Paris/August 22
From 2007.igem.org
(→Plasmids: MiniPrep Products) |
(→Preparing chemically competent cells) |
||
Line 118: | Line 118: | ||
*w121 | *w121 | ||
*FX85 | *FX85 | ||
+ | |||
+ | 1. Grow a 5ml overnight culture of cells in LB media. In the morning, dilute this culture back into 25-50ml of fresh LB media in a 200ml conical flask. You should aim to dilute the overnight culture by at least 1/100.<br> | ||
+ | 2. Grow the diluted culture to an OD600 of 0.5.<br> | ||
+ | 3. Put 500µL eppendorf tubes on ice so that they are cold when cells are aliquoted into them later. If your culture is X ml, you will need X tubes. At this point you should also make sure that your TSS is being chilled.<br> | ||
+ | 4. Split the culture into two 50ml falcon tubes and incubate on ice for 10 min. | ||
==Transformation of W121 and FX85 strains == | ==Transformation of W121 and FX85 strains == |
Revision as of 10:33, 22 August 2007
Contents |
Minipreps of Ligation transformation strains from yesterday
Plasmids: MiniPrep Products
Plasmids: MiniPrep Products | ||||
---|---|---|---|---|
Number | Name | Description | Products in use | Date |
L31 | Lox71>>B0015 Terminator | Ligation of B0015 Terminator behind Lox71 | L31.1, L31.3, L31.4 | August 20 |
L32 | B0015 Terminator>>Lox66 | Ligation of B0015 Terminator before Lox66 | L32.1, L32.2, L32.3 | August 20 |
L34 | Lox71-GFP-Ter dans J61002 | L34.1, L34.2, L34.3 | August 20 | |
L35 | AraC pBAD >> Lox71-GFP-Ter | L35.1, L35.2, L35.3 | August 20 | |
L36 | Lox66 >> mRFP | L36.1, L36.2, L36.3 | August 20 | |
L37 | Lox66 >> RBS-DapA Coli | L37.1, L37.2, L37.3 | August 20 | |
L39 | RBS DapA Coli BB dans pSB1A2 | L39.1, L39.2, L39.3 | August 20 | |
L40 | RBS DapA Subtilis BB dans pSB1A2 | L40.1, L40.2 | August 20 | |
L41 | CRE ORF >> lox71 FtsZ dans pSB1A2 (D47) | L41.1 | August 20 | |
L42 | CRE ORF >> lox71 FtsZ+A dans pSB1A2 (D47) | L42.1, L42.2, L42.3 | August 20 | |
L43 | RBS-DapA Subtilis FI >> CRE ORF dans pSB1A2 (D48) | L43.1, L43.2, L43.3 | August 20 |
Growth kinetic on w121 strains
In order to precise the growth behavior/kinetics of our strain W121 in smaller DAP concentration, we fit those last ones in function of our last kinetics results (06/08/07)
Kinetic Array :w121 kinetic as a function of DAP and supplemented medium (S0.x) | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | |
A | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 |
B | H20 | LB+0µM DAP | LB+5µM DAP | LB+8µM DAP | LB+10µM DAP | LB+12µM DAP | LB+15µM DAP | LB+17µM DAP | LB+20µM DAP | LB+30µM DAP | LB+40µM DAP | H20 |
C | H20 | S0.2+0µM DAP | S0.2+5µM DAP | S0.2+6µM DAP | S0.2+7µM DAP | S0.2+8µM DAP | S0.2+9µM DAP | S0.2+10µM DAP | S0.2+15µM DAP | S0.2+17µM DAP | S0.2+20µM DAP | H20 |
D | H20 | S0.4+0µM DAP | S0.4+2µM DAP | S0.4+3µM DAP | S0.4+4µM DAP | S0.4+5µM DAP | S0.4+8µM DAP | S0.4+10µM DAP | S0.4+12µM DAP | S0.4+15µM DAP | S0.4+20µM DAP | H20 |
E | H20 | S0.6+0µM DAP | S0.6+1µM DAP | S0.6+2µM DAP | S0.6+3µM DAP | S0.6+4µM DAP | S0.6+5µM DAP | S0.6+6µM DAP | S0.6+7µM DAP | S0.6+8µM DAP | S0.6+10µM DAP | H20 |
F | H20 | S0.8+0µM DAP | S0.8+0,5µM DAP | S0.8+1µM DAP | S0.8+2µM DAP | S0.8+3µM DAP | S0.8+4µM DAP | S0.8+5µM DAP | S0.8+6µM DAP | S0.8+7µM DAP | S0.8+10µM DAP | H20 |
G | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 |
H | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 | H20 |
The 96 well plate is surrounded by H2O in order to maintain humidity during the assay. In each slot, 200µL of the growth medium (LB or S0.x) is mixed with 2µL of w121 culture grown ON, and with different amount of DAP (see table). The growth profile is measured over a period of 20H, a DO measurement is acquired each 4min10s.
Preparing chemically competent cells
- w121
- FX85
1. Grow a 5ml overnight culture of cells in LB media. In the morning, dilute this culture back into 25-50ml of fresh LB media in a 200ml conical flask. You should aim to dilute the overnight culture by at least 1/100.
2. Grow the diluted culture to an OD600 of 0.5.
3. Put 500µL eppendorf tubes on ice so that they are cold when cells are aliquoted into them later. If your culture is X ml, you will need X tubes. At this point you should also make sure that your TSS is being chilled.
4. Split the culture into two 50ml falcon tubes and incubate on ice for 10 min.