Isolates of Xanthomonas translucens f .sp. oryzicola readily produced phenylalanine deaminase 1 day after inoculation and tyrosinase and 0-glucosidase 4 days after inoculation, but isolates of Xanthomonas oryzae showed no such enzymatic activities by the methods employed. These differences easily distinguish bacterial blight of rice (caused by X. oryzae) from leaf streak of rice (caused by X . translucens f.sp. oryzicola).In the tropics the two most common bacterial diseases of the rice plant are blight and leaf streak. Bacterial blight, known for many All the authors mentioned failed to differentiate the pathogens from one another by physiological characteristics. This paper reports a study aimed at determining whether specific enzymatic tests can readily distinguish one pathogen from the other.
MATERIALS AND METHODSBacterial cultures. Forty isolates of X. oryzae and 16 isolates of X. translucens f.sp. oryzicola were selected from the bacterial stock cultures of the Plant Pathology Department of the International Rice Research Institute, Manila. The cultures were maintained on Wakimoto (18) agar slants (potato, 300 g; Ca(N0, ), )*4H, 0, 0.5 g; Na, HPO, 12H, 0, 2.0 g; peptone, 5.0 g; sucrose, 15.0 g; agar, 20.0 g; distilled water, 1,000 ml; pH adjusted to 6.8 to 7.0) in a deep freezer at -30 C. Twenty-four-hour-old agar slant cultures were used in inoculating test media, and they were incubated at +28 C after inoculation.tained by the method of Thornley (17), and asparagine hydrolase was tested similarly with 1% L-asparagine, whereas arginine decarboxylase and phenylalanine deaminase were determined by using the procedures described by Skerman (14). Catalase was detected with 10 vol of H,O,, and oxidase was t e s t e d w i t h 1 5% N,N-d i m e t hyl-p-phenylenediammonium dichloride (Merck) according to Kovacs (9) and Ewing and Johnson (4). Similarly, tyrosinase was demonstrated with L-tyrosine (19) and 0-glucosidase with 0.5% arbutin (8) after 4 days of incubation. Esculin hydrolysis was observed by the method of Sneath (15). Lipase was detected by the method of Sierra (13), and urease was tested in Christensen urea-agar medium (2).Biochemical tests. Arginine hydrolase was ascer-