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Are these right?--won't take long..Moderator: BioTeam
4 posts • Page 1 of 1
Are these right?--won't take long..Had an exam yesterday and would just like to know if I am right in a few MCQs...I have just written out the ones I chose:
affinity chromatography is a purification technique that: separates proteins according to size explots an unique property of a protein separates proteins according to their hydrophilicity involves ion-exchange chromatography results in protein samples that are denatured cellulose acetate electrophoresis indicates that albumin: is -vely charged is +vely charged is a minor component of serum is a basic protein has a PI close to the ph of the electrophoresis buffer the rate of enzyme catalyzed rxns is usually determined by measuring the initial rate of rxns because: only the initial rate is simply related to the initial substrate concentration enzyme rxns are always fast at equlibrium the absorption of light will continue to increase otherwise the light absorption will go off the scale the initial rate is always the slowest Papain incubated with EDTA: Activates enzyme activity by binding divalent metal cationshave no effect on enzyme activty activate enzyme activty by modifying the casein substrate inhibit enzyme activty by binding divalent metal cations inhibit enzyme activty by binding divalent metal cations When acid is added to the rxn: ethanol + Nad+ <--> acetaldehyde + NADH + H+ the following is expected to happen: Increases the conc. of NADH interaction between cibacron blue and albumin is considered: Hydrophobic when the liver enzyme alcohol dehydrogenase oxidizes ethanol an increase in the absorbance of the solution occurs at 340nm. This is because: NADH is produced during the rxn In the lab where the enzyme papain is investigated, it was preincubated prior to assay to: ensure that the reactive site cysteine was in the reduced form I know there is heaps of q's but any1 that can tell me if they are wrong/right will be great...I just wanna make sure I have got the marks for these so having the ans. to this post will be MOST appreciated!! Thanks you to whoever answers!! b_06er
haha i wish i had a good memory then I would do better on exams!...we actually get to take the paper home
Re: Are these right?--won't take long..
The correct answer is "explots an unique property of a protein". The technique used to separate according to size is gel filtration chromatography.
EDTA binds metal ions through amine and carboxyl groups. However, i don't think papain has metal prosthetic groups. You can look that up and you will have your answer.
My guess is it would increase the rate of the backwards reaction, as the added H+ will increase the concentration of products. Don't know the answers to the others, or i consider your answers correct. Cheers. "I have no intention of stopping anytime soon. I want to understand the universe and answer the big questions, that is what keeps me going" - Stephen Hawking
4 posts • Page 1 of 1
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