2010
DOI: 10.1177/1934578x1000500329
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Toxicity of Non-protein Amino Acids to Humans and Domestic Animals

Abstract: Non-protein amino acids are common in plants and are present in widely consumed animal feeds and human foods such as alfalfa ( Medicago sativa), which contains canavanine, and lentil ( Lens culinaris), which contains homoarginine. Some occur in wild species that are inadvertently harvested with crop species. Some nonprotein amino acids and metabolites can be toxic to humans, e.g. Lathyrus species contain a neurotoxic oxalyl-amino acid. Some potential toxins may be passed along a food chain via animal intermedi… Show more

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Cited by 24 publications
(40 citation statements)
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“…Non-protein amino acids are plant secondary metabolites produced as a means to protect plants from environmental stresses, including herbivory [ 95 ]. Non-protein amino acids are structurally similar to proteinogenic amino acids which suggests both types of amino acids share similar synthetic metabolic pathways [ 96 ].…”
Section: Rumen Microbial Detoxification Of Plant Toxinsmentioning
confidence: 99%
“…Non-protein amino acids are plant secondary metabolites produced as a means to protect plants from environmental stresses, including herbivory [ 95 ]. Non-protein amino acids are structurally similar to proteinogenic amino acids which suggests both types of amino acids share similar synthetic metabolic pathways [ 96 ].…”
Section: Rumen Microbial Detoxification Of Plant Toxinsmentioning
confidence: 99%
“…Most legumes seeds such as the Canavalia species, Medicago sativa [34], and Vicia ervilia [35] consist of canavanine. The inhibition effect of canavanine on the development of insects is due to the competition for the irreplaceable amino acid arginine.…”
Section: Toxic Amino Acidsmentioning
confidence: 99%
“…The non-protein amino acid oxalyldiaminopropionic acid (ODAP) was originally derived from the legume Lathyrus sativus , a known neurotoxic compound and the primary component in the neurological disease lathyrism (Nunn et al 2010). Although ODAP does not form carbamates in the presence of CO 2 , or HCO 3 − , its structural similarities to glutamate causes ODAP to bind to ionotropic receptors and metabotropic receptors, causing cellular damage (Nunn et al 2010).…”
Section: Chemistrymentioning
confidence: 99%
“…Although ODAP does not form carbamates in the presence of CO 2 , or HCO 3 − , its structural similarities to glutamate causes ODAP to bind to ionotropic receptors and metabotropic receptors, causing cellular damage (Nunn et al 2010). Dissociation of ODAP results in the metabolite 2,3-diaminopropionate (2,3-DAP, Fig.4d).…”
Section: Chemistrymentioning
confidence: 99%