bestkeptsecret
New Member
OMG i left out the substrate haha whoops
meh oh well its over now
only religion left
meh oh well its over now
only religion left
Thats how i interpreted it too.Shuter said:Wait, didn't it say you can only measure it in ONE of the environments. I thought this meant that you had to have it at a pH of 7 and a temperature of between 50-55 degrees in order for you to effectively test both in the one environment.
What I wrote, even if I interpreted it wrong I shoulg get at least 6:~*HSC 4 life*~ said:it was a gay qu because it was woth 8 marks...i dont think i put as much content needed for 8 marks but meh, totally guessed it. i did temperature...but only 4 testtubes...whats with some of you guys doing 20 testtbes? yeah test tube plus enzyme plus substrate. 2 had enzyme x and two with enzyme e...then heat one to about 35 deg and one to about 55 bullshitted about seeing how enzymes work best at omptimum temp range etc
withoutaface said:What I wrote, even if I interpreted it wrong I shoulg get at least 6:
- 3 test tubes, one containing enzyme x, one with enzyme e and one control, all at 37'C, ph 8.5
- leave them for 10 minutes, then measure the bubbles produced by each with a ruler
- repeat several times
- test tubes should be same size, shape, materials etc, same volume and conc of substrate, same amount of each bacteria.
- stoppers should be put on test tubes as soon as bacteria are added to avoid them escaping, petri dishes and test tubes should be incinerated afterwards to avoid infection