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How Lipase(enzyme) can be affected with Substrate Concentration


Markee

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Keel, you know when you mentioned Amylase? And that it breaks down starch with iodine solution. Then that would mean, I would not use a lipid(butter) as my substrate concentration?

Well, if you use a different enzyme you obviously use a different substrate. Every enzyme's function is different.

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No..no..no..no..no XD

Independent Variable – Potato (you have to CONCENTRATION of X)

Dependent Variable – Activity of the Enzyme’s Reaction.

Controlled VariableS – Time, Amount of enzyme added, Amount of buffer solution, Temperature, Interval between testing..etc..etc anything you can think of.

-Concentration of Butter (Butter has got nothing to do with this! It's fat)

Basically : How can does Substrate Concentration affect the activity of Amylase?

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RQ: How does the change in concentration of starch affect the activity of amylase?

Independent Variable: Concentration of Starch - varied from xg per dm3 to yg per dm3

Dependent Variable: Time taken for solution to turn Benedict's solution from blue to brick red, OR time taken for solution to turn iodine solution black to red.

Control Variables: Concentration and Volume of Amylase, Volume of Starch, Temperature (room), pH of solution (buffer), Concentration and Volume of Inhibitors (0 g per dm3), Concentration and Volume of heavy metals (0 g per dm3), volume of Benedict's solution/iodine solution.

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"Time before testings"? How does that work?

So basically with this experiment, I would be using a Potato and the amylase+iodine solution mix em up whilst timing how long does it take for the color to change which should indicate the reaction is taking and has taken place?

(This thread will not reach 10 pages! XD )

Edited by Mark10B
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Errrmm...didn't really get that, but:

Why are you using potatoes? Just use starch solution! You are changing concentration, how are you going to change concentration of starch with potatoes?

Use starch solution and make 4 or 5 different concentrations.

As for testing:

I forgot what a thing is called so here's the apparatus you must have:

investigating-the-effect-of-ph-on-amylase-activity-170.jpg

The red in the tiles are drops of iodine solution, you are going to have tubes with the solution, buffer and enzyme. Every 30 seconds or so you are going to take two drops using the dropping pipette and drop it on to one tile. When it stops changing color..all the starch is digested.

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Lol, no..you are going to change the concentration of starch solution, not iodine.

Here it is:

TUBE 1: 100% starch + buffer solution + amylase.

TUBE 2: 75% starch + buffer solution + amylase.

etc

etc

etc.

You are going to do one tube at a time..take a sample every 30 seconds and drop it onto a dimple, keep doing that until the color stops changing.

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