UW-Stout/Hydrogen Peroxide SP22

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Revision as of 18:59, 4 May 2022 by Teagueb (talk | contribs) (Calibration Trial 1 Percent Series: 3%, 1%, 0.3%, 0.1%, 0.03%, 0.01%)
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Introduction

Hydrogen Peroxide (H2O2) is a very strong oxidizer and antiseptic that is often used in dilute forms. The overall compound is found in biological systems but is in short lived reactions due to it's high toxicity over time. The goal of our experiment was to test how multiple yeast strains with knockout genes would respond in the presence of varying concentrations of hydrogen peroxide.


Materials

  • Hydrogen Peroxide Solution 3% Concentration
  • Distilled water for dilutions
  • Wild Type and Knockout Yeast Strains


Equipment

  • P-200 Micropipette
  • P-20 Micropipette
  • P-10 Micropipette
  • Centrifuge Tubes
  • Yeast Test Well

Calibration Protocol

H2O2 Dilutions

  1. Vortex Yeast Strains
  2. Create 50ul Hydrogen Peroxide dilutions as required
  3. Mix dilutions With 50ul yeast cultures
  4. Put in individual wells to grow For 24 hours

Calibration Trial 1 Percent Series: 3%, 1%, 0.3%, 0.1%, 0.03%, 0.01%

revise1trial.png

Calibration Trial 2 Percent Series: 3%, 2%, 1.33%, 0.88%, 0.59%, 0.40%

2 2trial.jpg


Interpretation

Based on both calibration experiments, we determined that the concentration of hydrogen peroxide tested on the yeast would need to be much lower if we wanted to see consistent amounts of inhibition and compare them. The higher concentrations in calibration 2 yielded data was too close among the wells, so based on calibration 1 we settled on a dilution of 0.065%, as the range of 0.03% to 0.1% seemed to show the most observable differences in data.

Knockout Protocol

Procedure

  1. Vortex Yeast Strains
  2. Create 50ul Hydrogen Peroxide dilutions as required
  3. Mix dilutions With 50ul yeast cultures
  4. Put in individual wells to grow For 24 hours
  5. Place standard controls in each well to growth for 24 hours as comparison
  6. Plot growth data.