Team:Bielefeld-Germany/Labjournal
From 2011.igem.org
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- | [[Image:Bielefeld-Germany-2011|450px|thumb| | + | [[Image:Bielefeld-Germany-2011 6FAM-signaltobackgroundratio-490-530nm target.png|450px|thumb|left| '''Figure 11: Signal-to-background ratio (S/B) determination of 6-FAM labeled Molecular Beacon in its closed or open state at an extinction wavelength 495 nm and emission wavelength 530 nm. Molecular Beacons and the target were added one after another, each after equilibrium was reached (see gaps). Calculated S/B: 45,52 (n=3).''']] |
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+ | [[Image:Bielefeld-Germany-2011 6FAM-signaltobackgroundratio-490-530nm split-target.png|450px|thumb|right| '''Figure 12: Signal-to-background ratio (S/B) determination of 6-FAM labeled Molecular Beacon in its closed state at an extinction wavelength 495 nm and emission wavelength 530 nm. Molecular Beacons and the split target were added one after another, each after equilibrium was reached (see gaps). Calculated S/B: 3,36 (n=3).''']] | ||
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- | [[Image:Bielefeld-Germany-2011 | + | [[Image:Bielefeld-Germany-2011 TAMRA-signaltobackgroundratio-552-590nm target.png|450px|thumb|left| '''Figure 13: Signal-to-background ratio (S/B) determination of TAMRA labeled Molecular Beacon in its closed or open state at an extinction wavelength 552 nm and emission wavelength 590 nm. Molecular Beacons and the target were added one after another, each after equilibrium was reached (see gaps). Calculated S/B: 18,21 (n=3).''']] |
- | [[Image:Bielefeld-Germany-2011 | + | [[Image:Bielefeld-Germany-2011 TAMRA-signaltobackgroundratio-552-590nm split-target.png|450px|thumb|right| '''Figure 14: Signal-to-background ratio (S/B) determination of TAMRA labeled Molecular Beacon in its closed state at an extinction wavelength 552 nm and emission wavelength 590 nm. Molecular Beacons and the split target were added one after another, each after equilibrium was reached (see gaps). Calculated S/B: 2,31 (n=3).''']] |
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- | [[Image:Bielefeld-Germany-2011 | + | [[Image:Bielefeld-Germany-2011|450px|thumb|centre| '''Figure 10: Thermal profile of 6-FAM labeled Molecular Beacon alone and with either target or split target added (n=5).''']] |
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Revision as of 12:04, 26 August 2011
On this page we summarize the (successful) results and achievements of our teamwork.
Week 1: 2nd - 8th may
- cloning of <partinfo>K123000</partinfo> and <partinfo>K123001</partinfo> behind weak (<partinfo>J23103</partinfo>) and medium strong (<partinfo>J23110</partinfo>) constitutive promoter (each part and both parts polycistronic)
- cloning of fusionprotein between <partinfo>K123000</partinfo> and <partinfo>K123001</partinfo>, also assembly behind weak and medium strong constitutive promoter
- testing and establishing of HPLC method for [http://en.wikipedia.org/wiki/Bisphenol_A BPA] detection
- expression of the successfully assembled BPA degrading BioBricks in E. coli [http://openwetware.org/wiki/E._coli_genotypes#TOP10_.28Invitrogen.29 TOP10]
- successful PCR on the S-layer genes of [http://expasy.org/sprot/hamap/CORGL.html Brevibacterium flavum] and Corynebacterium crenatum
- successful cloning of the S-layer gene of B. flavum without TAT-sequence
Organizational:
- meeting with [http://www.bielefeld-marketing.de/de/index.html Bielefeld Marketing] to discuss our participation at the science festival [http://www.geniale-bielefeld.de/ GENIALE] in Bielefeld
Week 2: 9th - 15th may
Bisphenol A:
- assembly of <partinfo>K157011</partinfo> behind existing BPA degrading parts (for purification and testing of <partinfo>K123000</partinfo> and <partinfo>K123001</partinfo> in a cell free system)
- HPLC results: fusionprotein between <partinfo>K123000</partinfo> and <partinfo>K123001</partinfo> can degrade BPA and seems to work better than the polycistronic version (compare fig. 1)
S-layer:
- expression of the S-layer gene without TAT-sequence of B. flavum in E. coli [http://www.promega.com/products/cloning-and-dna-markers/cloning-tools-and-competent-cells/bacterial-strains-and-competent-cells/single-step-_krx_-competent-cells/ KRX] and [http://openwetware.org/wiki/E._coli_genotypes#BL21.28DE3.29 BL21-Gold(DE3)] after sequencing gave correct results
- successful PCR on the S-layer gene of [http://ijs.sgmjournals.org/cgi/content/abstract/54/3/779 Corynebacterium halotolerans]
Organizational:
- moving to our own room in the [http://www.cebitec.uni-bielefeld.de/ CeBiTec]
Week 3: 16th - 22nd may
Bisphenol A:
- successful PCR on the [http://www.brenda-enzymes.org/php/result_flat.php4?ecno=1.18.1.2 NADP oxidoreductase] gene from E. coli TOP10
S-layer:
- successful cloning of the complete S-layer gene cspB of B. flavum, C. crenatum and C. halotolerans
- successful cloning of the S-layer genes of B. flavum and C. halotolerans without TAT-sequence, without lipid anchor and without both (only self-assembly domain)
Organizational:
Week 4: 23rd - 29th may
Bisphenol A:
- establishing a new method for analysis of BPA concentrations (extraction + LC-ESI-QTOF-MS)
S-layer:
Organizational:
- arrange a BBQ for our workgroup in the CeBiTec to get to know our coworkers
- substantiating our contribution to the GENIALE
Week 5: 30th may - 5th june
Bisphenol A:
- beginning of first characterization experiments for BPA degrading BioBricks (<partinfo>K123000</partinfo> and <partinfo>K123001</partinfo>)
S-layer:
Organizational:
- meeting with Prof. [http://de.wikipedia.org/wiki/Alfred_Pühler Alfred Pühler] to plan our contribution to the [http://www.cebitec.uni-bielefeld.de/content/view/209/88/ CeBiTec symposium] in july
Week 6: 6th - 12th june
Organizational:
- presentation of the iGEM competition at the [http://www.bio.nrw.de/studentconvention 2nd BIO.NRW (PhD) Student Convention]
Week 7: 13th - 19th june
Bisphenol A:
- cloning of NADP oxidoreductase in [http://www.bioinfo.pte.hu/f2/pict_f2/pJETmap.pdf pJET1.2] finally successful -> waiting for sequencing results to remove illegal restriction sites
Week 8: 20th - 26th june
Organizational:
- finishing our first press release
- all devices (thermocycler etc.) and materials (competent cells, polymerase, kits) from our sponsors arrived
Week 9: 27th june - 3rd july
S-Layer:
- our synthesized S-Layers SgsE and SbpA finaly arrived
Week 10: 4th july - 10th july
Bisphenol A:
- experiments on the influence of temperature, promotor intensity and the characteristics of the fusion protein <partinfo>K123000</partinfo> || <partinfo>K123001</partinfo> on BPA degradation
Organizational:
- presenting our posters from the teams of 2010 and 2011 at the congress [http://www.biotechnologie2020plus.de/BIO2020/Navigation/DE/root,did=121262.html Biotechnologie2020+] in Berlin hosted by the "Bundesministerium für Bildung und Forschung" (Federal Ministry of Education and Research).
Week 11: 11th july - 17th july
Bisphenol A / S-Layer:
- our BioBrick order (some fluorescences proteins and cleavage sites) from iGEM HQ arrived
Organizational:
- presenting the iGEM competition and our team project at the secondary school [http://www.rg-herford.de/ Ravensberger Gynmasium] in Herford ([http://www.flickr.com/photos/igem-bielefeld/sets/72157627214780020/ Photos])
Week 12: 18th july - 24th july
Organizational:
- presenting our projects from 2010 and 2011 at the [http://www.cebitec.uni-bielefeld.de/content/view/209/88/ CeBiTec Symposium 2011] in Bielefeld
- meeting and having fun with the iGEM teams from Delft/NL, Edinburgh/UK, Odense/DK. Freiburg/DE and Ljubljana/SL at the Symposium ([http://www.flickr.com/photos/igem-bielefeld/sets/72157627300144576/ Photos])
Bisphenol A / S-Layer:
- removing illegal restiction sites to get valid BioBricks
- cloning the NAD+ dependent ligase from E. coli into BioBrick backbones
Week 13: 25th july - 31th july
S-Layer:
- fusing the synthesized S-Layers to a bunch of fluorescent proteins
Bisphenol A:
- testing new BPA extraction protocols for LC-MS including an internal standard (bisphenol F)
Week 14: 1st august - 7th august
Bisphenol A:
- BPA analysis with extraction and LC-MS finally works and is very accurate
- Better results for BPA degradation in E. coli -> our fusion protein (<partinfo>K123000</partinfo> to <partinfo>K123001</partinfo>) can completely degrade BPA
- Measuring characterization results for different BPA degrading BioBricks
Molecular Beacons:
- Successful characterization of two differently labeled Molecular Beacons as a preparation for the NAD+ bioassay including autonomously produced NAD+ dependent DNA ligase from E. coli
Week 15: 8th august - 14th august
Bisphenol A:
- BPA analysis with extraction and HPLC with UV detector leads to very similar results as the analysis with LC-MS (except for low BPA concentrations -> LOD / LOQ of LC-MS is lower than that of "normal" HPLC, compare figure 15)
- measuring of more samples from cultivations with BPA degrading BioBricks for further characterization
- we discovered some interesting results in our MS data - soon more
- testing methods to purify his-tagged BisdA and BisdB for cell free BPA degradation and further characterization of these proteins
- testing the influence of BPA on the growth of E. coli
- developing a modell for BPA degradation by E. coli (compare fig. 16)
S-layer:
- MALDI-TOF analysis of SDS-PAGEs to characterize the function of the TAT-sequence and the lipid anchor of PS2 (encoded by cspB gene) in E. coli
Week 16: 15th august - 21st august
S-layer:
- finally found our S-layer proteins in E. coli -> now we can plan purification strategy
- fusion of FPs to sgsE successful
Bisphenol A:
- all metabolites of natural BPA degradation pathway found during degradation of BPA in E. coli by LC-MS -> now MS/MS to check structure of these metabolites to be sure
- testing whether E. coli can grow on BPA as the only carbon source (on M9 plates)
Week 17: 22nd august - 28th august
S-layer:
- cultivation and purification of sgsE fusion proteins
Bisphenol A:
- purification of his-tagged BisdA and BisdB
- first characterization results entered into partsregistry