Difference between revisions of "Part:BBa K1197012"
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− | . | + | P-coumaric acid production: |
+ | The aim of modeling P-coumaric Acid production is to predict the amount and the activity of this enzyme ,Sam8, and the production of p-coumaric acid. The model was created mainly by designing ODEs and enzyme kinetics equations .Then; these equations were solved by the help of MATLAB software. | ||
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+ | In our circuit, Sam8 gene is transcribed with B. subtilis specific constituve promoter Pveg. SacB is transcribed with Sam8 gene for secretion out of cell. | ||
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+ | • We have calculated our enzyme activity according to our enzyme production rate. In 3500 s , 12E9 molecule of p-coumaric acid is produced according to our model. | ||
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+ | '''Sam8 activity:''' | ||
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+ | https://static.igem.org/mediawiki/parts/2/2d/P-coumaric_acid.jpg | ||
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+ | '''Sam8 amount''' | ||
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+ | https://static.igem.org/mediawiki/parts/c/c4/Sam8.jpg | ||
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+ | References: | ||
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+ | 1- https://static.igem.org/mediawiki/2009/6/6c/ODEs.pdf | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Latest revision as of 03:38, 5 October 2013
Pveg + RBS + Sam 8 + DT
P-coumaric acid production: The aim of modeling P-coumaric Acid production is to predict the amount and the activity of this enzyme ,Sam8, and the production of p-coumaric acid. The model was created mainly by designing ODEs and enzyme kinetics equations .Then; these equations were solved by the help of MATLAB software.
In our circuit, Sam8 gene is transcribed with B. subtilis specific constituve promoter Pveg. SacB is transcribed with Sam8 gene for secretion out of cell.
• We have calculated our enzyme activity according to our enzyme production rate. In 3500 s , 12E9 molecule of p-coumaric acid is produced according to our model.
Sam8 activity:
Sam8 amount
References:
1- https://static.igem.org/mediawiki/2009/6/6c/ODEs.pdf
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1053
Illegal BamHI site found at 1455 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 796
Illegal AgeI site found at 743
Illegal AgeI site found at 912 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 347
Illegal BsaI site found at 613