Pseudomonas syringae pv. tabaci 6605 possesses a genetic region involved in flagellin glycosylation. This region is composed of three open reading frames: orf1, orf2, and orf3. Our previous study revealed that orf1 and orf2 encode glycosyltransferases; on the other hand, orf3 has no role in posttranslational modification of flagellin. Although the function of Orf3 remained unclear, an orf3 deletion mutant (⌬orf3 mutant) had reduced virulence on tobacco plants. Orf3 shows significant homology to a 3-oxoacyl-(acyl carrier protein) synthase III in the fatty acid elongation cycle. The ⌬orf3 mutant had a significantly reduced ability to form acyl homoserine lactones (AHLs), which are quorum-sensing molecules, suggesting that Orf3 is required for AHL synthesis. In comparison with the wild-type strain, swarming motility, biosurfactant production, and tolerance to H 2 O 2 and antibiotics were enhanced in the ⌬orf3 mutant. A scanning electron micrograph of inoculated bacteria on the tobacco leaf surface revealed that there is little extracellular polymeric substance matrix surrounding the cells in the ⌬orf3 mutant. The phenotypes of the ⌬orf3 mutant and an AHL synthesis (⌬psyI) mutant were similar, although the mutant-specific characteristics were more extreme in the ⌬orf3 mutant. The swarming motility of the ⌬orf3 mutant was greater than that of the ⌬psyI mutant. This was attributed to the synergistic effects of the overproduction of biosurfactants and/or alternative fatty acid metabolism in the ⌬orf3 mutant. Furthermore, the amounts of iron and biosurfactant seem to be involved in biofilm development under quorum-sensing regulation in P. syringae pv. tabaci 6605.Pseudomonas syringae pv. tabaci 6605, an phytopathogenic bacterial isolate, causes wildfire disease on host tobacco plants and induces a hypersensitive reaction (HR) on nonhost plants.In previous studies, we demonstrated that flagellin, a component of the flagellar filament, is a major elicitor of HR by P. syringae pv. tabaci 6605 (30, 35). Flagellin of P. syringae pv. tabaci 6605 induces HR on nonhost plants but not on its host tobacco plant. Although the deduced amino acid sequence of P. syringae pv. glycinea race 4 flagellin (FliC) is identical to that of P. syringae pv. tabaci 6605 flagellin, the flagellin of P. syringae pv. glycinea does induce HR on tobacco plants, suggesting that posttranslational modification of flagellin determines the specificity to induce HR (34). We recently reported that genes existing upstream of fliC, which encodes flagellin protein, are involved in the glycosylation of flagellin in these two pathovars (33, 36). There are three open reading frames, namely, orf1, orf2, and orf3, in the glycosylation islands of P. syringae pv. tabaci and pv. glycinea (Fig. 1). Because the proteins encoded by orf1 and orf2 showed homology to a putative glycosyltransferase and the molecular mass of the flagellin of each orf1 and orf2 deletion mutant (⌬orf1 and ⌬orf2 mutants) was decreased, these genes are thought to encode the glycosyltransferases. I...