Types | DnaRegion
|
Roles | Regulatory
promoter
|
Description
We take advances in genetic engineering as synthetic biology, as viable solution to oil pollution cleanup. But for do this; we need to design and build an expression platform that works into our modified E.coli. For this, We choose four standardized biological parts from the Registry, those parts are: IPTG inducible promoter, Ribosomal Binding Site (RBS), GFP Reporter and Double Terminator; Were selected using rationale from molecular biology and genetic engineering to enable us to build up rationally-engineered, our expression platform. For the iGEM 2011, we will integrate and assembly those parts (P+RBS+GFP+T) along with our BioBrick part using the 3A Assembly Method, to bring up an expression device (P+RBS+rhlAB_BB+GFP+T) for rhamnolipid production in E. coli.
Notes
Those parts were assembled following the 3A assembly method.
Source
IPTG inducible Promoter with RBS
http://partsregistry.org/wiki/index.php?title=Part:BBa_J04500
GFP reporter plus Double terminator
http://partsregistry.org/wiki/index.php/Part:BBa_K653001