plasmid, restriction enzyme and dna...
TRANSCRIPT
3/14/2011
PLASMID, RESTRICTION ENZYME AND
DNA TRANSFORMATION
Lucia Dhiantika Witasari
http://dhiantika.staff.ugm.ac.id
3/14/2011
DNA cloning
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What is Plasmids ?• Extrachromosomal DNA • Having ori (origin of replication)• Very small• Carry genetic information• Can be isolated from bacterial cells• Important in a genetic engineering
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Using a plasmid vector, it would be possible to recover a single colony from an agar plate and to use this to produce a bacterial culture in which each cell carries a copy of the original
DNA fragment
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3/14/2011
Origin of replication The first requirement is that the plasmid must be able to replicate in the chosen host (in this case, E. coli).
Selectable markerit is necessary to be able to select those cells which have received the plasmid (transformants) :•one or more antibiotic resistance genes•b‐lactamase gene resistance to ampicillin
Cloning siteit must contain suitable recognition sites for cleavage by one or more restriction endonucleases. the circular plasmid can be opened up at that point and the ends ligated with the ends of the DNA fragment to be cloned
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3/14/2011Endang S. Rahayu
Fak.Teknologi Pertanian UGM
Antibiotic resistance genens and replicator genehttp://dhiantika.staff.ugm.ac.id
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Plasmid pBR322
pBR322• One of the original plasmids
used• Two selectable markers (Amp
and Tet resistance)• Several unique restriction sites
scattered throughout plasmid (some lie within antibiotic resistance genes = means of screening for inserts)
• ColE1 ORI
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pUC18• Derivative of pBR322• Advantages over pBR322:
• Smaller – so can accommodate larger DNA fragments during cloning (5‐10kbp)
• Higher copy # per cell (500 per cell = 5‐10x more than pBR322)
• Multiple cloning sites clustered in same location = “polylinker”
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POLYLINKER
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3/14/2011 Praktikum Biomol, 2008
pUC18
• Interruptable gene encoding for enzyme beta galactosidase (lacZ)
– Polylinker resides in the middle
– Enzyme activity can be used as marker for gene insertion
– Disrupted gene = nonfunctional
– Intact gene = functional
– Media containing XGAL chromagenic substrate used (blue colonies = intact; white colonies = disrupted)
• Amp resistance gene still present (= beta lactamase), Tet resistance gene omitted
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CLONING IN PLASMID VECTORS
IMPORTANT
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Restriction Enzymes
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DNA double helixes are cut at the axis of symmetry:
Although less efficient, blunt‐end ligation can be useful because it does not require the fragments to have been generated with the same enzyme
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CLONING BLUNT‐END MOLECULES
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DNA double helixes are cut : sticky end
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EcoR1 Recognition Site
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3/14/2011 http://dhiantika.staff.ugm.ac.id
3/14/2011 http://dhiantika.staff.ugm.ac.id
3/14/2011Endang S. Rahayu
Fak.Teknologi Pertanian UGMhttp://dhiantika.staff.ugm.ac.id
3/14/2011
TRANSFORMATION
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Basic procedure for plasmid transformation of E. coli
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Transformasi
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