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Molecular Biology and Biotechnology Quiz1, Quizzes of Biotechnology

Quiz questions and answers. True/False, short answer

Typology: Quizzes

2021/2022

Available from 03/05/2022

victoria-hart
victoria-hart 🇺🇸

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GBIO 434/534
Molecular Biology and Biotechnology
Quiz 1
True/False
1) The earliest manipulation of nature for human benefit was creation of recombinant DNA
technology.
False
2) Molecular Biotechnology arose out of an increased understanding of Genetics and
Molecular Biology.
True
3) Advances in knowledge in Genetics and Molecular Biology that helped lead to Molecular
Biotechnology included studies pre 1920 by Griffith/Avery/Hershey/Chase, Chargaff,
Franklin/Wilkins/Watson/Crick, and Cohen and post 1920 by Mendel, Darwin/Wallace,
Meischner, Sutton/Boveri, and Morgan.
False
4) Genetically Modified Organism crop plants could contain genes for insect resistance (Bt),
herbicide tolerance (Ht), drought resistance, or disease resistance.
True
5) Restriction enzymes are endonucleases that always leave overhangs (staggered ends).
False
6) The natural source of restriction enzymes is eukaryotic cells and their natural targets are
viruses that infect eukaryotic cells.
False
7) Recombinant DNA technology can be as simple as creating a plasmid using a restriction
enzyme to cut at a restriction site in the polylinker (cloning site) of the plasmid, cutting
out a gene from a larger DNA fragment using the same restriction enzyme, and using
DNA ligase to paste the gene into the plasmid.
True
8) “Competent” cells (bacteria), have been treated to make restriction enzymes.
False
9) Transformation can be used to describe the introduction of a plasmid into bacteria.
Selection of bacteria that carry the plasmid involves growth of colonies (cloning) on agar
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GBIO 434/

Molecular Biology and Biotechnology Quiz 1 True/False

  1. The earliest manipulation of nature for human benefit was creation of recombinant DNA technology. False
  2. Molecular Biotechnology arose out of an increased understanding of Genetics and Molecular Biology. True
  3. Advances in knowledge in Genetics and Molecular Biology that helped lead to Molecular Biotechnology included studies pre 1920 by Griffith/Avery/Hershey/Chase, Chargaff, Franklin/Wilkins/Watson/Crick, and Cohen and post 1920 by Mendel, Darwin/Wallace, Meischner, Sutton/Boveri, and Morgan. False
  4. Genetically Modified Organism crop plants could contain genes for insect resistance (Bt), herbicide tolerance (Ht), drought resistance, or disease resistance. True
  5. Restriction enzymes are endonucleases that always leave overhangs (staggered ends). False
  6. The natural source of restriction enzymes is eukaryotic cells and their natural targets are viruses that infect eukaryotic cells. False
  7. Recombinant DNA technology can be as simple as creating a plasmid using a restriction enzyme to cut at a restriction site in the polylinker (cloning site) of the plasmid, cutting out a gene from a larger DNA fragment using the same restriction enzyme, and using DNA ligase to paste the gene into the plasmid. True
  8. “Competent” cells (bacteria), have been treated to make restriction enzymes. False
  9. Transformation can be used to describe the introduction of a plasmid into bacteria. Selection of bacteria that carry the plasmid involves growth of colonies (cloning) on agar

plates containing an antibiotic. The plasmid must also contain a gene for resistance to that antibiotic. True

  1. In “blue/white” colony cloning of a gene inserted into a plasmid, disruption of the ampicillin resistance gene by the insert is desired, while expression of the beta galactosidase gene is uninterrupted (for selection of clones with insert). False
  2. After cloning a gene in a plasmid, picking a white colony (if doing blue/white cloning), and expanding the colony in culture, you can isolate larger amounts of the plasmid containing your gene. To test if it contains the insert, if your plasmid was 4kb and your insert was 3kb, you can digest plasmid DNA isolated from the large culture with the restriction enzyme used originally (e.g., as in #9). You should get a 4kb and 3kb band on a gel after electrophoresis. True
  3. The original DNA sequencing reactions (Sanger) used 4 tubes containing each dideoxyNTP (ddNTP). Later methods use reactions in a single tube with all 4 ddNTPs. True
  4. Not very much of the human genome contains noncoding DNA, but that’s ok, because it is “junk” …unimportant. False
  5. The Asilomar Conference sought to set guidelines for use of recombinant DNA technology in the 1970s. Scientists and others at the conference were interested in helping to ensure that the technology would be used only for the public good. There was also a self-imposed moratorium on use of the technology until guidelines were worked out. True
  6. “Pharming” involves production of pharmaceuticals in bacteria. False Short answer
  7. State the basic advances provided by any 3 of the scientists (or groups of scientists) listed in #3.
  1. Structure of DNA
  2. Restriction endonucleases
  3. DNA as hereditary material, not proteins

Choose the correct answer in the paragraph. (Answers separated by forward slashes) (Correct answers are in bold)

  1. The EPA, USDA, and FDA were developed ( before /after) recombinant DNA technology. They were largely developed to regulate (insects/ chemicals /microbes) released by the industry. The EPA generally regulates (Food, Drugs, Cosmetics/ Environment /Agriculture and Forestry). The FDA generally regulates ( Food, Drugs, Cosmetics /Environment/Agriculture and Forestry). The USDA generally regulates (Food, Drugs, Cosmetics/Environment/ Agriculture and Forestry ). For a GMO crop approval for commercialization (or exemption), it must go through lab testing, then field testing overseen and approved by the ( EPA or USDA /FDA). Approval of a field test looks for impact on nontarget organisms, origin and characteristics of inserted genes, product of transgenes and potential for (transfection/ introgression /suppression). A favorable (laboratory/ field ) test for a GMO leads to a finding of no significant impact (FONSI) and the GMO is eligible for final product testing by the FDA. Public comment periods occur between steps in the approval process. Additionally, the (FDA/ NIH Recombinant DNA advisory committee /USDA) grew from the Asilomar Conference and sets guidelines for NIH-funded GMO work and integrates it into a National Framework. Institutions also have Institutional Biosafety Committees that regulate NIH- funded GMO work at the local level.