Difference between revisions of "Part:BBa K3748011"

(→‎Team Estonia_TUIT characterization of BBa_K3748015 (pPAB1))
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pPAB1 promoter showed constitutive levels of Venus fluorescence throughout the experiment, confirming that it is a constitutive promoter. Compared to the background fluorescence of the DOM90 strain, pPAB1 showed a 19-fold higher level of fluorescence intensity (figure 1).
 
pPAB1 promoter showed constitutive levels of Venus fluorescence throughout the experiment, confirming that it is a constitutive promoter. Compared to the background fluorescence of the DOM90 strain, pPAB1 showed a 19-fold higher level of fluorescence intensity (figure 1).
  
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[[Image:PPAB1 Estonia TUIT.png|600px|thumb|center|'''Figure 1:''' <b>Graph depicting median fluorescence intensity of <i>pPAB1</i> and control strain</b>]]
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[[Image:PPAB1 Estonia TUITnew.png|600px|thumb|center|<b>Figure 1. The expression level of Venus is controlled by pREV1</b>. Bars indicate the mean fluorescence signal (AU), and error bars show the standard deviation.]]
  
 
<b>References:</b>
 
<b>References:</b>

Revision as of 04:24, 11 October 2022


pPAB1

S.cerevisiae medium strenght promoter.

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
    COMPATIBLE WITH RFC[1000]


Team Estonia_TUIT characterization of BBa_K3748011 (pPAB1)

Constitutive pPAB1 regulates the expression of an essential gene encoding for poly(A) binding protein, which is involved in the regulation of poly(A) tail length. Pab1 is localized to the nucleus and cytoplasm. It was shown that modulation of Pab1 levels can improve cell fitness under stress conditions (Martani et al., 2015).

We quantified the expression driven by the PAB1 promoter using fluorescent proteins as reporter genes. The expression cassettes were integrated into the yeast genome, and the fluorescence of the reporter proteins was monitored by quantitative time-lapse microscopy. The fluorescence levels were compared to the cell background fluorescence of the control DOM90 strain, which does not express any fluorescent proteins.

pPAB1 promoter showed constitutive levels of Venus fluorescence throughout the experiment, confirming that it is a constitutive promoter. Compared to the background fluorescence of the DOM90 strain, pPAB1 showed a 19-fold higher level of fluorescence intensity (figure 1).

Figure 1. The expression level of Venus is controlled by pREV1. Bars indicate the mean fluorescence signal (AU), and error bars show the standard deviation.

References:

  • Lee, M. E., DeLoache, W. C., Cervantes, B., & Dueber, J. E. (2015). A Highly Characterized Yeast Toolkit for Modular, Multipart Assembly. ACS Synthetic Biology, 4(9), 975–986. https://doi.org/10.1021/SB500366V/SUPPL_FILE/SB500366V_SI_002.ZIP
  • Martani, F., Marano, F., Bertacchi, S., Porro, D., & Branduardi, P. (2015). The Saccharomyces cerevisiae poly(A) binding protein Pab1 as a target for eliciting stress-tolerant phenotypes. Scientific Reports, 5, 18318. https://doi.org/10.1038/SREP18318