Biochemistry 1: Chapter 8A Nucleotides
9 Questions
0 Views

Choose a study mode

Play Quiz
Study Flashcards
Spaced Repetition
Chat to lesson

Podcast

Play an AI-generated podcast conversation about this lesson

Questions and Answers

Which statement regarding bases in DNA is false?

  • They have vertical stacking interactions.
  • Pyrimidines are aromatic; purines are not. (correct)
  • They absorb UV light.
  • They hydrogen bond between two or more complementary DNA strands.
  • What stabilizes the double helix in DNA?

    Metal cations shield negative charges of backbone phosphates and base stacking interactions between successive base pairs.

    What other name can be given to a nucleotide?

  • Glycosylated nucleoside (correct)
  • Purinated pentose
  • Deoxyribonucleotide
  • Nucleoside phosphate
  • Which of the following is NOT a pyrimidine base?

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

    Which of the following is NOT part of a deoxyribonucleotide?

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

    What name is given to the nucleotide found in DNA and NOT in RNA?

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

    A property of nucleotide bases that affects the three-dimensional structure of nucleic acids is:

    <p>Their existence in tautomeric forms depending on pH</p> Signup and view all the answers

    In a sample of DNA isolated from an unidentified species of bacteria, adenine makes up 28% of the total bases. Which statement is false about the relative proportions of the bases in the DNA sample?

    <p>G and C base pairs account for 44% of the bases</p> Signup and view all the answers

    Which statement is true about the three-dimensional structure of DNA?

    <p>The offset pairing of the two strands creates a major groove and a minor groove on the surface of the duplex</p> Signup and view all the answers

    Study Notes

    Nucleotides and Nucleic Acids

    • Nucleotides have three components: a nitrogenous base, a pentose, and one or more phosphates
    • A nucleoside is a molecule without a phosphate group
    • Nitrogenous bases include pyrimidines (cytosine, thymine, uracil) and purines (adenine, guanine)

    Nucleotide Bonds

    • N-β-glycosyl bond: covalently joins the 1′ carbon of the pentose to the base (at N-1 of pyrimidines and N-9 of purines)
    • Phosphate is esterified to the 5′ carbon

    Nitrogenous Bases

    • Major purine bases: adenine (A) and guanine (G)
    • Major pyrimidine bases: cytosine (C), thymine (T), and uracil (U)
    • Thymine is only found in DNA, while uracil is only found in RNA

    Nucleotide Nomenclature

    • Table 8-1 shows the nomenclature for nucleotides, nucleosides, and nucleic acids

    Nucleotide Pentoses

    • Two kinds of pentoses: 2′-deoxy-D-ribose (in DNA) and D-ribose (in RNA)
    • Both are in their β-furanose (closed five-membered ring) form

    Deoxyribonucleotides and Ribonucleotides

    • Deoxyribonucleotides are the structural units of DNA
    • Ribonucleotides are the structural units of RNA

    Phosphodiester Bonds

    • Phosphodiester linkage: a covalent bond that joins successive nucleotides of both DNA and RNA
    • Between the 5′-phosphate group of one nucleotide unit and the 3′-hydroxyl group of the next nucleotide

    Hydrolysis of DNA and RNA

    • Under alkaline conditions, RNA is rapidly hydrolyzed due to the presence of 2′-hydroxyl groups
    • DNA is not rapidly hydrolyzed

    Solubility of Nucleotides

    • Hydrophobic and relatively insoluble in pH 7.0 water
    • Leads to stacking interactions (van der Waals and dipole-dipole)
    • Charged and more soluble at acidic or alkaline pH values

    Studying That Suits You

    Use AI to generate personalized quizzes and flashcards to suit your learning preferences.

    Quiz Team

    Description

    This quiz covers the roles of nucleotides in cellular metabolism, including energy currency, response to hormones, and structural components of enzymes and metabolic intermediates.

    More Like This

    Use Quizgecko on...
    Browser
    Browser