Question

dh5α is a “cloning strain.” It is used to grow up plasmids (extra-chromosomal DNA) you want...

dh5α is a “cloning strain.” It is used to grow up plasmids (extra-chromosomal DNA) you want to use for other experiments. Why would you use dh5α and not K12 for this? (Note: all cloning strains are Rec- for this reason)

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

DH5alpha is a strain that is preferred for cloning genes using plasmids. It is a modified strain obtained from K12 strain of E.coli. It is preferred over K12 strain because it lacks the restriction modification system. Restriction/modification systems are known to prevent propagation of plasmids in wild type strains such as K12. This system cleaves any foreign DNA entering the cell. DH5 alpha strain also lacks endonuclease activity that can cleave plasmid DNA sequences. This strain also has mutations that allow it to take up large plasmids. Thus, large gene sequences can be inserted and cloned in this strain as compared to K12 strain. DH5 alpha is a RecA- strain and therefore cannot carry out homologous recombination. Thus, it prevents integration of plasmid DNA into chromosomal DNA. K12 is a wild type strain of E.coli that has lost its ability to grow in intestine. Thus, it is capable or recombination due to RecA expression.

Add a comment
Know the answer?
Add Answer to:
dh5α is a “cloning strain.” It is used to grow up plasmids (extra-chromosomal DNA) you want...
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
  • Cloning / Subcloning When subcloning engineering new plasmids, by inserting new DNA fragments (inserts) me plasmids...

    Cloning / Subcloning When subcloning engineering new plasmids, by inserting new DNA fragments (inserts) me plasmids (now called a vector because it will carry your gene of interest) it is important to considering existing genes / DNA elements. If a site is in the middle of a gene, you could lose or destroy that gene. If there are multiple sites for an enzyme, when you paste them together, multiple possible outcomes can arise. This is undesirable, because it confounds verification...

  • You have isolated a strain of brewer's yeast (Saccharomyces cerevisiae) in the lab for your second...

    You have isolated a strain of brewer's yeast (Saccharomyces cerevisiae) in the lab for your second job at a hip new microbrew (you make a great IPA). You find that this strain ferments more efficiently and adds a superior flavour profile to your brews. You want to clone the strain of yeast and generate a genomic library to determine the genes responsible for this finding. To do so you: 1. Obtain fragments of the whole yeast genome (DNA) through restriction...

  • How is PCR used in DNA cloning? Can you provide some real life examples of PCR...

    How is PCR used in DNA cloning? Can you provide some real life examples of PCR cloning? Why/When do we use PCR over alternative cloning techniques.

  • The following set of three separate experiments was conducted. Two strains of Escherichia coli are used....

    The following set of three separate experiments was conducted. Two strains of Escherichia coli are used. Strain 1 needs histidine added to the medium to grow. Strain 2 needs methionine added to the medium to grow. Experiment 1: After strain 1 and strain 2 are mixed in a culture flask containing a minimal medium (containing no added amino acids) and allowed to grow overnight. Results: It is possible isolate new strains that grow on the minimal medium. Experiment 2: Strains...

  • 7. Explain the procedure for cloning DNA fragment into the plasmid PBR322 (shown on the right) (S...

    7. Explain the procedure for cloning DNA fragment into the plasmid PBR322 (shown on the right) (S pts.). The gene fragment of interest was obtained by digestion of chromosomal DNA with the restriction enzyme Sall and subsequent purification using agarose gel electrophoresis. Which antiblotic would you use in the final step of the cloning procedure, and Pst why? EcoR Sal Ampicillin Tetracycline resistanica(Ter Amp) PBR322 4,361 bp) Origin of replicatiorn (ori Pvull 8. Assume that your gene fragment from question...

  • Genetics Yeast Lab The Awesome Power of Yeast Genetics Pre-lab questions Two weeks ago, you received...

    Genetics Yeast Lab The Awesome Power of Yeast Genetics Pre-lab questions Two weeks ago, you received three unknown yeast strains. One was lys- (it cannot synthesize its own lysine) while the other two were LYS+. Because they were LYS+, they should be sensitive to high levels of aminoadipate (AA) before spontaneous and/or induced mutations occur that may allow some cells to become AA resistant. The two LYS+ strains differ in the rate at which they accumulate mutations. Two weeks ago,...

  • Cloning 2 Below is the restriction map of a 10 kb piece of DNA. Also shown...

    Cloning 2 Below is the restriction map of a 10 kb piece of DNA. Also shown below is a cloning vector which has two unique restriction enzyme recognition sites, one for EcoRI (E) and one for HindIII (H). The location of the kanamycin (kan) and ampicillin (amp) resistance genes is also shown. Kanamycin and ampicillin are antibiotics that are commonly used to select transformed E. colicells (consult the Lab Manual for more information). Note that the HindIII site is located...

  • You have cut genomic DNA with AvrII and wish to ligate it into pBluescript. However, there...

    You have cut genomic DNA with AvrII and wish to ligate it into pBluescript. However, there is no AvrII site in the multiple cloning region of this plasmid. What other restriction enzyme could you use to cut the plasmid’s multiple cloning region that would produce compatible ends for ligation with your genomic DNA? (Hint: Look up the Compatible Cohesive Ends chart at New England Biolabs website and confer with pBluescript map) (1 point)

  • Hi, I like to make sure I am staying on track with the thought process and...

    Hi, I like to make sure I am staying on track with the thought process and was curious if anyone can help with A-D. Thank you so much for the help! 7. (12 pts) You have two Hfr strains of E. coli that carry the F plasmid integrated at different places in the chromosome. During conjugation, strain HfrA transfers the leucine biosynthetic operon only after the rest of the E. coli chromosome has been transferred. During conjugation, strain HfrB transfers...

  • You are a scientist studying DNA replication. You have the ability to introduce temperature-sensitive mutations into...

    You are a scientist studying DNA replication. You have the ability to introduce temperature-sensitive mutations into the bacteria that you are studying (temperature-sensitive mutations work normally at one temperature, but when you raise the temperature a little, the mutation exerts its effect. This allows you to grow colonies with mutations that would otherwise be lethal. The fact that these mutations are temperature sensitive has nothing to do with the problem, other than to make it accurate to how these would...

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
ADVERTISEMENT