1. Explain how bacterial cloning can help increasing the amount of DNA (DNA amplification) and when it is implemented in science or in medicine. Use a diagram if needed.
Bacterial cloning uses Plasmids and other vectors ( autonomously self-replicating DNA molecules ) in which foreign gene ( or exogenous DNA) can be inserted. Restriction endonucleases enzyme cleaves plasmid DNA at specific sites, creating sticky ends. This is where foreign DNA fragments that need to be cloned are inserted. DNA ligase enzyme joins the ends of the DNA fragment to the ends of plasmid DNA. These recombinant plasmids are introduced into the E.coli cells. Then, the E.coli cells are cultured and grown. In the E.coli cells, the recombinant plasmids replicate autonomously. Also, when the bacterial chromosomes replicate creating daughter cells each of them contains at least one recombinant plasmid. Thus, colonies of E.coli cells are formed where the foreign gene has amplified.
1. Explain how bacterial cloning can help increasing the amount of DNA (DNA amplification) and when...
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.
1. Descri be the process of a bacterial transformation. Explain how scientists can make bacteria take up DNA in a laboratory setting. (15 pts.) 2. Genetic transformations are not limited to bacteria. There are real-world applications where scientists have taken genes from one organism and inserted them into another organism. Give an example of how a genetically modified organism (can be any organ- ism, you are not limited to bacteria) have been used to solve real-world issues. Describe the organisms...
How can increasing the amount of competition (by encouraging more firms to enter an industry) aid innovation? How can increasing competition hinder innovation? Explain via a diagram.
1. Molecular cloning has made it possible to take a DNA fragment from nuclear DNA, containing an entire gene, and insert it into a cloning plasmid just behind a phage promoter. This means that the cloned gene can be transcribed in a test tube using a commercially available phage RNA polymerase protein. If you were to use agarose gel electrophoresis to separate RNA according to size, would the RNA produced in the test tube show any differences with RNA from...
You are interested in cloning a gene from the B. sanfranciscus genome, so you design PCR primers that should amplify a 1 kilobase pair (kbp) PCR product that contains the gene of interest. After amplification, you will see if the PCR was successful by loading the entire reaction onto an agarose gel and performing electrophoresis to see if a product of the expected size was generated. To visualize the DNA, you will stain the gel with a fluorescent dye called ethidium bromide, which...
Explain how comparing DNA fingerprints can help identify a person who has comitted a crime?
1. Explain how the plate count method can be an understatement for bacterial abundance and an overestimate for fungal abundance in the soil. 2. From an ecological standpoint, what can be shown from the buried slide technique that can not be shown by the plate count technique?
Scientists can use mutations in DNA sequences to help estimate the amount of time two species have been independently evolving, e.g., it serves as a "molecular clock". In the activity you studied how this works using numbers and types of mutations for DNA sequences of several related organisms, and saw how this information could help position them along a timeline for the lineage. Which of the below shows the correct position of these DNA sequences? (images for the answers to...
EXPLAIN each answer thoroughly. There are two common goals when using PCR to amplify DNA. A. Make lots of copies of a specific DNA sequence to use in cloning (preparative PCR) B. Detect the presence or relative amount of a specific gene under varying conditions (analytical PCR) *Remember: PCR is very similiar to DNA replication, but uses a DNA polymerase to amplify only specific parts of DNA sequence based on the sequence of the primers. 3. For which goal (A...
Now. you should be able to answer the following questions: • How the amplification will be done? - How you will determine your target sequence? How the amplification will be specific for certain segment? What are the requirements to carry PCR? • Suppose you perform a PCR that begins with one double-strand of the following DNA template: +5'-CTACCTGCGGGTTGACTGCTACCTTCCCGGGATGCCCAAAATTCTCGAG-3+ +3'-GATGGACGCCCAACTGACGATGGAAGGGCCCTACGGGTTTTAAGAGCTC-5'+ A. Draw one cycle of PCR reaction below the following diagram. B. Label the template DNA, the primers, and what is...