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Team:Bielefeld-CeBiTec/Notebook/Journal/Isobutanol/Sep
From 2014.igem.org
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| - | <ul><li>Until now we didn't purified Inserts out of the gel if the backbone had another antibiotic resistence. We were using the <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#DNAPurificationbyCentrifugation" target="_blank">PCR purification</a>. But because it didn't worked out, we analyzed all our cut samples by gelelectrophorese. Thereby we discovered that the pSB1K3_<i>alsS</i>_<i>ilvC</i>_<i>ilvD</i>_<i>kivD</i> has an illigal restriction side. <br> Because of the integration of RBS's between all genes in the <i>alsS</i>_<i>ilvC</i>_<i>ilvD</i>_<i>kivD</i>-Plasmid, a restriction side between <i>alsS</i> and a RBS occurs.</li></ul> | + | <ul><li>Until now we didn't purified Inserts out of the gel if the backbone had another antibiotic resistence. We were using the <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Protocols#DNAPurificationbyCentrifugation" target="_blank">PCR purification</a>. But because it didn't worked out, we analyzed all our cut samples by gelelectrophorese. Thereby we discovered that the pSB1K3_<i>alsS</i>_<i>ilvC</i>_<i>ilvD</i>_<i>kivD</i> has an illigal restriction side. <br> Because of the integration of RBS's between all genes in the <i>alsS</i>_<i>ilvC</i>_<i>ilvD</i>_<i>kivD</i>-Plasmid, a restriction side between <i>alsS</i> and a RBS occurs.<br>New primers were ordered: <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#rv_ilvC_alsS-new" target="_blank">rv_ilvC_alsS-new</a> and <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Primer#fw_alsS_ilvC-new" target="_blank">fw_alsS_ilvC-new</a></li></ul> |
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Revision as of 18:51, 15 October 2014
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September |
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- adhA
- This week we tried to verify the positive cutures that were identified last week by a restriction digest
- Plasmid isolation of pSB1K3_adhA
- Restriction digestion with EcoRI and PstI of pSB1K3_adhA
- Bands as expected (~1200 bp)
- Successful sequencing
Agarose gel from the restriction digestion with EcoRI and PstI. As a Ladder we used GeneRuler™ 1 kb DNA Ladder from Thermo Scientific.
- T7_alsS_ilvC_ilvD_kivD
- This week we tried to verify the positive cutures that were identified last week by a restriction digest
- Plasmid isolation of pSB1A2_T7_alsS_ilvC_ilvD_kivD
- Restriction digestion with EcoRI and PstI of pSB1A2_T7_alsS_ilvC_ilvD_kivD
- Bands not as expected (~7000bp)
- pSB1K3_alsS_ilvC_ilcD_kivD_adhA
- This week we tried to combine the pSB1K3_alsS_ilvC_ilvD_kivD with adhA
- BioBrick Assembly (Suffix)
- Colony PCR (fw-ilvD-kivD, rev-pSB1C3-adhA)
- Annealing temperature: 65 °C
- Bands not as expected (~ 3800 bp)
- pSB1C3_alsS_ilvC_ilvD_kivD
- This week we tried to reclone alsS_ilvC_ilvD_kivD into pSB1C3
- Restriction digestion of pSB1K3_alsS_ilvC_ilvD_kivD and pSB1C3_RFP with EcoRI and PstI
- Bands as expected
(~ 7500 bp for alsS_ilvC_ilvD_kivD and ~ 2200 bp for pSB1C3) - Clean up and Ligation as explained in the BioBrick Assembly
- Transformation with electrocompotetent cells
- Colony PCR (fw_ilvD_kivD, rv_pSB1C3_kivD)
- Annealing temperature: 65 °C
- Bands not as expected (~1800 bp)
- pSB1C3_alsS_ilvC_ilvD_kivD_adhA
- This week we tried to contruct the pSB1C3_alsS_ilvC_ilvD_kivD_adhA-Plasmid by NEB BioBrick Assembly
- Colony PCR (fw_ilvD_kivD , rev_pSB1C3_adhA)
- Annealing temperature: 65°C
- Bands not as expected (~3000 bp)
- pSB1C3_alsS_ilvC_ilvD_kivD
- This week we tried to reclone alsS_ilvC_ilvD_kivD into pSB1C3
- Restriction digestion of pSB1K3_alsS_ilvC_ilvD_kivD and pSB1C3_RFP with EcoRI and PstI
- Bands as expected
(~ 7500 bp for alsS_ilvC_ilvD_kivD and ~ 2200 bp for pSB1C3) - Clean up and Ligation as explained in the BioBrick Assembly
- Transformation with electrocompotetent cells
- Colony PCR (fw_ilvD_kivD, rv_pSB1C3_kivD)
- Annealing temperature: 65 °C
- Bands not as expected (~1800 bp)
- pSB1C3_adhA
- This week we tried to reclone adhA into pSB1C3
- Restriction digestion of pSB1K3_adhA and pSB1C3_RFP with EcoRI and PstI
- Bands as expected
(~ 1200 bp for adhA and ~ 2200 bp for pSB1C3) - Clean up and Ligation as explained in the BioBrick Assembly
- Transformation with electrocompotetent cells
- Colony PCR (fw_pSB1C3_adhA, rev_pSB1C3_adhA)
- Annealing temperature: 65 °C
- Bands not as expected (~ 1200 bp)
- pSB1A2_T7_adhA
- This week we tried to contruct the pSB1A2_T7_adhA-Plasmid
- BioBrick Assembly (Suffix)
- Colony PCR (fw_pSB1C3_adhA, rev_pSB1C3_adhA)
- Annealing temperature: 65 °C
- Bands not as expected (~ 1200 bp)
- pSB1C3_alsS_ilvC_ilvD_kivD_adhA
- This week we tried to contruct the pSB1C3_alsS_ilvC_ilvD_kivD_adhA-Plasmid by NEB BioBrick Assembly
- Colony PCR (fw_ilvD_kivD , rev_pSB1C3_adhA)
- Annealing temperature: 65°C
- Bands not as expected (~3000 bp)
- Until now we didn't purified Inserts out of the gel if the backbone had another antibiotic resistence. We were using the PCR purification. But because it didn't worked out, we analyzed all our cut samples by gelelectrophorese. Thereby we discovered that the pSB1K3_alsS_ilvC_ilvD_kivD has an illigal restriction side.
Because of the integration of RBS's between all genes in the alsS_ilvC_ilvD_kivD-Plasmid, a restriction side between alsS and a RBS occurs.
New primers were ordered: rv_ilvC_alsS-new and fw_alsS_ilvC-new
