Difference between revisions of "Part:BBa K2139002"
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<partinfo>BBa_K2139002 short</partinfo> | <partinfo>BBa_K2139002 short</partinfo> | ||
− | BBa_K2139000 encompass the coding region for an 1,4-beta-glucosidase gene known as Gluc1C. Gluc1C is a monomeric | + | BBa_K2139000 encompass the coding region for an 1,4-beta-glucosidase gene known as Gluc1C. Gluc1C is a monomeric enzyme capable of catalyzing the conversion of cellobiose into monomeric glucose at the non reducing end of the sugar polymer. It can be used in conjunction with an endoglucanase for the direct conversion of cellulose into monomeric 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 cresentus and is codon optimized to contain a high GC content. |
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 |
Revision as of 06:25, 14 October 2016
Coding Sequence of Gluc1C
BBa_K2139000 encompass the coding region for an 1,4-beta-glucosidase gene known as Gluc1C. Gluc1C is a monomeric enzyme capable of catalyzing the conversion of cellobiose into monomeric glucose at the non reducing end of the sugar polymer. It can be used in conjunction with an endoglucanase for the direct conversion of cellulose into monomeric 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 cresentus and is codon optimized to contain a high GC content.
Literature data for this part can be found http://www.sciencedirect.com/science/article/pii/S1046592812003154
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 264
- 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 1138