Abstract

ScopeThe Soybean (Glycine max) leghemoglobin c2 (LegHb) gene was introduced into Pichia pastoris yeast for sustainable production of a heme‐carrying protein, for organoleptic use in plant‐based meat. The potential allergenicity and toxicity of LegHb and 17 Pichia host‐proteins each representing ≥1% of total protein in production batches are evaluated by literature review, bioinformatics sequence comparisons to known allergens or toxins, and in vitro pepsin digestion.Methods and resultsLiterature searches found no evidence of allergenicity or toxicity for these proteins. There are no significant sequence matches of LegHb to known allergens or toxins. Eleven Pichia proteins have modest identity matches to minor environmental allergens and 13 Pichia proteins have significant matches to proteins from toxic sources. Yet the matched allergens and toxins have similar matches to proteins from the commonly consumed yeast Saccharomyces cerevisiae, without evidence of food allergy or toxicity. The demonstrated history of safe use indicates additional tests for allergenicity and toxicity are not needed. The LegHb and Pichia sp. proteins were rapidly digested by pepsin at pH 2.ConclusionThese results demonstrate that foods containing recombinant soy LegHb produced in Pichia sp. are unlikely to present an unacceptable risk of allergenicity or toxicity to consumers.

Highlights

  • Introduction introduced intoPichia pastoris yeast for sustainable production of a heme-carrying protein, for organoleptic use in plant-based meat

  • The leghemoglobin c2 (LegHb) and Pichia sp. proteins were rapidly digested by pepsin at pH 2. These results demonstrate that foods containing recombinant soy LegHb produced in Pichia sp. are unlikely to present an unacceptable risk of allergenicity or toxicity to consumers

  • Four major leghemoglobin (LegHb) isoproteins are generally found in root nodules, where atmospheric N2 is reduced to ammonia and assimilated in exchange for photosynthetically produced sugars.[4,5]

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Summary

Introduction

Pichia pastoris yeast for sustainable production of a heme-carrying protein, for organoleptic use in plant-based meat. The potential allergenicity and toxicity of LegHb and 17 Pichia host-proteins each representing ࣙ1% of total protein in production batches are evaluated by literature review, bioinformatics sequence comparisons to known allergens or toxins, and in vitro pepsin digestion. Methods and results: Literature searches found no evidence of allergenicity or toxicity for these proteins. There are no significant sequence matches of Hemoglobins (Hbs) are ubiquitous iron binding proteins in nature, present in bacteria, fungi, higher plants, and animals.[1] Consumption of these proteins serves as an efficient source of bioavailable iron, which is required for oxygen transport, respiration, and other metabolic functions.[2] Animal Hbs and myoglobins have long been widely

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