A system was developed for the formation of ethylene in vitro by an extract of Pseudomonas syringae pv. phaseolicola PK2. The ethylene-forming activity of a cell-free extract of this bacterium measured in a system reported previously was almost completely lost when the cell-free extract was dialysed against potassium phosphate buffer for 24 h at 4 "C. When the fraction of cell-free extract with a molecular mass < 10 kDa (SupI) was added back to the enzyme fraction after gel filtration of the cell-free extract, the enzymic activity increased to about four times that of the gel-filtered crude enzyme. The action of SupI could be reproduced by the addition of L-arginine. The complete system for the formation of ethylene under aerobic conditions in vitro required 0.25 mM-2-oxoglutarate, 0.2 mM-FeSO,, 2 mM-Dn, 10 mM-L-histidine and 0.2 mM-L-arginine. The cofactor specificity was examined by replacing L-arginine or L-histidine with various analogues, but none of them were effective. The components of this system, with the exception of L-histidine, were similar to those of a system derived from the ethylene-producing, plant pathogenic fungus Penicillium digitatum which also produced ethylene in vitro in a reaction dependent on 2-oxoglutarate. The intermediates in the ethylene-forming reaction are postulated and the roles of L-arginine and L-histidine in the formation of ethylene by Ps. syringae are discussed.