DH5α competent cells preparation

1. The day before the preparation, make overnight starters with 100 µL of bacterial cells diluted in 5 mL of LB in a 50 mL Erlenmeyer.
   
2. The next day, recover your starters and seed 1/60 bacterial cells in 200 mL of LB, then incubate at 37°C and 180 rpm.
   
3. Keep measuring the OD600. When it's between 0,4 and 0,6, recover your cells an pool them in cold 50 mL Falcon tubes.
   
4. Prepare buffers 1 and 2 and put them on ice. Put Eppendorf tubes and 50 mL Falcon tubes, and pipette tips at -80°C for future use.
   
5. Centrifuge tubes at 4000 rpm and 4°C for 10 minutes.
   
6. Discard supernatant and resuspend each Falcon tube in 20 mL of buffer 1. Afterward, centrifuge at 3500 rpm and 4°C for 5 minutes.
   
7. Discard supernatant and resuspend each Falcon tube in 8 mL of buffer 2.
   
8. Take 100 µL aliquots in Eppendorf tubes and stock them at -80°C.
   

Cloning

Digestion

1. Samples preperation

1. Incubate the mixture at 37°C for 3 hours.
   
2. Clean-up the product using the monarch kit.
   

Ligation

1. Incubate at 37°C for 5 hours.

Transformation

1. Recover the needed number of competent cells tubes, adding an additional negative control tube.
2. Add DNA (1µL) into the competent cells tubes.
3. Incubate tubes on ice for an hour.
4. Incubate tubes at 42°C for 2 minutes for thermal choc.
5. Leave tubes on ice for 5 minutes.
6. Leave tubes at room temperature for 5 minutes.
7. Add 1 mL of LB per tube, then incubate for 1 hour at 37°C and 180 rpm.
8. Spread cells on Petri dishes and incubate overnight at 37°C.

Monarch PCR and DNA cleanup kit

All centrifugation steps ~13000 rpm in a typical microcentrifuge. This ensures all traces of buffer are eluted at each step.

1. A starting sample volume of 50 μL is recommended. For smaller samples, nuclease-free water can be used to adjust the volume. Add 100 μL DNA Cleanup Binding Buffer to the 50 μL sample.
2. Insert a column into a collection tube, load sample onto the column and close the cap. Spin for 1 minute, then discard flow-through.
3. Re-insert column into the collection tube. Add 200 μL DNA Wash Buffer and spin for 1 minute. Discard flow-through.
4. Repeat Step 5. This step is recommended for removal of enzymes that may interfere with downstream applications.
5. Spin for 1 minute.
6. Transfer column to a clean 1.5 ml microfuge tube. Use care to ensure that the tip of the column does not come into contact with the flow-through. If in doubt, re-spin for 1 minute to ensure traces of salt and ethanol are not carried over to the next step.
7. Add 15 μL of hot water (70°C) to the center of the matrix. Wait for 1 minute, then spin for 1 minute to elute the DNA.
8. Repeat step 6.

Monarch miniprep kit

All centrifugation steps ~13000 rpm in a typical microcentrifuge. If precipitate has formed in Lysis Buffer (B2), incubate at 30–37°C, inverting periodically to dissolve. Store Plasmid Neutralization Buffer (B3) at 4°C after opening.

1. Pellet 1–5 mL bacterial culture (not to exceed 15 OD units) by centrifugation for 30 seconds. Discard supernatant.
2. Resuspend pellet in 200 μL Plasmid Resuspension Buffer (B1) (pink). Vortex or pipet to ensure cells are completely resuspended. There should be no visible clumps.
3. Lyse cells by adding 200 μL Plasmid Lysis Buffer (B2) (blue/green). Invert the tube immediately and gently 5–6 times until color changes to dark pink and the solution is clear and viscous. Do not vortex! Incubate for 5 minutes.
4. Neutralize the lysate by adding 400 μL of Plasmid Neutralization Buffer (B3) (yellow). Gently invert tube until the color is uniformly yellow and a precipitate forms. Do not vortex! Incubate for 2 minutes.
5. Clarify the lysate by spinning for 10 minutes at ~13000pm.
6. Carefully transfer supernatant to the spin column and centrifuge for 1 minute. Discard flow-through.
7. Re-insert column in the collection tube and add 200 μL of Plasmid Wash Buffer 1. Plasmid Wash Buffer 1 removes RNA, protein, and endotoxin. Centrifuge for 1 minute. Discard flow-through.
8. Add 400 μL of Plasmid Wash Buffer 2 and centrifuge for 1 minute.
9. Centrifuge for 1 minute one more time.
10. Transfer column to a clean 1.5 mL microfuge tube. Use care to ensure that the tip of the column has not come into contact with the flow-through. If there is any doubt, re-spin the column for 1 minute before inserting it into the clean microfuge tube.
11. Add ≥ 15 μL Hot Water (70°C) to the center of the matrix. Wait for 1 minute, then spin for 1 minute to elute DNA.

Beauveria bassiana competent blastospores

Ying, S.H., Feng, M.G., 2006. Novel blastospore-based transformation system for integration of phosphinothricin resistance and green fluorescence protein genes into Beauveria bassiana. Applied Microbiology and Biotechnology 72, 206–210

1. Dilute conidiospores in sabouraud dextrose medium and incubate for 2 days at 120 rpm and 25°C.
2. Transfer 5 mL aliquots into 50 mL medium with the following products (glucose 4%, NH4NO3 0,4%, KH2PO4 0,3%, and MgSO4 0,3%) and incubate for 1 day at 120 rpm and 25°C.
3. Filter conidiospores using lens paper and a steril erlenmeyer.
4. Centrifuge for 5 minutes at 660 g and 4°C.
5. Discard supernatant and wash in ddH2O twice by centrifugation for 5 minutes at 660 g and 4°C.
6. Resuspend in 1 mL of lithium acetate (0.1M).
7. Transfer into 15 mL Falcon tubes, then centrifuge for 5 minutes at 4°C and 4720 g.
8. Resuspend in 0.5 mL of lithium acetate (0,1M).
9. Take 100 μL aliquots in glycerol (90%).
10. Stock 50 μL aliquots at -80°C.

Sabouraud medium preperation

For solid medium, mix the following products in ddH2O while maintaining the pH at 5.6:
10 g/L of mycological peptone (enzymatic digest of casein and animal tissues).
40 g/L of glucose.
15 g/L of agar.

For liquid medium, don't add agar.

IPTG induced protein production

Production

1. Prepare 6 starters (20 mL LB and chloramphenicol): control BL21 (No plasmid), BL21 with the plasmid in duplicates, control DH5α (No plasmid), and DH5α with the plasmid in duplicates. Incubate overnight at 37°C and 180 rpm.
   
2. The next day, recover the overnight starters and measure the OD600.
   
3. Make 1/60 dilutions and incubate at 37°C to reach 0.7 in OD600.
   
4. Add (For one of the duplicates) IPTG (1M) (10µL for 20 mL) to induce the protein production in BL21 and DH5α with the plasmid.
   
5. Incubate at 16°C, 30°C, and 37°C for 5 hours.
   
6. Leave the remaining cultures at 37°C for 5 hours. Incubate the cultures at 16°C overnight.
   
7. After 5 hours, measure the OD600 and take 1 mL aliquots.
   
8. Centrifuge aliquots for 10 minutes at 13000 g. Discard supernatant and stock samples at -20°C.
   
9. For the remaining cultures, pour the remaining volumes into 50 mL Falcon tubes and centrifuge for 20 minutes at 4700 g and 4°C. Discard supernatant and stock samples at -20°C.
   
10. The next day, measure the OD600 of the culture at 16°C, take 1 mL aliquots, then repeat steps 8 and 9.
    

Electrophoresis gel migration

1. Add TSTD (1X) at 50 µL/OD unit to the 1 mL aliquots. Do not resuspend.
   
2. Put samples in the dry bath incubator for 20 minutes.
3. Prepare the migration apparel and charge the gel (20 µL for samples, and 5 µL for the ladders).
4. Start migration at 0.04 A for an hour.
5. Incubate gels in Coomassie blue for an hour.
6. Wash gels with acetic acid till they're transparent.
7. Once the gel is clear, add ddH2O and stock at 4°C.
   

Polymerase Chain Reaction (PCR)

Taq DNA polymerase

Setup the reaction mixture listed below on ice.

Q5 High-Fidelity 2X master mix

EconoTaq PLUS GREEN 2X master mix (For colony-PCR)

Exponential megapriming PCR (EMP)

Digest the PCR product (To cut the methylated GATC sites) as listed below

Inucubate at 37°C for 4 hours.

Protein purification

Cell lysis and protein extraction

1. Prepare a 1L starter cell cultures and incubate at the optimal conditions tested out during the first protein production.
   
2. Centrifuge for 20 minutes at 4500 rpm and 4°C . Discard supernatant.
   
3. Resuspend pellet in a lysis buffer (50 mM Tris-HCl (pH=8), 50 mM NaCl, 1 mM EDTA, 0.1 mg/L DNase, and an anti-protease tablet).
   
4. Put on agitator for 30 minutes at 4°C .
   
5. Disrupt the cells using the emulsiflex.
   
6. Ultracentrifuge for 35 minutes at 20000 rpm and 4°C .
   
7. Transfert supernatant into 50 mL Falcon tubes and discard pellets.
   

Protein purification

The purification uses the ÄKTA pure system with HisTrap™ columns.

1. Wash the column with 5 H2O volumes to eliminate all ethanol.
   
2. Wash the column with 5 buffer A (50 Mm Tris-HCl (pH=8), 50 mM NaCl) volumes.
   
3. Inject the supernatant from the protein extraction in the HisTrap™ column. Discard flowthrough.
   
4. Elute the column with 10 buffer A volumes. Discard flowthrough.
   
5. Using a 0 to 100% gradient, elute the column with buffer B (Buffer A + 500 mM imidazol). Collect flowthrough gradually in 1 mL fractions.
   
6. Recover the collected fractions and verify the purification on a SDS-PAGE gel.
   
7. Quantify the purified protein on the NanoDrop.
   

Western blot