When an enzyme is denatured the active site which allows it to catalyze reactions is destroyed, rendering the enzyme useless. This process is irreversible but the remains are recycled to form new enzymes.
Answer:
The shape of an enzyme determines which reaction it can catalyze.
Explanation:
Each enzyme is specific to one type of reaction. According to the structure of each enzyme, it has an active site capable of binding to a specific substrate, so the shape of the enzyme determines the type of reaction to be catalyzed.
Once the reaction occurs, the enzyme releases the product of the reaction and the enzyme is available for another reaction.
Regarding the other options:
- <em>The shape of an enzyme no depends on the reaction that it needs to catalyze.
</em>
- <em>Due to their specificity, enzymes can only catalyze one reaction at a time</em>
- <em>The shape of the enzyme is not altered after the reaction.</em>
Answer:
i would say they were skeptical
Explanation:
nobody really knows how test are going to work out, no one knows how intelligent marine life is at first. Im sure a lot of scientist doubted the idea of them being therapy animals
Answer:
Enzymes work best within specific temperature and pH ranges, and sub-optimal conditions can cause an enzyme to lose its ability to bind to a substrate. Temperature: Raising temperature generally speeds up a reaction, and lowering temperature slows down a reaction.
Explanation:
The process of fusing two or more DNA molecules to produce a hybrid is known as recombinant DNA. Restrictions endonucleases and ligases are two classes of enzymes that enable the technique.
When a restriction endonuclease detects a particular DNA sequence, it makes cuts inside or near that sequence. The recognition sequence of a restriction enzyme will haphazardly appear on every (1–4)n bases along a random DNA chain. The equation states how many fragments ends (measured in moles) are produced when a restriction enzyme cuts DNA.
Moles of DNA ends =2x(grams of DNA)/(number of bp)(660 g/mol / bp).
The equation describes how many ends are produced when circular DNA is digested by a restriction enzyme.
Mole ends=2x(moles DNA)x number of restriction sites.
The following equation can be used to determine how many ends are produced during the digestion of a linear molecule by a restriction endonuclease.
Mole ends=2x(molesDNA)number of restriction sites +[2x(moles of DNA)].
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