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Benders'dictionary of nutrition and food technology

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20that protein (chemical score). Most cereal proteins are limitedby lysine, <strong>and</strong> most animal <strong>and</strong> other vegetable proteins by thesum <strong>of</strong> methionine + cysteine (the sulphur amino acids). In completediets it is usually the sulphur amino acids that are limiting.amino acid pr<strong>of</strong>ile Amino acid composition <strong>of</strong> a protein.amino acids The basic units from which proteins are made. Chemicallycompounds with an amino group (—NH 2 ) <strong>and</strong> a carboxylgroup (—COOH) attached to the same carbon atom (see p. 22).Thirteen <strong>of</strong> the amino acids involved in proteins can be synthesisedin the body, <strong>and</strong> so are called non-essential or dispensableamino acids, since they do not have to be provided in thediet. They are alanine, arginine, aspartic acid, asparagine, cysteine,cystine, glutamic acid, glutamine, glycine, hydroxyproline,proline, serine <strong>and</strong> tyrosine.Nine amino acids cannot be synthesised in the body at all <strong>and</strong>so must be provided in the diet; they are called the essential orindispensable amino acids: histidine, isoleucine, leucine, lysine,methionine, phenylalanine, threonine, tryptophan <strong>and</strong> valine.Arginine may be essential for infants, since their requirement isgreater than their ability to synthesise it.Two <strong>of</strong> the non-essential amino acids are made in the bodyfrom essential amino acids: cysteine (<strong>and</strong> cystine) from methionine,<strong>and</strong> tyrosine from phenylalanine.A number <strong>of</strong> other amino acids also occur in proteins, includinghydroxyproline, hydroxylysine, γ-carboxyglutamate <strong>and</strong>methylhistidine, but are <strong>nutrition</strong>ally unimportant since theycannot be reutilised for protein synthesis. Other amino acidsoccur as intermediates in metabolic pathways, but are notrequired for protein synthesis <strong>and</strong> are <strong>nutrition</strong>ally unimportant,although they may occur in <strong>food</strong>s. These include homocysteine,citrulline <strong>and</strong> ornithine. Some <strong>of</strong> the non-protein amino acidsthat occur in plants are toxic.The amino acids are sometimes classified by the chemicalnature <strong>of</strong> the side chain. Two are acidic: glutamic acid (glutamate)<strong>and</strong> aspartic acid (aspartate) with a carboxylic acid(—COOH) group in the side chain. Three, lysine, arginine <strong>and</strong>histidine, have basic groups in the side chain. Three, phenylalanine,tyrosine <strong>and</strong> tryptophan, have an aromatic group in the sidechain. Three, leucine, isoleucine <strong>and</strong> valine, have a branchedchain structure. Two, methionine <strong>and</strong> cysteine, contain sulphur inthe side chain; although cysteine is not an essential amino acid,it can be synthesised only from methionine, <strong>and</strong> it is conventionalto consider the sum <strong>of</strong> methionine plus cysteine (the sulphuramino acids) in consideration <strong>of</strong> protein quality.

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