Difference between revisions of "Team:WashU StLouis/Proof"

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<h1>Proof of Concept</h1>  
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<h2>Measuring biotin production to calculate reduced electron donors</h2>
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<h1 class="lactionwords">Proof of Concept</h1>  
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<h2 class="speechwords">Measuring biotin production to calculate reduced electron donors</h2>
  
 
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After identifying the genes and constructing the electron donor overproducing plasmids, proper assays were necessary in order to see if our new cells produced usable forms of electron donors. Not only was it shown that the products were overproduced, but also significant data supported the claim that these products were usable in protein synthesis.  
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After identifying our genes of interest and constructing the electron donor overproducing plasmids, we performed an assay in order to see if our new cells produced usable forms of reduced electron donors. Our assay showed that not only were the products were overproduced, but also significant data supported the claim that these electron donors were usable in protein synthesis.
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<p>Since the results of the electron donor absorbance data showed promising evidence of electron donor production, we decided to go a step further to ensure that our electron donor constructs were producing reduced and usable electron donors. We performed an assay which showed that not only were the products being overproduced, but also that there was significant data supporting the claim that these electron donors were usable in <i>E. coli's</i> metabolism.  
 
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After analyzing the results of our absorbance data of electron donors, it was decided to go a step further to ensure that these construct produced usable electron donors. A biotin assay was found that offered an indirect way of measuring the amount of reduced electron donors present. Biotin, commonly know as vitamin B7, is produced by a pathway that uses reduced flavodoxin/ferredoxin,specifically the SAM pathway that turns dethiobiotin to biotin[1] (see diagram below).  
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Biotin, commonly know as vitamin B7, is produced via a pathway that uses reduced flavodoxin/ferredoxin. The SAM pathway, which turns dethiobiotin into biotin (see figure)<sup>1</sup> results in a 1:1 stoichiometric relationship between reduced electron donors and biotin molecules produced<sup>2</sup>. By measuring the amount of biotin in our cells, we will indirectly measure the amount of reduced electron donors present in our cells. This also shows that our 'Super Cell' could be used to increase the production of other valuable metabolic products that require reduced electron donors. We used a readily available biotin assay to conduct our proof of concept experiment.
 
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By measuring the amount of biotin in the new cells, and recognizing the 1:1 stoichiometric relationship between reduced electron donors and biotin molecules[2], the amount of electron donors present and used can be indirectly measured. Results showed that overall, our constructs worked to increase biotin production, as seen in the graphs below.
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Results showed that overall, our constructs worked to increase biotin production, as seen in the graphs below.
 
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<li>When our constructs were in DH10B cells, the fldA, fldA/pfo, petF, and petF/pfo strains produced more biotin than the control DH10B strain at some induction level</li>
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<li>When our constructs were in DH10B cells, the <i>fldA</i>, <i>fldA</i>-<i>pfo</i>, <i>petF</i>, and <i>petF</i>-<i>pfo</i> strains produced more biotin than the control DH10B strain at some induction level</li>
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<li>When our constructs were in the ΔaceE knockout cells, the fldA, fldA/pfo, and petF strains all produced more biotin than the control DH10B strain, control ΔaceE knockout strain, and DH10B+constructs strain (petF/pfo data is lacking due to its inability to grow)</li>
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<li>When our constructs were in the Δ<i>aceE</i> knockout cells, the <i>fldA</i>, <i>fldA</i>-<i>pfo</i>, and <i>petF</i> strains all produced more biotin than the control DH10B strain, control Δ<i>aceE</i> knockout strain, and DH10B+constructs strain (<i>petF</i>-<i>pfo</i> data is not present because it was not able to grow)</li>
 
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<p>Go to the <a herf="https://2016.igem.org/Team:WashU_StLouis/Conclusions">conclusions page</a> to see a complete summary of our results and proof of concept experiments.</p>
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<p>This experiment illustrates a proof of concept for our Super Cells. We have shown that the theory behind the Super Cells work: that overproducing certain co-factors will increase the amount of resulting product. Specifically, we overproduced biotin by overproducing reduced electron donors, which are needed in biotin synthesis.<p>
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<p>Go to the <a href="https://2016.igem.org/Team:WashU_StLouis/Conclusions">Conclusions page</a> for a complete summary of our findings.</p>
  
  

Latest revision as of 03:48, 20 October 2016

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Proof of Concept

Measuring biotin production to calculate reduced electron donors

Since the results of the electron donor absorbance data showed promising evidence of electron donor production, we decided to go a step further to ensure that our electron donor constructs were producing reduced and usable electron donors. We performed an assay which showed that not only were the products being overproduced, but also that there was significant data supporting the claim that these electron donors were usable in E. coli's metabolism.

Biotin, commonly know as vitamin B7, is produced via a pathway that uses reduced flavodoxin/ferredoxin. The SAM pathway, which turns dethiobiotin into biotin (see figure)1 results in a 1:1 stoichiometric relationship between reduced electron donors and biotin molecules produced2. By measuring the amount of biotin in our cells, we will indirectly measure the amount of reduced electron donors present in our cells. This also shows that our 'Super Cell' could be used to increase the production of other valuable metabolic products that require reduced electron donors. We used a readily available biotin assay to conduct our proof of concept experiment.

Results showed that overall, our constructs worked to increase biotin production, as seen in the graphs below.

  • When our constructs were in DH10B cells, the fldA, fldA-pfo, petF, and petF-pfo strains produced more biotin than the control DH10B strain at some induction level
  • When our constructs were in the ΔaceE knockout cells, the fldA, fldA-pfo, and petF strains all produced more biotin than the control DH10B strain, control ΔaceE knockout strain, and DH10B+constructs strain (petF-pfo data is not present because it was not able to grow)

This experiment illustrates a proof of concept for our Super Cells. We have shown that the theory behind the Super Cells work: that overproducing certain co-factors will increase the amount of resulting product. Specifically, we overproduced biotin by overproducing reduced electron donors, which are needed in biotin synthesis.

Go to the Conclusions page for a complete summary of our findings.

References

  1. Lin, Steven, and John E. Cronan. "Closing in on complete pathways of biotin biosynthesis." Molecular BioSystems 7.6 (2011): 1811-1821.
  2. Picciocchi, Antoine, Roland Douce, and Claude Alban. "Biochemical characterization of the Arabidopsis biotin synthase reaction. The importance of mitochondria in biotin synthesis." Plant physiology 127.3 (2001): 1224-1233.