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In the PCR, high temperatures are used in order to separate both strands of DNA readily. Normal DNA polymerases would "melt" (denature) under these conditions, whereas Taq DNA Polymerase does not (short from Thermus aquaticus, a bacteria that lives in very hot submarine springs).
At high temperatures, DNA denatures into single strands. A temperature around 95 degrees should work.
DNA is copied.
This is the phase in which DNA is replicated.
The Taq name is a shortened for Thermophilus aquaticus, a thermophilic bacteria that is the source of the particular DNA polymerase enzyme. The enzyme heat resistant property is desired because it could withstand the high temperature during the PCR process. -Kaitlin The Taq name is a shortened for Thermophilus aquaticus, a thermophilic bacteria that is the source of the particular DNA polymerase enzyme. The enzyme heat resistant property is desired because it could withstand the high temperature during the PCR process. -Kaitlin
This is because of Polymerase Chain Reaction (PCR). Basically, the problem is that you have a mixture of DNA, polymerase, primers etc, and you want to denature the DNA (separate both chains) - the denaturation happens at 94°C. Since the polymerase is present in the mixture, it has to withstand such temperature.
hydrogen bonds
Mammalian polymerase is heat labile. Which means, it denatures (or breaks up into fragments) at higher temperatures. Since PCR is a reaction what requires a high temperature for the DNA strands to denature, it would be more efficient to use a polymerase that could function at higher temperatures.
How is it that some bacteria live in the hot springs of Yellowstone Park at temperature up as high as 73 C? Extreme thermophiles have adapted unique ways to surviving harsh conditions. They're enzymes are specially designed to resist denaturing at high temperatures. What's really amazing is their DNA. Extremophile DNA is positively supercoiled (this describes the way it is twisted around itself) which makes it harder to separate the strands. DNA in most other species is negatively supercoiled (meaning it's wound up on itself in the opposite direction as positively supercoiled DNA). Since DNA is the building block of life, it makes sense that you need to be able to protect it from the environment. Extremophiles do just that by positively supercoiling it. It is much more resistant to heat denaturing than other DNA would be, which helps the bacteria to survive.
because they are more durable in high temperatures. Increasing the temperature is a way to increase the enzyme's production rate. Normally, a protein will denature at high temperatures. This way you can have the best of both worlds.
Heat denatures protein. DNA polymerase is an enzyme and a protein.
Heat anneals DNA strand i.e. separate two strands of DNA to build anti-codon to desired DNA strand
In the PCR, high temperatures are used in order to separate both strands of DNA readily. Normal DNA polymerases would "melt" (denature) under these conditions, whereas Taq DNA Polymerase does not (short from Thermus aquaticus, a bacteria that lives in very hot submarine springs).
DNA can determine if a person will have a heat attack to if you will be good at snowboarding
At high temperatures, DNA denatures into single strands. A temperature around 95 degrees should work.
During the S stage DNA synthesis occurs. (copying of the DNA)
what happen when dna letters are changed