Cyanobacteria are autotrophic prokaryotes which carry out oxygenic photosyn
thesis and accumulate glycogen as the major form of stored carbon. In this
research, we introduced new genes into a cyanobacterium in order to create
a novel pathway for fixed carbon utilization which results in the synthesis
of ethanol. The coding sequences of pyruvate decarboxylase (pdc) and alcoh
ol dehydrogenase II (adh) from the bacterium Zymomonas mobilis were cloned
into the shuttle vector pCB4 and then used to transform the cyanobacterium
Synechococcus sp. strain PCC 7942. Under control of the promoter from the r
bcLS operon encoding the cyanobacterial ribulose-1,5-bisphosphate carboxyla
se/oxygenase, the pdc and adh genes were expressed at high levels, as demon
strated by Western blotting and enzyme activity analyses. The transformed c
yanobacterium synthesized ethanol, which diffused from the cells into the c
ulture medium. As cyanobacteria have simple growth requirements and use lig
ht, CO2, and inorganic elements efficiently, production of ethanol by cyano
bacteria is a potential system for bioconversion of solar energy and CO2 in
to a valuable resource.