Enzyme Lab

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Pages: 6

Introduction:
Enzymes are a type of protein that initiate and assist every chemical reaction that occurs. Enzymes have the ability to do this with help from a few things. Increasing the temperature helps increase reaction rates however if you go past the optimum temperature it denaturizes the enzyme and the reaction rate decreases. PH can also have an effect on enzymes go past the optimum pH and it can disrupt the enzyme function in the interactions between excess hydrogen or hydroxide ions and amino acid side chains which also causes the reaction rate to decrease. An increase in substrate can increase the amount of enzymes which in turn can increase the reaction rate. This can also be seen if you increase the amount of enzymes the amount
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A piece of tape has ‘tube #4’ written on it, it was then placed on an empty tube. The liquids were converted from ml to μl. Guaiacol was converted from 0.1 ml to 100 μl and was extracted using a 200 μl pipette that was adjusted to 100 μl. Guaiacol was then placed in tube #4. The tip from the 200 μl was disposed of and a new one was placed on it. H202 was converted from 0.2 ml to 200 μl which was also extracted by the 200 μl pipette. H202 was also placed in tube #4. The tip from the 200 μl was disposed of and a new one was placed on it. DH20 was not converted from its 4.7 ml. DH20 was extracted by the 5 ml pipette and then placed in tube #4. Another piece of tape has ‘tube #5’ written on it, it was then placed on an empty tube. Turnip extract was converted from 1.0 ml to 1000 μl. Turnip extract was extracted by the 1000 μl pipette and was then placed in tube #5. The tip on the 1000 μl was disposed of and a new was placed on it. DH20 wasn’t converted from 4.0 ml and was extracted by the 5.0 ml pipette. DH20 was then placed in tube #5. Tube #4 and tube #5 are both placed in water that is heated at 72°c for five minutes. Each person in each group was assigned as a mixer, a reader, a timer and a data recorder. A timer was started and tube #4 was poured into tube #5 then this solution was poured into a cuvette to the line on it and then placed in the spectrophotometer and the first recording for this experiment is taken when the timer hit 20 seconds. For the next 10 minutes every 20 seconds the absorbance is recorded in table