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Team:Bielefeld-CeBiTec/Notebook/Journal/CO2-fixation/Sep
From 2014.igem.org
(Difference between revisions)
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<li>Backbone (digested with <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionDigestion" target="_blank"><i>EcoR</i>I</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionDigestion" target="_blank"><i>Xba</i>I</a>)</li> | <li>Backbone (digested with <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionDigestion" target="_blank"><i>EcoR</i>I</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionDigestion" target="_blank"><i>Xba</i>I</a>)</li> | ||
<ul> | <ul> | ||
| - | <li> | + | <li>pSB1C3_csoS1-4_GFP</li> |
</ul> | </ul> | ||
<li>Insert (digested with <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionDigestion" target="_blank"><i>EcoR</i>I</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionDigestion" target="_blank"><i>Spe</i>I</a>)</li> | <li>Insert (digested with <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionDigestion" target="_blank"><i>EcoR</i>I</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionDigestion" target="_blank"><i>Spe</i>I</a>)</li> | ||
<ul> | <ul> | ||
| - | <li> | + | <li>T7_sap</li> |
</ul> | </ul> | ||
</ul> | </ul> | ||
</ul> | </ul> | ||
| - | + | <ul> | |
| - | + | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Transformationviaelectroporation" target="_blank">Transformation</a> with electrocompotetent cells</li> | |
| + | </ul> | ||
| + | <ul> | ||
| + | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Transformationviaheatshock" target="_blank">Transformation</a> with chemocompetent cells</li> | ||
| + | </ul> | ||
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</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>T7_sap_csoS1-4_GFP</i></b></li> | ||
| + | <ul> | ||
| + | <li>We tried find the construct to use it for the microscopy.</li> | ||
| + | <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#Primer2" target="_blank">Primer2</a>) | ||
| + | </li> | ||
| + | <ul> | ||
| + | <li>Annealing temperature: 55 °C</li> | ||
| + | <li>Bands as expected (~3000 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_T7_sap_csoS1-4_GFP</li> | ||
| + | </ul> | ||
| + | <ul> | ||
| + | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#RestrictionDigestion" target="_blank">Restriction digestion</a> with <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionEnzymes" target="_blank"><i>Pst</i>I</a> and <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/KitsAndEnzymes#RestrictionEnzymes" target="_blank"><i>EcoR</i>I</a> </li> | ||
| + | <ul> | ||
| + | <li>Bands as expected (~2000 bp and ~4600 bp)</li> | ||
| + | </ul> | ||
| + | </ul> | ||
| + | |||
| + | |||
| + | |||
| + | </ul> | ||
| + | </ul> | ||
| + | |||
| + | |||
| + | |||
| + | <br> | ||
<ul> | <ul> | ||
<li><b><i>tkt</i></b></li> | <li><b><i>tkt</i></b></li> | ||
<ul> | <ul> | ||
| - | <li>This week we | + | <li>This week we wanted to purify the enzyme of <i>tkt</i> for the SBPase assay.</li> |
<ul> | <ul> | ||
<li>Cultivation of pet16b_tkt in 250 ml <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Media#LBmedium" target="_blank">LB medium</a></li> | <li>Cultivation of pet16b_tkt in 250 ml <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Media#LBmedium" target="_blank">LB medium</a></li> | ||
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</ul> | </ul> | ||
</ul> | </ul> | ||
| + | |||
| + | <br> | ||
| + | |||
<ul> | <ul> | ||
<li><b><i>fba</i></b></li> | <li><b><i>fba</i></b></li> | ||
<ul> | <ul> | ||
| - | <li>This week we | + | <li>This week we wanted to purify the enzyme of <i>fba</i> for the SBPase assay.</li> |
<ul> | <ul> | ||
<li>Cultivation of pet16b_fba in 250 ml <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Media#LBmedium" target="_blank">LB medium</a></li> | <li>Cultivation of pet16b_fba in 250 ml <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Media#LBmedium" target="_blank">LB medium</a></li> | ||
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</ul> | </ul> | ||
</ul> | </ul> | ||
| + | |||
| + | <br> | ||
| + | |||
<ul> | <ul> | ||
<li><b><i>glpX</i></b></li> | <li><b><i>glpX</i></b></li> | ||
<ul> | <ul> | ||
| - | <li>This week we | + | <li>This week we wanted to purify the enzyme of <glpX</i> for the SBPase assay.</li> |
<ul> | <ul> | ||
<li>Cultivation of pet16b_glpX in 250 ml <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Media#LBmedium" target="_blank">LB medium</a></li> | <li>Cultivation of pet16b_glpX in 250 ml <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Media#LBmedium" target="_blank">LB medium</a></li> | ||
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<li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Sodiumdodecylsulfatepolyacrylamidegelelectrophoresis (SDS-PAGE)" target="_blank">SDS-Page</a> of His-Tag purification result in correct bands at imidazol concentration of ...</li> | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Sodiumdodecylsulfatepolyacrylamidegelelectrophoresis (SDS-PAGE)" target="_blank">SDS-Page</a> of His-Tag purification result in correct bands at imidazol concentration of ...</li> | ||
</ul> | </ul> | ||
| - | + | <li>We also tried to bring <i>glpX</i> in the right vector pSB1C3.</li> | |
| + | <ul> | ||
| + | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Gibson" target="_blank">Gibson Assembly</a> with <i>glpX</i> and pSB1C3</li> | ||
| + | </ul> | ||
| + | <ul> | ||
| + | <li><a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#Transformationviaelectroporation" target="_blank">Transformation</a> with electrocompotetent cells</li> | ||
| + | </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#Primer1" target="_blank">Primer1</a>, <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#Primer2" target="_blank">Primer2</a>) | ||
| + | </li> | ||
| + | <ul> | ||
| + | <li>Annealing temperature: ... °C</li> | ||
| + | <li>Bands (not) as expected (~... bp)</li> | ||
| + | </ul> | ||
| + | </ul> | ||
| - | |||
| + | |||
| + | |||
| + | </ul> | ||
</ul> | </ul> | ||
Revision as of 10:38, 15 October 2014
 |
September |
 |
- glpX
- We tried to find and isolate pSB1K3_glpX.
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55 °C
- Bands as expected (~1300 bp)
- Plasmid isolation of pSB1K3_glpX
- csoS1-4
- We tried to amplify csoS1-4 (shell proteins) for a fusion with GFP.
- PCR amplification (fw-GFP-csoS1B, rv-rv-GFP-csoS1A)
- Annealing temperature: 54 °C
- Bands as expected (~4000 bp (~1800 bp csoS1-4, ~2200 bp pSB1C3))
- PCR products were purified
- csoS1-4 and GFP
- We tried to assemble the shell proteins of the carboxysome and GFP.
- Gibson Assembly with pSB1C3_csoS1-4 and GFP
- Transformation with electrocompotetent cells
- Colony PCR (fw-csoS1A-GFP, rv-csoS1B-GF)
- Annealing temperature: 68 °C
- Bands as expected (~1000 bp)
- Plasmid isolation of pSB1C3_csoS1-4_GFP
- Restriction digestion with NotI
- Bands as expected (~2000 bp and ~2400 bp)
Agarose gel from restriction digestion. As a Ladder we used GeneRuler™ 1 kb DNA Ladder from Thermo Scientific.
- csoS1-4_GFP and T7
- We tried to assemble our pSB1C3_csoS1-4_GFP construct with the T7 promotor.
- BioBrick Assembly (Suffix)
- Transformation with electrocompotetent cells
- Colony PCR (VF-Primer, rv_csoS4A_PstI)
- Annealing temperature: 55 °C
- Bands as expected (~320 bp)
- can and csoS1-4
- This week we tried to find positive clones of our transformation.
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55 °C
- Bands as expected (~3600 bp)
- Plasmid isolation of pSB1C3_can_csoS1-4
- Restriction digestion with EcoRI and PstI
- Bands as expected (~2100 bp and ~3300 bp)
Agarose gel from restriction digestion. As a Ladder we used GeneRuler™ 1 kb DNA Ladder from Thermo Scientific.
- can_csoS1-4 and csoS1D
- We tried to assemble our pSB1C3_can_csoS1-4 construct with csoS1D.
- BioBrick Assembly (Suffix)
- Transformation with electrocompotetent cells
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55 °C
- Bands as expected (~4300 bp)
- Plasmid isolation of pSB1C3_can_csoS1-4_csoS1D
- Restriction digestion with NotI
- Bands as expected (~2000 bp and ~4000 bp)
Agarose gel from restriction digestion. As a Ladder we used GeneRuler™ 1 kb DNA Ladder from Thermo Scientific.
- Hneap and T7
- This week we tried to assemble the T7 promotor with the Hneap.
- BioBrick Assembly (Suffix)
- Transformation with chemocompetent cells
- glpX and ptac
- This week we tried to bring glpX in the pSB1C3 backbone under the control of the ptac promotor.
- BioBrick Assembly (Suffix)
- Transformation with electrocompotetent cells
- Colony PCR (fw_pSB1_SBPase, rv_pSB1_SBPase)
- Annealing temperature: 54 °C
- Bands as expected (~2100 bp)
- Plasmid isolation of pSB1C3_ptac_glpX
- Restriction digestion with NotI
- Bands as expected (~2000 bp and ~2200 bp)
- Hneap and T7
- We tried to find positiv clones of pSB3A2_T7_Hneap.
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55 °C
- Bands as expected (~2000 bp)
- Plasmid isolation of pSB1A2_T7_Hneap
- Restriction digestion with EcoRI and PstI
- Bands as expected (~2000 bp and ~1800 bp)
Agarose gel from restriction digestion. As a Ladder we used GeneRuler™ 1 kb DNA Ladder from Thermo Scientific.
- sap
- We tried to assemble both parts of sap.
- PCR amplification on the pJet plasmid for sap_2 (sap_2_fwd, sap_2_rev)
- Annealing temperature: 55 °C
- Bands as expected (~1500 bp)
- Gibson Assembly with sap_1, sap_2 and pSB1C3
- Transformation with electrocompotetent cells
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55 °C
- Bands as expected (~3000 bp)
- Restriction digestion with EcoRI and PstI
- Bands as expected (~2000 bp (backbone) and ~2700 bp (insert))
- Restriction digestion with EcoRV
- Bands as expected (~1500 bp and ~3200 bp)
Agarose gel from restriction digestion. As a Ladder we used GeneRuler™ 1 kb DNA Ladder from Thermo Scientific.
- T7 and prkA
- This week we wanted to bring the prkA under the control of the T7 promotor.
- BioBrick Assembly (Suffix)
- Transformation with chemocompetent cells
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55 °C
- Bands as expected (~1400 bp)
- Plasmid isolation of pSB1A2_T7_prkA
- Restriction digestion with EcoRI and PstI
- Bands as expected (~2000 bp and ~1100 bp)
- T7 and sap
- We tried to bring the sap under the control of the T7 promotor.
- BioBrick Assembly (Suffix)
- Transformation with chemocompetent cells
- Colony PCR (VF-Primer, VR-Primer)
- Annealing temperature: 55 °C
- Bands as expected (~3000 bp)
- Plasmid isolation of pSB1A2_T7_sap
- Restriction digestion with EcoRI and PstI
- Bands as expected (~2800 bp and ~2000 bp)
- csoS1-4_GFP and T7_sap
- We tried to assemble our GFP construct with the shell associated protein sap and the T7 promotor.
- BioBrick Assembly (Prefix)
- Transformation with electrocompotetent cells
- Transformation with chemocompetent cells
- T7_sap_csoS1-4_GFP
- We tried find the construct to use it for the microscopy.
- Colony PCR (VF-Primer, Primer2)
- Annealing temperature: 55 °C
- Bands as expected (~3000 bp)
- Plasmid isolation of pSB1C3_T7_sap_csoS1-4_GFP
- Restriction digestion with PstI and EcoRI
- Bands as expected (~2000 bp and ~4600 bp)
- tkt
- This week we wanted to purify the enzyme of tkt for the SBPase assay.
- Cultivation of pet16b_tkt in 250 ml LB medium
- Induction with 1 mM IPTG at OD 0.8. Taking samples:t0, t1, t2, t3, t15, t17
- SDS-Page of cultivation result in correct bands at ~100kD
- His-Tag purification of tkt
- SDS-Page of His-Tag purification result in correct bands at imidazol concentration of ...
- fba
- This week we wanted to purify the enzyme of fba for the SBPase assay.
- Cultivation of pet16b_fba in 250 ml LB medium
- Induction with 1 mM IPTG at OD 0.8. Taking samples:t0, t1, t2, t3, t15, t17
- SDS-Page of cultivation result in correct bands at ~40kD
- His-Tag purification of fba
- SDS-Page of His-Tag purification result in correct bands at imidazol concentration of ...
- glpX
- This week we wanted to purify the enzyme of
- Cultivation of pet16b_glpX in 250 ml LB medium
- Induction with 1 mM IPTG at OD 0.8. Taking samples:t0, t1, t2, t3, t15, t17
- SDS-Page of cultivation result in correct bands at ~38kD
- His-Tag purification of glpX
- SDS-Page of His-Tag purification result in correct bands at imidazol concentration of ...
- We also tried to bring glpX in the right vector pSB1C3.
- Gibson Assembly with glpX and pSB1C3
- Transformation with electrocompotetent cells
- Transformation with chemocompetent cells
- Colony PCR (Primer1, Primer2)
- Annealing temperature: ... °C
- Bands (not) as expected (~... bp)
