UW-Stout/Ethanol FA22

Yeast Ethanol Stress Experiment

Introduction

We will add a sample of ethanol solution to a yeast culture and measure the growth afterward. This experiment is to determine what amounts of ethanol solution are best for the stress experiment on our class knockout genes.

Materials

• Corning COSTAR 96-well clear flat-bottom assay plate
• Wild-type yeast in 2x synthetic complete media at an OD600 of 0.1-0.2
• Ethanol concertation of 1M (labeled ETH01M)
• Sterile water

Procedure

1. Turn on the biological safety cabinet
2. Steralize your hands and other materials you need in the biological safety cabinet
3. Complete steps 4-20 in the biological safety cabinet
4. Make the ethanol solution in a 1.7 ml PCR tube by adding 942µl of water and 58µl of 100% ethanol
5. Collect well a clear flat-bottom assay plate
6. Vortex yeast culture for about 5 seconds
7. Put 50µl of the yeast culture into all 12 wells.
8. In the 1st well add 1µl of your ethanol solution and 49µl of H2O
9. In the 2nd well add 2µl of your ethanol solution and 48µl of H2O
10. In the 3rd well add 3µl of your ethanol solution and 47µl of H2O
11. In the 4th well add 4µl of your ethanol solution and 46µl of H2O
12. In the 5th well add 5µl of your ethanol solution and 45µl of H2O
13. In the 6th well add 8µl of your ethanol solution and 42µl of H2O
14. In the 7th well add 10µl of your ethanol solution and 40µl of H2O
15. In the 8th well add 20µl of your ethanol solution and 30µl of H2O
16. In the 9th well add 27µl of your ethanol solution and 23µl of H2O
17. In the 10th well add 35µl of your ethanol solution and 15µl of H2O
18. In the 11th well add 41µl of your ethanol solution and 9µl of H2O
19. In the 12th well add 50µl of your ethanol solution and 0µl of H2O
20. In E column 12th well add 0µl of your ethanol solution and 50µl of H2O
21. Put your well clear flat-bottom assay plate into the incubator and let sit.
22. Wait and observe the growth or death

Data

Analysis

Well 1 through 10 had roughly the same growth curve with linear movement from 25 minutes to 103 minutes. It plateaus starting at 103 minutes. Well 11 had a slow growth and the curve plateaued out just under 0.4 OD600. Well 12 also had a slow growth and the curve is concave down parabola shape that peaks at 0.37 OD600. Well 11 and 12 were our outliers because it did not fit into our expected curve.

Knockout Yeast Ethanol Stress Experiment

Introduction

Our class had some success with knocking out certain yeast genes. We take these genes, add the ethanol solution to a culture of said knockout genes and see how the yeast without those genes live or not.

Materials

• Corning COSTAR 96-well clear flat-bottom assay plate
• Wild-type yeast in 2x synthetic complete media at an OD600 of 0.1-0.2
• Ethanol concertation of 1M (labeled ETH01M)
• Sterile water

*BY-BY4735 (wild type)

• YJL133C-A yeast knockout strand
• YER186C yeast knockout strand
• YER076C yeast knockout strand
• YHR033W yeast knockout strand
• YCR095C yeast knockout strand

Procedure

1. Turn on biological safety cabinet
2. Steralize your hands and any other materials you need in the biological safety cabinet
3. Complete steps 4-13 in the biological safety cabinet
4. Make/find your ethanol solution, add 942µl of water and 58µl of neat ethanol in a 1.7ml PCR tube
5. Collect well a clear flat-bottom assay plate
6. Vortex yeast culture for about 5 seconds before adding to the wells
7. Add 50 µl of wild yeast culture and 50 ul of ethanol solution into well 1
8. Add 50 µl of knockout strain yeast culture and 50 ul of ethanol solution #1 into well 2
9. Add 50 µl of knockout strain yeast culture and 50 ul of ethanol solution #2 into well 3
10. Add 50 µl of knockout strain yeast culture and 50 ul of ethanol solution #3 into well 4
11. Add 50 µl of knockout strain yeast culture and 50 ul of ethanol solution #4 into well 5
12. Add 50 µl of knockout strain yeast culture and 50 ul of ethanol solution #5 into well 6
13. Put your well clear flat-bottom assay plate into the incubator and let sit
14. Wait and observe the growth

Data

Analysis

-Well 1 with the wild type had a steady growth throughout the experiment. Doubling time is 71.76

-Well 2 line lies on the middle of the overall growth curve.

-Well 3 is our outlier. We believe that this knockout strand had a slower growth because the missing gene affect that growth of the cell. We think Ethanol did not cause the large decrease in growth that we observed.

-Well 4 had the largest cell growth. -Well 5 is slightly above well 2 but has a similar curve. -Well 6 cell growth started off at a higher growth rate but decreased at an earlier rate.