Difference between revisions of "Part:BBa K901007"

 
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<partinfo>BBa_K901007 short</partinfo>
 
<partinfo>BBa_K901007 short</partinfo>
  
pLacI regulated GalU ([https://parts.igem.org/Part:BBa_K901004 BBa_K901004]: an enzyme that cleaves sucrose into glucose and fructose)
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GalU ([https://parts.igem.org/Part:BBa_K901004 BBa_K901004]) under control of the LacI promoter ([https://parts.igem.org/Part:BBa_J04500 BBa_J04500]): galU codes for UDP-Glucose phosphorylase, an <i>E. coli</i> enzyme that produces UDP-glucose.
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This expression construct is part of a 3 enzyme system designed to enhance the production and secretion of monosaccharide sugars in <i>Synechococcus elongatus</i>. This system is comprised of InvA ([https://parts.igem.org/Part:BBa_K901003 BBa_K901003]), Galu, and Glf ([https://parts.igem.org/Part:BBa_K901008 BBa_K901008]).
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GalU codes for UDP-glucose phosphorylase. This is an enzyme from <i>E. coli</i> that produces UDP-glucose. The presence of UDP-glucose enhances the native production of the disaccharide sucrose in <i>S. elongatus</i> in response to salt shock.
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Sucrose is then cleaved into glucose and fructose by Invertase A and secreted from the cell via the membrane bound transport protein Glf. These monosaccharides are sufficient nutriment for <i>E. coli</i> and will be used to feed a culture of engineered cells designed to produce high levels of acetic acid.
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 19:09, 2 October 2012

GalU Expression Construct

GalU (BBa_K901004) under control of the LacI promoter (BBa_J04500): galU codes for UDP-Glucose phosphorylase, an E. coli enzyme that produces UDP-glucose.

This expression construct is part of a 3 enzyme system designed to enhance the production and secretion of monosaccharide sugars in Synechococcus elongatus. This system is comprised of InvA (BBa_K901003), Galu, and Glf (BBa_K901008).

GalU codes for UDP-glucose phosphorylase. This is an enzyme from E. coli that produces UDP-glucose. The presence of UDP-glucose enhances the native production of the disaccharide sucrose in S. elongatus in response to salt shock.

Sucrose is then cleaved into glucose and fructose by Invertase A and secreted from the cell via the membrane bound transport protein Glf. These monosaccharides are sufficient nutriment for E. coli and will be used to feed a culture of engineered cells designed to produce high levels of acetic acid.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 272
    Illegal NgoMIV site found at 380
    Illegal NgoMIV site found at 929
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 707
    Illegal BsaI.rc site found at 980