Difference between revisions of "Part:BBa K2139008"
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<partinfo>BBa_K2139008 short</partinfo> | <partinfo>BBa_K2139008 short</partinfo> | ||
− | This part encompass the coding region for an endo-beta-1,4-glucanase known as G12. G12 catalyzes the conversion of cellulose into smaller fragments by making internal cuts in the cellulose chain. It can be used in conjunction with exoglucanases for the direct conversion of cellulose into monomeric glucose. The | + | This part encompass the coding region for an endo-beta-1,4-glucanase known as G12. G12 catalyzes the conversion of cellulose into smaller fragments by making internal cuts in the cellulose chain. It can be used in conjunction with exoglucanases and beta-1,4-glucosidases for the direct conversion of cellulose into monomeric glucose. The protein is monomeric with an optimal temperature of 50 degrees Celsius and an optimal pH ranging from 6 to 8. The genbank ascension number for this protein is ABK52392.1 (amino acid) and a PDB code of 1H0B_A (homolog). |
Literature data for this part can be found http://aem.asm.org/content/76/19/6360.full | Literature data for this part can be found http://aem.asm.org/content/76/19/6360.full |
Latest revision as of 20:09, 30 October 2016
G12 Expression Cassette
This part encompass the coding region for an endo-beta-1,4-glucanase known as G12. G12 catalyzes the conversion of cellulose into smaller fragments by making internal cuts in the cellulose chain. It can be used in conjunction with exoglucanases and beta-1,4-glucosidases for the direct conversion of cellulose into monomeric glucose. The protein is monomeric with an optimal temperature of 50 degrees Celsius and an optimal pH ranging from 6 to 8. The genbank ascension number for this protein is ABK52392.1 (amino acid) and a PDB code of 1H0B_A (homolog).
Literature data for this part can be found http://aem.asm.org/content/76/19/6360.full
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 864