Taurine (; IUPAC: 2-aminoethanesulfonic acid) is a natural product organic compound with the chemical formula , and is a non-proteinogenic sulfonic acid widely distributed in mammalian tissues and organs. Structurally, by containing a sulfonic acid group instead of a carboxylic acid group, it is not involved in protein synthesis but is still usually referred to as an amino acid. As non-proteinogenic amino sulfonic acid, it is not encoded by the genetic code and is distinguished from the protein-building α-amino acids.
Taurine is a major constituent of bile and can be found in the large intestine. It is named after Latin , meaning bull or ox, as it was first isolated from ox bile in 1827 by German scientists Friedrich Tiedemann and Leopold Gmelin.
Although taurine is abundant in human organs, it is not an essential human dietary nutrient and is not included among nutrients with a recommended intake level. Among the diverse pathways by which natural taurine can be biosynthesized, its human pathways (primarily in the human liver) are from cysteine and/or methionine.
Taurine is commonly sold as a dietary supplement, but there is no good clinical evidence that taurine supplements provide any benefit to human health. Taurine is used as a food additive to meet essential dietary intake levels for cats, and supplemental dietary support for dogs and poultry.
It is not an essential human dietary nutrient, resulting in the absence of taurine from compounds having a Reference Daily Intake. Its role in human physiology is unknown.
Taurine is a major constituent of bile, and can be found in the large intestine. Its concentrations in land plants are low or undetectable, but up to a substantial wet weight has been found in algae.
Taurine is also produced by the transsulfuration pathway, which converts homocysteine into cystathionine. The cystathionine is then converted to hypotaurine by the sequential action of three enzymes: cystathionine gamma-lyase, cysteine dioxygenase, and cysteine sulfinic acid decarboxylase. Hypotaurine is then oxidized to taurine as described above.
A pathway for taurine biosynthesis from serine and sulfate is reported in microalgae, developing chicken , and chick liver. Serine dehydratase converts serine to 2-aminoacrylate, which is converted to cysteic acid by 3-phosphoadenylyl sulfate:2-aminoacrylate C-sulfotransferase. Cysteic acid is converted to taurine by cysteine sulfinic acid decarboxylase.
In 1993, about of taurine were produced for commercial purposes: 50% for pet food and 50% in pharmaceutical applications.
In the laboratory, taurine can be produced by alkylation of ammonia with bromoethanesulfonate salts.
Taurine is partially destroyed by heat in processes such as baking and boiling. This is a concern for cat food, as cats have a dietary requirement for taurine and can easily become deficient. Either raw feeding or supplementing taurine can satisfy this requirement.
Both lysine and taurine can mask the metallic flavor of potassium chloride, a salt substitute.
A 2008 review found no documented reports of negative or positive health effects associated with the amount of taurine used in energy drinks, concluding, "The amounts of guarana, taurine, and ginseng found in popular energy drinks are far below the amounts expected to deliver either therapeutic benefits or adverse events".
Decreased plasma taurine concentration has been demonstrated to be associated with feline dilated cardiomyopathy. Unlike central retinal degeneration, the heart condition is reversible with supplementation.
Taurine is now a requirement of the Association of American Feed Control Officials (AAFCO) and any dry or wet food product labeled approved by the AAFCO should have a minimum of 0.1% taurine in dry food and 0.2% in wet food. Studies suggest the amino acid should be supplied at of bodyweight per day for domestic cats.
Taurine can be synthesized by chickens. Supplementation has no effect on chickens raised under adequate lab conditions, but seems to help with growth under stresses such as heat and dense housing.
The need of taurine in fish is conditional, differing by species and growth stage. The olive flounder, for example, has lower capacity to synthesize taurine compared to the rainbow trout. Juvenile fish are less efficient at taurine biosyntheis due to reduced cysteine sulfinate decarboxylase levels.
Discovery and name
In nature
Chemical and biochemical features
Biosynthesis
Chemical synthesis
In food
Breast milk
Energy drinks and dietary supplements
Research
Safety and toxicity
Animal dietary requirement
Cats
Other mammals
Birds
Fish
Derivatives
See also
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