Question

The polymerase chain reaction was originally designed/run using the polymerase from E. coli. What type of organisms gave rise

0 0
Add a comment Improve this question Transcribed image text
Answer #1

Thermophiles

Thermophiles are organisms that survive and grow at high temperatures ranging between 41oC and 122oC. These bacteria are tolerant to temperature and are evolved such that they can perform their metabolic processes normally at elevated temperatures.

The polymerase chain reaction is used for the purpose of amplification of DNA. IN PCR, a small amount of DNA can be amplified and billion copies of that DNA can be obtained. The procedure involved the steps of denaturation of the DNA strand, annealing of the PCR primers to the DNA strands and extension of the primer. For the extention of the primer, a DNA polymerase is required which extends the primer to produce the new DNA strand. The extension step is carried out at a tempertaure of 72oC. At this temperature, most of the proteins get denatured and loose their activity. The polymerase from E.coli was used for extension step primarily but there was a need for a polymerase which remains stable and active at tempertaure of 72oC.

Therefore, the DNA polymerase was derived from the thermophilic bacteria Thermus aquaticus and was called as Taq polymerase. Taq polymerase is active at 72oC and has been employed extensively for PCR procedures.

Add a comment
Know the answer?
Add Answer to:
The polymerase chain reaction was originally designed/run using the polymerase from E. coli. What type of...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Polymerase Chain Reaction (PCR) uses a special heat-stable DNA polymerase (Taq polymerase) that is slightly less...

    Polymerase Chain Reaction (PCR) uses a special heat-stable DNA polymerase (Taq polymerase) that is slightly less accurate than DNA polymerase (Pol I) purified from E. coli. Taq polymerase will therefore introduce wrong bases into a growing DNA chain more frequently than will Pol I. In which one or more of the following applications of PCR will this type of inaccuracy be a problem? Explain why. Detection of bacterial DNA in infected tissues from patients. Detection of viral RNA in infected...

  • Carolina Savirana Craz 3/12/20 GECC-Polymerase Chain Reaction 1. What is the purpose of the polymerase chain...

    Carolina Savirana Craz 3/12/20 GECC-Polymerase Chain Reaction 1. What is the purpose of the polymerase chain reaction? a. To repair damaged DNA b. To make copies of entire chromosomes c. To make copies of specific regions of DNA d. To prepare cells for cell division 2. The polymerase chain reaction is most comparable to what cellular process? a. Mitosis b. Replication c. Transcription d. Translation 3. When enzymes are elongating (building) a newly synthesized DNA strand in PCR, new nucleotides...

  • 1) What does PCR stand for and what does it do? a. Polymerase Chain Reaction; PCR...

    1) What does PCR stand for and what does it do? a. Polymerase Chain Reaction; PCR deletes DNA b. Polymerase Copying Repeats; PCR amplifies DNA c. Polymerase Copying Releats; PCR deletes DNA d. Polymerase Chain Reaction; PCR amplifies DNA 2) During gel electrophoresis, the DNA fragments are separated by ____ a. charge b. DNA fragments cannot be separated c. color d. size 3) Primers are a. double stranded DNA oligonucleotide (fragment) b. double stranded RNA oligonucleotide (fragment) c. single stranded...

  • Explain the polymerase chain reaction and include all starting materials required, what happens in each cycle,...

    Explain the polymerase chain reaction and include all starting materials required, what happens in each cycle, and how a scientific investigation might benefit from PCR.

  • Which is not one of the elements needed to amplify DNA by polymerase chain reaction (PCR)?...

    Which is not one of the elements needed to amplify DNA by polymerase chain reaction (PCR)? Question 16 options: A) Nucleoside triphosphates that serve as the source of the nucleotides A, T, C, and G needed in the synthesis of the new strands of DNA B) A restriction endonuclease enzyme that cleaves DNA at specific locations C) The segment of DNA that must be copied D) A DNA polymerase enzyme that will catalyze the synthesis of a complementary strand of...

  • A plasmid used as a cloning vector in E. coli must have… Does sequence similarity between...

    A plasmid used as a cloning vector in E. coli must have… Does sequence similarity between genes play an important role in assigning gene function? Successful insertion of a DNA fragment into the multi-cloning region (restriction sites) of a recombinant plasmid is detected by what changes? Understand the concept of (restriction enzyme produced) DNA fragment separation by gel electrophoresis. In addition to restriction enzymes, which enzyme(s) are required to insert a fragment of DNA into a cloning vector? What is...

  • Which of the following is the correct order of events in the polymerase chain reaction (PCR)?...

    Which of the following is the correct order of events in the polymerase chain reaction (PCR)? See Section 20.2 (Page 468) cooling to allow primers to attach; heating to separate double-stranded DNA; elongation of DNA strand as nucleotides are added elongation of the DNA strand as nucleotides are added; cooling to allow primers to attach; heating to separate double-stranded DNA heating to separate double-stranded DNA; cooling to allow primers to attach; elongation of DNA strand as nucleotides are added heating...

  • The gene machine program shows you what happens when lactose is present in E. coli, and...

    The gene machine program shows you what happens when lactose is present in E. coli, and how the lac operon is under negative control. However, the lac operon is also under positive control from a protein called CRP, eAMP Receptor Protein. The absence of the lac repressor is essential but not sufficient for effective transcription of the lac operon. RNA polymerase also depends on the presence of CRP. Like the lac repressor, which can bind to the DNA and lactose....

  • You are using PCR to amplify a 300 bp target sequence, a portion of Gene X,...

    You are using PCR to amplify a 300 bp target sequence, a portion of Gene X, from human genomic DNA isolated from patients' blood samples. The instructions for this procedure tell you to include Samples A and B, whose contents are listed below, with each batch of patient samples that you run. Ingredients Sample A Sample B 10x PCR Buffer (Tris,KCI,MgCl2,BSA) 5 mL 5 mL H2O 37.8mL 38.8mL dNTP's 3 mL 3 mL Taq DNA polymerase 0.2 mL 0.2 mL...

  • D. After you run your PCR reaction, what next steps would you perform to determine that...

    D. After you run your PCR reaction, what next steps would you perform to determine that the PCR amplified the region of interest? E. After your procedures in step D above, you decide to measure the concentration of DNA in your PCR product. Briefly explain how you would do this given the tools we have available. What values would you expect to confirm that you have a good DNA concentration and purity? F. Write and briefly describe a program you...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT