According to a third study, taurine consumption was estimated to vary between 40 and 400 mg/day. In another study, taurine intake was estimated to be generally less than 200 mg/day, even in individuals eating a high-meat diet. The mean daily intake from omnivore diets was determined to be around 58 mg (range from 9 to 372 mg) and to be low or negligible from a strict vegan diet. Taurine occurs naturally in fish and meat. Cysteic acid is converted to taurine by cysteine sulfinic acid decarboxylase. Serine dehydratase converts serine to 2-aminoacrylate, which is converted to cysteic acid by 3′-phosphoadenylyl sulfate:2-aminoacrylate C- sulfotransferase. Ī pathway for taurine biosynthesis from serine and sulfate is reported in microalgae, developing chicken embryos, and chick liver. Hypotaurine is then oxidized to taurine as described above. The cystathionine is then converted to hypotaurine by the sequential action of three enzymes: cystathionine gamma-lyase, cysteine dioxygenase, and cysteine sulfinic acid decarboxylase. Taurine is also produced by the transsulfuration pathway, which converts homocysteine into cystathionine. Hypotaurine is enzymatically oxidized to yield taurine by hypotaurine dehydrogenase. Cysteine sulfinic acid, in turn, is decarboxylated by sulfinoalanine decarboxylase to form hypotaurine. In this pathway, cysteine is first oxidized to its sulfinic acid, catalyzed by the enzyme cysteine dioxygenase. Mammalian taurine synthesis occurs in the pancreas via the cysteine sulfinic acid pathway. Taurine is naturally derived from cysteine. In the laboratory, taurine can be produced by alkylation of ammonia with bromoethanesulfonate salts. Most of these enterprises employ the ethanolamine method to produce a total annual production of about 3,000 tonnes. As of 2010, China alone has more than 40 manufacturers of taurine. In 1993, about 5,000–6,000 tonnes of taurine were produced for commercial purposes: 50% for pet food and 50% in pharmaceutical applications. A direct approach involves the reaction of aziridine with sulfurous acid. Synthetic taurine is obtained by the ammonolysis of isethionic acid (2-hydroxyethanesulfonic acid), which in turn is obtained from the reaction of ethylene oxide with aqueous sodium bisulfite. The sulfonic acid has a low p K a ensuring that it is fully ionized to the sulfonate at the pHs found in the intestinal tract. Taurine exists as a zwitterion H 3N +CH 2CH 2SO − 3, as verified by X-ray crystallography. It is an unusual example of a naturally occurring sulfonic acid. Taurine concentrations in land plants are very low or undetectable, but up to 1000 nmol/g wet weight have been found in algae. It is essential for cardiovascular function, and development and function of skeletal muscle, the retina, and the central nervous system. This compound has many biological roles, such as conjugation of bile acids, antioxidation, osmoregulation, membrane stabilization, and modulation of calcium signaling. It was discovered in human bile in 1846 by Edmund Ronalds. Taurine is named after Latin taurus ( cognate to Ancient Greek ταῦρος, taûros) meaning bull or ox, as it was first isolated from ox bile in 1827 by German scientists Friedrich Tiedemann and Leopold Gmelin. It is a major constituent of bile and can be found in the large intestine, and accounts for up to 0.1% of total human body weight. Taurine ( / ˈ t ɔː r iː n/), or 2-aminoethanesulfonic acid, is a non-proteinogenic amino sulfonic acid that is widely distributed in animal tissues.
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