From: Phytonanotechnology applications in modern agriculture
Abiotic stress | Nanomaterials (size) | Plant species | Ameliorative effects | References |
---|---|---|---|---|
Heat | MWCNTs (10–35 nm) | Tomato (Solanum lycopersicum L.) | Upregulated the expression of various stress-related genes including HSP90 | Khodakovskaya et al. [117] |
CeO2 NPs (~ 10 nm) | Maize (Zea mays L.) | Decreased production of hydrogen peroxide (H2O2) and upregulation of HSP70 | Zhao et al. [118] | |
TiO2 NPs (~ 16 nm) | Tomato (S. lycopersicum L.) | Enhanced photosynthesis, regulated energy dissipation, and induced stomatal opening | Qi et al. [119] | |
Ag NPs (10–20 nm) | Wheat (Triticum aestivum L.) | Protected plants against heat stress and improved plant growth significantly | Iqbal et al. [120] | |
Ag NPs (15–30 nm) | Wheat (T. aestivum L.) | Alleviated the harmful effects of salinity stress | Abou-Zeid and Ismail [121] | |
Se NPs (10–40 nm) | Tomato (S. lycopersicum L.) | Increased chlorophyll content, hydration of plants, and growth | Djanaguiraman et al. [122] | |
Cold | SiO2 NPs (10–15 nm) | Wheatgrass (Agropyron elongatum L.) | Overcame seed dormancy, enhanced seed germination and seedling weight | Azimi et al. [123] |
Na2SeO4 NPs (20–35 nm) | Tomato (S. lycopersicum L.) | Improved plant growth, chlorophyll, and leaf-relative water contents | Haghighi et al. [124] | |
TiO2 NPs (~ 20 nm) | Chickpea (Cicer arietinum L.) | Enhanced expression of Rubisco- and chlorophyll-binding protein genes | Hasanpour et al. [125] | |
ZnO NPs (~ 30 nm) | Rice (Oryza sativa L.) | Alleviated chilling stress by regulating the chilling response transcription factors | Song et al. [126 | |
Salinity | SiO2 NPs (~ 20 nm) | Tomato (S. lycopersicum L.) | Alleviated the effect of salinity on fresh weight, chlorophyll, and photosynthetic rate | Haghighi and Pourkhaloee [127] |
SiO2 NPs (~ 12 nm) | Squash (Cucurbita pepo L.) | Reduced levels of malondialdehyde (MDA), H2O2, and electrolyte leakage | Siddiqui et al. [76] | |
SiO2 NPs (~ 20 nm) | Tomato (S. lycopersicum L.) | Suppressed the effect of salinity on germination rate, root length, and fresh weight | Almutairi [128] | |
Chitosan NPs (~ 38 nm) | Maize (Z. mays L.) | Alleviated the harmful effects of salinity stress | Bruna et al. [129] | |
MWCNTs (30–100 nm) | Cabbage (Brassica oleracea L.) | Alleviated the harmful effects of salinity stress | Martinez-Ballesta et al. [130] | |
ZnO NPs (~ 20 nm) | Sunflower (Helianthus annuus L.) | Increased net CO2 assimilation rate, sub-stomatal CO2 content, and Fv/Fm ratio | Torabian et al. [131] | |
Fe2O3 NPs (~ 50 nm) | Peppermint (Mentha piperita L.) | Increased leaf dry weight, phosphorus, potassium, iron, zinc, and calcium contents | Askary et al. [132] | |
Fe2O3 NPs (~ 20 nm) | Wheat (T. aestivum L.) | Improved the growth of both root and shoot | Fathi et al. [133] | |
ZnO NPs (~ 20 nm) | Wheat (T. aestivum L.) | Improved the growth of both root and shoot | Fathi et al. [133] | |
SiO2 NPs (~ 10 nm) | Cucumber (Cucumis sativus L.) | Increased plant germination and growth characteristics | Alsaeedi et al. [134] | |
SiO2 NPs (20–30 nm) | Soybean (Glycine max L.) | Reduced oxidative damage due to expression of antioxidative enzymes | Farhangi-Abriz and Torabian [135] | |
Chitosan NPs (~ 25 nm) | Tomato (S. lycopersicum L.) | Alleviated the harmful effects of salinity stress | Hernandez-Hernandez et al. [136] | |
CeO2 NPs (~ 8.5 nm) | Cotton (Gossypium hirsutum L.) | Modulated α-amylase activities and ROS homeostasis | Khan et al. [137] | |
CeO2 NPs (~ 8 nm) | Rapeseed (Brassica napus L.) | Enabled better ability to maintain cytosolic K+/Na+ ratio | Liu et al. [138] | |
Drought | TiO2 NPs (~ 20 nm) | Wheat (T. aestivum L.) | Increased growth, yield, gluten, and starch content | Jaberzadeh et al. [139] |
ZnO NPs (~ 20 nm) | Soybean (G. max L.) | Increased germination percentage and rate, decrease in fresh and dry weights | Sedghi et al. [67] | |
Fe2O3 NPs (20–100 nm) | Sunflower (H. annuus L.) | Counteracted drought stress with no effect on proline and total amino acids | Martinez-Fernandez et al. [140] | |
TiO2 NPs (10–25 nm) | Lin seed (Linum usitatissimum L.) | Enhanced chlorophyll and carotenoid content, decreased H2O2 and MDA contents | Aghdam et al. [141] | |
MWCNTs (20–30 nm) | Barley (Hordeum vulgare L.) | Boosted seed water absorption and increased seedling water content | Karami and Sepehri [142] | |
CeO2 NPs (6–24 nm) | Soybean (G. max L.) | Enhanced growth, development, and yield | Cao et al. [143] | |
Fe NPs (40–53 nm) | Strawberry (Fragaria ananassa L.) | Enhanced acclimation and resistance of plants to drought | Mozafari et al. [144] | |
Heavy metal | Fe3O4 NPs (~ 20 nm) | Rice (O. sativa L.) | Reduced As transport from the root to the shoot | Huang et al.[145] |
Si NPs (~ 50 nm) | Wheat (T. aestivum L.) | Alleviated Cd toxicity by reducing Cd2+ uptake and enhancing antioxidative capacity | Ali et al. [146] | |
CuO NPs (9–22 nm) | Rice (O. sativa L.) | Reduced total As by 23% and 45% in roots and shoots | Wang et al. [147] | |
ZnO NPs (30–40 nm) | Rice (O. sativa L.) | Improved plant growth and alleviated the toxic effects of Cd | Zhang et al. [148] | |
SiO2 NPs (~ 100 nm) | Rice (O. sativa L.) | Inhibited As uptake into rice suspension cells via improving pectin synthesis | Cui et al. [149] | |
TiO2 NPs (36–140 nm) | Rice (O. sativa L.) | Reduced As toxicity and reduced As bioaccumulation in rice seedlings by 40–90% | Wu et al.[150] | |
Au NPs (~ 40 nm) | Rice (O. sativa L.) | Suppressed Cd uptake and alleviated Cd toxicity | Jiang et al. [151] | |
ZnO NPs (20–40 nm) | Rice (O. sativa L.) | Modulated early growth and enhanced physio-biochemical and metabolic profiles | Li et al. [65] | |
ZnO NPs (20–30 nm) | Rice (O. sativa L.) | Alleviated the As toxicity and decreased the accumulation of As |