In field experiments, increase the quantum efficiency of PSII (Fv/Fp), the Rfd-values (the chlorophyll fluorescence vitality indices) and the content of photosynthetic pigments in wheat leaves at pretreatment of wheat seeds with solutions of citrate nanoparticles has been shown. The green weight of plants at bacterial and phytoplasmas infecting at pretreatment with solutions of citrate nanoparticles, was increase, than without pre-treatment, in order: GeNPs>I-Se>SeNPs>VNPs as it has been shown. The Fv/Fp-values in leaves infected with phytoplasmas of plants at pretreatment of VNPs or I-Se solutions were more, than without pretreatment. The Fv/Fp-value in leafs with bacterial infecting at pretreatment of GeNPs with compared to infected plants without pretreatment was increased has been shown. The Rfd-value in leaves at pre-sowing treatment of GeNPs or I-Se and bacterial infecting compared to infected plants without the pr-treatment was more has been shown. This value at infected plants with phytoplasmas at pretreatment of GeNPs or VNPs, compared to infected plants without pretreatment, was increased. In greenhouse experiments, Fv/Fp-values of plants leaves infected of phytoplasmas, bacteria and wheat streak mosaic virus (WSMV) at pre-treatment of solutions of citrate nanoparticles compared to infected plants without pretreatment has been increased. The pretreatment with nanoparticles GeNPs caused grain production by 15.6% increased has been shown. The weight grains/10 in plants on variant with pretreatment with Ge

In greenhouse experiments changes in several metabolic parameters soybeans plants after inoculation by P. savastanoi pv. glycinea 9190, X. axonopodis pv. glycines 9192, BCMV, A. laidlawii on background pre-treatment by nanochelates (NHs) of V, Ge, Cu, Mo have been shown. The phenolic compounds content increased in leaves at inoculation by phytopathogens on background pre-treatment by NHs and without it. The content of H 2 O 2 in leaves increased in variants: BCMV (+VNHs, GeNHs, CuNHs), 9192 (+VNHs, CuNHs), 9190 (+GeNHs, CuNHs), A. laidlawii+MoNHs. But it decreased in the variants: BCMV + MoNHs, A. laidlawii + VNHs, 9190 + VNHs, 9192 (+ GeNHs, CuNHs) compared to controls. The peroxidase activity increased in variants: A. laidlawii, 9190, GeNHs + 9190, GeNHs + 9192, CuNHs, CuNHs (+ phytoplasmas, 9192), MoNHs (+ BCMV, phytoplasmas, 9190, 9192) with decreased catalase activity. The content of ABA in the leaves increased in variants: 9190, 9192 (+ VNHs, CuNHs), GeNHs + 9190, but the IAA content reduced. However, on variants MoNHs (+9190, 9192), GeNHs + 9192, A. laidlawii, A. laidlawii (+ GeNHs, CuNHs, MoNHs) the content of both phytohormones was decreased. The content of IAA and ABA in BCMV-infected leaves without treatment was increased, but on background of NHsit decreased