Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-23T21:28:29.276Z Has data issue: false hasContentIssue false

Role of novel protein sources in sustainably meeting future global requirements

Published online by Cambridge University Press:  26 January 2021

Andrew M. Salter*
Affiliation:
Division of Food, Nutrition and Dietetics, School of Biosciences & Future Food Beacon, University of Nottingham, Sutton Bonington Campus, LoughboroughLE12 5RD, UK
Carlos Lopez-Viso
Affiliation:
Division of Food, Nutrition and Dietetics, School of Biosciences & Future Food Beacon, University of Nottingham, Sutton Bonington Campus, LoughboroughLE12 5RD, UK
*
*Corresponding author: Andrew M. Salter, email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Global population growth, increased life expectancy and climate change are all impacting world's food systems. In industrialised countries, many individuals are consuming significantly more protein than needed to maintain health, with the majority being obtained from animal products, including meat, dairy, fish and other aquatic animals. Current animal production systems are responsible for a large proportion of land and fresh-water use, and directly contributing to climate change through the production of greenhouse gases. Overall, approximately 60% of the global protein produced is used for animal and fish feed. Concerns about their impact on both human, and planetary health, have led to calls to dramatically curb our consumption of animal products. Underutilised plants, insects and single-cell organisms are all actively being considered as alternative protein sources. Each present challenges that need to be met before they can become economically viable and safe alternatives for food or feed. Many plant species contain anti-nutritional factors that impair the digestion and absorption of protein and micronutrients. Insects represent a potentially rich source of high-quality protein although, questions remain relating to digestibility, allergenicity and biosecurity. Algae, fungi and bacteria are also a rich source of protein and there is growing interest in the development of ‘cultured meat’ using stem cell technology. For the foreseeable future, it appears likely that the ‘protein-economy’ will remain mixed. The present paper reviews progress and future opportunities in the development of novel protein sources as food and animal feed.

Type
Research Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Authors 2021. Published by Cambridge University Press

As the global population continues to rise, there is increasing concern over our ability to sustainably meet the nutritional demands of the most vulnerable individuals. In most Western, industrialised countries, overt malnutrition is relatively rare and recent decades have seen dramatic rises in obesity, and related diseases such as diabetes and CVD, associated with consumption of diets rich in saturated fat(1) and refined carbohydrate(Reference Jebb2). By contrast, in large parts of Africa and Asia, malnutrition and micronutrient deficiency are still common. Dietary protein, containing appropriate amounts of indispensable amino acids (IAA) is essential to maintain health and support pregnancy and growth(3). The WHO has estimated the average protein requirement for an adult is 0⋅66 g/kg bodyweight/d with a population safe level set at 0⋅83 g/kg bodyweight/d(3). Additional amounts are required to maintain growth in children and to support pregnancy and lactation.

Actual protein requirements are dependent on quality, as well as quantity, of protein consumed. The afore-mentioned WHO requirements assume a protein digestibility-corrected amino score of 1⋅0(3). Protein digestibility-corrected amino score represents both a measure of amino acid composition and protein digestibility and essentially compares a dietary protein source with an ‘ideal’ protein(3). Although values approaching 1 are commonly associated with animals sources, such as meat, milk and eggs, values associated with plant-based foods can be much more variable, both as a result of lower IAA contents and poorer digestibility, often associated with the presence of anti-nutritional factors such as trypsin inhibitors, phytates, saponins and tannins(Reference Gilani, Xiao and Cockell4). In more recent years, the value of the protein digestibility-corrected amino score has been questioned, primarily because it does not adequately take into account the bioavailability of individual amino acids(Reference Scaafsma5). In 2013, the FAO of the UN recommended that a new measure of protein quality, digestible indispensable amino acid score, should be used instead(6). The digestible indispensable amino acid score is based on determining the ileal digestibility of each individual IAA and basing the score on the least available one. However, as yet, only limited data are available on ileal digestibility of amino acids in human subjects, and although significant progress has been made in developing in vitro techniques for determining protein digestibility(Reference Sousa, Portmann and Dubois7), in vivo measurements in the pig are currently regarded as the best surrogate(Reference Hodgkinson, Stein and de Vries8).

When protein is being consumed from a variety of different sources, both omnivorous and vegetarian diets can usually supply protein in sufficient quantity, and of appropriate quality, to meet these needs. FAO Food Balance Sheets show that in most of the Western industrialised countries the amount of protein available for human consumption significantly exceeds requirements(9). In populations that have access to less variety of food types, and often obtain most of their protein from a single cereal crop, deficiency is still relatively common(9). This is particularly the case in Africa where the majority of protein-deficient countries are located(Reference Schönfeldt and Hall10).

Fig. 1 is based on data presented by Berners-Lee et al.(Reference Berners-Lee, Kennelly and Watson11) and demonstrates that, on a global scale, approximately five times more protein is produced than is required to feed the world. However, 60 % of this is not consumed directly by human subjects but by farmed animals. Ultimately, only 34 % protein produced (animal + plant) is directly consumed by people. Thus, the major concern relating to protein is not the overall amount currently produced, but the unequal distribution between different populations and the direct and indirect impacts of animal production on the environment(12Reference Salter14). Protein intake in Western countries has also been influenced by perceived health benefits of high-protein diets. Replacing refined carbohydrate with protein in the diet has been increasingly recommended as a potential way of reducing obesity, due to high satiating effects of protein(Reference Clifton15). Furthermore, high-protein diets are frequently recommended to improve athletic performance(Reference Witard, Garthe and Phillips16). However, both protein production and the excretion of nitrogen associated with excessive intake may negatively impact the environment(Reference Shibata, Galloway and Leach17).

Fig. 1. (Colour online) Global protein food chain, indicating the amount of protein (g/person/d), produced, harvested and consumed, indicating losses from the human food chain. Based on data presented by Berners-Lee et al.(Reference Berners-Lee, Kennelly and Watson11).

The impact of animal production on the environment has come under intense scrutiny in recent years(12Reference Salter14). Production of feed for animals is responsible for significant use of agricultural land. Animal agriculture is also responsible for a significant proportion of global fresh-water use. Effluent from animal production is a major source of pollution of waterways and ruminant animals, particularly cattle, contribute to global warming through the production of methane. Such concerns have led to calls for a major shift in dietary patterns across much of the developed world with much more emphasis on plant-based foods. A recent report(Reference Scheelbeek, Green and Papier18) suggests that this may be achieved in the UK by greater adherence to the national dietary guidelines (the Eatwell Guide) and this represents the basis of the One Blue Dot diet proposed by the British Dietetic Association(19). However, others suggest more radical solutions are required to address both the impact of diets on our health and that of the planet. One such example is the recent Planetary Diet proposed by the Eat Lancet Commission(Reference Willett, Rockström and Loken20) which describes major reduction in consumption of animal-based foods, particularly red meat, and suggests they should be replaced by a combination of protein-rich plant foods, including legumes, nuts and pulses. There is also increasing interest in the sustainable production of novel sources of high-quality protein that can be used both as human food and ingredients for animal feed. This includes currently underutilised plant sources, insects and single-celled organisms, including bacteria. The potential value of such sources is discussed next.

Alternative sources of protein for human consumption

Fig. 2 shows the sources of protein consumed across the world and is based on data presented by Gorissen and Witard(Reference Gorissen and Witard21). Overall, approximately 60 % of total protein consumed by human subjects is derived from plants. This does, however, vary substantially between different continents, from 75 % in Africa down to only 36 % in Oceania. The primary sources of plant protein consumed globally are the staple cereals (largely wheat, rice and maize). However, reliance on these can lead to deficiency of IAA, particularly lysine(Reference Pellett and Ghash22). By contrast, legumes, pulses and nuts provide only 11 % protein consumed by human subjects across the world. This does not, however, reflect their true contribution to human protein intake as 75 % soyabean crop produced actually goes into animal feed(Reference Gorissen and Witard21,Reference Fraanje and Garnett23) . The Eat Lancet report(Reference Willett, Rockström and Loken20) suggests that such sources should represent a much larger proportion of our daily protein intake, replacing a large proportion of the red meat currently consumed. Soyabeans certainly represent a protein-rich plant-based food which also contains high concentration of IAA. Similar to other legumes, they also contain a range of anti-nutritional factors that can impact the digestibility and bio-accessibility of the protein, although processing and cooking can often minimise their effects(Reference Gilani, Xiao and Cockell4). In the West, soyabeans have frequently been used to produce ‘meat analogues’, products which have been specifically designed to look like, and have the same sensory properties as, meat products such as burgers and sausages(Reference Malav, Talukder and Gokulakrishnan24). There has been a dramatic rise in popularity of such products in recent years(Reference Boukid25) and it could thus be argued that much of the soyabeans currently grown for animal feed could be repurposed for direct human consumption. However, there is increasing concern about the environmental impact of clearance of wild habitat, particularly in South America, for soyabean production on our ecosystems(Reference Gorissen and Witard21). Other plant proteins sources commonly used in the production of meat analogues include wheat gluten(Reference Kumar, Chatli and Mehta26), although this does have an inferior amino acid composition, and most recently, pea protein, which has the advantage of being produced in more moderate climates(Reference Schreuders, Dekkers and Bodnár27).

Fig. 2. (Colour online) Sources of protein consumed in each content of the world (g/capita/d). Based on data presented by Gorissen and Witard(Reference Gorissen and Witard21).

Increasing attention is being turned to alternative plant sources of protein which until recently have remained underutilised as sources of human food, with particular emphasis on tropical legumes which may help to meet the rising demands for protein in Africa and Asia(Reference Cheng, Raai and Zain28). Two such potential legumes are bambara groundnut and winged bean. Bambara groundnut is a drought-resistant, nitrogen-fixing legume which is commonly consumed by subsistence farmers in Western Africa(Reference Halimi, Barkla and Mayes29). However, for a variety of reasons, including the physical properties of the seeds, water absorption and further hardening during prolonged storage under hot and humid conditions, bambara is considered ‘hard to cook’(Reference Mubaiwa, Fogliano and Chidewe30). Similar to many legumes, the nutritional value of bambara is further impacted upon by the presence of anti-nutritional factors including trypsin inhibitors, tannins and phytic acid(Reference Halimi, Barkla and Mayes29). In many respects, the physical and chemical factors associated with reducing the nutritional value of bambara are not dissimilar to those associated with soyabean, which, as already mentioned, is now widely consumed across the world by both human subjects and animals. A number of processing methods, including soaking, fermentation or treatment with exogenous enzymes have been shown to reduce the anti-nutrient content of such legumes(Reference Halimi, Barkla and Mayes29,Reference Mubaiwa, Fogliano and Chidewe30) . This clearly shows that with appropriate investment in breeding and processing techniques, bambara has the potential to make an important contribution to the protein intake of some of the world's poorest populations, while having a relatively low impact on the environment and the capacity to grow in relatively arid conditions.

Winged bean represents another underutilised tropical legume that may have the potential to contribute to the protein requirements of future generations. It is a crop which grows under hot and humid conditions and is one of the richest sources of plant protein at almost 30 g/100 g. Similar to soyabean, and other legumes, it is also a relatively good source of IAA. Its low requirements for water and other external inputs make it an attractive source of sustainable protein, although further research is required to try and improve its relatively poor and variable yields(Reference Tanzi, Eagleton and Ho31). However, similar to bambara, with appropriate investment, winged beans may help to meet the future demands of the growing global population, particularly in tropical regions, while minimising the impact of protein production on the environment. As will be further discussed next, such underutilised crops may also help to replace soyabean meal commonly used as animal feed.

Insects as human food

In many parts of the world, including Africa, Asia and Central/Southern America, insects are commonly consumed as a traditional part of the human diet(Reference Mlcek, Rop and Borkovcova32). It has been estimated that over 2000 species of insect are consumed across 113 countries worldwide(Reference Dossey, Tatum, McGill, Dossey, Morales-Ramos and Rojas33). In most cases, the contribution of such insects to the overall nutritional intake of such populations is likely to be relatively small. However, in recent years there has been increasing interest in insects as a sustainable and healthy source of protein, and other nutrients for both people and farmed animals. Compared to conventional crops and animal-based foods, insects require less space and reduced input (of water and feed) and are reported to have a significantly reduced carbon footprint(Reference Hawkey, Lopez-Viso and Brameld34). Many insect species also have the potential capacity to be reared on substrates that would not be appropriate for consumption by either people or animals. In terms of protein content, they frequently exceed the 55 % (of DM) associated with soyabean meals and exhibit often superior IAA composition(Reference Hawkey, Lopez-Viso and Brameld34). A number of products have appeared within the Western market including protein bars, flours and cookies prepared from crickets. Currently, this remains a relatively niche market and there remain some safety concerns including allergenicity and the ability of insect to accumulate toxins or to host biopathogens(Reference Hawkey, Lopez-Viso and Brameld34). However, it appears that insect protein will be increasingly seen as a sustainable source of protein for direct human consumption and, as discussed next, as an ingredient of animal feed.

Single-cell sources of protein

Single-cell, or microbial, sources of protein include algae, fungi and bacteria. Some are already established sources of human food, such as mushrooms, and yeast and bacteria as components of various fermented foods(Reference Nangu and Bhatia35). In more recent years, Fusarium venenatum, a filamentous microfungus has been used to produce mycoprotein, the protein-rich ingredient of the meat analogue brand Quorn(Reference Finnigan, Phillips and Williams36). Quorn products are now widely available in over seventeen countries as a range of both red meat and poultry analogues. Mycoprotein is a highly digestible source of protein(Reference Dunlop, Kilroe and Bowtell37) which is relatively rich in IAA and has the advantage of being grown on a carbohydrate substrate with no need for an exogenous protein input(Reference Finnigan, Phillips and Williams36). Microalgae also represent a potential source of high value protein, with Spirulina platensis being one of the most promising candidates. Spirulina contains up to 630 g/protein per kg DM and has been reported to have a IAA composition close to that of animal protein and which exceeds most plant sources(Reference Lupatine, Colla and Canan38). Despite its potential as a source of high-quality protein, as yet limited use has been made of it as a component of the human diet, which may be associated with relatively high production costs and poor sensory properties. As already alluded to the use of bacteria to ferment foods has been an established part of human nutrition for many years. However, bacteria themselves also represent a rich source of high-quality protein. They have a very high-protein content (approximately 80 %) and are a good source of IAA(Reference Nangu and Bhatia35). However, they are also rich in nucleic acids, the consumption of which may be associated with raised serum uric acid and development of gout(Reference Calloway and Davis39). As such, if bacterial protein were to be considered as a significant component of the human diet, nucleic acid content would have to be reduced to acceptable levels. As with many of the novel protein sources described for potential human consumption, there is considerable interest in the development of bacteria as a source on animal/fish feed.

Cultured meat

One alternative to conventional animal products, that has received considerable attention in recent years, is cultured meat(Reference Post, Levenberg and Kaplan40). Cultured meat is derived from stem cells isolated from living animals. The cells are grown under laboratory conditions and can be differentiated into muscle or adipose cells. By growing them on a ‘biomaterial scaffold’ the cells can be assembled into complexes that look like meat. Potentially, a product can be made which has the nutritional value of meat but without negative environmental impacts of livestock production. Although still in relatively earlier stages, there has been considerable private investment in developing this technology as a more ethical and environmentally friendly alternative to livestock production. Should the industry overcome the challenges of producing material on an economically viable and commercial scale, such technology could potentially transform the world's agricultural and food industries. However, there are also a range of consumer concerns, which vary considerably between different demographics, that would also need to be addressed(Reference Bryant and Barnett41).

Alternative protein sources for animal feed and aquaculture

With an increasing global population, demand for animal-derived foods is increasing at an unsustainable rate(Reference Herrero and Thornton13,Reference Sánchez-Muros, Barroso and Manzano-Agugliaro42) . One of the major issues for animal production is the amount of protein needed, with feed representing 60–70 % total livestock production costs(Reference Khatoon, Banerjee and Guan Yuan43). This is even more dramatic for the aquaculture industry, which also depends on fishmeal (FM) and fish oil to meet the nutritional requirements of farmed fish(Reference Green and Pearsall44). Finding novel, sustainable and affordable alternative sources of protein has become a major priority for the animal feed industry. Diverse alternatives, including insects, non-human-edible plants and single-cell organisms (fungi, bacteria and algae) are all currently under consideration(Reference Malav, Talukder and Gokulakrishnan24,Reference Henchion, Hayes and Mullen45) .

The main protein source for feeding monogastric-farmed animals (poultry and pigs) is soyabean meal, with almost 250 million tonnes being produced in 2020(46). The majority of this was produced in China (30 %), United States (19 %), Argentina (14 %) and Brazil (13 %). The vast majority of the soyabean crop is processed for oil, directed towards human consumptions, with the remaining protein-rich cake being used in animal feed(Reference Fraanje and Garnett23). As already eluded to, there is considerable concern about clearance of natural habitat to grow soyabeans, and in particular its impact on deforestation in Argentina and Brazil(Reference Fraanje and Garnett23). There are also concerns relating to the environmental impact of soyabean production on greenhouse emissions, carbon footprint and residues(Reference Henchion, Hayes and Mullen45,Reference Tilman and Clark47) . As a result, there is increasing interest in finding alternative sources of protein of, at least, similar quality to soyabean meal.

The aquaculture industry produces about 50 % of the total fish consumed in the world and it is expected to keep increasing(Reference Gasco, Gai and Maricchiolo48). Although there are similarities between feeds for farmed terrestrial animals and fish, aquafeeds have specific requirements which are often met by the inclusion of FM and fish oil, especially for carnivorous fish(Reference Hardy49). As these are obtained from wild-fish captures, as wild populations decline, this is increasingly being seen as environmentally and economically unsustainable(Reference Hua, Cobcroft and Cole50Reference Naylor, Hardy and Bureau52). Although, in several species, at least part of the FM can be replaced with soyabean meal, the lower protein and higher carbohydrate content, together with the presence of a range of anti-nutritional factors, has limited its use, particularly in carnivorous species(Reference Zou, Ringo and Olsen53). In addition, other, non-human-edible, plants have also been tried as an alternative to FM, although these often show limited digestibility, with high concentrations of anti-nutritional factors(Reference Hardy49). Furthermore, gut inflammation and other pathologies have been reported as negative effects in fish fed on plant-based diets(Reference Baeverfjord and Krogdahl54,Reference Hu, Kortner and Gajardo55) . In some countries, processed animal proteins such as meat and bone, blood, feather and by-products derived from poultry have been used as a source of protein for aquaculture(Reference Gasco, Gai and Maricchiolo48), although the high variability of raw materials and biosecurity are significant issues.

Insects as a source of protein for animal and fish feed

Considerable interest has been shown in the use of insects as a protein source for monogastric animals, including poultry(Reference Biasato, De Marco and Rotolo56Reference Bovera, Piccolo and Gasco60) and pigs(Reference Spranghers, Michiels and Vrancx61,Reference Altmann, Neumann and Rothstein62) . In general, most research has focused on insect larvae, predominantly mealworm (Tenebrio molitor) or black soldier fly larvae (Hermetia illucens). Most of the published studies suggest that at least a proportion of soyameal can be replaced in the diets of poultry and pigs without negative impacts on growth(Reference Hawkey, Lopez-Viso and Brameld34). However, although significant progress is being made, establishing sustainable and economically-viable large scale insect production systems remains challenging.

Insects have also been actively considered as a protein source in aquaculture. The use of insects as an alternative source of protein has shown promising results by partial or total FM replacement in diets of different fish species such as rainbow trout (Oncorhynchus mykiss)(Reference Renna, Schiavone and Gai63), European seabass (Dicentrarchus labrax)(Reference Magalhães, Sánchez-lópez and Silva64), barramundi (Lates calcarifer)(Reference Kataya, Borsra and Ganesan65), Atlantic salmon (Salmo salar)(Reference Belghit, Liland and Gjesdal66), sea bream (Sparus aurata)(Reference Piccolo, Iaconisi and Marono67), and Nile tilapia (Oreochromis niloticus)(Reference Tubin, Paiano and de Hashimoto68). The most utilised insects in aquafeeds are mealworms, black soldier fly larvae and housefly (Musca domestica) larvae, which have been approved as feeds by the European Union regulation (Commission Regulation (EU) 2017/893 on 24 May 2017)(Reference Gasco, Gai and Maricchiolo48). Moreover, social perception and acceptance, which are important for the market, is positive, due to their natural relationship of predator-prey in the trophic chain(Reference Henry, Gasco and Piccolo69). To provide insect meal as a cost-efficient and sustainable protein source, they should, ideally, be reared on economically viable feedstuffs, which are not suitable for human or animal consumption(Reference Oonincx, van Broekhoven and van Huis70Reference Tomberlin, van Huis and Benbow72). As such, there is considerable interest in growing them on by-products from the food industry(Reference Van Huis, van Itterbeeck and Klunder73,Reference Gasco, Biancarosa and Liland74) , which would allow a circular economy based on sustainable, waste revalorisation. Insects generally have a relatively high fat content (15–50 % DM) which may not be suitable as a feed ingredient for fish and may thus require a defatted process. However, the extracted fat may have further economic value as a feed ingredient for other animal species, or as a biodiesel substrate(Reference Henry, Gasco and Piccolo69,Reference Makkar, Tran and Heuzé75Reference Li, Ji and Zhang77) . As with their use as human foods, there are potential safety concerns over the use of insects as feed, including possible heavy metals accumulation and allergenicity(Reference Belluco, Losasso and Maggioletti78). There is still research required on production scalability(Reference Rumpold and Schlüter79,Reference Carocci, Rovito and Sinicropi80) before the widespread commercial use of insects as a major source of protein for animal and fish agriculture.

Single-celled organisms as a source of protein for animal and fish feed

Further alternative protein sources are single-cell organisms including algae, fungi and bacteria, all of which are at various stages of research(Reference Ritala, Häkkinen and Toivari81). Currently, two species of microalgae (unicellular) are produced in Europe, Spirulina and Chlorella spp., and have been targeted for their high long-chain n-3 fatty acid content. At present, 30 % of the total algae produced is used for animal feed(Reference Van der Spiegel, Noordam and van der Fels-Klerx82) and it has been estimated that they could replace one-third of the soyabean meal used for chicken and pig feeding(Reference Bleakley and Hayes83,Reference Rosegrant, Paisner and Meijer84) . Additionally, marine macroalgae (multicellular organisms) have high growth rates, the ability to grow in saltwater, and no need of cultivable land. Moreover, macroalgae can provide monogastric animals with bioactive compounds. For example, red seaweed (Porphyra sp.) has shown potential as a feed ingredient for sea bream(Reference Henchion, Hayes and Mullen45,Reference Garcia-Vaquero and Hayes85,Reference Sampels86) . However, as an alternative source of protein, such sources frequently need to be processed and bio-refined, due to low total protein and IAA(Reference Øverland, Mydland and Skrede87).

Yeast and yeast-derived ingredients have shown some positive properties as a component of animal feed, including probiotic activity, and enhanced immune and stress response in both fish and terrestrial animals. Yeast also has a similar protein content compared to oilseed plants(Reference Shurson88). Moreover, as a by-product of the brewery industry, yeast potentially represent a sustainable feed ingredient(Reference Westendorf and Wohlt89).

There is growing interest in the production of bacteria as an alternative source of protein. Photosynthetic bacteria, such as Rhodopseudomonas faecalis, are reported to provide high-protein yield and are relatively rich in IAA, vitamins, carotenoids, lipids and PUFA(Reference Patthawaro and Saejung90,Reference Wang, Yang and Zhang91) . Furthermore, they can grow on wastewater, thus providing, a sustainable environmental solution for both animal feed requirements and waste management(Reference Alloul, Ganigué and Spiller92). Other bacteria of interest include Methylophilus methylotrophus (Reference Johnson93), methanotrophic bacteria(Reference Ritala, Häkkinen and Toivari81), Bacillus licheniformis (Reference Liu, Li and Song94) and Bacillus subtilis (Reference Wongputtisin, Khanongnuch and Kongbuntad95). A further advantage of single-cell organisms is their potential genetic modification in order to improve properties of interest, but, safety, regulations and social concerns are delaying their application and work is still required to produce economically viable, industrial scale production plants(Reference Ritala, Häkkinen and Toivari81).

Conclusions

Currently, enough human-edible protein is produced as is required to meet the nutritional requirements of the global population. However, this is inequitably distributed around the world, and large proportions are used to feed livestock. In the face of global population growth, and the uncertain impacts of climate change on our food systems, there is an urgent need to re-assess the ‘global protein balance sheet’. For most high-income countries, this should include an overall reduction in the consumption of animal products, particularly red meat, which would have major benefits for human health, as well as the environment. For many, this could simply mean reducing the excessive amount of protein they consume. For others, animal protein should be replaced with high-quality plant sources and, perhaps, other more novel sources including insects and single-cell organisms. In the future, ‘meat’ cultured from animal cells could also make a significant contribution. However, we must acknowledge that, for the foreseeable future, animal products will remain part of the human diet and in many low- and middle-income countries they represent a ‘safety net’ against malnutrition. However, we must try to replace traditional agricultural practices of feeding farm animals with human-edible protein sources (including soyabean meal) and the use of wild-caught FM in aquaculture. Insects and single-cell organisms, including bacteria, represent exciting, and with continued research and investment, economically and environmentally favourable alternatives. An overall reduction in the excessive amount of protein produced and, in richer countries, consumed could have a major impact on reducing greenhouse gas emissions, land and water pollution and help to preserve natural landscapes and biodiversity.

Acknowledgements

The authors thank Dr John Brameld, Dr Tim Parr and Ms Kerensa Hawkey, University of Nottingham for their useful discussions and valuable insight into the topics covered in this review.

Financial Support

C. L.-V. is supported by a postdoctoral fellowship awarded by the Future Food Beacon, University of Nottingham.

Conflict of Interest

None.

Authorship

Both authors wrote and approved the manuscript.

References

Scientific Advisory Committee on Nutrition (2019) Saturated fats and health. https://www.gov.uk/government/publications/saturated-fats-and-health-sacn-report.Google Scholar
Jebb, SA (2015) Carbohydrates and obesity: from evidence to policy in the UK. Proc Nutr Soc 74, 215220.CrossRefGoogle ScholarPubMed
World Health Organization (2007) Protein and amino acid requirements in human nutrition. https://apps.who.int/iris/bitstream/handle/10665/43411/WHO_TRS_935_eng.pdf?ua=1 (accessed December 2020).Google Scholar
Gilani, GS, Xiao, CW & Cockell, KA (2012) Impact of antinutritional factors in food proteins on the digestibility of protein and the bioavailability of amino acids and on protein quality. Br J Nutr 108, S315S332.CrossRefGoogle Scholar
Scaafsma, G (2012) Advantages and limitations of the protein digestibility-corrected amino acid score (PDCAAS) as a method for evaluating protein quality in human diets. Br J Nutr 108, S333S336.CrossRefGoogle Scholar
Food and Agriculture Organization of the United Nations (2013) Dietary protein quality evaluation in human nutrition. http://www.fao.org/ag/humannutrition/35978-02317b979a686a57aa4593304ffc17f06.pdf.Google Scholar
Sousa, R, Portmann, R, Dubois, S et al. (2020) Protein digestion of different protein sources using the INFOGEST static digestion model. Food Res Int 130, 108996.CrossRefGoogle ScholarPubMed
Hodgkinson, SM, Stein, HH, de Vries, S et al. (2020) Determination of true ileal amino acid digestibility in the growing pig for calculation of digestible indispensable amino acid score (DIAAS). J Nutr 150, 26212623.CrossRefGoogle Scholar
Schönfeldt, HC & Hall, NG (2012) Dietary protein quality and malnutrition in Africa. Br J Nutr 108, S69S76.CrossRefGoogle ScholarPubMed
Berners-Lee, M, Kennelly, C, Watson, R et al. (2018) Current global food production is sufficient to meet human nutritional needs in 2050 provided there is radical societal adaptation. Elem Sci Anth, 6, 52. https://doi.org/101.525/elementa.310.CrossRefGoogle Scholar
Foresight (2011) The Future of Food and Farming: Challenges and Choices for Global Sustainability. Final Project Report. London: The Government Office for Science.Google Scholar
Herrero, M & Thornton, PK (2013) Livestock and global change: emerging issues for sustainable food systems. Proc Natl Acad Sci USA 110, 2087820881.CrossRefGoogle ScholarPubMed
Salter, AM (2016) Improving the sustainability of global meat and milk production. Proc Nutr Soc 76, 2227.CrossRefGoogle ScholarPubMed
Clifton, P (2012) Effects of a high protein diet on body weight and comorbidities associated with obesity. Br J Nutr 108, S122S129.CrossRefGoogle ScholarPubMed
Witard, OC, Garthe, I & Phillips, SM (2019) Dietary protein for training adaptation and body composition manipulation in track and field athletes. Int J Sport Nutr Exerc Metab 29, 165174.CrossRefGoogle ScholarPubMed
Shibata, H, Galloway, JN, Leach, AM et al. (2017) Nitrogen footprints: regional realities and options to reduce nitrogen loss to the environment. Ambio 46, 129142.CrossRefGoogle ScholarPubMed
Scheelbeek, P, Green, R, Papier, K et al. (2020) Health impacts and environmental footprints of diets that meet the Eatwell Guide recommendations: analyses of multiple UK studies. BMJ Open, 10, e037554. https://doi:10.1136/bmjopen-2020-037554.CrossRefGoogle ScholarPubMed
British Dietetic Association (2020) Eating patterns for health and environmental sustainability. https://www.bda.uk.com/uploads/assets/539e2268-7991-4d24-b9ee867c1b2808fc/a1283104-a0dd-476b-bda723452ae93870/one%20blue%20dot%20reference%20guide.pdf (accessed November 2020).Google Scholar
Willett, W, Rockström, J, Loken, B et al. (2019) Food in the Anthropocene: the EAT–Lancet Commission on healthy diets from sustainable food systems. Lancet 393, 447492.CrossRefGoogle ScholarPubMed
Gorissen, SHM & Witard, OC (2018) Characterising the muscle anabolic potential of dairy, meat and plant-based protein sources in older adults. Proc Nutr Soc 77, 2031.CrossRefGoogle ScholarPubMed
Pellett, P & Ghash, S (2004) Lysine fortification: past, present, and future. Food Nutr Bull 25, 107113.CrossRefGoogle ScholarPubMed
Fraanje, W & Garnett, T (2020) Soy: food, feed, and land use change (Foodsource: Building Blocks). Food Climate Research Network, University of Oxford. https://www.leap.ox.ac.uk/article/soy-food-feed-and-land-use-change (accessed December 2020).Google Scholar
Malav, OP, Talukder, S, Gokulakrishnan, P et al. (2015) Meat analog: a review. Crit Rev Food Sci Nutr 55, 12411245.CrossRefGoogle ScholarPubMed
Boukid, F (2021) Plant-based meat analogues: from niche to mainstream. Eur Food Res Technol 247, 297308.CrossRefGoogle Scholar
Kumar, O, Chatli, MK, Mehta, N et al. (2017) Meat analogues: health promising sustainable meat substitutes. Crit Rev Food Sci Nutr 57, 923932.CrossRefGoogle ScholarPubMed
Schreuders, FKG, Dekkers, BL, Bodnár, I et al. (2019) Comparing structuring potential of pea and soy protein with gluten for meat analogue preparation. J Food Eng 261, 3239.CrossRefGoogle Scholar
Cheng, A, Raai, MN, Zain, NAM et al. (2019) In search of alternative proteins: unlocking the potential of underutilized tropical legumes. Food Sec 11, 12051215.CrossRefGoogle Scholar
Halimi, RA, Barkla, BJ, Mayes, S et al. (2019) The potential of the underutilized pulse bambara groundnut (Vigna subterranea (L.) Verdc.) for nutritional food security. J Food Comp Analysis 77, 4759.CrossRefGoogle Scholar
Mubaiwa, J, Fogliano, V, Chidewe, C et al. (2017) Hard-to-cook phenomenon in Bambara groundnut (Vigna subterranea (L.) Verdc.) processing: options to improve its role in providing food security. Food Rev Int 33, 147194.CrossRefGoogle Scholar
Tanzi, AS, Eagleton, GE, Ho, WK et al. (2019) Winged bean (Psophocarpus tetragonolobus (L.) DC.) for food and nutritional security: synthesis of past research and future direction. Planta 250, 911931.CrossRefGoogle ScholarPubMed
Mlcek, J, Rop, O, Borkovcova, M et al. (2014) A comprehensive look at the possibilities of edible insects as food in Europe – a review. Pol J Food Nutr Sci 64, 147157.CrossRefGoogle Scholar
Dossey, AT, Tatum, JT & McGill, WL (2016) Modern insect-based food industry: current status, insect processing technology, and recommendations moving forward. In Insects as Sustainable Food Ingredients: Production, Processing and Food Applications, pp. 113152 [Dossey, AT, Morales-Ramos, JA and Rojas, MG, editors]. Cambridge, MA: Academic.CrossRefGoogle Scholar
Hawkey, KJ, Lopez-Viso, C, Brameld, JM et al. (2021) Insects: a potential source of protein and other nutrients for feed and food. Ann Rev Anim Biosci 9, 333354.CrossRefGoogle Scholar
Nangu, A & Bhatia, R (2013) Microorganisms: a marvellous source of single cell protein. J Microbiol Biotechnol Food Sci 3, 1518.Google Scholar
Finnigan, TJA (2011) Mycoprotein: origins, production and properties. In Handbook of Food Proteins pp. 335352 [Phillips, GO and Williams, PA, editors]. Cambridge: Woodhead Publishing.CrossRefGoogle Scholar
Dunlop, MV, Kilroe, SP, Bowtell, JL et al. (2017) Mycoprotein represents a bioavailable and insulinotrophic non-animal-derived dietary protein source: a dose-response study. Br J Nutr 118, 673685.CrossRefGoogle Scholar
Lupatine, AL, Colla, LM, Canan, C et al. (2017) Potential application of microalga Spirulina platensis as a protein source. J Sci Food Agric 97, 724732.CrossRefGoogle Scholar
Calloway, DH (1974) The place of single cell protein in man's diet. In Single Cell Protein pp. 129146 [Davis, P, editor]. New York: Academic Press.Google Scholar
Post, MJ, Levenberg, S, Kaplan, DL et al. (2020) Scientific, sustainability and regulatory challenges of cultured meat. Nat. Food 1, 403415.CrossRefGoogle Scholar
Bryant, C & Barnett, J (2018) Consumer acceptance of cultured meat: a systematic review. Meat Sci 143, 817.CrossRefGoogle ScholarPubMed
Sánchez-Muros, MJ, Barroso, FG & Manzano-Agugliaro, F (2014) Insect meal as renewable source of food for animal feeding: a review. J Clean Prod 65, 1627.CrossRefGoogle Scholar
Khatoon, H, Banerjee, S, Guan Yuan, GT et al. (2016). Biofloc as a potential natural feed for shrimp postlarvae. Int Biodeterior Biodegrad 113, 304309.CrossRefGoogle Scholar
Green, K & Pearsall, D (2016) Fishmeal and fish oil facts and figures. Publ., Seafish, (December) Edinburgh.Google Scholar
Henchion, M, Hayes, M, Mullen, A et al. (2017) Future protein supply and demand: strategies and factors influencing a sustainable equilibrium. Foods 6, 53.CrossRefGoogle ScholarPubMed
Tilman, D & Clark, M (2014) Global diets link environmental sustainability and human health. Nature 515, 518522.CrossRefGoogle ScholarPubMed
Gasco, L, Gai, F, Maricchiolo, G et al. (2018) Fishmeal alternative protein sources for aquaculture feeds. In Feeds for the Aquaculture Sector-Current Situation and Alternative Sources, Springer Briefs in Chemistry of Food, pp. 128 Cham: Springer.CrossRefGoogle Scholar
Hardy, RW (2010) Utilization of plant proteins in fish diets: effects of global demand and supplies of fishmeal. Aquac Res 41, 770776.CrossRefGoogle Scholar
Hua, K, Cobcroft, JM, Cole, A et al. (2019) The future of aquatic protein: implications for protein sources in aquaculture diets. One Earth 1, 316329.CrossRefGoogle Scholar
The World Bank (2013) Fish to 2030 Prospects for Fisheries and Aquaculture. World Bank Report Number 83177-GLB.Google Scholar
Naylor, RL, Hardy, RW, Bureau, DP et al. (2009) Feeding aquaculture in an era of finite resources. Proc Natl Acad Sci 106, 1510315110.CrossRefGoogle Scholar
Zou, Z, Ringo, E, Olsen, RE et al. (2017) Dietary effects of soybean on gut microbiota and immunity of aquatic animals: a review. Aquacult Nutr 24, 644665.CrossRefGoogle Scholar
Baeverfjord, G & Krogdahl, A (1996) Development and regression of soybean meal induced enteritis in Atlantic salmon, Salmo salar L., distal intestine: a comparison with the intestines of fasted fish. J Fish Dis. 19, 375387.CrossRefGoogle Scholar
Hu, H, Kortner, TM, Gajardo, K et al. (2016) Intestinal fluid permeability in Atlantic salmon (Salmo salar L.) is affected by dietary protein source. PLoS ONE 11, e0167515.CrossRefGoogle ScholarPubMed
Biasato, I, De Marco, M, Rotolo, L et al. (2016) Effects of dietary Tenebrio molitor meal inclusion in free-range chickens. J Anim Physiol Anim Nutr (Berl) 100, 11041112.CrossRefGoogle ScholarPubMed
Ramos-Elorduy, J, Gonzalez, EA, Hernadez, AR et al. (2002) Use of Tenebrio molitor (Coleoptera: Tenebrionidae) to recycle organic wastes and as feed for broiler chickens. J Econom Entomol 95, 214220.CrossRefGoogle ScholarPubMed
De Marco, M, Martínez, S, Hernandez, F et al. (2015) Nutritional value of two insect larval meals (Tenebrio molitor and Hermetia illucens) for broiler chickens: apparent nutrient digestibility, apparent ileal amino acid digestibility and apparent metabolizable energy. Anim Feed Sci Technol 209, 211218.CrossRefGoogle Scholar
Oluokun, J. (2000) Upgrading the nutritive value of full-fat soyabeans for broiler production with either fishmeal or black solider fly larvae meal (Hermetia illucens). Niger J Anim Sci 3, 5161.Google Scholar
Bovera, F, Piccolo, G, Gasco, L et al. (2015) Yellow mealworm larvae (Tenebrio molitor, L.) as a possible alternative to soybean meal in broiler diets. Br Poult Sci 56, 569575.Google ScholarPubMed
Spranghers, T, Michiels, J, Vrancx, J et al. (2018) Gut antimicrobial effects and nutritional value of black soldier fly (Hermetia illucens L.) prepupae for weaned piglets. Anim Feed Sci Technol. 235, 3342.CrossRefGoogle Scholar
Altmann, BA, Neumann, C, Rothstein, S et al. (2019) Do dietary soy alternatives lead to pork quality improvements or drawbacks ? A look into micro-alga and insect protein in swine diets. Meat Sci 153, 2634.CrossRefGoogle ScholarPubMed
Renna, M, Schiavone, A, Gai, F et al. (2017) Evaluation of the suitability of a partially defatted black soldier fly (Hermetia illucens L.) larvae meal as ingredient for rainbow trout (Oncorhynchus mykiss Walbaum) diets. J Anim Sci Biotechnol 8, 57.CrossRefGoogle ScholarPubMed
Magalhães, R, Sánchez-lópez, A, Silva, R et al. (2017) Black soldier fly (Hermetia illucens) pre-pupae meal as a fish meal replacement in diets for European seabass (Dicentrarchus labrax). Aquaculture 476, 7985.CrossRefGoogle Scholar
Kataya, K, Borsra, MZS, Ganesan, D et al. (2017) Efficacy of insect larval meal to replace fish meal in juvenile barramundi, Lates calcarifer reared in freshwater. Int Aquat Res 9, 303312.CrossRefGoogle Scholar
Belghit, I, Liland, NS, Gjesdal, P et al. (2019) Black soldier fly larvae meal can replace fish meal in diets of sea-water phase Atlantic salmon (Salmo salar). Aquaculture 503, 609619.CrossRefGoogle Scholar
Piccolo, G, Iaconisi, V, Marono, S et al. (2017) Effect of Tenebrio molitor larvae meal on growth performance, in vivo nutrients digestibility, somatic and marketable indexes of gilthead sea bream (Sparus aurata). Anim Feed Sci Technol 226, 1220.CrossRefGoogle Scholar
Tubin, JSB, Paiano, D, de Hashimoto, GSO et al. (2020) Tenebrio molitor meal in diets for Nile tilapia juveniles reared in biofloc system. Aquaculture 519, 734763.CrossRefGoogle Scholar
Henry, M, Gasco, L, Piccolo, G et al. (2015) Review on the use of insects in the diet of farmed fish: past and future. Anim Feed Sci Technol 203, 122.CrossRefGoogle Scholar
Oonincx, DGAB, van Broekhoven, S, van Huis, A et al. (2015) Feed conversion, survival and development, and composition of four insect Species on diets composed of food by-products. PLoS ONE 14, e0222043.CrossRefGoogle Scholar
Van Huis, A. (2016) Edible insects are the future? Proc Nutr Soc 75, 294305.CrossRefGoogle ScholarPubMed
Tomberlin, JK, van Huis, A, Benbow, ME et al. (2015) Protecting the environment through insect farming as a means to produce protein for use as livestock, poultry, and aquaculture feed. J Insects Food Feed 1, 307309.CrossRefGoogle Scholar
Van Huis, A, van Itterbeeck, J, Klunder, H et al. (2013) Edible insects. Future Prospects for Food and Feed Security, vol. 171, pp. 1221. Rome: Food and Agriculture Organization of the United Nations.Google Scholar
Gasco, L, Biancarosa, I & Liland, NS (2020) From waste to feed: a review of recent knowledge on insects as producers of protein and fat for animal feeds. Curr Opin Green Sustain Chem 23, 6779.CrossRefGoogle Scholar
Makkar, HPS, Tran, G, Heuzé, V et al. (2014) State-of-the- art on use of insects as animal feed. Anim Feed Sci Technol 197, 133.CrossRefGoogle Scholar
Schiavone, A, Cullere, M, De Marco, M et al. (2017) Partial or total replacement of soybean oil by black soldier fly larvae (Hermetia illucens L.) fat in broiler diets: effect on growth performances, feed-choice, blood traits, carcass characteristics and meat quality. Ital J Anim Sci 16, 93100.CrossRefGoogle Scholar
Li, S, Ji, H, Zhang, B et al. (2016) Influence of black soldier fly (Hermetia illucens) larvae oil on growth performance, body composition, tissue fatty acid composition and lipid deposition in juvenile Jian carp (Cyprinus carpio var. Jian). Aquaculture 465, 4352.CrossRefGoogle Scholar
Belluco, S, Losasso, C, Maggioletti, M et al. (2013) Edible insects in a food safety and nutritional perspective: a critical review. Compr Rev Food Sci Food Saf 12, 296313.CrossRefGoogle Scholar
Rumpold, BA & Schlüter, OK (2013) Nutritional composition and safety aspects of edible insects. Mol Nutr Food Res 57, 802823.CrossRefGoogle ScholarPubMed
Carocci, A, Rovito, N, Sinicropi, MS et al. (2014) Reviews of environmental contamination and toxicology. Rev Environ Contam Toxicol 229, 118.Google Scholar
Ritala, A, Häkkinen, ST, Toivari, M et al. (2017) Single cell protein-state-of-the-art, industrial landscape and patents 2001–2016. Front Microbiol 8, 2009.CrossRefGoogle ScholarPubMed
Van der Spiegel, M, Noordam, MY & van der Fels-Klerx, HJ (2013) Safety of novel protein sources (insects, microalgae, seaweed, duckweed, and rapeseed) and legislative aspects for their application in food and feed production. Compr Rev Food Sci Food Saf 12, 662678.CrossRefGoogle ScholarPubMed
Bleakley, S & Hayes, M (2017) Algal proteins: extraction, application, and challenges concerning production. Foods 6, 33.CrossRefGoogle ScholarPubMed
Rosegrant, MW, Paisner, MS, Meijer, S et al. (2001) 2020 Global Food Outlook Trends, Alternatives, and Choices, pp. 124. Washington, DC: International Food Policy Research Institute (August).Google Scholar
Garcia-Vaquero, M & Hayes, M (2016) Red and green macroalgae for fish and animal feed and human functional food development. Food Rev Int. 32, 1545.CrossRefGoogle Scholar
Sampels, S. (2014) Towards a more sustainable production of fish as an important protein source for human nutrition. J Fish Livest Prod 2, 119.Google Scholar
Øverland, M, Mydland, LT & Skrede, A (2019) Marine macroalgae as sources of protein and bioactive compounds in feed for monogastric animals. J Sci Food Agric 99, 1324.CrossRefGoogle ScholarPubMed
Shurson, GC. (2017) Yeast and yeast derivatives in feed additives and ingredients: sources, characteristics, animal responses, and quantification methods. Anim Feed Sci Technol 235, 6076.CrossRefGoogle Scholar
Westendorf, ML & Wohlt, JE (2002) Brewing by-products: their use as animal feeds. Vet Clin North Am – Food Anim Pract 18, 233252.CrossRefGoogle ScholarPubMed
Patthawaro, S & Saejung, C (2019) Production of single cell protein from manure as animal feed by using photosynthetic bacteria. Microbiol Open. 8, 120.CrossRefGoogle ScholarPubMed
Wang, H, Yang, A, Zhang, G et al. (2017) Enhancement of carotenoid and bacteriochlorophyll by high salinity stress in photosynthetic bacteria. Int Biodeterior Biodegrad 121, 9196.CrossRefGoogle Scholar
Alloul, A, Ganigué, R, Spiller, M et al. (2018) Capture-ferment-upgrade: a three-step approach for the valorization of sewage organics as commodities. Environ Sci Technol 52, 67296742.CrossRefGoogle ScholarPubMed
Johnson, EA (2013) Biotechnology of non-Saccharomyces yeasts – the ascomycetes. Appl Microbiol Biotechnol 97, 503517.CrossRefGoogle ScholarPubMed
Liu, B, Li, Y, Song, J et al. (2014) Production of single-cell protein with two-step fermentation for treatment of potato starch processing waste. Cellulose 21, 36373645.CrossRefGoogle Scholar
Wongputtisin, P, Khanongnuch, C, Kongbuntad, W et al. (2014) Use of Bacillus subtilis isolates from Tua-nao towards nutritional improvement of soya bean hull for monogastric feed application. Lett Appl Microbiol 59, 328333.CrossRefGoogle ScholarPubMed
Figure 0

Fig. 1. (Colour online) Global protein food chain, indicating the amount of protein (g/person/d), produced, harvested and consumed, indicating losses from the human food chain. Based on data presented by Berners-Lee et al.(11).

Figure 1

Fig. 2. (Colour online) Sources of protein consumed in each content of the world (g/capita/d). Based on data presented by Gorissen and Witard(21).