Difference between revisions of "Part:BBa K3192019"

 
 
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<partinfo>BBa_K3192019 short</partinfo>
 
<partinfo>BBa_K3192019 short</partinfo>
  
This gene encodes styE, a gene essential for the biochemical pathway degrading styrene into phenyl acetic acid.  
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<p>This part contains the styE gene taken from <i>Pseudomonas putida S12 </i>. This encodes the putative styrene transporter protein. This protein works to help shuttle the styrene molecules across the cell membrane into the cytoplasm to begin styrene degradation. It contains a 24 residue peptide for signaling to transport styrene. This is vital in the gene cluster styABCDE to allow the cell to metabolize styrene.<sup>1</sup> </p>
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<h3> References: </h3>
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<p> 1) Mooney, A., Oleary, N. D. & Dobson, A. D. W. Cloning and Functional Characterization of the styE Gene, Involved in Styrene Transport in Pseudomonas putida CA-3. <i> Applied and Environmental Microbiology </i> 72,1302–1309 (2006). </p>
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 22:23, 21 October 2019


styE

This part contains the styE gene taken from Pseudomonas putida S12 . This encodes the putative styrene transporter protein. This protein works to help shuttle the styrene molecules across the cell membrane into the cytoplasm to begin styrene degradation. It contains a 24 residue peptide for signaling to transport styrene. This is vital in the gene cluster styABCDE to allow the cell to metabolize styrene.1

References:

1) Mooney, A., Oleary, N. D. & Dobson, A. D. W. Cloning and Functional Characterization of the styE Gene, Involved in Styrene Transport in Pseudomonas putida CA-3. Applied and Environmental Microbiology 72,1302–1309 (2006).


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BamHI site found at 1040
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 125