Difference between revisions of "Part:BBa K3930014"
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<h2>Introduction</h2>
 
<h2>Introduction</h2>
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<p>The promoter TetO7 is an doxycycline-inducible promoter. It must be used with the part coding for the activator protein rtTA advanced (BBa_K3930019). The sequence comes from the publication (Garí et al. 1997)</p>
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<p>The promoter TetO7 is an doxycycline-inducible promoter. It must be used with the part coding for the activator protein rtTA advanced (BBa_K3930019). The sequence comes from the publication Garí et al. (1997).</p>
 
<h2>Results</h2>
 
<h2>Results</h2>
  
 
<h3>Production of &beta;-carotene (BBa_K3930003)</h3>
 
<h3>Production of &beta;-carotene (BBa_K3930003)</h3>
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<p> The part (BBa_K3930002) was linearized and transformed into the <i>S.cerevisiae</i> LycoYeast strain. The production of &beta;-carotene was measured by HPLC. Figure 1 shows the chromatogram of a induced strain with 10 &mu;g.ml-1 of doxycycline.</p>
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<p> All the experiments that characterized this part are related to the final construct <a href="https://parts.igem.org/Part:BBa_K3930003" class="pr-0" target="_blank">(BBa K3930003) </a>, which was cloned into the <i>S. cerevisiae</i> LycoYeast strain. For more information on the experimental background, please refer to this part.</p>
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<p>The promoter controls in the pFRAMBOISE-notfused construct the expression of the CrtY gene, which converts lycopene to &beta;-carotene. The production of &beta;-carotene is therefore a control of the functionality when the expression is induced with doxycycline. The carotenoids produced by the LcyE part of our enzymatic fusion, are contained in the cells. They were extracted using the method described by López et al. (2020). Yeast cells were lysed in acetone using glass beads and the supernatant obtained after lysis was analyzed by RP-HPLC on a C18 column. In the LycoYeast-pVIOLETTE strains (which express the LcyE-ofCCD1 fusion), Figure 1 shows that lycopene is converted into a new product with a higher retention time. Considering the &beta;-ionone production results, we concluded this new peak most likely corresponds to &beta;-carotene. Nonetheless, the peak is also observed in the condition with no induction. It seems like there is no negative regulation of the promoter TetO7.</p>
 
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Revision as of 17:24, 16 October 2021


Doxycycline inducible promoter Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 282
    Illegal XhoI site found at 239
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


Introduction

The promoter TetO7 is an doxycycline-inducible promoter. It must be used with the part coding for the activator protein rtTA advanced (BBa_K3930019). The sequence comes from the publication Garí et al. (1997).

Results

Production of β-carotene (BBa_K3930003)

All the experiments that characterized this part are related to the final construct (BBa K3930003) , which was cloned into the S. cerevisiae LycoYeast strain. For more information on the experimental background, please refer to this part.

The promoter controls in the pFRAMBOISE-notfused construct the expression of the CrtY gene, which converts lycopene to β-carotene. The production of β-carotene is therefore a control of the functionality when the expression is induced with doxycycline. The carotenoids produced by the LcyE part of our enzymatic fusion, are contained in the cells. They were extracted using the method described by López et al. (2020). Yeast cells were lysed in acetone using glass beads and the supernatant obtained after lysis was analyzed by RP-HPLC on a C18 column. In the LycoYeast-pVIOLETTE strains (which express the LcyE-ofCCD1 fusion), Figure 1 shows that lycopene is converted into a new product with a higher retention time. Considering the β-ionone production results, we concluded this new peak most likely corresponds to β-carotene. Nonetheless, the peak is also observed in the condition with no induction. It seems like there is no negative regulation of the promoter TetO7.



Figure 1: Production of β-carotene upon doxycycline activation

β-caroteneis produced in vivo by our strain. On the right are presented the mass spectra that correspond between the standard and the observed peak


This promoter TetO7 isn't negatively regulated and is always actived under those lab conditions.


References

  1. Garí E, Piedrafita L, Aldea M, Herrero E. 1997. A set of vectors with a tetracycline-regulatable promoter system for modulated gene expression in Saccharomyces cerevisiae. Yeast. 13(9):837–848. doi:10.1002/(SICI)1097-0061(199707)13:9<837::AID-YEA145>3.0.CO;2-T.