The effects of tabtoxinine-,8-lactam (T-,i-L) on nitrate uptake and glutamine synthetase (GS) and nitrate reductase (NR) activities in roots of Avena sativa seedlings were determined. Seven-day-old oat seedlings placed in a 10 mm KNO3 and 0.5 mm T-,B-L solution for 24 hours took up T-f,-L and lost approximately 90% of their root GS activity. 1H1T-,B-L taken up by roots of seven-day-old oat seedlings was associated with GS immunoprecipitated from the extract of these roots. Total nitrate uptake and in vivo NR activity were decreased approximately 50% in the T-,B-L treated roots. However, T-,6-L uptake did not affect the induction phases of nitrate uptake or reduction, nor did it inhibit in vitro NR activity. Thus, the decrease in nitrate uptake and reduction is a secondary effect of T-Ot-L action. Roots of seven-day-old oat seedlings were inoculated with Pseudomonas syringae pv tabaci (Tox+) and the pathogen population in the rhizosphere was estimated by dilution plate count; 6 x 10" bacteria were recovered after 3 days, as compared to the original inoculation with 7 x 10' bacteria, indicating a significant growth of the pathogen in the rhizosphere. The bacteria recovered from the rhizosphere caused chlorosis in tobacco leaves and produced T-,j-L in culture; I x 10i4 bacteria were recovered from roots of seedlings inoculated with P. syringae pv tabaci (Tox-) using the same inoculation and assay procedure as for the pv tabaci(Tox+). Extracts of surface-sterilized roots previously inoculated with P. syringae pv tabaci (Tox+) did not produce viable bacterial cultures when plated out on a complete medium. Oat seedlings growing in sand culture and inoculated with P. syringae pv tabaci (Tox+) had developed chlorosis, and root GS activity had declined to less than 10% of controls after 3 days. Conversely, seedlings inoculated with P. syringae pv tabaci (Tox-) never developed chlorosis and maintained normal levels of GS activity. All oat plants inoculated with P. syringae pv tabaci (Tox+) died within 7 days after inoculation as compared to the plants inoculated with P. syringae pv tabaci (Tox-) which grew to maturity.The phytopathogenic bacterium Pseudomonas syringae pv tabaci and several closely related pathovars produce tabtoxin which when hydrolyzed to tabtoxinine-#-lactam (18) (2-amino-4-[3-hydroxy-2-oxo-azacyclobutan-3-yl]-butanoic acid) (T-,B-L)2 is an irreversible inhibitor of GS (EC 6.3.2.1.) in vivo (7, 16). T-,B-L is not a host-selective toxin and inactivates GS purified from a variety of sources (4, 7).