"
Team:Heidelberg/Notebook/Killing II/12thweek
From 2008.igem.org
(Difference between revisions)
(→Wednesday 10/22/2008) |
(→Wednesday 10/22/2008) |
||
| Line 582: | Line 582: | ||
**after adjustment of the OD of the different cultures (killer, reference killer, prey), mixtures of different rations were done and transfered to a 96 well plate for ON measurement after following schemes | **after adjustment of the OD of the different cultures (killer, reference killer, prey), mixtures of different rations were done and transfered to a 96 well plate for ON measurement after following schemes | ||
[[Image: 081022_killer_prey_legend.jpg | 600 px | center]] | [[Image: 081022_killer_prey_legend.jpg | 600 px | center]] | ||
| - | [[Image: 081022_killer_prey.jpg | | + | |
| + | |||
| + | [[Image: 081022_killer_prey.jpg | 900 px | center]] | ||
==Thursday 10/23/2008== | ==Thursday 10/23/2008== | ||
Revision as of 13:53, 28 October 2008
12th week
Contents |
Monday 10/20/2008
pSB1A3-Receiver-Colicin cloning
- Minipreps of colE1/E9/E9lys-Receiver with QiaCube, Qiagen
- Send probes to GATC for sequencing
Sender cloning: constitutive promotor-sender
- Minipreps of J23107-Receiver with QiaCube, Qiagen
- Send probe to GATC for sequencing
Tuesday 10/21/2008
Sequencing results of ready cloned BioBrick parts
| EcoRI-site mutation | PstI-site 1 mutation | PstI-site 2 mutation | PstI-site 3 mutation | Prefix | Suffix | complete sequence | |
|---|---|---|---|---|---|---|---|
| colE1_BB_57-1 | + | + | + | + | + | + | + |
| colE1_BB_57-2 | + | + | + | + | + | + | + |
| colE1_BB_57+2 | ? | + | + | ? | + | ? | missing sequence |
| colE1_BB_67+1 | + | + | + | + | + | ? | sequencing failure |
| colE9_BB_(2) | + | XXX | XXX | XXX | + | + | + |
| colE9lys_BB | XXX | XXX | XXX | XXX | + | + | + |
| sender_BB | XXX | XXX | XXX | XXX | + | + | + |
--> colE1_BB_57-1, colE9_BB_(2), colE9lys_BB and sender_BB gave positive sequencing results in all criteria and will be sent to the registry
Controldigestion of parts with EcoRI and PstI
- colE1_BB_57-1, colE9_BB_(2), colE9lys_BB and sender_BB was digested with EcoRI and PstI: 1h 30 min -> 37 °C
0.5 µl EcoRI (NEB) 0.5 µl PstI (NEB) 3.0 µl DNA 2.0 µl EcoRI Buffer (NEB) 2.0 µl BSA 10x 12.0 µl H2O ------- 20.0 µl
- Gelresults: The digestion pattern looks like expected. 1% Agarose, 135 V, 30 min
Control of antibiotics resistance
- LB-media containing tetracycline, chloramphenicol, ampicilin or kanamycin was inoculated with the different parts to the theri antibiotics resistance.
Wednesday 10/22/2008
- Antibiotics test: Each part only grew in ampicilin media as expected
- packaging and shipping of all standardized BioBrick parts to MIT
- Characterization: Colicin activity test
- after adjustment of the OD of the different cultures (killer, reference killer, prey), mixtures of different rations were done and transfered to a 96 well plate for ON measurement after following schemes
Thursday 10/23/2008
pSB1A2-Receiver-Colicin cloning
HisTag cloning of Colicins for purification
Colicin activity test
Friday 10/24/2008
Sender activity test
Constitutive sender and amplifier ([http://partsregistry.org/Part:BBa_I15030 BBa_I15030]) activity test
- over the day:
- 7x Inoculation of 8 ml TB media with 160 µl from sender ONC
- 7x Inoculation of 8 ml TB media with 160 µl from amplifier ONC
- Inoculation of 7 ml TB media with 7 ml from GFP-receiver ONC
- every hour (starting at t = 0 h until t = 7 h)
- Measurement of optical density (OD) of ONC dilutions
- Two different adequate dilutions of the diluted ONC were plate on LB Agar plates for cfu determination
- Creation of supernatant of the measured probe by sterile filtration (storage of the supernatant at 4 °C)
- evening: Measurement of the amount of produced AHL in the supernatants of the different timepoints
- each: 400 µl of the respective supernatant + 400 µl fresh TB media + 200 µl T9002 cells
- reference: T9002 cells + different concentrations of AHL
- plate scheme:
Saturday 10/25/2008
Results of the Sender activity test
Characterization: ColicinE1-Receiver Activitytest: Killer-prey system test and lysis test of killer cells
- afternoon: Inoculation of the following cultures:
- constitutive Sender with GFP(J23107-F1610 + I20260)(TB-Kana_Amp)
- ColE1Rec pBAD-mCherry (TB-Kana-Amp-Arab)
- T9002 without GFP pBAD-mCherry (TB-Kana-Amp-Arab)
- ColE1Rec + I20260 (TB-Kana-Amp)
- T9002 without GFP + I20260 (TB-Kana-Amp)
- 8.30 pm: Preparing mixtures for the plate:
- for colE1-Receiver killer-prey test (left part of the plate):
- 1:4 100 µl Sender + 400 µl Receivercells
- 1:1 100 µl Sender + 100 µl Receivercells + 300 µl TB media
- 5:1 100 µl Sender + 20 µl Receivercells + 380 µl TB media
- 10:1 100 µl Sender + 10 µl Receivercells + 390 µl TB media
- 25:1 100 µl Sender + 4 µl Receivercells + 396 µl TB media
- 50:1 100 µl Sender + 2 µl Receivercells + 398 µl TB media
- 100:1 100 µl Sender + 0.4 µl Receivercells + 400 µl TB media
- for colE1-Receiver lysis test (right part of the plate)
- colE1 + I20260: 250 µl colE1 cells + 250 µl TB-Amp-Kana
- T9002 without GFP + I20260: 250 µl T9002 without GFP + I20260 cells + 250 µl TB-Amp-Kana
- plate scheme:
Theoretical work for documentation
Sunday 10/26/2008
Theoretical work for documentation.
