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MIB2603 Exam Revision – Complete Question-and-Answer Study Pack

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A full revision document containing all key MIB2603 exam questions with clear, summed-up answers from all study units. Covers bacterial genetics, DNA replication, gene expression, genetic variation, immunity, epidemiology and public-health microbiology. Designed for fast study, accurate exam preparation and streamlined consolidation of the module’s core concepts.

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‭MIB 2603 EXAM REVISION‬

📘
‭ STUDY UNIT 1 – Chapter 13: Bacterial Genome Replication‬
‭and Expression‬

‭Learning Outcomes‬
‭By the end of this learning unit you should be able to:‬

‭●‬ B ‭ riefly describe the experiments of Griffiths, Avery and colleagues as well as Hershey and‬
‭Chase.‬
‭●‬ ‭Discuss the control experiments that these researchers included in their experiments to‬
‭support virulence transformation and the identification of DNA as the genetic material.‬
‭●‬ ‭Describe the contributions that Miescher, and Mirsky and Ris have made to our‬
‭understanding of DNA.‬
‭●‬ ‭Describe the central dogma and discuss the results of Hershey and Chase’s experiment‬
‭from this viewpoint.‬
‭●‬ ‭Draw the DNA helix taking note of the major and minor grooves.‬
‭●‬ ‭Explain the effect of the difference in the number of hydrogen bonds between G and C‬
‭bases compared to those between A and T bases.‬
‭●‬ ‭Discuss similarities and differences between the structure of DNA and that of RNA.‬
‭●‬ ‭Access and read the 1953 Nature article written by Crick and Watson.‬
‭●‬ ‭Describe the experiments involving the incorporation of radioactive label into progeny‬
‭DNA strands that were used to support the concept of semiconservative replication of‬
‭DNA.‬
‭●‬ ‭Discuss the consequences of DNA vs. RNA polymerase proofreading ability.‬
‭●‬ ‭Read the legend to figure 13.12 in Prescott (2014) describing replication activities at the‬
‭replication fork.‬
‭●‬ ‭Define the terms “downstream” and “upstream” in the context of DNA sequences.‬
‭●‬ ‭Describe the process of transcription in bacteria.‬
‭●‬ ‭Describe the structure and catalytic activity of DNA-dependent RNA polymerase.‬
‭●‬ ‭Describe bacterial promoters.‬
‭●‬ ‭Translate a given mRNA sequence.‬
‭●‬ ‭Explain the difference between a codon and an anticodon.‬
‭●‬ ‭Describe reading frames.‬
‭●‬ ‭Describe the function of tRNA.‬
‭●‬ ‭Describe how the ribosome interacts with macromolecules.‬
‭●‬ ‭Describe translation including initiation, elongation and termination.‬
‭●‬ ‭Describe the function of initiation, elongation and termination factors.‬

,‭Question a)‬

‭ riefly describe the experiments of Griffiths, Avery and colleagues as well as Hershey and Chase.‬
B
‭Include diagrams of these experiments.‬

‭Answer:‬

‭●‬ G
‭ riffith (1928): Demonstrated transformation using‬‭Streptococcus pneumoniae‬‭. Heat-killed‬
‭virulent (S) + live non-virulent (R) = mouse dies.‬

‭●‬ A
‭ very et al. (1944): Showed DNA is the transforming factor using DNase, RNase, and‬
‭protease.‬

‭●‬ H
‭ ershey & Chase (1952): Used radioactive ³²P-labeled DNA and ³⁵S-labeled protein in‬
‭bacteriophages. Only DNA entered the host cell, proving DNA is genetic material.‬


📌
‭ ‬‭See Prescott Figures 13.1 to 13.3 for visuals.‬




‭Question b)‬

‭ iscuss the control experiments that these researchers included in their experiments to support‬
D
‭virulence transformation and the identification of DNA as the genetic material.‬

‭Answer:‬

‭●‬ A
‭ very’s team used specific enzymes (DNase, RNase, protease) to confirm only DNA was‬
‭responsible for transformation.‬

‭●‬ H
‭ ershey & Chase used isotopic labeling (³²P for DNA, ³⁵S for protein) to track which‬
‭molecule entered the bacterial cell.‬




‭Question c)‬

‭ ey into Google the names of the following researchers: Miescher (1878) as well as Mirsky and‬
K
‭Ris (1949). Then describe the contributions that these researchers have made to our‬
‭understanding of DNA.‬

,‭Answer:‬

‭●‬ M
‭ iescher (1878): Discovered nuclein (DNA) in the nuclei of white blood cells, identifying‬
‭DNA as a distinct molecule.‬

‭●‬ M
‭ irsky and Ris (1949): Demonstrated that DNA content is constant in somatic cells and‬
‭varies between species, supporting DNA’s role as the genetic material.‬




‭Question d)‬

‭ ater in this learning unit, I will describe a flow of genetic information from DNA to RNA to protein.‬
L
‭In your own words, describe the central dogma and discuss the results of Hershey and Chase’s‬
‭experiment from this viewpoint.‬

‭ nswer:‬
A
‭The central dogma describes the flow of genetic information: DNA → RNA → Protein. Hershey‬
‭and Chase confirmed that DNA—not protein—enters the host and directs viral replication,‬
‭reinforcing DNA’s central role in this process.‬




‭Question a)‬

‭Draw the DNA helix taking note of the major and minor grooves.‬

‭ nswer:‬
A
‭The DNA double helix is right-handed, with two grooves:‬

‭●‬ ‭Major groove: Wide; allows protein binding‬

‭●‬ M
‭ inor groove: Narrow; less accessible‬
‭These grooves are essential for regulatory protein-DNA interactions.‬




‭Question b)‬

‭ xplain the effect of the difference in the number of hydrogen bonds between G and C bases‬
E
‭compared to those between A and T bases.‬

, ‭Answer:‬

‭●‬ ‭G-C pairs have 3 hydrogen bonds‬

‭●‬ A
‭ -T pairs have 2 hydrogen bonds‬
‭G-C rich DNA is more stable and requires more energy to denature due to the extra bond.‬




‭Question c)‬

‭Discuss similarities and differences between the structure of DNA and that of RNA.‬

‭Answer:‬


‭Feature‬ ‭DNA‬ ‭RNA‬

‭Sugar‬ ‭Deoxyribose‬ ‭Ribose‬

‭Bases‬ ‭A, T, G, C‬ ‭A, U, G, C‬

‭Strands‬ ‭Double-stranded‬ ‭Single-stranded‬

‭Stability‬ ‭High‬ ‭Less stable‬

‭Function‬ ‭Long-term storage‬ P
‭ rotein synthesis, regulation,‬
‭catalysis‬




‭Question d)‬

‭Access and read the 1953 Nature article written by Crick and Watson (Nature 171, 737-738).‬

‭ nswer:‬
A
‭Watson and Crick described the double helix model: two antiparallel DNA strands held together‬
‭by specific base pairing (A-T, G-C). This structure explained replication, mutation, and genetic‬
‭coding.‬




‭Question a)‬

‭ se Google to access details of the experiment of Meselson and Stahl (1958) and Cairns (1963).‬
U
‭Describe these experiments involving the incorporation of radioactive label into progeny DNA‬
‭strands that were used to support the concept of semiconservative replication of DNA.‬
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