Difference between revisions of "Part:BBa K1758332"

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<partinfo>BBa_K1758332 parameters</partinfo>
 
<partinfo>BBa_K1758332 parameters</partinfo>
 
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===Results===
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<h2><i>in vivo</i> characterization </i></h2></br>
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<p>In addition to the other heavy metal sensors, we constructed a sensor for lead detection. It consists of the repressor PbrR which binds at the operator box downstream of the <i>pbrAP </i>promoter. The binding of the repressor is reversible in the presence of Pb<sup>2+</sup> Ions. Those ions can weakened the repressors binding and hence, all genes downstream of the <i>pbrAP</i> promoter can be expressed. Like the former sensors this one encloses a sfGFP for detection via fluorescence. So if no lead is present in the media, the repressor binds to the operator box and the <i>pbrAP</i> promoter is blocked meaning that the transcription of <i>sfGFP</i> is prevented. No fluorescence signal is the results. By supplementation of lead, the repressor is separated from the operator box and the genes downstream of the promoter can be expressed.  </p>
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<p>The <i>pbrAP </i>promoter, the operator box and the PbrR repressor are parts of the chromosomal lead operon of <i>Cupriavidus metallidurans</i> (figure 1). This was cloned and transformed into <i>E.coli</i> KRX. This operon includes now the promoter <i>pbrAP</i> (<a href="https://parts.igem.org/Part:BBa_K1758332" target="_blank"> BBa_K1758332 </a>)), which is regulated by the repressor PbrR. The PbrR belongs to the MerR family, of metal-sensing regulatory proteins, and is Pb2+-inducible. Our sensor system comprises <i>pbrR</i> (<a href="https://parts.igem.org/Part:BBa_K1758330" target="_blank"> BBa_K1758330 </a>) BBa_K1758330 ), which is under the control of a constitutive Promoter and <i>pbrAP</i> and a 5’ untranslated region, which controls the transcription of a sfGFP and increases the fluorescence. Fluorescence implemented by sfGFP protein is the measured output signal (figure 2 and figure 3).  </p>
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<figure>
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<a><img src="https://static.igem.org/mediawiki/2015/a/a3/Bielefeld-CebiTec_in_vivo_Lead.jpeg" alt="genetical approach" width="80%"></a>
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<figcaption>Figure 1: The concept of our in vivo lead sensor  (<a href="https://parts.igem.org/Part:BBa_K1758332" target="_blank"> BBa_K1758332</a>)which consists of the repressor under the control of a constitutive promoter  (<a href="https://parts.igem.org/Part:BBa_K1758330" target="_blank"> BBa_K17583230</a>) and the operator and promoter sequence of the lead 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_K1758332" target="_blank"> BBa_K1758332</a>).</figcaption>
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<figure>
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<a><img src="https://static.igem.org/mediawiki/2015/d/d5/Bielefeld-CeBiTec_Biolector_lead.jpg" width="80%"></a>
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<figcaption>Figure 2: Time course of the induction of a lead biosensor with sfGFP for different lead concentrations <i>in vivo</i>. The data are measured with BioLector and normalized to the OD<sub>600</sub>. Error bars represent the standard deviation of two biological replicates. </figcaption>
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<figure>
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<a><img src="https://static.igem.org/mediawiki/2015/a/aa/Bielefeld-CeBiTec_Biolector_lead_Balkendiagramm.jpeg" width="80%"></a>
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<figcaption>Figure 3: Fluorescence levels at three different stages of cultivation. Shown are levels after 60 minutes, 150 minutes and 650 minutes. Error bars represent the standard deviation of two biological replicates. </figcaption>
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</figure>
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<p>The kinetic of our sensors response to different lead concentrations is shown in figure 2. The first 40 hours show a strong increase in fluorescence. After that the increase in fluorescence reaches a plateau. For better visualization the kinetics of figure 2 are represented as bars in figure 3. A fluorescence level difference for 60 min, 150 min and 650 min is represented.</p>
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<p> The results of the lead sensor show no significant differences between the different concentrations (figure 3). This might be due to the <i>pbrAP’s</i> weak promoter strength in <i>E. coli.</i> Further reasons are most likely in the weak repressor binding to its operator.  So, we suggest for the usage of this sensor, it has to be optimized. Moreover we were lacking time for further in vivo characterizations and different experimental setups. Hence, we did not use this sensor in further experiments regarding Cell-free-Protein-synthesis (CFPS). In the future a characterization in the CFPS systems would be desirable.  </p>
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Revision as of 05:54, 19 September 2015

PbrA-5-UTR-sfGFP Lead repressor under control of constitutive promoter and strong RBS

Lead promoter with 5´untranslated reigion and sfGFP for detection


Usage and Biology

For our biosensor we use parts of the chromosomal lead operon of Cupriavidus metallidurans (Ralstonia metallidurans). The promoter that we use is PbrA. This part of the operon is regulated by the repressor pbrR.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 133


Results

in vivo characterization


In addition to the other heavy metal sensors, we constructed a sensor for lead detection. It consists of the repressor PbrR which binds at the operator box downstream of the pbrAP promoter. The binding of the repressor is reversible in the presence of Pb2+ Ions. Those ions can weakened the repressors binding and hence, all genes downstream of the pbrAP promoter can be expressed. Like the former sensors this one encloses a sfGFP for detection via fluorescence. So if no lead is present in the media, the repressor binds to the operator box and the pbrAP promoter is blocked meaning that the transcription of sfGFP is prevented. No fluorescence signal is the results. By supplementation of lead, the repressor is separated from the operator box and the genes downstream of the promoter can be expressed.

The pbrAP promoter, the operator box and the PbrR repressor are parts of the chromosomal lead operon of Cupriavidus metallidurans (figure 1). This was cloned and transformed into E.coli KRX. This operon includes now the promoter pbrAP ( BBa_K1758332 )), which is regulated by the repressor PbrR. The PbrR belongs to the MerR family, of metal-sensing regulatory proteins, and is Pb2+-inducible. Our sensor system comprises pbrR ( BBa_K1758330 ) BBa_K1758330 ), which is under the control of a constitutive Promoter and pbrAP and a 5’ untranslated region, which controls the transcription of a sfGFP and increases the fluorescence. Fluorescence implemented by sfGFP protein is the measured output signal (figure 2 and figure 3).

genetical approach
Figure 1: The concept of our in vivo lead sensor ( BBa_K1758332)which consists of the repressor under the control of a constitutive promoter ( BBa_K17583230) and the operator and promoter sequence of the lead inducible promoter. An untranslated region in front of the sfGFP, which is used for detection, enhances its expression ( BBa_K1758332).
Figure 2: Time course of the induction of a lead biosensor with sfGFP for different lead concentrations in vivo. The data are measured with BioLector and normalized to the OD600. Error bars represent the standard deviation of two biological replicates.
Figure 3: Fluorescence levels at three different stages of cultivation. Shown are levels after 60 minutes, 150 minutes and 650 minutes. Error bars represent the standard deviation of two biological replicates.

The kinetic of our sensors response to different lead concentrations is shown in figure 2. The first 40 hours show a strong increase in fluorescence. After that the increase in fluorescence reaches a plateau. For better visualization the kinetics of figure 2 are represented as bars in figure 3. A fluorescence level difference for 60 min, 150 min and 650 min is represented.

The results of the lead sensor show no significant differences between the different concentrations (figure 3). This might be due to the pbrAP’s weak promoter strength in E. coli. Further reasons are most likely in the weak repressor binding to its operator. So, we suggest for the usage of this sensor, it has to be optimized. Moreover we were lacking time for further in vivo characterizations and different experimental setups. Hence, we did not use this sensor in further experiments regarding Cell-free-Protein-synthesis (CFPS). In the future a characterization in the CFPS systems would be desirable.