Difference between revisions of "Part:BBa K1129046"

 
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<h2>Experimental Data</h2>
 
<h2>Experimental Data</h2>
  
 
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4-CMH under the constitutive promoter (<html><b><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_J23118">BBa_J23118</b></a></html>) were transformed into ''E.coli 10G'' cells. An overnight culture of these cells harboring (<html><b><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K1129046">BBa_K1129046</b></a></html>)was inoculated into a fresh culture of 5mL minimal media containing tyrsoine.  Cells  and were harvested for GC-MS after 7 hours of growth.
  
  
 
<p align=center>https://static.igem.org/mediawiki/2013/5/5f/PhpGF9BoJPM%281%29.jpg</p>
 
<p align=center>https://static.igem.org/mediawiki/2013/5/5f/PhpGF9BoJPM%281%29.jpg</p>
  
4-CMH under the constitutive promoter (<html><b><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_J23118">BBa_J23118</b></a></html>) were transformed into ''E.coli 10G'' cells. An overnight culture of these cells harboring (<html><b><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K1129046">BBa_K1129046</b></a></html>)  and were harvested for GC-MS after 7 hours of growth.
 
 
Ech and fcs genes( <html><b><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K1129022">BBa_K1129022</b></a></html> and <html><b><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_K1129024">BBa_K1129024</b></a></html>), both of which are under constitutive promoters (<html><b><a href="https://parts.igem.org/wiki/index.php?title=Part:BBa_J23118">BBa_J23118</b></a></html>), were ligated into one pSB1C3 plasmid. An overnight culture of ''E.coli 10G'' cells harboring this plasmid was inoculated into a fresh culture of 5mL minimal media containing ferulic acid. Cells were then harvested for GC-MS after 7 hours of growth.
 
  
Figure 3. Compound generation identification by GC-MS. Chromatograms and mass spectra for select peaks are shown. Structures represent predictions based on library matching or comparison to standards. Controls represent plasmids missing the gene of interest. A) Internal control using caffeic acid. B) Conversion of p-coumaric acid to caffeic acid by constitutive expressed 4-CMH. C) Possible conversion of p-coumaric acid to caffeic acid by inducibly expressed 4CMH. The mass spectrum however is confounded by another compound.
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Figure 3. Compound generation identification by GC-MS. Chromatograms and mass spectra for select peaks are shown. Structures represent predictions based on library matching or comparison to standards. Controls represent plasmids missing the gene of interest. A) Internal control using caffeic acid. B) Conversion of p-coumaric acid to caffeic acid by constitutively expressed 4-CMH. C) Possible conversion of p-coumaric acid to caffeic acid after induction by arabinose on 4CMH under the control by the arabinose promoter. The mass spectrum however is confounded by another compound.

Latest revision as of 02:20, 29 October 2013

4-coumarate 3-hydroxylase under pTET constitutive promoter


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 100
    Illegal NgoMIV site found at 108
    Illegal NgoMIV site found at 858
    Illegal NgoMIV site found at 1031
    Illegal NgoMIV site found at 1433
    Illegal NgoMIV site found at 1437
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 632


Background

4-coumarate 3-hydroxylase is an enzyme in the vanillin pathway. 4-coumarate 3-hydroxylase (4-CMH) hydrolyses p-coumaric acid to caffeic acid. It is the 2nd enzyme in the biosynthetic pathway of vanillin bioproduction from the amino acid tyrosine. 4-CMH is biobrick (BBa_K238007) from KULeuven iGEM 2009



Experimental Data

4-CMH under the constitutive promoter (BBa_J23118) were transformed into E.coli 10G cells. An overnight culture of these cells harboring (BBa_K1129046)was inoculated into a fresh culture of 5mL minimal media containing tyrsoine. Cells and were harvested for GC-MS after 7 hours of growth.


PhpGF9BoJPM%281%29.jpg


Figure 3. Compound generation identification by GC-MS. Chromatograms and mass spectra for select peaks are shown. Structures represent predictions based on library matching or comparison to standards. Controls represent plasmids missing the gene of interest. A) Internal control using caffeic acid. B) Conversion of p-coumaric acid to caffeic acid by constitutively expressed 4-CMH. C) Possible conversion of p-coumaric acid to caffeic acid after induction by arabinose on 4CMH under the control by the arabinose promoter. The mass spectrum however is confounded by another compound.