This cheat sheet summarizes key experiments proving DNA as genetic material, highlighting objectives, methods, results, and conclusions.
|
Information:
|
Contains instructions to build an organism.
|
|
Replication:
|
Capable of accurate copying (DNA replication).
|
|
Transmission:
|
Passed from parent to offspring and between cells during division.
|
|
Variation:
|
Accounts for differences within and between species.
|
|
Early Hypotheses (Late 1800s):
|
August Weismann and Karl Nägeli proposed a biochemical basis for inheritance.
|
|
Chromosome Insight:
|
Chromosomes, composed of proteins and DNA, identified as carriers of genetic information.
|
|
Experiment Background:
|
Studied Streptococcus pneumoniae:
Type S (smooth, virulent) strains produce a polysaccharide capsule. Type R (rough, non-virulent) strains lack this capsule. |
|
Step 1:
|
Injected live type R bacteria into a mouse → Mouse survived, no live bacteria found.
|
|
Step 2:
|
Injected live type S bacteria into a mouse → Mouse died, live type S bacteria found in blood.
|
|
Step 3:
|
Injected heat-killed type S bacteria into a mouse → Mouse survived, no live bacteria found.
|
|
Step 4:
|
Mixed heat-killed type S with live type R bacteria → Injected into a mouse → Mouse died, live type S bacteria found in blood.
|
|
Living type R bacteria transformed into type S, gaining the ability to produce a capsule.
|
|
This transformation indicated transfer of genetic material.
|
|
Focus:Investigated bacterial transformation, following up on Griffith's observations to identify the biochemical nature of the genetic material.
|
|
Question: What substance from dead type S bacteria transforms live type R bacteria?
|
|
Purification Process: Purified macromolecules (proteins, DNA, RNA) from type S Streptococcus pneumoniae.
Found only purified DNA could convert type R to type S bacteria initially. |
|
Step 1:
|
Mixed purified DNA from type S bacteria with type R bacteria.
Allowed DNA uptake by type R bacteria, converting some to type S. |
|
Step 2:
|
Enzyme Treatments :
DNase: Digests DNA. RNase: Digests RNA. Protease: Digests proteins. |
|
Step 3:
|
Aggregated type R cells (non-transformed) removed by centrifugation.
|
|
Step 4:
|
Type S cells (transformed) remain in the supernatant.
|
|
Step 5:
|
Supernatant plated on growth media to observe bacterial colony formation.
|
|
Step 6:
|
Control plates (without DNA extract) showed no type S colonies.
|
|
DNA from type S bacteria alone could convert type R bacteria to type S, proving DNA as the genetic material.
|
|
Elimination of transformation with DNase confirmed DNA's essential role.
|
|
Goal: To identify which component, DNA or protein, enters the bacterial cell and directs the synthesis of new viruses.
|
|
Labeling:
|
DNA labeled with 32P (radioactive phosphorus).
Protein labeled with 35S (radioactive sulfur). |
|
Infection Process:
|
E. coli cells are infected with either 32P-labeled phage or 35S-labeled phage.
|
|
Shearing Force:
|
Use a blender to detach phage coats from bacterial cells after allowing the phages to inject their genetic material.
|
|
Centrifugation:
|
Separate heavier bacterial cells (pellet) from lighter phage coats (supernatant).
|
|
Detection:
|
Measure the radioactivity in the pellet and supernatant using a Geiger counter.
|
No comments yet.
Cheatography n. The art of mapping complex subjects into clear, instantly navigable reference guides.