Iron deficiency impairs chlorophyll biosynthesis and chloroplast development. In leaves, most of the iron must cross several biological membranes to reach the chloroplast. The components involved in the complex internal iron transport are largely unknown. Nitric oxide (NO), a bioactive free radical, can react with transition metals to form metal-nitrosyl complexes. Sodium nitroprusside, an NO donor, completely prevented leaf interveinal chlorosis in maize (Zea mays) plants growing with an iron concentration as low as 10 m Fe-EDTA in the nutrient solution. S-Nitroso-N-acetylpenicillamine, another NO donor, as well as gaseous NO supply in a translucent chamber were also able to revert the iron deficiency symptoms. A specific NO scavenger, 2-(4-carboxy-phenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, blocked the effect of the NO donors. The effect of NO treatment on the photosynthetic apparatus of iron-deficient plants was also studied. Electron micrographs of mesophyll cells from iron-deficient maize plants revealed plastids with few photosynthetic lamellae and rudimentary grana. In contrast, in NO-treated maize plants, mesophyll chloroplast appeared completely developed. NO treatment did not increase iron content in plant organs, when expressed in a fresh matter basis, suggesting that root iron uptake was not enhanced. NO scavengers 2-(4-carboxy-phenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide and methylene blue promoted interveinal chlorosis in iron-replete maize plants (growing in 250 m Fe-EDTA). Even though results support a role for endogenous NO in iron nutrition, experiments did not establish an essential role. NO was also able to revert the chlorotic phenotype of the iron-inefficient maize mutants yellow stripe1 and yellow stripe3, both impaired in the iron uptake mechanisms. All together, these results support a biological action of NO on the availability and/or delivery of metabolically active iron within the plant.Iron deficiency impairs chlorophyll biosynthesis and chloroplast development in both dicotyledonous and monocotyledonous species. Therefore, iron availability maintains a direct correlation with plant productivity. Chlorosis because of unavailability of iron in calcareous soils (high pH) is a major agricultural problem that results in diminished crop yields in an estimated 30% of calcareous soils worldwide (Mori, 1999).Iron deficiency responses involve several physiological plant adaptations (Guerinot and Yi, 1994;Mori, 1999). Under iron deficiency, plants have evolved two separate strategies for iron acquisition. Non-graminaceous plants (strategy I) enhance acidification of the extracellular medium and increase both root ferric-reducing capacity and uptake of ferrous iron. In contrast, graminaceous plants possess the ability to secrete phytosiderophores to enhance iron uptake from soils (strategy II). However, when iron availability is under a threshold level, both strategies I and II are not sufficient to support the iron requirement for plant development, and stress symptoms beco...