BMOL20090 Molecular Genetics and Biotech Assignment 1 2026 | UCD

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Published: 26 Aug, 2026
Category Assignment Subject Science
University University College Dublin Module Title BMOL20090 Assignment 1

BMOL20090 Assignment 1

This  assignment  is  “open  book”. All  five  questions  should  be  attempted. You  must compose  your  answers  without  assistance  from  any  other  person.  The  completed assignment should be uploaded to Brightspace as a single PDF or Word file. Diagrams should  be  hand-drawn  and  clearly  labelled,  then  photographed  or  scanned.  The resulting image files should be embedded in the text of the relevant answer. 

1. The molecule below (Figure 1) is used as an antiviral prodrug. What is/are the likely mode/s of action? 

Figure 1. Structure of antiviral prodrug 

2. Assume that the spacecraft “Tianwen-2” landed on Mars and has found a new life  form  that  resembles  bacteria  and  contains  a  molecule  like  DNA.  The spacecraft can carry out simple experiments. To study replication, the Meselson-Stahl  experiment  is  repeated.  After  1  round  of  replication,  there  are  DNA molecules  with  different densities; 50% is light DNA and  50%  is heavy DNA. What mode of replication do you predict the Martian bacterium uses, and why did you reach that conclusion? If you are correct, what would the DNA look like after two rounds of replication?

3. The sequence below (Figure 2) shows the coding strand plus regulatory regions of a bacterial gene that encodes a single 38-residue protein.  You can use tools like https://web.expasy.org/translate/ to help you identify the protein coding sequence.

a) Label the promoter sequence.

b) What are the first 10 amino acids generated?

c) Label and describe a possible transcriptional terminator. 

4. The classic experiment by Hershey and Chase used a bacteriophage labelled with radioactive isotopes 32P and 35S. What was the aim of this experiment and what did it reveal? Why were 3H or 14C not used as radioactive labels?

5. Aminoacylation  is  the  attachment  of  an  amino  acid  to  the  3′  end  of  a  tRNA molecule. This occurs  in  two  steps  that are catalyzed by  an  aminoacyl-tRNA synthetase (not covered in lectures). In the first step, the amino acid reacts with ATP to form a 5′-aminoacyl adenylate (Figure 3). In the second step, the amino acid migrates from AMP onto the tRNA. Schematic diagrams of a typical tRNA and its acceptor stem are shown in Figure 4.

There are two ways in which amino acids are attached to the adenosine at the extreme  3′  end  of  the  tRNA.  Draw  diagrams  showing  the  linkages  between amino acyl residue and the tRNA in both types of aminoacyl-tRNA. What is the difference between them?  

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