Try it on paper first. A hint, the key idea and the worked solution are here when you need them.
In an experiment like that of Avery, MacLeod and McCarty, an extract of heat-killed S cells was split into four parts. One part was left alone as the control. The other three were treated with an enzyme, then mixed with live R cells and spread on plates. The plates were counted for S colonies.
| Plate | Treatment | S colonies |
|---|---|---|
| 1 | none (control) | 180 |
| 2 | protease | 176 |
| 3 | RNase | 182 |
| 4 | DNase | 3 |
Have you tried it?
Work it out on paper first. It is fine to get stuck or make a mistake: that is how we learn. When you are ready, go through the solution one step at a time, and check each step against your own.
Given. Control: colonies. Plates 2, 3 and 4: , and .
Plan. Each plate is a share of the control, so divide by and multiply by .
Step 1. (a) .
Step 2. (b) .
Step 3. (c) .
Step 4. (d) Protease and RNase leave the power to transform almost unchanged, and only DNase takes it away. So the carrier is DNA. A few colonies are left because the enzyme does not digest every DNA molecule.
Answer: ; ; ; DNA.
Check. Plates 2 and 3 are close to , and a small difference from the control is chance. Plate 4 is far below.
Watch out. A count above does not mean that RNase helps the transformation. It is a variation of the count.
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Griffith found that heat-killed S cells change live R cells into S cells. Avery, MacLeod and McCarty found that only DNase stops this change. Hershey and Chase tagged DNA with 32P and protein with 35S. The 32P went into the bacteria, and the 35S stayed outside.
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