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Maghemite Nanoparticles Acts as Nanozymes, Improving Growth and Abiotic Stress Tolerance in Brassica napus
Nanoscale Research Letters volume 12, Article number: 631 (2017)
Yttrium doping-stabilized γ-Fe2O3 nanoparticles were studied for its potential to serve as a plant fertilizer and, through enzymatic activity, support drought stress management. Levels of both hydrogen peroxide and lipid peroxidation, after drought, were reduced when γ-Fe2O3 nanoparticles were delivered by irrigation in a nutrient solution to Brassica napus plants grown in soil. Hydrogen peroxide was reduced from 151 to 83 μM g−1 compared to control, and the malondialdehyde formation was reduced from 36 to 26 mM g−1. Growth rate of leaves was enhanced from 33 to 50% growth compared to fully fertilized plants and SPAD-measurements of chlorophyll increased from 47 to 52 suggesting improved agronomic properties by use of γ-Fe2O3 nanoparticles as fertilizer as compared to chelated iron.
Food security is of paramount importance and a pressing issue of our changing world. A changing climate and growing population are steering plant scientists and agricultural engineers to innovate improved tools to secure food production with less environmental impact. Nanotechnologies are one such novel tool that can be explored to solve this longstanding problem [1,2,3]. Nanotechnology has been predicted to become an important and integral part of the food production chain, serving, for example, a role in crop protection [4,5,6], fertilizers [7, 8], biosensors and precision farming , and food packaging and safety . Nanoparticles are ubiquitous in nature, and plants have evolved exposed to various nanoparticles . Iron oxide nanoparticles (IONs) constitute an important part of naturally occurring nanoparticles . There is evidence that plants and soil microbes produce IONs [11, 13, 14]. While some researchers have been concerned with the toxicity to plants of engineered IONs [15, 16], others have focused on the possibility of using IONs as a fertilizer [17,18,19,20,21,22]. Magnetic nanoparticles of magnetite Fe3O4 and maghemite γ-Fe2O3 structure have been suggested to be effective nanozymes of both peroxidase mimetic ability (at low pH) and catalase mimetic ability (at neutral pH) [23,24,25]. It has been shown that, at certain concentrations, nano iron oxide increases plant growth compared to the addition of equivalent amounts of ferrous ions in chelated form . We hypothesize that the enzymatic abilities of nano iron oxide can stimulate growth in plants above that of just iron fertilization. Further, we suggest that this should aid plants during common abiotic stresses such as drought, where catalase and peroxidase becomes important for scavenging of reactive oxygen species (ROS) being released. Here, we present investigations to test this hypothesis on γ-Fe2O3 and oil seed rape, grown in soil and controlled environment.
Effect of Particles on Plant Traits
By adding IONs, we increased growth of oilseed rape compared to just adding an adequate amount of chelated iron. Leaf length showed a statistically significant increase compared to the control, suggesting an increase in either cell division or cell elongation (Fig. 1a). Before the plants were subjected to drought there was a statistically significant increase in chlorophyll content as measured by SPAD-meter, suggesting an increased fitness of these plants compared to control (Fig. 1b).
Water loss did not show statistically significant difference but there was a tendency towards greater water retention in treatments with IONs (Fig. 2a). Fresh weights, which also take into account the growth of the plants, always showed higher values for ION treatments (Fig. 2b) and were statistically significant in some cases. For example, one experiment with extended drought can be seen in Fig. 3.
Considering that control also has adequate amount of iron, big differences in fresh weight would be exceptional. It was observed that the plants treated with IONs coped better than control during drought and recovered better after rewatering (Fig 4).
Effects of IONs on Leaf Hydrogen Peroxide Concentration
The amount of hydrogen peroxide in the leaf after drought was substantially reduced when IONs were added to the nutrient solution used for watering. Variation was high in the 0.8 mg ml−1 treatment; hence, difference towards the other treatments is not statistically significant. However, the difference between control and the highest concentration of 2 mg ml−1 is statistically significant with a p value of 0.004 and a mean 84% greater in the control treatment (Fig. 5).
Effects of IONs on Lipid Peroxidation
Lipid peroxidation with MDA levels as proxy was reduced by addition of IONs, with 36% lower mean concentration of MDA in the leaves of plants with 200 mg of IONs added. We added a positive control with the same molar concentration of iron (III) ions; however, the variation was too big to make any conclusions. The mean of the lower ION concentration was also lower than control, showing a trend towards reduced lipid peroxidation in the leaves of oil seed rape (Fig. 6).
Plant Particle Uptake
To investigate particle uptake into leaf tissue, we measured the iron content of the leaves with inductively coupled plasma atomic emission spectroscopy (ICP-AES). Indeed, a statistically significant increase of iron was observed in treatments with maghemite nanoparticles. Interestingly, the concentration of iron was reduced in leaves irrigated with superfluous iron (III) ions (Fig. 7).
To further corroborate the increased iron content as proof of particle uptake, we measured the low-temperature magnetization in the same leaves. A larger magnetization was observed in control under a strong magnetic field, but without magnetic field, the remanent magnetization was larger in leaves treated with maghemite nanoparticles (Figs. 8 and 9). Due to small sample size and great variation, the differences are not statistically significant but the trend clearly shows a presence of superparamagnetic IONs since the magnetization is higher in control under high magnetic fields but lower when there is no magnetic field. It is clouded by variation, but in certain samples, the presence of IONs was clearly visible (Additional file 1: Figure S2). On one hand, at low enough temperature and at high enough magnetic field, the magnetization for iron ions will be larger than that of ferrimagnetic IONs. On the other hand, at the same low temperature but at zero magnetic field, the remanent magnetization will be larger for IONs due to blocked nanoparticle magnetic moments.
The IONs produced by the method of Cui et al. (2013) formed a gel, indicating successful production of nanoparticles on the order of ~ 1–10 s nm. The dried gel was ground into a powder. The low resolution SEM cannot show individual particles but the hierarchical structure of the powder is evident; the EDS of the sample did not detect any Y, only iron (Fig. 7).
When dispersed in water, the particles form aggregates, with a hydrodynamic size of up to 500 nm, however 84% of the aggregated particles are smaller than 300 nm and at least 11% are smaller than 50 nm. In absolute values, according to the Nanosight measurements, there are 4.28 × 106 particles smaller than 20 nm ml−1, in the 50 times diluted dispersion needed for measurement (Fig. 8). Calculating back, that means that there are approximately 2 × 108 particles smaller than 20 nm ml−1 in the treatments.
The images made by AFM show a similar pattern as the NTA combined with XRD vide infra, with particle sizes from a few nanometers to aggregates of several hundred nanometers (Fig. 9).
The XRD of the particles was acquired 1 year after production and still shows a clear pattern of maghemite structure, evidence for successful maghemite stabilization (Fig. 10). The crystallite size was calculated to be 3.8 nm by use of Scherrer equation. Even though the structure is conserved, the introduction of 13% of Y by weight, of course, affects the vibrational states of the atoms (Additional file 1: Figure S3).
The proposed use of IONs as an iron fertilizer has been investigated before in other systems [17,18,19]. In this investigation, it was for the first time tested whether there is an enzymatic effect of a similar fertilizer, additional to the effect of providing the micro nutrient, iron, to an important crop species. The control was given an adequate amount of chelated iron. We also tested, a positive control, in which a molar equivalent amount of iron (III) ions was supplemented to the negative control with an adequate amount of plant available iron. Hence, the positive effects from IONs seen in our experiments arise from the properties of the IONs. We would like to suggest that it is the known enzymatic effects of IONs that are at play [23, 25, 26]. Other mechanisms can still not be excluded—IONs could also interact with proteins, lipids, and other biomolecules , or it can be that the nanoparticles absorb native iron ions onto the surface and hence reduce harmful Fenton reactions. The fact that the hydrogen peroxide levels of leaves were reduced in the ION-treatments is in itself an indirect proof of nanoparticle uptake. Together with increased concentration of iron and changed magnetization in maghemite the picture becomes more complete. The positive control with iron (III) ions had a reduced concentration of iron content in the leaves, indicating that the plants have capability to reduce iron ion uptake as a defense mechanism. This further suggests that the increased concentration of iron in the leaves in maghemite treatments are indeed nanoparticles, which are not as toxic to the plant as elevated levels of iron ions can be. The magnetic measurements show a superparamagnetic behavior and blocked nanoparticle magnetic moments at low temperature typical of very small γ-Fe2O3 in the leaves treated with maghemite , clearly demonstrating nanoparticle uptake. The miniscule amount of Y administered should not produce any effect on the plants; there is little known about the effects of Y on plants, but Fu et al. (2014) established that 2 mg L−1 Y was the median lethal dose (LD50) in a hydroponic system, and Maksimovic et al. (2014) started seeing toxic effects at 10−5 mol L−1 Y [29, 30]. In the highest concentration used in our experiments, an approximate amount of 50 mg (5.6 10−4 mol) of Y was added per pot by irrigation to the soil, from which only a fraction can be expected to be taken up. What is taken up should not be readily available as ions, but rather be bound in the maghemite particles. The purpose of introducing Y into the synthesis is to reduce the solubility of maghemite nanoparticles and also to prevent transformation into hematite, a less enzymatic form of iron oxide. Undoubtedly, it is beneficial to have increased catalase activity during stress conditions , since a whole range of stress conditions are known to cause toxic accumulations of H2O2 . Further, it has become increasingly evident that H2O2 also serve as a signaling molecule for stress [32, 33]. Increased biomass production is yet to be corroborated, preferably looking into the oil seed yields and quality, as well. Other features, such as increased speed of leaf growth, a very good property in agricultural setting where competition against weeds is crucial, can readily be taken into consideration. It has been shown in Arabidopsis that nano zero valent iron particles can induce extrusion of protons into the apoplast of leaves and thereby allowing turgor-driven cell-wall expansion . The same effect was also observed in roots, which could also be beneficial during drought stress . They also observed an increase in stomatal openings of the leaves which could lead to water loss, but when they measured, there was only a marginal difference compared to the control. It is a known paradox that the relationship between stomatal opening and water transpiration is not linear . This relationship is also highly affected by the environment by, for example, relative humidity or wind . Although, zero valent nanoparticles are of course not to be considered the same as maghemite, the mechanism for leaf elongation seen in our experiments must be investigated. Ghafariyan et al. (2013) observed, as we did, an increase in chlorophyll concentration in the leaves upon addition of IONs compared to a negative control with no iron at all. When they compared to chelated iron there was no difference. However, adding equal amounts of chelated iron as IONs will result in more plant available iron, since in the case of particles great parts of the iron is stored in the crystal structures. Hence, there is a possibility that the plants only fertilized with IONs where actually suffering iron deficiency. We found higher amounts of chlorophyll in the leaves (according to SPAD-measurements, see Fig. 1) when IONs were added auxiliary to the chelated iron. We also measured a reduced amount of hydrogen peroxide and MDA in the leaves, after drought, when we added IONs. Rui et al. (2016) did not measure hydrogen peroxide but MDA and enzymes related to oxidative stress. They suggested that oxidative stress does not occur from addition of IONs, and indeed, they did as well find a reduced amount of MDA in the leaves, compared to chelated iron, on 10 mg kg−1 concentration. In the roots, they saw a reduction of MDA as they increased concentration of IONs. They also measured a reduced amount of superoxide dismutase and peroxidase activity compared to chelated iron suggesting that our hypothesis that IONs can work as reactive oxygen scavengers, in vivo, might be right. Reactive oxygen scavenging was further demonstrated by our measured reduction of hydrogen peroxide in the leaves of Brassica napus. This explains the increased resistance to drought that is observed upon addition of IONs.
Our experiments have provided evidence for the mechanism of IONs acting as nanozymes in planta, revealing coupling between a decrease in hydrogen peroxide contents in the leaves of Brassica napus and introduction of IONs. The increased resistance to drought that is observed upon addition of IONs can thus be related to relieved oxidative stress.
Experimental Conditions and Design
Brassica napus seeds, of the spring rape variety Larissa (Scandinavian Seed AB, Lidköping, Sweden), were sterilized and germinated on agar plates for 3 days before seedlings of similar sizes were transferred to pots with sterilized S-Soil (Hasselfors garden, Örebro, Sweden). It is a soil for professional growth of seedlings with low amount of all macro and micro nutrients, perlite for aeration, growth-stimulating humic acids and a pH of 6. The plants were allowed to establish in the pots for 7 days, irrigated with deionized water. Before treatments were initiated, plants were distributed between trays, so that plant size was as consistent as possible. From day seven, after transfer to pots, the plants were irrigated with nutrient solution, nutrient solution with extra FeCl3 or nutrient solution with different concentrations of γ-Fe2O3 IONs. Each pot was irrigated with 40 ml every day. The plants were grown in a growth chamber with 16-h light (180 μE m−2 s−1) and 8-h darkness. Temperature was set to 25 °C during irradiation and 22° during darkness and relative humidity to 65%. Plants were grown in 8 × 8 cm pots in trays harboring eight pots each. Every treatment had two trays and 16 biological replicates. The trays were moved in a rotating order every day to compensate for any variation in the chamber. The treatment went on for 5 days adding in total 200 ml of either 0.5, 0.8, 1, or 2 mg ml−1, totally 100, 160, 200 or 400 mg per plant, respectively. After the 5 days of adding IONs, all treatments were watered with nutrient solution (Additional file 1: Table S1), for another 5 days before 4 days of drought was initiated. After 4 days of drought, hydrogen peroxide and lipid peroxidation measurements were performed and the plants were again watered with the same nutrient solution for 3 days to study the recovery. The experiment was replicated four times.
Nanoparticle Synthesis and Characterization
The maghemite particles were produced according to the method of  with approximately 13% weight of yttrium (Y) and characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM), nanoparticle tracking analysis (NTA), infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and atomic force microscopy (AFM). The SEM images were acquired with a Hitachi TM1000, with Oxford μDeX electron dispersive x-ray spectrometer (EDS). Hydrodynamic size was measured through nano tracking analysis (NTA) on the Nanosight 300 (Fig. 11). A Perkin-Elmer Spectrum 100 was used to do Fourier transform infrared spectroscopy (FTIR) in potassium bromide (KBr) pellets. For thermogravimetric analysis (TGA), a Perkin-Elmer Pyris 1 was used and for atomic force microscopy (AFM), a Bruker FastScan (Fig. 12). The XRD was performed on a Bruker Smart ApexII multipurpose diffractometer with molybdenum source; the crystallite size was calculated with sherrer equation using the greatest peak at 2θ° angle 16,197 with a full width half maximum (FWHM) of 1.01358489355378 calculated by Origin software peak finder function (Fig. 13). The dried IONs were suspended in a nutrient solution, with 3.4 mg L−1 chelated iron, the same used as control. For a complete list of all the nutrients, see Additional file 1: Table S1.
Plant Trait Measurements
Before treatment was started, the length of the longest leaf, the first true leaf, on each plant was measured. Later, after the 5 days of sequential irrigation with IONs in nutrient solution or nutrient solution alone, the same leaf was measured again. The results are reported as percentage increase. Leaf chlorophyll was assessed by SPAD-measurements with Minolta SPAD-meter, before during and after treatment and subsequently after drought. Three measurements, on two leaves per plant, were averaged for each of the 16 biological replicates. Finally, above ground biomass of all plants were weighed up and placed into aluminum foil to be dried at 110 °C for 72 h.
Iron Content and Magnetic Measurements
After five days of drought, the experiment was ended and all above ground plant tissue was ashed at 450 °C for 24 h. After the ash had been homogenized, 10 mg was weighed up per sample and dissolved in 3 ml of hydrochloric acid 36% on a shaker overnight. Then, the samples were diluted with 44.74 ml of 10% ethanol in Milli-Q water and subsequently measured for iron with ICP-AES at 238.204 nm. For magnetic measurements, the same ash was placed into sample holder and the exact weight for each sample was weighed up with a precision balance. Then, the sample was cooled down to 2 K, and a magnetic field sweep from 10,000 to 0 Oersted was performed on a superconducting quantum interference device (SQUID) magnetometer. The magnetic moment due to the sample holder was subtracted from the measured magnetic moment prior to normalizing with the weight of iron in the sample.
Hydrogen Peroxide Measurements
Hydrogen peroxide in the leaves were measured by the eFOX method reported by . The 16 plants were pooled into four biological replicates with four plants each. Fifty milligrams was taken from the youngest and still fresh leaf of each plant. Then, 200 mg of leaf material was powdered in a precooled mortar in liquid nitrogen. To the powder, we added 4 ml of 100 mM phosphate buffer (pH 6.9) and mortared the ice into a homogenous liquid. From this homogenous liquid, we transferred 1900 μl into a 2-ml Eppendorf tube and added 20 μl of 25 mM ferrous ammonium sulphate (Mohrs salt), 20 μl of 10 mM sorbitol, 20 μl of 10 mM xylenol orange, 20 μl of 99% ethanol, and 20 μl of 250 mM sulfuric acid. A full visible absorbance spectrum was taken for each sample, but the difference between 550 and 800 nm was used for hydrogen peroxide quantification. A calibration curve from 2 to 40 μM hydrogen peroxide was made with R 2 value of 0.9946.
Lipid peroxidation was measured according to the method of . Samples were harvested in the same manner as for hydrogen peroxide measurements, except that they were homogenized in 4 ml 0.1% w/v trichloroacetic acid (TCA). The absorbance was measured at 532 nm and corrected for nonspecific turbidity by subtracting the absorbance at 600 nm. The extinction coefficient of 155 mM cm−1 was used to calculate malondialdehyde concentration (MDA).
All statistics were performed in Minitab 17 software. All data was run through a one-way ANOVA with Fisher test for grouping. Student’s t test was performed to find specific p values between groups found to have statistically significant differences.
Misra P, Shukla PK, Pramanik K, Gautam S, Kole C (2016) Nanotechnology for crop improvement. In: Kole C, Kumar DS, Khodakovskaya MV (eds) Plant nanotechnology: principles and practices. Springer International Publishing, Cham, pp 219–256
Mani PK, Mondal S (2016) Agri-nanotechniques for plant availability of nutrients. In: Kole C, Kumar DS, Khodakovskaya MV (eds) Plant nanotechnology: principles and practices. Springer International Publishing, Cham, pp 263–303
Wang P, Lombi E, Zhao F-J, Kopittke PM (2016) Nanotechnology: a new opportunity in plant sciences. Trends Plant Sci 21(8):699–712
Kah M, Beulke S, Tiede K, Hofmann T (2012) Nanopesticides: state of knowledge, environmental fate, and exposure modeling. Crit Rev Environ Sci Technol 43(16):1823–1867
Khot LR, Sankaran S, Maja JM, Ehsani R, Schuster EW (2012) Applications of nanomaterials in agricultural production and crop protection: a review. Crop Prot 35:64–70
Servin A, Elmer W, Mukherjee A, De la Torre-Roche R, Hamdi H, White J et al (2015) A review of the use of engineered nanomaterials to suppress plant disease and enhance crop yield. J Nanopart Res 17(2):1–21
DeRosa MC, Monreal C, Schnitzer M, Walsh R, Sultan Y (2010) Nanotechnology in fertilizers. Nat Nano 5(2):91
Solanki P, Bhargava A, Chhipa H, Jain N, Panwar J (2015) Nano-fertilizers and their smart delivery system. In: Rai M, Ribeiro C, Mattoso L, Duran N (eds) Nanotechnologies in food and agriculture. Springer International Publishing, Cham, pp 81–101
Wong MH, Giraldo JP, Kwak S-Y, Koman VB, Sinclair R, Lew TTS, et al. Nitroaromatic detection and infrared communication from wild-type plants using plant nanobionics. Nat Mater. 2016;advance online publication
Duncan TV (2011) Applications of nanotechnology in food packaging and food safety: barrier materials, antimicrobials and sensors. J Colloid Interf Sci 363(1):1–24
Sharma VK, Filip J, Zboril R, Varma RS (2015) Natural inorganic nanoparticles—formation, fate, and toxicity in the environment. Chem Soc Rev 44(23):8410–8423
Guo H, Barnard AS (2013) Naturally occurring iron oxide nanoparticles: morphology, surface chemistry and environmental stability. J Mater Chem A 1(1):27–42
Bharde A, Rautaray D, Bansal V, Ahmad A, Sarkar I, Yusuf SM et al (2006) Extracellular biosynthesis of magnetite using fungi. Small 2(1):135–141
Makarov VV, Makarova SS, Love AJ, Sinitsyna OV, Dudnik AO, Yaminsky IV et al (2014) Biosynthesis of stable iron oxide nanoparticles in aqueous extracts of Hordeum vulgare and Rumex acetosa plants. Langmuir 30(20):5982–5988
Wang H, Kou X, Pei Z, Xiao JQ, Shan X, Xing B (2011) Physiological effects of magnetite (Fe3O4) nanoparticles on perennial ryegrass (Lolium perenne L.) and pumpkin (Cucurbita mixta) plants. Nanotoxicology 5(1):30–42
Zhu H, Han J, Xiao JQ, Jin Y (2008) Uptake, translocation, and accumulation of manufactured iron oxide nanoparticles by pumpkin plants. J Environ Monitor 10(6):713–717
Rui M, Ma C, Hao Y, Guo J, Rui Y, Tang X et al (2016) Iron oxide nanoparticles as a potential iron fertilizer for peanut (Arachis hypogaea). Front Plant Sci 7:815
Ghazi Harsini M, Habibi H, Hosein Talaei G. Effect of nano iron foliar application on quantitative characteristics of new line of wheat 2014
Ghafariyan MH, Malakouti MJ, Dadpour MR, Stroeve P, Mahmoudi M (2013) Effects of magnetite nanoparticles on soybean chlorophyll. Environ Sci Technol. 47(18):10645–10652
Li J, Hu J, Ma C, Wang Y, Wu C, Huang J et al (2016) Uptake, translocation and physiological effects of magnetic iron oxide (γ-Fe2O3) nanoparticles in corn (Zea mays L.) Chemosphere 159:326–334
Li J, Hu J, Xiao L, Gan Q, Wang Y (2017) Physiological effects and fluorescence labeling of magnetic iron oxide nanoparticles on citrus (Citrus reticulata) seedlings. Water Air Soil Pollut 228(1):52
Wang Y, Hu J, Dai Z, Li J, Huang J (2016) In vitro assessment of physiological changes of watermelon (Citrullus lanatus) upon iron oxide nanoparticles exposure. Plant Physiol Bioch 108:353–360
Wei H, Wang E (2013) Nanomaterials with enzyme-like characteristics (nanozymes): next-generation artificial enzymes. Chem Soc Rev 42(14):6060–6093
Roy A, Sahoo R, Ray C, Dutta S, Pal T (2016) Soft template induced phase selective synthesis of Fe2O3 nanomagnets: one step towards peroxidase-mimic activity allowing colorimetric sensing of thioglycolic acid. RSC Adv 6(38):32308–32318
Chen Z, Yin J-J, Zhou Y-T, Zhang Y, Song L, Song M et al (2012) Dual enzyme-like activities of iron oxide nanoparticles and their implication for diminishing cytotoxicity. ACS Nano 6(5):4001–4012
Lin S-S, Gurol MD (1998) Catalytic decomposition of hydrogen peroxide on iron oxide: kinetics, mechanism, and implications. Environ Sci Technol. 32(10):1417–1423
Monopoli MP, Walczyk D, Campbell A, Elia G, Lynch I, Baldelli Bombelli F et al (2011) Physical−chemical aspects of protein corona: relevance to in vitro and in vivo biological impacts of nanoparticles. J Am Chem Soc 133(8):2525–2534
Morales MP, Veintemillas-Verdaguer S, Montero MI, Serna CJ, Roig A, Casas L et al (1999) Surface and internal spin canting in γ-Fe2O3 nanoparticles. Chem Mater 11(11):3058–3064
Fu Y, Li F, Xu T, Cai S, Chu W, Qiu H et al (2014) Bioaccumulation, subcellular, and molecular localization and damage to physiology and ultrastructure in Nymphoides peltata (Gmel.) O. Kuntze exposed to yttrium. Environ Sci Pollut Res 21(4):2935–2942
Maksimovic I, Kastori R, Putnik-Delic M, Borišev M (2014) Effect of yttrium on photosynthesis and water relations in young maize plants. J Rare Earths 32(4):372–378
Sofo A, Scopa A, Nuzzaci M, Vitti A (2015) Ascorbate peroxidase and catalase activities and their genetic regulation in plants subjected to drought and salinity stresses. Int J Mol Sci 16(6):13561
Kar RK (2011) Plant responses to water stress: role of reactive oxygen species. Plant Signal Behav 6(11):1741–1745
Cuypers A, Hendrix S, Amaral dos Reis R, De Smet S, Deckers J, Gielen H et al (2016) Hydrogen peroxide, signaling in disguise during metal phytotoxicity. Front Plant Sci. 7(470). https://www.frontiersin.org/articles/10.3389/fpls.2016.00470/full.
Kim J-H, Oh Y, Yoon H, Hwang I, Chang Y-S (2015) Iron nanoparticle-induced activation of plasma membrane H+-ATPase promotes stomatal opening in Arabidopsis thaliana. Environ Sci Technol. 49(2):1113–1119
Kim J-H, Lee Y, Kim E-J, Gu S, Sohn EJ, Seo YS et al (2014) Exposure of iron nanoparticles to Arabidopsis thaliana enhances root elongation by triggering cell wall loosening. Environ Sci Technol 48(6):3477–3485
Franks PJ, Farquhar GD (2001) The effect of exogenous abscisic acid on stomatal development, stomatal mechanics, and leaf gas exchange in Tradescantia virginiana. Plant Physiol 125(2):935–942
Bange GGJ (1953) On the quantitative explanation of stomatal transpiration. Acta Botanica Neerlandica 2(3):255–297
Cui H, Liu Y, Ren W (2013) Structure switch between α-Fe2O3, γ-Fe2O3 and Fe3O4 during the large scale and low temperature sol–gel synthesis of nearly monodispersed iron oxide nanoparticles. Adv Powder Technol 24(1):93–97
Cheeseman JM (2006) Hydrogen peroxide concentrations in leaves under natural conditions. J Exp Bot 57(10):2435–2444
Heath RL, Packer L (1968) Photoperoxidation in isolated chloroplasts. Arch Biochem Biophys 125(1):189–198
The authors would like to acknowledge Johan Meijer for the support in the development of the experimental set up. We want to thank Jean Pettersson for help with ICP-AES. Finally, we would like to extend our gratitude to Matthew Gentry for proof reading the manuscript.
This work was funded by The Swedish Research Council FORMAS, through grant number 2012-581.
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A complete list of nutrients, in the solution, that was used as control and medium for ION application. Nitrogen is divided into ammonia and nitrate. All micronutrients are chelated. No cadmium, chloride or sodium was present. Figure S1. Oilseed rape plants after 5 days of drought. A. Control plants treated with nutrient solution (Table S1). B. Plants treated with nutrient solution supplemented with IONs. Figure S2. Two selected plots of magnetic susceptibility to demonstrate the superparamagnetic behavior present in the maghemite treatment. The selected control is of general behavior for the group while the maghemite is the sample showing most pronounced superparamagnetism. Figure S3. Infrared absorbance spectrum of yttrium directed maghemite nanoparticles. Wavenumber of the peaks are annotated in the graph. (DOCX 4838 kb)
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Palmqvist, N.M., Seisenbaeva, G.A., Svedlindh, P. et al. Maghemite Nanoparticles Acts as Nanozymes, Improving Growth and Abiotic Stress Tolerance in Brassica napus . Nanoscale Res Lett 12, 631 (2017) doi:10.1186/s11671-017-2404-2
- Maghemite nanoparticles
- Drought stress
- Catalase activity
- Iron oxide nanoparticles
- Nano agriculture
- Agrobio nanotechnology
- Growth promotion
- Reactive oxygen species scavenging