bacterial transformation
DESCRIPTION
Bacterial Transformation. AP Biology/Honors Genetics Ms. Gaynor. What does it mean to transform a cell?. To insert a foreign piece of DNA into a cell. How would a living organism be transformed?. Using a cloning vector/ plasmid. Give it different DNA. DNA. RNA. Protein. Trait. - PowerPoint PPT PresentationTRANSCRIPT
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Bacterial TransformationAP Biology/Honors Genetics
Ms. Gaynor
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What does it mean to transform a cell?
How would a living organism be transformed?
To insert a foreign piece of DNA into a cell
Using a cloning vector/ plasmid
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DNA RNA Protein Trait
Don’t Forget…
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Bacterial Transformation•Step 1 DNA Isolation
– Isolation of Your Gene of Interest (GFP)
•Step 2 Recombinant DNA– Insertion of foreign DNA into bacterial
plasmid using restriction enzymes and DNA ligase
• http://www.dnalc.org/resources/animations/transformation1.html
•Step 3 Transformation– Insertion of recombinant DNA into
bacteria by making bacteria competent• Use CaCl2 and heat shock techniques• http://www.dnalc.org/resources/animations/transformation2.html
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Step 1: DNA Isolation digesting the ”gene of interest” with restriction
enzyme•In the lab, this has been done for you!
•How did they do it?
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After Isolating GFP from a jellyfish
… Step 2: Make Recombinant DNA
Amp
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Need to use Restriction Enzymes to Make Recombinant DNA
• Act as molecular scissors
• Naturally found in bacteria – Used to decompose
viral & phage DNA
• Act as ENDOnucleases (cut WITHIN the DNA strand)
• ~3,000 known enzymes
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Step 3 TransformationRECALL WHAT THE PLASMID (pGLO)
LOOKS LIKE…
CaCl2
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Step 3 Transformation
pGLO
Amp resistance
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Transformed Bacteria!
When will this happen?
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What is an operon?-Clusters of genes located together and transcribed from ONE promoter usually found only in bacteria
-3 arabinose genes are present in a natural (not recombined) plasmid: araB, araA, araD
-All 3 genes dependent on 1 promoter (called pBAD)
-Interaction with arabinose (sugar) changes the shape of the promoter & enables RNA polymerase to bind to the DNA coding strand for transcription
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Visualize the Operon
araB araDaraA
= ARABINOSE (a sugar needed to make room
for RNA polymerase)
Promoter called Pbad
araAaraBRNA
Polymerase
araDPbad
Repressor
Repressor
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Visualize the pGLO recombinant DNA
What was changed?araB araDaraAPbad
GFP gene RNA
Polymerase
amp genePbad
Repressor
RNA
Polymerase
Also on the pGLO plasmid
but NOT in place of the ara operon!
Pamp
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pGLO plasmid contains:1)ampR gene2)GFP gene 3)Arabinose operon and promoter (pBAD)
operonpromoter
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Materials
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Lab Procedure-Brief Overview1. Label micro test tubes (+pGLO and –pGLO)2. Transfer 250 μL (0.25 mL) of transformation
solution (CaCl2) to each tube place on ice
Transformation Solution (CaCl2)
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Lab Procedure-Brief Overview3. Use sterile inoculating loop to transfer ~2 “fat”
colonies of bacteria to +pGLO tube spin loop to remove bacteria from loop to CaCl2 solution
4. Use a DIFFERENT sterile inoculating loop to transfer ~2 “fat” colonies of bacteria to -pGLO tube
NO chunks!
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Lab Procedure-Brief OverviewLAB PRCEDURE REVISION
5. I will have some pGLO plasmid in a labeled micro test tube…
• You (a lab group member) will come to the front of the room and retrieve your 9 μL of pGLO plasmid• I will add plasmid using a
micropipette • Cap the +pGLO microtest tube and
mix the plasmid into the cell suspension by inverting tube.
• Return this test tube to the ice. • DO NOT add plasmid DNA to the
–pGLO tube.
You are NOT doing this method!!!
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Lab Procedure-Brief Overview
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Lab Procedure-Brief Overview6. Incubate both +pGLO and –pGLO tubes on ice
for 10 minutes
+p
GL
O+
pG
LO
-pG
LO
-pG
LO10:0
0
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Lab Procedure-Brief OverviewWhile the tubes are sitting on ice…7. Label your 4 LB Nutrient agar plates on the
bottom (not the lid) as follows: • Label one LB/amp plate: + pGLO • Label the LB/amp/ara plate: + pGLO • Label the other LB/amp plate: - pGLO • Label the LB plate: -pGLO
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Lab Procedure-Brief OverviewTIME TO HEAT SHOCK…
8. Use foam rack as a holder, transfer both the +pGLO and -pGLO tubes into the water bath, set at 42°C, for exactly 50 seconds. • Make sure to push the tubes all the way
down in the rack so the bottoms of the tubes stick out and make contact with the warm water.
When the 50 seconds are done, RAPIDLY place both tubes back on ice. Incubate tubes on ice for 2 minutes
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Lab Procedure-Brief Overview9. Remove the rack with tubes from ice and place
on lab bench. Open a tube and, using a new sterile pipet, add 250
µl of LB nutrient broth to EACH tube and reclose it. • Use a new sterile pipet for the other tube.
Incubate tubes for 10 minutes at room temperature.
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Lab Procedure-Brief Overview9. Remove the rack with tubes from ice and place
on lab bench. Open a tube and use a new sterile pipet, add 250 µl
of LB broth to EACH tube and reclose it. • Use a new sterile pipet for the other tube.
Incubate the tubes for 10 minutes at room temperature.
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Lab Procedure-Brief Overview10. After 10 min have passed, tap the closed tubes
with your finger to mix. Using a new sterile pipet for each tube, pipet 100 µl of liquid onto the appropriate LB agar plates
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Lab Procedure-Brief Overview11. Use a new sterile loop for each plate. Spread
liquid evenly around surface of LB agar using streaking method.
DO NOT PRESS TOO DEEP INTO THE AGAR.
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Streaking Plates with bacteria
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Lab Procedure12. Stack up your plates and
tape them together. Put your group name and class period on the tape and place the stack of plates upside down in Ms. Gaynor’s transfer box.
She will put all plates in the 37°C incubator upside
down for 24 hours.
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Reasons for Performing Transformation Step
1. Transformation solution = CaCI2-Positive charge of Ca++ ions shields negative
charge of DNA phosphates & helps neutralize cell membrane so plasmid can get in
2. Incubate on ice-Slows movement of cell membrane so Ca++ can bind & plasmid can slip into bacterial cell
3. Heat-shock-Increases movement of membranes (heat)- Then closes up holes in membranes
4. Nutrient broth incubation-Allows bacteria to be feed
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Review… What does the following mean?
• +pGLO• a cell contains the pGLO plasmid (transformed cell)• pGLO plasmid contains 2 genes: AMP and GTP
• -pGLO•a cell without the plasmid (“normal” cell)
•LB•Luria Broth (LB or Agar) sugar needed for E.Coli to live (feeds on this sugar solution)
•amp• Ampicillin an liquid antibiotic added to the LB•Normally KILLS bacteria by breaking down cell wall peptidoglycan
•ara•Arabinose sugar needed to turn on operon containing the GFP gene; needed to make glow protein
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Petri Dish Label
What do this dish have on
it?
Hypothesis: Will the bacteria
grow on the dish? Y or N
Hypothesis: Will the bacteria
GLOW green on the dish?
Y or N+pGLO
LB/amp+pGLO
LB/amp/ara-pGLO
LB/amp-pGLO
LB
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Petri Dish Label
What do this dish have on
it? **they all
have E. coli
Hypothesis: Will the bacteria
grow on the dish? Y or N
Hypothesis: Will the bacteria
GLOW green on the dish?
Y or N+pGLO
LB/amp
Plasmid (with pGLO & AMPR),
Luria Broth (Agar), ampicillin
YES- colony growth
NO
+pGLO
LB/amp/ara
Plasmid, Luria Broth,
ampicillin, arabonose
Yes-
Colony growth Yes
-pGLO
LB/amp
No plasmid, Luria Broth, ampicillin
No No
-pGLO
LB
No plasmid, Luria broth
Yes- Lawn growth No
NEGATIVE CONTROL
POSITIVE CONTROL
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Results
+ control - control