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3-methyl-1-butanol (3MB) from captured CO2 via photosynthesis
PCC 6803 (hereinafter referred to as PCC 6803) avoids the use of harmful chemicals and metal inducers. We previously reported the development of light-regulated gene expression systems in cyanobacteria

A green light-induced alcohol production system has been successfully integrated into cyanobacteria to produce value-added chemicals without the use of expensive chemical inducers. Green-light regulated production of isobutanol and 3-methyl-1-butanol from CO2 is environmentally friendly and cost-effective. This study demonstrates that light regulation is a potential tool for producing chemicals and increasing the viability of cyanobacterial biological processes.

Therefore, in this study, we used the CcaS/CcaR two-component system [13] to produce isobutanol and 3-methyl-1-butanol (3MB) in Synechocystis sp. PCC 6803 (hereinafter referred to as PCC 6803) avoids the use of harmful chemicals and metal inducers. We previously reported the development of light-regulated gene expression systems in cyanobacteria

Protocol for green light-induced ethanol production in Synechocystis sp. PCC6803 (PCC6803). a Biosynthetic pathway for the production of isobutanol and 3-methyl-1-butanol (3MB) from captured CO2 via photosynthesis in PCC 6803. A CcaS/CcaR two-component system derived from PCC6803 was used to regulate the gene expression levels of ketoacid decarboxylase (kdc) and alcohol dehydrogenase (adh), which are involved in the production of isobutanol and 3-methyl- Required for 1-butanol.

In this study, we demonstrate the green light-induced production of isobutanol and 3-methyl-1-butanol in PCC 6803 using the CcaS/CcaR two-component system. The expression of kdc and adh genes was induced by green light irradiation. Under the control of PcpcG2, isobutanol and 3-methyl-1-butanol were successfully produced. Furthermore, additional expression of ccaR resulted in the production of 238 mg L-1 isobutanol and 75 mg L-1 3-methyl-1-butanol within 5 days. This study demonstrates the potential use of the CcaS/CcaR system for chemical production in cyanobacteria.