Difference between revisions of "Part:BBa K1758323"
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| − | + | <img src="https://static.igem.org/mediawiki/2015/b/b2/Bielefeld-CebiTec_in_vivo_Copper.jpeg" width="100%"> | |
<figcaption>Figure 2: The concept of our <i>in vivo</i> copper sensor (<a href="https://parts.igem.org/Part:BBa_K1758324" target="_blank">BBa_K1758324</a>), which consists of the activator under the control of a constitutive promoter (<a href="https://parts.igem.org/Part:BBa_K1758320" target="_blank">BBa_K1758320</a>) and the operator and promoter sequence of the copper inducible promoter. An untranslated region in front of the sfGFP, which is used for detection, enhances its expression (<a href="https://parts.igem.org/Part:BBa_K1758323" target="_blank">BBa_K1758323</a>). </figcaption> | <figcaption>Figure 2: The concept of our <i>in vivo</i> copper sensor (<a href="https://parts.igem.org/Part:BBa_K1758324" target="_blank">BBa_K1758324</a>), which consists of the activator under the control of a constitutive promoter (<a href="https://parts.igem.org/Part:BBa_K1758320" target="_blank">BBa_K1758320</a>) and the operator and promoter sequence of the copper inducible promoter. An untranslated region in front of the sfGFP, which is used for detection, enhances its expression (<a href="https://parts.igem.org/Part:BBa_K1758323" target="_blank">BBa_K1758323</a>). </figcaption> | ||
</figure> | </figure> | ||
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| − | + | <img src="https://static.igem.org/mediawiki/2015/9/90/Bielefeld-CeBiTec_Biolector_copper.jpg" width="100%"> | |
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<figcaption>Figure 3: Time course of the induction of a copper biosensor with sfGFP for different copper concentrations <i>in vivo</i>. The data are measured with BioLector and normalized on OD<sub>600</sub>. Error bars represent the standard deviation of two biological replicates.</figcaption> | <figcaption>Figure 3: Time course of the induction of a copper biosensor with sfGFP for different copper concentrations <i>in vivo</i>. The data are measured with BioLector and normalized on OD<sub>600</sub>. Error bars represent the standard deviation of two biological replicates.</figcaption> | ||
</figure> | </figure> | ||
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| − | <figure | + | <img src="https://static.igem.org/mediawiki/2015/4/4e/Bielefeld-CeBiTec_Biolector_copper_Balkendiagramm.jpeg"width="100%"></a> |
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<figcaption>Figure 4: Fluorescence levels at three different stages of cultivation. Shown are levels after 60 minutes, 150 minutes and 650 minutes. </figcaption> | <figcaption>Figure 4: Fluorescence levels at three different stages of cultivation. Shown are levels after 60 minutes, 150 minutes and 650 minutes. </figcaption> | ||
</figure> | </figure> | ||
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<p>We tested our <i>in vivo</i> copper sensor with <i>sfGFP</i> as reporter gene, to test the functionality of the system. Moreover, we tested different copper concentrations. The kinetic of our sensors response to different copper concentrations is shown in figure 3. The first ten hours show a strong increase in fluorescence. After that the increase in fluorescence is slower. For better visualization the kinetics of figure 3 are represented as bars in figure 4. A fluorescence level difference for 60 min, 150 min and 650 min is represented.</p> | <p>We tested our <i>in vivo</i> copper sensor with <i>sfGFP</i> as reporter gene, to test the functionality of the system. Moreover, we tested different copper concentrations. The kinetic of our sensors response to different copper concentrations is shown in figure 3. The first ten hours show a strong increase in fluorescence. After that the increase in fluorescence is slower. For better visualization the kinetics of figure 3 are represented as bars in figure 4. A fluorescence level difference for 60 min, 150 min and 650 min is represented.</p> | ||
<p><i>In vivo</i> we could show that the adding different concentrations of copper has effects on the transcription levels of <i>sfGFP</i>.</p> | <p><i>In vivo</i> we could show that the adding different concentrations of copper has effects on the transcription levels of <i>sfGFP</i>.</p> | ||
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<p>The shown data suggest that sensing copper with our device is possible even if the detectable concentrations are higher than the desireble sensitivity limits. Therfore we tested the copper sensor in our <i>in vitro</i> transcription translation approach.</p> | <p>The shown data suggest that sensing copper with our device is possible even if the detectable concentrations are higher than the desireble sensitivity limits. Therfore we tested the copper sensor in our <i>in vitro</i> transcription translation approach.</p> | ||
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<h2><i>in vitro</i></h2> | <h2><i>in vitro</i></h2> | ||
<p>For the characterization of the copper sensor with CFPS we used parts differing from that we used in vivo characterization. For the <i>in vitro</i> characterization we used a cell extract out of cells which contain the plasmid (<a href="https://parts.igem.org/Part:BBa_K1758320" target="_blank">BBa_K1758320</a>) (figure 5), so that the resulting extract is enriched with the activator CueR. To this extract we added plasmid-DNA of the copper specific promoter <i>copAP</i> with 5’-UTR-<i>sfGFP</i> under the control of T7-promoter (<a href="https://parts.igem.org/Part:BBa_K1758325" target="_blank">BBa_K1758325</a>) to the cell extract. The T7-promoter is needed to get a better fluorescence expression. </p> | <p>For the characterization of the copper sensor with CFPS we used parts differing from that we used in vivo characterization. For the <i>in vitro</i> characterization we used a cell extract out of cells which contain the plasmid (<a href="https://parts.igem.org/Part:BBa_K1758320" target="_blank">BBa_K1758320</a>) (figure 5), so that the resulting extract is enriched with the activator CueR. To this extract we added plasmid-DNA of the copper specific promoter <i>copAP</i> with 5’-UTR-<i>sfGFP</i> under the control of T7-promoter (<a href="https://parts.igem.org/Part:BBa_K1758325" target="_blank">BBa_K1758325</a>) to the cell extract. The T7-promoter is needed to get a better fluorescence expression. </p> | ||
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| − | + | <img src="https://static.igem.org/mediawiki/2015/0/05/Bielefeld-CeBiTec_in_vitro_CueR-part.jpeg"width="100%"><figcaption> Figure 5: To produce the cell extract for <i>in vitro</i> characterization a construct (<a href="https://parts.igem.org/Part:BBa_K1758320" target="_blank">BBa_K1758320</a>) with copper activator under the control of a constitutive promoter and strong RBS (BBa_K608002) is needed. | |
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</figcaption> | </figcaption> | ||
</figure> | </figure> | ||
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| − | + | <img src="https://static.igem.org/mediawiki/2015/1/15/Bielefeld-CebiTec_in_vitro_T7-copAP-UTR-sfGFP.jpeg"><figcaption>Figure 6: T7-copAP-UTR-sfGFP <a href="https://parts.igem.org/Part:BBa_K1758325" target="_blank">BBa_K1758325</a> used for <i>in vitro</i> characterization. </figcaption> | |
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</figure> | </figure> | ||
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<p>The results presented in figure 7 illustrate the influences of different copper concentrations on the cell extract. </p> | <p>The results presented in figure 7 illustrate the influences of different copper concentrations on the cell extract. </p> | ||
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<!-- Einfluss von Kupfer auf den Zellextrakt, keinen negative Einfluss auf das CFPS so mit kann gezeigt werden dass dieses System relativ stabil gegenüber verschiedenen Kupferkonzentratione ist --> | <!-- Einfluss von Kupfer auf den Zellextrakt, keinen negative Einfluss auf das CFPS so mit kann gezeigt werden dass dieses System relativ stabil gegenüber verschiedenen Kupferkonzentratione ist --> | ||
| − | <figure | + | <figure> |
| − | + | <img src="https://static.igem.org/mediawiki/2015/3/37/Bielefeld-CeBiTec_Influence_of_copper_on_the_cell_extract.jpeg" width="100%"></a> | |
<figcaption>Figure 7: Influence of different copper concentrations on our crude cell extract. Error bars represent the standard deviation of three biological replicates. </figcaption> | <figcaption>Figure 7: Influence of different copper concentrations on our crude cell extract. Error bars represent the standard deviation of three biological replicates. </figcaption> | ||
| − | </figure | + | </figure> |
<p>As shown in figure 7 copper has no negative influence on the functionality of our cell extract. Therefore, a relatively stable system for copper sensing is provided. | <p>As shown in figure 7 copper has no negative influence on the functionality of our cell extract. Therefore, a relatively stable system for copper sensing is provided. | ||
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<!-- Induktion mit Kupfer im Kupfer spezifischen Extrakt --> | <!-- Induktion mit Kupfer im Kupfer spezifischen Extrakt --> | ||
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| − | + | <img src="https://static.igem.org/mediawiki/2015/4/45/Bielefeld-CeBiTec_induction_copper_in_CueR_cell-extract.jpeg" width="100%"></a> | |
| − | + | <figcaption>Figure 8: Copper specific cell extract made from <i>E. coli</i> cells which have already expressed the activator before cell extract production. Induction of copper inducible promoter without T7 upstream of the operator site with different copper concentrations. Error bars represent the standard deviation of three biological replicates.</figcaption> | |
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| − | <figcaption>Figure 8: Copper specific cell extract made from <i>E. coli</i> cells which have already expressed the activator before cell extract production. Induction of copper inducible promoter without T7 upstream of the operator site with different copper concentrations. Error bars represent the standard deviation of three biological replicates. | + | |
</figure> | </figure> | ||
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| − | + | <figure> | |
| − | + | <img src="https://static.igem.org/mediawiki/2015/4/4c/Bielefeld-CeBiTec_correction_induction_copper_in_cueR_cell-extract.jpeg" width="100%"></a> | |
<figcaption>Figure 9: Copper specific cell extract made from <i>E. coli</i> cells which have already expressed the activator before cell extract production. Induction of copper inducible promoter without T7 in front of the operator site with different copper concentrations. Error bars represent the standard deviation of three biological replicates. Data are normalized on coppers influence to the cell extract.</figcaption> | <figcaption>Figure 9: Copper specific cell extract made from <i>E. coli</i> cells which have already expressed the activator before cell extract production. Induction of copper inducible promoter without T7 in front of the operator site with different copper concentrations. Error bars represent the standard deviation of three biological replicates. Data are normalized on coppers influence to the cell extract.</figcaption> | ||
</figure> | </figure> | ||
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<p>In addition,we measured the operator device under the control of T7 promoter as described before.</p> | <p>In addition,we measured the operator device under the control of T7 promoter as described before.</p> | ||
| − | <p>Fluorescence was normalized to influence of copper on the the cell extract (figure 10 and figure 11).< | + | <p>Fluorescence was normalized to influence of copper on the the cell extract (figure 10 and figure 11).</p> |
<!--obrige Abbildung durch den errechneten Korrekturfaktor angepasst, da verschiedene Faktoren auf Zellextrakt wirken und so diesen beeinflussen.--> | <!--obrige Abbildung durch den errechneten Korrekturfaktor angepasst, da verschiedene Faktoren auf Zellextrakt wirken und so diesen beeinflussen.--> | ||
<!-- Es wurde auch das Konstrukt mit einen T7 davor eingesetzt, es zeichen sich unterschhiede inder Flurescens ausbeute, so mit ist für das CFPS system ein vorgeschalteter T7 sinnvoll zur besseren sensitivität des Systems. --> | <!-- Es wurde auch das Konstrukt mit einen T7 davor eingesetzt, es zeichen sich unterschhiede inder Flurescens ausbeute, so mit ist für das CFPS system ein vorgeschalteter T7 sinnvoll zur besseren sensitivität des Systems. --> | ||
| − | + | <figure> | |
| − | + | <img src="https://static.igem.org/mediawiki/2015/c/ce/Bielefeld-CeBiTec_induction_T7-copAP_copper_in_cueR_cell-extract.jpeg" width="100%"></a> | |
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<figcaption>Figure 10: Copper specific cell extract made from <i>E. coli</i> cells which have already expressed the activator before cell extract production. Induction with different copper concentrations. Error bars represent the standard deviation of three biological replicates. </figcaption> | <figcaption>Figure 10: Copper specific cell extract made from <i>E. coli</i> cells which have already expressed the activator before cell extract production. Induction with different copper concentrations. Error bars represent the standard deviation of three biological replicates. </figcaption> | ||
</figure> | </figure> | ||
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| − | + | <img src="https://static.igem.org/mediawiki/2015/0/01/Bielefeld-CeBiTec_correction_induction_T7-copAP_in_cueR_cell-extract.jpeg" width="100%"> | |
<figcaption>Figure 11: Copper specific cell extract made from <i>E. coli</i> cells which have already expressed the activator before cell extract production. Induction of copper inducible promoter with different copper concentrations. Error bars represent the standard deviation of three biological replicates. Data are normalized on coppers influence to the cell extract. </figcaption> | <figcaption>Figure 11: Copper specific cell extract made from <i>E. coli</i> cells which have already expressed the activator before cell extract production. Induction of copper inducible promoter with different copper concentrations. Error bars represent the standard deviation of three biological replicates. Data are normalized on coppers influence to the cell extract. </figcaption> | ||
</figure> | </figure> | ||
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<p>Compared to the former fluorescence levels the T7 reporter device showed higher levels. Therefore, a reporter device under the control of T7 promoter is more suitable for our CFPS.</p> | <p>Compared to the former fluorescence levels the T7 reporter device showed higher levels. Therefore, a reporter device under the control of T7 promoter is more suitable for our CFPS.</p> | ||
Revision as of 06:18, 19 September 2015
UTR-sfGFP under control of Copper responsive promoter
Copper induceble promoter with an untranslated region and sfGFP for detection via fluorescence
Usage and Biology
CopAP is the central component in obtaining copper homeostasis, which exports free copper from cytoplasm to the periplasm. This is enabled by copper induced activation of the operon transcription via CueR. The CueR-Cu+ is the DNA-binding transcriptional dual regulator which activates transcription (Yamamoto, Ishihama 2005). In our project this part is essential for the in vitro characterization of our copper sensor. We started characterizing it with this device, but data suggested that we could reach higher fluorescence level using a T7 promoter, which was realized in BBa_K1758325.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 29
Illegal SapI.rc site found at 179
Results
in vivo
Our sensor for copper detection consists of CueR a MerR like activator and the copper specific promoter copAP. The promoter is regulated by CueR, which binds Cu 2+ ions. We also used a sfGFP downstream the promoter for detection through a fluorescence signal.
For our copper sensor we used the native operator of cooper homeostasis from E.coli K12. We constructed a part (BBa_K1758324) using the basic genetic structur shown in our biosensors.The operator sequence, which includes the promoter (copAP), is regulated by the activator CueR. In BBa_K1758324 we combined a codon optimized version of cueR (BBa_K1758320) under the control of a constitutive promoter with sfGFP under the control of the corresponding promoter copAP (BBa_K1758321)(figure 2). Through the addition of a 5’ UTR upstream of the sfGFP we optimized the expression of sfGFP and increased fluorescence.
We tested our in vivo copper sensor with sfGFP as reporter gene, to test the functionality of the system. Moreover, we tested different copper concentrations. The kinetic of our sensors response to different copper concentrations is shown in figure 3. The first ten hours show a strong increase in fluorescence. After that the increase in fluorescence is slower. For better visualization the kinetics of figure 3 are represented as bars in figure 4. A fluorescence level difference for 60 min, 150 min and 650 min is represented.
In vivo we could show that the adding different concentrations of copper has effects on the transcription levels of sfGFP.
The shown data suggest that sensing copper with our device is possible even if the detectable concentrations are higher than the desireble sensitivity limits. Therfore we tested the copper sensor in our in vitro transcription translation approach.
in vitro
For the characterization of the copper sensor with CFPS we used parts differing from that we used in vivo characterization. For the in vitro characterization we used a cell extract out of cells which contain the plasmid (BBa_K1758320) (figure 5), so that the resulting extract is enriched with the activator CueR. To this extract we added plasmid-DNA of the copper specific promoter copAP with 5’-UTR-sfGFP under the control of T7-promoter (BBa_K1758325) to the cell extract. The T7-promoter is needed to get a better fluorescence expression.
The results presented in figure 7 illustrate the influences of different copper concentrations on the cell extract.
As shown in figure 7 copper has no negative influence on the functionality of our cell extract. Therefore, a relatively stable system for copper sensing is provided. First tests with specific cell extract and different copper concentrations lead to further tests and normalizations, illustrated in figure 8.
In addition,we measured the operator device under the control of T7 promoter as described before.
Fluorescence was normalized to influence of copper on the the cell extract (figure 10 and figure 11).
Compared to the former fluorescence levels the T7 reporter device showed higher levels. Therefore, a reporter device under the control of T7 promoter is more suitable for our CFPS.
After normalizing on coppers influence to the cell extract these differences were even more obvious.