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Alanine solubility

Alitame (trade name Adame) is a water-soluble, crystalline powder of high sweetness potency (2000X, 10% sucrose solution sweetness equivalence). The sweet taste is clean, and the time—intensity profile is similar to that of aspartame. Because it is a stericaHy hindered amide rather than an ester, ahtame is expected to be more stable than aspartame. At pH 2 to 4, the half-life of aUtame in solution is reported to be twice that of aspartame. The main decomposition pathways (Fig. 6) include conversion to the unsweet P-aspartic isomer (17) and hydrolysis to aspartic acid and alanine amide (96). No cyclization to diketopiperazine or hydrolysis of the alanine amide bond has been reported. AUtame-sweetened beverages, particularly colas, that have a pH below 4.0 can develop an off-flavor which can be avoided or minimized by the addition of edetic acid (EDTA) [60-00-4] (97). [Pg.280]

Acrylamide readily undergoes polymerization by conventional free radical methods, ionizing radiation, ultrasonic waves, and ultraviolet radiation. The base-cata-lized hydrogen transfer polymerization of acrylamide yields poly-/3-alanine (Nylon 3) a water insoluble polymer that is soluble in certain hot organics. All current industrial production is believed to be by free radical polymerization. [Pg.65]

Tropoelastin is the soluble precursor of elastin and consists of alternating hydrophobic and hydrophilic peptide domains. The most common amino acids in the hydrophobic domains are Gly, Val, Ala, and Pro, which are often present in repeats of tetra-, penta-, and hexapeptides, such as Gly-Gly-Val-Pro, Gly-Val-Gly-Val-Pro, Gly-Val-Pro-Gly-Val, and Gly-Val-Gly-Val-Ala-Pro, respectively [3, 4]. The hydrophilic domains are mainly composed of lysines interspersed by alanines. [Pg.73]

Unlike the end products of purine catabolism, those of pyrimidine catabolism are highly water-soluble COj, NH3, P-alanine, and P-aminoisobutyrate (Figure 34-9). Excretion of P-aminoisobutyrate increases in leukemia and severe x-ray radiation exposure due to increased destruction of DNA. However, many persons of Chinese or Japanese ancestry routinely excrete P-aminoisobutyrate. Humans probably transaminate P-aminoisobutyrate to methylmalonate semialdehyde, which then forms succinyl-CoA (Figure 19-2). [Pg.300]

Since the end products of pyrimidine catabolism are highly water-soluble, pyrimidine overproduction results in few clinical signs or symptoms. In hypemricemia associated with severe overproduction of PRPP, there is overproduction of pyrimidine nucleotides and increased excretion of p-alanine. Since A, A -methyl-ene-tetrahydrofolate is required for thymidylate synthesis, disorders of folate and vitamin Bjj metabofism result in deficiencies of TMP. [Pg.300]

Finally, the solubility of the amino acids is also important. Only those amino acids that are readily soluble in water, such as glycine, alanine, valine, and proline, can be employed to construct the present family of 3d-4f amino acid compounds. [Pg.212]

Endothelial NOS was found to be associated with cell membranes and this property was associated with the finding that the cDNA contained the structure for binding myristic acid55. Busconi and Michel56 used bovine aortic endothelial cells to demonstrate that the myristoylated protein was found. When the second amino acid, glycine, was converted to alanine, the addition of myristic acid was prevented and the enzyme remained soluble. Sessa and coworkers51 carried out the same experiments simultaneously and found the same results. However, in both cases the enzyme was not purified, although the protein... [Pg.977]

Keefer, R.M. Interaction of ions and dipolar ions. IV. The solubility of cupric iodate in glycine and in alanine solutions, J. Am. Chem. Soc., 70(2) 476-479, 1948. [Pg.1677]


See other pages where Alanine solubility is mentioned: [Pg.61]    [Pg.165]    [Pg.61]    [Pg.165]    [Pg.77]    [Pg.5]    [Pg.518]    [Pg.530]    [Pg.83]    [Pg.142]    [Pg.14]    [Pg.16]    [Pg.105]    [Pg.339]    [Pg.210]    [Pg.268]    [Pg.196]    [Pg.208]    [Pg.201]    [Pg.155]    [Pg.489]    [Pg.53]    [Pg.173]    [Pg.30]    [Pg.348]    [Pg.354]    [Pg.38]    [Pg.202]    [Pg.230]    [Pg.322]    [Pg.5]    [Pg.77]    [Pg.72]    [Pg.118]    [Pg.61]    [Pg.450]    [Pg.33]    [Pg.371]    [Pg.32]    [Pg.161]    [Pg.1490]    [Pg.204]    [Pg.70]   
See also in sourсe #XX -- [ Pg.357 , Pg.415 ]

See also in sourсe #XX -- [ Pg.266 ]




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