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