Homologs of the genes for indole-3-acetic acid (IAA) biosynthesis from Pseudomonas syringae pv. savastanoi were retrieved from a genomic library of P. syringae pv. syringae, and their nucleotide sequences were determined. Sequence relatedness between the P. syringae pv. syringae and P. syringae pv. savastanoi iaa operons is greater than 901% within the iaaM and iaaH loci but declines dramatically at a position approximately 200 bp 5' of the iaaM translation initiation codon. A third open reading frame was detected downstream of iaaH. Production of LIA was undetectable in mutant strain Y30-53.29, which was generated by transposition of TnS into the iaaM gene of P. syringae pv. syringae Y30. The IAA-deficient (LA-) mutant retained the ability to colonize the bean phylloplane and induced disease symptoms on bean which were similar to those produced by the parental strain. However, the population dynamics of the IAA-strain during the parasitic phase in leaves differed from those of both the parental strain and the mutant genetically restored for IAA biosynthesis. The mutant was capable of inducing disease symptoms when established in bean tissues at a lower initial cell density than either LIA-producing strain. Syringomycin biosynthesis by the IAA-strain was diminished in comparison with the parental strain or the mutant genetically restored for LIA production. The results indicate that bacterially derived IAA, or its biosynthesis, is involved in the regulation of in planta growth and in the expression of other factors that affect the host-pathogen interaction.The ability to produce indole-3-acetic acid (IAA) is widespread among soil and plant-associated microorganisms (17,25). Among phytopathogenic bacteria, production of IAA has been shown to play a causal role in the development of hyperplastic disease symptoms that are induced by certain species of bacteria. Production of IAA by plant cells after transformation with Agrobacterium tumefaciens and Agrobacterium rhizogenes is directed by the T-DNA genes and was shown to be a determinant for induction of hypertrophic plant growth after incorporation and expression within the host cells (1,51,55). These transformed plant cells produce IAA from L-tryptophan via the intermediate indole-3-acetamide (IAM). In this pathway, the enzyme tryptophan-2-monooxygenase catalyzes the conversion of tryptophan to IAM, and the conversion of IAM to IAA is catalyzed by the enzyme indoleacetamide hydrolase. Pseudomonas syringae pv. savastanoi also induces hyperplasia on its plant host, with symptoms varying from knots on oleander and olive to bark blisters and wart-like formations on ash (19). Induction of tumor formation by P. syringae pv. savastanoi on olive and oleander requires bacterial production of IAA (12, 49). As observed for crown gall cells, P. syringae pv. savastanoi produces IAA via the IAM pathway, and the genetic determinants for tryptophan-2-monooxygenase and indoleacetamide hydrolase (iaaM and iaaH, respectively) are part of an operon with iaaM promoter proximal (59). E...