PREBIOTIC DIPEPTIDE FORMATION BY CYCLO-TRIPHOSPHATE
Hideko Inoue, Yoshinobu Baba, Mitsutomo Tsuhako
Abstract
Open-access reader
Hideko Inoue, Yoshinobu Baba, Mitsutomo Tsuhako
Abstract
Open-access reader
The reaction of glycine (Gly) or L-α-alanine (Ala) with inorganic sodium cyclo-triphosphate hexahydrate (P3m), Na3P3O9·6H2O, gave dipeptide [glycylglycine (GlyGly) or alanylalanine (AlaAla)] and the phosphorylated products of amino acids. Maximum yields of GlyGly and AlaAla were 17.9 and 5.6%, at pH9 and room temperature, respectively. Four kinds of dipeptide (GlyGly, AlaAla, GlyAla, and AlaGly) were produced in the reaction of P3m with the mixture of Gly and Ala.
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The reaction of glycine (Gly) or L-α-alanine (Ala) with inorganic sodium cyclo-triphosphate hexahydrate (P3m), Na3P3O9·6H2O, gave dipeptide [glycylglycine (GlyGly) or alanylalanine (AlaAla)] and the phosphorylated products of amino acids. Maximum yields of GlyGly and AlaAla were 17.9 and 5.6%, at pH9 and room temperature, respectively. Four kinds of dipeptide (GlyGly, AlaAla, GlyAla, and AlaGly) were produced in the reaction of P3m with the mixture of Gly and Ala.
Key concepts: Glycylglycine, Dipeptide, Glycine, Chemistry, Alanine, Amino acid, Stereochemistry, Sodium