ABSTRACT The rice bacterial blight resistance gene, Xa22(t), provides resistance to a broad spectrum of Xanthomonas oryzae pv. oryzae isolates. Here, we localize the gene to a small 100-kb fragment of chromosome 11 by a combination of genetic recombination analysis and physical mapping. Mapping was done with two F(2) populations from the cross between Zhachanglong and Zhenzhuai. The first population consisted of 248 random individuals and 404 highly susceptible individuals selected from an F(2) population of more than 2,000 individuals and was used to construct a linkage map around the Xa22(t) locus. For the second F(2) population, 7,680 plants were examined with simple sequence repeat markers flanking the Xa22(t) locus to identify recombinants useful for fine-genetic mapping. Two large-insert bacterial artificial chromasome (BAC) libraries (from cvs. Teqing and Minghui63) were screened with a marker (R1506) which cosegregated perfectly with Xa22(t) in the first population. Restriction mapping of the resulting BAC clones enabled a physical map of the area to be constructed, and subclones from the BAC clones provided additional restriction fragment length polymorphism probes which could be placed on the fine-structure genetic map using the recombinants from the second mapping population. The Xa22(t) locus was mapped to a approximately 100-kb interval delimited by the R1506 marker and a subclone from the M3H8 BAC clone.