Restriction Enzyme Vector Ligase Enzyme Recombinant DNA DNA Construct Digestion ligation.

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Restrict ion Enzyme Vecto r Ligase Enzyme Recombina nt DNA DNA Construct Digest ion ligat ion

description

DNA cloning The recombinant plasmids are then mixed with bacteria which have been treated to make them “competent”, or capable of taking in the plasmids This insertion is called transformation There are two methods for transforming E.coli cells with plasmid DNA; Chemical Transformation Electroporation There are two methods for transforming E.coli cells with plasmid DNA; Chemical Transformation Electroporation

Transcript of Restriction Enzyme Vector Ligase Enzyme Recombinant DNA DNA Construct Digestion ligation.

Page 1: Restriction Enzyme Vector Ligase Enzyme Recombinant DNA DNA Construct Digestion ligation.

Restriction Enzyme Vector

Ligase Enzyme

Recombinant DNA

DNA Construct

Digestion

ligation

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Electroporation in cloning

presented by:vidahomayouni

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DNA cloning

• The recombinant plasmids are then mixed with bacteria which have been treated to make them “competent”, or capable of taking in the plasmids

• This insertion is called transformation

There are two methods for transforming E.coli cells with plasmid DNA; •Chemical Transformation •Electroporation

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Electroporation

• Most efficient method of transforming bacteria • •A strong electrical impulse renders bacterial cell walls

transiently permeable • •Efficiency: 10⁷ to 10¹⁰colonies per μg DNA • •Salts used in vector preparation may interfere with the

electroporation process • •Washed E. coli are mixed with plasmid DNA. • •The E.coli + plasmid mix is then placed into a plastic

cuvette. • •A short electric pulse is applied to the cells causing

small holes in the plasma membrane through which the plasmid enters.

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