Plant-Based Alkaline Fermented Foods as Sustainable Sources of Nutrients and Health-Promoting Bioactive Compounds

Owusu-Kwarteng, James; Agyei, Dominic; Akabanda, Fortune; Atuna, Richard Atinpoore; Amagloh, Francis Kweku

doi:10.3389/fsufs.2022.885328

REVIEW article

Front. Sustain. Food Syst., 14 June 2022

Sec. Sustainable Food Processing

Volume 6 - 2022 | https://doi.org/10.3389/fsufs.2022.885328

This article is part of the Research Topic Food Bioactives: Implications for Meeting Sustainable Development Goals View all 8 articles

Plant-Based Alkaline Fermented Foods as Sustainable Sources of Nutrients and Health-Promoting Bioactive Compounds

$\nJames Owusu-Kwarteng$ James Owusu-Kwarteng¹^*

Dominic Agyei²

Fortune Akabanda³

Richard Atinpoore Atuna³

Francis Kweku Amagloh³

¹Department of Food Science and Technology, University of Energy and Natural Resources, Sunyani, Ghana
²Department of Food Science, University of Otago, Dunedin, New Zealand
³Department of Food Science and Technology, University for Development Studies, Tamale, Ghana

Traditional food fermentation is a practice that precedes human history. Acidic products such as yogurts and sourdoughs or alcoholic beverages produced through lactic acid or yeast fermentations, respectively, are widely described and documented. However, a relatively less popular group of fermented products known as alkaline fermented foods are common traditional products in Africa and Asia. These products are so called “alkaline” because the pH tends to increase during fermentation due to the formation of ammonia resulting from protein degradation by Bacillus species. Plant-based alkaline fermented foods (AFFs) are generally produced from legumes including soybean, non-soybean leguminous seeds, and other non-legume plant raw materials. Alkaline fermented food products such as natto, douchi, kinema, doenjang, chongkukjang, thua nao, meitauza, yandou, dawadawa/iru, ugba, kawal, okpehe, otiru, oso, ogiri, bikalga, maari/tayohounta, ntoba mbodi, cabuk, and owoh are produced at small industrial scale or household levels and widely consumed in Asia and Africa where they provide essential nutrients and health-promoting bioactive compounds for the population. Alkaline food fermentation is important for sustainable food security as it contributes to traditional dietary diversity, significantly reduces antinutritional components in raw plant materials thereby improving digestibility, improves health via the production of vitamins, and may confer probiotic and post-biotic effects onto consumers. In this review, we present currently available scientific information on plant-based AFFs and their role as sustainable sources of nutrients and bioactive compounds for improved health. Finally, we provide perspectives on research needs required to harness the full potential of AFFs in contributing to nutrition and health.

Overview of Traditional Alkaline Fermented Foods

Food fermentation is a practice that precedes human history and will continue to be with us far into the future as populations around the world today obtain a considerable portion of their nutritional needs and incomes through fermented foods processing (Hesseltine and Wang, 1980; Tamang et al., 2020). When applied to foods, fermentation has a much broader meaning as opposed the strict biochemical definition of “an ATP-generating process in which organic compounds act as both donors and acceptors of electrons” (Kim et al., 2012). Thus, fermented foods and beverages include “foods that are made through desired microbial growth and enzymatic conversions of food components” (Marco et al., 2021). It is estimated that over 5,000 varieties of fermented foods and beverages are produced and consumed around the world from diverse raw materials (substrates) such as cereals, roots and tubers, meat, dairy products, fish, fruits, vegetables and legumes (Owusu-Kwarteng et al., 2012, 2020; Akabanda et al., 2013; Tamang et al., 2016a, 2020; Agyei et al., 2020).

Traditional fermented foods and their associated microbes are diverse depending on the substrate and the methods used for the fermentations. Whether they are produced by uncontrolled natural fermentation or with controlled starter cultures, fermented foods attain their characteristic taste, flavor, consistency, improved nutritional, and functional properties through the effects of microbial assimilation, metabolites production, and enzymatic activities (Owusu-Kwarteng et al., 2015, 2020; Marco et al., 2021). Microbial communities in natural (spontaneous) fermented foods are principally determined by dispersal and selection. Thus, in traditional spontaneous fermentation of foods, naturally occurring autochthonous microorganisms adapt to the complex food substrate and the fermentation environment leading to competitive selection of the microbial species that are more effectively adapted and positively respond to the in-situ conditions (Ouoba et al., 2007; Illeghems et al., 2012; Walsh et al., 2016; Einson et al., 2018). Consequently, an active change in the microbial community and metabolic profile gets established, leading to a stable fermented food ecosystem with characteristic microbiota structure and composition, metabolome, organoleptic properties, and nutritional and health benefits (Giraffa, 2004; Wolfe and Dutton, 2015; Marco et al., 2021). However, the desired outcomes and final properties of fermented foods do not only depend on the microbial-led conversion of substrates but also on a range of physicochemical parameters such as water activity, temperature, pH, oxidation-reduction potential and substrate accessibility. Therefore, effective management of both the intrinsic and extrinsic parameters during fermentation is critical in achieving the desired characteristics and final properties of fermented food products (Terefe and Augustin, 2020).

Throughout the world, lactic acid fermented products such as yogurts and sourdoughs, acetic acid fermented vinegar or alcoholic beverages produced by lactic acid bacteria, acetic acid bacteria or yeast fermentations, respectively, are widely described and their suggested nutritional and health benefits documented. This has contributed, in part, to consumer interest and the popularity of these fermented food products (Dimidi et al., 2019; Staudacher and Nevin, 2019). However, a relatively less popular yet rich diverse group of fermented products known as alkaline fermented foods (AFFs) which form an essential part of the diets and culture of people in parts of Africa and Asia (Ouoba et al., 2004; Azokpota et al., 2006; Parkouda et al., 2009; Owusu-Kwarteng et al., 2020; Tamang et al., 2020) have received relatively little attention. Figure 1 shows a comparison of studies published on the Scopus database with the terms “lactic acid fermentation” and “alkaline fermentation” in title, abstract or keywords. Active research in the area of “alkaline food fermentation” only began to “take off” in the late 1980s, whereas lactic acid fermentation had benefited from detailed scientific research dated as far back as in 1950. Indeed, pioneering scientific research on African alkaline fermented foods only started in 1980s with the microbiology works on iru (Odunfa, 1981), dawadawa (Campbell-Platt, 1980), ogiri (Odunfa, 1983, 1985), and ugba (Odunfa and Oyewole, 1986).

FIGURE 1

Figure 1. Comparison of cumulative publication outputs in Scopus database on the search terms “lactic acid fermentation” and “alkaline fermentation” (Search done on 23rd February 2022).

These so called “alkaline fermented foods” tends to have their pH increasing during fermentation. Thus, the predominant Bacillus spp. in these alkaline fermentations degrade the endogenous proteins in the raw plant into peptides and amino acids (Odunfa, 1985; Ouoba et al., 2003). As shown in equation 1, the free amino acids are further utilized by the Bacillus spp. as carbon and nitrogen sources to produce ammonia/ammonium hydroxide, resulting in the high pH values and the associated atypical odor of these fermented condiments (Ouoba et al., 2003, 2005; Parkouda et al., 2009; Amoa-Awua et al., 2014).

\begin{array}{l} R C H (N H_{3}^{+}) C O O^{-} + n O_{2} \to n C O_{2} + n H_{2} O + N H_{4}^{+} + O H^{-} \end{array}

AFFs of Africa and Asia are produced from a range of protein-rich substrates such as Glycine max (soybeans), Parkia biglobosa (African locust bean) seeds and other non-leguminous plant parts. Plant-based AFFs of Asia are almost exclusively produced from soybean as the substrate, giving credence to the first domestication of soybean in Asia particularly in the eastern half of north China in 1,000 BC, and the importance and agricultural sustainability of soybean across the Asian region (Tamang et al., 2020). In Africa, however, several wild as well as cultivated legumes and non-leguminous plants are used as substrates to produce AFFs. Asian AFFs produced from soybean include natto from Japan (Kanno and Takamatsu, 1987), douchi from China (Fan et al., 2009), kinema and similar products from Nepal and neighboring countries such as Bengal, India, and Bhutan (Tamang et al., 2002), doenjang and chongkukjang from Korea (Park, 2000; Kim, 2002; Park and Jung, 2005; Baek et al., 2008; Park et al., 2010), thua nao from Thailand (Leejeerajumnean, 2000), and meitauza and yandou from China (Zhu et al., 2008; Xu et al., 2012; Qin et al., 2013). On the other hand, African locust bean [Parkia biglobosa (Jacq. Benth)] is a common substrate for AFF condiments in Africa under different local names such as dawadawa in Ghana and Nigeria, soumbala in Burkina Faso (Ouoba et al., 2004), afitin, iru or sonru in Benin (Azokpota et al., 2006), nététou in Senegal (N'Dir et al., 1994), kinda in Sierra Leone and iru among the Yoruba tribe of Southwestern Nigeria (Sanni et al., 2000). Similarly, roselle seeds [Hibiscus sabdariffa (Linn.)] is used to produce AFF condiment such as bikalga in Burkina Faso (Ouoba et al., 2008), yanyanku and ikpiru in Benin (Agbobatinkpo et al., 2013) and mbuja in Cameroon (Mohamadou et al., 2013). Other plant based AFFs in Africa include okpehe from Prosopis africana seeds (Achi, 1992; Oguntoyinbo et al., 2010), otiru from African yam bean (Jeff-Agboola, 2007), oso from Cathormion altissimum seeds (Popoola et al., 2004), ugba from Pentaclethra macrophylla seeds (Sanni et al., 2002; Ahaotu et al., 2013), maari and tayohounta from Baobab seed (Parkouda et al., 2010; Chadare et al., 2011; Kaboré et al., 2012), ogiri from melon/castor oil seeds (Odunfa, 1985; Ademola et al., 2018), owoh from cotton seeds (Gossypium hirsutum) seeds (Sanni and Ogbonna, 1991; Ezekiel et al., 2015), mantchoua and kantong from Kapok tree (Ceiba pentadra) seed (Kpikpi et al., 2014; Kere-Kando et al., 2020) and ntoba mbodi from cassava leaves (Louembe et al., 2003; Mbozo et al., 2017; Moutou-Tchitoula et al., 2018). A range of plant species used for the processing of AFFs in Asia and Africa are shown in Figure 2.

FIGURE 2

Figure 2. Diversity and distribution of plant species used for the production of alkaline fermented foods in Africa and Asia.

Being predominantly produced from locally cultivated and wild plants, AFFs and the microorganisms therein provide sustainable diets serving as sources of nutrients and health promoting bioactive molecules thereby contributing toward achieving the United Nations Sustainable Development Goals (SGD), specifically SGDs 2 and 3. In addition to the general benefits associated with fermentation such as improvement in shelf-life, organoleptic quality and safety, alkaline food fermentations play a significant role in nutritional intake of several traditional communities in Africa and Asia where these fermentation processes transforms somewhat inedible, unpalatable, potentially toxic and undigestible plant materials into diverse desirable food products that delivers essential nutrients such as proteins, amino acids, vitamins and minerals within otherwise marginal diets (Wang and Fung, 1996; Parkouda et al., 2009; Reddy et al., 2018). Furthermore, AFFs and their associated microorganisms have been associated with several putative health-promoting effects that can positively impact human health via mechanisms such as including nutritive alteration of raw components, biosynthesis of bioactive compounds, modification of the human gut microbiota, and development and modification of the immune system (Shin et al., 2001; Sarkar et al., 2002; Hosoi et al., 2003; Suzuki et al., 2004; Zhang et al., 2006; Wang et al., 2008; Tolhurst et al., 2012; Tamang et al., 2016a; Araki et al., 2020). However, except for natto which has received at least one Randomized Control Trial (RCT), evidence of nutritional and health promoting effects of AFFs or their inherent microorganisms have so far been limited to laboratory chemical analysis and animal/cell model studies in contrast to other fermented foods such as yogurts and cultured milk which have their health benefits reported through at least 20 RTCs for both healthy and patient population groups (Dimidi et al., 2019; Araki et al., 2020; PraŽnikar et al., 2020; Savaiano and Hutkins, 2021). In this review, we demonstrate based on reported scientific information, the potential contribution of plant-based AFFs toward achieving the UN-SDGs as these foods serve as a sustainable source of healthy and nutritious diets for many traditional communities in Africa and Asia. Finally, we present future perspective on the need to apply holistic, meta-omics methods (metagenomics, meta-transcriptomics, meta-proteomics and metabolomics) to characterize traditional AFFs as well as conduct properly designed large placebo-controlled RCTs that will provide a better understanding of the health benefits of traditional AFFs.

Predominant Microorganisms in AFFs

In order to appreciate the scope of AFFs in nutrition and health, it is necessary to acknowledge the diversity and origin of predominant microorganisms responsible for the fermentation of these products. In general, traditional AFFs of Africa and Asia are processed by spontaneous fermentation (depends on autochthonous or resident microorganism present in the raw substrate and/or surrounding environment) to initiate the fermentation processes in these products (Parkouda et al., 2009; Owusu-Kwarteng et al., 2020; Tamang et al., 2020). In assessing their microbial ecology, the gold standard culture dependent phenotypic approaches complemented by molecular tools such as internal transcribed spacer PCR (ITS-PCR), random amplification polymorphic DNA-PCR (RAPD-PCR), repetitive sequence-based PCR (rep-PCR), pulsed field gel electrophoresis (PFGE), as well as sequencing of 16S rRNA, gyrA, gyrB, and rpoB genes, have shown that plant-based AFFs of Africa and Asia are characterized by complex microbial communities. Despite this complexity, Bacillus subtilis and related species are the predominant functional microbiota in a wide-range of plant-based AFFs of Africa and Asia (Ouoba et al., 2004, 2010; Meerak et al., 2007, 2008; Oguntoyinbo et al., 2007; Parkouda et al., 2009, 2010; Chukeatirote et al., 2010; Kamada et al., 2015; Owusu-Kwarteng et al., 2020). Predominant microbial species associated with the fermentation of plant-based AFFs in Asia and Africa are shown in Table 1. Frequently identified species of Bacillus and related genera associated with plant-based AFFs are Bacillus subtilis, Bacillus cereus, Bacillus megaterium, Bacillus endophyticus, Bacillus licheniformis, Bacillus borstelensis, Bacillus pumilus, Bacillus coagulans, Bacillus circulans, Paenibacillus polymyxa, Lysinibacillus sphaericus, and Lysinibacillus fusiformis (Odunfa, 1981; Sarkar et al., 2002; Ouoba et al., 2004, 2010; Azokpota et al., 2007; Parkouda et al., 2009).

TABLE 1

Table 1. Overview of predominant microorganisms occurring in plant-based AFFs in Africa and Asia.

Irrespective of raw material or geographic location of production, B. subtilis remains the dominant functional species in most AFFs in Africa and Asia. B. subtilis is reported as the predominant species in the fermentation of dawadawa and soy-daddawa in Ghana and Nigeria (Dakwa et al., 2005; Amoa-Awua et al., 2006; Ezeokoli et al., 2016), soumbala, bikalga, maari and mantchoua in Burkina-Faso (Bengaly, 2001; Ouoba et al., 2004, 2007, 2010; Parkouda et al., 2010; Kaboré et al., 2012; Kere-Kando et al., 2020), kawal in Sudan and Chad (Mbaiguinam et al., 2005), soumbara in Côte d'Ivoire (Adjoumani et al., 2019), afitin, sonru, and iru in Benin (Azokpota et al., 2007), tayohounta, yanyanku, and ikpiru in Benin (Chadare et al., 2011; Agbobatinkpo et al., 2013), mbuja in Cameroon (Mohamadou et al., 2013), kinda in Sierra Leone (Meerak et al., 2008), and okpehe, oso, ugba, iru, and owoh in Nigeria (Sanni et al., 2000, 2002; Popoola et al., 2004; Oguntoyinbo et al., 2010; Adewumi et al., 2013, 2014; Ahaotu et al., 2013; Ezekiel et al., 2015; Ademola et al., 2018). Similarly, Asian AFFs produced from soybean such as kinema produced in Nepal, thua nao in Thailand, chongukukjang and doenjang in Korea, meitauza in China, and natto in Japan are produced by B. subtilis (Tamang et al., 2016b).

The B. subtilis species complex is a tight assemblage of related species that includes B. subtilis subsp. subtilis BEST195, the starter strain used for natto fermentation which is thought to have been isolated from a traditionally prepared natto and was therefore originally named Bacillus natto. However, Bacillus natto was re-classified and included in B. subtilis in 1970 supported by phylogenetic analyses using 16S rRNA genes (Tamang et al., 2002; Kubo et al., 2011). Since its isolation, further characterization including entire genome information (Kiuchi et al., 1987; Sulistyo et al., 1988; Nishito et al., 2010) have led to the development of B. subtilis subsp. subtilis BEST195 starter strain used for natto production in Japan. Natto starter cultivation generally targets genes regulating the metabolic pathways of secondary metabolites that affect texture, aroma, sensitivity to bacteriophages, spore formation and germination, and high productivity of ⋎PGA via the pgs operon (Ashiuchi and Misono, 2002; Beckett, 2009; Kubo et al., 2011) which imparts a sticky texture onto natto. In plant-based African AFFs, B. subtilis play technological and functional roles such as Production of Aroma/flavor compounds (Owens et al., 1997; Ouoba et al., 2005; Nwokeleme and Ugwuanyi, 2015; Akanni et al., 2018), amino acids synthesis (Ouoba et al., 2003; Azokpota et al., 2006), degradation of carbohydrates and oils (Kiers et al., 2000; Ouoba et al., 2003, 2007; Azokpota et al., 2006), production of antimicrobial peptides (Ouoba et al., 2007; Savadogo et al., 2011; Kaboré et al., 2012, 2013; Compaore et al., 2013), and reduction of anti-nutritional factors and toxic compounds (Okafor, 1977; Odunfa, 1985; Abban et al., 2013).

Being produced predominantly by spontaneous fermentation processes, the microbial ecology of traditional plant-based AFFs of Africa and Asia are generally characterized by mixed populations of different species of bacteria, yeasts and molds (Dirar et al., 1985; Sarkar et al., 1994; Dakwa et al., 2005; Jeff-Agboola, 2007; Parkouda et al., 2009, 2010; Sohliya et al., 2009; Ouoba et al., 2010; Kim et al., 2011a; Rashad et al., 2011; Tamang et al., 2012; Adewumi et al., 2013; Owusu-Kwarteng et al., 2020). Thus, in addition to Bacillus and related species, other groups of microorganisms including other aerobic endospore-forming bacteria (AEB), lactic acid bacteria (LAB), yeasts and molds have been frequently identified as members of the microbial consortia of traditional plant-based AFFs. However, the contribution of these so-called “secondary microbiota” to technological and functional properties of AFFs have been sparsely reported. Lactic acid bacterial may enhance the safety of AFFs through the production of antimicrobial compounds (Kaboré et al., 2012). Yeasts such as Candida parapsilosis and Geotrichum candidum have also been shown to significantly lower the levels of free fatty acids, while contributing to the production of free amino acids as well as enhance the formation of flavor compounds in traditional AFFs (Sarkar et al., 1996; Kim et al., 2011b; Rashad et al., 2011).

Nutritional and Dietary Value of Plant-Based AFFs

Plant-based AFFs play significant roles in the nutritional intake and are important in achieving dietary sufficiency in several traditional communities where they are produced and consumed. Two main features of alkaline fermentation process are particularly significant in relation to national and dietary impacts of AFFs. Firstly, enzymes produced by predominant bacteria during alkaline fermentation hydrolyses macronutrient molecules i.e., complex carbohydrates, proteins, and fats, thereby enhancing nutrient bioavailability and digestibility of the fermented product compared with the unfermented substrate (Wang and Fung, 1996). For example, B. subtilis fermentation has been shown to effectively hydrolyse soybean proteins and polysaccharides, resulting in low-molecular-weight, water-soluble products that require little further degradation by gastrointestinal enzymes (Kiers et al., 2000). Secondly, enzymatic degradation during fermentation significantly reduces naturally occurring toxic components, allergens, and antinutritional components in the raw food substrate, thereby transforming otherwise inedible, difficult to digest or potentially toxic raw materials into palatable and culturally desirable food products that deliver essential nutrients. In Africa, several of such alkaline fermented food products are produced in each country or region, thus contributing to a complex rich traditional dietary diversity, with important food security and sustainability implications (Iwuoha and Eke, 1996; Parkouda et al., 2009).

Soybean, the most common plant substrate for AFFs produced in Asia, is nutritious with high levels of protein and fat (Bouchenak and Lamri-Senhadji, 2013). However, unprocessed soybean contains high levels of complex oligosaccharides and antinutrients (Reddy and Pierson, 1994), as well as potential allergens (Phromraksa et al., 2008). The presence of antinutritional factors such as tannins, trypsin inhibitors and phytic acid tend to limit the digestibility and bioavailability of essential nutrients in unprocessed soy products (Ghavidel and Prakash, 2007). Therefore, in order to liberate the essential nutrients from soybean for human digestion and absorption, some form of processing is necessary. Fermentation has proven to reduce antinutrient levels, improving the nutritional and organoleptic properties of fermented food products (Osman, 2004; Eltayeb et al., 2007; Atuna et al., 2022).

During the production of soy-based natto (Figure 3A), biochemical changes occurring as a result of fermentation has been shown to improve the content of protein, lipids and minerals such as iron, zinc and calcium (Table 2). Hu et al. (2010) reported 1.1-fold increase in protein content of natto after fermentation. It has been suggested that microorganisms increase the protein content of samples on which they grow due to microbial synthesis of protein (Hu et al., 2010). Crude fat and total ash contents of natto ranges from 18–24.7 to 4.7–4.6%, respectively (Table 2). Although fermentation is reported to have little effect on the crude fat content of natto, there appears to be strain-specific influence by the fermenting microorganism which may result in increased or decreased fat content. For example, the lipid content of natto decreased by 1.1-times from 25.41% in raw soybeans inoculated with the “Itobiki” strain of B. natto while the NRRL B-3383 strain of B. natto increased lipid content by 1.1-fold (Wei and Chang, 2004). Thus, different B. natto strains have different capabilities to synthesize lipid or utilize carbohydrates during fermentation (Wei and Chang, 2004). Another notable compositional change in natto is the significant increase in vitamin K content after fermentation. The extraordinary increase in vitamin K in natto has been attributed to vitamin K2 (menaquinone-7 or MK-7) synthesis by B. subtilis natto (Kouris-Blazos and Belski, 2016). Epidemiological studies have also shown that increased consumption of Japanese natto is positively correlated with bone density among Japanese females as a result of increases in serum vitamin K and ⋎-carboxylated osteocalcin, both of which facilitate bone mineralization (Tsukamoto et al., 2000; Katsuyama et al., 2002). For water-soluble vitamins, fermentation was reported to increase thiamine and riboflavin contents by 3-folds and a 5-fold increase in vitamin B12 content compared to the raw substrate (Reddy et al., 1983).

FIGURE 3

Figure 3. Examples of traditional AFFs in Africa and Asia. (A) Natto (Photograph credit: Chichi Wang), (B) Kinema (Photograph from Tamang et al., 2016a), (C) Doenjang (Photograph by Maangchi), (D) Douchi (Photograph by Xin-Mei Fang), (E) Dawadawa (Photograph by R. A. Atuna), and (F) Thua nao (Photograph by puechkaset).

TABLE 2

Table 2. Summarized nutritional information previously reported for some AFFs.

Kinema (Figure 3B), a fermented-soy condiment, is a traditional delicacy produced in Nepal and parts of India. Kinema not only possesses exceptional flavor but has a significant dietary importance as a relatively cheap substitute for meat (Sarkar et al., 1994). Like other soy-based fermented products, kinema is a rich source of protein (43.4–48.7%), fat (16.1–22.7%), carbohydrates (27.4–29.6%), and minerals (Table 1). The nutrient composition of kinema has previously been reported (Sarkar and Tamang, 1995; Sarkar et al., 1997b, 1998). Total protein content of kinema increases by about 1% while free amino acid content increases by 60-fold compared to raw soybeans. However, for its dietary role as meat substitute, tryptophan, cysteine, and methionine are the main limiting amino acids in kinema, although protein quality has been reported to be comparable to animal source protein (Sarkar et al., 1994, 1997b). B-vitamins in kinema varies from the raw soybean substrate with general increases in levels of riboflavin and niacin, but a decrease in thiamine (Sarkar et al., 1998). The minerals content of kinema was also reported to be lower than raw soybean. The decline in the mineral level in kinema has been attributed to the preparation process where soybeans are soaked, cooked, and the water discarded (Sarkar et al., 1998).

Doenjang (Figure 3C) is an indigenous alkaline fermented soybean paste which serves as an important protein source and seasoning agent in the traditional diets of the people of Korea. Doenjang is considered a nutritious food that provides essential amino acids, fatty acids, minerals, and vitamins, associated with various nutritional benefits. Proximate composition of doenjang include 54.7% water, 13.8% crude protein, 8.0% crude lipid, 14.4% (Park and Jung, 2005). Amino acids composition of doenjang include glutamic acid, leucine, alanine, histidine, lysine, proline, and valine (Park and Jung, 2005). Fermentation of doenjang for 80 days results in relative increases in methionine and threonine levels compared to raw soybeans. However, these amino acids are still limiting in doenjang and therefore other dietary strategies such as complementation would ensure adequate intake of essential amino acids (Namgung et al., 2010). Like doenjang, chongkukjang is another traditional Korean soy-based fermented food, similar to Japanese natto, but different in usage (Chukeatirote, 2015). Chongkukjang, commonly consumed for its perceived health-promoting properties, is also regarded as a rich source of proteins, lipids, amino acids, vitamins, and minerals (Ali et al., 2018). Fermentation of soybean into chongkukjang with higher concentrations (5–7%) of B. subtilis enhances the minerals content of the product (Ali et al., 2018). The significant improvement of minerals content has been attributed to microbial involvement and interaction with metabolites breakdown (Ali et al., 2018). Fermentation is also reported to degrade antinutritional factors during chongkukjang processing, invariably improving the bioavailability of minerals (Ali et al., 2018). The microorganisms' strains in the fermentation process significantly influence the product's value. The total mineral contents in chongkukjang fermented with Bacillus amyloliquefaciens RWL-1 increased by about 33% compared with the quantity obtained from the conventional B. subtilis (Shahzad et al., 2020).

Douchi (Figure 3D), a nutrient-rich fermented soy-based food product, is widely used seasoning in China and other Asian countries to enhance appetite (Li and Ma, 2014). During douchi production, a series of complex biochemical reactions enhance chemical and nutritional components in the raw soybeans. During fermentation, proteins are converted to peptides and amino acids, lipid to fatty acids, starch to reducing-sugars and ethanol, and various aroma components by salt-tolerant microorganisms (Li and Ma, 2014). The crude protein and fat content of douchi ranges from 35.9–40.4 to 19.9–23.9%, respectively (Table 1). The crude protein content of pre-fermented douchi slightly increased and then decreased by 1.2-fold after four (4) weeks of ripening (Wang et al., 2016). The fermentation process is also reported to increase the product's mineral content and bio-accessibility (Liu et al., 2020).

Meitauza is produced from okara (a by-product from the production of soybean foods such as soymilk and tofu) in China. Crude protein content of meitauza declines by almost 6% due to the interaction between microbes and the fermenting media. However, total free amino acids significantly increased during the fermentation process (Xu et al., 2012). Strong-tasting amino acids such as glutamic acid and glycine increase by over 10-folds; and aspartic acid, alanine and arginine increased several-fold. Similarly, amino acid with sweet taste: leucine, valine, serine, and methionine significantly increase during fermentation, improving the taste and overall nutritional value of the fermented product. Although okara contains high moisture content (>80%), the water is linked to dietary fiber, resulting in the pasty texture of the by-product (Redondo-Cuenca et al., 2008). The fiber, largely insoluble cellulose and hemicellulose, form a more significant part of the dry matter content (40–60%). Fermentation can increase the soluble fiber level in okara, improving its nutritional quality and processibility (Sharma et al., 2020). It also induces a significant decrease in lipid and lignin contents in okara. These compositional changes have led to a pleasant and delicate taste, as well as a smooth and rubbery texture (Colletti et al., 2020).

Dawadawa (Figure 3E) is the most important protein-rich food condiment in West and Central African, primarily used as a meat substitute or to enhance the organoleptic qualities of traditional staple foods. Dawadawa is known by different local names depending on the country of production; dawadawa in Ghana, iru (Nigeria), nététu (Senegal), kinda (Sierra Leone), afitin, iru, or sonru (Benin) and soumbala (Burkina Faso). Varying nutritional composition have been reported for dawadawa because a range of raw materials including locust bean, bambara groundnuts [Vigna subterranean (L.) Verdc.], and soybean serve as substrates for the fermentation (Achi, 2005). In general, locust bean is inedible and could be toxic to humans (Wang and Fung, 1996). However, a significant reduction in the anti-nutrient content and enhanced amino acid profile has been reported for alkaline fermented locust bean (Ijarotimi and Keshinro, 2012). Generally, dawadawa produced from African locust beans contain about 49.7% protein, 26.9% lipids, 4.3% total ash, and 7.4% carbohydrates (Appiah et al., 2012). Alkaline fermentation of African locust bean resulted in an increase in total protein content and an improvement in the amino acid profile (Urua et al., 2013). This increase in free amino acids levels due to the proteolytic activities by the fermentative microorganisms have been reported for dawadawa (Odunfa, 1981; Akabanda et al., 2018). Additionally, fermentation of locust bean results in a 6-fold increase in thiamine and 3-fold increase in riboflavin contents, but a reduction (30%) in niacin content. Similar reduction in niacin content was reported for ugba, fermented condiment from African oil bean seeds, corresponding to progressive reduction in cyanide, phytate, tannin and oxalate contents (Ogueke et al., 2013). Sulfur-containing amino acids are generally limiting in locust bean dawadawa (Campbell-Platt, 1980) and ogiri produced by alkaline fermentation of melon seeds, but these could be complemented through the consuming the AFFs with cereal-based staples (Wang and Fung, 1996). For soy-dawadawa, fermentation protein, carbohydrates and fat contents are reported to be 43.2–47.4, 16.2, and 19.9–26.7%, respectively (Table 2). The major biological changes occurring during soy-dawadawa processing include hydrolyses of protein, fat, and carbohydrate, with the fermentation leading to increased contents of protein and amino acids such as lysine, arginine, proline, phenylalanine, isoleucine, and leucine (Dakwa et al., 2005; Terlabie et al., 2006).

In Congo and parts of central Africa, cassava (Manihot esculenta Crantz) leaves are fermented to produce ntoba mbodi (Louembe et al., 2003). Ntoba mbodi is relatively rich in protein although a slight reduction in free nitrogen occurs during fermentation, probably due to liberation of hydrogen cyanide. Extensive cellulase activity, through fermentation, further enhances the bioavailability of carbohydrates and increases magnesium, calcium, and potassium contents in notba nbodi compared to raw cassava leaves. However, methionine and phenylalanine are the limiting amino acids in ntoba nbodi (Mokemiabeka et al., 2011). Another product similar to ntoba nbodi is kawal produced by the fermentation of sickle pod [Senna obttusifolia (L.) H.S/Irwin & Barneby] leaves in Chad and Sudan where it serves as meat substitute and flavoring agent soups and stews (Dirar, 1984; Harper and Collins, 1992). While Dirar (1984) reported a decrease in crude protein content of after fermentation, Harper and Collins (1992) reported increased crude protein content of kawal. Although about 50% protein loss during the fermentation of kawal has been observed, the loss is overshadowed by the substantial increase in digestibility and palatability of the fermented product. Limiting amino acids in kawal include cysteine, histidine, and threonine. However, kawal is consumed with cereals foods which may provide complementary proteins (Mbaiguinam et al., 2005).

Health Promoting Effects of AFFs

Production of Vitamins

All vitamins are essential for human growth—meaning human cannot synthesize adequate quantities of vitamins de novo, if at all. Therefore, human diet must contain adequate quantities of these vitamins in order to maintain normal growth and bodily functions. These vitamins act as co-factors or pre-cursors to important metabolic processes and enzymes in living organisms. Fermentation is touted as a natural process for the in-situ biosynthesis of vitamins in food materials (Odunfa, 1986). As shown in Table 3, examples of vitamins whose levels have been significantly increased after fermentation are Vitamin K and the B-vitamins (e.g., thiamine (B₁), riboflavin (B2), niacin (B3), pantothenic acid (B5), pyridoxal (B6), biotin (B7), folate (B9), and cobalamins (B12).

TABLE 3

Table 3. Improvement in vitamin availability of some AFFs.

The biosynthetic pathways for the production of vitamins B2 (Burgess et al., 2009), B12 (Burgess et al., 2009), B9 (Rossi et al., 2011), and other B-type vitamins have been widely reported in lactic acid bacteria (LeBlanc et al., 2011). Among alkaline-fermenting bacterial strains, B. subtilis (Bacher et al., 1980; Bretzel et al., 1999; Li et al., 2013; Man et al., 2014), B. tequilensis (Abdulla et al., 2016), B. abortus (García-Angulo, 2017), B. amyloliquefaciens (Vitreschak et al., 2002), and B. halodurans (Averianova et al., 2020) are the most studied species.

Most food-grade microorganisms, including those found in alkaline fermented foods have the genetic wherewithal to synthesize vitamins during growth on organic materials. The class of genes needed for the biosynthetic of these vitamins differ for each vitamin but can be intricately linked, as is the case for vitamin B2, B9, and B12 (Gu and Li, 2016). In B. subtilis, the production of Vitamin B2 begins with the expression of ribA gene which encodes for the bifunctional enzyme guanosine 5′-triphosphate (GTP) cyclohydrolase II/3,4-dihydroxy-2-butanone 4-phosphate synthase responsible for the conversion of GTP to 5-amino-6-ribityl-amino-2,4(1H,3H) pyrimidinedione (ArP), and ribulose 5-phosphate (Ribu5P) to 3,4-dihydroxy-2-butanone-4-phosphate (DHBP). ArP and DHBP are the two substrates of riboflavin (Vitamin B2) (Averianova et al., 2020). Plant-based food products whose riboflavin levels have been significantly improved via alkaline fermentation include dawadawa (Oguntoyinbo et al., 2016), kinema (Sarkar et al., 1998), and tempe (Mani and Ming, 2017).

The production of folate also begins with GTP which acts as a precursor for 6-hydroxymethyl-7,8-dihydropterin pyrophosphate (DHPPP) through a series of four enzymatic conversion steps. Another important substrate for folate production is para-aminobenzoic acid (pABA) which is produced from erythrose 4-phosphate and phosphoenolpyruvate through the shikimate pathway (Bermingham and Derrick, 2002). The coupling together of DHPP and pABA, and subsequent glutamylation of the final product gives polyglutamate forms of dihydrofolate (DHF), and tetrahydrofolate (THF) (Rossi et al., 2011).

Cobalamin (Vitamin B12) has an intricate and complex structure. It is no wonder that as many as 30 genes are required for its biosynthesis (Gu and Li, 2016). One of the few Bacillus species known to synthesis Vitamin B12 de novo is B. megaterium where the synthesis occurs through an anaerobic route (Fang et al., 2017). B. megaterium is considered a producer of Vitamin 12 at the industrial scale (Vary, 1994; Mohammed et al., 2014). In this species, uroporphyrinogen III is first converted to precorrin-2 and then subsequently to cobyric acid. The transformation of precorrin-2 to cobyric acid occurs through a series of reactions involving eight methylations, six amidations, insertions of cobalt, and decarboxylation and contraction of the porphyrin ring (Moore and Warren, 2012). Cobyric acid is converted to cobinamide, and then to cobalamin.

Kwak et al. (2008) reported the Vitamin B12 contents of traditionally fermented Doenjang and Chungkookjang, two Korean soybean-based fermented foods, and found levels of 1.85 mg/100 g and 0.69 mg/100 g, respectively. These levels were significantly higher than those found in factory-made versions of the products which had 0.04–0.86 mg/100 g and 0.06–0.15 mg/100 g, respectively. The high levels of Vitamin B12 in the traditional fermentation process could be due to the fact that the traditional process to prepare Doenjang and Chungkookjang is relatively long (~ about 10 months) and uses “wild-type” multiple microorganisms found in nature (Kwak et al., 2010).

Vitamin B12 production to levels of about 91.43 mg/100 dw in in fermented soybean, Thua nao (Figure 3F) using mixed culture fermentation using mixed cultures of B. amyloliquefaciens. and Klebsiella spp. have been reported (Yongsmith et al., 2016). The levels of Vitamin B12 in tempeh (i.e., 0.7–8.0 mg/100 g), (Watanabe et al., 2014). The levels of Vitamin B12 in natto has been reported to be over five times that in cooked soybeans (Wang and Fung, 1996).

The fact that the aforementioned vitamins are abundant in alkaline fermented plant-based foods suggest that fermentation can be considered as suitable chemical-free production route for these vitamins, for use in supplements and food fortification programs (Gu and Li, 2016). Further, in some cases (such as in riboflavin synthesis) production of these vitamins via fermentation leads to products with higher chemical purity, compared with chemically synthesized alternatives (Bretzel et al., 1999).

Improved Digestibility

In general, plant-based foods are comparatively less digestible than animal-based foods, when subjected to the human digestive system. The low digestibility of plant materials is due to factors such as the presence of cellulose cell wall that decrease access by enzymes to target molecules (Holland et al., 2020), the inability of human gastro intestinal enzymes to digest cellulose (Cummings, 1984), restrictive structural features of target molecules (e.g., hydrophobicity and folding patterns of plant proteins), presence of “antinutritive” compounds or secondary metabolites that inhibit human gastric enzyme activities (Sarwar Gilani et al., 2012), complexation of target molecules with other compound (e.g., starch-lipid conjugates) (Qin et al., 2019), among others. All of these aforementioned phenomena decrease the digestion, bioaccessibility, and bioavailability of nutrients in plant-based foods. The ability of alkaline fermentation to improve the digestibility of plant foods therefore strongly depends largely on microbial metabolic processes that affects one or more of the above-mentioned factors. The description (with examples) of two pathways through which fermentation increases the digestibility of certain alkaline-fermented foods is given below.

Partial Hydrolysis and Release of Hydrolytic Products and Their Metabolites

The action of alkaline fermentation leads to the generation of a host of factors that directly or indirectly causes partial hydrolysis or softening of plant matrix. For example, microbial enzymes produced in situ during fermentation can utilize biomolecules in plant matrices as substrates, leading to the generation of partially-hydrolysed plant microstructures and release of hydrolysis products. Case in point, proteolysis is considered the most important metabolic activity in alkaline fermentation (Parkouda et al., 2009), and increased protease activity during alkaline fermentation is well-reported (Ouoba et al., 2003; Owusu-Kwarteng et al., 2020). Proteolysis is mostly caused by Bacillus spp. (Ouoba et al., 2003), and this biochemical process leading to the formation of peptides and free amino acids that improve the nutritional qualities of the fermented product. The levels of essential amino acids such as methionine, cysteine, leucine, tyrosine, phenylalanine, and lysine have been reported to increase after alkaline fermentation (Ouoba et al., 2003; Owusu-Kwarteng et al., 2020). The released free amino acids are further metabolized by the microorganisms to ammonia, giving rise to the characteristic pungent “ammonia-like” odors of some traditional fermented foods such as dawadawa (Parkouda et al., 2009). High pH is known to degrade cellulose and lignocellulose (Glaus and Van Loon, 2008). Therefore, the production of ammonia and accompanying high pH during alkaline fermentation can be expected to indirectly “soften” plant compounds, making them more susceptible to the actions of subsequent food processing and gastrointestinal enzymes.

Reduction in Levels of Antinutritional Factors and Flatus-Forming Oligosaccharides

Plant materials are rich in antinutritional factors such as lectins, tannins, saponins, protease inhibitors, oxalic acid, cyanogenic glycosides, and phytic acid. These antinutritional factors can reduce the bioavailability of key nutrients (such as vitamins and minerals), or interfere with the activities of gastro-intestinal digestion. Some antinutritional compounds (e.g., hydrocyanic acid released from cyanogenic glycosides) can be toxic to humans.

The seeds of African locust bean (Parkia biglobosa), used in the preparation of dawadawa contains antinutrients such as nitrates, tannins, cyanide, phytates, and oxalates (Termote et al., 2022). Urua et al. (2013), in their work on the effect of processing on three accessions of African locust bean reported that fermentation reduced the levels of phytic acid and oxalates respectively by up to 44.4 and 50.9% each; whereas boiling reduced the levels of these antinutrient by up to 33.3 and 4.4%, respectively. The oxalate contents in two of the accessions actually increased by 140.8 and 78.1%, respectively (Urua et al., 2013). In another study, trypsin inhibitor activity, tannins, and phytic acids in African locust bean seed were reduced significantly by 89.0, 59.8, and 62.5%, respectively after 72 h of alkaline fermentation (Esenwah and Ikenebomeh, 2008). In other reports, alkaline fermentation of soy beans into kinema has been shown to reduce the levels of tannins, phytic acids, trypsin inhibitor activity, and haemagglutinating activity by 100, 61, 71, and 100%, respectively (Sharma et al., 2015). Kobawila et al. (2005) have demonstrated that the cyanogenic glycoside content reduced significantly by 70–75% during alkaline fermentation of cassava leaves (Kobawila et al., 2005). These examples demonstrate that alkaline fermentation degrades antinutritional compounds, thereby reducing or eliminating them from the fermented food.

Improved Health Benefits via the Actions of Probiotics and Post-biotics

Many of the Bacillus strains predominant in alkaline fermented foods are also used commercially as probiotics. Some of these strains include B. cereus, B. clausii, B. coagulans, B. licheniformis, B. polyfermenticus, B. pumilus, and B. subtilis—all of which exhibit probiotic activities in both spores and vegetative forms (Lee et al., 2019). Compared to probiotic lactic acid bacteria, Bacillus probiotic strains have better survival rates and stability to processing conditions such heat, cold, moisture, dehydration, as well as gastric conditions (Lee et al., 2019). This feature of Bacillus probiotics is largely due to their ability to form spores (Nicholson et al., 2000). In fact, the ability of Bacillus spores to germinate and grow in the gastro-intestinal tract has been reported (Hoa et al., 2000). This means that fermented pant-based foods could be used as carriers for the delivery of Bacillus probiotics into the mammalian digestive systems.

The influence of probiotics on human gut microbiome is well-reported (Thursby and Juge, 2017; Kawai et al., 2018), but the focus of has mostly been on lactic acid bacteria probiotics. Whereas, the impact of individual Bacillus strains on gut microbiome of some animal model (e.g., chicken and pigs) have been studied (Poulsen et al., 2018; Jacquier et al., 2019), little is known on how specific Bacillus strains influence the human gut microbiome. It is however known that, as probiotics, Bacillus strains stimulate antimicrobial, anticancer, antihypertensive, antioxidant, fibrinolytic, and immunomodulating activities in vitro and in vivo (Lee et al., 2019). These biological properties can be stimulated by the metabolic process of probiotics and post-biotics in alkaline fermenting foods.

Post-biotics are the bioactive soluble by-products released following either through the metabolic processes of probiotics or through lysis of probiotics (Wegh et al., 2019). A technical definition of post-biotics, as proposed by The International Scientific Association of Probiotics and Pre-biotics (ISAPP) is “preparation of inanimate microorganisms and/or their components that confers a health benefit on the host” (Salminen et al., 2021).

There is a growing number of studies reporting the health properties of post-biotics (Wegh et al., 2019; Zółkiewicz et al., 2020; Salminen et al., 2021) but these studies do not discriminate the source of these post-biotics, i.e., whether from acid or alkaline fermentation. However, examples of post-biotics that can be expected to be produced following alkaline fermentation of plant-based foods are soluble proteins, protein hydrolysates, bacteriocins, free amino acids, vitamins, soluble dietary fiber, exopolysaccharides, non-viable cells, and cell fragments. As presented earlier (see Sections Nutritional and Dietary Value of Plant-Based AFFs), alkaline fermentation leads to the production of several probiotics-derived biomolecules, many of which can be expected to have bioactive properties. Some of the mechanisms through which post-biotics mediate health in hosts includes mediating growth and metabolic activities of gut microbiota, modulating systemic metabolism, mediating signaling in nervous system, enhancing epithelial barrier function, modulating immune responses, triggering bioactive properties such as anti-adhesion, anti-biofilm, antidiabetic, antiviral, immunomodulatory, antihypertensive, hypocholesterolemic, and antioxidant effects (Tangyu et al., 2019; Wegh et al., 2019; Nataraj et al., 2020; Zółkiewicz et al., 2020; Salminen et al., 2021). A schematic of the nutrition and health impact of alkaline fermentation on plant-based foods is shown in Figure 4.

FIGURE 4

Figure 4. Impact of alkaline fermentation on plant-based foods.

Conclusion and Future Outlook

As shown in the preceding discussion, alkaline fermentation of plant-based foods offers several sensorial, nutritional, and health benefits. For example, guided selection of starter cultures and probiotic strains could be used to stimulate the in situ biofortification of plant-based foods through alkaline fermentation as a strategy to prevent deficiencies in nutrients such as vitamins, minerals, and proteins. However, as demonstrated in this review, the scientific underpinnings of the microbial metabolic factors and health-promoting effects of AFFs are not as well-studied as other fermented foods produced via lactic acid fermentation. For example, a careful search of the literature shows that only a few Bacillus species have been studied for their vitamin production potential, with B. subtilis being the most studied. Even then, most of the fundamental scientific studies on vitamin-producing alkaline fermenters were performed at laboratory scale using genetically modified strains, and in chemically defined media. The production of vitamins by alkaline fermenters in situ in plant-based foods needs more investigation.

Moreover, perspectives for improving the traditional production processes of AFFs to ensure consistency in safety and quality should be researched. Research is needed to unravel the genome sequences of microorganisms in AFFs. This will help with proper identification and taxonomic classification of species responsible for the generation of desired properties. Genomic sequences of microbiota in AFFs will also allow the selection of genes that can be targeted and altered by metabolic engineering strategies, to improve desired traits such as the production of post-biotics (e.g., enzymes, vitamins, bacteriocins, and exopolysaccharides), or to isolate and exclude genes responsible for the production of biogenic amines and antibiotic resistance genes. Another important area that needs attention is the generation of clinical evidence on how the composite microbial species in AFFs alter human gut microbiome. For reasons such as relatively low cost of production and the aforementioned nutritional and health promoting benefits, AFFs are expected to play a huge role in meeting the food, dietary, and health requirements of consumers, going forward.

Author Contributions

JO-K designed the manuscript. JO-K and DA critically revised and corrected the manuscript. JO-K, DA, FA, RA, and FKA wrote the manuscript. All authors contributed to the article and approved the submitted version.

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

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