Synthetic biology has developed numerous parts for building synthetic gene circuits. However, few parts have been described for prokaryotes to integrate two signals at a promoter in an AND fashion, i.e. the promoter is only activated in the presence of both signals. Here we present a new part for this function: a split intein T7 RNA polymerase. We divide T7 RNA polymerase into two expression domains and fuse each to a split intein. Only when both domains are expressed does the split intein mediate protein trans-splicing, yielding a full-length T7 RNA polymerase that can transcribe genes via a T7 promoter. We demonstrate an AND gate with the new part: the signal-to-background ratio is very high, resulting in an almost digital signal. This ha...
Synthetic genetic programs are built from circuits that integrate sensors and implement temporal con...
Synthetic genetic systems share resources with the host, including machinery for transcription and t...
Split inteins are powerful tools for seamless ligation of synthetic split proteins. Yet, their use r...
Synthetic genetic sensors and circuits enable pro-grammable control over the timing and conditions o...
Synthetic genetic sensors and circuits enable pro-grammable control over the timing and conditions o...
Microorganisms use genetic circuits to integrate environmental information. We have constructed a sy...
Developing the next generation of medical, agricultural and sustainability biotechnology is limited ...
Recent advances in nucleic acids engineering introduced several RNA-based regulatory components for ...
Bennett* Split T7 RNA polymerase provides new avenues for creating synthetic gene circuits that are ...
T7 RNA polymerase is the foundation of synthetic biological circuitry both <i>in vivo</i> and <i>in ...
textIn this work, we seek to expand synthetic in vitro biological systems by using water-in-oil emul...
Information processing using biochemical circuits is essential for survival and reproduction of natu...
Synthetic genetic systems share resources with the host, including machinery for transcription and t...
textT7 RNA polymerase is a single protein capable of driving transcription from a simple promoter in...
Synthetic genetic systems share resources with the host, including machinery for transcription and t...
Synthetic genetic programs are built from circuits that integrate sensors and implement temporal con...
Synthetic genetic systems share resources with the host, including machinery for transcription and t...
Split inteins are powerful tools for seamless ligation of synthetic split proteins. Yet, their use r...
Synthetic genetic sensors and circuits enable pro-grammable control over the timing and conditions o...
Synthetic genetic sensors and circuits enable pro-grammable control over the timing and conditions o...
Microorganisms use genetic circuits to integrate environmental information. We have constructed a sy...
Developing the next generation of medical, agricultural and sustainability biotechnology is limited ...
Recent advances in nucleic acids engineering introduced several RNA-based regulatory components for ...
Bennett* Split T7 RNA polymerase provides new avenues for creating synthetic gene circuits that are ...
T7 RNA polymerase is the foundation of synthetic biological circuitry both <i>in vivo</i> and <i>in ...
textIn this work, we seek to expand synthetic in vitro biological systems by using water-in-oil emul...
Information processing using biochemical circuits is essential for survival and reproduction of natu...
Synthetic genetic systems share resources with the host, including machinery for transcription and t...
textT7 RNA polymerase is a single protein capable of driving transcription from a simple promoter in...
Synthetic genetic systems share resources with the host, including machinery for transcription and t...
Synthetic genetic programs are built from circuits that integrate sensors and implement temporal con...
Synthetic genetic systems share resources with the host, including machinery for transcription and t...
Split inteins are powerful tools for seamless ligation of synthetic split proteins. Yet, their use r...