74. Culture of BL21DE3
75. Dephosphorylation of pET43.1a(+)
76. Digestion of the new inserts
77. Electrophoresis on agarose gel
78. Ligation of the inserts
79. Transformation of competent cells
80. Results of the culture of BL21DE3 (July 11, 2016)
81. Protein gel
82. Extraction of pET43.1a(+)
Aim:Make a growth curve and induce the production of protein. We will start producing our protein in bacterial cells. In order to do that we need to have an idea of the growth profile of the cells with this construct inside. This will determine at what time we can induce the expression of our protein. Protocol: follow in this link What we did in the lab: Materials: • Erlenmeyer flasks 250 ml capacity, IPTG (Iso-propyl β thio galactopyranoside) 0.5 M, LB media, carbenicillin at 50 mg/ml, shaking incubator (Infors HT), spectrophotometer. Method: 1. 2 x 250 ml Erlenmeyer, put 25 ml of LB and 25 µl of carbenicillin at 50 mg/ml 2. then add in one colony of BL21DE3 pLys S with C2 1.2 and in the other flask add one with C 1.1 3. put them 1 hour at 37°C and 180 RPM 4. Store the master plate (reference) at -4°C and make a copy plate grown at 37°C, then stored at 4°C. 5. Measure absorbance at 600 nm (Abs 600 nm) to make a growth curve (Ultrospec 3100 pro, GE Lifesciences) using plain plastic cuvettes, 1 cm path length.
| Time | C2 1.1 Abs 600 nm | C2 1.2 Abs 600 nm |
|---|---|---|
13h59 |
0.128 | 0.044 |
| 14h25 | 0.168 | 0.095 |
| 14h50 | 0.282 | 0.188 |
| 15h17 | 0.387 | 0.262 |
| 15h32 | 0.722 | 0.620 |
| 16h07 | 0.675 |
Aim:after the digestion we dephosphorylated it to prevent that pET43.1 to religates without the insert. Protocol: follow in this link What we did in the lab: Method: In a 1 ml Eppendorf, we put: - 25 µl of pET43.1 (3 µg/50 µl) - 2 µl of buffer Cutsmart 10X - 1 µl of SAP TOTAL = 28 µl
Aim:Integrate the inserts into the plasmid Protocol:follow in this link
Aim:Purify the digested inserts (C1/C2/B1/B2) and the plasmid before the ligation. Protocol: follow in this link What we did in the lab: Method: 1. make a 0.7% agarose gel 2. do an electrophoresis following the deposit table L1: ladder (Gene Ruler) L3: B1 L5: B2 L7: C1 L9: C2 3. we extract the DNA purified o the gel with QIAGEN extraction kit. We follow the kit step Gel mass: B1: 304 mg B2: 382 mg C1: 378 mg C2: 451 mg
Aim:To Prepare our plasmids for the transformation. Protocol: follow in this link What we did in the lab: Method: For each insert, we make two samples.
| 1:1 | 1:3 | |
|---|---|---|
DNA (200 ng) |
4 µl | 4 µl |
Insert B1/B2/C1/C2 (version 2) |
4 µl | 12 µl |
T4 ligase |
1 µl | 1 µl |
Buffer 10X |
2 µl | 2 µl |
H20 |
9 µl | 1 µl |
TOTAL |
20 µl | 20 µl |
Aim:Transform our plasmids into competent cells to amplify the DNA. Protocol: follow in this link What we did in the lab: Method: Moreover, we spread the competent cells from July 7,2016 on petri dishes to have new colonies.
Aim:Check if the bacteria that were induced by IPTG have produced the protein (weight = 30 kDa). What we did in the lab: Materials: • mini protean TGX 4-15% precast gels (BioRad) • TGS Buffer 10X • Electrophoresis chamber • Samples of our culture C2 1.1 (-) IPTG C2 1.1 (+) IPTG C2 1.2 (-) IPTG C2 1.2 (+) IPTG Method: 1. Put the gel in the electrophoresis chamber, take off the green parts off the gel before 2. Fill the chamber with the buffer 1X 3. Follow the deposit table: L1: 8 µl ladder protein Thermofisher (PAGE Ruler plus) L3: 17 µl of C2 1.1 (-) IPTG L6: 17 µl of C2 1.1 (+) IPTG L8: 17 µl of C2 1.2 (-) IPTG L10: 17 µl C2 1.2 (+) IPTG In each eppendorg we added: - 10 µl of protein solution - 10 µl of laemli 2X Heat the samples at 95°C for 5 min to denature the protein 4. start of migration at 130 V 5. Stop the migration about one hour later 6. Open the plastic content to get back the gel 7. Wash three times five minutes in distilled H20 8. Fill a cuve with Bleu de Coomassie and let color the gel during 30 minutes. Let one hour more if required 9. Wash distilled H20 until the bands appear Results: It seems to have a slight band for C2 11 (+) IPTG that could be our protein but this band doesn’t appear in C2 1.2 (+) IPTG. We decided to let it the whole weekend in distilled H20 to analyze the bands.
Aim:To get back the plasmid from the cultures made on the July 11, 2016. Protocol: follow in this link What we did in the lab: Method: Once, the DNA has been pelleted let the Eppendorf open to evacuate the ethanol (all the week-end).
