The organic catalyst breaks down due to the reduction taking place in the peroxide solution. The inorganic catalyst does not deform in the solution.
2007-03-05 14:29:57
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answer #1
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answered by bestguessing 3
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Enzymes are a subclass of proteins. So mess with substance "x" in a manner that selectively objectives proteins. there are a style of issues you're able to do to screw with proteins, however the main obtrusive is to deal including your substance with proteases (trypsin, chymotrypsin, pepsin, etc). Proteases are a subclass of enzymes which destroy down proteins via breaking peptide bonds. So, deal including your substance with a protease and spot if it may nonetheless catalyze the reaction. If substance "x" is an enzyme, it is going to now no longer paintings. Denaturation is, as you stated, yet another decision, yet i'm uncertain how inorganic catalysts would be laid low with denaturing brokers. One decision would be something that reduces disulfide bonds -- which i will no longer be able to think of would impact inorganic catalysts. some reagents for this incorporate DTT, performic acid, and TCEP. you additionally can use a detergent to denature, like SDS, yet I back do no longer understand if that could inhibit different catalysts. *There are some organic and organic catalysts referred to as ribozymes that are RNA quite than protein, yet you're in all possibility no longer coping with one here. If protease would not inhibit "x"s activity, then you definately would desire to handle "x" with RNase quite of protease. RNase breaks down RNA.
2016-12-14 09:54:32
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answer #2
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answered by vannostrand 4
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