Q. What will be the fate of a Seq A mutant E. Coli?

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Q. At which end are the new DNA bases added?

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Q. How many prokaryotic DNA polymerases have 5’->3’ proofreading activity?

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Q. Which is the most processive of prokaryotic DNA polymerases?

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Q. Bacterial polymerases are slower than eukaryotic polymerases.

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Q. In an experiment you take a DNA in vitro and attempt to replicate it. Which combination will you add to your DNA to get the maximum replication product?

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Q. In an experiment you use DNA pol I – Klenow fragment. When all other requisites for replication are added, then what will be the effect on the newly replicated DNA? Consider leading strand only.

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Q. You take a circular ssDNA and to it you attach a small labeled complimentary fragment. You add different reagents and try to get free labeled probe. Which of this reagent will give you your desired result?

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Q. Which of this subunit is not a part of core DNA polymerase?

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Q. Rolling circle mode of replication is ________

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Q. What constitutes Primosome?

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Q. If we mutate the DNA ligase and observe the length of the replicated strands in different time slots after replication initiation, what will we observe?

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Q. If we mutate the DNA ligase and observe the length of the replicated strands in different time slots after replication initiation, what will we observe?

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Q. DNA replication in the two strands proceed in opposite direction as they are aligned oppositely with respect to 3’ and 5’ ends
( 5’——————————-3’
3’——————————-5’).

In this context which of the following is true.

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Q. In case of eukaryotes replication initiates at ________

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Q. Here are names of some factors necessary for prokaryotic replication. Which of these or their homologue is unnecessary for eukaryotes?

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Q. You wanted to find out the importance of the DNA polymerases. So, you mutated the polymerases one by one and checked for survival. In which of these mutant cases will you see least survival rate?

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Q. You design a circular ssDNA with a labeled RNA primer (alpha-P³² labeling). You add polymerase epsilon and required enzymes for replication to the fragment. What will you expect to see on autoradiography after gel electrophoresis?

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Q. You design a plasmid with a gene for Histidine synthesis and a fragment containing ARS. You introduce it yeast culture and try to grow then in Histidine deficit media. What will be your observation?

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Q. Deletion of which domain of ARS would give the least replication rate in eukaryotes?

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