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• W1866244218 endingPage "81" @default.
• W1866244218 startingPage "67" @default.
• W1866244218 abstract "The tissues of animals do not normally contain D-amino acids, and before an animal can utilize an ingested D-amino acid, it must convert the amino acid in the L form. This conversion, known as inversion, consists of two steps: (1) oxidative deamination of the α-keto analog; and (2) transamination of an amino group from glutamate. Amino acids differ greatly in the extent to which they can be inverted by animals and consequently, in the degree to which the D forms are bioavailable. Some amino acids are readily inverted and may be completely bioavailable, whereas others do not undergo inversion and therefore cannot be utilized by animals. In general, with the exception of tryptophan, avian species invert D-amino acids more efficiently than mammalian species do. Bioavailabilities of amino acid isomers and analogs include arginine, cystine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, tyrosine, and valine. Most research on 2-hydroxy-4-methylthiobutyric acid, often referred to as methionine hydroxy analog (OH-M), has involved poultry, for which this methionine analog is an important commercial product. It is sold as either free OH‑M, a liquid, or OH‑M (Ca), a solid consisting of 2 mol of OH‑M bound to calcium by the two carboxyl carbons. Considerable controversy has surrounded the biological availability of DL‑OH‑M relative to DL-methionine. Recent research by Chung and Baker has indicated that young pigs utilize DL‑OH‑M with the same free molar efficiency as L-methionine." @default.
• W1866244218 created "2016-06-24" @default.
• W1866244218 creator A5004977506 @default.
• W1866244218 creator A5039190928 @default.
• W1866244218 date "1995-01-01" @default.
• W1866244218 modified "2023-09-23" @default.
• W1866244218 title "Bioavailability of D-amino acids and DL-hydroxy-methionine" @default.
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