chapter 16 microbial genomics “if we should succeed in helping ourselves through applied genetics...
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Restriction Endonuclases (enzymes) “Sticky” Ends Blunt EndsTRANSCRIPT
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Chapter 16 Microbial Genomics
“If we should succeed in helping ourselves through applied genetics before vengefully or accidentally exterminating ourselves, then there will have to be a new definition of evolution, one that recognizes a process nolonger directed by blind selection but by choice.”
Genetic engineering: the manipulation of DNA to introducenew genes to an organism or to modify existinggenes
--- transgenic, an organism carrying genes froma different individual
--- can occur naturally among the bacteria--- generally requires human intervention
among eukaryotes
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Most DNA manipulation is done in bacteria
Bacterial Advantages:
1.) rapid growth on simple substrates2.) stable extrachromosomal DNA (plasmids)3.) molecular tools, some model bacteria, particularly E. coli,
are very well understood at the cellular level
The most significant molecular tool was the discovery of restriction endonucleases.
--- discovered in the early 1970’s--- cut dsDNA only at specific nucleotide sequences--- several hundred known--- it has recently become possible to design RE’s
to cut at particular sequences --- are part of host restriction system, a way for bacteria
to protect themselves from “foreign” DNA,relies on methylation to mark their own DNA
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Restriction Endonuclases (enzymes)
“Sticky” Ends
Blunt Ends
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Plasmid Cloning
Cut (RE)
Ligate
Screen
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Polymerase Chain Reaction (PCR)
--- another way to get insert DNA for plasmid cloning--- basically PCR is DNA replication outside of a cell--- requires some knowledge of nucleotide sequence
of the target DNA (primers)--- uses a thermo-stable DNA polymerase--- each cycle doubles the amount of target DNA (2n)
Heat Denaturation (95 C)
Elongation (polymerization)(72 C)
Annealing (50-55 C) (primer binding)
Start
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Transformation
Cloning
PCR
cDNA
OR
Cloning a Eukaryotic Gene
--- ultimately want geneIn an expression vector
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Computer Based Sequence Annotation:
--- pretty good, but not perfect
E. Coli K-12 (MG1655):
Genome size: 4.6 MbpPredicted ORF’s (genes): 5,295 ( 88% of genome) Unknown function: 38%
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DNA Microarray Data
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