Phytoremediation of Cadmium Contaminated Soil Using Sesbania sesban L. in Association with Bacillus anthracis PM21: A Biochemical Analysis

: Sustainable food production to feed nine to 10 billion people by 2050 is one of the greatest challenges we face in the 21st century. Due to anthropogenic activities, cadmium (Cd) contamination is ubiquitous with deleterious effects on plant and soil microbiota. In the current study, the phytoremediation potential of Sesbania sesban L. was investigated in Cd-spiked soil inoculated with Bacillus anthracis PM21. The Cd-spiked soil drastically reduced important plant attributes; how-ever, inoculation of B. anthracis PM21 signiﬁcantly ( p ≤ 0.05) enhanced root length (17.21%), shoot length (15.35%), fresh weight (37.02%), dry weight (28.37%), chlorophyll a (52.79%), chlorophyll b (48.38%), and total chlorophyll contents (17.65%) at the Cd stress level of 200 mg/kg as compared to the respective control. In addition, bacterial inoculation improved superoxide dismutase (11.98%), peroxidase (12.16%), catalase (25.26%), and relative water content (16.66%) whereas it reduced proline content (16.37%), malondialdehyde content (12.67%), and electrolyte leakage (12.5%). Inoculated plants showed signiﬁcantly ( p ≤ 0.05) higher Cd concentration in the S. sesban root (118.6 mg/kg) and shoot (73.4 mg/kg) with a translocation (0.61) and bioconcentration factor (0.36), at 200 mg/kg Cd. Surface characterization of bacteria through Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) predicted the involvement of various functional groups and cell surface morphology in the adsorption of Cd ions. Ampliﬁcation of the CzcD gene in strain PM21, improved antioxidant activities, and the membrane stability of inoculated S. sesban plants conferred Cd tolerance of strain PM21. In addition, the evaluated bacterial strain B. anthracis PM21 revealed signiﬁcant plant growth-promoting potential in S. sesban ; thus, it can be an effective candidate for phyto-remediation of Cd-polluted soil. the preparation of 0.1 M phosphate buffer of 6.5 One-percent hydrogen peroxide was made in phosphate buffer (0.1 M) of pH 6.5. By using 10 mL of phosphate buffer of pH 6.5, a fresh shoot (1 g) sample was crushed, then spun, and the supernatant was obtained. A spectrophotometer was adapted to zero and values were recorded at 430 nm. H 2 O 2 (0.5 mL) was added and mixed for each sample in the test cuvette. The absorbance of the supernatant was recorded at 430 nm for a consecutive 3 min to observe changes in the absorbance values. The absorbance change per minute at 430 nm was taken as one unit of peroxides. The protocol suggested by [45] was implemented to determine catalase activity by H 2 O 2 decomposition.


Introduction
Sustainability and food security are the main challenges of the current era. Environmental pollution is drastically increasing due to anthropogenic activities [1]. As a result of anthropogenic activities, the contamination of heavy metals (HMs) causes serious threats to the environment [1]. Being non-degradable and persistent in nature, HMs can easily bio-accumulate in the food chain and eventually induce ill effects on the health of humans. Sesban (Sesbania sesban L.) belongs to the Fabaceae or Leguminosae family, which has huge medicinal importance and is widely distributed in tropical regions worldwide [31]. It is also used for fodder and fuel purposes and has high biomass. S. sesban is reported to survive in contaminated environments [32]. S. sesban could be an effective option for reclamation due to the potential of nitrogen fixation in root nodules [33]. Researchers have also conducted genetic studies to understand the mechanisms adopted by microorganisms for the remediation of heavy metals. For example, the gene cadA, which encodes the cadmium efflux system, was explored and has been commonly observed in Gram-positive bacteria species [34]. In B. subtilis, the cadA gene has a role against Cd [35]. Two other genes (TrkA and czcD) in bacteria detoxify metals, and their recombinant boosts the efficiency of Escherichia coli [36]. Genes for the biosynthesis of bacilli thiol (BSH) in the genus Bacillus are an efficient mechanism for metal decontamination. The lack of BSH in B. subtilis increases its sensitivity against Cd [37]. We assessed the biosorption capacity of a plant growth-promoting bacterium, B. anthracis PM21, for sorption of Cd under different operational conditions. This research work was mainly focused on highlighting the ability of B. anthracis PM21 to tolerate Cd as well as its ability in bacterial-assisted phytoremediation of Cd-spiked soil. Additionally, we evaluated the differential effects of B. anthracis PM21 inoculation on important morphological, physiological, and biochemical attributes of S. sesban under different Cd concentrations.

Materials and Methods
Bacillus anthracis PM21 with NCBI accession number (OK255528) was previously isolated from the rhizosphere of tomato and was found to play a role as plant growth-promoting rhizobacteria. The isolated bacterial strain was tested for growth under different concentrations of Cd for 7 days. According to previous findings, the growth of Bacillus anthracis PM21 remained negatively proportional to heavy metal concentrations. The maximum growth for the B. anthracis PM21 strain was observed at the sixth day of incubation [27].

Antibiotic Resistance of Bacillus Anthracis PM21
The disk diffusion method was used for the detection of antibiotic resistance [38]. Bacterial culture was allowed to grow in broth for 24 h. The antibiotic discs were fixed on LB agar plates on 24 h grown culture (100 µL). Incubation of inoculated Petri plates was done overnight at 35 • C. Bacterial resistance to antibiotics was quantified by measuring the diameter of the inhibition zone around the antibiotic disks.

Inoculum Preparation and Seed Treatment
A 250 mL conical flask containing 100 mL LB broth was used to multiply B. anthracis PM21 inoculum. A shaking incubator (DKS-1020, N-Biotek, Bucheon-si, Korea) was set at 30 • C with 120 rpm for 24 h to keep the prepared inoculum. The value of optical density was recorded at 600 nm and 1.00 was obtained that showed bacteria as a 10 9 colony forming unit (CFU/mL). S. sesban seeds were initially soaked for 5 min in 75% ethanol and then in HgCl2 (0.1%) for 1 min for sterilization purposes [39]. The seeds were washed 5 to 6 times with double-distilled water (DDW). Seed priming was carried out via immersion in bacterial inoculum for 3-4 h. The control treatment contained seeds that were soaked only in double-distilled water.

Greenhouse Experiment
Soil was collected from an agricultural and non-contaminated field of the National Agricultural Research Center, Islamabad, Pakistan (33.6701 • N, 73.1261 • E). The collected soil was autoclaved at 121 • C for 1 h. The nature of the soil was found to be loamy. The properties of the experimental soil prior to the experiment were determined (Table 1). Experimental pots each having 23 cm diameter and 19 cm length were filled with autoclaved soil (5 kg). Cadmium was applied in dried form in two levels (100 and 200 mg/kg) in pot treatments. Treatments containing Cd were thoroughly mixed for two weeks for metal solution stabilization to maintain an even metal concentration in the soil before sowing [38]. A completely randomized design with three replications was implemented to manage the experimental treatments. Initially, 10 seeds per pot were sown, and after germination 4-5 plants were left per pot. Moreover, one pot was considered as a replication. Experimental treatments included control (T0), B. anthracis PM21 (T1), Cd 100 mg/kg (T2), Cd 100 mg/kg + B. anthracis PM21 (T3), Cd 200 mg/kg (T4), and Cd 200 mg/kg + B. anthracis PM21 (T5).

Growth and Photosynthetic Pigments of Sesbania sesban L.
Growth variables were observed in the plants just after harvesting for the experimental treatment. The root and shoot length, fresh (FW), and dry weight (DW) were recorded as plant growth traits. Plant parts were kept in an oven at 70 • C for complete removal of moisture and the dry weight was estimated [27]. The photosynthetic pigments were isolated and estimated by the method used by [41]. Small pieces (0.5 g) of fresh leaves were suspended in falcon tubes containing 5 mL dimethyl-sulfoxide (DMSO) reagent with lids. The combination was incubated in a water bath at 65 oC until the extraction of pigments. Centrifugation (Pro Economy, Centurion Scientific, Chichester UK) of the extract was done and assorted supernatant in 6 mL of C 3 H 6 O was added followed by centrifugation again. The samples (extracts) were then quantitatively estimated at wavelengths of 663 and 645 nm by means of the formula by [41] for various chlorophyll contents as follows:

Electrolyte Leakage (ELL) and Relative Water Content (RWC)
Fresh leaves (0.5 g) from each treatment were kept in water at 4 • C for 4 h to evaluate relative water content. Similarly, plant samples were dried in an oven (80 • C) to obtain the dry weight (DW) [42]. The protocol suggested by [42] was implemented to measure electrolyte leakage (ELL) via the formula given below: electrolyte leakage (ELL) = Electrical conductivity 1 Electrical conductivity 2 × 100 (1)

Estimation of Proline Content, Malondialdehyde (MDA), and Antioxidant Enzyme Activity
The proline content was determined using ninhydrin [38]. A total of 4 mL of sulphosalicylic acid (3%) was used to grind the leaf sample (0.5 g) and placed overnight. Cen-trifugation (Pro Economy, Centurion Scientific, Chichester UK) of the ground samples was done for 5 min at 3000 rpm and then glacial acetic acid and ninhydrin was added to the suspension. The obtained mixture was heated at 100 • C for 1 h in a water bath. The mixture was transferred to an ice bath to cool it. Toluene was used for extraction of the mixture and its absorbance was noted at 520 nm. A standard curve was used to measure proline concentration and expressed in mmol g −1 . A fresh leaf sample of 0.5 g was ground in 10 mL of 0.1% trichloroacetic acid (TCA) to measure MDA [43]. The sample was centrifuged at 15,000× g for 15 min. The supernatant was separated and mixed with 4 mL of 0.5% TBA (Thiobarbituric acid) and 20% TCA. The samples were centrifuged (Pro Economy, Centurion Scientific, Chichester UK) at 10,000× g for 10 min and absorbance was noted at 440, 532, and 600 nm, respectively. The MDA equivalents were estimated using the formula given below.
Superoxide dismutase (SOD) was recorded as a reduction in superoxide nitro blue tetrazolium complex absorbance through enzymes [44]. The following buffers were prepared: (a) adding 15.6 g monosodium dihydrogen phosphate to 500 mL of distilled water, and (b) adding 53.65 g disodium hydrogen phosphate to 600 mL of distilled water. For the preparation of the buffer solution of pH 7, 183 mL of Na 2 HPO 4 disodium monohydrogen phosphate and 117 mL of NaHPO 4 monosodium dihydrogen phosphate was allowed to mix to make the last volume of 0.6 L and the pH was adjusted to 7. For the preparation of buffer solution of pH 7.8, both the buffers were mixed by taking 275.5 mL of Na 2 HPO 4 disodium monohydrogen phosphate and 25.5 mL of NaHPO 4 monosodium dihydrogen phosphate. The last volume was made in a quantity of 0.6 L and the pH was adjusted to 7.8. The superoxide dismutase level was assessed by utilizing the method of [44]. The plant sample (0.2 g) was crushed in a solution (4 mL) formed by adding PVP (1 g) along with disodium EDTA (0.028 g) in 0.1 L of phosphate buffer of pH 7. The mixture was centrifuged for 10 min at 4 • C. The supernatant was collected, and the volume was upgraded to 8 mL using phosphate buffer (pH 7). Na 2 EDTA (0.0278 g), methionine (1.5 g), and nitro blue tetrazolium chloride (NBT) (0.04 g) were added in phosphate buffer of pH 7.8 (100 mL). A total of 10 mL was taken in another flask and its volume was increased up to 50 mL. Riboflavin (0.00113 g) was added to the phosphate buffer (100 mL). A total of 20 mL was taken in another flask and its volume was increased up to 50 mL with DH 2 O. Then reference, blank, and reaction mixtures were prepared, each containing 2 mL of solution, 0.5 mL of solution two, and 0.5 mL of enzyme extract. The reference treatment was placed in darkness and the reaction mixture was kept in a light chamber. Absorbance was noted as 560 nm. The activity of SOD was presented as unit/100 g of fresh weight.
The following formula was used to determine SOD activity. R 1 , R 2 , and R 3 represent the OD of the reference, OD of the blank, and OD of the sample, respectively. R 4 = R 3 − R 2 and Final = R 4 /A In a similar way, peroxidase (POD) activity was observed by following [44]. A total of 4.45 g Na 2 HPO 4 disodium monohydrogen phosphate and 3.9 g NaHPO 4 monosodium dihydrogen phosphate was taken in 0.5 L distilled water for the preparation of 0.1 M phosphate buffer of 6.5 pH. One-percent hydrogen peroxide was made in phosphate buffer (0.1 M) of pH 6.5. By using 10 mL of phosphate buffer of pH 6.5, a fresh shoot (1 g) sample was crushed, then spun, and the supernatant was obtained. A spectrophotometer was adapted to zero and values were recorded at 430 nm. H 2 O 2 (0.5 mL) was added and mixed for each sample in the test cuvette. The absorbance of the supernatant was recorded at 430 nm for a consecutive 3 min to observe changes in the absorbance values. The absorbance change per minute at 430 nm was taken as one unit of peroxides. The protocol suggested by [45] was implemented to determine catalase activity by H 2 O 2 decomposition. Disodium monohydrogen phosphate (5.963 g) and monosodium dihydrogen phosphate (5.226 g) were added to 500 mL distilled water to make 0.067 M phosphate buffer of pH 7.0. Hydrogen peroxide (12.6 µL) was added to 100 mL of phosphate buffer to make 2 mM hydrogen peroxide solution. Plant tissues (0.5 g) were measured and crushed in 8 mL of phosphate buffer. The extract was spun, and the supernatant obtained was used for the enzyme assay. A total of 40 µL supernatant was mixed completely in 3 mL of 2 mM hydrogen peroxide solution already prepared by using 0.067 M phosphate buffer (100 mL phosphate buffer + 26.5 µL H 2 O 2 ). The absorbance of the samples was recorded at 240 nm while taking phosphate buffer as blank. The optical density was measured at 240 nm using a spectrophotometer (752N UV-VIS, Beijing, China).

Metal Analysis of Plants by Wet Acid Digestion
Cadmium (Cd) uptake was achieved by employing the method of wet acid digestion [46]. Plant material (1 g) was finely ground via pestle and mortar and transferred to a 0.1 L conical flask. About 10 mL nitric acid and perchloric acid (HNO 3 -HClO 4 in a 3:1 ratio) were kept in the flask and kept overnight in a fume hood. Then the flasks were kept in a fume hood for 60 min, maintaining the temperature of 70 • C. During this process, brown fumes turned white. The flasks containing mixture were permitted for a few seconds to cool. Distilled water was added to dilute the mixture. The obtained extract was filtered through Whatman No. 42 and double-distilled water was added to raise the total volume up to 50 mL. These samples were utilized to quantify Cd concentration with the help of the flame atomic absorption spectrometry method (Varian FAAS-240, Triad Scientific, New York, NJ, USA). To assure quality, the FAAS instrument was calibrated with standards (R 2 = 0.9999) given by the firm (SRM 3108 for cadmium). Periodic calibration of the FAAS instrument using metal standards at intervals of 10 samples ensured the accuracy of the Cd readings. The FAAS instrument has a detection limit of 0.002 µg/L for Cd.

Bioconcentration Factor (BCF) and Translocation Factor (TF)
The bioconcentration factor (BCF) was determined to evaluate the metal uptake capacity that occurred from the soil to plant tissues. The BCF was calculated for individual plant parts i.e., roots and shoots. The translocation factor (TF) determined the ability of a given plant species as a phytoremediator. The translocation factor is the ratio between the concentration (Conc.) of Cd present in the plant shoot to the root. The formulae proposed by [47] were used to calculate BCF and TF.

BCF =
Conc. of metal in root Conc. of metals in shoot (2) TF = Conc. of metal in shoot Conc. of metals in root (3)

Fourier Transform Infrared Spectroscopy (FT-IR) Analysis
The functional groups involved in the adsorption of Cd ions on the surface of bacterial cells were identified through Fourier transform infrared spectrophotometric (FTIR) analysis. Initially, bacterial culture was inoculated in LB broth with and without the amendment of Cd (100-200 mg/L). After an incubation of 24 h, B. anthracis PM21 culture was centrifuged for 10 min at 8000 rpm by maintaining a temperature of 4 • C. Supernatant was discarded and pelleted bacterial cells were separated. Bacterial cells were washed three times with sodium chloride solution (0.85%) followed by de-ionized (DDI) H 2 O and then oven dried at 50 • C [48]. Furthermore, 1 mg of crushed dried bacterial cells were mixed with 400 mg of KBr (potassium bromide). Thoroughly mixed cells were ground into fine powder and a manual hydraulic press at 100 kg/cm2 pressure was applied for 10 min to obtain transparent sample disks. Fixation of the disks was done in FTIR (Nicolet TM, Thermo Scientific, Waltham, MA, USA) to observe specific functional groups at a wavelength ranging from 400 to 4000 cm [49].

Scanning Electron Microscopy (SEM)
SEM was executed to examine the impact of Cd on bacterial cell morphology. Bacteria were grown at 30 • C for 24 h at 120 rpm in LB broth in the presence (200 mg/L) and absence of Cd. The LB broth that did not contain Cd was considered a control treatment. Centrifugation of the bacterial cells was performed at 4 • C for 10 min at 8000 rpm after 24 h of incubation. Phosphate buffer saline (PBS) was used to wash pelleted bacterial cells thrice. Glutaraldehyde (2.5%) was used to pre-fix the washed bacterial cells for 4-6 h at 4 • C [50]. The PBS (pH 7.2) was again used to wash the pre-fixed bacterial cells twice. Osmium tetroxide (1%) was used for post-fixation purposes for 1 h followed by PBS washing and dehydration with acetone (v/v) at 20%, 40%, 60%, 80%, and 100%. Bacterial cells were dried with the help of a critical point dryer (CPD) and platinum-coated ion sputter coater (JFC 1600 Auto Fine Coater, JEOL, Tokyo, Japan) and analyzed under SEM (JSM-6490LV, JEOL) to investigate the morphological changes in bacterial cells treated with or without Cd.

Amplification of Heavy Metal Resistance CzcD Gene
The CzcD gene responsible for cadmium resistance was amplified in B. anthracis PM21. The sequence of the CzcD primer set is F-CAGGTCACTGACACGACCAT, R-CATGCTGATGAGATTGATGATC, with an amplicon size of about 398 base pairs [51]. Reactions were performed in the sequence of denaturation at 95 • C for 5 min, followed by 34 cycles at 94 • C for 90 s, 52 • C for 90 s, 72 • C for 2 min, and a final extension step of 72 • C for 7 min [52].

Re-Isolation of Inoculated Strain
Re-isolation was performed as reported by [53]. The re-isolation experiment was performed for the confirmation of inoculated strain PM21.

Statistical Analysis
Normality of the data was calculated through the Shapiro-Wilk test using SPSS software (IBM SPSS Statistics 21) (Table S1) [54]. The experiment was organized as a completely randomized design (CRD) in triplicate. Statistix version 8.1 was used to perform the analysis of variance (ANOVA) ( Table S2). Data are presented as means ± standard error; statistical significance between the treatments was calculated using a least significant difference (LSD) value of p ≤ 0.05.

Antibiotic Resistance of Bacillus Anthracis PM21
The bacterial strain was tested using the disk method for antibiotic resistance. The strain was resistant against the maximum number of antibiotics applied. A total of 20 antibiotics were tested and the appearance of a halo zone around the disk was considered a sign of susceptibility to bacterial strain. The antibiotic resistance ability of the strain is shown in (Table S3). The B. anthracis PM21 was highly resistant and showed resistant against 15 antibiotics.

Growth and Photosynthetic Pigments of Sesbania sesban L.
A significant increase in the root length of S. sesban L. was observed in Cd-stressed and non-stressed treatments with the inoculation of B. anthracis PM21 (Table 2). Both Cd contamination levels, 100 and 200 mg/kg (T2), significantly decreased root length (47.68%) and shoot length (33.29%) compared to the control. Inoculation of strain PM21 increased shoot and root length in both non-stress and Cd-stress treatments (  Figure 1). A significant reduction in photosynthetic pigments was noted in Cd-contaminated treatments of S. sesban compared to control treatment (Table 2). Chlorophyll a and b and total chlorophyll content were reduced by 27.34, 62.79, and to 43.71%, respectively, at a Cd stress level of 200 mg/kg compared to control treatment. Chlorophyll a and b and total chlorophyll contents were considerably improved due to the application of strain PM21 compared to the respective control. Enhanced chlorophyll a (60.08) and b (48.38%) and total chlorophyll contents (17.65%) were noted with the application of strain PM21 at the level of Cd stress of 200 mg/kg.

Relative Water Content, Electrolyte Leakage, MDA, and Proline
Reduced RWC and enhanced electrolyte leakage was noted in Cd-contaminated treatments compared to control (Figure 2). The Cd stress at 200 mg/kg significantly reduced RWC (16.66%) and enhanced membrane electrolyte leakage (14.28%) compared to control treatment (Figure 2a,b). Inoculation of B. anthracis PM21 under Cd stress at 200 mg/kg enhanced RWC (16.66%) and reduced ELL (12.5%). The Cd contamination enhanced the proline and MDA content of S. sesban (Figure 2c,d). The Cd stress at 200 mg/kg recorded maximum proline (37.75%) and MDA content (41.04%) compared to control. Bacterium inoculation under Cd stress at 200 mg/kg observed maximum reduction in proline (16.37%) and MDA content (12.65%).

Tolerance Index, Translocation Factor (TF), and Bioconcentration Factor (BCF)
The enhanced Cd tolerance and high biomass values were noted in plants inoculated with strain PM21 compared to control (Table 3). S. sesban L. plants shown a high Cd absorption upon exposure to increased levels of Cd (Table 3). The application of strain PM21 showed high Cd absorption, resulting in the best cadmium contents in inoculated Cd 200 plants. In all treatments, plant roots had higher Cd than shoots. In comparison to roots of un-inoculated S. sesban L., strain PM21-inoculated plants had 12

Scanning Electron Microscope (SEM)
Compared to unexposed cells having a smooth cell surface, bacterial cells subjected to Cd stress became rough, exhibited surface depression, and showed increased cell size (Figure 5a,b).

Amplification of Heavy Metal Resistance CzcD Gene
The bacterial strain PM21 was screened for the Cd resistance gene (CzcD) by performing PCR amplification of genomic DNA. Bacillus anthracis PM21 possessed the resistant gene for Cd (CzcD) (Figure 6).

Discussion
Agricultural soil contaminated with Cd poses major risks to crop productivity [55]. Microbial-assisted phytoremediation is considered an effective approach for the reclamation of polluted soils [56,57]. The inoculation of stress-tolerant PGPR can reduce the detrimental impact of heavy metals (HMs) in sustainable agriculture [27]. Bacteria can tolerate HMs and can enhance plant growth by producing antioxidants [57]. The current investigation explained S. sesban phytoremediation potential for Cd with and without bacterial inoculation (B. anthracis PM21) to analyze the potential regulation of physiological parameters, biochemical parameters, and antioxidant enzymes. The application of HM-tolerant bacteria can be used as a promising technique to induce a Cd stress-tolerance mechanism in plants [27,42].
Antibiotic-resistant PGPR can be utilized in the form of inoculum to reduce competition. In the current study, B. anthracis PM21 showed resistance against 15 antibiotics. Ref. [58] reported that bacteria can benefit from antibiotic resistance to enhance their colonization and niche with plants compared to others. Genes responsible for antibiotic resistance are considered to provide a key role in the mechanism proposed for antibiotic resistance. The genes are located either in chromosomes or in plasmid. The presence of multifunctional proteins involved in functions such as efflux of metals or molecules are considered for antibiotic resistance [59].
The application of strain PM21 increased agro-morphological traits, including fresh weight (FW), dry weight (DW), root length (RL), and shoot length (SL), of the S. sesban plant in the presence and absence of Cd stress. The RL (47.68%), SL (33.29%), FW (44.95%), and DW (62.48%) of S. sesban were significantly decreased in Cd-spiked soil compared to control treatment. Previous results reported that plants at 150 µM Cd reduced root length (27.56%), shoot length (30.95%), fresh weight (28.46%), and dry weight (32.24%) compared to control [60]. Several studies have shown that Cd hampers various biological processes in plants, including impregnation through ammonia and other compounds. Cadmium stress also brings negative physiological, biochemical, and genetic changes in plants, which might be a reason for the decreased growth parameters of S. sesban L. under Cd stress [42]. Furthermore, Cd levels above the permissible limit may cause the inhibition of enzymatic functions, leaf chlorosis, reduced plant fresh and dry weight, and sometimes death [61].
The increased growth parameters of S. sesban was observed through the inoculation of strain PM21 at the concentration of 200 mg/kg Cd. Inoculation of strain PM21 significantly increased RL, SL, FW, and DW up to 38.39, 32.67, 43.48, and 50.84%, respectively, under 200 mg/kg of Cd compared to control ( Table 2). This could be due to the modulation of antioxidant mechanisms and photosynthetic pigments of the studied plant with the application of strain PM21 [62]. It has been well documented that inoculating Cd-stressed Serratia marcescens BM1 to soyabean enhanced root (14.58%) and shoot length (21.51%) and fresh (11.11%) and dry weight (5.11%) [63]. Usually, applied bacteria benefit plants in phytoremediation under abiotic stress conditions by increasing metal solubility with the synthesis of various organic acids, ACC deaminase enzyme, and exopolysaccharides produced by bacteria [26]. Moreover, a reduction in plant growth and biomass of Solanum nigrum was examined when plants were under stress with Cd contamination only, but the application of Serratia sp. RSC-14 significantly reduced Cd stress and facilitated plant growth [64].
Chlorophyll a (27.34%) and b (62.79%) and total chlorophyll content (43.71%) of S. sesban was significantly decreased in Cd-spiked soil compared to control treatment. In the same way, in an investigation conducted by [65], chlorophyll a (29.25%) and b (43.22%), and total chlorophyll content (61.73%) were decreased under Cd stress. Low synthesis of photosynthetic pigments could be due to a change in structural compounds and gas exchange factors that are blocked under stress conditions [46]. This reduction in chlorophyll content of the S. sesban plant could be due to the activation of chlorophyll and membrane damage [26,66]. On the other hand, the chlorophyll a (60.08%), chlorophyll b (48.38%), and total chlorophyll content (17.65%) were positively improved with the application of strain PM21 ( Table 2). The chlorophyll contents, including chlorophyll a (28.26%), chlorophyll b (30.54%), and total chlorophyll (58.01%), of the maize plant were increased by bacterial inoculation under 30 µM of Cd [36,67]. Plant growth-promoting bacteria could enhance chlorophyll that upsurges nutrient uptake in plants through PSB and exudates essential substances that have a role in the synthesis of photosynthetic pigments required for photo assimilation [68,69]. In comparison with the reported literature, our results showed significant improvement in the following growth parameters: root length, shoot length, fresh weight, dry weight, and chlorophyll a, chlorophyll b, and total chlorophyll.
In the current study, the electrolyte leakage (ELL) (14.28%) and relative water content (RWC) (16.66%) were significantly decreased upon exposure to Cd compared to control. Similar findings were observed with decreased ELL (20.14%) and RWC (29.44%) under Cr 200 mg/kg [38]. A positive correlation among enhanced ELL and a decrease in RWC represented membrane damage in S. sesban upon exposure to Cd [26]. The present investigation demonstrated that the inoculation of strain PM21 reduced ELL (12.5%) and enhanced RWC (16.66%). In comparison, inoculation of B. xiamenensis PM14 to S. sesban minimized ELL (2.73%) and improved RWC (25.79%) [38]. Bacterium inoculation enhanced water absorption due to improved root surface area, which resulted in improved physiological parameters of the host plant [70]. Under Cd exposure, proline (37.75%) and MDA content (41.01%) were significantly decreased in S. sesban. In the same way, physiological parameters proline (37.75%) and MDA contents (34.84%) were decreased in S. sesban when exposed to Cd [38]. Cadmium stress produced ROS that led to plant oxidative stress with increased ELL and lipid peroxidation [71]. Malondialdehyde content is an indication of cell membrane damage due to its reaction with protein amino groups [25]. Improved physiological mechanisms like malondialdehyde (MDA) and proline content have been documented in bacterial-inoculated plants [38]. Increased proline content (16.37%) could be due exopolysaccharide synthesis by strain PM21 under Cd stress condition [38]. Bacterialinoculated S. sesban plants showed a significant decrease in MDA content (12.65%), which could have been due to the mitigation of Cd stress by the application of ACC deaminase, producing microbial solution. The results presented by [38] are in line with current results, in which proline (12.33%) was improved and MDA (29.53%) was decreased with B. xiamenensis PM14 in S. sesban. Plants can tolerate Cd stress with the production of antioxidant enzymes that scavenge produced reactive oxygen species (ROS). Maximum oxidative stress in S. sesban was triggered with Cd stress applied at the level of 200 mg/kg, which led to the enhanced production of important antioxidant activities (SOD, POD, and CAT) (Figure 3) [72]. However, inoculation with strain PM21 significantly improved the antioxidants activities of SOD (11.98%), POD (12.16%), and CAT (4.46%) at 200 mg/kg of Cd (Figure 3). It was previously reported that SOD (24.54%), POD (26.03%), and CAT (30.54%) at a 30 µM Cd stress level increased by bacterial inoculation [72]. The acinetobacter controls the activities of antioxidant enzymes, as reported in a previous research study, due to the initiation of antioxidant enzyme mRNA expression [73]. As one of the mitigation strategies to deal with the drastic effects of metal stress, particularly in susceptible ones, improved antioxidant enzymes under abiotic stress using PGPR could be predicted [74]. Enhanced activities of SOD, POD, and CAT in inoculated chickpea improved plant growth through the protection of chloroplasts and other organelles in which important metabolic mechanisms occur [60].
Both bioconcentration factor (BCF) and translocation factor (TF) can be used as possible tools to identify the ability of plants to absorb metal ions. The TF and BCF of the strain PM21-inoculated S. sesban plants are shown in Table 3. Compared to the control plants, inoculated S. sesban showed increased root (118.6 mg/kg), shoot (73.4 mg/kg), TF (0.61), and BCF (0.36), respectively. It was previously reported that accumulation of Cd increased in root (57.2 mg/kg) and shoot (9.02 mg/kg), resulting in higher TF (0.18) and BAF (0.06) values of Sesbania sesban [75]. Because of their growth-promoting biochemicals and boosting nutrient uptake capabilities, PGPR can co-currently enhance phytoremediation and plant growth [76]. It was observed that the tolerance index (TI) of strain PM21-inoculated plants was 97.11% with 200 mg/kg of Cd. The tolerance index was 49.6% and 48.14%, respectively, as reported by [77]. The growth and phytoextraction of S. sesban were improved by inoculating B. anthracis PM21. Moreover, plant growth-promoting rhizobacteria boosted bioaccumulation, bioavailability, and plant biomass in inoculated plants [78,79]. Bacteria can produce chelating biochemicals, siderophores, and phosphate solubilization, which have a role in improved Cd uptake and alleviation of stress-inoculated plants [80]. The current study suggests that strain PM21 is involved in bioavailability in Cd, due to which accumulation and uptake of Cd is enhanced in S. sesban [79]. In accordance with the reported literature, our results revealed a considerable improvement in Cd uptake of the root, shoot, TF, BCF, and TI of S. sesban. The FTIR spectral results of strain B. anthracis PM21 demonstrated that treatments showed a clear shift in the peaks of the hydroxyl functional group present in alcohol, alkene, nitro compounds, alkane, sulfonyl chloride, alkyl aryl ether, and primary alcohol groups of bacterial biomasses. These functional groups are supposed to relate to polysaccharides and proteins found on the cell surface during their interaction with Cd, as demonstrated by [81]. The peaks observed at 3280.89 cm −1 and 2922.60 cm −1 resulted from the O-H stretching form of alcohol. The overlap of alcohol and hydroxyl stretching on the surface of cells has been clearly observed [81]. However, in Cd stress-exposed cells, an unchanged absorption peak was observed at 2929.53 cm −1 , suggesting the O-H stretching of lipids, nucleic acid, proteins, and polysaccharides in the cell wall. A small difference in the peak of absorption from lower (1633.93 cm −1 ) to higher (1637.79 cm −1 ) was also observed, suggesting C = C stretching primarily associated with the mode of deformation of C = C [82]. Scanning electron microscopy of strain B. anthracis PM21 revealed clear adsorption of Cd. The SEM results revealed the changes in cell surface morphology, which was Cd concentration dependent. It might be due to different surface responses against Cd stress applied at 200 mgL −1 . Extracellular adsorption, including surface complexation, could affect its structure, increasing in cell surface roughness [82]. However, these changes help with adaptation to stressful conditions [83]. Previously, it was also noted that a relative decrease in bacterial cell surface area could reduce the toxic effects of pollutants [83,84]. The CzcD operon that is responsible for Cd resistance is owned by the bacterial strain PM21. The CzcD operon is used to detoxify Cd by exporting it into the extracellular medium from the cytoplasm and/or periplasm [84].

Conclusions
Bacterial-assisted phytoremediation is considered an effective approach to reclaim polluted soils for sustainable food production. Phytoremediation in combination with inoculation of PGPR can be used efficiently to manage soil polluted under metal stress. Our findings highlighted remarkable improvements after inoculation of plants with the B. anthracis PM21 strain as a plant growth-promoting rhizobacteria. Application of B. anthracis PM21 significantly (p ≤ 0.05) enhanced root length (26.77%), shoot length (12.65%), fresh weight (37.02%), dry weight (28.37%), chlorophyll a (52.79%), chlorophyll b (48.38%), and total chlorophyll contents (17.65%) compared to uninoculated ones. Application of B. anthracis PM21 significantly (p ≤ 0.05) enhanced Cd concentration in root (118.6 mg/kg) and shoot (73.4 mg/kg), and the translocation (0.61) and bioconcentration factor (0.36). The PGPR, like B. anthracis PM21, has bioremediation potential and can be utilized to decontaminate HM-contaminated soil. B. anthracis PM21 was also applied for the first time in bacterial-assisted phytoremediation that enhanced plant growth of S. sesban under Cd stress. It is evident that B. anthracis PM21 showed Cd tolerance through the amplification of the CzcD gene. SEM and FTIR analysis conferred surface moieties for the adsorption of Cd on cell surface, growth, and antioxidant improvement.
Supplementary Materials: The following are available online at https://www.mdpi.com/article/10 .3390/su132413529/s1, Table S1: Shapiro-Wilk test showed normal distribution for all the studied parameters, Table S2: Analysis of variance revealed highly significant difference for the studied parameters, Table S3: Antibiotic resistance of Bacillus anthracis PM21.