Lipase investigation.

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Lipase investigation

I am going to use five different kinds of milk as I think that this is a suitable number to give me a varied amount of fat concentrations. My different milks are:

They will be kept at room temperature 22°C and the enzyme concentration level will stay the same.

Safety:

As with all experiments there will be an element of danger, to avoid this I will do the following:

-Wear goggles

-Wear a lab coat

-Walk and not run

-Make sure all things loose are kept away e.g. Tie and

-General common sense throughout the experiment

Equipment:

-Range of five different milks

-Boiling tubes

-Boiling tube rack

-5% Lipase solution

-Sodium carbonate solution

-Phenolphthalein

-Stirring rod

Method:

I will set up a boiling tube rack with five boiling tubes each contain a different type of milk. Then I will add 7mls of sodium carbonate solution and 5 drops of phenolpharium. I will stir with my stirring rod and when I add The 1ml of lipase solution I will start timing Then I will wait until the solution has turned from pink to white and record the results. I will repeat the experiment three times. The solution will turn white because when the lipase and fat get in  they produce fatty acids and glycerol, sodium carbonate makes the solution alkaline (pink) to start with but as more acids are produced the pH drops and the solution turns white.

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Prediction:

Enzymes are biological catalysts, they speed up the chemical reactions that happen in living things. Enzymes carry out their  at an extremely efficient rate. Enzymes are formed inside cells and after they are formed they leave their cells to carry out their  outside. Enzymes that act on lipids are called lipases.

The picture below shows simply how enzymes work. Molecules are continuously  around and therefore they bump into each other. When a substrate molecule bumps into the corresponding enzyme, it fits neatly into a  on the enzyme, this is called the active site. The reaction takes place here and ...

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