Difference between revisions of "Part:BBa K3183100"

(→‎Part characterisation by Oxford iGEM 2019)
(→‎Part characterisation by Oxford iGEM 2019)
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Summary</b><br>
 
Summary</b><br>
 
We have used this part as a reporter of transformation success in our work on <i>L. reuteri</i>, and as a positive control for protein expression.
 
We have used this part as a reporter of transformation success in our work on <i>L. reuteri</i>, and as a positive control for protein expression.
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Methods</b><br>
 
Methods</b><br>
 
The composite part was inserted into the pTRKH3 (<partinfo>BBa_K3183050</partinfo>) vector by Gibson Assembly and transformed into <i>L. reuteri</i> 10023c by electroporation. The transformants were used in a fluorometric assay using excitation at 500 nm and detecting emission at 520 nm; the assay was used to show the relationship between exogenous protein expression and bacterial growth rate by comparing the OD600 and relative fluorescence of wild type and transformed bacteria. In addition, the part was used in fluorescence microscopy using the same absorption and emission wavelengths to determine the cytoplasmic protein distribution/morphology:
 
The composite part was inserted into the pTRKH3 (<partinfo>BBa_K3183050</partinfo>) vector by Gibson Assembly and transformed into <i>L. reuteri</i> 10023c by electroporation. The transformants were used in a fluorometric assay using excitation at 500 nm and detecting emission at 520 nm; the assay was used to show the relationship between exogenous protein expression and bacterial growth rate by comparing the OD600 and relative fluorescence of wild type and transformed bacteria. In addition, the part was used in fluorescence microscopy using the same absorption and emission wavelengths to determine the cytoplasmic protein distribution/morphology:
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Results:</b>
 
Results:</b>
 
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<li>The MRS medium in which the cells were grown has very high background fluorescence, such that its intrinsic noise significantly overshadowed the signal and most frequently led to negative values. </li>
 
<li>The MRS medium in which the cells were grown has very high background fluorescence, such that its intrinsic noise significantly overshadowed the signal and most frequently led to negative values. </li>
 
<li>The optical density of the solution due to light scattering by bacteria led to a significant drop in signal intensity, which would have been extremely difficult to correct for at large ODs</li>
 
<li>The optical density of the solution due to light scattering by bacteria led to a significant drop in signal intensity, which would have been extremely difficult to correct for at large ODs</li>
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<li>The vastly different chemical properties (e.g. ionic strength, the presence of quenchers etc.)of the cytosolic environment from regular buffer solutions likely result in very different spectroscopic properties of the fluors, such as quantum yield and maximal absorption/emission wavelengths, thus reducing the feasibility of comparison of our sample to the calibration curve based on fluorescein.</li>
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<li>The vastly different chemical properties (e.g. ionic strength, the presence of quenchers etc.)of the cytosolic environment from regular buffer solutions likely result in very different spectroscopic properties of the fluorophores, such as quantum yield and maximal absorption/emission wavelengths, thus reducing the feasibility of comparison of our sample to the calibration curve based on fluorescein.</li>
 
Therefore, we argue that the data we obtained cannot be used to quantitatively assess the strength of the promoters and has, at most, qualitative value. Therefore, we suggest that in the future more rigorous assays performed by purifying the enzyme and measuring its fluorescence after the buffer was exchanged to one similar to that of the fluorescein solution.  
 
Therefore, we argue that the data we obtained cannot be used to quantitatively assess the strength of the promoters and has, at most, qualitative value. Therefore, we suggest that in the future more rigorous assays performed by purifying the enzyme and measuring its fluorescence after the buffer was exchanged to one similar to that of the fluorescein solution.  
 
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Revision as of 15:25, 21 October 2019


Erythromycin Promoter Reporter Gene

Erythromycin Promoter fused with mGFP5


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 BsaI.rc site found at 928


Part characterisation by Oxford iGEM 2019

Reporter of constitutive expression in L. reuteri

Summary
We have used this part as a reporter of transformation success in our work on L. reuteri, and as a positive control for protein expression.

Methods
The composite part was inserted into the pTRKH3 (BBa_K3183050) vector by Gibson Assembly and transformed into L. reuteri 10023c by electroporation. The transformants were used in a fluorometric assay using excitation at 500 nm and detecting emission at 520 nm; the assay was used to show the relationship between exogenous protein expression and bacterial growth rate by comparing the OD600 and relative fluorescence of wild type and transformed bacteria. In addition, the part was used in fluorescence microscopy using the same absorption and emission wavelengths to determine the cytoplasmic protein distribution/morphology:

Results:

Fig. 1: Transformant Fluorescence: Normalized fluorescence of the cell cultures was determined by calculating the ratio of raw fluorescence to the optical density at 600 nm to ensure that the fluorescence levels measured are a result of reporter gene expression and not simply due to cell growth. The observed drop in fluorescence/OD600 across the time period can be accounted for by considering the large background fluorescence signal of MRS, such that the fluorescence stays nearly constant, while the OD increases markedly as a result of cell proliferation.
Fig. 2: Fluorescence Microscopy: top row: micrographs of normalised exposure show the relative levels of exogenous protein expression in 3 strains of Lactobacillus reuteri 100-23c: wild type, pTRKH3-erm-GFP and pTRKH3-erm-slpMod CD27L_mClover. Bottom row: the corresponding bright field imaging mode. As expected, no fluorescent protein expression is detected in the wild type strain, while significant levels are observable in the GFP transformants. However, the CD27L shows low level expression concentrated in inclusion body-like structures.



Discussion:
The results section shows that the blank corrected fluorescence intensity signals often have negative values. This is likely because, instead of purifying the protein and exchanging the buffer, we performed our assays on living cells; this had a number of consequences on the accuracy of our results:

  • The MRS medium in which the cells were grown has very high background fluorescence, such that its intrinsic noise significantly overshadowed the signal and most frequently led to negative values.
  • The optical density of the solution due to light scattering by bacteria led to a significant drop in signal intensity, which would have been extremely difficult to correct for at large ODs
  • The vastly different chemical properties (e.g. ionic strength, the presence of quenchers etc.)of the cytosolic environment from regular buffer solutions likely result in very different spectroscopic properties of the fluorophores, such as quantum yield and maximal absorption/emission wavelengths, thus reducing the feasibility of comparison of our sample to the calibration curve based on fluorescein.

    • Therefore, we argue that the data we obtained cannot be used to quantitatively assess the strength of the promoters and has, at most, qualitative value. Therefore, we suggest that in the future more rigorous assays performed by purifying the enzyme and measuring its fluorescence after the buffer was exchanged to one similar to that of the fluorescein solution.