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Cystin

As constituents of proteins the amino-acids are important constituents of the food of animals. Certain amino-acids can be made in the body from ammonia and non-nitrogenous sources others can be made from other amino-acids, e.g. tyrosine from phenylalanine and cystine from methionine, but many are essential ingredients of the diet. The list of essential amino-acids depends partly on the species. See also peptides and proteins. [Pg.29]

HSCH -CHNHj-COjH. Cysteine is a reduction product of cystine. It is the first step in the breakdown of cystine in the body, one molecule of cystine splitting to give two molecules of cysteine. Cysteine is soluble in water but the solution is unstable, and is reoxidized to cystine. [Pg.124]

A) Amino-aliphatic carboxylic acids. Glycine, tyrosine cystine. ... [Pg.318]

Tyrosine and cystine have been included primarily for students of biochemistry, physiology and medicine these two amino-acids might, however, be omitted by other students. [Pg.318]

Glycine or amino-acetic acid, NHjCHjCOOH tyrosine, />-HOC<.H4CH2CH(NH2)COOH cystine, [ SCH2CH(NH2)COOH]2. [Pg.380]

A) AMINO-ALIPHATIC CARBOXYLIC ACIDS. Glycine, tyrosine, cystine. [Pg.380]

Tyrosine and cystine are colourless solids almost insoluble in water gfid in ethanol (tyrosine dissolves in hot water). They are readily soluble in dilute caustic alkali solution, in ammonia and mineral acids, but not in acetic acid. They are also classed as neutral ampholytes. ... [Pg.381]

Action of nitrous acid. To a few ml. of 20% NaNO, solution add a few drops of cold dil. acetic acid. Pour the mixture into a cold aqueous solution of glycine, and note the brisk evolution of nitrogen. NH CH COOH -h HNO2 = HO CH2COOH + N + H O. Owing to the insolubility of cystine in acetic acid use a suspension in dU. acetic acid for this test. In each case care must be taken not to confuse the evolution of nitrogen with any possible thermal decomposition of the nitrous acid cf. footnote, p, 360). [Pg.381]

Tyrosine and cystine are insoluble in water therefore place about 0 2 g. in the test-tube A, dissolve in the dil. NaOH solution, add phenolphthalein as before and then add dil. HCl until pink colour is iust not discharged then proceed as above. [Pg.381]

Many amino-acjds are easily identified as their 3,5-dinitroben2oyl derivatives (Saunders, Biochem. Jour., 1934, 28, 580 1942, 36, 368). Cystine, however, forms a gelatinous derivative, but is readily identified by special tests. Tyrosine does not form a derivative under these conditions. [Pg.381]

Niiroprusside test. Dissolve about o-i g. of cystine in a few ml. of dilute ammonia and then add a few drops of potassium cyanide solution. This reduces cystine to cysteine,... [Pg.383]

Almost insoluble in cold water. Higher alcohols (including benzyl alcohol), higher phenols (e.g., naphthols), metaformaldehyde, paraldehyde, aromatic aldehydes, higher ketones (including acetophenone), aromatic acids, most esters, ethers, oxamide and domatic amides, sulphonamides, aromatic imides, aromatic nitriles, aromatic acid anhydrides, aromatic acid chlorides, sulphonyl chlorides, starch, aromatic amines, anilides, tyrosine, cystine, nitrocompounds, uric acid, halogeno-hydrocarbons, hydrocarbons. [Pg.404]

Peptide chain with two cystine residues (R = -CHgSH)... [Pg.330]

Tertiary structure also refers to the overall shape of a molecule, especially to structures stabilized by disulfide bridges (cystine) formed by the oxidation of cysteine mercapto groups. [Pg.19]

Keratin is the protein of hair and wool. These proteins are insoluble because of the disulfide cross-linking between cystine units. Permanent waving of... [Pg.19]

LPC Product Quality. Table 10 gives approximate analyses of several LPC products. Amino acid analyses of LPC products have been pubhshed including those from alfalfa, wheat leaf, barley, and lupin (101) soybean, sugar beet, and tobacco (102) Pro-Xan LPC products (100,103) and for a variety of other crop plants (104,105). The composition of LPCs varies widely depending on the raw materials and processes used. Amino acid profiles are generally satisfactory except for low sulfur amino acid contents, ie, cystine and methionine. [Pg.469]

The sulfur amino acid content of soy protein can be enhanced by preparing plasteins from soy protein hydrolysate and sources of methionine or cystine, such as ovalbumin hydrolysate (plastein AB), wool keratin hydrolysate (plastein AC), or L-methionine ethyl ester [3082-77-7] (alkaU saponified plastein) (153). Typical PER values for a 1 2 mixture of plastein AC and soybean, and a 1 3 mixture of alkah-saponified plastein and soybean protein, were 2.86 and 3.38, respectively, as compared with 1.28 for the soy protein hydrolysate and 2.40 for casein. [Pg.471]


See other pages where Cystin is mentioned: [Pg.28]    [Pg.124]    [Pg.124]    [Pg.233]    [Pg.383]    [Pg.383]    [Pg.406]    [Pg.407]    [Pg.553]    [Pg.440]    [Pg.663]    [Pg.865]    [Pg.346]    [Pg.330]    [Pg.275]    [Pg.275]    [Pg.275]    [Pg.275]    [Pg.275]    [Pg.275]    [Pg.275]    [Pg.142]    [Pg.142]    [Pg.143]    [Pg.144]    [Pg.144]    [Pg.146]    [Pg.151]    [Pg.152]    [Pg.18]    [Pg.469]    [Pg.476]    [Pg.448]   
See also in sourсe #XX -- [ Pg.132 ]

See also in sourсe #XX -- [ Pg.132 , Pg.301 , Pg.358 ]

See also in sourсe #XX -- [ Pg.68 ]

See also in sourсe #XX -- [ Pg.13 ]

See also in sourсe #XX -- [ Pg.132 , Pg.301 , Pg.358 ]




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2-Cystine

2-Cystine

B-Cystine

Bleached hair, cystine

Cross-linking cystine bridges

Crystal structures cystine

Cyclo Cystine

Cyclopentanone Cystine

Cystein, cystin

Cysteine Cystine

Cysteine and Cystine

Cysteine cystine equivalency

Cysteine sulfoxides Cystine

Cysteine, from cystine

Cysteine-cystine identification

Cysteine-cystine interconversion

Cystine Friedmann

Cystine Residues in Bovine Serum Albumin

Cystine absorption spectra

Cystine amalgam reduction

Cystine ammonia

Cystine analyses

Cystine and methionine

Cystine association with methionine

Cystine biosynthesis

Cystine catabolism

Cystine constitution

Cystine cross-links

Cystine crystalls

Cystine decarboxylase

Cystine decomposition

Cystine deficiency

Cystine degradation

Cystine dehydrogenase

Cystine derivatives

Cystine disulfoxide

Cystine disulfoxide oxidation

Cystine electrochemical oxidation

Cystine excretion

Cystine function

Cystine heart agar blood

Cystine hemoglobin

Cystine hydrogenation

Cystine in proteins

Cystine in the urine

Cystine in wool

Cystine isolation

Cystine lactoglobulin

Cystine ligands

Cystine linkage

Cystine lipids

Cystine lyase

Cystine manufacture

Cystine mixtures

Cystine ninhydrin reaction

Cystine nucleophilic cleavage

Cystine occurrence

Cystine oxidase

Cystine oxidation

Cystine peptides

Cystine peptides separation

Cystine peptides, cyclic

Cystine production

Cystine purification

Cystine racemization

Cystine reductase

Cystine reduction

Cystine requirements

Cystine residues

Cystine residues elimination

Cystine residues lipoamide dehydrogenase

Cystine residues ribonuclease

Cystine residues thioredoxin

Cystine residues, beta elimination

Cystine resolution

Cystine rotation

Cystine seleno

Cystine separation from tyrosine

Cystine solubility

Cystine solutions

Cystine stereochemistry

Cystine stones

Cystine sulfur, oxidation, direct

Cystine sulphite with

Cystine supplementation

Cystine synthesis

Cystine taurine

Cystine terms Links

Cystine titration

Cystine toxins

Cystine ultraviolet absorption

Cystine urolithiasis

Cystine with Liberation of Hydrogen Sulfide

Cystine with peptides

Cystine, cyanide reaction with

Cystine, determination

Cystine, disulfide reduction

Cystine, plasma concentration

Cystine, properties

Cystine, reactions

Cystine, structure

Cystine-binding protein

Cystine-containing peptides, protein

Cystine-copper complex

Cystinuria Cystine stone

DL-Cystine

Dibenzoyl cystine

Disulfide Interchange and Its Avoidance during the Synthesis of Peptides Containing Cystine

Disulfide cystine

Elimination reactions beta, of cystine residues

Glutathione reductase cystine residues

Half-cystin

I-Cystine

Intermediate oxidation products cystine

Keratins cystine determination

Keratins cystine reactivity

L-Cystine

L-cystine derivative

Lipid cystine residues

Methionine cystine from

Methionine cystine synthesis

Of L-cystine

Of cystine

Oxidation of Cystine Sulfur

Proteins blocking cystine residues

Proteins cystine

Pyruvic acid from cystine

Serum cystine

Sulfhydryl groups Cystine

Thioredoxin reductase cystine residues

Tryptophane separation from cystine

Tyrosine, removal from cystine

Urine cystine

Z-Cystine

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