Biology
Biology
5th Edition
ISBN: 9781260487947
Author: BROOKER
Publisher: MCG
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Chapter 11, Problem 6TY

Meselson and Stahl were able to demonstrate semiconservative replication in E. coli by

  1. a. using radioactive isotopes of phosphorus to label the original strand and visually determining the relationship of original and new DNA strands.
  2. b. using different enzymes to eliminate old strands from DNA.
  3. c. using isotopes of nitrogen to label the DNA and determining the relationship of original and new DNA strands by density differences of the new DNA molecules.
  4. d. labeling viral DNA before it was incorporated into a bacterial cell and visually determining the location of the DNA after centrifugation.
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You are studying a colony of cells and determine that some of these cells have a mutated DNA polymerase I that results in loss of function of this enzyme. A)   What will the effect of the mutation in DNA polymerase I be on DNA replication? In your answer make sure to describe what would be observed in the leading and lagging strand and explain your reasoning.  B)   Will this mutation in DNA polymerase I have an impact on another step in DNA replication? In your answer make sure to indicate whether DNA replication will be impacted or not. If it is not, explain why. If it is impacted, then describe the step that is impacted and name the molecule or enzyme involved.
Which of the following statements BEST DESCRIBES the main findings of the Meselson-Stahl experiment?   A. DNA can be separated using centrifugation   B. The semiconservative model of DNA replication is more accurate than the dispersive or conservative models of DNA replication   C. Using 14N in experiments is an effective way of tracking nitrogen molecules   D. Bacteria grown in the presence of a heavier nitrogen isotope (15N) will replicate at a slower rate than those that utilise a lighter nitrogen isotope (14N)   E. Both strands of each new DNA double helix are brand new and synthesized from individual nucleotides
Which of the following best describes the process of DNA seqencing. a. DNA is seperated on a gel and the different bands are labled with flouroscent nucleotides and scanned with a laser. b. A laser is used to flurorescently label the nucleotides present with in the DNA , the DNA is run on a gel and then the DNA is droken into fragments  c. Nucleotides are scanned with a laser and incrprorated into the DNA that has been seperated on a gel and then DNA is amplified with PCR. d. fragments of DNA are produced in a reaction that lables them with any of four different fluroscent dyes and the fragmented then are run on a gel and scanned with laser e. DNA is broken down into its constituents nucleotides and the nucleotides are then run on a gel and purified with a laser
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