Application of FaRLiP

Regulation of FaRLiP Gene Cluster

What applications could FaRLiP in cyanobacteria have? Is it possible to transfer it to enable other species to utilize far-red light? We are dedicated to applying the genes and mechanisms of FaRLiP in synthetic biology research. This includes, but is not limited to, identifying promoters that can be regulated by far-red light and establishing systems that can be controlled by far-red light in cyanobacteria, as well as potentially in other bacteria or organisms.

Relative Publications:

Screening Far-red light Promoters

We analyze the transcriptome of FaRLiP cyanobacterial strains under far-red light, identifying genes induced by far-red light. Through our established fluorescent protein reporter system, we test potential upstream promoter sequences of these genes. Promoters such as PchlFJSC1 are significantly induced by far-red light.

Selected Publication:

Establish FRL Regulation Systems

Through the FRL promoter and the regulators rfpABC, which control the expression of the FaRLiP gene cluster, we can express eYPF under far-red light and deactivate the expression system in the absence of light. Currently, we are working on applying this system to other cyanobacteria or organisms that cannot utilize far-red light for photosynthesis.

Relative Publication:

Explore the possibilities of FaRLiP applications

Cyanobacteria are widely used in applications such as bioenergy and compound synthesis. Issues like insufficient light can arise as cell density increases in bioreactors. By enabling cells to perform photosynthesis using far-red light, it can effectively address the lighting problems in bioreactors  and extend the operation field of cyanobacteria bioreactor.