Difference between revisions of "Part:BBa K523002"
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===Usage and Biology=== | ===Usage and Biology=== | ||
| − | The product protein is believed to be periplasmic. | + | The product protein is believed to be periplasmic. β-glucosidase cleaves β(1→4) bonds, i.e. those found in the disaccharide cellobiose. |
The SignalP program predicts that a 20 amino acid localisation signal (at the N terminal) is cleaved off before the protein reaches its mature form. | The SignalP program predicts that a 20 amino acid localisation signal (at the N terminal) is cleaved off before the protein reaches its mature form. | ||
Revision as of 20:29, 16 September 2011
RBS + bglX (E. coli perisplasmic β-glucosidase)
This is the E. coli β-glucosidase gene bglX. The part contains the native Ribosome Binding Site.
The part was made using the strategy outlined in BBa_K523000, and therefore contains 4 extra bases at the 5' end which generate a BglII restriction site.
Usage and Biology
The product protein is believed to be periplasmic. β-glucosidase cleaves β(1→4) bonds, i.e. those found in the disaccharide cellobiose.
The SignalP program predicts that a 20 amino acid localisation signal (at the N terminal) is cleaved off before the protein reaches its mature form.
Edinburgh 2011 carried out some experiments on this part under the control of the lac promoter - see details at part BBa_K523014.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1658
Illegal AgeI site found at 1880
Illegal AgeI site found at 2069 - 1000COMPATIBLE WITH RFC[1000]