DNA and Protein Synthesis Review

By Jessica Long,2014-06-01 16:42
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DNA and Protein Synthesis Review

    DNA and Protein Synthesis Review ANSWERS!!!

1. What are nucleotides? Describe their structure.

    They are the monomers (“building blocks”) of nucleic acid. They are made up of a 5-carbon sugar (ribose in RNA or deoxyribose in DNA), a phosphate, and a nitrogen base (A, C, G, T [DNA] or U [RNA]). The sugar and phosphate make up the backbone of the structure. The nitrogen base is bonded to the sugar.

    2. Summarize the Hershey and Chase experiment and explain what their results suggested. The Hershey-Chase blender experiment: 35- Took viruses called a bacteriophages (will infect bacteria) and labeled their protein with heavy sulfur (S).

    The bacteriophages infected the bacteria. After centrifugation, the radioactive protein was found to be in the supernatant, NOT in the pellet with the bacteria. 32- Labeled the nucleic acid of the bacteriophage with heavy phosphorus (P) and carried out the experiment as

    stated above. The radioactive phosphorus was found in the pellet, which indicated that it was injected into the bacteria.

    - Hershey and Chase concluded that the viral DNA was the genetic material, not the protein, that was taking over the bacteria.

    3. Chargaff made an important contribution to uncovering the structure of DNA. What were his findings and what do they indicate? He found that in every species that he studied, if there were a certain number of adenines, then there was an equal number of thymine. The same was true for guanine and cytosine. This indicated that A must bond with T and C with G….complementary base pairing!

4. Who proposed the “double helix” model for the DNA molecule? Watson and Crick

    5. Describe how DNA and RNA differ in their composition, structure, function, and location.

    Nucleic Acid Composition Structure Function Location

    Deoxyribose DNA double helix Master “blueprint” nucleus thymine

    Ex. mRNA, tRNA, Ribose single segments or Mainly outside the RNA primer during DNA uracil strands nucleus replication…

6. What is meant when we say that DNA replication is complementary? A-T,C-G

7. Why is DNA replication important for every cell? Each daughter cell needs a complete set of DNA in order to

    properly functionb.

8. Compare the amount of DNA in a muscle cell with that in a brain cell. It is the exact same.

9. What is meant by saying that DNA replication is semi-conservative? Each daughter molecule has one parent (old)

    strand and one daughter (new) strand.

10. Briefly describe the steps in DNA replication.

    Here we go…

    - Helicase unwinds the DNA, and the replication fork is held open by single-strand binding proteins. - DNA polymerase III creates a daughter strand of DNA in the 5’ to 3’ direction via complementary base pairing.

    - The leading strand is formed in a simple, continuous fashion. The lagging strand is formed via segments called Okazaki fragments.

    - To create the lagging strand, primase creates and RNA primer from which DNA polymerase III will then create an Okazaki fragment in the 5’ to 3’ direction.

    - When the DNA polymerase III reaches the RNA primer of a previous Okazaki fragment, it detaches and DNA Polymerase I bonds to the nucleic acid and replaces the RNA primer with DNA.

    - The gap between the two Okazaki fragments is then sealed by ligase.

    11. Why is replication on one strand of DNA continuous, while on the other strand the replication must be discontinuous? The strands of DNA are antiparallel and complementary strands can only be constructed in a 5’ to 3’ direction. At the 3’ end there is a free hydroxyl group and in order to bond the next nucleotide (which, while floating in the cytosol, has three phosphates in total!!), two phosphates have to be lost so that the energy released can be used to form a bond. This bond forms between the remaining phosphate and the terminal sugar on the growing daughter strand.

12. What functional group is at the 5' end of a DNA molecule? Phosphate

    13. Proofreading enzymes scan DNA to check for base pairing errors. Explain why these enzymes are important. They minimize the number of mutations when replicating the DNA.

14. Why is the making of exact copies of DNA called replication rather than duplication? Because calling it DNA

    duplication would make it sound like the parent DNA strands stays together and that the new DNA is entirely made of daughter DNA. This terminology would support the CONSERVATIVE model, not the


     915. If human DNA contains approximately 3x10 base pairs, and DNA polymerase can work at the rate of about 50

    nucleotides per second, how can our DNA be replicated so quickly? There are a number of origins of replication;

    replication will occur in both directions within a replication bubble AND on both strands, all at the same time!

    16. If 27 percent of the bases in a certain segment of DNA were adenine, what would be the percentages of thymine (27%), cytosine (23%), and guanine (23%)?

17. A segment of chromosomal DNA which contains instructions for one protein is a ____gene_________.

18. Describe the technique of DNA fingerprinting.

    Since DNA contains some sequences that are unique to individuals, this information can be used to identify someone just like a regular fingerprint can. Restriction enzymes are used to cut the DNA of an individual at specific sites such that they have DNA divided into varying lengths. These segments of DNA are then divided during a process called gel electrophoresis, and the pattern of the bands in the gel is unique to one person.

    19. As a research biologist, you know of a bacterium that produces an antifungal treatment that is quite effective against a certain crop plant fungus. There would be great economic importance in enabling the plant to resist the fungus. How might you use DNA technology to accomplish this?

    Using recombinant DNA!! The bacterial DNA coding for the antifungal treatment is inserted to the plant DNA. The resulting plant will be resistant to the fungus.

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