Team:Buenos Aires/ protocols

From 2013.igem.org

(Difference between revisions)
(Materials)
 
(4 intermediate revisions not shown)
Line 1: Line 1:
<div id="external">
<div id="external">
-
= MINIPREP =
+
= Miniprep =
==Materials==
==Materials==
Line 12: Line 12:
==Procedure==
==Procedure==
-
 
# Centrifuge for 5 minutes at 5000 rpm 1,5 ml of bacteria culture.
# Centrifuge for 5 minutes at 5000 rpm 1,5 ml of bacteria culture.
# Take the pellet and add 250 ul of resuspension buffer and pipet up and down a few times.(make sure that all is properly mixed)
# Take the pellet and add 250 ul of resuspension buffer and pipet up and down a few times.(make sure that all is properly mixed)
Line 27: Line 26:
# Let the tube open until it is dried. The pellet must turn from white to transparent.
# Let the tube open until it is dried. The pellet must turn from white to transparent.
# Add 20 ul of dH2O and freeze.
# Add 20 ul of dH2O and freeze.
-
 
-
 
=Transformation=
=Transformation=
We have E. Coli DH5α strain competent bacteria, with a transformation efficiency of 10
We have E. Coli DH5α strain competent bacteria, with a transformation efficiency of 10
-
 
'''Important!''' Competent bacteria should always be on ice.
'''Important!''' Competent bacteria should always be on ice.
-
 
# If the plasmid comes from the kit or is a product of ligation, add 2μl of plasmidic DNA into 50μl  
# If the plasmid comes from the kit or is a product of ligation, add 2μl of plasmidic DNA into 50μl  
-
 
of competent bacteria. If it’s a plasmid that comes from a miniprep, use a mass in function of  
of competent bacteria. If it’s a plasmid that comes from a miniprep, use a mass in function of  
-
 
the efficiency of the bacteria.
the efficiency of the bacteria.
-
 
# Incubate for 20 min on ice.
# Incubate for 20 min on ice.
-
 
# Heat Shock: 42°C for exactly 1’30’’, then immediately place on ice.
# Heat Shock: 42°C for exactly 1’30’’, then immediately place on ice.
-
 
# Incubate for 5 min on ice.
# Incubate for 5 min on ice.
-
 
# Recovery: Add 950μl of LB without antibiotic, incubate from 30 min to an hour at 37°C
# Recovery: Add 950μl of LB without antibiotic, incubate from 30 min to an hour at 37°C
-
 
# Pellet the bacteria by centrigue at 10000rpm for 5 minutes. Discard the supernatant of LB.  
# Pellet the bacteria by centrigue at 10000rpm for 5 minutes. Discard the supernatant of LB.  
 +
# Resuspend the bacteria in the remnant LB.
 +
# Plaque onto plates with LB and the desired antibiotic.
 +
# Incubate overnight in a stove at 37°C
-
Resuspend the bacteria in the remnant LB.
 
-
# Plaque onto plates with LB and the desired antibiotic.
+
=Digestion=
 +
 
 +
'''Important!''' In order to determine the appropriate buffer when digesting with more than one enzyme, refer to the universal selection chart by Invitrogen.
 +
 
 +
#Place in a tube the required volume of plasmidic DNA, up to 1 μg of DNA.
 +
#Add milliQ water to 17 μl.
 +
#Add 2 μl of 10X buffer. This way, the final concentration in 20 μl will be 1X.
 +
#Finally add 1 μl of each enzyme.
 +
#Incubate at least 1 hour at 37°C.
-
# Incubate overnight in a stove at 37°C
 
=Ligation=
=Ligation=
Line 63: Line 60:
# Add 2μl of digested plasmid backbone (or the equivalent of 25ng).
# Add 2μl of digested plasmid backbone (or the equivalent of 25ng).
-
 
# Add equimolar amount of EcoR1-HF Spe1 digested fragment (less than 3μl).
# Add equimolar amount of EcoR1-HF Spe1 digested fragment (less than 3μl).
-
 
# Add equimolar amount of Xba1 Pst1 digested fragment (less than 3μl).
# Add equimolar amount of Xba1 Pst1 digested fragment (less than 3μl).
-
 
# Add 2μl of T4 DNA ligase buffer (final concentration should be 1x).
# Add 2μl of T4 DNA ligase buffer (final concentration should be 1x).
-
 
# Add 0.5μl of T4 DNA ligase.
# Add 0.5μl of T4 DNA ligase.
-
 
# Add water to 10μl.
# Add water to 10μl.
-
 
# Ligate at 16°C for 30 min, then heat kill 80°C for 20min.
# Ligate at 16°C for 30 min, then heat kill 80°C for 20min.
-
 
+
# Transform with 1–2 μl of product.
-
# Transform with 1 – 2 μl of product.
+
=LB & LB agar=
=LB & LB agar=
-
# Liquid LB (1 litre)
+
'''Liquid LB (1 litre)'''
-
 
+
# 10g of bacto peptone (peptone, triptone or bactereologic triptone)
# 10g of bacto peptone (peptone, triptone or bactereologic triptone)
-
 
# 5g of yeast extract
# 5g of yeast extract
-
 
# 10g of NaCl
# 10g of NaCl
-
 
# Fill with dH2O
# Fill with dH2O
-
Autoclave.
 
-
TIP: if it is not going to be autoclaved in the next few hours water should not be added (because even
 
-
when in the fridge it will get contaminated), in which case everything can be measured and left ready to
+
'''LB agar (1 litre)'''
-
 
+
-
just add the water.
+
-
 
+
-
# LB agar (1 litre)
+
# 10g of bacto peptone (peptone, triptone or bactereologic triptone)
# 10g of bacto peptone (peptone, triptone or bactereologic triptone)
-
 
# 5g of yeast extract
# 5g of yeast extract
-
 
# 10g of NaCl
# 10g of NaCl
-
 
# 15g of agar
# 15g of agar
-
 
# Fill with dH2O
# Fill with dH2O
'''IMPORTANT''': agar does not dissolve if not heated so if Erlen-Meyers are prepared with LB agar, add LB in  
'''IMPORTANT''': agar does not dissolve if not heated so if Erlen-Meyers are prepared with LB agar, add LB in  
-
 
liquid form and then add the agar to the Erlen-Meyer according to the volume.
liquid form and then add the agar to the Erlen-Meyer according to the volume.
-
 
-
Autoclave.
 
-
 
-
'''TIP''': if it is not going to be autoclaved in the next few hours water should not be added (because even
 
-
 
-
when in the fridge it will get contaminated), in which case everything can be measured and left ready to
 
-
 
-
just add the water.
 
-
 
-
 
Line 160: Line 125:
1x until it is completely covered.
1x until it is completely covered.
 +
 +
= Fluorescene measurement =
 +
 +
# Take  1.5 ml aliquots of selected cultures.
 +
# Pellet the aliquots in a microcentrifuge (5 minutes 5000 g).
 +
# Resuspend the pellet in 500 µl MilliQ water.
 +
# Measure cell density (OD 600 nm).
 +
# Sonicate samples: four rounds of 15 seconds with 20% amplitude.
 +
# Measure fluorescence with a fluorimeter.
 +
# Normalize results by the culture density of the aliquots.
</div>
</div>

Latest revision as of 18:37, 27 September 2013

Contents

Miniprep

Materials

  1. Resuspension buffer
  2. Lysis buffer
  3. Neutralization buffer
  4. Isopropanol
  5. 70% Etanol
  6. dH2O
  7. Ice (in ice bucket/container)

Procedure

  1. Centrifuge for 5 minutes at 5000 rpm 1,5 ml of bacteria culture.
  2. Take the pellet and add 250 ul of resuspension buffer and pipet up and down a few times.(make sure that all is properly mixed)
  3. Add 250 ul of Lysis buffer and invert the tubes 5 times to mix. Let rest 5 minutes. The mix must turn transparent.
  4. Add 250 ul of cold Neutralization buffer and invert the tubes 5 times to mix. The mix must turn turbid.
  5. Centrifuge at 13.000 rpm for 15 minutes.
  6. Transfer the supernatant to a new clean eppendorf tube.
  7. Add isopropanol (the same volume that is in the tube). Mix many times and put it in ice for 20 minutes.
  8. Centrifuge at 13.000 rpm for 20 minutes.
  9. Eliminate the supernatant (be carefull that the pellet does not go with it)
  10. Add 1 ml of etanol 70% and use a vortex to ensure the pellet mixes with the etanol.
  11. Centrifuge at 13.000 rpm for 5 minutes.
  12. Eliminate all the supernatant with a pipette (be carefull that the pellet does not go with it)
  13. Let the tube open until it is dried. The pellet must turn from white to transparent.
  14. Add 20 ul of dH2O and freeze.

Transformation

We have E. Coli DH5α strain competent bacteria, with a transformation efficiency of 10 Important! Competent bacteria should always be on ice.

  1. If the plasmid comes from the kit or is a product of ligation, add 2μl of plasmidic DNA into 50μl

of competent bacteria. If it’s a plasmid that comes from a miniprep, use a mass in function of the efficiency of the bacteria.

  1. Incubate for 20 min on ice.
  2. Heat Shock: 42°C for exactly 1’30’’, then immediately place on ice.
  3. Incubate for 5 min on ice.
  4. Recovery: Add 950μl of LB without antibiotic, incubate from 30 min to an hour at 37°C
  5. Pellet the bacteria by centrigue at 10000rpm for 5 minutes. Discard the supernatant of LB.
  6. Resuspend the bacteria in the remnant LB.
  7. Plaque onto plates with LB and the desired antibiotic.
  8. Incubate overnight in a stove at 37°C


Digestion

Important! In order to determine the appropriate buffer when digesting with more than one enzyme, refer to the universal selection chart by Invitrogen.

  1. Place in a tube the required volume of plasmidic DNA, up to 1 μg of DNA.
  2. Add milliQ water to 17 μl.
  3. Add 2 μl of 10X buffer. This way, the final concentration in 20 μl will be 1X.
  4. Finally add 1 μl of each enzyme.
  5. Incubate at least 1 hour at 37°C.


Ligation

Important! Before starting the ligation process, make sure that the restriction enzymes are inactive.

  1. Add 2μl of digested plasmid backbone (or the equivalent of 25ng).
  2. Add equimolar amount of EcoR1-HF Spe1 digested fragment (less than 3μl).
  3. Add equimolar amount of Xba1 Pst1 digested fragment (less than 3μl).
  4. Add 2μl of T4 DNA ligase buffer (final concentration should be 1x).
  5. Add 0.5μl of T4 DNA ligase.
  6. Add water to 10μl.
  7. Ligate at 16°C for 30 min, then heat kill 80°C for 20min.
  8. Transform with 1–2 μl of product.


LB & LB agar

Liquid LB (1 litre)

  1. 10g of bacto peptone (peptone, triptone or bactereologic triptone)
  2. 5g of yeast extract
  3. 10g of NaCl
  4. Fill with dH2O


LB agar (1 litre)

  1. 10g of bacto peptone (peptone, triptone or bactereologic triptone)
  2. 5g of yeast extract
  3. 10g of NaCl
  4. 15g of agar
  5. Fill with dH2O

IMPORTANT: agar does not dissolve if not heated so if Erlen-Meyers are prepared with LB agar, add LB in liquid form and then add the agar to the Erlen-Meyer according to the volume.


Electrophoresis Gel

TAE 1x (diludde from TAE stock solution – 50x)

Agarose

Remember to use gloves during the entire process, being mindful not to have direct contact with

ethidium bromide.

  1. Add the necessary agarose into an Erlenmeyer flask and then add TAE, and fill with water. The

final concentration of agarose may depend on the type of gel needed, but usually will be 1%.

  1. Heat the flask, while covered, in a microwave until completely dissolved (should take no more

than 3 minutes at maximum potency)

  1. Add the necessary volume of Ethidium Bromide (about 10 μl for each 100g of gel)

IMPORTANT: Ethidium Bromide is carcinogenic. It should be handled with gloves, and these,

such as anything that has come in direct contact with Ethidium Bromide must be discarded

separately in an assigned discard bag.

  1. Pour the melted gel, with Ethidium Bromide, slowly into the gel tray. Add the combs and leave

until solified. Remove the combs. Rinse the flask with abundant water.

  1. Place the gel tray inside the gel box being mindful of the direction in which gel will run. Add TAE

1x until it is completely covered.


Fluorescene measurement

  1. Take 1.5 ml aliquots of selected cultures.
  2. Pellet the aliquots in a microcentrifuge (5 minutes 5000 g).
  3. Resuspend the pellet in 500 µl MilliQ water.
  4. Measure cell density (OD 600 nm).
  5. Sonicate samples: four rounds of 15 seconds with 20% amplitude.
  6. Measure fluorescence with a fluorimeter.
  7. Normalize results by the culture density of the aliquots.