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Amino acids identifying

Is the following structure a d amino acid or an i. amino acid Identify it. [Pg.1053]

Figure 7.5 The Edman degradation method, by which the sequence of a peptide/polypeptide may be elucidated. The peptide is incubated with phenylisothiocyanate, which reacts specifically with the N-terminal amino acid of the peptide. Addition of 6 mol l-1 HCl results in liberation of a phenylthiohydantoin-amino acid derivative and a shorter peptide, as shown. The phenylthiohydantoin derivative can then be isolated and its constituent amino acid identified by comparison to phenylthiohydantoin derivatives of standard amino acid solutions. The shorter peptide is then subjected to a second round of treatment, such that its new amino terminus may be identified. This procedure is repeated until the entire amino acid sequence of the peptide has been established... Figure 7.5 The Edman degradation method, by which the sequence of a peptide/polypeptide may be elucidated. The peptide is incubated with phenylisothiocyanate, which reacts specifically with the N-terminal amino acid of the peptide. Addition of 6 mol l-1 HCl results in liberation of a phenylthiohydantoin-amino acid derivative and a shorter peptide, as shown. The phenylthiohydantoin derivative can then be isolated and its constituent amino acid identified by comparison to phenylthiohydantoin derivatives of standard amino acid solutions. The shorter peptide is then subjected to a second round of treatment, such that its new amino terminus may be identified. This procedure is repeated until the entire amino acid sequence of the peptide has been established...
A similar ion-exchange resin method was used by Ling in 1955 (LI) for the examination of combined amino acids in urine. According to this procedure urine was desalted and simultaneously freed from amino acids by using Amberlite IR-112, H+-form resin. The effluent collected from the column was then fractionated on Amberlite IRA, OH--form resin, by successive elution with 0.16 N acetic acid, 0.08 N formic acid, 0.25 N formic acid, 0.08 N hydrochloric acid, and finally with 0.16 N formic acid. The solutions of all acids contained 10% of acetone. The collected fractions were hydrolyzed with hydrochloric acid and the liberated amino acids identified by means of paper chromatography. [Pg.130]

The isolated proteinaceous surfactants, obtained from commercial agarose powder and forest soil extract, were found to have extremely similar total amino acid compositions. Table 4.2 summarizes the amino acid values obtained from four determinations for each of the two surfactant preparations it can be seen that the rather unusual amino acid ratios obtained (among 17 different amino acids) for the two separate cases closely resemble one another. Specifically, in both of these cases the relative amounts of the different amino acids identified (excluding tryptophan which is completely destroyed during acid hydrolysis) were as follows glycine serine > aspartic acid (and/or aspara-... [Pg.76]

The Miller-Urey reaction has been quite successful in duplicating these results. All 20 amino acids identified in meteorites, and 12 others, were produced by electric discharges on CH4-NH3-H2O-H2 mixtures, in the presence of an aqueous phase (Ring et al., 1972 Wolman et al., 1972). Even the proportions of the various amino acids resemble those in Murchison to within 1-2 orders of magnitude. [Pg.15]

Amino acids identified in both total DOM (as THAA) and HMWDOM (as DCAA) include aspartic acid, glutamic acid, serine, histidine, glycine, threonine, alanine, arginine, tyrosine, valine, isoleucine, phenylalanine, leucine, and tryptophan (e.g., McCarthy et al., 1996 Yamashita and Tanoue, 2003). Figure 3.5A shows the mole percent distribution of these amino acids in DOM and HMWDOM. AU... [Pg.108]

Rogers (1983) defined a relationship where the total peptidoglycan-N content of a sample could be estimated based on its D-Ala content (peptidoglycan-N = 5.7 X D-Ala-N). Based on this relationship it was estimated that peptidoglycan contributed 7 =b 2% of THAA-N in Arctic rivers, 53 11% of THAA-N in the deep waters of the Arctic Ocean (Dittmar et al, 2001), and 20—25% of the THAA-N (and 2.5% of the total DON) in North Atlantic surface waters (Perez et ai, 2003). McCarthy et al. (1998) calculated a peptidoglycan-N content of 4.5—16% in HMWDON. However, intact peptidoglycans have not been isolated from any fraction of DOM, and D-amino acids identified in DOM could be present in other peptides. [Pg.115]

McCleUand, J. W., HoU, C. M., and Montoya, J. P. (2003). Nitrogen sources to zooplankton in the Tropical North Atlantic Stable isotope ratios of amino acids identify strong couphng to N2-fixation. Deep-Sea Res. I 50, 849—861. [Pg.1299]

Figure 16.2 Schematic representation of the crystal structure of CYP2D6 [44] illustrating the position of amino acids identified as key by model building. Hydrogen bonds identified by modeling between Asp301 and the main chain amides of Vail 19 and Phel20 are denoted by dashed lines. (Image produced using Pymol [15].) See color plates. Figure 16.2 Schematic representation of the crystal structure of CYP2D6 [44] illustrating the position of amino acids identified as key by model building. Hydrogen bonds identified by modeling between Asp301 and the main chain amides of Vail 19 and Phel20 are denoted by dashed lines. (Image produced using Pymol [15].) See color plates.
Table 11.2. Ranking of amino acids according to results from stabilization assays of 0/X7 libraries on MHC H-2K1 molecules (31). Amino acids O are classified for Iheir influence on stabilization (destabilizing upper part (a) stabilizing lower part (b)). Motif amino acids identified by sequence analysis of natural peptide libraries [33] are underlined. Table 11.2. Ranking of amino acids according to results from stabilization assays of 0/X7 libraries on MHC H-2K1 molecules (31). Amino acids O are classified for Iheir influence on stabilization (destabilizing upper part (a) stabilizing lower part (b)). Motif amino acids identified by sequence analysis of natural peptide libraries [33] are underlined.
Amino acids identified by paper or column chromatography after acid hydrolysis of the glycopeptide or peptido-oligosaccharide fractions. Amino acids present in trace quantities are shown in italics. [Pg.447]

Table lV.A-1 summarizes the numbers of carboxylic acids and amino acids identified to date in tobacco and tobacco smoke. Their listing and references are presented in subsequent tables. [Pg.317]

Yambe H, Kitamura S, Kamio M, Yamada M, Matsunaga S, Fusetani N, Yamazaki F (2006) L-Kynurenine, an amino acid identified as a sex pheromone in the urine of ovulated female masu salmon. Proc Natl Acad Sci USA 103 15370-15374... [Pg.412]

Draw structural formulas for the foUowing amino acids, identify the chiral carbon atom in each one, and circle the four different groups attached to the chiral carbon. [Pg.319]

Alcohols, aldehydes, oxo-acids, and amino acids identified in yeast [1]... [Pg.219]


See other pages where Amino acids identifying is mentioned: [Pg.29]    [Pg.58]    [Pg.5]    [Pg.175]    [Pg.487]    [Pg.33]    [Pg.219]    [Pg.483]    [Pg.219]    [Pg.97]    [Pg.440]    [Pg.88]    [Pg.223]    [Pg.115]    [Pg.142]    [Pg.65]    [Pg.88]    [Pg.120]    [Pg.164]    [Pg.94]    [Pg.318]    [Pg.727]    [Pg.1131]    [Pg.482]    [Pg.125]    [Pg.54]    [Pg.217]   
See also in sourсe #XX -- [ Pg.450 ]




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