Difference between revisions of "Part:BBa K3332013"
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− | We anchor GRHPR protein onto membranes through Lpp-OmpA to catalyze the reaction of reducing glyoxalic acid and consuming NADPH. We use <partinfo>BBa_K880005</partinfo> to construct the expression system and anchor GRHPR on the surface of ''E.coli''. | + | We anchor GRHPR protein onto membranes through Lpp-OmpA to catalyze the reaction of reducing glyoxalic acid and consuming NADPH. We use <partinfo>BBa_K880005</partinfo> to construct the expression system and anchor GRHPR on the surface of ''E.coli''. |
Revision as of 16:33, 27 October 2020
Lpp-OmpA-GRHPR
We anchor GRHPR protein onto membranes through Lpp-OmpA to catalyze the reaction of reducing glyoxalic acid and consuming NADPH. We use BBa_K880005 to construct the expression system and anchor GRHPR on the surface of E.coli.
Biology
Lpp-OmpA is an anchor protein from E. coli, which can anchor its passenger protein to the cell membrane. It has been widely used in cell-surface display. GRHPR, a Glyoxylate reductase from human liver, can reduce glyoxylic acid when NADPH is used as cofactor. GRHPR is fused at N terminal with Lpp-OmpA so that GRHPR can be displayed on the surface of E. coli.[1][2]
- Fig 1. mechanism.
Usage
Here, we used BBa_K880005 to construct the expression system and demonstrate the effect of Lpp-OmpA-GRHPR on the surface of E. coli. We obtained the composite part BBa_K3332058. Due to the limited time, we didn’t get the gene in time. As a result, there is a lack of data about this part. The progress of this part remains in the stage of design.
- Fig 2. Gene circuit of Lpp-OmpA-GRHPR.
References
- ↑ Rumsby G, Cregeen D P. Identification and expression of a cDNA for human hydroxypyruvate/glyoxylate reductase[J]. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1999, 1446(3): 383-388.
- ↑ http://2016.igem.org/Team:TJUSLS_China
Sequence and Features
- 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 1012
- 1000COMPATIBLE WITH RFC[1000]