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1 Proteins perform many different functions in the body. 2 H + │ H3N—C—COO− │ H glycine CH3 + │ H3N—C—COO− │ H alanine 3 Amino acids are classified as • nonpolar (hydrophobic) with hydrocarbon side chains. • polar (hydrophilic) with polar or ionic side chains. • acidic (hydrophilic) with acidic side chains. • basic (hydrophilic) with –NH2 side chains. Nonpolar Polar Acidic Basic 4 Amino acids • are chiral except glycine. • have Fischer projections that are stereoisomers. • that are L are the only amino acids used in proteins. COOH COOH H2N H CH3 L-Alanine H NH2 CH3 D-Alanine COOH H2N H CH2SH L-Cysteine COOH H NH2 CH2SH D-Cysteine 5 A zwitterion • has charged −NH3+ and COO– groups. • forms when both the –NH2 and the –COOH groups in an amino acid ionize in water. • has equal + and – charges at the isoelectric point (pI). O ║ NH2—CH2—C—OH glycine O ║ + H3N—CH2—C—O– zwitterion of glycine 6 In solutions more basic than the pI, • the —NH3+ in the amino acid donates a proton. + H3N—CH2—COO– zwitterion at pI Charge: 0 OH– H2N—CH2—COO– Negative ion pH > pI Charge: 1- 7 In solution more acidic than the pI, • the COO- in the amino acid accepts a proton. + H3N—CH2 zwitterion at pI Charge: 0 H+ —COO– + H3N—CH2—COOH Positive ion pH< pI Charge: 1+ 8 H+ + H3N–CH2–COOH positive ion low pH OH– + H3N–CH2–COO– zwitterion pI H2N–CH2–COO– negative ion high pH 9 When an electric current is used to separate a mixture of amino acids • the positively charged amino acids move towards the negative electrode. • the negatively charged amino acids move toward the positive electrode. • an amino acid at its pI does not migrate. • the amino acids are identified as separate bands on the filter paper or thin layer plate. 10 With an electric current, a mixture of lysine, aspartate, and valine are separated. 11 CH3 | + H3N—CH—COOH CH3 | H2N—CH—COO– (1) (2) Which structure represents: A. Alanine at a pH above its pI? B. Alanine at a pH below its pI? 12 CH3 | + H3N—CH—COOH CH3 | H2N—CH—COO– (1) (2) Which structure represents: A. Alanine at a pH above its pI? (2) B. Alanine at a pH below its pI? (1) 13 14 Alanine has a methyl group for the “R” Has 3 carbons (glycine had just 2) NOT essential NOT essential Essential Essential Valine is a branched chain amino acid. An "ideal protein" would contain 70% as much isoleucine as lysine. A rare, inherited metabolic disease in which there is a failure of oxidative decarboxylation (breakdown) of valine, leucine and isoleucine results in maple syrup urine disease, named because of a characteristic odor of the urine. Leucine is abundant in corn protein and many other grain proteins, and is not therefore a concern to supplement. Only the L isomer has biological value. "Ideal protein" would contain 100% as much leucine as lysine. Isoleucine is a branched chain amino acid. An "ideal protein" would contain one-half as much isoleucine as lysine. A rare, inherited metabolic disease in which there is a failure of oxidative decarboxylation (breakdown) of valine, leucine and isoleucine results in maple syrup urine disease, named because of a characteristic odor of the urine. Phenylalanine is not tolerated by people with inborn errors of PHE metabolism so they must avoid it. Babies are given a PKU (phenylketonuria) test at birth to detect phenylalanine metabolites in the urine, so they can be treated in order to avoid a dangerous condition. PHE is combined with ASP (aspartic acid, another amino acid) in the common non-nutritive sweetner aspertame. Equal is another trade name. Methionine is a sulfur-containing amino acid. A portion of the methionine requirement can be met from cystine, another sulfur-containing amino acid. An "ideal protein" would contain one- half as much methionine + cystine as lysine. Unlike most amino acids, both the d and l isomers of methionine are biologically active. Consequently, it has been synthesized and can be economically purchased for adding to diets. Methionine participates in acting as a methyl donor, and is involved in the synthesis of many important compounds in the body, including epinephrine and choline. Cysteine Cystine Tryptophan is the second most limiting amino acid in corn diets for pigs. Tryptophan can be used to from the Vitamin niacin but since feeds are usually low in tryptophan and the synthesis is insufficient to meet daily needs, it is not relied upon to meet the animal's need. Useful in aiding sleep, tryptophan supplements have been banned by FDA as dangerous. Skatole and indole can be formed from its breakdown in the large intestine by bacteria, producing foul odors. Arginine is a precursor of urea in the body. Urea is the form in which nitrogen is removed from mammals, so normal breakdown of protein and deamination of amino acids will result in urea formation, requiring arginine. Histidine contains an imidazole group. It is a precursor of histamine. An "ideal protein" would contain 33% as much histidine as lysine. Lysine is the most limiting amino acid in corn and most grains for swine and poultry. Diets balanced for lysine will contain most of the other amino acids in excess of requirement if natural sources of good quality proteins are used. It can be supplemented in the synthetic form and this is often economical, replacing a portion of the protein needed. Only the L isomer is biologically active. Phenylalanine Methionine Valine Histidine Threonine Arginine Tryptophan Lysine Isoleucine Leucine 1. General Features Nitrogen Balance & Metabolic Pools 2. Degradation Transamination & Glutamate Dehydrogenases 3. Urea Cycle 4. Sulfur-containing amino acids 5. Creatine & Creatinine 30 31 32 Formation of Peptides 33 A peptide bond • is an amide bond. • forms between the carboxyl group of one amino acid and the amino group of the next amino acid. 34 35 Write the dipeptide Ser-Thr. 36 Write the dipeptide Ser-Thr. 37 A dipeptide • is named from the free amine (NH3+) using a -yl ending for the name. • names the last amino acid with the free carboxyl group (COO-) by its amino acid name. 38 Write the three-letter abbreviations and names of the tripeptides that could form from two glycine and one alanine. 39 Write the names and three-letter abbreviations of the tripeptides that could form from two glycine and one alanine. Glycylglycylalanine Gly-Gly-Ala Glycylalanylglycine Gly-Ala-Gly Alanylglycylglycine Ala-Gly-Gly 40 What are the possible tripeptides formed from one each of leucine, glycine, and alanine? 41 Tripeptides possible from one each of leucine, glycine, and alanine: Leu-Gly-Ala Leu-Ala-Gly Ala-Leu-Gly Ala-Gly-Leu Gly-Ala-Leu Gly-Leu-Ala 42 Write the three-letter abbreviation and name for the following tetrapeptide. CH3 │ CH3 S │ │ CH–CH3 SH CH2 │ │ │ CH3 O H CH O H CH2O H CH2 O +│ ║ │ │ ║ │ │ ║ │ │ ║ H3N–CH–C–N–CH–C–N–CH–C–N–CH–CO– 43 Ala-Leu-Cys-Met Alanylleucylcysteinylmethionine CH3 │ CH3 S │ │ CH–CH3 SH CH2 │ │ │ CH3 O H CH O H CH2O H CH2 O +│ ║ │ │ ║ │ │ ║ │ │ ║ H3N–CH–C–N–CH–C–N–CH–C–N–CH–CO– Ala Leu Cys Met 44 Qualitative Tests for Amino Acids • There are a number of qualitative tests to detect the presence of amino acids • These are largely dependent on the nature of R-group. Exp. 1 Ninhydrin Reaction • A color reaction given by amino acids and peptides on heating with the chemical ninhydrin. • The technique is widely used for the detection and quantitation (measurement) of amino acids and peptides. • Ninhydrin is a powerful oxidizing agent which reacts with all amino acids between pH 4-8 to produce a purple colored-compound. • The reaction is also given by primary amines and ammonia but without the liberation of Co2 • The amino acids proline and hydroxyproline also reacts but produce a yellow color. Exp. 1 Ninhydrin Reaction ■ Method: • 1 ml AA + 1 ml NH • heat in boiling WB for 5min. • Purple color. Exp. 1 Ninhydrin Reaction ■ Method: • α-amino acid + 2 ninhydrin ---> CO2 + aldehyde + final complex (purple) + 3H2O • In summary, ninhydrin, which is originally yellow, reacts with amino acid and turns deep purple. It is this purple color that is detected in this method. Exp. 2 Xanthoproteic Reaction • This reaction involves the nitration of benzene nucleus in alkaline medium. As a result AAs that contain aromatic nucleus undergo this reaction. • Aromatic AAs form yellow nitro derivative on heating with conc. nitric acid, the salts of these derivatives are orange. Phenylalanine Tryptophan Tyrosine Exp. 2 Xanthoproteic Reaction ■ Method: • • • • 1 ml AA + 1 ml conc. HNO3 heat the mixture in WB for 30s cool add drop-wise 40% NaOH to render the solution alkaline • Yellow to orange color. Exp. 2 Xanthoproteic Reaction Tryptophan Tyrosine (a)Nitrated tyrosine and tryptophan (b) Exp. 3 Millon Reaction • This reaction is used to detect the presence of phenol (hydroxybenzene) which reacts with Millon's reagent to form red complexes. • The only phenolic AA is tyrosine. Tyrosine Exp. 3 Millon Reaction ■ Method: • • • • • 1 ml AA + 5 drops of Millon reagent heat the mixture in BWB for 10min cool too room temp add 5 drops of NaNO2 Brick red color. Exp. 4 Hopkin-cole Reaction • This reaction is used to detect the presence of indol group • The indol group of tryptophan reacts with glyoxalic acid in the presence of conc. H2SO4 to give purple color. Tryptophan Exp. 4 Hopkin-cole Reaction ■ Method: • 1 ml AA + 1 ml Hopkin-cole reagent • mix well • Carefully pour conc. H2SO4 down the side of the tube so as to form two layers • Purple ring at the interface. Exp. 5 Sulfur Reaction • This reaction is specific to detect the presence of sulfur. • The sulfur of cystein and cystine is converted to inorganic sulfide with conc. NaOH. Lead acetate is added and a ppt of black lead sulfide indicates a +ve reaction. Cystein Exp. 5 Sulfur Reaction • 2 ml AA + 1 ml 40% NaOH + 1-3 drops of lead acetate solution • heat the mixture in WB for 3min • Cool • observe any change • Black ppt. Exp. 6 Sakaguchi Reaction • This reaction is used to detect the presence of guanidine group. • The only AA that contains guanidine group is arginine which reacts with α-naphthol and an oxidizing agent such as bromide water to give a red color. Arginine Exp. 6 Sakaguchi Reaction • 2 ml AA + 1 ml 2M NaOH + 1 ml ethanolic 0.02% α-naphthol • mix well • cool in ice • add 1 ml of alkaline hypochlorite solution • Red color