| Literature DB >> 26677142 |
Dennis Binder1, Claus Bier2, Alexander Grünberger3, Dagmar Drobietz2, Jennifer Hage-Hülsmann1, Georg Wandrey4, Jochen Büchs4, Dietrich Kohlheyer3, Anita Loeschcke1, Wolfgang Wiechert3, Karl-Erich Jaeger1,3, Jörg Pietruszka2,3, Thomas Drepper5.
Abstract
Controlling cellular functions by light allows simple triggering of biological processes in a non-invasive fashion with high spatiotemporal resolution. In this context, light-regulated gene expression has enormous potential for achieving optogenetic control over almost any cellular process. Here, we report on two novel one-step cleavable photocaged arabinose compounds, which were applied as light-sensitive inducers of transcription in bacteria. Exposure of caged arabinose to UV-A light resulted in rapid activation of protein production, as demonstrated for GFP and the complete violacein biosynthetic pathway. Moreover, single-cell analysis revealed that intrinsic heterogeneity of arabinose-mediated induction of gene expression was overcome when using photocaged arabinose. We have thus established a novel phototrigger for synthetic bio(techno)logy applications that enables precise and homogeneous control of bacterial target gene expression.Entities:
Keywords: caged compounds; gene expression; optogenetics; photochemistry; synthetic biology
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Year: 2016 PMID: 26677142 DOI: 10.1002/cbic.201500609
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164