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Question
Plasmid pBR322 has Pst I restriction enzyme site within gene ampR that confers ampicillin resistance. If this enzyme is used for inserting a gene for $\beta$-galactoside production and the recombinant plasmid is inserted in an E.coli strain
It will be able to produce a novel protein with dual ability
It will not be able to confer ampicillin resistance to the host cell
The transformed cells will have the ability to resist ampicillin as well as produce $\beta$-galactoside
It will lead to lysis of host cell

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