Difference between revisions of "Part:BBa K2139010"

 
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<partinfo>BBa_K2139010 short</partinfo>
 
<partinfo>BBa_K2139010 short</partinfo>
  
Ba_K2139010 encompass the coding region for an 1,4-beta-glucosidase known as Gluc1C along with a double terminator. Gluc1C is a monomeric enzyme capable of catalyzing decomposition of cellobiose down to two glucose monomers. It can be used in conjunction with an exo-beta-1,4-glucanase and endo-beta-1,4-glucanase for the conversion of cellulose to glucose. The genbank ascension number for this protein is JQ713769.1 (DNA), AFQ36783.1 (amino acid), and a PDB code of 2O9R_A. This construct was synthesized for use in Caulobacter crescentus and is codon optimized to contain a high GC content.
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Ba_K2139010 encompass the coding region for an 1,4-beta-glucosidase known as Gluc1C along with a double terminator. Gluc1C is a monomeric enzyme capable of catalyzing decomposition of cellobiose down to two glucose monomers. It can be used in conjunction with an exo-beta-1,4-glucanase and endo-beta-1,4-glucanase for the conversion of cellulose to glucose. The genbank ascension number for this protein is JQ713769.1 (DNA), AFQ36783.1 (amino acid), and a PDB code of 2O9R_A. This construct was synthesized by IDT for use in Caulobacter crescentus and is codon optimized.
  
 
Literature data for this part can be found http://www.sciencedirect.com/science/article/pii/S1046592812003154
 
Literature data for this part can be found http://www.sciencedirect.com/science/article/pii/S1046592812003154

Latest revision as of 21:04, 30 October 2016


Gluc1C with Terminator

Ba_K2139010 encompass the coding region for an 1,4-beta-glucosidase known as Gluc1C along with a double terminator. Gluc1C is a monomeric enzyme capable of catalyzing decomposition of cellobiose down to two glucose monomers. It can be used in conjunction with an exo-beta-1,4-glucanase and endo-beta-1,4-glucanase for the conversion of cellulose to glucose. The genbank ascension number for this protein is JQ713769.1 (DNA), AFQ36783.1 (amino acid), and a PDB code of 2O9R_A. This construct was synthesized by IDT for use in Caulobacter crescentus and is codon optimized.

Literature data for this part can be found http://www.sciencedirect.com/science/article/pii/S1046592812003154

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 264
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 1138