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56 Wild Edible Plants
FIGURE 2.4 Classification of proteins by raw material origin.
Source: Adapted according to Healy & Tiwari (2023).
the time of harvest. Seaweeds harvested in summer contain more protein than those harvested in winter. Seaweeds contain all the amino acids required for human nutrition, especially rich in glycine, alanine, arginine, glutamic, pro­line, and aspartic acids (Thiviya et al., 2022).
Isolates from mushrooms. Mushrooms are a source of protein with a balanced amino acid composition, polysaccharides, dietary ber, phenolic compounds, fats, chitin and cellulose. Mushroom proteins make up 19– 35% of dry weight and have all the properties inherent in proteins: foaming, emulsifying, and sta­bilizing effects. Mushroom proteins have a high branched- chain amino acids (BCAA) content, which are commonly found only in animal- based protein sources (Ayimbila & Keawsompong, 2023).
Unconventional plant proteins. This group includes proteins isolated from green biomass, leaves, grass, stems, and forage legumes. Fresh green leaves comprise 1.6%– 8.2% protein, depending on the type of species and cultivars. However, if you process large quantities of them, the yield becomes signicant (Tiwari & Healy, 2023). Wild plants should be considered in this group.
Edible plants usually contain globular proteins, but by changing the processing conditions, pH, ionic strength, temperature, and physical impact on the system, it is possible to achieve the desired form of proteins: globular, unfolded into bers or formed into a spatial network (McClements & Grossmann, 2024). In addition, it is important whether they are classied as albumin, globulin, prolamine, or glutelin. This classica­tion has more to do with their water solubility (Figure 2.5).
Wild Edible Plants in the Development of Emulsion-Based Foods 57
FIGURE 2.5 Soluble- based classification of plant proteins.
Source: Adapted according to A. Zhang et al. (2022) and X. Zhang et al. (2023).
Therefore, not only physicochemical, but also a whole range of technological prop­erties directly depend on the structure of the protein. The most well- known sources of proteins are seeds, nuts, and beans, so let’s start our review with them. An example of a wild plant whose seeds are rich in protein is wild almond (Amygdalus scoparia) (Table 2.1).
The authors (Amirshaghaghi et al., 2017) managed to extract 56% of protein from almond seeds. This protein contains 17 amino acids. Aspartic and glutamic acids are the most abundant. Differential scanning calorimetry has shown that almond protein denatures at 80°C. The isoelectric point of protein is 3.8, and its solubility in water in the pH range of 3.5– 4.0 is minimal due to the aggregation of protein macromolecules accompanied by system separation. Studies of the protein’s ability to emulsify at concentrations of 0.1% and 1.0% in the pH range 2– 10 showed that the emulsifying ability increased at pH<4 and also at pH>4.5. It is important to note that for all pH values, the emulsifying activity index was higher for the 0.1% solution than for the
1.0% solution. It can be explained by the concentration factor: at a low concentration, during the homogenization process, the protein chains unfold, exposing their hydro­phobic fragments, which causes better adsorption on the surface of the oil droplet. On the other hand, near the isoelectric point, the distance between molecules is minimal due to the weakening of electrostatic repulsion, which creates optimal conditions for protein adsorption on the surface of oil droplets and the formation of a stable emulsion (Mwasaru et al., 2000).
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TABLE 2.1 The use of polysaccharides of some wild plants in the creation of food emulsions and emulsion- like foods
PLANT
PLANT PAR T
PROTEIN CONTENT, % DW FUNCTIONAL PROPERTIES
FOOD APPLICATION REFERENCE
Amygdalus scoparia Nuts 56 Emulsifier, foaming agent Suitable cost- effective
protein isolates
Cyperus esculentus L.Grassy part,
nut
Duckweed Aquatic plants 20- 35 (RuBisCo
Chenopodium
Seeds 14 Emulsifier, stabiliser, foaming
quinoa
Chenopodium
Seeds 13.12 Emulsifier, foaming agent,
album
Irvingia gabonensis Seeds 10,9
1.0- 1.4 (grassy part)
protein)
Emulsifier Addition to local corn or
millet dishes
Emulsifier, foaming and
Emulsified sauces, desserts (Appenroth et al., 2017;
gelling agent
and gelling agent
Bakery, jellies and sauces (Mir et al., 2020)
gelling agent
Structure forming agent Commercial raw materials (Giami et al., 1994)
7.60
Diyan kwakwa Nuts 27.1 Structure forming agent Traditional dishes, sauces, Muricin giginya Young shoots 15.4
and baking
Tsamiya biri Fruits 11.6 Yari Lichensmixture 5.3 Ximenia americana Leaves 7.87 Structure forming agent Sauces, snacks, Amaranthus viridus Leaves 18.4 Corchorus tridens Leaves 19.0
confectionery, additives to traditional food
Hibiscus sabdarifa Leaves 16.9 Maerua crassifolia leaves 15.5 Moringa oleifera Leaves 17.1 Leptadenia hastate Leaves 14.0 Amaranthus Seeds 14 Emulsifier, foaming and
gelling agent, antioxidant
Gluten- free food,
drinks, gels, artificial meat
58 Wild Edible Plants
(Amirshaghaghi et al., 2017;
Mwasaru et al., 2000)
(Alabi A. O. et al., 2024;
Pelegrín et al., 2022)
Di Stefano et al., 2018; H. Zhou et al., 2024)
(Shi et al., 2019)
(Glew et al., 2005)
(Freiberger et al., 1998)
(X. Zhang et al., 2023)
Wild Edible Plants in the Development of Emulsion-Based Foods 59
A promising source of protein is the walnut residue (Juglans regia L.), which contains more than 50% of it. However, the problem is that most of this protein is insol­uble and is lost during cooking.
Therefore, it is reasonable to use the walnut protein isolate nanoparticles (WPINPs) obtained by the US- pH- cycling method. The average particle size of WPINPs was 108 nm. The composition included 80.2% protein, 2.2% ash, 7.8% water and 0.9% fat. Liu et al. (2023) studied the effect of WPINPs’ concentration (0.5– 2.5%) on the stability of o/ w emulsions with an oil content of 20– 70%. The optimal ratio was 2.0% WPINPs to 60% oil. Such a pickling emulsion exhibited the highest stability and was characterized by a particle size of 3.33 µm and an elastic structure. The formation of a mesh elastic structure provided good thermal stability and high stability of the emulsions during storage for 15 days.
Tiger nut (Cyperus esculentus L.), a herbaceous perennial known for its ‘bulbs’, like ground almonds, can also be a source of protein, fat and ber. It is now actively cultivated, but in some countries wild species are also used. The addition of tiger nut bers to ‘ogi’, a specic emulsion porridge made from corn, sorghum, or millet that is a traditional product in Nigeria, increases its protein content, extends its shelf- life and increases its energy value (Alabi et al., 2024). The protein content in the herbaceous part of this plant is 1.0– 1.4% (Pelegrín et al., 2022).
Many Asian and African cultures actively use amaranth extracts, derived mainly from the seeds of Amaranthus spp., as a source of protein. The protein of amaranth has been studied in depth. The total protein content is up to 14– 16%. Amaranth protein consists mainly of albumin fraction (19– 23% of the total content) and globulin (~19%). Glutelin and prolamin are quite small (Dai et al., 2022; Tovar- Pérez et al., 2019). It should be noted that amaranth protein is quite balanced in its amino acid composition compared to other cereals. It is relatively rich in essential amino acids such as lysine and tryptophan, unlike cereal grains, which are low in lysine. This protein can be suc­cessfully used for the production of edible lms, beverages, baked goods, and vegetable meat, but it is not the best option for emulsion system technology (X. Zhang et al.,
2023). The protein fraction of amaranth has worse emulsifying and foaming properties than casein or soy protein (Tömösközi et al., 2008).
In addition to amaranth, quinoa (Chenopodium quinoa L.) can be a great source of protein. Although quinoa is usually cultivated, it is also found in the wild. Quinoa has all nine essential amino acids, making it a balanced source of protein. The protein content of quinoa is about 14%. Regarding the amino acid prole, quinoa protein has a well­balanced conguration with high levels of essential amino acids, lysine and histidine, which makes it represents a valuable source to supplement cereals (Shi et al., 2019). Quinoa protein has the typical processing properties of proteins: emulsifying ability and stability, pH dependence of solubility, foaming and gelling properties. Moreover, quinoa protein is characterized by a foaming capacity similar to that of soy protein (Abugoch et al., 2008) and a gel- forming ability similar to that of amaranth protein (Bejarano- Luján et al., 2010). In addition, it was shown that emulsions stabilized with quinoa protein showed higher resistance to oxidation than those with amaranth protein (Gürbüz et al., 2018).
A member of the Amaranthaceae family of the genus Chenopodium, in addition to actively cultivated quinoa, is album (Chenopodium album L.). This is a wild and
60 Wild Edible Plants
fast- growing plant. Chenopodium album L. like quinoa and amaranth, can also be classied as pseudo- cereal crops. Compared to classical cereals, album and quinoa seeds have a better amino acid composition, biological index and nutritional index for humans (Mir et al., 2021). Chenopodium album L. seeds contain about 13.1% protein and have an excellent amino acid balance with a high content of lysine and methionine (Mir et al., 2020). The quinoa protein isolates had the best rheological and structural properties. The denaturation temperature is higher for album proteins.
An interesting source of protein can be the seeds of the wild mango Irvingia gabonensis, which is widely used in Niger as a avoring and consistency regulator for some dishes. According to Giami et al. (1994) the protein content in the seeds is
10.9%, and the fat content is from 54 to 67%, so it is more likely to be ranked as an oilseed. Other researchers (Ekpe et al., 2007) indicate that mango seeds contain 66.6% fat, which ts into the previous interval, but only 7.6% protein, which is less than the previous values. The amino acid prole consists of 18 amino acids, with a predominant content of proline and leucine. It is clear that due to the low protein content, Irvingia gabonensis seeds are not an interesting object for protein- enriched products, but due to their high fat content, they are a potential raw material for the production of vegetable oil, which is also an essential component of food emulsion systems.
African cuisine has a centuries- long tradition of using plants for food. Many local recipes are passed down from generation to generation and are based on the use of local plant ingredients. Many African countries have a favorable climate for a wide range of plant crops. Seasonal vegetables and fruits are available throughout the year, which facilitates their constant use in the diet. Growing, and even more so, harvesting plants requires signicantly fewer resources compared to poultry and livestock. Moreover, the inclusion of wild fruits and vegetables in the diet can alleviate some of the problems associated with vitamin and mineral deciencies in the population (Bvenura & Afolayan,
2015). This is critical in regions with limited economic opportunities, not only in Africa but also in other parts of the world (Ding et al., 2021). However, there is still no single general list of edible plants not only on the African continent, but even in individual regions (Welcome & Van Wyk, 2019).
Examples include African wild plants diyan kwakwa (nut of the coconut palm, Cocos nucifera L.), muricin giginya (young shoot of Borassus aethiopum), tsamiya biri (fruit of the tree, Tamarindus indica L.), and yari (a mixture of lichens, mainly Rimelia reticulate) that grows on ebony trees (Diospyros mespiliformis L.), whose nutritional composition has been described (Glew et al., 2005) (Table 2.1).
It is interesting to note that the raw materials used for these studies were purchased in local stores. The study of the amino acid composition of proteins showed that a high protein content does not always correlate with its quality. For example, diyan kwakwa contained 24.7% protein, but it contained only three of the eight categories of essen­tial amino acids. In contrast, the amino acid composition of muricin giginya protein (15.4%) was very close to the WHO recommended value, differing only in the content of tryptophan. A study of another group of wild plants (Table 2.1), whose leaves are used to make sauces, snacks, and other food products, showed that these raw materials are quite rich in protein (Freiberger et al., 1998).
Moreover, the leaves of Moringa oleifera, Maerua crassifolia, and Leptadenia hastata are characterized by the highest proportions of essential amino acids (94– 97%
Wild Edible Plants in the Development of Emulsion-Based Foods 61
of the WHO standard). However, the amino acid composition of the protein of other plants was less balanced, with a pronounced deciency of methionine, which is gener­ally typical for raw materials obtained from leaves.
Although it is not obvious to the average consumer, a high amount of protein can be contained in the stems and leaves of plants. The article by H. Zhou et al. (2024) describes the potential for replacing egg raw materials with Ribulose- 1,5­bisphosphate carboxylase- oxygenase (RuBisCO) protein, which can be sourced from both cultivated and wild leafy raw materials, in particular, duckweed. This protein exists in four forms. Form I makes up 50% of leaf proteins and can be used as a functional ingredient (Di Stefano et al., 2018). Notably, the amino acid compos­ition of duckweed protein is very close to that recommended by the WHO: 4.8% Lys, 2.7% Met + Cys and 7.7% Phe + Tyr (Appenroth et al., 2017). However, the extraction process of plant proteins is very complex and may limit their use in food products (Di Stefano et al., 2018). At concentrations of about 12.5% by weight, this protein exhibits powerful emulsifying and gelling properties and can be used in combination with vegetable dyes to mimic the structure of egg yolk. To study the gelation processes, O/ W emulsions based on corn oil with droplet sizes of 0.2, 1 and 15 µm were prepared and then heated to the gelation temperature. The lightness and hardness of the resulting gel depended on the particle size: it was higher, the smaller the droplet size of the initial emulsion (H. Zhou et al., 2024). Thus, heating before emulsication increases the strength and stability of the emulsion formed with RuBisCo. Maximum foaming occurs in the region of the isoelectric point. An increase in pH causes an increase in the emulsifying capacity of the protein (Di Stefano et al., 2018).
If the nutrients are extracted from the green part of the plant (leaves, stems), it is more efcient to use dried and ground plants rather than fresh ones. It is clear that removing moisture serves as a way to concentrate all the nutrients. An example of such a plant is the well- known nettle Urtica dioica. Its shoots contain 90% moisture and rests are proteins (3.7%), fat (0.6%), ash (2.1%), dietary ber (6.4%), and total carbo­hydrate (7.1%). Dry our consists of crude protein (33.8%), crude ber (9.1%), crude fat (3.6%), total ash (16.2%), and carbohydrates (37.4%). It is important that the energy value of dry nettle our is low (307 kcal/ 100 g) compared to wheat and barley ours (Adhikari et al., 2016).
The European continent is also rich in wild plants that can be a source of components for emulsion systems. It is well known that both cultivated and wild legumes contain high levels of ber, protein, and polysaccharides. The researchers (Elamine et al., 2022) conducted a study of 23 species of Mediterranean legumes. In Table 2.2, only those plants that are used for human consumption are listed. The composition of proteins in legumes is very close to the WHO recommended values. These proteins have a high nutritional value and can be a source of essential amino acids, which the human body usually gets from meat products. However, most proteins derived from legumes are lacking in sulphur- containing amino acids such as methionine and cysteine. Legume seeds are characterized by the presence of a signicant content of free non- protein amino acids, especially sanavanine, an analog of arginine (Elamine et al., 2022).
Thus, we can summarize that wild plants can be a valuable source of protein, especially in regions where access to traditional sources of protein, such as meat or
62 Wild Edible Plants
cultivated crops, is limited (Bvenura & Afolayan, 2015). Wild plant proteins can have a high nutritional value, just like animal proteins. However, the selection and combination of raw materials to achieve an optimal amino acid composition is important (Martins et al., 2022). Plants that contain protein are often rich in minerals and trace elements, contain ber and vitamins, and have antioxidant properties. Often, the same plants can be both a source of protein and polysaccharides. The combination of these factors can be used successfully in the development and creation of new food emulsion products.
2.3.2 Polysaccharides
Water- soluble polysaccharides, especially non- starches, are becoming increas­ingly used in the food industry. The reason for this is their high structure- forming ability, which allows them to form strong spatial structures that are mostly thermally stable. Polysaccharides are an integral component of all food emulsions. Depending on the expected result, they are used together or in a mixture. In emulsion systems, polysaccharides act as thickening, gelling, or stabilizing agents (Dickinson, 2013). It is well known that the properties of plant polysaccharides depend signicantly on their botanical nature. Polysaccharides differ signicantly in the types of glycosidic bonds, composition of monosaccharides, degree of polymerization, and presence of certain functional groups (Ma et al., 2017). In addition, this is due to a signicant increase in consumer interest in environmentally friendly products made with natural emulsiers instead of synthetic ones. Therefore, attention is growing to the possibility of extracting polysaccharides from unconventional raw materials, which are actually waste (Ramadan & Mörsel, 2003). An example could be the leaves that remain after brewing and infusing drinks on them (Chen et al., 2022).
Many of the polysaccharides discussed below contain not only sugar units, but also proteins and other substances in their macromolecular chains. Such conjugates can exhibit more powerful or, in contrast, worse emulsifying properties than indi­vidual proteins and polysaccharides, and therefore generate increased interest among scientists. For this reason, the term ‘hydrocolloids’ is used and understood by scientists and technologists. It unites a large group of polymers that consist mainly of polysac­charide chains, but may also contain cross- linked protein fragments (Pirsa & Hafezi,
2023). The presence of proteins, non- covalent bonds and other additional interactions at certain concentrations causes a powerful synergistic effect, accompanied by the for­mation of strong gels. It is worth noting that small concentrations of hydrocolloids are sufcient to obtain the required structure and texture of food products: less than 1% (Gao et al., 2024).
The diversity of botanical species can provide a high variety of polysaccharides. Moreover, the source of polysaccharides can be not only plants (plant seeds, fruit rinds, tree secretion) but also fungi and algae (Figure 2.6).
There is no established classication of polysaccharides, they are generally divided into low- molecular weight and gums (long- chain high- molecular weight polysaccharides). Polysaccharide gums are promising ingredients for foods designed for appetite control (Carnachan et al., 2019). Interestingly, the lion’s share of researchers focuses on the isolation and purication of polysaccharides and the precise determin­ation of their chemical composition. Most polysaccharides are considered to be sugar
Wild Edible Plants in the Development of Emulsion-Based Foods 63
FIGURE 2.6 Classification of hydrocolloids by origin.
Source: Adapted according to Gao et al. (2024).
substitutes and components of antidiabetic drugs, antioxidants, anticoagulants, and encapsulating agents (Fuentes- Ortega et al., 2017; Inngjerdingen et al., 2013; Potin et al., 1992). However, the prospects for their use in the food industry are practically not considered. In view of the ancient traditions of Oriental medicine, much attention is paid to plants (roots, leaves, owers, and fruits) from China, Japan, and India. Below, we will review the properties and prospects for the use of some of the wild plants as sources of polysaccharides, taking into account the part of the plant from which these polysaccharides are extracted. The main focus will be on the opportunities for using these compounds in food emulsion technology (Table 2.2).
2.3.2.1 Polysaccharides isolated from mucilage and gums
In addition to the well- known botanical polysaccharides, such as cellulose, humiarabic, starch, pectin, or marine polysaccharides (agar, carrageenan, alginate), there are many others that are often classied by country of origin. Polysaccharides from New Zealand Native Plants may be unique and different from other plant polysaccharides due to the geographical isolation of this region (Carnachan et al., 2019). Most polysaccharides are found in the gum or mucilage of plants, which they produce in response to external inuences: plant disease, injury to the trunk, and other factors. Some of the most researched polysaccharides in New Zealand are Mamaku, Houhere, Puka, and Harakeke.
Puka gum is a water- soluble polysaccharide (type II arabinogalactan- protein) extracted from the gum exudate of the native New Zealand puka tree (Meryta sinclairii) (Wee et al., 2019). Puka gum (PG) is actually a protein conjugate. It contains up to 2% protein, so it has broad application prospects as an emulsier and stabilizer at the same time. Puka gum exhibits Newtonian behavior at concentrations below 4%, but at higher
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TABLE 2.2 The use of polysaccharides of some wild plants in the creation of food emulsions and emulsion- like foods
PLANT PLANT SOURCE HYDROCOLLOID
Apocynum
venetum
Leaves Polysaccharide conjugates
(ATPC- A)
tea
Meryta
Gum Puka gum Emulsifier, stabilizer 4– 15% soybean
sinclairii
FUNCTIONAL PROPERTIES RESEARCH OBJECT
Emulsifier Stabilizer O/ W emulsion
2 and 3% ATPC- A pH = 7– 8
oil emulsion
FOOD APPLICATION REFERENCE
Emulsion- like
functional foods
Emulsion- like
functional foods
Cyathea
medullaris
Leaf stem core Glucuronomannan
backbone with branched sugar side- chains of galactose, arabinose, non- methylesterified glucuronic acid and other
Shear- thickening Wiesenberger effect Rheological properties
are very sensitive to the cation valence and concentrations
Mamaku
gum water suspensions
Emulsion- like
functional foods
simple sugars
11% non- starch
polysaccharide, 10.3% starch, 49% sugars, 2.2% crude protein and 18% ash and 0.2% fat
Prosopis
trees
Mesquite gum
Prosopis gum Exudate
l- arabinose, β- dgalactose, and
4- O- methyl- d- glucuronic acid in a molar ratio of 4:2:1 with a small amount
Emulsifier, foaming
agent
Encapsulated
sesame oil
functional foods of
emulsion type
Emulsion- like
functional foods
of protein from 2.0% to
4.8%
64 Wild Edible Plants
(Chen et al.,
2022)
(Riana et al.,
2022; Wee et al., 2019)
(Bisht
et al., 2024; Jaishankar et al., 2015; Wee et al.,
2015)
(Fuentes-
Ortega et al.,
2017)
Verbascum
nigrum L.
Amana
edulis
Echinops
setifer
Dioscorea
opposita
Thunb
Passiflora
foetida
Flowers Saponins with hydrocarbon
chains
Flowers Polysaccharides with different
protein content and uronic acid
CHSS 1.5 × 105, CASS 2.6 ×
6
10
Shekartighal
Green part
76.85% carbohydrates,
9.24% protein, 4.91% fat, 1.74% ash, 7.26% moisture
Four
polysaccharides Root vegetable
PFP1 Fruit
Polysaccharide conjugate with
protein, catecholamine and leucoanthocyanidins
8 sugars, but the highest
content of galactose (32.46%) and mannose (48.83%)
Emulsifier O/ W emulsion of
rapeseed oil
Thickeners, emulsifier
1% aqueous
solutions of individual components
Emulsifier, stabilizer,
O/ W emulsion Mayonnaise- type
antioxidant, moisture
absorbing agent
Emulsifier 0.2; 0.4; 0.6; 0.8;
1 % aqueous solutions of individual polysaccharides. Emulsions with medium chain
triglyceride (1:1) Antioxidant, immunomodulator
Emulsion- like
functional foods
sauces
Beverage
industry
Food
supplements
(Amrouche
et al., 2022; Jarzębski et al., 2018)
(Ji et al., 2019)
(Nemati &
Hesarinejad,
2024)
(Ma et al.,
2017)
(Song et al.,
2019)
(continued)
Wild Edible Plants in the Development of Emulsion-Based Foods 65