Lecture #11- DNA Chemistry and Replication Flashcards
1
Q
properties of genetic material and why wasn’t DNA thought to be the universal hereditary material
A
- carry info
- replicated faithfully and transmit info
- have variation
- proteins with 20 possible monomers seems more likely because of the variation
2
Q
explain the Griffiths Transformation Experiment
A
- 1928
- showed that non-living component of cells was able to transform other cells
- “is there a transforming principle?”
- Experiment: took 2 strains of bacteria (same species with different properties)
1. Rough (R) strain -> non- virulent (non-disease causing)
2. S (smooth) strain -virulent (disease causing) - conclusion: there is an abiotic transforming principle
3
Q
explain the Avery, MacLeod and McCarty experiment
A
- “what is the transforming principle?”
- use different enzymes to specifically degrade cellular components
- Pipases or sucrases, RNase, Protase, DNase
- conclusion: DNA is the transforming principle
4
Q
Explain Hershey and Chase (Phage-in-a-blender)
A
- uses a phage (virus that infect bacteria)
- use radioactivity as a was to trace DNA and protein
- P32 tracks DNA, S35 tracks protein
- P32, there was radioactivity the pelle, DNA entered the bacteria to transform it
- conclusion: DNA is the universal transforming principle
5
Q
Explain Meselson- Stahl experiment and draw it out
A
- attempted to determine which hypothetical process of DNA replication was correct - semi-conservative, conservative or dispersive
- used radioactive to change the molecular mass of - compared the expected to the observed
- conclusion: DNA replicates semi-conservatively
6
Q
3 rules to understand DNA replication
A
- DNA is antiparallel 5’ -> 3’ and 3’ -> 5’
- DNA polymerase only extends 5’ -> 3’
- DNA poly requires an existing 3’ OH
- DNA poly catalyze phosphodiester bond formation
7
Q
Draw and label, replication bubble, direction of the fork opening, leading strand, Okazaki fragments, lagging strand
A
pg 10
8
Q
Draw DNA Replication in detail, include helicase, SSB’s, primase, DNA polymerase III, DNA poly I, ligase
A