Plant growth promoting rhizobacterium Stenotrophomonas maltophilia BJ01 augments endurance against N2 starvation by modulating physiology and biochemical activities of Arachis hypogea

Arachis hypogea (Peanut) is one of the most important crops, and it is harvested and used for food and oil production. Being a legume crop, the fixation of atmospheric nitrogen is achieved through symbiotic association. Nitrogen deficiency is one of the major constrains for loss of crop productivity. The bacterium Stenotrophomonas maltophilia is known for interactions with plants. In this study, characteristics that promote plant growth were explored for their ability to enhance the growth of peanut plants under N2 deficit condition. In the presence of S. maltophilia, it was observed that fatty acid composition of peanut plants was influenced and increased contents of omega-7 monounsaturated fatty acid and omega-6 fatty acid (γ-Linolenic acid) were detected. Plant growth was increased in plants co-cultivated with PGPR (Plant Growth Promoting Rhizobacteria) under normal and stress (nitrogen deficient) condition. Electrolyte leakage, lipid peroxidation, and H2O2 content reduced in plants, co-cultivated with PGPR under normal (grown in a media supplemented with N2 source; C+) or stress (nitrogen deficient N+) conditions compared to the corresponding control plants (i.e. not co-cultivated with PGPR; C–or N–). The growth hormone auxin, osmoprotectants (proline, total soluble sugars and total amino acids), total phenolic-compounds and total flavonoid content were enhanced in plants co-cultivated with PGPR. Additionally, antioxidant and free radical scavenging (DPPH, hydroxyl and H2O2) activities were increased in plants that were treated with PGPR under both normal and N2 deficit condition. Overall, these results indicate that plants co-cultivated with PGPR, S. maltophilia, increase plant growth, antioxidant levels, scavenging, and stress tolerance under N2 deficit condition. The beneficial use of bacterium S. maltophilia could be explored further as an efficient PGPR for growing agricultural crops under N2 deficit conditions. However, a detail agronomic study would be prerequisite to confirm its commercial role.

The narrow region of soil that is closest to the plant root and is directly influenced by root exudates and associated-microorganisms is known as the rhizosphere. Rhizosphere is considered highly nutritive, therefore is highly competitive for soil microbes. Soil bacteria that inhabitant in the rhizosphere and enhance the plant growth are known as plant growth promoting rhizobacteria (PGPR). PGPR colonize the root surface and induce these positive effects on the plant, and act as (1) bio-fertilizers (increasing plant nutrient availability via phosphate solubilization and siderophore production), (2) phytostimulators (by promoting plant growth through phytohormones), (3) rhizo-remediators (degrading organic pollutants) and (4) biopesticides (controlling diseases through production of antibiotics, antifungal metabolites and biofilms) [27]. PGPR have enormous potential to increase crop productivity under normal as well as stressful environmental conditions.
Stenotrophomonas is a genus of Gram negative bacteria and belongs to Xanthomonadaceae family. A species of Stenotrophomonas, S. maltophilia was isolated from the rhizosphere of Cyperus laevigatus and demonstrated to present different bioactivities including anti-quorum sensing and antibiofilm [28], biological control of fungal plant diseases, and bioremediation [29]. Cyperus laevigatus is a species of sedge which grows in the coastal saline area and harbors beneficial rhizospheric bacteria such as Delftia tsuruhatensis and Exiguobacterium indicum [30,31]. Plant growth promoting potential of S. maltophilia has been reported in wheat plants along with resistance against biotic and abiotic stress [32].
Arachis hypogaea (peanut) is an economically important crop which is utilized for oil, food, fiber and fodder for livestock. Peanut seeds contain approximately 40-60% oil, 20-40% protein and 10-20% carbohydrate, and many vitamins and minerals [33]. India ranks second worldwide in terms of peanut production (6-7 million tons per year) after China, but its production has declined immensely because of various environmental stresses including nitrogen deficiency in the soil. Some transgenic approaches have been employed for developing abiotic stress tolerant peanut [34][35][36]. However, developing a transgenic peanut is time consuming and laborious method, ethical and environmental issues make it difficult [37]. Subsequently, it is clear that an environment friendly and natural method is preferred for the enhanced productivity of crops. It has been noted that CO 2 -fixing bacterial communities were observed as part of the peanut rhizosphere which hints at the possibility of peanut-microbe interactions [38].
Nitrogen deficiency in the soil is one of the major causes that leads to low productivity and health of the crop. Reclamation of these type of soils requires the excessive application of chemical fertilizers, however, PGPR have the potential to protect plants under such conditions. In this study, we observed the interaction of S. maltophilia BJ01 with peanut plants, and effect on morphology and plant growth, changes in physiology, production of ROS, and different activities (antioxidant and scavenging) of peanut plants were analyzed under normal and nitrogen deficit conditions.

Plant material, bacterial strain and treatment
Peanut seeds (cultivar GG-20) were obtained from the Junagadh Agricultural University, Junagadh (Gujarat), India. Dry and mature peanut seeds were washed with 70% (v/v) aqueous-ethanol followed by surface sterilization with 0.1% mercuric chloride for 10 min with gentle shaking [35]. The seeds were thoroughly washed with sterile water (five to six times) and soaked for 3 h in water. Seeds of uniform size were placed on sterilized cotton in tissue culture bottles containing ½ Murashige and Skoog ( [28], and deposited at Indian marine microbial culture collection of CSMCRI, Bhavnagar with culture collection number IMMCC255. To check nitrogen fixing ability of the bacteria, nitrogen-free semisolid (NFb) medium with malate as a carbon source was used for growth. Further total DNA of the bacterium, S. maltophilia BJ01 were isolated, the nifH gene was amplified using degenerate primers [39]. Polymerase chain reaction (PCR) amplified products were analyzed on an agarose gel and purified using the QIAquick gel extraction kit (Qiagen, Germany). The purified PCR amplicons were cloned in pGEM-T Easy cloning vector (Promega, USA) and transformed into Escherichia coli DH5α competent cells. Positive clones were selected, confirmed and sequenced (M/s Macrogen Inc., South Korea).
For the bacterial inoculum preparation, the bacterial strain was streaked on DYGS (dextrose 1.0 g L -1 ; malate 1.0 g L -1 ; peptone 1.5 g L -1 ; yeast extract 2.0 g L -1 ; MgSO 4 .7H 2 O 0.5 g L -1 ; L-glutamic acid 1.5 g L -1 ; pH 6.0) agar plate and incubated for 16 hr at 30˚C. Single colony from the plate was inoculated in 5 mL DYGS broth media and incubated overnight at 30˚C and 180 rpm in an incubator shaker. Overnight grown culture was diluted to OD 600nm 0.01 in 150 mL of DYGS medium and grown up to OD 600nm 0.6 in an incubator shaker (30˚C and 180 rpm). Freshly grown 150 mL (OD 600 0.6) bacterial culture was centrifuged at 4000 x g for 10 min. Pellet was re-suspended in 300 mL ½ MS media supplemented with or without nitrogenous component. The ½ MS media containing all macronutrients, micronutrients and vitamins is considered control media/ condition with nitrogenous source (C), whereas MS media that did not contain any nitrogenous constituents/ ingredients (such as ammonium nitrate and potassium nitrate from macronutrients, and vitamins) was considered media without nitrogenous source or nitrogen deficit media/ condition (N) Seven days old germinated seedlings were transferred to hydroponics condition in a glass beaker containing 300 mL ½ MS media supplemented with (C) or without nitrogenous component (N). The experiment was first divided in two sets, i) control (C: control plants grown in a media supplemented with nitrogen source) and stress (N: plants grown under nitrogen deficient condition) followed by further division in two sub-sets; C-and C+ (control plants grown without or with PGPR), and N-and N+ (plants under nitrogen deficient without and with bacteria). Seedlings were transferred to the particular growth condition for twenty-one days at 25 ± 2˚C temperature, 16 h/ 8 h light/dark cycle, and 170±25 μmol m -2 s -1 light intensity. Corresponding media were replenished every seven days, and different morphology characteristics including shoot length, root length and fresh weight were recorded, and images were captured for each plant. After completion of 21 days, growth characteristics, physio-biochemical properties and metabolic activities were studied.

Fatty acid profiling
Total lipid was extracted from 300 mg plant samples (fresh leaves) using chloroform-methanol-phosphate buffer (1:2:0.9 v/v/v, pH 7.5; 10 mL), and fatty acids were converted to corresponding methyl esters (FAMEs) by transmethylation. For transmethylation, 1 mL of NaOH (1% v/v in methanol) was added, and mixture was incubated at 55˚C for 15 min, after that 2 mL of methanolic HCl (5% v/v) was added and further incubated at 55˚C for 15 min. Finally 3 mL of deionized water-hexane mixture (1:2 v/v) was added. FAMEs were extracted in three times in hexane, samples were pooled together and dried under vacuum. Dried sample was resuspended in 200 μl hexane and analyzed by using a RTX 5MS capillary column in GCMS-QP2010 (Shimadzu, Japan) coupled with an auto-sampler (AOC-5000) [6].

Chlorophyll and carotenoid content
Leaf chlorophyll and total carotenoid contents were estimated according to the methods described by Arnon and Chamovitz et al. [40,41]. Briefly, leaf tissues (100 mg) were homogenized in 80% acetone, incubated for 6hrs in the dark, centrifuged at 10000 x g and absorbance of supernatant was recorded at 461, 645, 663, and 664nm. Total carotenoid and chlorophyll contents were calculated using the following equations:

Electrolyte leakage
Leaves of equal size and age were harvested from primary branch (toward the distal end) of each experimental plant and washed thoroughly with deionized water to remove surfaceadhered electrolytes. Samples were kept in deionized water (10 mL) and incubated at 25˚C on a rotary shaker for 24 h. The electrical conductivity (EC) of the solution (L 1 ) was determined using a conductivity meter (Seven Easy, Mettler Toledo, USA). Samples were autoclaved at 120˚C for 20 min, cooled at 25˚C, and electrical conductivity (L 2 ) was determined [42]. The electrolyte leakage was estimated with the following equation:

Membrane stability index
To determine the membrane stability index (MSI), thoroughly washed leaf samples (equal size and age) were kept in 10 mL deionized water, incubated at 40˚C for 30 min, and EC (L 1 ) was recorded. Samples were boiled at 100˚C for 20 min, then they were cooled at 25˚C, and EC (L 2 ) was recorded to calculate MSI [43]. Following equation were used for the calculation:

Lipid peroxidation
Lipid peroxidation was determined by quantifying the malondialdehyde (MDA) content according to method described by Hodges et al. [44]. In brief, leaf samples (100 mg) were homogenized in liquid nitrogen and extracted. In one set of reaction, leaf extract was mixed with an equal volume of thiobarbituric acid reagent containing thiobarbituric acid (TBA) and trichloroacetic acid (TCA) (TBA; 1 mL of 0.5% w/v prepared in 20% w/v TCA). In another set of reaction, extract was mixed with an equal volume of TCA (20% w/v). Reaction mixtures were incubated at 95˚C for 30 min, cooled at 25˚C, and centrifuged at 10000 x g for 5 min. Absorbance of the supernatant was recorded at 440 nm, 532 nm, and 600 nm. MDA content was quantified using the following equation:

Total H 2 O 2 content
Leaf samples (100 mg) were extracted in 80% cold acetone and hydrogen peroxide was determined by the modified method described by Mukherjee and Choudhuri [45]. Absorbance was measured at 415 nm. Total H 2 O 2 content of samples was calculated by a standard curve drawn with the known concentration of H 2 O 2 .

Auxin content
For the quantification of auxin contents, Leaf samples were homogenized in liquid nitrogen and extracted with 95% ethanol. Colorimetric assay was performed with Salkowski reagent and the absorbance was recorded at 535nm [46].

Proline content
Free proline contents of harvested leaf samples were quantified by acid ninhydrin reagent as described by Bates et al. [47]. One hundred mg plant leaves were homogenized in liquid nitrogen and extracted in aqueous sulphosalicylic acid. An equal volume of the extract and the acid ninhydrin reagent are mixed together and incubated at 100˚C for 1 h. Reaction was terminated by cooling the sample in an ice bath. Toluene was added after cooling the sample mix, vortexed, and upper phase was aspirated to measure the absorbance at 520nm. Total proline content was calculated using a standard curve of known concentration of proline. Total amino acid content. Total amino acid content of plant samples was determined by previously described method [48]. Plant leaf samples (100 mg) were extracted with 80% ethanol, and extract was treated with an equal volume of 0.2 M citrate buffer (pH 5) along with ninhydrin reagent (1% ninhydrin). The reaction mixture was incubated at 95˚C in a water bath for 15 min. Samples were cooled to room temperature centrifuged and the absorbance was read at 570 nm.
Total soluble sugars. Total soluble sugar contents were calculated according to the previously described method [49]. One hundred microgram leaf samples were homogenized with liquid nitrogen and extracted in 1 mL of 80% ethanol. Three milliliter freshly prepared anthrone reagent (150 mg anthrone in 100 mL of 72% v/v H 2 SO 4 ) was added to 100 μL extract, kept at 100˚C in water bath for 10 min. Reaction mixtures were cooled at room temperature and the absorbance was measured at 625 nm Extract preparation for the analysis of metabolic activities. Five gram leaves were harvested from control and treated plants, powdered by homogenizing in liquid N 2 , and added to the aqueous methanol (70% v/v). After 16 hr of incubation sample were centrifuged at 10000 x g for 10 min, supernatant was collected in fresh reagent bottle and aqueous methanol was again added to the sample for re-extraction. After double extraction supernatant was pooled, concentrated under vacuum using a rotary evaporator (Büchi, Switzerland), and lyophilized at -80˚C (VirTis Sentry, USA) and stored at -20˚C until further use.
Total phenolic content. Total phenolic content of the samples was estimated by the Folin-Ciocalteu reagent. The Plant extract was added in 2.5 mL Folin-Ciocalteu reagent (0.2M; Sigma-Aldrich, USA) mixed and incubated at room temperature. After 5 min of incubation, 2 mL sodium carbonate (Na 2 CO 3 ; 75 g L -1 ) were mixed in the reaction mixture and incubated in dark at room temperature for 90 min. The absorbance was measured at 760 nm, and the total phenolic content was calculated as gallic acid equivalent (GAE) from a standard curve plotted with the known concentration of gallic acid [50,51].
Total flavonoid content. Total flavonoid content was measured as described by Zhishen et al. [52]. Plant extracts were mixed with NaNO 2 (5% w/v), incubated at room temperature for 5 min, followed by addition of AlCl 3 (10% v/v). After 6 min, 1M NaOH was added to reaction mixture, mixed well by vortex and absorbance was measured at 510 nm. The total flavonoid content was calculated from a standard curve of quercetin.
Total antioxidant activity. Total antioxidant activity was measured by 2,2 0 -azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) free radical (ABTS + ) scavenging ability of the extracts of To generate the free radicals, ABTS diammonium salt (7 mM) solution was mixed with potassium persulfate (2.45 mM), and incubated overnight in the dark at room temperature. After the generation of stable free radicals, absorbance of ABTS + radical solution was adjusted to A 734nm = 0.70 ± 0.02 and equilibrated at 30˚C. Different concentrations of the extract (10-50 μg mL -1 ) or the standard (1-5 μg mL -1 ) were added to the ABTS + radical solution and absorbance was measured at 734 nm after 5 min. Trolox was used as standard and percentage inhibition of absorbance was calculated [53].
DPPH free radical scavenging assay. To check the free radical scavenging of extract, 2,2 0diphenyl-1-picrylhydrazyl (DPPH) was used as free radical. The DPPH solution (0.024% w/v) was prepared in methanol and absorbance was adjusted to Abs 517 nm 0.98 ± 0.02 using methanol. Different concentrations of extracts (10-80 μg mL -1 ) were mixed in DPPH solution (Abs 517 nm 0.98 ± 0.02) and incubated for 15 min at room temperature in the dark. The absorbance was measured at 517 nm and the radical scavenging activities were estimated [54].
Reducing power assay. To check reducing capacity different concentrations of the plant extracts (100-1000 μg mL -1 ) were mixed with 1 mL phosphate buffer (0.2 M, pH 6.6). Thereafter 1 mL of K 3 Fe(CN) 6 (10 mg mL -1 ) was added to the reaction and incubated at 50˚C in water bath (Julabo, Germany). After 20 min of incubation, 1 mL trichloroacetic acid (100 mg L -1 ) was added to terminate the reaction. Reaction mixtures were cooled at room temperature, centrifuged at 7000 x g for 10 min and the supernatant was collected. In the next step 1 mL supernatant was mixed with 0.2 mL freshly prepared FeCl 3 (0.1% w/v), incubated for 10 min at room temperature, absorbance was measured at 700 nm. Ascorbic acid was used as standard [49,51].
Hydrogen peroxide scavenging activity. The hydrogen peroxide scavenging activity of different concentration of plant extracts was evaluated by previously described method [6,48,49,51]. Plant extracts (0.1-0.5 mg mL −1 ) were mixed with 0.4 mL phosphate buffer (50 mM, pH 7.4) and 43 mM hydrogen peroxide (0.6 mL; prepared in phosphate buffer) added to the reaction mixture, and absorbance was recorded at 230 nm (T1). After 10 min incubation, absorbance of reaction mix was recorded at 230 nm (T2) and scavenging activity was calculated using following formula: Hydroxyl radical scavenging assay. Hydroxyl radical scavenging activity was performed with different concentrations (10-100 μg) of plant extracts using Fenton reaction (Fe 3+ -ascorbate-EDTA-H 2 O 2 ) as described by Saeed et al. [54]. Plant extracts were mixed with 500 μL of 2.8 mM 2-deoxyribose prepared in 50 mM potassium phosphate buffer (pH 7.4). Thereafter, 200 μL of 100mM FeCl 3 and 100mM EDTA solution (1:1 v/v) and 100 μL of 200 mM H 2 O 2 were added to reaction mixture. Reaction was started by adding 100 μL of 300mM ascorbic acid to the reaction mixture and incubated for 1 h at 37˚C. After incubation, 500 μL reaction mixture was added to the 1 mL of TCA solution (2.8% w/v) followed by addition of 1 mL of aqueous TBA solution (1% prepared in 0.025 M NaOH containing 0.02% BHA) and incubated at 99˚C in water bath (Julabo, Germany) for 15 min. Reactions were cooled at room temperature and absorbance was recorded at 532 nm. The following formula was used to calculate percent scavenging activity.

Statistical analysis
Statistical analysis was performed by GraphPad Prism software. One-way ANOVA followed by Tukey post-hoc test was applied to compare the test and controls. Values are expressed as the mean ± SE, and statistically significant differences are marked with different stars.

Nitrogen fixing ability of Stenotrophomonas maltophilia BJ01
The bacterium S. maltophilia was grown in nitrogen-free semisolid NFb medium with malate as a carbon source to confirm the nitrogen-fixing ability of the bacterial strain. Further, an amplicon of expected 360 bp was obtained with degenerate nifH primers [55,56], which confirmed the presence of the nifH gene in the bacterium (S1 Fig). The sequence analysis showed 99% query coverage and 99.44% homology with uncultured bacterium dinitrogenase reductase (nifH) gene (JN162497) and also showed 99% query coverage and 83.29% homology with nifH gene of culturable bacterium Bradyrhizobium japonicum (GQ289567). The nifH gene sequence of S. maltophilia BJ01 was submitted to NCBI (GenBank: JX545230).

Stenotrophomonas maltophilia BJ01 alters the plant fatty acid composition
Fatty acid composition of peanut seedling was highly influence by the interaction with S. maltophilia (Table 1). Under control condition (with N 2 source), about 84.75% heptadecenoic acid was detected followed by hexadecanoic acid (6.74%) and pentadecenoic acid (6.6%), whereas other fatty acids were negligible. In contrast, heptadecenoic acid was not detected when plants were grown with nitrogenous source and bacterium. Furthermore, hexadecanoic acid (37.5%) detected utmost followed by heptadecanoic acid (33.43%) and 6,9,12-octadecatrienoic acid (28.62%). Under N 2 deficit condition, the maximum content of heptadecanoic acid (76.54%) was detected in control plants (without N 2 source) followed by hexadecanoic acid (11.65%) and 6,9,12-octadecatrienoic acid (8.07%). High content of tetradecanoic acid (C14:0; 41.11%) was observed in the plants grown under N 2 deficit condition along with bacterial inoculum, followed by 9-hexadecenoic acid (30.15%), hexadecanoic acid (15.94%), pentadecanoic acid (9.26%) and 6,9,12-octadecatrienoic acid (2.16%). A change in the fatty acid composition was observed due to interaction between S. maltophilia and peanut under control and stress condition. Peanut is an edible oil-yielding plant and grown worldwide for commercial edible-oil production. Its fatty acid composition is considered beneficial for human health and widely used in the human diet. It was observed that PGPR S. maltophilia interaction altered fatty acid composition while interacting with peanut plants under both normal and N 2 stress conditions ( Table 1). Palmitoleic acid or 9-Hexadecenoic acid is an omega-7 monounsaturated fatty acid, which is biosynthesized from palmitic acid, and an enhanced concentration was detected in plants grown with PGPR under N 2 stress condition. Monounsaturated fats are well known to provide membrane fluidity and thus protect against cardiovascular disease. Similarly, 6,9,12-Octadecatrienoic acid, also known as Gamma-linolenic acid or GLA (γ-Linolenic acid) is an omega-6 fatty acid, and its concentration increased after PGPR interaction. GLA has been reported to reduce atopic dermatitis in a double-blind, placebo-controlled clinical trial [57]. It was also noticed that content of mono-saturated fatty acids increased in plants during PGPR inoculation. It was shown that saturated fatty acid has no effect on blood cholesterol levels [58] whereas some saturated fatty acids have antibacterial activity [59]. Similar to this study, inoculation of PGPR Bradyrhizobium japonicum altered the fatty acids composition of soybean [60]. It was established that fatty acids content regulates the cell-membrane fluidity, and therefore alleviates the plant tolerance to different stress condition [61]. Surprisingly, Cagide et al. [62] did not find any change in the fatty acid composition of Soybean grown with Bradyrhizobium elkanii and Delftia sp. Strains. A similar result was also observed with alfalfa plants cocultivated with S. meliloti [63]. It was speculated that inoculation of PGPR S. maltophilia may have altered the fatty acid composition of peanut plants, resulted in the improved plant-tolerance to N 2 deficit condition by modulating membrane fluidity.

Plant growth and photosynthetic pigments are influenced by S. maltophilia BJ01
The total chlorophyll, (about 0.7 mg g −1 Fw), Chl a (about 0.3 mg g −1 Fw), Chl b (about 0.4mg g −1 Fw), and carotenoid (about 14 μg g −1 Fw) content were comparable between control plants (media supplemented with nitrogenous source) grown with (C+) or without (C-) bacterial inoculum (Fig 1). Under N 2 deficit conditions, chlorophyll (total, a and b) and carotenoid contents decreased in stressed plants grown without bacteria (N-) compared to control plants (Fig  1). PGPRs are widely used in agriculture for enhanced growth and productivity of crops, and the most common beneficial bacteria are Azospirillum spp. and rhizobia [64]. It is hypothesized that PGPRs influence the content of photosynthesis pigments, and thus control the plant growth and yield. Growth characteristics of the control and treated plants did not show significant changes (S2 Fig), however, plants grown with bacterium inoculum showed dense root morphology (Fig 2). Overall, plants grown with bacterium showed better morphology (overall plant growth e.g. plant height-shoot and root length, and number of leaves) compared to their corresponding control plants (Fig 2). Chlorophylls and carotenoids are pigments which are involved in photosynthesis, they absorb light and provide the energy [65]. They are also involved in the regulation of plant growth [66]. Our results suggest that bacterial inoculation promotes plants to grow under control and stress conditions compared to corresponding plants grown without bacteria (Figs 1 and 2). Previously, an increase in the content of photosynthetic pigments was observed in wheat and Arabidopsis thaliana plants by inoculation with Azospirillum brasilense [67,68].

Interaction of S. maltophilia regulates the physiology and biochemical status of Arachis hypogea
Electrolyte leakage, membrane stability, lipid peroxidation and hydrogen peroxide production were measured for control and stressed plants, grown with or without bacteria (Fig 3). No significant electrolyte leakage was observed in the control plants (C) grown with (C+; 8.2%) or without (C-; 7.7%) bacteria. However, under nitrogen deficit condition, electrolyte leakage decreased significantly in the plants grown with bacteria (N+; 6%) compared to those that grown without bacteria (N-; 9.8%). Similarly, lower H 2 O 2 content was estimated in the treated plants (C+ and N+; grown with bacteria) compared to plants grown without bacterial inoculum (C-and N-). About 7.4 μmol g -1 Fw H 2 O 2 were measured in the plants grown without bacteria (C-), which decreased significantly to 6.3 μmol g -1 Fw in the plants grown with bacteria (C+). Under nitrogen stress condition, H 2 O 2 production further decreased significantly, and 5.5 and 4.4 μmol g -1 Fw H 2 O 2 were estimated in the plants grown without (N-) or with bacteria (N+). In contrast, lipid peroxidation (measured by MDA content which is a product of lipid peroxidation and accumulated in the cells) increased under N 2 stress condition but a quenching effect (mitigation of lipid peroxidation) was observed when plants were grown with bacteria under both normal and N 2 stress condition. About 1.36 (C-) and 2.56 (N-) μmol g -1 Fw MDA contents were measured in control and N 2 stressed plants grown without bacteria, which reduced to 0.83 (C+) and 1.73 (N+) μmol g -1 Fw in the plants grown with bacteria inoculum. The membrane stability indices (0.8-0.9) were almost similar for control and N 2 stressed plants grown with or without bacteria inoculum.
The biochemical status of plants was studied by measuring auxin, proline, total aminoacids and total sugar contents of control and N 2 stressed plants grown with or without bacteria inoculum (Fig 4). Auxin content was increased significantly in the plants grown with bacteria inoculum, about 0.28 mg g -1 Fw auxin was detected in control and N 2 stressed plants (C-and N-) grown without bacteria which reached to about 0.4 mg g -1 Fw in the plants grown with bacteria inoculum. In contrast, lower proline accumulation was observed in the plants grown  Accumulation of osmoprotectants such as proline, total amino acids and total sugars can protect plants and scavenge the free hydroxyl radicals [69]. Rhizobacterium Enterobacter cloacae is reported to protect plants under biotic and abiotic stress conditions [1]. In the present study, plants co-cultivated with PGPR S. maltophilia showed improved physiology and biochemical status under normal as well as N 2 stress condition (Figs 3 and 4). Environmental Stress tolerance by PGPR stress promotes the generation of ROS which leads to enhanced lipid peroxidation, assessed by observation of an increase in the MDA contents [70,71]. The decrease in MDA content confirms that bacterial inoculation protects peanut plants under control and stress conditions. Higher accumulation of auxin in inoculated plants further supports the plant growth due to PGPR under normal as well as stress condition.

Bacterium interaction influences the antioxidant and scavenging activities of Arachis hypogea
Total phenolic (TPC) and total flavonoid (TFC) contents were increased in the plants when grown with bacteria. About 6.24 μg mg -1 gallic acid equivalent (GAE) TPC was estimated in the control plants grown without bacteria which increased significantly after bacterial inoculation (21.29 μg mg -1 GAE). Under N 2 stress condition, about 95.76 μg mg -1 GAE TPC was measured in the plants grown without bacteria, which further increased and reached maximum (103.25 μg mg -1 GAE) when grown with bacterial inoculum (Fig 5). Similarly, total flavonoid content was increased and maximum content (95.35 μg QE) was estimated in the plants grown under N 2 deficit condition with bacterial inoculum (Fig 5). Plants co-inoculated with S. maltophilia showed higher content of phenolic-compounds and total flavonoids under normal and stress condition compared to corresponding controls. These results suggest that peanut plants modify their metabolism in response to bacterium inoculum and thus produce a higher amount of TPC and TFC. Further, total phenolic-compounds and total flavonoids influence the plant defence against free radicals under normal and N 2 stress condition.
The N 2 deficit condition may lead to free radical formation during nitrogen fixation, therefore different antioxidant and scavenging activities were studied under normal and stress condition. Total antioxidant and scavenging (DPPH, hydrogen peroxide and hydroxyl ions) activities were found concentration dependent (S3 Fig). Total antioxidant and scavenging activities were increased concomitantly with the increasing concentration of plants extracts, and maximum activity (except DPPH scavenging) was noticed for the N 2 stressed plants grown with bacterial inoculum (N+). In contrast, maximum DPPH scavenging activity was observed with stressed plant extracts grown without bacterial inoculum (S3 Fig). The half maximal effective concentration (EC 50 ) was estimated for the different antioxidant and scavenging activities (Fig 5). The EC 50 for total antioxidant was lower for stressed plants grown with bacteria (N+; 90 μg mL -1 ) compared to control plants grown with bacteria (C+; 104 μg mL -1 ), followed by control plants grown without bacteria (C-; 139 μg mL -1 ) and stressed plants grown without bacteria (N-; 167 μg mL -1 ). Similarly, for hydroxyl ions scavenging activity, the lowest EC 50 of 210 μg mL -1 was detected for N+, followed by C+ (236 μg mL -1 ), C-(412 μg mL -1 ) and N-(551 μg mL -1 ). Plants grown under N 2 deficit condition showed maximum H 2 O 2 scavenging activity compared to plants grown under control condition. In contrast, a decrease in the DPPH scavenging activity was observed in plants after bacterial interaction under both control and stress condition. In addition bacterial interaction showed maximum antioxidant and scavenging activities that required the lowest EC 50 dose (Fig 5).
Phenolic, flavonoids and secondary metabolites are plant-derived compounds which play a key role in defence under stress condition [72]. Phenolic-compounds are considered precursors of several signalling molecules which are involved in plant growth, redox reactions and stress tolerance [73,74]. In legumes, flavonoids (like daidzein and genistein) and coumestrol trigger the nodule formation [75,76]. In this study, an enhanced total phenolic and flavonoid contents were detected in plants which are co-cultivated with bacterium inoculum (Fig 5).
Generation of free radicals lead to auto-oxidation, and maintain oxidation/reduction equilibrium which is important for plant growth and stress tolerance [77]. TPC and TFC are known for their antioxidant and scavenging potential [78], as well as our results showed that PGPR S. maltophilia improves the antioxidant and scavenging activities of peanut plants by enhancing the TPC and TFC. Similarly, soybean plants inoculated with PGPR also enhanced antioxidant and scavenging activities [59,79,80].

Conclusion
In the study, the PGPR effect of Stenotrophomonas maltophilia BJ01 strain was evaluated by co-cultivating with Arachis hypogaea GG20 (peanut) plants under normal and nitrogen deficient conditions. Plants use metabolites, especially secondary metabolites (alkaloids, flavonoids and phenolics), as their defence system in the face of various biotic and abiotic stresses. Earlier studies have shown the changes in metabolic profile and essential oils of host plant after interaction with microbes. We have demonstrated that metabolites and fatty acid content were altered in peanut after interaction with S. maltophilia BJ01 strain under nitrogen starvation condition. The data presented herein highlight the understanding of different aspects of connection between induced systemic resistance ISR, signaling and metabolic pathways which can play a major role in plant-microbe interaction. Interaction of plants with PGPR's improve the plant health and soil fertility in many aspects but the systemic information about host plant at metabolic and genetic level is still in infancy which needs an extensive research.   Estimation of phenolic (TPC) and flavonoid (TFC) contents, and half maximal effective concentration of different activities (total antioxidant and scavenging-DPPH, H 2 O 2 and OH − and reducing) in peanut plants grown under nitrogen supplement (C) or nitrogen deficit (N) conditions with inoculum (C+ and N +) or without inoculum (C-and N-). Bars represent means ± SE, and ' � ', ' �� ' and ' ��� ' Indicate significant differences at P < 0.05, P < 0.01 and P < 0.001, respectively, while 'ns' means no significant difference.