Concept explainers
Interpretation:
The elution order of given amino acids with
Concept introduction:
Ion-exchange chromatography is used to separate mixture of amino acids on the basis of their overall charge by using cation or anion-exchange resins.
Dowex-1 is an anion-exchange resins with less polar used for anion-exchange chromatography.
Anion-exchange chromatography separate amino acids according to their
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EBK ORGANIC CHEMISTRY
- 22-49 Based on your knowledge of the chemical properties of amino acid side chains, suggest a substitution for leucine in the primary structure of a protein that would probably not change the character of the protein very much.arrow_forward22-61 Polyglutamic acid (a polypeptide chain made only of glutamic acid residues) has an a-helix conformation below pH 6.0 and a random-coil conformation above pH 6.0. What is the reason for this conformational change?arrow_forward22-71 Which amino acid side chain is most frequently involved in denaturation by reduction?arrow_forward
- 22-6 The members of which class of proteins are insoluble in water and can serve as structural materials?arrow_forward22-45 Proteins are least soluble at their isoelectric points. What would happen to a protein precipitated at its isoelectric point if a few drops of dilute HCl were added?arrow_forwardExplain why a protein is least soluble in an aqueous medium that has a pH equal to the isoelectric point of the protein.arrow_forward
- Identify the following amino acid at pH = 7 (aqueous form): (COO-)–CH(NH3+)–CH2–(COO-) aspartic acid asparagine histidine arginine lysine Describe the amino acid illustrated above (at pH = 7.0). it is a non-polar, positively-charged amino acid it is a polar, positively-charged amino acid it is a polar, uncharged amino acid it is a polar, negatively-charged amino acid it is a non-polar, negatively-charged amino acid How many chiral carbons are present in the above amino acid (in aqueous form)? zero chiral carbons one chiral carbon two chiral carbons three chiral carbons four chiral carbons How many optical isomers (stereoisomers) are possible for the above amino acid (aqueous form)? 21 = 2 optical isomers 22 = 4 optical isomers 23 = 8 optical isomers 24 = 16 optical isomers 25 = 32 optical isomersarrow_forwardWrite down the structure of glutamic acid in each pH range from acidic to basic. It is known that pKa1 = 2.5 pKa2 = 3.5 pKa3 = 8.7 and draw the titration curve of glutamic acid titrated with a strong base, such as NaOH.arrow_forwardFor aspartic and glutamic acids, the isoelectric point occurs at a pH where the net charge on the two carboxyl groups is -1 and balances the charge of +1 on the a-amino group. Calculate pI for these amino acids.arrow_forward
- All amino acids have two ionizable functional groups: an α‑amino group (average pKa of 9.4) and an α‑carboxylic acid group (average pKa of 2.2). Aspartic acid has an ionizable side chain (R group) with a pKa of about 3.8. One of the possible ionization states of aspartic acid is shown in the image. At what pH would the structure be the predominant ionization state? Consider the ionization state of all three of the functional groups.arrow_forward4 An aqueous solution of an amino acid with a dissociable side chain is found to have the following side chain ratio at pH 4.0: K=[A- ]/[HA]=0.01. What is the identity of the amino acid?arrow_forwardConsider the following peptide : Phe – Glu – Ser – Met and Val – Trp – Cys – Leu. Do these peptides have different net charges at (a) pH 1? (b) pH 7? Indicate the charges at both pH valuesarrow_forward
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