Problem Sheet BIOL1XX7 Module1 2021
Problem Sheet BIOL1XX7 Module1 2021
For each Lecture questions that focus on part A should be above the **** and part B below the
line. Try these out, the plan is to go over some these questions in the Live Q&A sessions (there will
be an upvoting option available on canvas in Padlet to vote for which questions – if for some
reason that doesn’t work properly will use a Zoom poll at the beginning of the session) focussing
on lectures 2-4 in the first Q&A session and 5-7 in the second session (with room for other
questions from anywhere in the second half of each Q&A).
Lecture 2
A) B) C)
D) E) F)
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7) What are the five main types of molecules used in Biology and what are their uses?
10) What are the differences between amino acids and nucleotides?
11) What chemical properties can different amino acids have (name at least 3)?
Lecture 3
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4) Which nucleobases basepair with each other (A,C,G,T,U), which are considered to have
stronger basepairing and why?
5) What properties of RNA mean that it is less suitable as a source of genetic material than
DNA?
6) Make a sketch of the dsDNA helix (B-DNA) showing (and labelling) the following features (NB
not asking for chemical formula or precise dimensions etc just enough detail so that you can
point out where these features appear):
A. sugar-phosphate backbone
B. Base-pairing
C. Base-stacking
D. Major groove
E. Minor groove
F. Directions of each strand
Lecture 4
1) According to the central dogma of molecular biology, which of the following flows of
information can take place directly in biology?
A. DNA to RNA
B. Protein to RNA
C. DNA to Protein
D. DNA to DNA
E. RNA to DNA
F. Protein to DNA
G. Protein to Protein
H. RNA to RNA
2) Match the type of information containing biopolymer to its main role in the central dogma
of Molecular Biology:
Molecule Role
1. DNA A. Doing molecules
2. RNA B. Genetic Store
3. Protein C. Messenger
3) Consider muscle cells and skin cells from the same individual. In general terms describe the
genome, transcriptome and proteome for each cell type (are they the same or different and
if different how/why are they different).
4) What are the main differences between genomes and chromosomes from bacteria and
eukaryotes?
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5) What is the “start codon” and what amino acid does it encode?
6) What peptide sequence does the following mRNA sequence encode [hint: find the start
codon first and use the codon table above]?
UCAUGGGUUGGACUCUUUAACCG
Lecture 5
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Lecture 6
1) How do tRNA and aminoacyl RNA synthetases work together to correctly translate an mRNA
sequence translated into a protein/peptide sequence?
2) What roles does the ribosome have in protein synthesis initiation, elongation and
termination?
3) True or False: Release Factor is a tRNA that binds to the stop codon to terminate protein
synthesis
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4) What are the differences between primary, secondary, tertiary and quaternary structure of
proteins?
5) What types of bonds and forces hold protein structure held together?
6) Describe how an element of protein secondary structure can complement dsDNA structure
to allow protein-DNA interactions.
Lecture 7
2) What does it mean if a reaction is under kinetic rather than thermodynamic control?
3) True or False? A reaction (Substrate <-> Product) can be driven to the right by adding more
substrate or removing the product.
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4) Consider this graph from Lecture 7B where we saw faster initial reaction rates when twice as
much enzyme was added. What would happen to these two curves if we let the reactions
run for a long time?
5) What are three properties of enzymes that are important for biology and/or medicine?
6) How can the hydrolysis of pyrophosphate drive unfavourable interactions?