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Fighting Against Plant Saline Stress: Development of a Novel Bioactive Composite Based on Bentonite and L-Proline

Published online by Cambridge University Press:  01 January 2024

Danila Merino*
Affiliation:
Facultad de Ingeniería, Grupo de Materiales Compuestos Termoplásticos (CoMP), Instituto de Investigaciones en Ciencia y Tecnología de Materiales (INTEMA), Universidad Nacional de Mar del Plata (UNMdP) y Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. Colón 10850, (7600) Mar del Plata, Mar del Plata, Argentina Present Address: Present Address: Smart Materials Group, Itailian Institute of Technology (HT), Vai Morego 30, 16163 Genoa, Italy
María J. Iglesias
Affiliation:
Facultad de Ciencias Exactas y Naturales, Instituto de Investigaciones Biológicas, UE CONICET-UNMDP, Universidad Nacional de Mar del Plata, (7600) Mar del Plata, 3250, Deán Funes, Argentina
Andrea Y Mansilla
Affiliation:
Facultad de Ciencias Exactas y Naturales, Instituto de Investigaciones Biológicas, UE CONICET-UNMDP, Universidad Nacional de Mar del Plata, (7600) Mar del Plata, 3250, Deán Funes, Argentina
Claudia A. Casalongué
Affiliation:
Facultad de Ciencias Exactas y Naturales, Instituto de Investigaciones Biológicas, UE CONICET-UNMDP, Universidad Nacional de Mar del Plata, (7600) Mar del Plata, 3250, Deán Funes, Argentina
Vera A. Alvarez
Affiliation:
Facultad de Ingeniería, Grupo de Materiales Compuestos Termoplásticos (CoMP), Instituto de Investigaciones en Ciencia y Tecnología de Materiales (INTEMA), Universidad Nacional de Mar del Plata (UNMdP) y Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. Colón 10850, (7600) Mar del Plata, Mar del Plata, Argentina
*
*E-mail address of corresponding author: danila.merino@fi.mdp.edu.ar danila.merino@iit.it
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Abstract

Soil salinity is one of the most critical environmental stresses that affects crop productivity. In a context in which world demand for food is growing continuously, this problem requires urgent attention. Actions that go beyond traditional agricultural practices are needed. The objective of the current study was to develop a bioactive, economic, and sustainable compound that can increase the tolerance of cultivated plants in saline-stress situations by combining the hosting capacity of natural bentonite nanoclay (Bent) with a phytoactive osmoprotective compound, L-Proline (Pro). The Bent-Pro nanocomposite synthesis method, its final chemical structure, and in vitro bioactivity were addressed here. The results indicated that Bent can retain a maximum of 14.4% (w/w) of Pro. The (001) X-ray diffraction (XRD) peak of Bent shifted to smaller angles in the pattern of Bent-Pro, indicating that Pro has a monolayer arrangement between the Bent layers. The results of transmission electron microscopy (TEM) also supported this result. Pro was also retained on the edges or external surfaces of Bent, as indicated by thermogravimetric analysis (TGA) and scanning electron microscopy (SEM). In addition, Pro functional groups identified by Fourier-transform infrared (FTIR) spectroscopy indicated that it was present in its zwitterionic form. The role of Bent-Pro as a protector against plant saline stress was assayed using Arabidopsis thaliana (A. thaliana) as a model, demonstrating that it mitigates the detrimental effects of NaCl-mediated salt stress on seed germination and the leaf chlorophyll level, thus highlighting the relevance of this contribution and the versatility and broad applicability of clays.

Type
Article
Copyright
Copyright © Clay Minerals Society 2021

Introduction

Phyllosilicates are nanostructured inorganic lamellar materials available widely in nature and usually referred to as nanoclays. They are layered aluminosilicates, which means that their crystalline structure is formed by Al and Si oxide sheets stacked on top of each other. The specific spatial organization of two, three, or up to four sheets of [SiO4]4– and/or [AlO3(OH)3]6– leads to the formation of the different 1:1, 2:1, and 2:1:1 types of phyllosilicates (Pédro Reference Pédro1965). A clear representation of these nanoclay crystalline structures can be found in a previous study (Pédro Reference Pédro1965). Among them, 2:1 phyllosilicates are of particular importance as they include the smectite group, an expansible kind of clay, used widely due to its great versatility and multiple applications.

In line with this classification, the montmorillonite (Mnt) mineral belonging to the smectite group is the most commonly used nanoclay for chemical modification. It is the main component of bentonite (Bent), which is widely available in Argentina, having quartz and feldspar as impurities. The Bent layers present negative charges resulting from isomorphic substitutions which occur naturally and refer to the replacement of an element by a similar one without altering the mineral’s chemical structure. The negative charges generated due to this natural process are compensated by incorporating inorganic cations such as Na+, K+, Mg2+, and Ca2+ in the interlamellar space. These cations are also known as “exchangeable cations” as others, including organic cations, can replace them (McConnell Reference McConnell1950).

Naturally occurring clays are often modified to provide them with specific functions or properties (Pédro Reference Pédro1965). The idea of using nanosystems for the retention and release of active substances has been used widely in the fields of medicine and cosmetics (Patel et al. Reference Patel, Somani, Bajaj and Jasra2006; Ruiz-Hitzky et al. Reference Ruiz-Hitzky, Aranda, Darder and Rytwo2010), polymer science (Alexandre and Dubois Reference Alexandre and Dubois2000; Merino and Alvarez Reference Merino and Alvarez2020; Merino et al. Reference Merino, Ollier, Lanfranconi and Alvarez2016; Wu et al. Reference Wu, Gaharwar, Schexnailder and Schmidt2010), and, of late, has also been used in agriculture (Sanhez-Martin et al. Reference Sanchez-Martin, Rodriguez-Cruz, Andrades and Sanchez-Camazano2006; Gamba et al. Reference Gamba, Flores, Madejová and Torres Sánchez2015; Merino et al. Reference Merino, Mansilla, Casalongué and Alvarez2018, Reference Merino, Tomadoni, Salcedo, Mansilla, Casalongué and Alvarez2020; Mansilla et al. Reference Mansilla, Salcedo, Colman, Chevalier, Lanfranconi, Alvarez and Casalongué2020). These carrier systems lead to greater application efficiency and less associated contamination. In general, these include the possibility of reducing the volume of the doses applied and offer protection against drug environmental degradation, evaporation, and leaching (Grillo et al. Reference Grillo, Mattos, Antunes, Forini, Monikh and Rojas2021).

In the context of the projected increase in crop production to meet the growing demand for food (~ 50% more by 2030 according to the Food and Agriculture Organization of the United Nations (2017)), agricultural nanotechnologies are urgently required. Nanoclays are inexpensive, non-toxic, abundant materials and offer the possibility of functionalization. The number of publications reporting their use for the controlled release of agrochemicals such as fertilizers, pesticides, herbicides, and biostimulants and fertilizers has increased over recent decades (e.g. Celis et al. Reference Celis, Hermosín, Carrizosa and Cornejo2002; Lagaly Reference Lagaly2001; Li et al. Reference Li, Li and Dong2008; Mansilla et al. Reference Mansilla, Salcedo, Colman, Chevalier, Lanfranconi, Alvarez and Casalongué2020; Merino et al. Reference Merino, Mansilla, Casalongué and Alvarez2018, Reference Merino, Tomadoni, Salcedo, Mansilla, Casalongué and Alvarez2020; Ni et al. Reference Ni, Liu, Lü, Xie and Wang2011).

Soil salinity is one of the most critical environmental stresses that impacts the growing demand for food crops as the majority of the plant species consumed worldwide are susceptible to salt stress. The amount of irrigated land estimated to be affected by salinity is ~ 45 million hectares, resulting in ~ US$ 12 billion of annual losses in agricultural production (Negrão et al. Reference Negrão, Schmöckel and Tester2016; Shahid et al. Reference Shahid, Zaman, Heng, Zaman, Shahid and Heng2018). Salinity affects crops by limiting their ability to take up water, leading to poor germination and seedling establishment, in addition to Na+ toxicity, which has detrimental effects in multiple plant-cell responses at the molecular, biochemical, and physiological levels (Golldack et al. Reference Golldack, Li, Mohan and Probst2014; Zhu Reference Zhu2002).

When exposed to salinity, many plants induce the accumulation of osmoprotectants or compatible solutes consisting of low-molecular-weight secondary metabolites such as the amino acid L-Proline (Pro). These osmoprotectants ameliorate osmotic stress by maintaining turgor pressure and plasma membrane ion efflux, and by controlling transpiration rate (Ashraf and Foolad Reference Ashraf and Foolad2007; Kaur and Asthir Reference Kaur and Asthir2015). Stress-tolerant plant species, therefore, have been associated with greater concentrations of Pro compared to salt stress-sensitive plants. In addition to its role as a compatible osmolyte, Pro action has been associated with the stabilization of sub-cellular structures, the scavenging of harmful free radicals generated by the stress, and the modulation of gene expression (Per et al. Reference Per, Khan, Reddy, Masood, Hasanuzzaman, Khan and Anjum2017; Szabados and Savouré Reference Szabados and Savouré2010). Given that the action of Pro in plants is highly sensitive to its application doses, it is essential to optimize the concentration and treatment time according to the requirements of the individual crops (Ashraf and Foolad Reference Ashraf and Foolad2007). The incorporation of Pro in Bent could offer advantages for its protection against possible biological degradation together with the administration of controlled doses and its sustained release over a certain period. Taking into account the potential of the exogenous application of Pro as a scavenger for reactive oxygen species (ROS) and also as an inductor of the antioxidative enzymes (Hayat et al. Reference Hayat, Hayat, Alyemeni, Wani, Pichtel and Ahmad2012), the support and carrying of Pro in a nanoclay would potentially improve the bioefficacy of the product against stressful environments on plant crops.

The objective of the current study was to develop a bioactive, economic, and sustainable compound that can increase the tolerance of cultivated plants to saline stress. The hypothesis presented here is that Bent nanoclay can act as a vehicle for an osmoprotective compound, such as Pro, and that this ‘Bent-Pro’ nanocomposite can contribute to maximizing the yield of cultures. Arabidopsis thaliana (A. thaliana) was used as a suitable model for studying responses to saline stress. Promising results were obtained, emphasizing the relevance of this contribution toward a sustainable future in agriculture and highlighting the versatility and broad applicability of clays.

Materials and Methods

Materials

The clay used here was a bentonite obtained from Minarmco S.A. (Neuquén, Argentina), consisting of Mnt with quartz and feldspar as the main impurities and was used without further treatment (XRD data given in Fig. 1). The Bent CEC was determined by the methylene blue method to be 105 meq/100 g of clay (Merino et al. Reference Merino, Mansilla, Casalongué and Alvarez2018). The amino acid Pro (≥ 99.0% purity) was acquired from Biopack (Buenos Aires, Argentina).

Fig. 1 XRD pattern of the natural bentonite

Preparation of Bent-Pro

Various syntheses were carried out in order to optimize the relative amounts of the reagents involved and the reaction times that enable the maximum retention capacity of Pro in Bent. For this, a 1 wt.% suspension of Bent in distilled water was kept under stirring, together with varied amounts of Pro for 2 h at 20°C. Then, the solutions were centrifuged at 10,733 × g for 15 min. The supernatant was collected for the subsequent determination of Pro, and the modified nanoclay was washed three times with distilled water. The samples were frozen at –20°C and lyophilized at 40 Torr and −55°C for 72 h using a Columbia International freeze dryer (Irmo, South Carolina, USA) to obtain them in fine powder form. The resulting nanoclays were designated: Bent/0.5Pro2H, Bent/1.0Pro2H, Bent/1.5Pro2H, Bent/2.0Pro2H, Bent/4.0Pro2H, and Bent/8.0Pro2H, where the number preceding Pro is the CEC fraction (f) representing the amount of Pro used and 2H indicates the reaction time, 2 h. The Pro mass to be incorporated, M Pro , was calculated using Eq. 1:

(1) M Pro = f · C E C · X · M M · 10 - 3

where the CEC is 105 meq/100 g of clay, X is the amount of clay to be used, and MW is the molecular weight of Pro (115.13 g/mol). Finally, the effect of reaction time on the amount of Pro retained by Bent was studied. For this, f = 2 was used, and times ranged from 0.5 to 8 h.

Pro is an amphoteric molecule and can, therefore, act as an acid or a base depending on the pH. This species can also be neutralized internally, forming a zwitterion. The isoelectric point of Pro occurs at pH 6.3 (McKee and McKee Reference McKee and McKee2003); in the pH of the distilled water (~ 5.8, slightly acidic due to the effect produced by the dissolution of atmospheric CO2) it would exist in an ionized form and with a slight prevalence of positive charge. In the present study, a decision was made not to reduce the pH further, in order to increase the proportion of species with positive charge as it has been described previously that zwitterionic species can be intercalated in the Mnt interlayer space (Zhu et al. Reference Zhu, Zhang, Qing, Wen, Su, Ma, Wei, Liu, He and Xi2017). In addition, a strong acid medium could damage the structure of the clay (Komadel and Madejová Reference Komadel, Madejová, Bergaya, Theng and Lagaly2006); furthermore, a new reagent included in the production process would add more cost.

Pro Quantification

The organic mass contents of Pro supported by Bent were determined using the method described by Bates et al. (Reference Bates, Waldren and Teare1973), according to which 3 μL of the Bent-Pro synthesis supernatants was brought to a final volume of 300 μL using a 3 wt.% aqueous solution of sulfosalicylic acid (99% purity, Sigma-Aldrich, St. Louis, Missouri, USA). One volume of this fraction was mixed with equal volumes of glacial acetic acid (≥ 99.7% purity, JT Baker, Phillipsburg, New Jersey, USA) and a 2.5 wt.% solution of ninhydrin (99% purity, Sigma-Aldrich, St. Louis, Missouri, USA) in acetic acid and incubated at 100°C for 30 min. Subsequently, the absorbance at 540 nm was measured using an Ultrospec 1100 spectrophotometer (Amersham Biosciences, Amersham, UK), and the Pro content was determined from its calibration curve.

Characterization Techniques

FTIR.

The FTIR spectra were measured by attenuated total reflectance (ATR) using a Perkin Elmer 100 infrared spectrophotometer (Akron, Ohio, USA), in the range 600–4000 cm–1, with 16 scans at a resolution of 4 cm–1.

XRD.

The Bent and Bent-Pro powder samples were analyzed using a Malvern X-Pert Pro diffractometer (Malvern, UK), operating at 40 kV and 40 mA, with CuKα radiation (λ = 1.54 Å), at a scanning speed of 1º2θ/min and size of step of 0.02º2θ. The interlamellar spacings (d 001 values) were calculated from the 2θ values using the Bragg equation (Eq. 2) (Bragg and Bragg Reference Bragg and Bragg1913).

(2) n λ = 2 d sin θ

TEM.

The shape, size, and arrangement of the Bent and Bent-Pro layers were investigated using a Jeol JEM 2100 (Tokyo, Japan) transmission electron microscope at a magnification of 150,000 × . The operating voltage was 200 kV, and a B6La filament was used. The sample was dispersed in acetone, and then a drop was placed on a perforated copper grid covered with carbon.

TGA.

The TGA was performed using a TA Instrument HI-Res thermal analyzer (New Castle, Delaware, USA) at a heating rate of 10°C/min and from room temperature to 900°C in airflow. The mass of all the samples was in the range 20–30 mg. The degradation temperatures were obtained from the maximum of each event in the curves derived from TGA (DTGA).

SEM.

The morphology of Bent and Bent-Pro nanoclays was analyzed under a FESEM Supra55 Zeiss microscope (Oberkochen, Germany) with an acceleration voltage of 3 kV. The samples were coated with a thin layer of gold in order to ensure electrical conduction.

Bioassays

Plant Material, Growth, and Treatments.

A. thaliana seeds from the Columbia (Col-0) ecotype were surface sterilized in 30 vol.% of sodium hypochlorite (commercial concentration of 55 g of Cl/L, Ayudín, Clorox Argentina SA, Buenos Aires, Argentina) and 0.2 vol.% of Tween-20 (> 99% purity, Sigma-Aldrich, St. Louis, Missouri, USA), for 10 min, followed by three washing steps with sterilized distilled water. The seeds were sowed under laminar flow on Murashige and Skoog (MS) medium (Sigma-Aldrich, St. Louis, Missouri, USA) with 0.8 wt.% agar (BD-Difco, Sparks, Maryland, USA) in Petri plates and stratified at 4°C for 2 − 3 days in the dark. Then, seeds were germinated in a growth chamber at 23°C under 250 μmol photons/m2s, with 16:8 h light:dark cycles.

Germination Assay.

Approximately 50 seeds per technical replicate per treatment were sown on plates containing 20 mL of MS medium supplemented with 150 mM NaCl (> 99.0% purity, JT Baker, Phillipsburg, New Jersey, USA) in combination with increasing concentrations of Bent-Pro (0.01, 0.1, and 1 mg/mL), or the respective concentrations of free Pro (based on ~ 10% of Pro incorporation in Bent-Pro nanosystem), as a reference of the active compound. Bent (1 mg/mL) was used as the negative control. After stratification, the seeds were transferred to the growth chamber for two days. The percentage of germination was scored according to seeds in the 0.5 stage (Boyes et al. Reference Boyes, Zayed, Ascenzi, McCaskill, Hoffman, Davis and Görlach2001). Four independent experiments with two replicates each (n = 800 seeds) were performed. The working NaCl concentration used for this assay (150 mM) corresponds to the concentration required for 50% inhibition of germination of wild-type seeds and was already set up in previous studies (Iglesias et al. Reference Iglesias, Terrile, Bartoli, D'Ippólito and Casalongué2010).

Chlorophyll Content.

Ten-day-old seedlings grown on MS medium agar plates were transferred to 50 mL of liquid MS medium or MS containing 200 mM NaCl, supplemented with Bent-Pro (0.1 mg/mL), Pro (0.01 mg/mL), or Bent (0.1 mg/mL) for 2 days. Leaves (0.5 g) were ground in liquid N2, and the powder was extracted with 80% acetone for 30 min in the dark. Plant extracts were centrifuged at 10,000 × g for 20 min. The amounts of chlorophyll A and B were measured spectrophotometrically at 645 and 663 nm (Arnon Reference Arnon1949). Three independent experiments with two technical replicates each (n = 240 seedlings) were performed. The working NaCl concentration used for this assay (200 mM) corresponded to the condition required for control seedlings to show a 50% reduction in their chlorophyll content. These experimental conditions were established previously by Iglesias et al. (Reference Iglesias, Terrile, Bartoli, D'Ippólito and Casalongué2010).

Statistical Analysis.

The values shown in Figs. 7 and 8 are mean ± standard errors (SE) of the corresponding independent experiments. The data were subjected to analysis by the Student-t test against the control in GraphPad Prism version 5.01 software (*p < 0.05, **p < 0.01).

RESULTS AND DISCUSSION

Optimization of the Bent-Pro Synthesis Conditions

The adsorption of amino acids on clays depends on several conditions, including temperature, relative concentration among reactants, exchangeable cations present in the clay, type of clay, and pH (Petra et al. Reference Petra, Billik and Komadel2015). In the present study, the effects of various proportions of Bent and Pro and the reaction time under the conditions mentioned in the Materials and Methods section were studied.

First, the Bent-Pro nanocomposite preparation was studied at a fixed reaction time (2 h), and the effect of the initial amount of Pro, f, was studied. Values of f = 0.5, 1, 1.5, 2, 4, and 8 were studied, and the amount of Pro retained in Bent increased with increasing f until reaching f = 2 and then decreased with larger f values (Fig. 2). In general, the amount of Pro incorporated was slightly greater than the CEC of the clay, and excess Pro failed to produce significant increases in the amount retained. The results found here were superior to those reported by Petra et al. (Reference Petra, Billik and Komadel2015) for the amino acids cysteine and glutamic acid loaded on Mnt. Those authors worked at pH 4, conditions that favor a cation exchange process, and thus limited the maximum amount of amino acids retained to the value of the CEC of the clay.

Fig. 2 Amount of Pro incorporated in Bent (g of Pro/100 g of Bent-Pro) depending on a the reaction time (h), and b the initial amount of Pro (f)

Next, the effect of reaction time on the incorporation of Pro in Bent was studied. For this, the variable f was set at 2, and the amount of Pro that was incorporated in Bent was studied as a function of reaction time: 0.5, 1, 1.5, 2, 3, and 4 h. The results showed that the amount of Pro retained increased with reaction time until 2 h was reached, where retaining ~ 1.2 × the value of the CEC of the clay was possible, which is equivalent to 14.4 wt.% of Pro. Longer times produced smaller amounts of Pro loading (Fig. 2).

At least two amino acid-adsorption mechanisms operate on smectites, such as Bent, according to Parbhakar et al. (Reference Parbhakar, Cuadros, Sephton, Dubbin, Coles and Weiss2007). While cation-exchange mechanisms predominate at low amino acid concentrations and pH, adsorption at higher concentrations has been observed. In the present study, note that the pH of the reaction medium was not reduced and the predominant form of the Pro amino acid was zwitterionic. The observed effect as a function of time could, therefore, be related to the molecular rearrangements of Pro between the Bent layers. The loading of a given substance in Bent occurs as a process of ‘self-assembly’ governed by the following forces: (1) the electrostatic interaction between the protonated amino group of Pro and the internal and external surfaces of Bent; (2) the electrostatic repulsion between the carboxylate group of Pro and the Bent layers; (3) the electrostatic interaction between the interlamellar cations present in Bent and Pro; (4) the electrostatic interaction among Pro molecules; and (5) the interaction between all the compounds mentioned with the water molecules of the solvent. The way that these components are organized in space, resulting in the Bent-Pro nanoclay, is determined mainly by the combination of these factors, and will be further discussed below (Zhu et al. Reference Zhu, Zhang, Qing, Wen, Su, Ma, Wei, Liu, He and Xi2017).

Physicochemical Properties of Bent-Pro Nanoclay

The incorporation of Pro in Bent was reflected in new stretching bands in the FTIR spectrum of Bent. The new bands were centered at 1700 cm–1 (υ C = O), 1557.2 cm–1 (the NH2 + δ in-plane), and 1418.6 cm–1 (υ symmetric COO) (Devi et al. Reference Devi, Lawrence, Ramesh Babu, Selvanayagam, Stoeckli-Evans and Ramamurthi2009). A reduction in the intensity of the absorption band centered at 3390.6 cm–1 (υ of OH and NH overlapping) and a shift of the stretching band of the Si–O group in Bent toward higher wavenumbers (Chen et al. Reference Chen, Chen, Huang, Wang and Wang2018), from 996.1 to 1009.1 cm–1 (Fig. 3), were observed.

Fig. 3 FTIR spectra of a Bent, b Bent-Pro, and c Pro

The stretching bands of COO and NH2 + in the Bent-Pro spectrum indicated that the Pro molecules were intercalated in their zwitterionic form. The existence of a small peak at 1700 cm–1 could also indicate the presence of carboxylic acid groups and, consequently, a partial contribution of cation exchange. The isoelectric point of Pro occurs at pH 6.3; so at the pH of deionized water (~ 5.8) it has a small positive charge (McKee and McKee Reference McKee and McKee2003). Nevertheless, the absence of other bands associated with carboxylic groups, such as OH stretching at 3500 cm–1, and bending between 1200 and 1300 cm–1, suggest that Pro was intercalated preferentially in its zwitterionic form.

The intercalation mechanism of a zwitterion between the Mnt layers was described previously by Zhu et al. (Reference Zhu, Zhang, Qing, Wen, Su, Ma, Wei, Liu, He and Xi2017) who explained that the intercalation mechanism occurs in two stages: the first being the electrostatic interaction; and the second, a co-adsorption process that refers to a Van der Waals-type interaction process between the hydrophobic chains of the rest of the zwitterions (Zhu et al. Reference Zhu, Zhang, Qing, Wen, Su, Ma, Wei, Liu, He and Xi2017). Thus, specific rearrangements in time probably result in a reduced Pro in Bent retention when the reaction extends for > 2 h.

The Bent-Pro XRD pattern showed a shift in the position of the (001) diffraction peak (Fig. 4a), which is related to the distance between the clay layers. Such shifting to lower angles (smaller values of 2θ) is related to an increase in interlamellar spacing and indicates that the amino acid is partially intercalated between the Bent layers (Patel et al. Reference Patel, Somani, Bajaj and Jasra2006).

Fig. 4 a Bent and Bent-Pro XRD pattern between 2 and 10°2θ. b Representative scheme of the orientation of a Pro molecule (3.7 Å) confined in the interlamellar space of Bent, in its zwitterionic form, in the presence of a Na+ cation and a water molecule; c TEM images of a Bent and b Bent-Pro

The interlamellar spacing of Bent was 11.5 Å, and after the reaction with Pro, this parameter was increased by 3.4 Å, which indicated that some of the amino acid was incorporated in the interlamellar space. Similar results were found for the modification of Mnt with the amino acids valine, leucine, isoleucine, methionine (Mallakpour and Dinari Reference Mallakpour and Dinari2011), and arginine (Shokri et al. Reference Shokri, Yegani and Akbarzadeh2017). On the other hand, the molecular size calculations carried out with the Chem3D Pro program showed an approximate value of 3.7 Å for the Pro molecule. The results indicated, therefore, that Pro would be oriented in a monolayer between Bent layers (Fig. 4b).

Transmission electron microscopy allowed direct observation of the changes produced in the interlamellar spacing of the clay after its modification. Examination of the laminar structure of clays is not straightforward, however (Mallakpour and Dinari Reference Mallakpour and Dinari2011). In general, it is believed that the high energy of the electron beam could remove the water of hydration of the cations present in the Bent interlayer space, causing the layers to collapse. The same might even be observed for the modified clays; the images needed to be captured quickly. The observed spacings were of the order of 11.8 Å for Bent and 13.9 Å for Bent-Pro (Fig. 4c), in agreement with the results observed by XRD.

The thermal stability of the Bent-Pro nanoclay and the mechanisms involved in its thermal degradation, which are related directly to their assembly, were analyzed by TGA.

The nanoclay Bent presented three events in the curve of DTGA (Fig. 5a) with maximum temperatures at 63, 110, and 624°C. The associated mass losses were 6.6, 0.9, and 3.6%, respectively. These events are related directly to the evaporation of slightly adsorbed water, water present in the interlayer space, and the dehydroxylation process that leads to the collapse of the interlayer of the clay, respectively, as previously reported (Mallakpour and Dinari Reference Mallakpour and Dinari2011; Merino et al. Reference Merino, Ollier, Lanfranconi and Alvarez2016).

Fig. 5 DTGA (%/°C) vs. Temperature (°C) for a Bent, b Bent-Pro, and c Pro

By incorporating Pro into Bent, significant changes were observed in the appearance of the DTGA curves, suggesting a smaller moisture content and the presence of organic matter (Mallakpour and Dinari Reference Mallakpour and Dinari2011). Notably, three events were observed in the DTGA curve for Bent-Pro (Fig. 5b). The first was associated with the evaporation of slightly adsorbed water (49°C, 5.5%) with less interlamellar water than in Bent overlapped in this same event. According to previous publications, this observation agrees with the expected results after Bent loading with an organic compound (Mallakpour and Dinari Reference Mallakpour and Dinari2011; Merino et al. Reference Merino, Ollier, Lanfranconi and Alvarez2016). Some of the water molecules in Bent were displaced during the intercalation of Pro and are more weakly bonded, demonstrating that Bent hydrophilicity was reduced slightly.

The second event was related to the thermal degradation of Pro. It occurred in two stages associated with the maximum temperatures, 297.4 and 364.6°C, in overlapping events. The thermal analysis of free Pro (Fig. 5c) revealed a single maximum degradation step at 251°C, thus suggesting a strong interaction between Pro and Bent in the Bent-Pro nanocomposite. Because Pro can be found in three different spaces, namely, intercalated between the clay layers, adsorbed at the edges, or adsorbed on the external surfaces, it is expected to degrade over a wide temperature range (Mallakpour and Dinari Reference Mallakpour and Dinari2011; Merino et al. Reference Merino, Ollier, Lanfranconi and Alvarez2016). As explained by Zhu et al. (Reference Zhu, Zhang, Qing, Wen, Su, Ma, Wei, Liu, He and Xi2017), when the amount of compound to be intercalated exceeds the CEC, the surplus can be retained by Van der Waals type interactions, causing the appearance of a new peak in the DTGA at a lower temperature than that noticed for the intercalated Pro. In this way, the appearance of two temperatures of degradation for Pro in Bent-Pro could indicate that Pro is in at least two different environments and that some of the Pro retained is interacting by electrostatic forces, while the rest is interacting via weaker forces such as dipole–dipole or Van der Waals type. An estimation of the amount of Pro retained by Bent was also carried out by comparing the areas under the DTGA curves for Bent and Bent-Pro in the 200–800°C range, giving a 17% Pro intercalated, slightly more than the amount determined by the analytical method of Bates et al. (Reference Bates, Waldren and Teare1973). Finally, the third event was attributed to the dehydroxylation of the clay with a maximum degradation rate at 631°C.

The morphology of the materials developed was observed by SEM. After loading Pro in Bent, the surface of Bent (Fig. 6a) initially smooth and compact, changed subtly to a more spongy and rough morphology in Bent-Pro (Fig. 6b), suggesting that some of the amino acid could be found on the edges or external surfaces of the clay (Merino et al. Reference Merino, Mansilla, Casalongué and Alvarez2018), in line with the results from TGA analysis. These results are consistent with those of Chen et al. (Reference Chen, Chen, Huang, Wang and Wang2018) who observed a rougher surface after the intercalation of the amino acid cysteine into Bent.

Fig. 6 SEM images of: a Bent and b Bent-Pro

Characterization of the Biological Action of Bent-Pro in the Protection of A. thaliana Against Salinity

Salinity affects the growth and production of plants by reducing the water potential of the soil solution, decreasing water availability. At the same time, an ionic imbalance is established, interfering with mineral nutrition and cellular metabolism. Multiple effects at various scales are possible, including reduction of turgency and growth, loss of cell structure due to membrane disorganization, and inhibition of enzymatic activity as the consequence of the combination of water stress, ionic toxicity, and nutritional imbalance (Saha et al. Reference Saha, Brauer, Sengupta, Popescu, Gupta and Gupta2015). The most significant effects at physiological and biochemical levels, however, are the inhibition of seed germination and chlorosis (loss of photosynthetic pigments in leaves) (Saha et al. Reference Saha, Brauer, Sengupta, Popescu, Gupta and Gupta2015).

In this context, the protective role of Bent-Pro nanoclays in the protection of the model plant A. thaliana against salinity was investigated. This plant species is sensitive to moderate levels of NaCl and has been suggested as a good model for the study of plant responses against salt stress (Zhang et al. Reference Zhang, Creelman and Zhu2004). Under salt-stress-free conditions, the germination rate of this species was ~ 98%. After a 48-h treatment on 150 mM NaCl-supplemented medium, the germination rate dropped to 32% (Fig. 7). Seeds sown in 150 mM NaCl in combination with increasing levels of Bent-Pro germinated at increasingly improved rates, reaching ~ 47% with a 0.1 mg/mL optimum dose of Bent-Pro, which was slightly greater than for equivalent doses of free Pro (Fig. 7).

Fig. 7 Bar chart showing the effects of Bent-Pro on seed germination under salt stress. A. thaliana seeds were sown on MS medium supplemented with 150 mM NaCl (black bar) or 150 mM NaCl combined with various concentrations of Bent-Pro (dark gray bars), Pro (light gray bars) or Bent (white bars). Germination was scored after 48 h. The percentage of germination with respect to the control for each treatment is shown. 100% indicates that the seeds germinated under control conditions (without NaCl). The data are mean values (± SE) of four independent experiments. (n = 800; t-Test * p ≤ 0.05 **p ≤ 0.01)

Because Bent addition showed no biological effects on seed germination under salinity, the action of Bent-Pro is probably associated with the bioactive effect of Pro within the Bent nanoclay. Plants are highly sensitive to Pro application doses, which is why optimizing the concentrations and time of application according to the crop that is to be treated and studied is essential (El Moukhtari et al. Reference El Moukhtari, Cabassa-Hourton, Farissi and Savouré2020). A similar result was reported by Deivanai et al. (Reference Deivanai, Xavier, Vinod, Timalata and Lim2011) for the optimal concentration of exogenously applied Pro to alleviate the effect of NaCl on rice-seed germination.

To analyze further the putative protection effect of Bent-Pro against salinity in photosynthetic organs, the levels of chlorophyll were measured in 10-day-old A. thaliana seedlings treated with NaCl for 48 h in a hydroponic system (method of Iglesias et al. Reference Iglesias, Terrile, Bartoli, D'Ippólito and Casalongué2010, Reference Iglesias, Terrile, Windels, Lombardo, Bartoli, Vazquez, Estelle and Casalongué2014). Salinity led to the loss of 50% of the chlorophyll content in leaves from plants subjected to NaCl-mediated stress for 48 h (Fig. 8). Leaves from plants exposed to salinity in combination with Bent-Pro showed only a very slight decrease in chlorophyll content, however, thus providing evidence of a protection against salt stress. When analyzing chlorophyll levels, Bent-Pro performed better in terms of the protection of A. thaliana plants from chlorosis symptoms than did free Pro, in accord with the germination results, suggesting emerging properties of the proposed bioactive nanocomposite. These results could be associated with a release of Pro from Bent-Pro for a more prolonged time period favoring plant uptake and a spatiotemporal induction of Pro-mediated signaling mechanisms (Jafarbeglou et al. Reference Jafarbeglou, Abdouss, Shoushtari and Jafarbeglou2016).

Fig. 8 Effects of Bent-Pro on seedlings grown under salt. 10-day-old A. thaliana seedlings grown in MS agar medium were transferred to liquid MS medium (control, -) or medium supplemented with 200 mM NaCl (+ NaCl) in combination with 0.1 mg/mL Bent-Pro, 0.01 mg/mL Pro, and 0.1 mg/mL Bent for 48 h. The chlorophyll content was measured spectrophotometrically and related to control NaCl-treated seedlings. The data are mean values (± SE) of three independent experiments, (n = 240; t-Test * p ≤ 0.05 **p ≤ 0.01)

In agreement with the findings of the current study, Nanjo et al. (Reference Nanjo, Fujita, Seki, Kato, Tabata and Shinozaki2003) reported that A. thaliana transgenic plants suppress Pro degradation and consequently accumulate higher levels of Pro and show reduced symptoms of salt stress in terms of chlorophyll levels. The contribution of Pro to salt-stress tolerance using transgenic plants has been the approach of agro-biotechnology investigations for many years (Per et al. Reference Ruiz-Hitzky, Aranda, Darder and Rytwo2017). Transgenic tobacco, sorghum, pigeon-pea, and citrumelo plants that synthesize enhanced levels of Pro also presented an increased tolerance to salinity (de Campos et al. Reference de Campos, de Carvalho, de Souza, Marur, Pereira, Filho and Vieira2011; Kishor et al. Reference Kishor, Hong, Miao, Hu and Verma1995; Surekha et al. Reference Surekha, Kumari, Aruna, Suneetha, Arundhati and Kavi Kishor2014; Surender Reddy et al. Reference Surender Reddy, Jogeswar, Rasineni, Maheswari, Reddy, Varshney and Kavi Kishor2015). The potential effects on the environment and human health of transgenic biotechnology have led to questions amongst members of the public, however (Lu Reference Lu2016). An alternative and quicker approach for the improvement of salt-stress tolerance indicates that the exogenous application of Pro exerts osmoprotection and favors crop productivity (Per et al. Reference Per, Khan, Reddy, Masood, Hasanuzzaman, Khan and Anjum2017), but the use of Bent-Pro offers a new approach to improving plant protection even more against salinity.

Conclusions

Biological tests indicated that Bent-Pro protected A. thaliana plants from NaCl-mediated inhibition of seed germination and the loss of chlorophyll, two typical physiological and biochemical markers of salt-mediated detrimental effects on plants. The method for obtaining optimal Bent-Pro nanoclay was described. Using twice the CEC of Bent as the initial amount of Pro led to ~ 14 wt.% of Pro being retained in the Bent and the reaction time influenced the intercalation reaction, with maximum retention of Pro being achieved after 2 h of reaction. Based on FTIR and TGA tests (and supported by SEM), Pro was present mainly in its zwitterionic form intercalated in the Bent interlayer space and on the edges or surfaces of its plates. The XRD and TEM analysis, together with the molecular-size calculations, confirmed intercalation of the Pro in Bent and indicated a monolayer arrangement of the Pro molecules in the Bent interlayer space. The results obtained indicated that the reaction mechanism consisted predominantly of the incorporation of Pro as a zwitterion due to its electrostatic interaction with Bent and the interlaminar cations. Bent-Pro thus constitutes an innovative bioactive nanocomposite that can improve the protection of plants against salinity.

ACKNOWLEDGMENTS

This study was supported by Agencia Nacional de Investigaciones Científicas y Técnicas (ANPCyT, PICT Start up Nº 0008 and PICT 4363 Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Universidad Nacional de Mar del Plata. M.J.I., A.Y.M., and C.A.A. are researchers from CONICET. The authors thank ID. Ezequiel Macri for his support with the Bent and Bent-Pro schemes.

Funding

Funding sources are as stated in the Acknowledgments.

Declarations

Conflict of Interest

The authors declare that they have no conflict of interest.

Footnotes

(AE: Yael G. Mishael)

References

Alexandre, M., & Dubois, P. (2000). Polymer-layered silicate nanocomposites: preparation, properties and uses of a new class of materials. Materials Science and Engineering: R: Reports, 28, 163.CrossRefGoogle Scholar
Arnon, D. I. (1949). Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiology, 24, 115.CrossRefGoogle ScholarPubMed
Ashraf, M., & Foolad, M. R. (2007). Roles of glycine betaine and proline in improving plant abiotic stress resistance. Environmental and Experimental Botany, 59, 206216.CrossRefGoogle Scholar
Bates, L. S., Waldren, R. P., & Teare, I. D. (1973). Rapid determination of free proline for water-stress studies. Plant and Soil, 39, 205207.CrossRefGoogle Scholar
Boyes, D. C., Zayed, A. M., Ascenzi, R., McCaskill, A. J., Hoffman, N. E., Davis, K. R., & Görlach, J. (2001). Growth stage–based phenotypic analysis of Arabidopsis. The Plant Cell, 13, 1499LP1510.Google ScholarPubMed
Bragg, W. H., & Bragg, W. L. (1913). The reflection of X-rays by crystals. Proceedings of the Royal Society of London A: Mathematical, Physical and Engineering Sciences, 88, 428438.Google Scholar
Celis, R., Hermosín, M. C., Carrizosa, M. J., & Cornejo, J. (2002). Inorganic and organic clays as carriers for controlled release of the herbicide hexazinone. Journal of Agricultural and Food Chemistry, 50, 23242330.CrossRefGoogle ScholarPubMed
Chen, H., Chen, Q. S., Huang, B., Wang, S. W., & Wang, L. Y. (2018). High-potential use of l-Cysh modified bentonite for efficient removal of U(VI). from aqueous solution. Journal of Radioanalytical and Nuclear Chemistry, 316, 7180.CrossRefGoogle Scholar
de Campos, M. K. F., de Carvalho, K., de Souza, F. S., Marur, C. J., Pereira, L. F. P., Filho, J. C. B., & Vieira, L. G. E. (2011). Drought tolerance and antioxidant enzymatic activity in transgenic ‘Swingle’ citrumelo plants overaccumulating proline. Environmental and Experimental Botany, 72, 242250.CrossRefGoogle Scholar
Deivanai, S., Xavier, R., Vinod, V., Timalata, K., & Lim, O. F. (2011). Role of exogenous proline in ameliorating salt stress at early stage in two rice cultivars. Journal of Stress Physiology & Biochemistry, 7, 157174.Google Scholar
Devi, T. U., Lawrence, N., Ramesh Babu, R., Selvanayagam, S., Stoeckli-Evans, H., & Ramamurthi, K. (2009). Synthesis, crystal growth and characterization of l -Proline lithium chloride monohydrate: A new semiorganic nonlinear optical material. Crystal Growth & Design, 9, 13701374.CrossRefGoogle Scholar
El Moukhtari, A., Cabassa-Hourton, C., Farissi, M., & Savouré, A. (2020). How does proline treatment promote salt stress tolerance during crop plant development? Frontiers in Plant Science, 11, 1127.CrossRefGoogle ScholarPubMed
Food and Agriculture Organization of the United Nations. (2017). The future of food and agriculture: Trends and challenges. http://www.fao.org/3/I8429EN/i8429en.pdfGoogle Scholar
Gamba, M., Flores, F. M., Madejová, J., & Torres Sánchez, R. M. (2015). Comparison of imazalil removal onto montmorillonite and nanomontmorillonite and adsorption surface sites involved: an approach for agricultural wastewater treatment. Industrial & Engineering Chemistry Research, 54, 15291538.CrossRefGoogle Scholar
Golldack, D., Li, C., Mohan, H., & Probst, N. (2014). Tolerance to drought and salt stress in plants: unraveling the signaling networks. Frontiers in Plant Science, 5, 151.CrossRefGoogle ScholarPubMed
Grillo, R., Mattos, B. D., Antunes, D. R., Forini, M. M. L., Monikh, F. A., & Rojas, O. J. (2021). Foliage adhesion and interactions with particulate delivery systems for plant nanobionics and intelligent agriculture. Nano Today, 37, 101078.CrossRefGoogle Scholar
Hayat, S., Hayat, Q., Alyemeni, M. N., Wani, A. S., Pichtel, J., & Ahmad, A. (2012). Role of proline under changing environments: a review. Plant Signaling & Behavior, 7, 14561466.CrossRefGoogle ScholarPubMed
Iglesias, M. J., Terrile, M. C., Bartoli, C. G., D'Ippólito, S., & Casalongué, C. A. (2010). Auxin signaling participates in the adaptative response against oxidative stress and salinity by interacting with redox metabolism in Arabidopsis. Plant Molecular Biology, 74, 215222.CrossRefGoogle ScholarPubMed
Iglesias, M. J., Terrile, M. C., Windels, D., Lombardo, M. C., Bartoli, C. G., Vazquez, F., Estelle, M., & Casalongué, C. A. (2014). MiR393 regulation of auxin signaling and redox-related components during acclimation to salinity in Arabidopsis. PLoS ONE, 9, e107678.CrossRefGoogle ScholarPubMed
Jafarbeglou, M., Abdouss, M., Shoushtari, A. M., & Jafarbeglou, M. (2016). Clay nanocomposites as engineered drug delivery systems. RSC Advances, 6, 5000250016.CrossRefGoogle Scholar
Kaur, G., & Asthir, B. (2015). Proline: a key player in plant abiotic stress tolerance. Biologia Plantarum, 59, 609619.CrossRefGoogle Scholar
Kishor, P. B. K., Hong, Z., Miao, G. H., Hu, C. A. A., & Verma, D. P. S. (1995). Overexpression of δ-pyrroline-5-carboxylate synthetase increases proline production and confers osmotolerance in transgenic plants. Plant Physiology, 108, 1387LP1394.CrossRefGoogle ScholarPubMed
Komadel, P., & Madejová, J. (2006). Acid activation of clay minerals. In Handbook of Clay Science (Bergaya, F., Theng, B.K.G., and Lagaly, G., (Ed.), Developments in Clay Science. (Vol. 1, pp. 263287). Elsevier.CrossRefGoogle Scholar
Lagaly, G. (2001). Pesticide–clay interactions and formulations. Applied Clay Science, 18, 205209.CrossRefGoogle Scholar
Li, J., Li, Y., & Dong, H. (2008). Controlled Release of Herbicide Acetochlor from Clay/Carboxylmethylcellulose Gel Formulations. Journal of Agricultural and Food Chemistry, 56, 13361342.CrossRefGoogle ScholarPubMed
Lu, B.-R. (2016). Challenges of transgenic crop commercialization in China. Nature Plants, 2, 16077.CrossRefGoogle ScholarPubMed
Mallakpour, S., & Dinari, M. (2011). Preparation and characterization of new organoclays using natural amino acids and cloisite Na+. Applied Clay Science, 51, 353359.CrossRefGoogle Scholar
Mansilla, A. Y., Salcedo, M. F., Colman, S. L., Chevalier, M. T., Lanfranconi, M. R., Alvarez, V. A., & Casalongué, C. A. (2020). Characterization of functionalized bentonite as nanocarrier of salicylic acid with protective action against Pseudomonas syringae in tomato plants. European Journal of Plant Pathology, 158, 211222.CrossRefGoogle Scholar
McConnell, D. (1950). The crystal chemistry of montmorillonite. American Mineralogist, 35, 166172.Google Scholar
McKee, T., & McKee, J. (2003). Biochemistry: The Molecular Basis of Life. McGraw-Hill.Google Scholar
Merino, D., & Alvarez, V. A. (2020). Thermal degradation of poly (ε-caprolactone). nanocomposites with soy lecithinmodified bentonite fillers. Thermochimica Acta, 689, 178638.CrossRefGoogle Scholar
Merino, D., Ollier, R., Lanfranconi, M., & Alvarez, V. (2016). Preparation and characterization of soy lecithin-modified bentonites. Applied Clay Science, 127, 1722.CrossRefGoogle Scholar
Merino, D., Mansilla, A. Y., Casalongué, C. A., & Alvarez, V. A. (2018). Preparation, characterization, and in vitro testing of nanoclay antimicrobial activities and elicitor capacity. Journal of Agricultural and Food Chemistry, 66(12), 31013109.CrossRefGoogle ScholarPubMed
Merino, D., Tomadoni, B., Salcedo, M. F., Mansilla, A. Y., Casalongué, C. A., & Alvarez, V. A. (2020). Nanoclay as carriers of bioactive molecules applied to agriculture. Pp. 122 in: Handbook of Nanomaterials and Nanocomposites for Energy and Environmental Applications (O.V. Kharissova, L.M.T. Martínez, and B.I. Kharisov). Springer, Berlin.Google Scholar
Nanjo, T., Fujita, M., Seki, M., Kato, T., Tabata, S., & Shinozaki, K. (2003). Toxicity of free proline revealed in an arabidopsis T-DNA-tagged mutant deficient in proline dehydrogenase. Plant & Cell Physiology, 44, 541548.CrossRefGoogle Scholar
Negrão, S., Schmöckel, S. M., & Tester, M. (2016). Evaluating physiological responses of plants to salinity stress. Annals of Botany, 119, 111.CrossRefGoogle ScholarPubMed
Ni, B., Liu, M., , S., Xie, L., & Wang, Y. (2011). Environmentally Friendly Slow-Release Nitrogen Fertilizer. Journal of Agricultural and Food Chemistry, 59, 1016910175.CrossRefGoogle ScholarPubMed
Parbhakar, A., Cuadros, J., Sephton, M. A., Dubbin, W., Coles, B. J., & Weiss, D. (2007). Adsorption of l-lysine on montmorillonite. Colloids and Surfaces A: Physicochemical and Engineering Aspects, 307, 142149.CrossRefGoogle Scholar
Patel, H. A., Somani, R. S., Bajaj, H. C., & Jasra, R. V. (2006). Nanoclays for polymer nanocomposites, paints, inks, greases and cosmetics formulations, drug delivery vehicle and waste water treatment. Bulletin of Materials Science, 29, 133145.CrossRefGoogle Scholar
Pédro, G. (1965). La constitution cristallochimique des phyllosilicates. Sa signification et ses conséquences. Bulletin du Groupe français des argiles, 16, 3747.CrossRefGoogle Scholar
Per, T. S., Khan, N. A., Reddy, P. S., Masood, A., Hasanuzzaman, M., Khan, M. I. R., & Anjum, N. A. (2017). Approaches in modulating proline metabolism in plants for salt and drought stress tolerance: Phytohormones, mineral nutrients and transgenics. Plant Physiology and Biochemistry, 115, 126140.CrossRefGoogle ScholarPubMed
Petra, L., Billik, P., & Komadel, P. (2015). Preparation and characterization of hybrid materials consisting of highenergy ground montmorillonite and α-amino acids. Applied Clay Science, 115, 174178.CrossRefGoogle Scholar
Ruiz-Hitzky, E., Aranda, P., Darder, M., & Rytwo, G. (2010). Hybrid materials based on clays for environmental and biomedical applications. Journal of Materials Chemistry, 20, 93069321.CrossRefGoogle Scholar
Saha, J., Brauer, E. K., Sengupta, A., Popescu, S. C., Gupta, K., & Gupta, B. (2015). Polyamines as redox homeostasis regulators during salt stress in plants. Frontiers in Environmental Science, 3, 21.CrossRefGoogle Scholar
Sanchez-Martin, M. J., Rodriguez-Cruz, M. S., Andrades, M. S., & Sanchez-Camazano, M. (2006). Efficiency of different clay minerals modified with a cationic surfactant in the adsorption of pesticides: influence of clay type and pesticide hydrophobicity. Applied Clay Science, 31, 216228.CrossRefGoogle Scholar
Shahid, S. A., Zaman, M., & Heng, L. (2018). Introduction to soil salinity, sodicity and diagnostics techniques. Pp. 142 in: Guideline for Salinity Assessment, Mitigation and Adaptation Using Nuclear and Related Techniques (Zaman, M., Shahid, S.A., and Heng, L., editors). Springer International Publishing, Cham.Google Scholar
Shokri, E., Yegani, R., & Akbarzadeh, A. (2017). Novel adsorptive mixed matrix membranes by embedding modified montmorillonite with arginine amino acid into polysulfones for As(V) removal. Applied Clay Science, 144, 141149.CrossRefGoogle Scholar
Surekha, C., Kumari, K. N., Aruna, L. V., Suneetha, G., Arundhati, A., & Kavi Kishor, P. B. (2014). Expression of the Vigna aconitifolia P5CSF129A gene in transgenic pigeonpea enhances proline accumulation and salt tolerance. Plant Cell. Tissue and Organ Culture (PCTOC), 116, 2736.CrossRefGoogle Scholar
Surender Reddy, P., Jogeswar, G., Rasineni, G. K., Maheswari, M., Reddy, A. R., Varshney, R. K., & Kavi Kishor, P. B. (2015). Proline over-accumulation alleviates salt stress and protects photosynthetic and antioxidant enzyme activities in transgenic sorghum [Sorghum bicolor (L.). Moench]. Plant Physiology and Biochemistry, 94, 104113.CrossRefGoogle Scholar
Szabados, L., & Savouré, A. (2010). Proline: a multifunctional amino acid. Trends in Plant Science, 15, 8997.CrossRefGoogle ScholarPubMed
Wu, C.-J., Gaharwar, A. K., Schexnailder, P. J., & Schmidt, G. (2010). Development of biomedical polymer-silicate nanocomposites: A materials science perspective. Materials, 3, 29863005.CrossRefGoogle Scholar
Zhang, J. Z., Creelman, R. A., & Zhu, J.-K. (2004). From laboratory to field. Using information from Arabidopsis to engineer salt, cold, and drought tolerance in crops. Plant Physiology, 135, 615LP621.CrossRefGoogle ScholarPubMed
Zhu, J.-K. (2002). Salt and drought stress signal transduction in plants. Annual Review of Plant Biology, 53, 247273.CrossRefGoogle ScholarPubMed
Zhu, J., Zhang, P., Qing, Y., Wen, K., Su, X., Ma, L., Wei, J., Liu, H., He, H., & Xi, Y. (2017). Novel intercalation mechanism of zwitterionic surfactant modified montmorillonites. Applied Clay Science, 141, 265271.CrossRefGoogle Scholar
Figure 0

Fig. 1 XRD pattern of the natural bentonite

Figure 1

Fig. 2 Amount of Pro incorporated in Bent (g of Pro/100 g of Bent-Pro) depending on a the reaction time (h), and b the initial amount of Pro (f)

Figure 2

Fig. 3 FTIR spectra of a Bent, b Bent-Pro, and c Pro

Figure 3

Fig. 4 a Bent and Bent-Pro XRD pattern between 2 and 10°2θ. b Representative scheme of the orientation of a Pro molecule (3.7 Å) confined in the interlamellar space of Bent, in its zwitterionic form, in the presence of a Na+ cation and a water molecule; c TEM images of a Bent and b Bent-Pro

Figure 4

Fig. 5 DTGA (%/°C) vs. Temperature (°C) for a Bent, b Bent-Pro, and c Pro

Figure 5

Fig. 6 SEM images of: a Bent and b Bent-Pro

Figure 6

Fig. 7 Bar chart showing the effects of Bent-Pro on seed germination under salt stress. A. thaliana seeds were sown on MS medium supplemented with 150 mM NaCl (black bar) or 150 mM NaCl combined with various concentrations of Bent-Pro (dark gray bars), Pro (light gray bars) or Bent (white bars). Germination was scored after 48 h. The percentage of germination with respect to the control for each treatment is shown. 100% indicates that the seeds germinated under control conditions (without NaCl). The data are mean values (± SE) of four independent experiments. (n = 800; t-Test * p ≤ 0.05 **p ≤ 0.01)

Figure 7

Fig. 8 Effects of Bent-Pro on seedlings grown under salt. 10-day-old A. thaliana seedlings grown in MS agar medium were transferred to liquid MS medium (control, -) or medium supplemented with 200 mM NaCl (+ NaCl) in combination with 0.1 mg/mL Bent-Pro, 0.01 mg/mL Pro, and 0.1 mg/mL Bent for 48 h. The chlorophyll content was measured spectrophotometrically and related to control NaCl-treated seedlings. The data are mean values (± SE) of three independent experiments, (n = 240; t-Test * p ≤ 0.05 **p ≤ 0.01)

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