; Duerr, I.; McNaughton, J.L.; Johnson, A.B. The Effects of a Quillaja and Yucca Combination on Performance and Carcass Traits of Coccidia-Vaccinated Broilers Exposed to an Enteric Disease Challenge. Poult. Sci. 2021, 100, 101391. [CrossRef]
  66. Stefanello, C.; Moreira, B.; Gräf, W.M.; Robalo, S.; Costa, S.T.; Vieira, I.M.; Miranda, D.J. Effects of a Proprietary Blend of Quillaja and Yucca on Growth Performance, Nutrient Digestibility, and Intestinal Measurements of Broilers. J. Appl. Poult. Res. 2022, 31. [CrossRef]
  67. Boutakiout, A.; Elothmani, D.; Hanine, H.; Mahrouz, M.; Le Meurlay, D.; Hmid, I.; Ennahli, S. Effects of Different Harvesting Seasons on Antioxidant Activity and Phenolic Content of Prickly Pear Cladode Juice. J. Saudi Soc. Agric. Sci. 2018, 17, 471–480. [CrossRef]
  68. González-Monroy, A.D.; Kaur Kataria, T.; Olvera-Cervantes, J.L.; Corona-Chávez, A.; Ozuna, C.; Rodríguez-Hernández, G.; Sosa-Morales, M.E. Dielectric Properties of Beverages (Tamarind and Green) Relevant to Microwave-Assisted Pasteurization. J. Food Sci. 2018, 83, 2317–2323. [CrossRef]
  69. Liguori, G.; Gentile, C.; Gaglio, R.; Perrone, A.; Guarcello, R.; Francesca, N.; Fretto, S.; Inglese, P.; Settanni, L. Effect of Addition of Opuntia Ficus-Indica Mucilage on the Biological Leavening, Physical, Nutritional, Antioxidant and Sensory Aspects of Bread. J. Biosci. Bioeng. 2020, 129, 184–191. [CrossRef]
  70. Dick, M.; Limberger, C.; Cruz Silveira Thys, R.; de Oliveira Rios, A.; Hickmann Flôres, S. Mucilage and Cladode Flour from Cactus (Opuntia Monacantha) as Alternative Ingredients in Gluten-Free Crackers. Food Chem. 2020, 314, 1–9. [CrossRef]
  71. Mata, A.; Ferreira, J.P.; Semedo, C.; Serra, T.; Duarte, C.M.M.; Bronze, M.R. Contribution to the Characterization of Opuntia Spp. Juices by LC-DAD-ESI-MS/MS. Food Chem. 2016, 210, 558–565. [CrossRef]
  72. Betancourt, C.; Cejudo-Bastante, M.J.; Heredia, F.J.; Hurtado, N. Pigment Composition and Antioxidant Capacity of Betacyanins and Betaxanthins Fractions of Opuntia Dillenii (Ker Gawl) Haw Cactus Fruit. Food Res. Int. 2017, 101, 173–179. [CrossRef]
  73. Otálora, M.C.; de Jesús Barbosa, H.; Perilla, J.E.; Osorio, C.; Nazareno, M.A. Encapsulated Betalains (Opuntia Ficus-Indica) as Natural Colorants. Case Study: Gummy Candies. Lwt 2019, 103, 222–227. [CrossRef]
  74. Bouazizi, S.; Montevecchi, G.; Antonelli, A.; Hamdi, M. Effects of Prickly Pear (Opuntia Ficus-Indica L.) Peel Flour as an Innovative Ingredient in Biscuits Formulation. Lwt 2020, 124, 1–7. [CrossRef]
  75. Yao, X.; Hu, H.; Qin, Y.; Liu, J. Development of Antioxidant, Antimicrobial and Ammonia-Sensitive Films Based on Quaternary Ammonium Chitosan, Polyvinyl Alcohol and Betalains-Rich Cactus Pears (Opuntia Ficus-Indica) Extract. Food Hydrocoll. 2020, 106, 1–9. [CrossRef]
  76. Gengatharan, A.; Dykes, G.A.; Choo, W.S. The Effect of PH Treatment and Refrigerated Storage on Natural Colourant Preparations (Betacyanins) from Red Pitahaya and Their Potential Application in Yoghurt. LWT - Food Sci. Technol. 2017, 80, 437–445. [CrossRef]
  77. de Souza, A.C.; Fernandes, A.C.F.; Silva, M.S.; Schwan, R.F.; Dias, D.R. Antioxidant Activities of Tropical Fruit Wines. J. Inst. Brew. 2018, 124, 492–497. [CrossRef]
  78. Amjadi, S.; Ghorbani, M.; Hamishehkar, H.; Roufegarinejad, L. Improvement in the Stability of Betanin by Liposomal Nanocarriers: Its Application in Gummy Candy as a Food Model. Food Chem. 2018, 256, 156–162. [CrossRef]
  79. Hsu, C.T.; Chang, Y.H.; Shiau, S.Y. Color, Antioxidation, and Texture of Dough and Chinese Steamed Bread Enriched with Pitaya Peel Powder. Cereal Chem. 2019, 96, 76–85. [CrossRef]
  80. Som, A.M.; Ahmat, N.; Abdul Hamid, H.A.; Azizuddin, N.M. A Comparative Study on Foliage and Peels of Hylocereus Undatus (White Dragon Fruit) Regarding Their Antioxidant Activity and Phenolic Content. Heliyon 2019, 5, 1–13. [CrossRef]
  81. Zambrano, C.; Kerekes, E.B.; Kotogán, A.; Papp, T.; Vágvölgyi, C.; Krisch, J.; Takó, M. Antimicrobial Activity of Grape, Apple and Pitahaya Residue Extracts after Carbohydrase Treatment against Food-Related Bacteria. Lwt 2019, 100, 416–425. [CrossRef]
  82. Utpott, M.; Ramos de Araujo, R.; Galarza Vargas, C.; Nunes Paiva, A.R.; Tischer, B.; de Oliveira Rios, A.; Hickmann Flôres, S. Characterization and Application of Red Pitaya (Hylocereus Polyrhizus) Peel Powder as a Fat Replacer in Ice Cream. J. Food Process. Preserv. 2020, 44, 1–10. [CrossRef]
  83. Leticia García-Cruz; Valle-Guadarrama, S.; Guerra-Ramírez, D.; Martínez-Damián, M.T.; Zuleta-Prada, H. Cultivation, Quality Attributes, Postharvest Behavior, Bioactive Compounds, and Uses of Stenocereus: A Review. Sci. Hortic. (Amsterdam). 2022, 304, 0304–4238. [CrossRef]
  84. Cejudo-Bastante, M.J.; Hurtado, N.; Muñoz-Burguillos, P.; Heredia, F.J. Stenocereus Griseus (Haw) Pitaya as Source of Natural Colourant: Technological Stability of Colour and Individual Betalains. Int. J. Food Sci. Technol. 2019, 54, 3024–3031. [CrossRef]
  85. Pérez-Armendáriz, B.; Cardoso-Ugarte, G.A. Traditional Fermented Beverages in Mexico: Biotechnological, Nutritional, and Functional Approaches. Food Res. Int. 2020, 136. [CrossRef]
  86. de la Rosa, O.; Flores-Gallegos, A.C.; Muñíz-Marquez, D.; Nobre, C.; Contreras-Esquivel, J.C.; Aguilar, C.N. Fructooligosaccharides Production from Agro-Wastes as Alternative Low-Cost Source. Trends Food Sci. Technol. 2019, 91, 139–146. [CrossRef]
  87. Sáyago-Ayerdi, S.G.; Zamora-Gasga, V.M.; Venema, K. Changes in Gut Microbiota in Predigested Hibiscus Sabdariffa L Calyces and Agave (Agave Tequilana Weber) Fructans Assessed in a Dynamic in Vitro Model (TIM-2) of the Human Colon. Food Res. Int. 2020, 132, 1–8. [CrossRef]
  88. Enríquez-Salazar, M.I.; Veana, F.; Aguilar, C.N.; De la Garza-Rodríguez, I.M.; López, M.G.; Rutiaga-Quiñones, O.M.; Morlett-Chávez, J.A.; Rodríguez-Herrera, R. Microbial Diversity and Biochemical Profile of Aguamiel Collected from Agave Salmiana and A. Atrovirens during Different Seasons of Year. Food Sci. Biotechnol. 2017 264 2017, 26, 1003–1011. [CrossRef]
  89. Gutiérrez-Uribe, J.A.; Figueroa, L.M.; Martín-del-Campo, S.T.; Escalante, A. Pulque; Elsevier Inc., 2017; ISBN 9780128023099.
  90. Villarreal-Morales, S.L.; Muñiz-Márquez, D.B.; Michel-Michel, M.; González-Montemayor, Á.M.; Escobedo-García, S.; Salas-Tovar, J.A.; Flores-Gallegos, A.C.; Rodríguez-Herrera, R. Aguamiel a Fresh Beverage from Agave Spp. Sap with Functional Properties. Nat. Beverages Vol. 13 Sci. Beverages 2019, 179–208. [CrossRef]
  91. Attallah, N.G.M.; El-Sherbeni, S.A.; El-Kadem, A.H.; Elekhnawy, E.; El-Masry, T.A.; Elmongy, E.I.; Altwaijry, N.; Negm, W.A. Elucidation of the Metabolite Profile of Yucca Gigantea and Assessment of Its Cytotoxic, Antimicrobial, and Anti-Inflammatory Activities. Mol. 2022, Vol. 27, Page 1329 2022, 27, 1329. [CrossRef]
  92. Morales-Figueroa, G.-G.; Pereo-vega, G.D.; Reyna-murrieta, M.E.; Pérez-morales, R.; López-mata, M.A.; Sánchez-escalante, J.J.; Tapia-rodriguez, M.R.; Ayala-zavala, J.F.; Juárez, J.; Quihui-cota, L. Antibacterial and Antioxidant Properties of Extracts of Yucca Baccata , a Plant of Northwestern Mexico , against Pathogenic Bacteria. 2022, 2022, 1–8.
  93. Mokbli, S.; Nehdi, I.A.; Sbihi, H.M.; Tan, C.P.; Al-Resayes, S.I.; Rashid, U. Yucca Aloifolia Seed Oil: A New Source of Bioactive Compounds. Waste and Biomass Valorization 2018, 9, 1087–1093. [CrossRef]
  94. Song, W.; Lagmay, V.; Jeong, B.G.; Jung, J.; Chun, J. Changes in Physicochemical and Functional Properties of Opuntia Humifusa during Fermentation with Cellulolytic Enzyme and Lactic Acid Bacteria. Lwt 2022, 159, 113192. [CrossRef]
  95. Abd El-Moaty, H.I.; Sorour, W.A.; Youssef, A.K.; Gouda, H.M. Structural Elucidation of Phenolic Compounds Isolated from Opuntia Littoralis and Their Antidiabetic, Antimicrobial and Cytotoxic Activity. South African J. Bot. 2020, 131, 320–327. [CrossRef]
  96. Chahdoura, H.; Barreira, J.C.M.; Barros, L.; Dias, M.I.; Calhelha, R.C.; Flamini, G.; Soković, M.; Achour, L.; Ferreira, I.C.F.R. Bioactivity, Hydrophilic, Lipophilic and Volatile Compounds in Pulps and Skins of Opuntia Macrorhiza and Opuntia Microdasys Fruits. Lwt 2019, 105, 57–65. [CrossRef]
  97. García-Cayuela, T.; Gómez-Maqueo, A.; Guajardo-Flores, D.; Welti-Chanes, J.; Cano, M.P. Characterization and Quantification of Individual Betalain and Phenolic Compounds in Mexican and Spanish Prickly Pear (Opuntia Ficus-Indica L. Mill) Tissues: A Comparative Study. J. Food Compos. Anal. 2019, 76, 1–13. [CrossRef]
  98. da Silveira Agostini-Costa, T. Bioactive Compounds and Health Benefits of Pereskioideae and Cactoideae: A Review. Food Chem. 2020, 327, 1–14. [CrossRef]
  99. Sandate-Flores, L.; Rodríguez-Rodríguez, J.; Velázquez, G.; Mayolo-Deloisa, K.; Rito-Palomares, M.; Torres, J.A.; Parra-Saldívar, R. Low-Sugar Content Betaxanthins Extracts from Yellow Pitaya (Stenocereus Pruinosus). Food Bioprod. Process. 2020, 121, 178–185. [CrossRef]
  100. König, J. Functional Foods. Encycl. Imdustrial Chem. 2016, 1, 492–499. [CrossRef]
  101. Jiang, L.L.; Gong, X.; Ji, M.Y.; Wang, C.C.; Wang, J.H.; Li, M.H. Bioactive Compounds from Plant-Based Functional Foods: A Promising Choice for the Prevention and Management of Hyperuricemia. Foods 2020, 9. [CrossRef]
  102. Ramírez-Pulido, B.; Bas-Bellver, C.; Betoret, N.; Barrera, C.; Seguí, L. Valorization of Vegetable Fresh-Processing Residues as Functional Powdered Ingredients. A Review on the Potential Impact of Pretreatments and Drying Methods on Bioactive Compounds and Their Bioaccessibility. Front. Sustain. Food Syst. 2021, 5. [CrossRef]
  103. Pinela, J.; Carocho, M.; Dias, M.I.; Ceja, C.; Barros, L.; Ferreira, I. Wild Plant - Based Functional Foods , Drugs , and Nutraceuticals. Wild Plants, Mushrooms Nuts 2017, 1, 315–351. [CrossRef]
  104. Tanna, B.; Mishra, A. Metabolites Unravel Nutraceutical Potential of Edible Seaweeds: An Emerging Source of Functional Food. Compr. Rev. Food Sci. Food Saf. 2018, 17, 1613–1624. [CrossRef]
  105. Gutiérrez-García, G.J.; Quintana-Romero, L.A.; Morales-Figueroa, G.G.; Esparza-Romero, J.; Pérez-Morales, R.; López-Mata, M.A.; Juárez, J.; Sánchez-Escalante, J.J.; Peralta, E.; Quihui-Cota, L.; et al. Effect of Yucca Baccata Butanolic Extract on the Shelf Life of Chicken and Development of an Antimicrobial Packaging for Beef. Food Control 2021, 127. [CrossRef]
  106. García-Lucas, K.A.; Méndez-Lagunas, L.L.; Rodríguez-Ramírez, J.; Campanella, O.H.; Patel, B.K.; Barriada-Bernal, L.G. Physical Properties of Spray Dryed Stenocereus Griseus Pitaya Juice Powder. J. Food Process Eng. 2016, 40, 1–9. [CrossRef]
Figure 1. Arid zone plants a) Agave spp. b) Yucca spp. c) Yucca flowers d) Opuntia cladodes and fruit, e) Pitahaya, and f) Pitaya.
Figure 1. Arid zone plants a) Agave spp. b) Yucca spp. c) Yucca flowers d) Opuntia cladodes and fruit, e) Pitahaya, and f) Pitaya.
Preprints 139020 g001
Figure 2. Traditional food uses of arid zone plants a) Pulque, b) Pulque bread, c) Yucca flower dish, d) Nopales dish, e) Artisanal fermented prickly pear juice (Colonche), f) Pitaya wine, g) Dragon fruit (Pitahaya), and h) Pitaya fruit (“tuna de pitaya”).
Figure 2. Traditional food uses of arid zone plants a) Pulque, b) Pulque bread, c) Yucca flower dish, d) Nopales dish, e) Artisanal fermented prickly pear juice (Colonche), f) Pitaya wine, g) Dragon fruit (Pitahaya), and h) Pitaya fruit (“tuna de pitaya”).
Preprints 139020 g002
Table 1. Macronutrient composition of Arid zone plants.
Table 1. Macronutrient composition of Arid zone plants.
Component (%) Agave spp Yuccaflowers Opuntia spp Opuntia fruit Hylocereus Stenocereus
Moisture 6.44-8.5 50-70 90.1 89.96 87-88.01 85.8
Carbohydrate 60-74 9.77 8.17 1.35 9.34-11 12.33
Proteins 2.5-8.35 0.31 0.36 1.18 0.18-1.1 1.29
Lipids 0.3 17.55 0.14 0.76 0.4-0.45 0.12
Fiber 5-8 19.23 2.75 2.84 0.45-3 3.23
Ashes 6-8 1.60 1.32 6.75 0.96 0.46
Authors [16,33] [34] [35] [36] [37] [38]
Table 2. Bioactive compounds found in arid zone plants and their functionality.
Table 2. Bioactive compounds found in arid zone plants and their functionality.
Plants Bioactive compounds Functional activity Author
Agave spp. Polyphenols (flavonoids), Terpenoids, Steroids, Glycosides, Fructans, Inulin, Oligosaccharides (fructooligosaccharides). Prebiotic activity
Antioxidant activity
Anti-inflammatory activity
Antimicrobial activity
Antifungal activity
Improvement of nutritional, rheological, thermal, and sensory properties
[51,57,58,59,60,61,62,63,64]
Yucca spp. Polyphenols (Gallic acid, 4-hydroxybenzoic acid, Vanillic acid, Chlorogenic acid, Caffeic acid, 4-Coumaric acid, Ferulic acid, Rutin, Quercetin 3-D-galactoside, Quercetin 3-glucoside, Trans-cinnamic acid, Quercetin, Kaempferol), saponins. Antioxidant activity
Ant—inflammatory activity
Antimicrobial activity
[34,65,66]
Opuntia spp (Cladodes) Phenols (gallic acid, epicatechin gallate, vanillic acid, chlorogenic acid, procyanidin B2, epicatechin, vanillin, p-coumaric acid, epigallocatechin, ferulic acid, synapic acid, benzoic acid, ellagic acid, hyperoside, isoquercetin, rutin, chloridzine, quercetin, vitamin C & E, and flavonoids; Caempferol, Hyperoside, Prociadin), Terpenoids (β-carotene, α-carotene, lutein, zeaxanthin). Antioxidant activity
Hypoglycemic activity
Antibacterial activity
[23,53,67,68,69,70]
Opuntia spp (fruit) Phenols (vitamin A, C & E, flavonoids; rutin, quercetin glucoside, isorhamnetin glucosyl-dirhamnoside, isorhamnetin pentosyl-rutinoside, isorhamnetin pentosyl-glucoside, isorhamnetin pentosyl-rhamnoside, isorhamnetin rutinoside, isorhamnetin glucoside, quercetin), Betalains (betaxanthins, muscaaurin, indicaxanthin isomer I, indicaxanthin isomer II, betacyanins, betanin, betanidin-5-O-β-glucoside, gomphrenin, betanidin isobetanin, indicaxanthin isomer, indicaxanthin, betanin isomer), Terpenoids (carotenoids), and Organic acids (malic acid, quinic acid, citric acid, succinic acid, piscidic acid derivative I, piscidic acid derivative II, piscidic acid, 2-Feruloyl piscidic acid, hydroxybenzoic acid, eucomic acid, ferulic acid glucoside, caffeic acid, and fumaric acid) Antioxidant activity
Antimicrobial activity
Anti-inflammatory activity
Hypoglycemic activity
Antiulcerogenic activity
[71,72,73,74,75]
Hylocereus spp. Phenols (vitamins, flavonoids, phenolic acids, and betalains; betacyanins, betanin, isobetanin, betanidin, phyllocactin and hylocerenin), Terpenoids, Fatty acids and sterols
Antioxidant activity
Antimicrobial activity
Prebiotic activity
[47,76,77,78,79,80,81,82]
Stenocereus spp. Phenols and betalains (isobetanin, betanidin, 17-Decarboxy-neobetanin, isobetanidin, neobetanin, 2-Decarboxy-neobetanin, betacyanins and betaxanthines). Antioxidant potential [31,83,84]
Table 3. Use of arid zone plants in foods with functional potential and/or improvement of physical properties.
Table 3. Use of arid zone plants in foods with functional potential and/or improvement of physical properties.
Plants Food or additive Functional contribution Bioactive compound Author
Agave spp Powdered extract of Agave salmiana fructans Prebiotic activity and Anti-inflammatory activity Fructans [63]
Cookies with Agave angustifolia fructans as a fat substitute Improved rheological properties Fructans [59]
Reduced fat cheeses Improved nutritional qualities Fructans [61]
Ice cream Improved thermal properties Fructans [62]
Dehydrated apple enriched with prebiotics Prebiotic activity and sensory properties Fructans [64]
Yucca spp. Antimicrobial control in food
Food packaging development
Antimicrobial activity
Saponins [105]
Opuntia spp (Cladodes) Pasta with flour from Opuntia cladodes Antioxidant activity Hypoglycemic activity Fiber [45]
Prickly pear cladode juice Antioxidant activity Gallic acid, epicatechin gallate, vanillic acid, procyanidin B2, epicatechin, p-Coumaric acid, epigallocatechin, ferulic acid, sinapic acid, benzoic acid, hyperoside, isoquercetin, rutin, quercetin [67]
Cookies gluten-free with flour from cactus Antioxidant activity Fiber soluble and insoluble, flavonoids, phenolic acids, leutin. β-carotene, zeaxanthin, α-carotene [70]
Bread with Opuntia ficus-indica mucilage Antioxidant activity Mucilage [69]
Pigment Antioxidant activity Betacyanins, betaxanthins [72]
Opuntia spp (fruit) Gummy candy Antioxidant activity Betalains [73]
Cookies enriched with prickly pear peel flour Antioxidant activity Carotenoids, betalains, betacyanins, betaxantins [74]
Edible films Antioxidant activity and antimicrobial activity Betalains [75]
Yogurt Antioxidant activity Betacyanins; betanin, isobetanin, betanidin, phyllocactin,hyloccerenin [76]
Wine Antioxidant activity Succinic acid, citric acid, acetic acid, [77]
Hylocereus spp. Gummy candy Antioxidant activity Betalains [78]
Chinese steamed bread enriched with pitaya peel powder Antioxidant activity Batacyanin [79]
Reduced-fat ice cream Antioxidant activity
Technological and physicochemical properties
Betacyanins, fiber and minerals [82]
Natural colourant Antioxidant activity Betalains, isobetanin, betanidin, 17-Decarboxy-neobetanin, isobetanidin, neobetanin, 2-Decarbaxy-neobetanin [84]
Pitaya juice powders Antioxidant activity Betalains, fructose, glucose, sucrose, citric acid, malic acid and tartaric acid [106]
Stenocereus spp. Low-sugar food colorant Antioxidant and antimicrobial activity Betaxantinas [99]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
Copyright: This open access article is published under a Creative Commons CC BY 4.0 license, which permit the free download, distribution, and reuse, provided that the author and preprint are cited in any reuse.
Prerpints.org logo

Preprints.org is a free preprint server supported by MDPI in Basel, Switzerland.

Subscribe

Disclaimer

Terms of Use

Privacy Policy

Privacy Settings

© 2025 MDPI (Basel, Switzerland) unless otherwise stated