"
Team:Bielefeld-CeBiTec/Notebook/Journal/rMFC/Sep
From 2014.igem.org
(Difference between revisions)
| Line 260: | Line 260: | ||
</ul> | </ul> | ||
<ul> | <ul> | ||
| - | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Gibson" target="_blank">Gibson Assembly</a> of PCR products and <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionEnzymes" target="_blank"><i>Dpn</i>I</a> | + | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Gibson" target="_blank">Gibson Assembly</a> of PCR products and <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionEnzymes" target="_blank"><i>Dpn</i>I</a> digestion to remove the template |
</ul> | </ul> | ||
<ul> | <ul> | ||
| Line 275: | Line 275: | ||
<ul> | <ul> | ||
<li><b><i>ccm</i></b></li> | <li><b><i>ccm</i></b></li> | ||
| + | <ul> | ||
| + | <li> This week we tried to get the <i>ccm</i> into the correct backbone </li> | ||
<ul> | <ul> | ||
<li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Gibson" target="_blank">Gibson Assembly</a> with <i>ccm</i> and pSB1C3</li> | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Gibson" target="_blank">Gibson Assembly</a> with <i>ccm</i> and pSB1C3</li> | ||
| Line 313: | Line 315: | ||
</ul> | </ul> | ||
</ul> | </ul> | ||
| - | |||
| - | |||
</ul> | </ul> | ||
| - | |||
| - | |||
| - | |||
</ul> | </ul> | ||
</ul> | </ul> | ||
<br> | <br> | ||
| - | |||
| - | |||
</div> | </div> | ||
</div> | </div> | ||
| Line 340: | Line 335: | ||
</div> | </div> | ||
<div class="content" style="margin-right:10%; margin-left:10%"> | <div class="content" style="margin-right:10%; margin-left:10%"> | ||
| + | <ul> | ||
| + | <li><b><i>FumA</i></b></li> | ||
| + | <ul> | ||
| + | <li> This week we removed the the mutation of <i>FumA</i> by PCR </li> | ||
| + | <ul> | ||
| + | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#PCR" target="_blank">PCR amplification</a> of <i>FumA</i> using a gradient(<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#FumA_mut_fwd" target="_blank">FumA_mut_fwd, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#FumA_mut_rev" target="_blank">FumA_mut_rev</a>)</li> | ||
| + | <ul> | ||
| + | <li>Annealing temperature: 50°C to 60°C</li> | ||
| + | <li>Bands as expected (~4000 bp)</li> | ||
| + | </ul> | ||
| + | </ul> | ||
| + | <ul> | ||
| + | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Gibson" target="_blank">Gibson Assembly</a> with <i>FumA</i> and pSB1C3 and digestion with <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionEnzymes" target="_blank"><i>Dpn</i>I</a> to remove the template | ||
| + | </ul> | ||
| + | <ul> | ||
| + | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Transformationviaheatshock" target="_blank">Transformation</a> with chemocompetent cells</li> | ||
| + | </ul> | ||
| + | <ul> | ||
| + | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#ColonyPCR" target="_blank">Colony PCR</a> (<a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#VF-Primer" target="_blank">VF-Primer</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#VR-Primer" target="_blank">VR-Primer</a>) | ||
| + | </li> | ||
| + | <ul> | ||
| + | <li>Annealing temperature: 55°C</li> | ||
| + | <li>Bands as expected (~2100 bp)</li> | ||
| + | </ul> | ||
| + | </ul> | ||
| + | <ul> | ||
| + | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#PurificationPromega" target="_blank">Plasmid isolation</a> of pSB1C3_<i>FumA</i></li> | ||
| + | </ul> | ||
| + | <ul> | ||
| + | <li> | ||
| + | Sequencing of pSB1C3_<i>FumA</i> confirmed the correct construct</i> | ||
</div> | </div> | ||
</div> | </div> | ||
Revision as of 13:59, 15 October 2014
 |
September |
 |
- FumA
- This week we assembled FumA with different constitutive promotors
- Restriction digestion with EcoRI and PstI
- Bands as expected (~2070 bp and ~1800 bp) for pSB1C3_T7_FumA
- BioBrick Assembly (Suffix)
- Transformation of all constructs with electrocompotetent cells
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55 °C
- Bands as expected (~2100 bp) for all constructs
- Plasmid isolation of the positive colonies
- Restriction digestion with EcoRI and PstI
- Bands as expected (~2070 bp and ~1800 bp)
- ccm
- Gibson Assembly with ccm and pSB1C3
- Transformation of pSB1C3_ccm with electrocompotetent cells
- GSU 3274
- This week we assembled GSU 3274 with different promotors
- BioBrick Assembly (Suffix)
- Transformation of all constructs with electrocompotetent cells
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55°C
- Bands as expected (~ bp) for pSB1C3_ptac and pSB1A2_T7
- Electrobiochemical reactor system
- This week we arranged the complete H-cell reactor for the first time to start first trials. Therefore we prepare the H-cell buffers and the Nafion® membrane which ensures the division of the two compartments.
- NAD/NADH Assay
- This week we startet the first test with the Promega NAD/NADH-Glo™ Assay to evaluate later cultivations respectively.
- frd (E.coli)
- This week we transform pSB1C3_T7_frd with different E.coli strains for the characterization of it respectively
- Transformation of pSB1C3_T7_frd with electrocompotetent cells of KRX ΔdcuB::oprF, JW4084-1 as well as JW0506-1 from the KEIO collection
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55 °C
- Bands as expected (~3600 bp)
- Restriction digestion of all constructs with EcoRI and PstI
- Bands (not) as expected (~... bp)
- Expression of frd (E.coli) for SDS-Page
- Induction was carried out with 0.1 % Rhamnose and 1 mM IPTG
- For the release of the periplasmatic protein fraction a cold osmotic shock was performed
- ccm
- Plasmid isolation of pSB1C3_ccm
- Restriction digestion with NotI
- Bands not as expected (~6611 bp)
- frd (E. coli)
- This week we removed the first illegal restriction site (PstI at 144 bp)
- PCR amplification (frd_cut1
- Annealing temperature: 55 °C
- Bands as expected (~... bp)
- Gibson Assembly of PCR products and DpnI digestion to remove the template
- Transformation with electrocompotetent cells
- Plasmid isolation for a restriction digestion with PstI afterwards
- PCR amplification (frd_cut1
- ccm
- This week we tried to get the ccm into the correct backbone
- Gibson Assembly with ccm and pSB1C3
- Transformation with electrocompotetent cells and Transformation with chemocompetent cells
- Plasmid isolation of ccm and Restriction digestion with EcoRI and PstI
- Bands mainly not as expected (~6281 bp and ~2070 bp ) because additional bands are visible.
- Therefore a restriction digestion with EcoRV and HindIII was done
- Bands not as expected because only two bands were visible
- Colony PCR with new primer(ccm_con1, VR-Primer)
- Annealing temperature: 55°C
- Bands as expected (~880 bp)
- Plasmid isolation of pSB1C3_ccm and restriction digestion with EcoRI and PstI
- Bands not as expected (~6281 bp and ~2070 bp)
- PCR amplification of ccm backbone(pSB1C3_pre_ccm, pSB1C3_suf_ccm)
- Annealing temperature: 61°C
- Bands as expected (~6281 bp)
- FumA
- This week we removed the the mutation of FumA by PCR
- PCR amplification of FumA using a gradient(FumA_mut_fwd, FumA_mut_rev)
- Annealing temperature: 50°C to 60°C
- Bands as expected (~4000 bp)
- Gibson Assembly with FumA and pSB1C3 and digestion with DpnI to remove the template
- Transformation with chemocompetent cells
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55°C
- Bands as expected (~2100 bp)
- Plasmid isolation of pSB1C3_FumA
- Sequencing of pSB1C3_FumA confirmed the correct construct
