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What did you write for this question...How could you modify the experiment to find out the activity of enzymes at different temperatures?xtremeforums: looking at mark schemes, they normally provide a range of values which are acceptable. However, if they required a very accurate answer, yours would be correct.
prepare 4 water baths ( 20, 40,60,80) using cold water ,hot water and a thermometer. Label four large test tubes accordinlgy and put 10 seeds of the same size in each test tube. and add to them 3 cc of sucrose solution. leave in the approriate water bath for 20 mins.. then extract 2cc of each solution and add to it 2cc of Benedicts. put in a boiling water bath and observe the first color change.... the least time taken for the color to change would mean the highest enzyme activity ( which would probably be at 40 degrees)What did you write for this question...How could you modify the experiment to find out the activity of enzymes at different temperatures?
me too, and at the end i wrote, plot a graph of time taken for initial colour change against temp..prepare 4 water baths ( 20, 40,60,80) using cold water ,hot water and a thermometer. Label four large test tubes accordinlgy and put 10 seeds of the same size in each test tube. and add to them 3 cc of sucrose solution. leave in the approriate water bath for 20 mins.. then extract 2cc of each solution and add to it 2cc of Benedicts. put in a boiling water bath and observe the first color change.... the least time taken for the color to change would mean the highest enzyme activity ( which would probably be at 40 degrees)
i wrote smth like that
everything else was easy, el7 so i guess we r done...What other questions are there left to discuss?
InshAllah!everything else was easy, el7 so i guess we r done...
good luck with p1 inshallah it'll be a good one
ThanksInshAllah!
Good luck to you too.
same here but i haven't rlly killed the book as many times as u mashallahUmm, let's see:
Benedict's solution was supposed to be kept anywhere between 80 and 100 degrees (anything written in between would be acceptable)
You're supposed to take 2 cm3 from each solution and 2cm3 (or more) from benedict's
Table:
Headings: concentrations of R, volume of solution, volume of water
0.4---10---0.0
0.3---7.5---2.5
0.2---5.0---5.0
o.1---2.5---7.5
0.0---0.0---10
Describing trend of change in pH for leaves: sharply increases until pH of 5.3 then sharply decreases (although decrease is less steep than increase)
Explaining trend in activity between pH between 5.3 and 6.4: the relatively higher concentrations of OH- ions could interact with the protein structure (by forming hydrogen bonds with the polypeptides) and denature the enzymes. So activity decreases.
And I think that's all. Good luck to everyone on paper 1 this Monday. How are you guys preparing? I've killed the book already (more than 10 times) studying for paper 2, and right now I'm solving all past papers from 2007 - 2012, starting from the most recent. I'll try to be on the paper 1 thread as much as possible
me! but i joined the points by lines, i did not make a curve!On the x axis, pH... And on the y axis, Activity of enzyme...
and we were suppose to make two line graphs, and label each one clearly, eg. leaves or bark.
Did anyone else do this?
yah u were supposed to join them by straight lines...me! but i joined the points by lines, i did not make a curve!
Great!yah u were supposed to join them by straight lines...
and no extrapolation.
That depends on whether u have ur concepts clear or not...same here but i haven't rlly killed the book as many times as u mashallah
what abt the older years ( 2002-2006) are u gonna solve them??
and do u think its important that we finish the syllabus for p1 or do u think pps are enough??
ok,, thanks for the adviceThe syllabus changed completely at 2007, so they're getting different questions starting May/June '07.
I'd recommend doing both past papers and studying the syllabus. If you don't have time to do both, then I would prefer if you study the syllabus rather than solving past papers. If you really have no time for that, then you'll have to read notes. Then just solve one or two past papers just so you could know what they could type of questions they could throw at you. Good luck
yup, exactly =)
exactly what I wroteCalibration:
Every unit on the stage micrometer was 0.01 mm
The stage micrometer was 4 units long on the eyepiece graticule
So you're supposed to divide 0.1 mm by 4 to get 0.0025 mm
Also, you're supposed to convert it to a more suitable unit by multiplying 0.0025 mm by 1000 to get 2.5 micrometres.
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