Research Article | Open Access
Hassiba Bouazzi, Kaouthar Feki, Nabil Zouari, Mouna Sahnoun, Faical Brini, Walid Saibi, "Causal Enzymology and Physiological Aspects May Be Accountable to Membrane Integrity in Response to Salt Stress in Arabidopsis thaliana Lines", BioMed Research International, vol. 2019, Article ID 3534943, 13 pages, 2019. https://doi.org/10.1155/2019/3534943
Causal Enzymology and Physiological Aspects May Be Accountable to Membrane Integrity in Response to Salt Stress in Arabidopsis thaliana Lines
Apart from their significance in the protection against stress conditions, the plant cell membranes are essential for proper development of the diverse surface structures formed on aerial plant organs. In addition, we signal that membrane remodeling and integrity are function of some of causal physiological and enzymological aspects such as the MDA, the ion leakage and also the monitoring of some phytozymes involved in lipid and cellulose metabolisms. Those last ones are related to the membrane structure (lipases and cellulases), that were assessed in durum wheat dehydrin transgenic context (YS, K1-K2, DH2, and DH4), proline metabolic mutant () per comparison with the wild-type plant (Wt). We report also the docking data reinforcing the fact that the membrane integrity seems to be function of causal enzymological behaviors, through the molecular dynamic investigation resulting from the dehydrin-phytozyme interactions and also from the inhibition effect of the durum wheat LTP4 on the lipase activity.
At the beginning, it is crucial to note that as much as one-half of the irrigated areas of the world are affected by high salinity. Furthermore, the one distinctive feature of most plants growing in saline environments is that they accumulate increased amounts of low-molecular-weight water-soluble solutes in their cells. The last process is called osmotic adjustment. It has been repeatedly inferred, but never proven, that there might be a relationship between salt tolerance and osmotic adjustment [1–4].
The best characterized biochemical response of plant cells to osmotic stress is the accumulation of organic osmolytes like proline [2, 3, 5, 6]. The accumulation of this atypical amino acid in leaves was first observed  and since then its cardinal role as an osmoprotectant effector under various stress conditions, especially under salt stress, has been shown . The effect of salt stress on plants depends on the salt concentration, the duration of exposure, and also the plant genotype [7, 9]. The presence of salt in the environment induces water deficit in plants because of the lowered external water potential, while ion toxicity and nutritional alterations disturb ion transport systems [9, 10]. In addition, salt stress causes membrane damage, alters levels of growth regulators, inhibits some enzymes, and also disrupts photosynthesis, and may thus lead to plant death [2, 11, 12]. It is important to note as well that proline is described as playing catalytic role miming the aldolation reaction [1, 8]. Indeed, the proline-catalyzed aldol reaction mechanism has stimulated considerable debate; at least various mechanisms have been discussed. The Hajos-Parrish-Eder-Sauer-Wiechert reaction represents not only the first asymmetric aldol reaction invented by chemists but also the first highly enantioselective organocatalytic transformation [1, 13].
On the other hand, one of the known plant responses to salt stress is ROS production [5, 12]. Plant cells need to regulate ROS production as excess ROS is potentially harmful to nucleic acids, proteins, and lipids and may therefore lead to cell injury and death [1, 3, 14, 15]. ROS produced through NADPH oxidase activity was shown to be mediated by phospholipid signaling [12, 15]. The second messenger phosphatidic acid is a phospholipid which targets specific proteins to bring about cellular and physiological changes that allow plants to adapt to abiotic stresses . Phosphatidic acid is formed when phospholipase D hydrolyses structural phospholipids at the terminal phosphoesteric bond with release of the hydrophilic head group. In plants, phospholipase D is predominant among the phospholipase families . Their activity upgrades rapidly in response to various environmental stresses like cold, drought, salinity, and wounding ones [11, 18, 19]. It is also very interesting to point out that proline accumulation was shown to be negatively regulated by phospholipase D activity in Arabidopsis thaliana [1, 19].
On the other hand, we note that lipid transfer proteins (LTPs) are abundant small members of the family of pathogenesis-related proteins (PR-14) and believed to be involved in plant defense responses. A number of biological roles including antimicrobial defense, signaling, cell wall loosening, and involvement in salt tolerance process acquisition have been proposed and proved. Substantially, LTPs may be important components of direct defense against fungal pathogens and also in some of abiotic stress like salinity [20–22].
Here, the present study deals with the identification of the roles of some physiological parameters and also causal enzymological behaviors that may explain the membrane integrity in case of response of Arabidopsis thaliana lines (wild type (Wt), transgenic and metabolic mutant) to salt stress treatment. Hence, we report the potential contribution of phytozymes involved in membrane remodeling and integrity such as lipases and cellulases and also the impact of the tolerance level on the MDA and the ion leakage. Moreover, the in silico studies reinforce the role played by transgenic context through the study of the molecular dynamics of the interaction between phytozymes (lipases) and dehydrin or one of these active regions. Eventually, it is basic to note the inhibition role that can be played by the LTP4 during the in vitro lipase assessment.
2. Experimental Section
2.1. Plant Material, Growth Conditions, and Salinity Treatments
Arabidopsis thaliana ecotype Columbia (Col-0) is the wild type (Wt) used in this study. Hence, Wt, the transgenic Arabidopsis lines overexpressing durum wheat dehydrin Dhn-5 gene (DH2 and DH4), and the truncated forms (YS, K1-K2) have been previously described by [23–25] and also the proline metabolic mutant lines () were grown on MS agar medium  for one week under light/dark cycle condition of 16-hour light/8-hour dark cycle at 22°C and then transferred to MS medium supplemented or not with NaCl at the concentration of 100 mM. After 8 days of salt stress application, the effect of the addition of NaCl in the medium was determined by measuring some catalytic activities and also some other physiological parameters such as H2O2 amount, MDA, and ion leakage.
2.2. Enzymatic Extract Preparation
Aliquots of frozen fresh shoot material (0.5 g) were ground to a fine powder with liquid nitrogen and homogenized in a cold solution containing 100 mM Tris-HCl buffer (pH 8), 10 mM EDTA (ethylenediaminetetraacetic acid), 50 mM KCl, 20 mM MgCl2, 0.5 mM PMSF (Phenyl-Methyl-Sulfonyl-Fluoride), and 2 % (w/v) PVP. The homogenate was centrifuged at 14.000 × g for 30 min at 4°C and the supernatant was used for determination of the enzyme activities . Protein concentration was determined according to Bradford method .
2.3. Potentiometric pH-stat Assay of Lipase Activities
As indicated by , lipase activities were measured potentiometrically at 40°C and pH 8 meaning automatically titrating the free fatty acids released from purified egg L-α-phosphatidylcholine (Sigma) as substrate, as previously described [11, 19, 27]. Lipase activities were measured with mechanically stirred triglyceride emulsions . The inhibitory effect of the LTP4 on the lipase activity is monitored by adding the purified durum wheat LTP4 to the reaction mixture at the concentration of 40 μg.mL−1.
2.4. The Assessment of β-Glucosidase Activity
As indicated in materials and methods section of Saibi and Gargouri , β-glucosidase activity is monitored by incubating 0.2 mL of p-nitrophenyl-β-D-glucopyranoside as substrate (in 0.1 M sodium acetate buffer pH 5) with the enzymatic preparation at the appropriate dilution for 15 min at 50°C. The reaction was stopped by adding 0.6 mL of 0.4 M glycine-NaOH buffer pH 10.8. The p-nitrophenol liberated was measured at 400 nm. The molecular extinction coefficient of p-nitrophenol was 18,000 M−1.cm−1. One unit of enzymatic activity was monitored as the amount of enzyme required to release 1 μmol of p-nitrophenol per min under the assay conditions.
2.5. Membrane Lipid Peroxidation Assays
Levels of lipid peroxidation were assessed by measuring the amount of malondialdehyde (MDA) in tissue. Fresh leaf and root samples were homogenized in 10% TCA. The homogenate was centrifuged at 15,000g for 20 min at 4°C. The supernatant was collected and mixed with 0.5% thiobarbituric acid in 20% TCA. Samples were heated at 95°C for 25 min in a water bath and then cooled on ice. The samples were centrifuged at 10,000g for 10 min and the absorbance of solutions at 532 and 600 nm was recorded. The MDA level was calculated using the extinction coefficient for MDA (ε = 155 μM cm−1) expressed in nmol MDA g−1 DW [9, 11].
2.6. Electrolyte Leakage Assay
Five leaf discs (0.5 cm diameter) were cut from leaves derived from the studied Arabidopsis thaliana lines and placed in glass tubes containing 5 ml of deionised water. Thereafter, tubes were kept at room temperature with gentle agitation for 24 h. Electrolyte leakage was determined by measuring the electrical conductivity of the glass tube solution using a conductivity meter and data were expressed as mS.cm−1 like described by .
2.7. Molecular Modeling and Docking Analysis
The unique available sequences of the phospholipid/glycerol acyltransferase (AT4G00400), lipase class 3 family protein (AT1G02660), and thioesterase family protein (AT1G08310) were modeled by the modeling server, phyre 2 (Protein Homology/analogY Recognition Engine V.2). The crystal structure of the 1-acyl-sn-glycerophosphate (lpa)2 acyltransferase, plsc, from Thermotoga maritima (PDB: c5kymA) was utilized to model the phospholipid/glycerol acyltransferase. The fungal lipase (PDB: d3tgla) was selected as a template to generate the lipase class 3 family. The crystal structure of murine soluble epoxide hydrolase 2 (PDB: c1cr6A) was used as a structure template for the thioesterase. The dehydrin ORF was modeled using collagen i alpha 1(PDB: c1ygvA) as template. The generated models were then refined by two-step atomic-level energy minimization through the ModRefiner tool available at http://zhanglab.ccmb.med.umich.edu/ModRefiner/. Ramachandran plots were then created by the online tool RAMPAGE (http://mordred.bioc.cam.ac.uk/~rapper/rampage.php) to evaluate and validate models . The PyMol Molecular Graphics System (DeLano Scientific, San Carlos, CA, http://www.pymol.org) was used to visualize the constructed model structure and generate graphical figures. Protein-protein docking of dehydrin and the most three partners’ interacting protein was performed using the GRAMM-X server available at (http://vakser.bioinformatics.ku.edu/resources/gramm/grammx) web site . GRAMM-X analyzes the input structures and chooses the best course of action automatically.
2.8. Statistical Analysis
Data were analyzed using one-way analysis of variance and treatment mean separations were performed using Duncan’s multiple range tests at the 5 % level of significance .
3. Results and Discussion
At the beginning, it is basic to indicate that membranes are one of the most important structural components of the cell. Hence, they are the protecting layer of the cell bounding the protoplasm and provide the interface for interaction between the outer and the inner components . They have very important functions such as receiving signals, involved in transport of chemicals inwards and outwards. At the same case and in addition to cellulose and hemicellulose, the membrane contains lipids, phospholipids, and galactolipids [11, 27]. In particular, those last compounds were judged playing very important roles on the membrane integrity and also functionality against various biotic and abiotic stresses [11, 31].
On the other hand, it is fundamental to add that durum wheat dehydrin (named DHN-5) is one of the LEA-group 2 family members that was isolated and characterized to be studied and to understand their physiological roles . Furthermore, DHN-5 overexpression in Arabidopsis thaliana was realized by our team . Indeed, we proved that DHN-5 confers salinity tolerance to the dehydrin transgenic Arabidopsis lines (DHE 2, DH4, and K1-K2), through the modulation of some of metabolic pathways such as ROS scavenging system, proline metabolism one, and also some of phytozymes like proteases (cysteine and aspartyl proteases) [3, 5].
3.1. Rating of the Transcriptional Investigations Leads to Persuasive Salt Tolerance Process
In addition and according to our previous studies at transcriptional level , our team proved also the denivelation of 77 genes up or downregulated in DH4 line submitted to salt stress treatment. Indeed, Figure 1 illustrates some properties of phospholipid/glycerol acyltransferase (AT4G00400) which was upregulated as indicated in the list of upregulated genes in transgenic Arabidopsis seedlings overexpressing DHN-5  and also lipase class 3 family protein (AT1G02660) and moreover esterase/lipase/thioesterase family protein (AT1G08310) that were downregulated, as indicated in the microarray analysis realized under salt stress and that appeared in the list of downregulated genes in transgenic Arabidopsis line (DH4) . Hence, it is important to point out that those three proteins (phospholipid/glycerol acyltransferase, the lipase class 3 family proteins, and the esterase/lipase/thioesterase family protein) are involved in the lipid metabolism that is strongly related to the membrane structure and so with the level of membrane integrity . To achieve this fact, we note that there is another important member named LTP4 (AT5G59310) and it is an upregulated one.
As a point of fact and as indicated in Figure 1, the first one (AT4G00400) is composed of 500 amino acids having an apparent molecular weight of 55.866 kDa and a computed isoelectric point of 9.31. The second one (AT1G02660) consists of 713 amino acids, 78.345 kDa, and a computed isoelectric point of 4.96. The third one (AT1G08310) consists of 318 amino acids, 36.810 kDa, and a computed isoelectric point of 9.4. The last one (AT5G59310) consists of 112 amino acids having a molecular weight of 11.405 kDa and a computed isoelectric point of 9.11.
3.2. MDA and Ion Leakage Findings Reflect the Membrane Integrity
It is well established that various abiotic stresses lead to damage to plants through oxidative stress due to the generation of ROS [5, 6]. Thus, the amount of MDA and ion leakage were assessed in both the transgenic Arabidopsis seedlings overexpressing DHN-5 full length (DH2 and DH4), YS and K1-K2 Quiet sequences, Wt and lines under unstressed and salt stress conditions. In this case and as indicated in Figure 2, MDA content increased obviously in mutant, transgenic, and Wt plants after salt stress. Indeed, the level of MDA in transgenic lines was significantly lower (5.4, 5.5, and 5.4 mmol.g−1(FW) in DH2, DH4, and K1-K2, respectively) than in Wt, YS, and (11.35 and 9.7 mmol.g−1, 0 mmol.g−1 (FW), respectively). In addition to this fact, it is crucial to note that the MDA level of the mutant line under salt stress treatment is considered to be zero because of the inability of the described strain to grow under salt stress conditions used in these studies .
On the other hand and as shown in Figure 3, we illustrate the fact that Wt, YS, , DH2, DH4, and K1-K2 lines presented the same ion leakage level in conventional medium. Under salt stress condition, the Wt, YS, presented 1.51-, 1.46-, and 1.79-fold higher electrolyte leakage than DH4 line, respectively. Those findings indicated that the transgenic plants produce significantly lower levels of ROS. This fact suggests that overexpression of DHN-5 leads to efficient scavenging system, hence better membrane stability.
3.3. Advancement of the Lipase Activity
Table 1 summarizes a clear value reconciliation of the lipase level in full length dehydrin transgenic lines (DH2, DH4), the truncated dehydrin transgenic ones (YS and K1-K2) compared to the wild-type (Wt) and the proline metabolic mutant (). Indeed, under MS medium Table 1 shows 1.41, 1.40, 1.39, and 1.41 U. mg−1 (FM), respectively. At the same case but under salt stress treatment (NaCl 100 mM), the studied activity is more decreased in the case of the transgenic Arabidopsis seedlings overexpressing DHN-5 (DH2, DH4, and K1-K2) which followed 1.30, 1.31, and 1.30 U.mg−1 (FM). Concerning both the wild type and , the activity levels were indicated in the table because of the sensitivity of the first one and the hypersensitivity of the second one to grow properly under salt stress. Looking for those findings, it seems that the acquisition of the salt tolerance is accompanied with the decrease of the lipase activity . This fact can be explained through the fact that the membrane structure and integrity must be more protected and this protection seems to be realized via the dehydrin transgenic context by decreasing the lipase activity.
3.4. Furtherance of the β-Glucosidase Activities
The analysis of data illustrated in Table 2 proves a clear value reconciliation of the β-glucosidase level in both used strains such as transgenic lines (DH2, DH4, YS and K1-K2) in addition to the wild type (Wt) and the proline metabolic mutant () under conventional standard conditions (MS medium). Indeed, the described lines present 0.52, 0.51, 0.50, 0.49, 0.49, and 0.50 U.mg−1 (FM), respectively. At the same case but under salt stress treatment, β-glucosidase activity is more decreased in the case of the transgenic Arabidopsis seedlings overexpressing DHN-5 (DH2, DH4, and K1-K2) which followed 0.40, 0.39, and 0.40 U.mg−1 (FM). Concerning both wild type and , the activity levels were not really monitored in the table and we stop it to put zero because of the sensitivity of the first one and the hypersensitivity of the last one to grow properly under salt stress. Eventually and according to those results, it seems that it is plausible to explain the fact that the membrane structure and integrity must be more protected and this protection is plausibly realized via the dehydrin transgenic context by decreasing the β-glucosidase activity .
3.5. Interactome Findings Analysis
The study of protein interaction of the three target proteins (phospholipid/glycerol acyltransferase (AT4G00400), lipase class 3 family protein (AT1G02660), and esterase/lipase/thioesterase family protein (AT1G08310)), taken alone, with the proteome of Arabidopsis thaliana showed, as follows in Figures 4(a), 4(b), and 4(c), that each one has a range of potential partners, clearly indicated in Tables 3, 4, and 5, respectively. Among phospholipid/glycerol acyltransferase (AT4G00400) partners, we can cite more than a partner involved in metabolism related to tenacity and good membrane structuring and integrity (Table 3). We guess that the positive implication of this enzyme on the tolerance acquisition process in the dehydrin transgenic Arabidopsis lines (DH4) is due to their involvement in the maintaining of the membrane stability through the dynamic stability in lipid and phospholipid metabolism in plant .
The same case was observed with lipase class 3 family protein (AT1G02660) and esterase/lipase/thioesterase family protein (AT1G08310)) that were downregulated (Tables 4 and 5). Those two enzymes are implicated as downexpressed proteins. Hence, they should have moderate activities in relation to the level of tolerance and sensitivity of the plant under salt stress conditions [39–41]. We can say that the transgenic context gives to the plant a tolerance to salt stress through its multifactorial interactions, following two types of modulation, positive and negative regulations. This modulation may be dictated by the disordered aspect of the DHN-5 and its multifunctionality, already proven [24, 25, 37, 42].
3.6. In Silico Studies
To better understand the implication of the transgenic context in the development of the salinity tolerance process through the interaction of DHN-5 with these candidate phytozymes, we used the study of protein-protein interaction. It is within this framework that we have adopted molecular modeling to cool the maximum of data used to reinforce our suggestions.
Accordingly, the phospholipid/glycerol acyltransferase, lipase class 3 family, thioesterase, dehydrin obtained models were refined by ModRefiner and checked by the corresponding Ramachandran plots. Furthermore, the models analysis showed that more than 98% of residues were in the favored and allowed regions. Consequently, these models were validated and retained. Particularly, the dehydrin shows a disordered structure . Moreover, the dehydrin structural model [23, 25, 37] contains the K-segment domain present in two copies as Lys-Ileu-Lys-Glu-Lys-Leu-Pro-Gly sequence. The consensus sequence Asp-Glu-Tyr-Gly-Asn-Pro is also conserved in the N-terminal region as well as the (SSSSSSSS) sequence recognized as the S-(Ser-rich tract) segment. The docking analysis between the dehydrin and those proteins showed that the dehydrin was more effective for lipase class 3 than acyltransferase and thioesterase in terms of interaction hydrogen bonds number (Figures 5(a), 5(b), and 5(c)). Indeed the atomic contact energies of dehydrin-protein complexes were -297 kcal/mol, -148 kcal/mol, while they reached -69.96 kcal/mol for lipase, the acyltransferase, and the thioesterase, respectively. The approximate interface areas of dehydrin for lipase, acyltransferase, and thioesterase were 1316 Å2, 1277Å2, and 1136 Å2, respectively (Tables 6, 7, and 8, respectively). Eventually, those in silico findings reinforce the data collected through the analysis of the transcriptional one realized by our group  and moreover argue about the strong implication of causal enzymology in the process of membrane integrity
3.7. The Plausible Involvement of LTP4 in Salt Tolerance Process
The lipid transfer protein 4 (LTP4) is involved in various biotic and abiotic stresses such as water deprivation, abscisic acid stimulus, and salt stress. It was described also as an inhibitor of some of enzymes involved in lipid metabolism and also as inhibitor of some glycosyl hydrolase ones . In addition, LTP4 represents an upregulated protein as indicated in . Moreover, it is important to signal that the LTP4 was described as an inhibitor of some of enzymes implicated in the carbohydrate and other metabolisms related to the membrane integrity . Based on this fact, it seems that LTP4 can play a protective role during the acquisition of the salt tolerance process by remodeling some of the involved phytozymes in the described process . In this case, it is crucial to test the effect of the durum wheat LTP4 on the lipase activity. Furthermore, the assessment of the last one in presence of the described protein gives birth to the results indicated in Figure 6.
Eventually, the inhibition effect of the durum wheat LTP4 observed on the lipase activity can explain the acquisition of the salt tolerance under salt treated condition (MS-NaCl). Indeed, the decease of the lipase activity under stress condition can protect the membrane structure and so the membrane integrity against the damage that can be caused by the lipolytic activity.
4. Concluding Remarks
Eventually and according to the findings followed here, it is fundamental to indicate that the membrane integrity may be explained through some causal enzymological and also physiological aspects due to looking for the acquisition of salt tolerance process in Arabidopsis thaliana lines. Given that DHN-5 is a multifunctional protein through its crucial roles played as thermoactivator and thermostabilizator of biocatalysts [5, 37, 42] and also its ability to chelate metals , it seems to be a key protein playing a heat protective role and also interacts with multiple partners involved in different pathways (such as proline) and other metabolites (like sucrose and trealose). In addition, through its multifunctionality , dehydrin may be a good candidate to interact with the catalysts involved in proline metabolism such as P5CS one. All these findings reinforce the importance of this protein in plant stress response. Finally and to give opportunity to new strategies of research and investigation, we can dare to ask the following question: could proline affect salt tolerance process through a catalytic scene?
No data were used to support this study.
Conflicts of Interest
The authors note that there is no conflict of interest.
This work was in part financially supported by a grant from the Tunisian Ministry of Higher Education and Scientific Research contract program_2015-2018 CBS-LBAP/code: LR15CBS03.
- W. Saibi, K. Feki, I. Yacoubi, and F. Brini, “Bridging between proline structure, functions, metabolism, and involvement in organism physiology,” Applied Biochemistry and Biotechnology, vol. 176, no. 8, pp. 2107–2119, 2015.
- C. Di Martino, R. Pizzuto, M. L. Pallotta, A. De Santis, and S. Passarella, “Mitochondrial transport in proline catabolism in plants: the existence of two separate translocators in mitochondria isolated from durum wheat seedlings,” Planta, vol. 223, no. 6, pp. 1123–1133, 2006.
- H. Bouazzi, K. Feki, F. Brini, and W. Saibi, “Is duality between proline metabolic mutation (p5cs 1-4) and durum wheat dehydrin transgenic contexts a “pacemaker” for salt tolerance process in Arabidopsis thaliana?” Acta Physiologiae Plantarum, vol. 41, no. 3, p. 36, 2019.
- C. Ghoulam, A. Foursy, and K. Fares, “Effects of salt stress on growth, inorganic ions and proline accumulation in relation to osmotic adjustment in five sugar beet cultivars,” Environmental and Experimental Botany, vol. 47, no. 1, pp. 39–50, 2002.
- W. Saibi, N. Zouari, K. Masmoudi, and F. Brini, “Role of the durum wheat dehydrin in the function of proteases conferring salinity tolerance in Arabidopsis thaliana transgenic lines,” International Journal of Biological Macromolecules, vol. 85, pp. 311–316, 2016.
- W. Saibi, K. Feki, R. Ben Mahmoud, and F. Brini, “Durum wheat dehydrin (DHN-5) confers salinity tolerance to transgenic Arabidopsis plants through the regulation of proline metabolism and ROS scavenging system,” Planta, vol. 242, no. 5, pp. 1187–1194, 2015.
- A. R. Kemble and H. T. Macpherson, “Liberation of amino acids in perennial rye grass during wilting,” Biochemical Journal, vol. 58, no. 1, pp. 46–49, 1954.
- L. Szabados and A. Savouré, “Proline: a multifunctional amino acid,” Trends in Plant Science, vol. 15, no. 2, pp. 89–97, 2010.
- K. Feki, F. J. Quintero, H. Khoudi et al., “A constitutively active form of a durum wheat Na+/H+ antiporter SOS1 confers high salt tolerance to transgenic Arabidopsis,” Plant Cell Reports, vol. 33, no. 2, pp. 277–288, 2014.
- M. M. Julkowska and C. Testerink, “Tuning plant signaling and growth to survive salt,” Trends in Plant Science, vol. 20, no. 9, pp. 586–594, 2015.
- A. Ben Othman, H. Ellouzi, S. Planchais et al., “Phospholipases Dζ1 and Dζ2 have distinct roles in growth and antioxidant systems in Arabidopsis thaliana responding to salt stress,” Planta, vol. 246, no. 4, pp. 721–735, 2017.
- K. Ben Rejeb, C. Abdelly, and A. Savouré, “How reactive oxygen species and proline face stress together,” Plant Physiology and Biochemistry, vol. 80, pp. 278–284, 2014.
- B. List, L. Hoang, and H. J. Martin, “New mechanistic studies on the proline-catalyzed aldol reaction,” Proceedings of the National Acadamy of Sciences of the United States of America, vol. 101, no. 16, pp. 5839–5842, 2004.
- S. S. Gill and N. Tuteja, “Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants,” Plant Physiology and Biochemistry, vol. 48, no. 12, pp. 909–930, 2010.
- S. S. Gill and N. Tuteja, “Polyamines and abiotic stress tolerance in plants,” Plant Signaling and Behavior, vol. 5, no. 1, pp. 26–33, 2010.
- W. Zhao, D. Qian, S. Zhang et al., “Fullerene-free polymer solar cells with over 11% efficiency and excellent thermal stability,” Advanced Materials, vol. 28, no. 23, pp. 4734–4739, 2016.
- F. McLoughlin, S. A. Arisz, H. L. Dekker et al., “Identification of novel candidate phosphatidic acid-binding proteins involved in the salt-stress response of Arabidopsis thaliana roots,” Biochemical Journal, vol. 450, no. 3, pp. 573–581, 2013.
- S. Mahajan and N. Tuteja, “Cold, salinity and drought stresses: an overview,” Archives of Biochemistry and Biophysics, vol. 444, no. 2, pp. 139–158, 2005.
- C. Testerink and T. Munnik, “Phosphatidic acid: A multifunctional stress signaling lipid in plants,” Trends in Plant Science, vol. 10, no. 8, pp. 368–375, 2005.
- H. Safi, W. Saibi, M. M. Alaoui et al., “A wheat lipid transfer protein (TdLTP4) promotes tolerance to abiotic and biotic stress in Arabidopsis thaliana,” Plant Physiology and Biochemistry, vol. 89, pp. 64–75, 2015.
- F. Brini, I. Amara, K. Feki, M. Hanin, H. Khoudi, and K. Masmoudi, “Physiological and molecular analyses of seedlings of two Tunisian durum wheat (Triticum turgidum L. subsp. Durum [Desf.]) varieties showing contrasting tolerance to salt stress,” Acta Physiologiae Plantarum, vol. 31, no. 1, pp. 145–154, 2009.
- A. DeBono, T. H. Yeats, J. K. Rose et al., “Arabidopsis LTPG Is a glycosylphosphatidylinositol-anchored lipid transfer protein required for export of lipids to the plant surface,” The Plant Cell, vol. 21, no. 4, pp. 1230–1238, 2009.
- F. Brini, M. Hanin, I. Mezghani, G. A. Berkowitz, and K. Masmoudi, “Overexpression of wheat Na+/H+ antiporter TNHX1 and H+-pyrophosphatase TVP1 improve salt- and drought-stress tolerance in Arabidopsis thaliana plants,” Journal of Experimental Botany, vol. 58, no. 2, pp. 301–308, 2006.
- M. Drira, W. Saibi, I. Amara, K. Masmoudi, M. Hanin, and F. Brini, “Wheat dehydrin K-segments ensure bacterial stress tolerance, antiaggregation and antimicrobial effects,” Applied Biochemistry and Biotechnology, vol. 175, no. 7, pp. 3310–3321, 2015.
- M. Drira, W. Saibi, F. Brini, A. Gargouri, K. Masmoudi, and M. Hanin, “The K-Segments of the Wheat Dehydrin DHN-5 are Essential for the Protection of Lactate Dehydrogenase and β-Glucosidase Activities In Vitro,” Molecular Biotechnology, vol. 54, no. 2, pp. 643–650, 2013.
- T. Murashige and F. Skoog, “A revised medium for rapid growth and bio assays with tobacco tissue cultures,” Physiologia Plantarum, vol. 15, no. 3, pp. 473–497, 1962.
- I. Belhaj, S. Amara, G. Parsiegla et al., “Galactolipase activity of Talaromyces thermophilus lipase on galactolipid micelles, monomolecular films and UV-absorbing surface-coated substrate,” Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, vol. 1863, no. 9, pp. 1006–1015, 2018.
- M. M. Bradford, “A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding,” Analytical Biochemistry, vol. 72, no. 1-2, pp. 248–254, 1976.
- I. B.-B. Romdhane, A. Fendri, Y. Gargouri, A. Gargouri, and H. Belghith, “A novel thermoactive and alkaline lipase from Talaromyces thermophilus fungus for use in laundry detergents,” Biochemical Engineering Journal, vol. 53, no. 1, pp. 112–120, 2010.
- W. Saibi and A. Gargouri, “Hydroxyl distribution in sugar structure and its contributory role in the inhibition of Stachybotrys microspora β-glucosidase (bglG),” Carbohydrate Research, vol. 346, no. 13, pp. 1848–1854, 2011.
- R. Djemal and H. Khoudi, “TdSHN1, a WIN1/SHN1-type transcription factor, imparts multiple abiotic stress tolerance in transgenic tobacco,” Environmental and Experimental Botany, vol. 131, pp. 89–100, 2016.
- D. Xu and Y. Zhang, “Improving the physical realism and structural accuracy of protein models by a two-step atomic-level energy minimization,” Biophysical Journal, vol. 101, no. 10, pp. 2525–2534, 2011.
- S. C. Lovell, I. W. Davis, W. B. Arendall III et al., “Structure validation by Cα geometry: ϕ, ψ and Cβ deviation,” Proteins: Structure, Function, and Bioinformatics, vol. 50, no. 3, pp. 437–450, 2003.
- A. Tovchigrechko and I. A. Vakser, “GRAMM-X public web server for protein-protein docking,” Nucleic Acids Research, vol. 34, supplement 2, pp. W310–W314, 2006.
- D. B. Duncan, “Multiple range tests for correlated and heteroscedastic means,” Biometrics, vol. 13, no. 2, pp. 164–176, 1957.
- R. F. Evert, Esau's Plant Anatomy: Meristems, Cells, and Tissues of The Plant Body: Their Structure, Function, And Development, John Wiley & Sons, 2006.
- W. Saibi, M. Drira, I. Yacoubi, K. Feki, and F. Brini, “Empiric, structural and in silico findings give birth to plausible explanations for the multifunctionality of the wheat dehydrin (DHN-5),” Acta Physiologiae Plantarum, vol. 37, no. 3, p. 52, 2015.
- F. Brini, A. Yamamoto, L. Jlaiel et al., “Pleiotropic effects of the wheat dehydrin DHN-5 on stress responses in arabidopsis,” Plant & Cell Physiology (PCP), vol. 52, no. 4, pp. 676–688, 2011.
- H. U. Kim, P. Vijayan, A. S. Carlsson, L. Barkan, and J. Browse, “A mutation in the LPAT1 Gene suppresses the sensitivity of fab1 plants to low temperature,” Plant Physiology, vol. 153, no. 3, pp. 1135–1143, 2010.
- M. Ferro, D. Salvi, S. Brugière et al., “Proteomics of the chloroplast envelope membranes from Arabidopsis thaliana,” Molecular & cellular proteomics : MCP, vol. 2, no. 5, pp. 325–345, 2003.
- C. Xu, B. Yu, A. J. Cornish, J. E. Froehlich, and C. Benning, “Phosphatidylglycerol biosynthesis in chloroplasts of Arabidopsis mutants deficient in acyl-ACP glycerol-3-phosphate acyltransferase,” The Plant Journal, vol. 47, no. 2, pp. 296–309, 2006.
- F. Brini, W. Saibi, I. Amara, A. Gargouri, K. Masmoudi, and M. Hanin, “Wheat dehydrin DHN-5 exerts a heat-protective effect on β-glucosidase and glucose oxidase activities,” Bioscience, Biotechnology, and Biochemistry, vol. 74, no. 5, pp. 1050–1054, 2014.
- S. Sarowar, Y. J. Kim, K. D. Kim, B. K. Hwang, S. H. Ok, and J. S. Shin, “Overexpression of lipid transfer protein (LTP) genes enhances resistance to plant pathogens and LTP functions in long-distance systemic signaling in tobacco,” Plant Cell Reports, vol. 28, no. 3, pp. 419–427, 2009.
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