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Questions and Answers

What is the main role of amino acids in biological systems?

  • They are involved in DNA replication.
  • They serve as a primary energy source.
  • They facilitate nerve signal transmission.
  • They are the building blocks of proteins. (correct)
  • Which group is not attached to the α-carbon atom of an amino acid?

  • Amino group (-NH2)
  • Hydroxyl group (-OH) (correct)
  • R-group (side chain)
  • Carboxyl group (-COOH)
  • What is the significance of the isoelectric point (IEP) of an amino acid?

  • It is the pH at which the amino acid acts only as a base.
  • It represents the maximum solubility of the amino acid.
  • It is the pH at which the zwitter ion is formed. (correct)
  • It indicates the melting point of the amino acid.
  • Which of the following statements about zwitter ions is true?

    <p>Zwitter ions are electrically neutral.</p> Signup and view all the answers

    Which of these classifications does not apply to amino acids?

    <p>Structural classification</p> Signup and view all the answers

    Which amino acids are classified as aliphatic amino acids?

    <p>Valine and Isoleucine</p> Signup and view all the answers

    Which of the following groups of amino acids contains a hydroxyl group (-OH) in their R group?

    <p>Serine and Threonine</p> Signup and view all the answers

    Which amino acids are considered basic because they contain an amino group (-NH2) in their R group?

    <p>Lysine and Arginine</p> Signup and view all the answers

    Which amino acids contain sulfur in their R group?

    <p>Methionine and Cysteine</p> Signup and view all the answers

    Which of the following amino acids forms a ring structure due to its side chain?

    <p>Proline</p> Signup and view all the answers

    Study Notes

    Amino Acids Overview

    • Approximately 300 amino acids exist in nature
    • Only 20 (or 22) occur in proteins

    Importance

    • Amino acids are the fundamental building blocks of proteins

    Structure

    • Each amino acid has four distinct groups attached to a central carbon atom (α-carbon), adjacent to the carboxyl group
    • These groups are:
      • Amino group (-NH₂)
      • Carboxyl group (-COOH)
      • Hydrogen atom (-H)
      • Side chain (R-group)

    General Formula

    • A central carbon atom (α-carbon) bonded with:
      • Carboxyl group (-COOH)
      • Amino group (-NH₂)
      • Hydrogen atom (-H)
      • Variable side chain (R-group)

    Physical Properties

    • All amino acids are soluble in water, dilute acids, dilute alkalis, and ethanol.
    • Amino acids possess high melting points (above 200°C), indicating substantial stability

    Amphoteric Properties

    • Amino acids exhibit amphoteric (acid-base) behavior
    • In neutral aqueous solutions, a proton typically shifts from the carboxyl group to the amino group, resulting in a zwitterion
    • Zwitterions bear both positive and negative charges

    Zwitterion

    • A zwitterion is electrically neutral (net charge zero)
    • It cannot migrate in an electric field

    Isoelectric Point (IEP)

    • The pH at which the zwitterion forms
    • Example: Alanine's IEP is 6

    Classification of Amino Acids

    • Based on side chain properties:
      • Nature of side chain ("R-group")
      • Polarity of side chain ("R-group")
      • Nutritional classification
      • Metabolic classification

    1/ Aliphatic Amino Acids

    • Includes Glycine (Gly) and Alanine (Ala), Valine (Val), Leucine (Leu), and Isoleucine (Ile)

    2/ Hydroxyl Amino Acids

    • Includes Serine (Ser), Threonine (Thr), and Tyrosine (Tyr)

    3/ Sulfur Amino Acids

    • Includes Methionine (Met) and Cysteine (Cys)
    • Cystine is formed by two cysteine molecules linked by a disulfide bond

    4/ Acidic Amino Acids

    • Includes Glutamic Acid (Glu) and Aspartic Acid (Asp)

    5/ Basic Amino Acids

    • Includes Histidine (His), Lysine (Lys), and Arginine (Arg)

    6/ Aromatic Amino Acids

    • Includes Phenylalanine (Phe), Tyrosine (Tyr), and Tryptophan (Trp)

    7/ Imino Acids

    • Includes Proline (Pro)

    Classification by Polarity

    • Polar Amino Acids:

      • Side chains contain polar hydrophilic groups
      • Form hydrogen bonds with water
      • Subtypes: Hydroxyl groups (OH), SH, Amide group (NH₂) (basic amino acids: lysine, arginine, histidine) or COOH (acidic amino acids)
    • Non-Polar Amino Acids:

      • Side chains are alkyl hydrophobic groups
      • Cannot form hydrogen bonds with water
      • Examples: Glycine, Alanine, Valine, Leucine, Isoleucine, Phenylalanine, Tryptophan, Proline, Methionine

    Nutritional Classification

    • Essential Amino Acids:
      • Cannot be synthesized by the body and must be obtained from the diet
      • Examples: Isoleucine, Leucine, Lysine, Methionine, Phenylalanine, Threonine, Tryptophan, Valine
    • Semi-essential Amino Acids:
      • Can be synthesized by the body but not in sufficient amounts, especially for children
      • Examples: Arginine, Histidine
    • Non-essential Amino Acids:
      • Can be synthesized by the body in sufficient amounts
      • Remaining amino acids

    Metabolic Classification

    • Ketogenic Amino Acids:
      • Metabolized to form ketone bodies
      • Examples: Lysine, Leucine
    • Mixed Ketogenic & Glucogenic Amino Acids:
      • Metabolized to form both ketone bodies and glucose
      • Examples: Isoleucine, Phenylalanine, Tyrosine, Tryptophan
    • Glucogenic Amino Acids:
      • Metabolized to form glucose
      • Examples: Rest of the amino acids

    Deficiency in Selected Foods

    • Certain foods lack specific amino acids
      • Wheat/Rice: Lysine deficiency
      • Corn: Lysine, Tryptophan deficiency
      • Beans: Methionine, Tryptophan deficiency
      • Peas: Methionine deficiency

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