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When an enzyme is frozen, it only slows down activity. Unlike boiling an enzyme, it does not stop it from working.
Destroying the active site of an enzyme would no longer allow a substrate to bind to it, therefore stopping the enzyme from working.
yes, enzymes can be inhibited by other enzymes.
extremely high temperatures can decrease the rate of enzyme action very quickly ,the enzyme becomes deactivated (enzyme does not work)
1. Some solvents 2. Temperature changes (when exposed to high temperatures, the protein will denature, rendering it inactive)
It is to neutralize the solution and to stop the hydrolysis.
This serves two functions; first, it stops the enzyme-catalyzed reaction by changing the pH to one unsuitable for the enzyme (the enzyme is denatured at high pH and so unable to function). Second, it deprotonates the p-nitrophenol to give the yellow colored p-nitrophenylate.
prohibitors are used to enzyme reaction
to freeze the reaction mixture, means to stop the further hydrolysis of ethyl acetate so that our readings couldn't interrupt.
When an enzyme is frozen, it only slows down activity. Unlike boiling an enzyme, it does not stop it from working.
When an enzyme is frozen, it only slows down activity. Unlike boiling an enzyme, it does not stop it from working.
Destroying the active site of an enzyme would no longer allow a substrate to bind to it, therefore stopping the enzyme from working.
stop speaking jiberish dumbo
A change in pH can denature an enzyme, meaning the reaction would stop.
If an enzyme in a sequence of enzyme-controlled reactions is missing or defective then the process will stop at that point. So respiration could proceed until it reached the reaction which needed the missing or defective enzyme at which point it would stop.
If an enzyme in a sequence of enzyme-controlled reactions is missing or defective then the process will stop at that point. So respiration could proceed until it reached the reaction which needed the missing or defective enzyme at which point it would stop.
H2SO4 is used to denature the enzyme and stop the reaction instantly. by adding H2SO4,it will prevent further reaction of the enzyme onto the substrate and the rate of enzyme reaction can be measured in the specific time