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Review

Peach Palm (Bactris gasipaes Kunth.): Ancestral Tropical Staple with Future Potential

by
Nancy González-Jaramillo
1,2,
Natalia Bailon-Moscoso
3,
Rodrigo Duarte-Casar
4 and
Juan Carlos Romero-Benavides
2,*
1
Maestría en Alimentos, Facultad de Ciencias Exactas y Naturales, Universidad Técnica Particular de Loja, Loja 110108, Ecuador
2
Departamento de Química, Facultad de Ciencias Exactas y Naturales, Universidad Técnica Particular de Loja, Loja 110108, Ecuador
3
Facultad de Ciencias de la Salud, Universidad Técnica Particular de Loja, Loja 110108, Ecuador
4
Departamento de Turismo y Gastronomía, Facultad de Ciencias Administrativas y Económicas, Universidad Técnica de Manabí, Portoviejo 130105, Ecuador
*
Author to whom correspondence should be addressed.
Plants 2022, 11(22), 3134; https://doi.org/10.3390/plants11223134
Submission received: 26 October 2022 / Revised: 8 November 2022 / Accepted: 13 November 2022 / Published: 16 November 2022
(This article belongs to the Special Issue Phytochemicals: Antioxidant, Antitumoral and Anti-inflammatory Activity)
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Abstract

:
A pre-Columbian staple, Bactris gasipaes Kunth. is a palm tree domesticated around 4000 years ago, so appreciated that a Spanish chronicler wrote in 1545, “only their wives and children were held in higher regard” by the Mesoamerican natives. The peach palm is an integral part of the foodways and gastronomy of Ecuador, Colombia, Bolivia, Peru, Brazil, and other tropical American countries; meanwhile, it is almost unknown in the rest of the world, except for hearts of palm. Although abundant, the species faces anthropogenic threats. The purpose of this study is to describe and summarize the physicochemical, nutritional, and bioactive characteristics of the peach palm and its two main alimentary products: hearts of palm and fruits, highlighting the functional and antioxidant potential of the latter, showing both ancestral and modern uses. There is active research on peach palm products and coproducts that aim for better, more sustainable uses of its traditional and recently found properties. The review and presentation of studies on this strategically relevant species can motivate the protection of endangered populations and stimulate new lines of research to advance development in the food, pharmaceutical, and cosmetic industries, with fair trade, sustainable development goals, and adaptation to climate change in mind.

1. Introduction

The Amazon is a multicultural and multiethnic space where natural resources have been used ancestrally to provide housing, medicine, and food to its inhabitants [1]. Some of these are fruits that are currently considered promising for their sensory, nutritional, and ethnomedicinal characteristics [2,3,4]. Among these important species, palms are an important family. Palm trees are considered to be more useful to mankind than any other family, inspiring the tree of life motif [5]. An important palm in the Amazon and tropical America is Bactris gasipaes Kunth., in the Areacaceae family, the most important pre-Columbian American palm [6], a polyvalent pre-Columbian staple. This species, among many others, is expected to undergo changes in the land area suitable for cultivation due to climate change, with loss of current cultivation areas and the emergence of new ones [7]. This would not be the first climate event in Amazonia [8], and B. gasipaes overcame earlier events.
There is abundant research published on B. gasipaes, including excellent review articles [9,10]. We found the need for an integrated, updated view that presents the current knowledge of the food and phytochemical study of the species. Most research on the species centers on its biology and agriculture.
This article discusses the ancestral and modern uses of B. gasipaes: food, pharmacological, and others, with emphasis on the fruit of the species. We aim to find research and application opportunities in food and industrial production in the face of the food crisis that favors a return to more ecological agroecosystems [11]. We also provide material for action on the following Sustainable Development Goals (SDG): 1 No poverty, 2 Zero hunger, 9 Industry, innovation and infrastructure, 12 Responsible consumption and production, 13 Climate action, and 15 Life on land.

2. Methods

A narrative literature review was performed consulting the published literature in English, Spanish, and Portuguese for “Bactris gasipaes” in the title, abstract, and keywords; the last two languages were included because they are the main languages spoken in the countries where the species grows. The scientific databases consulted were Scopus (413 results), Web of Science (218), Crossref (494), Dimensions (505), and SciELO (136). Among the documents returned by the searches, those having to do with history, domestication, ancestral and modern food, and feed uses, ethnopharmacology, cultural aspects, phytochemical composition, sustainability, and innovation were included in the review. Results from the last fifty years were included in the search. Ad hoc searches were performed as needed to supplement the information and relevant, earlier publications are also mentioned.

3. Taxonomy and Distribution

Bactris gasipaes Kunth. Belongs to the Bactris Jacq. ex Scop. genus of spiny palms in the Arecaceae family, Cocoseae tribe. The genus includes seventy-nine species, of which several are edible. B. gasipaes is the most used species as a food resource in the genus. There are two accepted varieties of the species: Bactris gasipaes var. chichagui (H. Karst.) A.J. Hend. [12], and Bactris gasipaes var. gasipaes [13,14]. The chichagui variety is mostly wild with smaller, oilier fruit, and the gasipaes variety is cultivated, with larger and starchier fruit [15].
B. gasipaes currently extends throughout the Amazon basin and other humid lowlands of the neotropics, with one population up to 1800 m above sea level in Colombia. The species has been introduced to countries such as Australia, Indonesia, Malaysia, Reunion island, and Hawaii [16,17,18] to relieve the pressure on local palms endangered by non-sustainable production, especially where hearts of palm are produced.
Common names for this species vary depending on the region, some of which are presented in Table 1. Figure 1 shows the distribution of B. gasipaes in tropical America by country, both as a native and as an introduced species.

4. Morphological Description

The species is characterized by being cespitose, i.e., several trunks (one to fifteen) with heights from six to twenty meters stemming from the point of origin, smooth in appearance, with evident internodes, surrounded by a ring of black thorns (Figure 2A) [16,20]. The leaves, located at the top of the trunk, are arched and long (up to 100 cm), their sheath covered with small white or dark brown spines; inflorescences appear in intrafoliar clusters and are monoecious: female and male flowers emerge from the same stem; with some structures, such as the peduncle, covered with spines. The species can produce up to ten inflorescences per year [17,21].
Inside the trunk, the heart of palm can be found, a vegetable considered a delicacy: cylindrical and sweet-tasting, it consists of the apical meristem, divided into basal, central and apical with marked differences in texture due to the arrangement of the structural fibers; its harvest results in the death of some species [22,23], but not in Bactris spp., and other cespitose palms. This is why it has become a more sustainable prime source for hearts of palm, together with Euterpe oleracea (Açai).
The fruits are spherical or ovoid in shape, and come in a variety of sizes; the largest are up to10 cm long and up to 6 cm in diameter, they are clustered, green when unripe, and from yellow to orange when ripe [5,24]. The inside of the pulp is floury or oily depending on the variety, and in the center, there is a seed that resembles a very oily small coconut (Figure 2B). According to the weight of the fruit, B. gasipaes is categorized as microcarpa (<20 g), mesocarpa (>21 g, <70 g) and macrocarpa (>70 g) (Figure 2C), and also as orange, yellow, and lately, white varieties [25,26]. The fruit presents low polyphenol oxidase activity, which makes it suitable for minimally processed products [18].
The similarity with other species suggests the species was domesticated in areas of the Amazon through hybridization [5,27,28]. Its food use is mainly for its oil content, plus the harvesting process has ethnic, cultural, and traditional value [5,15,28,29]; in addition, it is attractive as a promising industrial resource for new products derived from the same species (chonta, palm heart, wood) [30,31].

5. Mythical Origins

There are several related origin myths for B. gasipaes in the traditions of Peruvian (Asháninka), Colombian (Yukuna Matapi), and Ecuadorian (Shuar Achuar) native peoples [32,33,34,35]. A common motif is that chonta and maize come from the otherworld, stolen by human or demigod visitors. In a Catío myth, the immortals of Armucurá, a planet below earth, feed on the vapors of B. gasipaes, but it is the human visitors that return with seeds for human cultivation and consumption [35]. In these stories, practical elements are transmitted: the quality of the wood for the making of proper weapons; the food value of the species; and the importance of not throwing the seeds away but saving them for cultivation. The interdependence of the cultivated palm and humans is shown in these stories, pointing to a domesticated species, no longer able to survive in the wild. Another example of how ingrained B. gasipaes is in the local cultures is the calendar use: “Pupunha summer” is part of the calendar of the indigenous peoples of the Tiquié river in Brazil [36], and the harvest season between December and March is an important event. Today, chonta festivities that reenact these myths survive and are becoming a community tourism product [37].

6. History

The origin of the species is unclear, but consensus points to the Bolivian amazon as a possible origin [5]. Three hypotheses coexist: a southwestern Amazon domestication, a northwestern South America domestication, and that of multiple origins. Two dispersals are supported by genetic diversity patterns: one along the Ucayali river, northwestern South America, and into Central America with a starchy, fermentable fruit used as a staple; another, along the Madeira river into central and eastern Amazonia in which the smaller, starchy, and oily fruit is used for snacking [15]. Similarity with other species suggests the species was domesticated in areas of the Amazon through hybridization, with highest genetical diversity in northern Peruvian and Ecuadorian Amazon. The domestication of the species is tentatively dated between 4000 and 3000 years BP, coincident with the establishment of sedentary communities in Amazonia [5,27,28]. The earliest archaeological remains of the species, presumably already cultivated, are dated 2300–1700 BC in Costa Rica [38].
The records about the species date back to the fifteenth century, and it is presumed that the beginning of its production under the Spanish was as timber, not as a food resource. During the Spanish conquest, native crops such as B. gasipaes lost importance, due to the massive native population loss [8] and the adoption of European productive systems. The European contact in the fifteenth–sixteenth centuries in Central America is marked by the awe of the Spaniards towards how appreciated the species was. Spanish chronicler Godínez Osorio wrote in 1575 that, “only their wives and children were held in higher regard” [39]. The timber of B. gasipaes was used in the early 1540s by the Spaniards to build fortifications because of its hardness and the fact that the trunk is naturally covered by thorns. It was also used as a weapon: more than 30,000 palms were cut down to submit the natives to hunger [40]. The same chronicle attests to the consumption of hearts of palm by a Chichimeca army under the orders of the Spaniards. Before the Spanish invasion, the fruit of B. gasipaes was a staple, and the harvest was one of the most important events of the year, with most births taking place nine months after it. Even today, 500 years later, the use of the species has not reached back to its pre-Hispanic level [15,17,41]. B. gasipaes fruit has been relegated pejoratively as a “fruit of the Indians”, a forgotten, neglected fruit [39,42]; however, in times of scarcity it has been used to provide food security [43], and it still is today [9].

7. Traditional Uses

The main use of this species is timber. It is suggested that domestication of the species was primarily because of its wood [32]. The species is also an important part of the Amazonian and Central American foodways and ethnopharmacology, and material and social uses are also listed [44]. The main morphological structure from an ethnopharmacological perspective is the root, used to reduce inflammation and infections, and both to promote female fertility and act as an aid during pregnancy [20].
From the alimentary perspective, the main products are hearts of palm and fruits. The palm heart, already documented in the sixteenth century, is today one of the most important non-timber products in South America [45], and probably the best-known part of B. gasipaes worldwide, used in the preparation of salads, pizza, and even ceviche [46]. B. gasipaes hearts of palm are replacing those of other species, often endangered by overharvesting, mainly Euterpe spp. Being a cespitose species, the plant is not killed by prudent harvesting and thus a more sustainable product can be obtained. Canned hearts of palm are currently exported by several American countries. Ecuador and Bolivia are the largest exporters [47].
The fruit, despite not being produced in the same proportion, is a popular traditional food that needs to be processed prior to consumption, due to its high oxalate and other antinutrient content [48]: cooked fruit, flour, fermented chicha, slowly fermented silage [38], and oil are among the traditional uses. The fruit and its processing byproducts have also been used as animal and fish feed [5,49,50,51]. Larger fruit is less palatable than smaller fruit, due to a coarse, dry texture. To compensate, the fruit is frequently consumed with mayonnaise or sour cream.
An indirect alimentary use of the species is the use of the decomposing trunk after felling the palm to raise chontacuros, the larvae of Rhynchophorus palmarum L., a “…delicious, butter-tasting” delicacy [52] in the Ecuadorian and Peruvian Amazonia rich in protein, vitamin E, and minerals, also used against cough, asthma, and other respiratory affections [53,54,55].
Some Indigenous communities, such as the Colombian Uitoto, do not have access to table salt, so they make “bush salt,” obtained from burning, dissolving, filtering, and drying plant material, including the barkless stem of B. gasipaes. This process yields a mixture of salts: chloride, sulfate, and carbonate are the main anions, and potassium is the main cation. These salts are not particularly good tasting because of the high carbonate and low sodium content: their taste was described by Spanish chronicler Juan de Castellanos in the sixteenth century as “almost having the taste of sardines and herrings.” There is also a cosmic, alchemical, significance for communities, where extracting salt is considered to be the cleansing of the evil and disease and converting them into human food [56].
In other uses, the wood is used in the manufacture of flooring, marimbas, bows and arrows, spears, knives, and building material, the thorns are used as needles, the leaves for roofing, the fruit is used together with Clibadium surinamense L. leaves to make fish poison [53]. Table 2 summarizes traditional ethnomedical, alimentary, and other uses of B. gasipaes. The use of the wood is so present that the verb achuntar (to hit the mark) has entered the Spanish language from chunta, the quechua name for B. gasipaes, referring to the use of the wood to make arrows [57].

8. Modern Uses

Aside from the traditional uses, new applications are being found for B. gasipaes. Chonta pulp, in combination with other materials, is being implemented in the decontamination of water of minerals such as lead and cadmium [29,60]. Sensory evaluation and consumer acceptance analysis has been performed: oily fruit is more attractive and less averse than starchy fruit [61]. This may influence genetic development of the species and also guide the manufacture of food products from the fruit. Food products are being produced and marketed other than hearts of palm: jam, jelly, wine, flour and flour products (bread, pudding, pasta, etc.) [62,63].
There is a variety of alimentary and industrial applications and new uses for B. gasipaes, both as product and from the industry byproducts: functional food ingredients, brewing, dyes, and others. Some examples are listed in Table 3.

9. Nutritional Composition

The fruit of the peach palm, macrocarpa variety, is a starchy, ancestral staple, while meso and microcarpa varieties are used as snacks due to their smaller size, and to obtain oil. In order to consume the fruit, it is necessary to ferment or cook it for 1–3 h, usually in salt water, to remove the irritating oxalate crystals usually found in red drupes and reduce other antinutrients, such as phytates and tannins [20,71,72]. The nutritional composition of the fruit is summarized in Table 4 and that of the flour in Table 5.
The fruit of B. gasipaes is characterized by the amount of carbohydrates and fats contained that tend to increase when cooked. The oil obtained from the mesocarp is rich in unsaturated fatty acids, particularly oleic acid, while saturated fatty acids such as lauric acid are found in the seed [73,74]. The fruit is also high in dietary fiber, and although the protein content is low, all essential amino acids are present. Essential minerals are also present: K (12%), Se (9%), and Cr (9%) are the most abundant [5,24]. In addition, the bromatological characterization of the epicarp or peel shows: protein, 2.3%; ash, 2.3%; raw fiber, 8.2%; detergent acid fiber, 13.4%; and detergent neutral fiber, 63.6%. This composition supports the use as raw material for the production of flour [75,76].
The industrialization of products derived from this fruit has been increasing in recent years. The production of flour obtained from the mesocarp of the fruit, in combination with other flours such as wheat, corn, or quinoa and technological adjuvants, are acceptable by consumers and can be used in different matrices (sandwiches, cakes, pasta), the high carotenoid content makes the flour a potentially functional ingredient [66,77,78]. Nutritional composition of fruit from different origins is summarized in Table 4.
There is variability in the nutritional values that can be explained by the different B. gasipaes varieties, size, and starch–oil composition of the fruit. The nutritional parameters of flours from different origins are shown in Table 5. Flour from macrocarpa and seedless varieties show higher carbohydrate content. Additionally, flour from seedless fruits has a higher protein content.
The oil obtained from B. gasipaes is rich in mono and polyunsaturated fatty acids, particularly oleic, with the presence of ω-3 and ω-6 acids and bioactive lipids. It can be considered a heart-healthy oil [82,83].

10. Biological Activity

The information derived from research on the biological activity of the fruit of B. gasipaes (pulp, seed, peel, or whole fruit) has been summarized in Table 6—antioxidant activity, and Table 7—other biological activity. Most studies focus on antioxidant and protective activity, due to the presence of carotenoids. There are other studies on its biological activity that are not related to its traditional use. Within these activities we can mention the hypoglycemic capacity, modulation of lipid metabolism, cytotoxic activity, and its effect on sperm motility [84].

11. Phytochemical Composition

According to the bibliographic data collected; the phytochemical composition of fruit pulp in concentrations greater than 1 mg/100 g, comprises 16 phytochemical compounds (Table 8 and Figure 3), which include: one ester, one aldehyde, four alcohols, four carotenoids, five fatty acids, and one aromatic compound. However, compounds in nanogram quantities have also been identified through ultra-high performance liquid chromatography coupled to tandem mass spectrometry with quadrupole analyzer (UHPLC–MS/MS), i.e., protocatechuic acid (30 ng/g), chlorogenic acid (20 ng/g), p-coumaric acid (16.6 ng/g), ferulic acid (160 ng/g). In addition, flavonoids such as myricetin (20 ng/g), apigenin (2.1 ng/g) [85], and also rutin, catechin [90], vicenin-2, and schaftosides [26].
The analysis carried out by [82] from the pulp oil analyzed by gas chromatography, identified minoritarian fatty acids: myristic acid (0.10%), margaric acid (0.11%), arachidonic acid (0.24%), and linolenic acid (1.17%). Fatty acid composition changes by variety [91]
In the comparisons among the lipid extraction from of pulp (2 g) of four varieties of Colombia, obtained by Soxhlet extraction using hexane and analyzed by gas chromatography (GC) with flame ionization detector, shows that the fatty acids present, respectively, are: lauric (0.014 and 0. 015%), myristic (0.12, 0.14, 0.13, and 0.10%), palmitic (34.9, 34, 39.9, and 34.5%), palmitoleic (7.9, 8.3, 9.5, and 10.8%), stearic (1.5, 1.6, 1.4, and 1%), oleic (51.9, 45.8, 38, and 46.4%), linoleic (2.4, 8, 8.6, and 5.3%), linolenic (0.2, 0.9, 1.5, and 0.9%), saturated fatty acids (36.8, 36.1, 41.7, and 36.2%), and polyunsaturated fatty acids (2.6, 8.9, 10.1, and 6.2%) [92].
Today there is an interest in the food industry in replacing synthetic dyes such as tartrazine (yellow-orange color) as additives due to adverse reactions related to hypersensitization to salicylic acid, complications in respiratory diseases, and long-term genotoxic effects [93] of dyes such as β-carotenes, although they are not as stable in extreme conditions [94,95]. However, carotenes have an added value due to the great diversity of biological activities they present, mainly as antioxidants. From the raw and cooked pulp, α-carotene, E-γ-carotene, and E-lycopene have been identified using high-resolution liquid phase chromatography with a diode network detector and visible ultraviolet spectroscopy (HPLC-DAD-UV/Vis) [86], and HPLC with a photodiode-array detector (PDA) coupled to mass spectrometry with an ion trap analyzer (MS) and ultraviolet spectroscopy (UV/Vis). The concentration of these components varies according to the place of origin of the sample, where the ones originating in Bolivia are those that presented higher concentrations [96,97], while Santos [98] have reported the identification of lutein (11.9 mg/Kg) and cis lutein (2.22 mg/Kg) using HPLC-PDA-UV/Vis.
A comparison of carotenoid extraction from pulp, between supercritical fluids, traditional methods of methanolic extraction, and the Soxhlet extraction method using petroleum ether was performed [99]. The highest extract yield was that obtained by Soxhlet extraction, followed by methanolic extraction, and finally supercritical fluids with extraction conditions of 300 bar and −60 °C. The concentration of carotenoids (mg/g of extraction) differs from the yield, with the order of highest to lowest extraction: Soxhlet, supercritical fluids, and methanolic extraction. However, the antioxidant activity evaluated by spectroscopic techniques compared to caffeic acid and quercetin show that the best antioxidant activity is that of the extract using the Soxhlet extraction, then methanolic extraction, and finally supercritical fluids, most likely the type of carotenoids obtained differs with the type of extraction.
Another promising method is ultrasound-assisted extraction, in this case to obtain total carotenoids from the peel of the chonta fruit and optimize extraction conditions: ultrasonic intensity (1528 W/m2), temperature (35 °C), and time (30 min), obtained 163.47 mg carotenoids per 100 g fruit [100], which is considered a significant amount of carotenoids.

12. Sustainable Development Goals (SDG)

B. gasipaes cultivation and uses are linked to several SDGs through food and non-food initiatives. Examples include farming, products recovered from waste, and food safety are shown in Table 9. The main SDGs are Responsible Consumption and Production (nine publications), Life on Land (five), and Climate action (three).

13. Major Concerns

Even though the species is widely spread, there is concern for the loss of populations due to soybean cultivation, forest clearance, and road building [109], as well as genetic erosion due to centuries of neglect [38]. Lately the forest fires due to anthropogenic action and climate change have risen as a concern. The modification of current cultivation areas, with an allover descent in surface due to the climate crisis [7] is also a major concern.

14. Conclusions

The peach palm is a very important species in tropical America, especially as a food source that not only provides food safety but also several opportunities for sustainable industrial production. The fruit is a rich source of bioactive compounds with significant antioxidant capacity, and nutritional, both macro and micronutrient, and functional properties.
Prudent cultivation and use of B. gasipaes in a way respectful of traditional methods, coupled with sustainable innovation has potential for advancing the SDGs.
Despite its widespread cultivation area, populations, and genetic diversity of the species, they are at risk due to deforestation, neglect, and the climate crisis.

Author Contributions

N.G.-J.: research, draft writing. N.B.-M.: conceptualization, manuscript review. R.D.-C.: research, translation, figures. J.C.R.-B.: conceptualization, manuscript review, overview. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by Universidad Tecnica Particular de Loja (UTPL).

Data Availability Statement

Not applicable.

Acknowledgments

We are grateful to the Universidad Técnica Particular de Loja (UTPL) for supporting this research and open access publication.

Conflicts of Interest

The authors declare no conflict of interest.

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Plants 11 03134 g001 550
Figure 1. Distribution of Bactris gasipaes Kunth., in tropical Central and South America. Grey: native; light blue: introduced (Trinidad and Tobago, El Salvador). Source: [19]. Shaded areas, main complexes: red: Occidental; green: Maracaibo; brown: Upper Amazonia; yellow: Eastern Amazonia. Source: [20].
Figure 1. Distribution of Bactris gasipaes Kunth., in tropical Central and South America. Grey: native; light blue: introduced (Trinidad and Tobago, El Salvador). Source: [19]. Shaded areas, main complexes: red: Occidental; green: Maracaibo; brown: Upper Amazonia; yellow: Eastern Amazonia. Source: [20].
Plants 11 03134 g001
Plants 11 03134 g002 550
Figure 2. Morphology of Bactris gasipaes: (A). Trunks showing internodes covered with thorns. Source: David Stang (CC BY-SA 4.0); (B). Difference between macrocarpa and microcarpa fruits; (C). B. gasipaes fruit, microcarpa variety, Cali Colombia. Source: Michael Hermann (CC BY-SA 3.0).
Figure 2. Morphology of Bactris gasipaes: (A). Trunks showing internodes covered with thorns. Source: David Stang (CC BY-SA 4.0); (B). Difference between macrocarpa and microcarpa fruits; (C). B. gasipaes fruit, microcarpa variety, Cali Colombia. Source: Michael Hermann (CC BY-SA 3.0).
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Plants 11 03134 g003 550
Figure 3. Phytochemical composition of Bactris gasipaes fruit. Major compounds.
Figure 3. Phytochemical composition of Bactris gasipaes fruit. Major compounds.
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Table
Table 1. Common names of Bactris gasipaes according to location.
Table 1. Common names of Bactris gasipaes according to location.
CountryNames
BrazilPapunha; Pupunha; Pupunheira; Popunha.
BoliviaChonta; Palma de Castilla; Tembe; Chima; Anua; Mue; Huanima; Pupuña; Tëmbi; Eat; Tempe.
ColombiaCachipay; Chantaduro; Chenga; Chonta; Chontaduro; Chichagai; Pijiguay; Pupunha; Pupuña; Pejibá; Jijirre; Macanilla; Contaruro; Have; Pipire.
Costa RicaPejibaye; Pejivalle.
EcuadorChonta; Chonta dura; Chontaduro; Chonta palm; Palmito; Chantaduro, Puka chunta; Shalin chunta
GuyanaParipie; Parepon.
PeruChonta; Ruru; Pejwao; Pifuayo; Chonta Duro; Joó; Uyai; Mee; Pijuayo; Pisho-Guayo; Sara-Pifuayo.
SurinameAmana; Paripe; Paripoe.
VenezuelaBobi; Cachipaes; Macana; Peach; Pijiguao; Pixabay; Rancanilla; Gachipaes; Pichiguao; Piriguao; Cachipay; Pachigaro.
Adapted from [16,19].
Table
Table 2. Traditional uses of B. gasipaes ordered by plant organs.
Table 2. Traditional uses of B. gasipaes ordered by plant organs.
Plant OrganApplicationsRef.
Ethnomedical
FruitBody and head aches, inflammation of eyes and gall bladder, galactagogue, infertility, cough, colds, psoriasis, tuberculosis.[19]
LeafEar pain, epilepsy, baths that prevent premature birth, energy cleansing.[19]
Palm, heart of palmStomach, ear, menstrual and muscle pain, eye inflammation, inguinal hernia, malaria, chickenpox, hepatitis, childbirth problems, infertility, and uterine infections, anemia, antiophidic, prevention of baldness, galactagogue, sedative, hot hearts of palm are rubbed on children to dispel panic attacks.[19,53]
SeedStomach pain, cancer[19]
RootUrinary and menstrual problems, inguinal hernia, uterine infections, colds and pneumonia, epilepsy, body, stomach, and ear pains, diarrhea (decoction), eye inflammation, vermicide, postpartum depression, galactagogue (washed with cooked root), contraceptive, prevention of baldness, hepatitis, malaria, mastitis, prevention of abortions, hemorrhages in childbirth, fertility, and aphrodisiac.[19,53,58]
Alimentary
FruitCooked, roasted, dried, canned, jams and preserves, flour. Drinks: “chucula” (mixed with banana), “chicha” and juices. Oil for human consumption.[19,53]
PalmIt is consumed preferentially cooked due to the antinutrient content: as a side dish, salad, filling, ceviche. Consumed dry or canned in brine.[19,46,53,58]
SeedCooking oil, dried and ground to prepare a coffee-like drink, toasted as a snack.[19,53]
Other
FruitCosmetic, fuel, and lubricating oil, fertilizer, hunting and fishing bait, dye, animal feed, fish poison mixed with Clibadium surinamense leaves.[19,53,58]
SeedCosmetic and soapmaking oil, body adornment, toy (marbles), handicrafts.[19]
LeafBody adornment, thatching, baskets, mats, and fan weaving, dying, wrapping, fuel, animal feed, paper, fertilizer.[19,53,58]
WoodManufacture of marimbas, knives, blowguns, spears, good luck charms, vessels, bows, arrows, looms, pylons, macanas, walls and wall sidings, corrals, canoes, beds, weaving spindles, flooring (parquet), fishing rods and traps, ceremonial tables, and altars of healing, hollow trunk as a conduit or trough, manufacture of paper and fertilizers.[53,58]
ThornRemoval of other thorns, sewing needles, witchcraft.[53,58,59]
Table
Table 3. Modern uses for B. gasipaes.
Table 3. Modern uses for B. gasipaes.
Plant OrganUseRef.
FruitMicrowave assisted extraction, extract emulsified for improved carotenoid bioavailability.[64]
FruitFermentable substrate for lager beer brewing.[65]
PeelNatural food dye from peel flour.[66]
PeelEmulsified flavoring paste.[67]
Peel, pulpFunctional food additives.[68]
PlantB. gasipaes industrial waste as substrate for xylanase production.[69]
PlantB. gasipaes and Theobroma cacao residues used as substrate for edible mushroom cultivation.[70]
PulpIn combination with other materials, heavy metal decontamination of water.[29,60]
Table
Table 4. Nutritional composition of B. gasipaes fruit from different origins.
Table 4. Nutritional composition of B. gasipaes fruit from different origins.
Parameter (per 100 g Cooked Fruit)Colombia [79]Costa Rica [71]Peru [80]Brazil [63]Brazil, White [25]
Energy (Cal)358185–196184-266.6
Carbohydrates (%)19.037.6–41.141.024.05–44.1643.76 ± 1.76
Moisture (%)48.250.5–52.252.347.98–63.9628.85 ± 0.57
Lipids (%)25.74.4–4.63.22.62–6.887.80 ± 1.85
Protein (%)6.32.6–3.32.82.00–3.905 ± 1
Fiber (%)12.71.0–1.41.3-10 ± 1
Calcium (mg)8114–232321.8 ± 2.4150 ± 18
Phosphorus (mg)47-20-86 ± 12
Iron (mg)0.70.7–1.00.65-2.3 ± 0.57
Table
Table 5. Nutritional parameters, B. gasipaes flour.
Table 5. Nutritional parameters, B. gasipaes flour.
Parameter (per 100 g Flour)Microcarpa [63]Mesocarpa [63]Macrocarpa [63]Seedless [81]
Carbohydrates (%)67.32 ± 0.466.68 ± 0.9275.02 ± 0.2376.2 ± 0.8
Moisture (%)12.21 ± 0.4112.58 ± 0.519.60 ± 0.176.94 ± 0.04
Lipids (%)7.40 ± 0.204.73 ± 0.043.95 ± 0.137.8 ± 0.7
Protein (%)4.62 ± 0.033.20 ± 0.022.46 ± 0.026.9 ± 0.1
Fiber (%)5.47 ± 0.7010.82 ± 0.437.67 ± 0.18
Energy (kcal)300.07 ± 2.46326.67 ± 2.01321.28 ± 1.64403 ± 2
Table
Table 6. Antioxidant activity of B. gasipaes.
Table 6. Antioxidant activity of B. gasipaes.
MSMaterialModelMethodResultRef.
PulpAqueous ethanolic extractIn vitroABTS88 ± 1%; SC50 30.5 ± 0.6 μg/mL CE[85]
H-ORACFL602 ± 20 μmol TE/g DE
Dehydrated pulpHexane extractIn vitroH-ORAC45.56 ± 1.96 μmol TE/g of dehydrated fruit[71]
Raw and cooked pulpVarieties of countriesIn vitroDPPH (IC50)Crude: Costa Rican variety 16.3 μg carotenoids/mL
Cooked: Bolivian variety 24.1 μg carotenoids/mL		[86]
MS: Morphological structure. DPPH: 2,2-diphenyl-1-picrylhydrazyl. IC50: Maximum inhibitory concentration (50%). ABTS: 2,2 azino bis (3-ethylbenzothiazolin-6-sulfonic acid). CE: Crude extract. H-ORACFL: Absorbance capacity of hydrophilic oxygen radicals–fluorescein. TE: Trolox equivalents. DE: Dry extract.
Table
Table 7. Biological activity of Bactris gasipaes.
Table 7. Biological activity of Bactris gasipaes.
ActivityMSProduct/ModelMechanismResultRef.
HypoglycemicPulpIn vivo
Healthy individuals (18–51 years)		Post-prandial glucose measured at 30, 60, 90 and 120 min after ingesting 25 g of pulp.Smaller Glycemic index than bread
80 ± 9 mg/dl-60 to 90 min		[87]
HDL increasePulverized fruitCommercial rat food supplemented with red B. gasipaes fruit
/Rats		Daily feeding with the mixture for 30 days.Infant group: <weight gain and BMI, cholesterol and >HDL cholesterol
Post-infant group: <triglycerides and >HDL cholesterol		[88]
HypolipemiantPulp and seedFruit flour and lysine
In vivo
16 pigs, fattening phase for 35 days		Percentage of flour (0, 16, and 32) and lysine (0 and 0.27)
<lipid content
Improves the properties of lean meat		Addition of flour in 16% and lysine 0.17%-meat with >dry matter content and moisture <[89]
CytotoxicityPulpETHOS
In vitro
MCR-5 cells		Viability of MCR-5 when exposing cells to concentrations of 6.25 to 200 μg/mL/72 hCauses death in normal lung cells.[85]
Effect on sperm motilityPulverized pulpAqueous extract
In vitro
Sperm		Progressive agglutination of sperm
Reduces its rectilinear velocity and linearity index.		Non-permanent action, thermolabile at 100 °C for 1 min[84]
Liver protectionPulpAcetone extract
In vivo
5 Sprague–Dawley rats 		Liver tissue of each rat subjected to oxidative stress with HPTB and then measure the reactive substances to thiobarbituric acid—the final product of lipid peroxidation.Hepatoprotective effect against oxidative stress
<CI50 with a concentration of 10.9 μg carotenoids/mL		[87]
Note. The acronyms correspond to: SM: Morphological structure. min: Minutes. N: Number. BMI: body mass index. ETHOS: Microwave extraction with aqueous ethanol solution. MCR-5: A cell line of human lung fibroblasts. h: Hours.
Table
Table 8. Phytochemical composition of the fruit of Bactris gasipaes.
Table 8. Phytochemical composition of the fruit of Bactris gasipaes.
No.CompoundIAPOMethodReference
Ester
1Methyl salicylatex Raw pulp ETHOS; HS-SPME/GC-MS[85]
Aldehyde
2Nonanal Raw pulpETHOS; HS-SPME/GC-MS[85]
Alcohols
32-phenylethanolx Raw pulpETHOS; HS-SPME/GC-MS[85]
41-Hexanolx Raw pulpETHOS; HS-SPME/GC-MS
52,3-Butanodiolx Raw pulpETHOS; HS-SPME/GC-MS
61-Nonanolx Raw pulpETHOS; HS-SPME/GC-MS
Carotenoids
7β-carotenex Raw and boiled pulpHPLC-DAD-UV/Vis[86]
8Xanthophyllx Raw and boiled pulpHPLC-DAD-UV/Vis
9γ-carotene x Raw and boiled pulpHPLC-DAD-UV/Vis
10Lycopenex Raw and boiled pulpHPLC-DAD-UV/Vis
Fatty acids
11Stearic acidx Pulp (oil)SOX; GC-MS[82]
12Oleic acidx Pulp (oil)SOX; GC-MS
13Linoleic acidx Pulp (oil)SOX; GC-MS
14Palmitic acidx Pulp (oil)SOX; GC-MS
15Palmitoleic acidx Pulp (oil)SOX; GC-MS
Other
16β-iononex Raw pulpETHOS; HS-SPME/GC-MS[85]
Note. I: identified; A: isolated; PO: plant organ. Methods are indicated with an acronym, corresponding to: ETHOS: Microwave extraction with aqueous ethanol solution. HS-SPME/GC-MS: Microextraction in solid phase in headspace mode (HS-SPME) coupled to gas chromatography/mass spectrometer. HPLC-DAD-UV/Vis: high resolution liquid phase chromatography (HPLC) and visible ultraviolet spectroscopy (UV/Vis). SOX: Soxhlet (solid liquid) extraction method, using petroleum ether. GC-MS: gas chromatography coupled to mass spectrometry.
Table
Table 9. Sustainable Development Goals (SDG) initiatives including B. gasipaes.
Table 9. Sustainable Development Goals (SDG) initiatives including B. gasipaes.
InitiativeSDGRef.
Agroforestry indigenous farming1, 2, 13, 15[101]
Recovery of biological pigments with alternative solvents9[102]
B. gasipaes recovered carotenoid supplements9, 12[103]
Production of antioxidant xylooligosaccharides from B. gasipaes waste12[104]
Ethanol production12[105]
Dietary diversity through underutilized species1, 15[106]
Materials for jewelry13[107]
Integration into circular economy12[108]
SDG: 1-No poverty; 2-Zero hunger; 9-Industry, innovation, and infrastructure; 12-Responsible consumption and production; 13-Climate action; 15-Life on land.
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González-Jaramillo, N.; Bailon-Moscoso, N.; Duarte-Casar, R.; Romero-Benavides, J.C. Peach Palm (Bactris gasipaes Kunth.): Ancestral Tropical Staple with Future Potential. Plants 2022, 11, 3134. https://doi.org/10.3390/plants11223134

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González-Jaramillo N, Bailon-Moscoso N, Duarte-Casar R, Romero-Benavides JC. Peach Palm (Bactris gasipaes Kunth.): Ancestral Tropical Staple with Future Potential. Plants. 2022; 11(22):3134. https://doi.org/10.3390/plants11223134

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González-Jaramillo, Nancy, Natalia Bailon-Moscoso, Rodrigo Duarte-Casar, and Juan Carlos Romero-Benavides. 2022. "Peach Palm (Bactris gasipaes Kunth.): Ancestral Tropical Staple with Future Potential" Plants 11, no. 22: 3134. https://doi.org/10.3390/plants11223134

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