Difference between revisions of "Template:Heidelberg/best basic"

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A triple mutant of this part has already been applied in the successful synthesis of organosilicons as a proof-of-concept.
 
A triple mutant of this part has already been applied in the successful synthesis of organosilicons as a proof-of-concept.
 
As a next step, this part can be implemented in the directed evolution approach of phage-assisted continuous evolution (PACE) or in the phage-related discontinuous evolution (PREDCEL) approach to improve organosilicon synthesis by cytochrome engineering.
 
As a next step, this part can be implemented in the directed evolution approach of phage-assisted continuous evolution (PACE) or in the phage-related discontinuous evolution (PREDCEL) approach to improve organosilicon synthesis by cytochrome engineering.
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{{Heidelberg/templateus/Imagesection|https://static.igem.org/mediawiki/2017/9/92/T--Heidelberg--GCAnilineCompound.png|Figure 4:|Gas chromatogram for the reaction of educt (1) and (5) to the product (3). 11.7 minutes retention time, indicates product formation. Unconverted educts converge 6.9 and 7.2, 7.4 minutes|}}
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{{Heidelberg/templateus/Imagesection|https://static.igem.org/mediawiki/2017/1/16/T--Heidelberg--MSAnilineCompound.png|Figure 5:|Mass chromatogram shows the breakdown of the product (3) <i>ethyl 2-((4-aminophenyl)dimethylsilyl)propanoate</i>. The product itself corresponds to a mass of 251 dalton|}}
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{{Heidelberg/templateus/Imagesection|https://static.igem.org/mediawiki/2017/e/ef/T--Heidelberg--GCNonAninlineCompound.png|Figure 6:|Gas chromatogram for the reaction of educt (2) and (5) to the product (4). 9.2 minutes retention time indicates product formation.|}}
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{{Heidelberg/templateus/Imagesection|https://static.igem.org/mediawiki/2017/2/2b/T--Heidelberg--MSNonAnilineCompound.png|Figure 7:|Mass chromatogram shows the breakdown of the product (4) <i>ethyl 2-(dimethyl(phenyl)silyl)propanoate</i>. The product itself corresponds to a mass of 236 dalton|}}
 
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Revision as of 16:52, 1 November 2017

BBa_K2398000

We present as best basic part the codon-optimized version of the cytochrome c protein that is able to convert silicon educts to organosilicon products.
Circularization Construct
{{{5}}}
This cytochrome c variant provides an easy to use tool that is accessible to everyone in the synthetic biology community and allows the user to harness the vast potential of organosilicons. This basic part exhibits a strong tendency to form silicon-carbon bonds and is, therefore, a valuable addition to perform controlled organic chemistry in microorganisms. A triple mutant of this part has already been applied in the successful synthesis of organosilicons as a proof-of-concept. As a next step, this part can be implemented in the directed evolution approach of phage-assisted continuous evolution (PACE) or in the phage-related discontinuous evolution (PREDCEL) approach to improve organosilicon synthesis by cytochrome engineering.
Figure 4:
Gas chromatogram for the reaction of educt (1) and (5) to the product (3). 11.7 minutes retention time, indicates product formation. Unconverted educts converge 6.9 and 7.2, 7.4 minutes
Figure 5:
Mass chromatogram shows the breakdown of the product (3) ethyl 2-((4-aminophenyl)dimethylsilyl)propanoate. The product itself corresponds to a mass of 251 dalton
Figure 6:
Gas chromatogram for the reaction of educt (2) and (5) to the product (4). 9.2 minutes retention time indicates product formation.
Figure 7:
Mass chromatogram shows the breakdown of the product (4) ethyl 2-(dimethyl(phenyl)silyl)propanoate. The product itself corresponds to a mass of 236 dalton