Enzyme core practical Flashcards

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1
Q

what is the independent variable

A

Enzyme concentration (trypsin)

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2
Q

how do you vary the independent variable

A

Have 0.5%, 0.4%, 0.3% and 0.2% of trypsin

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3
Q

what is used as a control

A

distilled water in cuvette that you put in the colorimeter between each enzyme concentration

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4
Q

how do you measure the dependent variable

A

use a colorimeter calibrated to 440nm wavelength

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5
Q

what are the procedural variables and how are they controlled

A

volume of trypsin and milk used that were mixed together (2cm3 of each into cuvette)- control this by using a graduated pipette#

time between measurements- use a stopwatch to time 10 seconds between each transmission

wavelength of colorimeter- set it to 440nm

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6
Q

what are the environmental variables and how should they be controlled

A

age of milk - make sure milk is in date and has been stored correctly

temperature of trypsin and milk used in experiment- use a water bath set at 37 degrees to control temperature

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7
Q

what are the organism variables and how are they controlled

A

if an organism is used as source of enzyme then the age and mass of enzyme should be considered as a control

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8
Q

what repeats should be carried out

A

repeat practical 5 times for each concentration of trypsin used
calculate the mean average of results for an enzyme concentration to get one figure

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9
Q

how is this investigation made reliable

A

use the same volumes of solution in cuvette of milk and trypsin (2cm3 of each) measured by a graduated pipette

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10
Q

how is this investigation made valid

A

make sure you can get the same results if you were to attempt again
using the most accurate equipment to measure volumes of trypsin and milk (graduated pipette

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11
Q

conclusion that would be drawn from the results

A

as the enzyme concentration increases so does the rate of reaction
higher enzyme concentration mean there are more frequent collisions happening between the enzyme and the substrate meaning E-S complexes
if the enzyme concentration is too high then the reaction plateaus since the substrate becomes the limiting factor.

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