Preparation of competent Bacterial cells

Preparation of the Bacterial culture

1. Recuperate the overnight bacterial culture
2. Determine the OD600 in a 1 mL Tank Spectro, dilute a 100µl of culture in 900µl of distilled LB
3. In 1L Erlenmeyer add 200 ml of LB and an appropriate volume of culture to have an OD600 = 0.1
4. Put the Erlenmeyer in an incubator for about an hour at 37˚C.
5. Test the OD600 for the new culture
6. The OD600 should be between 0.4 and 0.6

All the handling done in a 15cm radius of an open flame for optimal sterility

Preparation of Buffer Tbf1 and Tbf2

Some solution aren’t available directly and are prepared by dissolving the solid compound

Sterilize the flask prepared after weighing in an autoclave. When preparing Tbf1 and Tbf2 should be in proximity of an open flame

Preparation of Competent Bacterial cells

1. Transfer the Bacterial culture in 50 ml Falcon tubes
2. Centrifuge for 10 minutes at 3500 rpm in cold
3. Remove the supernatant then re-suspend the pellet in 20 ml of Tbf1 for each falcon tube
4. Poll in all bacterial culture in two Falcon tubes with 40 ml each
5. Centrifuge for 5 minutes at 3500 rpm in cold
6. Remove the supernatant then re-suspend the pellet in 4 ml of Tbf2 for each falcon tube
7. Allocate 220 µl of competent Bacterial cells in each eppendorf tube
8. Instant freeze the eppendorf tubes in liquid nitrogen
9. Conserve the tubes at -80˚C

NOTE: all handling done in a cold room. To re-suspend the pellet a hard jerking action applied on the tube. Alternatively, put on wheel for 10 minute.

Transformation protocol

Sensitivity test of competent bacterial cells

1. Heat up LB-agar in micro oven at 300Watt for 19 minutes for 400 mL of LB-agar loosen cap before heating to let steam out
2. Transfer 80 mL of LB-agar in to Erlenmeyer one for every antibiotic
3. Pour 20 mL and spread the LB-agar in petri dishes, let it dry out
4. Prepare petri dishes:

25µL of competent strain spread with glass beads in all four antibiotic and one without antibiotic as negative test

Handling is done near an open flame, sterile environment

Preparation of DNA material from iGEM kit

1. Pierce plate at the desired location
2. Hydrate by injecting 10µL of ddH2O
3. Let it soak for 5 minutes until red coloration is highly visible
4. pipet up-down to homogenize the solution
5. Transfer the solution into an eppendorf tube set it on ice

No special conditions needed when manipulating just respect sterility

Transformation of bacterial cells with plasmid/ligation

1. Add an adequate quantity of DNA in eppendorf tube
2. Add 100 µL(50 µL) of competent bacterial cells
3. Put on ice for 20 minutes
4. Put tubes in thermomixer at 42˚C for 45 seconds
5. Put on ice for 5 minutes
6. Add 450 µL (900 µL) of LB
7. Incubate tube for 1 hour at 37˚C
8. Centrifuge for 5 minutes at 5000rpm (normal centrifuge will work)
9. Remove 400 µl(850 µL) of supernatant
10. Re-suspend pellet in the 150 µL of remaining medium pipet up-down
11. Spread total volume on petri dish with the appropriate antibiotic
12. Put petri dishes in an incubator overnight at 37˚C

For a negative control repeat procedure without adding plasmid

Handling is done near an open flame, sterile environment

Procedures

1. Digest vector with restriction enzyme(s) overnight, and purify the linearized vector with a commercial PCR purification kit. Elute the DNA with elution buffer or 10mM TrisCl, pH 8.0-8.5. Do not elute the DNA with water or TE. Measure the concentration of the vector.

2. Amplify your gene pf interest by PCR using primer with ≥ 15 mer homology extension to the linearized vector end. We usually use 15bp homology for single fragment cloning, and 20 bp homology for multiple fragment cloning. Purify the linearized vector with a commercial PCR purification kit. Elute the DNA with elution buffer or 10 mM TrisCl, pH 8.0-8.5. Do not elute the DNA with water or TE. Measure the concentration of the insert(s).

3 .Mix the linearized vector and insert at a molar ratio of 1:2 in a 1.5 ml tube. An example is shown as follows. (Vector to insert molar ratio of 1:1 to 1:7 works well, but we usually use 1:2 for single fragment cloning 1:2:2 for multiple fragments cloning. An example of 3 fragment cloning is shown below with vector: insert 1: insert 2 molar ratio is 1:2:2 as shown

4 .Add 0.2 µL of T4 DNA polymerase (3 U/µL,NEB) to the mixture and incubate at room temperature for 2.5 min. we found that 0.5µL(1.5 U) of T4 DNA polymerase gives the best result, But 0.2 µL gives more than sufficient number of colonies.

5 . Put the reaction mixture on ice immediately to stop the reaction and incubate on ice for 10 min

6 .Thaw chemically competent E.coli cells on ice for ~ 10 min

7 .For single fragment cloning, gently mix the cells with 1-2 µL of the reaction mixture and incubate the cells on ice for 20 min. for multiple fragments cloning, mix the cells with 3-5 µL of the reactant.

8 .Incubate the cells on ice for 20 min.

9 .Heat shock the cells at 42˚C for 45 sec

10 .Incubate the cells on ice for 2 min.

11 .Add 900 (or 950) µL of LB broth to 100 (or 50) µl of cells and transfer the cells to 15 ml round-bottom tube.

12 .Incubate the cells at 37˚C for 1 hour

13 .Plate the cells on agar plates containing suitable antibiotics (eg.100 µg/mL ampicillin). We usually spread 10 to 20 µL of cells onto an agar plate to get optimal number of colonies per plate for single fragment cloning, and 100 µL per plate for multiple fragments cloning. In case of 10-20 µL spreading, cells needs to be further silted with 80~ 90 µL LB broth for suitable spreading.

14 .Incubate the plates at 37˚ for 16 hr and analyze the colonies

Reaction setup

• Add the following component as listed below

• Assemble all reaction components on ice and quickly transfer the reactions to thermocycle preheated to 94°C and begin thermocycling

Hint: make a premix of the components mentioned without DNA template and allocate appropriately 12 µL in each pcr tube

Thermocycling conditions for a routine PCR

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Re-suspending gene fragments

1. Centrifuge for 5 seconds at 3000g
2. Add 20 µL of H₂O to the tube for a final concentration of 10ng/µL
3. Briefly vortex and centrifuge
4. Tube can be stored at -20˚C

Digest with the restriction endonucleases

• Add the following components

• Incubate for 45 minutes at 37˚C
• Incubate for 20 minutes at 80˚C

Gene Fragment and vector digested separately

Ligation

• Add the following components in the order listed below

• calculate insert to vector quantities by this equation :required mass insert (ng) = desired insert/vector molar ratio x mass of vector (ng) x ratio of insert to vector lengths

• Centrifuge for 5 seconds at 3000g
• Incubate at 16˚C overnight

Transformation

• Reapeat protocol as mentioned previously

Digestion protocol for biobrick assembly

• prepare the compounds as mentioned separately in eppendorf tubes

Upstream Part digest :

Downstream part digest :

Destination plasmid digest :

Incubate all three-restriction digest reactions at 37˚C for 30 minutes and then heat inactivate at 80˚C for 20 minutes. Short spin to recuperate water condensation

Ligation protocol for biobrick assembly

Incubate at room temperature for 10 minutes Transform 2 µL of the ligation product into 50 µL of competent bacterial cells

1- Preparing the agarose gel

• Measure 0.8g of agarose powder and add 100 mL of TAE 1X
• Melt in a micro oven until solution becomes clear
• Let it cool; swirl occasionally to cool evenly until warm to the touch
• Pour the melted agarose solution into the casting tray and let cool until it is solid

2- Loading the gel

• Add enough TAE 0.5 buffer so that there is about 2-3 mm of buffer over the gel
• Add 1X loading dye to each PCR reaction
• Record the order each sample will be loaded on the gel
• Pipette each sample into separate wells in the gel
• Pipette 5µL of DNA ladder standard into at least one well

3- Running the gel

• Turn on the power supply to about 135 volts let it run for about 25 minutes
• Check to make sure that the current is running in the correct direction by observing the movement of the dye

4- Revelation

• Soak into gel red for 10 minutes
• Put the gel under UV
• Make a copy of the image

Mini prep protocol

1-Material preparation

• Centrifuge Lyse bleu and RNase samples
• Add 20 µL of Lyse to 20 ml of Buffer P1
• Add 200 µL of RNase to previous mix

This mix is considered as buffer P1

2- Culture preparation

• Centrifuge for 2 minutes at 13000 rpm bacterial culture, remove supernatant
• Re-suspend pellet with 250 µL of P1 buffer, pipette up-down
• Add 250 µL of P2 buffer mix thoroughly by inverting the tubes 4-6 times
• Add 350 µL of N3 buffer mix immediately and thoroughly by inverting the tubes 4-6 times
• Centrifuge at 9000 rpm for 10 minutes

3- DNA material separation process

• Transfer 800µL of supernatant to the spin column that should be in a tube
• Centrifuge at 9000 rpm for 45 seconds, discard flow through
• Add 0.5 ml of PB buffer
• Centrifuge at 9000 rpm for 45 seconds ,discard flow through
• Add 0.75 ml of PE buffer
• Centrifuge at 9000 rpm for 45 seconds ,discard flow through
• Centrifuge at 9000 rpm for 1 minute , discard collection tube
• Transfer column to a new eppendorf tube
• Add 50 µL of H2O let stand for 1 minute
• Centrifuge at 9000 rpm for 1 minute
• Keep flow through, discard column

No special condition while preparation. After adding P2, mix N3 in less than 5 minutes

Gel and PCR Clean up

Wash buffer NT3 preparation

1- Adjust DNA binding condition/Excise DNA fragment

• Mix one volume of sample with 2 volumes of buffer NT1 for PCR sample
• Add 200 µL of NT1 buffer for each 100mg of agarose gel
• Incubate sample for 5-10 minutes at 50˚C. vortex if needed to completely dissolve gel

2- Bind DNA

• Place PCR Clean up column into collection tube 2 mL
• Load up to 700 µl of sample with NT1 buffer
• Centrifuge for 30 seconds at 11 000 g
• Discard flow through and place column back

3- Wash silica membrane

• Add 700 µL of NT3 buffer
• Centrifuge for 30 seconds at 11000 g
• Discard flow through and place column back

4- Dry silica membrane

• Centrifuge for 1 minute at 11 000 g
• Discard flow through

5- Elute DNA

• Place column into new 1.5 mL micro centrifuge tube
• Add 15-30 µL of ddH2O
• let it settle for 1 minutes
• Centrifuge for 1 minutes at 11 000 g

Note don’t discard flow through

5’- Elute DNA > 1000 bp

• Heat ddH2O to 70˚C
• Incubate ddH2O on column for 5 minutes
• Add 20-30µL of ddH2O
• Centrifuge for 1 minute at 30-50 g
• Centrifuge for 1 minute at 11 000 g
• Repeat elution 2 to 3 times for the best result

Phages in soil duration protocol

Preparation :

We need a 2 OD of F+ E.Coli : Dilute bacteria 10x to read and incubate till getting 0.2 DO. vvv Our phage concentration have to be lower than the bacterial concentration, we’ll use a 2.10⁸ pfu of bacterias. So we will use 10µL of 100x times diluted phage mix : 10⁷ pfu phages per use.

Bacteriophages counting test :

Add 1 mL of bacterias solution + 100µL of phage 10⁸ pfu/mL solution Incubate for 1h at room temperature (25°C) + 300 rpm agitation Spread 150µL of mix on Kanamycin plate (LBA) and let it grow ON Count colonies

Soil preparation :

Pickup ~250 g of soil Sift it to get only soil and discard rocks and heavier objects : keep only 200g Store it in a 500 mL erlenmeyer with a cap that allows air to go through and place it near sunlight to imitate natural conditions. Use the diluted virus mix (1,42 µL of 7.10⁸ phages in 50 ml) and add it to soil erlenmeyer, agitate to mix

T+ / T- :

T⁺ : soil extract (without phage) + added phage right before incubating T⁻ : soil extract (without phage) T- : Water

Recuperation :

Add 10g of soil + 20 mL of sterile water in a 50mL falcon tube Spin 1 500 g : 10 min and transfer supernatant into an ultracentrifugation tube Spin for 10 min at 10 000g and transfer supernatant into filter unit (0,22µm) In 2 1,5 mL tubes, put 500 µL of the filtrated solution and 500µL of DO=2 GM1 bacteria Incubate for 30 min at 25°C with slow shaking Spin at 5000 rpm for 10 min Discard 925µL of supernatant Resuspend pellet of the first tube Transfer into the second Resuspend Spray on kanamycin dish Incubate overnight

Production of large quantities of helper phage

Requirement :

110 mL PEG/NaCl (from powder : 16 g NaCl + 22 g PEG 8000) - 14 mL PBS - 3 mL H-top Agar - LB - 2,5 mL Kanamycin 10 - 1 plate without antibiotics.

Prepare a TG1 starter from glycerol or plate

Overnight

Needed DO = 0,4-0,5 : dilute in LB and put at 37°C for 20 min In an eppendorf tube, infect 200µL bacteria with 10µL phage solution Incubate for 30 min without shaking In a 15mL Falcon tube, add 3 mL of H-top agar (42°C) Spread on LBA plate (no antibiotics)

Overnight

Make a 0,4 DO TG1 5 ml starter, pick a small plaque at let it grow for 2h at 37°C with shaking in the starter In a 2L flask : pour the starter and add 500 mL of 2YT (TB) Add 2,5 mL of kanamycin

Overnight

In a 500 mL tube, spin for 45 min at 5000 g (10800 15 min) Recover 400 mL of supernatant in an 1L erlenmeyer Add 100 mL of PEG/NaCl From now, every step has to be on ice or at 4°C Spin for 1h30 at 5000 g in the 500mL tubes (10800 g 30 min) Throw away supernatant Resuspend pellet in 8 mL PBS and add 2 mL of PEG/NaCl Vortex for 30s Put in a 15 mL Falcon Let in ice for 30 min Spin for 30 min at 3300g Remove supernatant Add 5 mL of PBS Resuspend pellet Spin for 30 min at 5000 g (11000 g 10 min) Add 500µL of chloroform Spin for 30 min at 5000 g Keep supernatant Add 10µL of chloroform

Storage : 15% glycerol at -80°C

Mesure of biofilm density

• Add a drop of CV in each well (pipette). I let colore 10 minutes at 30°C
• Blow the liquide
• Rince twice with water MiliQ
• Add 250µl physiologic water (0.9% NaCl) + ethanol 60%
• Agitation during 2 minutes
• Mesure OD570nm and OD600nm plaque bottom TECAN
• Agitation during 2 minutes (amplitude 3mm orbitale)
• Mesure OD600 above through the plaque (25 flashes)
• The OD600 is proportional to biofilm production

Creation of phage-fluorescence with carboxyfluorescein

Requirement: 200µL of Napi 0.5M - 500µL of DMSO (diméthyl sulfoxyde) - 100 mg of carboxyfluorescein - 28 ml of PBS 1X

Prepare a solution of 1 mL of purified phages with a concentration of 7x10^8
Dilute 100 mg of carboxyfluorescein in 500µL of DMSO in an eppendorf wrap up with foil.
Add 20µL of fluorophore solution in phages solution
Keep at 4°C during 1 hour
Transfer the complete solution in a dialyse membrane (cutoff 30 kDa) set in a 15mL falcon tube containing 14ml of PBS.
Agitate for 1h30 then change the buffer solution. Let it dialyze overnight. The excess of fluorochrome which will not be fixed on phages will pass the membrane.