Abstract: The present invention discloses a membrane-less reactor design for microbial electrosynthesis of alcohols from carbon dioxide (CO2). The membrane-less reactor design thus facilitates higher and efficient CO2 transformation to alcohols via single pot microbial electrosynthesis. The reactor design operates efficiently avoiding oxygen contact at working electrode without using membrane, in turn there is an increase in CO2 solubility and its bioavailability for subsequent CO2 conversion to alcohols at faster rate. The present invention further provides a process of operation of the reactor for biotransformation of the carbon dioxide.

Abstract: The present invention discloses a membrane-less reactor design for microbial electrosynthesis of alcohols from carbon dioxide (CO2). The membrane-less reactor design thus facilitates higher and efficient CO2 transformation to alcohols via single pot microbial electrosynthesis. The reactor design operates efficiently avoiding oxygen contact at working electrode without using membrane, in turn there is an increase in CO2 solubility and its bioavailability for subsequent CO2 conversion to alcohols at faster rate. The present invention further provides a process of operation of the reactor for biotransformation of the carbon dioxide.

Abstract: The invention relates to a fused gene containing: the promoter sequence of (a) gene(s) encoding the resistance to one or several metal(s) or encoding the catabolism of one or several xenobiotic compound(s), said promoter being inducible in the presence of said metal(s) or xenobiotic compound(s), or both, and downstream the promoter, a gene producing a detectable signal such as light emitting gene, said gene being under the control of said promoter, said gene producing a detectable signal being located at a position such that the induction of the promoter causes the transcription of the gene producing a detectable signal and such that there is no terminator between the promoter and the gene producing a detectable signal.