BIL 250 Lecture Notes - Lecture 7: Multiple Cloning Site, Molecular Cloning, Dna Ligase

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Recombinant dna technology began with two key tools: restriction enzymes and dna cloning vectors. Produced by artificially joining dna from different biological sources not found together in nature. Used to study structure and orientation of dna. Technology used to isolate, replicate, and analyze genes. Produced by bacteria as a defense mechanism against bacteriophages. Bind to dna at specific recognition sequence and cleaves dna to produce restriction fragments. More than 3500 types of restriction enzymes exists and 250 are commercially available. Nucleotide enzymes cut dna in characteristic cleavage pattern. Blunt ends: fragments produced with double stranded ends. Dna ligase seals the nicks in the dna backbone, covalently bonding the two strands. Can replicate cloned dna fragments in host cell. Have several restriction enzyme sites to allow insertion of dna fragment. Carry selectable gene marker to distinguish host cells that have taken them up from those that have not. Genetically modified bacterial plasmids first vectors develop.

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