how to bioengineer a novel system? obtain a sequence by pcr, then clone it into a suitable plasmid

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How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid We’re adding DNA, but want E. coli to make a protein!

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How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid We ’ re adding DNA, but want E. coli to make a protein!. In bacteria transcription and translation are initially coupled. In Bacteria transcription and translation are initially coupled - PowerPoint PPT Presentation

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Page 1: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

How to bioengineer a novel system?Obtain a sequence by PCR, then clone it into a suitable plasmid•We’re adding DNA, but want E. coli to make a protein!

Page 2: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

1) In bacteria transcription and translation are initially coupled

Page 3: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

1) In Bacteria transcription and translation are initially coupled• RNA polymerase quits if ribosomes lag too much

Page 4: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

1) In Bacteria transcription and translation are initially coupled• RNA polymerase quits if ribosomes lag too much• Recent studies show that ribosomes continue translating once

mRNA is complete; i.e after transcription is done

Page 5: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Bacteria have > 1 protein/mRNA (polycistronic)http://bmb-it-services.bmb.psu.edu/bryant/lab/Project/Hydrogen/index.html#section1•euk have 1 protein/mRNA

Page 6: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Bacteria have > 1 protein/mRNA (polycistronic)•Mutations can have polar effects: mutations in upstream genes may affect expression of perfectly good downstream genes!

Page 7: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Regulating transcription

Telling RNA pol to copy a DNA sequence

Page 8: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Regulating transcription

Telling RNA pol to copy a DNA sequence

Transcription factors bind promoters & control initiation of transcription

Page 9: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Regulating transcription

Telling RNA pol to copy a DNA sequence

Transcription factors bind promoters & control initiation of transcription

1/signal gene senses

Page 10: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Regulating transcriptionTelling RNA pol to copy a DNA sequenceTranscription factors bind promoters & control initiation of transcription

1/signal gene senses1 binding site/signal gene senses

Page 11: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Transcription factorsBind surface -> base-pairs form unique patterns in major & minor grooves

Page 12: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Transcription factorsBind surface -> base-pairs form unique patterns in major & minor groovesScan DNA for correct pattern

Page 13: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Transcription factorsBind surface -> base-pairs form unique patterns in major & minor groovesScan DNA for correct patternneed 15 - 20 H-bonds = 5-8 base-pairs

Page 14: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Transcription

Prokaryotes have one RNA polymerase

makes all RNA

core polymerase = complex of 5 subunits (’)

Page 15: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Transcription

Prokaryotes have one RNA polymerase

makes all RNA

core polymerase = complex of 5 subunits (’)

not absolutely needed, but cells lacking are very sick

Page 16: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Initiating transcription in Prokaryotes1) Core RNA polymerase is promiscuous

Page 17: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Initiating transcription in Prokaryotes1) Core RNA polymerase is promiscuous2) sigma factors provide specificity

Page 18: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Initiating transcription in Prokaryotes1) Core RNA polymerase is promiscuous2) sigma factors provide specificity• Bind promoters

Page 19: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Initiating transcription in Prokaryotes1) Core RNA polymerase is promiscuous2) sigma factors provide specificity• Bind promoters• Different sigmas bind different promoters

Page 20: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Initiating transcription in Prokaryotes1) Core RNA polymerase is promiscuous2) sigma factors provide specificity• Bind promoters3) Once bound, RNA polymerase “melts” the DNA

Page 21: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Initiating transcription in Prokaryotes3) Once bound, RNA polymerase “melts” the DNA4) rNTPs bind template

Page 22: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Initiating transcription in Prokaryotes3) Once bound, RNA polymerase “melts” the DNA4) rNTPs bind template5) RNA polymerase catalyzes phosphodiester

bonds, melts and unwinds template

Page 23: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Initiating transcription in Prokaryotes3) Once bound, RNA polymerase “melts” the DNA4) rNTPs bind template5) RNA polymerase catalyzes phosphodiester

bonds, melts and unwinds template6) sigma falls off after ~10 bases are added

Page 24: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Structure of Prokaryotic promotersThree DNA sequences (core regions)

1) Pribnow box at -10 (10 bp 5’ to transcription start)5’-TATAAT-3’ determines exact start site: bound by factor

Page 25: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Structure of Prokaryotic promotersThree DNA sequences (core regions)

1) Pribnow box at -10 (10 bp 5’ to transcription start)5’-TATAAT-3’ determines exact start site: bound by factor

2)” -35 region” : 5’-TTGACA-3’ : bound by factor

Page 26: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Structure of Prokaryotic promotersThree DNA sequences (core regions)

1) Pribnow box at -10 (10 bp 5’ to transcription start)5’-TATAAT-3’ determines exact start site: bound by factor

2)” -35 region” : 5’-TTGACA-3’ : bound by factor3) UP element : -57: bound by factor

Page 27: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Structure of Prokaryotic promotersThree DNA sequences (core regions)

1) Pribnow box at -10 (10 bp 5’ to transcription start)5’-TATAAT-3’ determines exact start site: bound by factor

2)” -35 region” : 5’-TTGACA-3’ : bound by factor3) UP element : -57: bound by factor

Page 28: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Structure of Prokaryotic promotersThree DNA sequences (core regions)

1) Pribnow box at -10 (10 bp 5’ to transcription start)5’-TATAAT-3’ determines exact start site: bound by factor

2)” -35 region” : 5’-TTGACA-3’ : bound by factor3) UP element : -57: bound by factorOther sequences also often influence transcription! Eg Trp operator

Page 29: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Prok gene regulation5 genes (trp operon) encode trp enzymes

Page 30: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Prok gene regulationCopy genes when no trpRepressor stops operon if [trp]

Page 31: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Prok gene regulationRepressor stops operon if [trp] trp allosterically regulates repressor can't bind operator until 2 trp bind

Page 32: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

lac operonSome operons use combined “on” & “off” switches E.g. E. coli lac operon Encodes enzymes to use lactose

lac Z = -galactosidaselac Y= lactose permeaselac A = transacetylase

Page 33: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

lac operon

Make these enzymes only if:

1) - glucose

Page 34: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

lac operon

Make these enzymes only if:

1) - glucose

2) + lactose

Page 35: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

lac operon

Regulated by 2 proteins

1) CAP protein : senses [glucose]

Page 36: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

lac operonRegulated by 2 proteins1) CAP protein : senses [glucose]2) lac repressor: senses [lactose]

Page 37: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

lac operonRegulated by 2 proteins1) CAP protein : senses [glucose]2) lac repressor: senses [lactose]

encoded by lac i geneAlways on

Page 38: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

lac operon2 proteins = 2 binding sites1) CAP site: promoter isn’t active until CAP binds

Page 39: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

lac operon2 proteins = 2 binding sites1) CAP site: promoter isn’t active until CAP binds2) Operator: repressor blocks transcription

Page 40: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

lac operonRegulated by 2 proteins1) CAP only binds if no glucose -> no activation

Page 41: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

lac operonRegulated by 2 proteins1) CAP only binds if no glucose -> no activation2) Repressor blocks transcription if no lactose

Page 42: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

lac operonRegulated by 2 proteins1) CAP only binds if no glucose 2) Repressor blocks transcription if no lactose3) Result: only make enzymes for using lactose if lactose is present and glucose is not

Page 43: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid
Page 44: How to bioengineer a novel system? Obtain a sequence by PCR, then clone it into a suitable plasmid

Result[-galactosidase]rapidly rises if noglucose & lactoseis presentW/in 10 minutes is 6% of total protein!