Chapter 13 & 14 Vocabulary & Important Concepts

Cards (118)

  • Frederick Griffith

    Discovered transformation while searching for how bacteria made people sick
  • Griffith's Experiment
    Experimented with harmless rough strain bacteria and pneumonia-causing S strain bacteria; dead S strain can make R strain dangerous by altering its genes (transformation)
  • transformation
    process in which one strain of bacteria is permanently changed by genes from another strain
  • Oswald Avery

    Discovered that DNA stores and transmits genetic info
  • Avery's experiment

    Avery treated biological molecules (ex. nucleic acids, lipids, etc.) with enzymes to destroy them; transformation does not occur without DNA
  • Alfred Hershey and Martha Chase

    further proved that DNA is the molecule of genetic material
  • Hershey-Chase experiment

    An experiment involving bacteriophages, which a component of enters the bacteria to transfer its genetic material; Radioactive phosphorus-32 marked DNA and sulfur-35 marked proteins; Phosphorus-32 was found in the supernate of the bacteria - the DNA entered the bacteria to transfer its genetic material
  • bacteriophage
    a kind of virus that infects bacteria
  • nucleotides
    the basic building block of nucleic acids
  • nitrogenous bases

    adenine, thymine, uracil, guanine, cytosine
  • two types of nitrogenous bases
    purines and pyrimidines
  • purine
    double-ring nitrogenous base; adenine and guanine
  • pyrimidine
    single-ring nitrogenous base; thymine and cytosine
  • Chargaff's Rule

    [A] = [T] and [C] = [G]
  • Rosalind Franklin

    Used X-ray diffraction to photograph DNA; the photo allowed Watson and Crick to build a model of DNA
  • Watson and Crick
    Used Franklin's x-ray photo and Chargraff's Rule to produce a model of DNA
  • Watson and Crick's model

    double helix (as in Franklin's photo); purines hydrogen bonded to pyrimidines (explains Chargraff's rule); sugar-phosphate backbone; antiparallel
  • 5' (five prime)

    End of the DNA strand where the fifth carbon is bonded to the phosphate group
  • 3' (three prime)

    End of the DNA strand where there is no phosphate group
  • hydrogen bonds in DNA
    hold base pairs together; weak enough to split the double helix for replication
  • Number of hydrogen bonds between A and T
    two
  • Number of hydrogen bonds between G and C
    three
  • complementary
    bases are paired in a specific way that fits its counterpart
    ex. original has A, complementary has T
  • Structure of DNA and replication

    Double helix and complementary base pairing facilitate replication
  • replication
    process of copying DNA that occurs during the S (synthesis) stage of interphase; used to duplicate DNA for cell division
  • origin of replication

    Site where the replication of a DNA molecule begins; typically in area rich with A-T pairs b/c its 2 hydrogen bonds are weaker than G-C's 3
  • replication bubble

    Region of DNA where helicase has split the double helix
  • helicase
    enzyme that unwinds DNA by breaking hydrogen bonds; results in replication bubble, replication forks, and ssDNA
  • ssDNA
    single-stranded DNA; unwound DNA
  • SSB
    single-stranded binding proteins; stabilizes ssDNA by keeping the strands apart (they were unstable b/c they want to become the double helix again)
  • RNA primase

    Enzyme that adds RNA primers
  • RNA primer

    short segments of RNA nucleotides (about 10) that are complementary to the DNA; needed because DNA polymerase needs a foundation to add on; initiates addition of DNA nucleotides
  • DNA polymerase III

    Enzyme that adds nucleotides to the 3' side of the template strand (new strand is made from 5' to 3' b/c they are antiparallel); proofreads new DNA
  • template strand

    Original strand that the new strand complements
  • reason for leading and lagging strands

    Nucleotides can only be added to the 3' end of the template strand, but the strands are still antiparallel
  • leading strand
    New strand where nucleotides are added continuously (toward replication fork)
  • lagging strand

    New strand where nucleotides are added discontinuously (away from replication fork); segments of RNA primer added (RNA primase more active), then Okazaki fragments added
  • Okazaki fragments

    Fragments of DNA (~100-200 nucleotides) added to the lagging strand
  • semiconservative
    describes DNA replication; in each new DNA molecule, there is one original strand and one new strand
  • DNA polymerase I
    Enzyme that replaces RNA primer with DNA in the lagging strand; exonuclease removes RNA primer