Team:UST-Beijing/Project
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chimeric nuclear receptors. Through directed molecular evolution, a harmonious signal network regulating | chimeric nuclear receptors. Through directed molecular evolution, a harmonious signal network regulating | ||
metabolism of both prokaryocytes and their host eukaryocytes in the digestive tract is feasible. | metabolism of both prokaryocytes and their host eukaryocytes in the digestive tract is feasible. | ||
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+ | PR,whichisaabbreviationofproteorhodopsin,wasdiscoveredin2000throughshortgunsequencingofseawateroffthecoastofCalifornia.Itisaakindofmenbraneproteinsthatgeneratesaprotonmotiveforce(pmf)thatcanbeusedforadenosinetriphosphate(ATP)synthesisasalight-activatedprotonpump.Inourexperiment,wereplacedthePR’sprecusorsequencewiththatofcytochromeoxidasesubunit4isoform1,mitochondrialprecursor(Homosapiens).SoPRcanbefixedintheinnermembraneofmitochrondria.Meanwhile,allthecodonsareoptimizedaccordingtocodonusagebiasforHomosspiens.Then,thegeneofPRisconstructedinpSG5vectorforeukaryoticexpression. | ||
+ | FunctionalPRrequiresthecovalentbindingofretinal,whichissynthesizedfrom-carotene. | ||
== Project Details== | == Project Details== |
Revision as of 09:28, 4 September 2011
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Gene H-transfer: bile acid receptor in E.coli & proteorhodpsin in mitochindrial inner membrane
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We are engineering a bile acid sensor in E.coli and others
Using lacI DNA-binding domain and LXRbeta ligand-binding domain, we made an artificial bile acid receptor which can regulate expression of target gene within a natural lacI operon. As proof of principle, we
demonstrate that regulation of bacteria gene expression by host eukaryocyte metabolites is achievable using chimeric nuclear receptors. Through directed molecular evolution, a harmonious signal network regulating metabolism of both prokaryocytes and their host eukaryocytes in the digestive tract is feasible.
PR,whichisaabbreviationofproteorhodopsin,wasdiscoveredin2000throughshortgunsequencingofseawateroffthecoastofCalifornia.Itisaakindofmenbraneproteinsthatgeneratesaprotonmotiveforce(pmf)thatcanbeusedforadenosinetriphosphate(ATP)synthesisasalight-activatedprotonpump.Inourexperiment,wereplacedthePR’sprecusorsequencewiththatofcytochromeoxidasesubunit4isoform1,mitochondrialprecursor(Homosapiens).SoPRcanbefixedintheinnermembraneofmitochrondria.Meanwhile,allthecodonsareoptimizedaccordingtocodonusagebiasforHomosspiens.Then,thegeneofPRisconstructedinpSG5vectorforeukaryoticexpression. FunctionalPRrequiresthecovalentbindingofretinal,whichissynthesizedfrom-carotene.