Introduction

The sixth most common transition metal and the seventh most prevalent element in the earth’s crust is chromium (Cr) [1]. Due to the weathering of the earth’s crust and the deposition of waste from industrial operations, including the chemical (leather, pigments, electroplating, and other industries) and metallurgical (mostly steel and metal) sectors, it is present in the environment [2]. Environmental conditions severally effect on the growth and development of the plants [3, 7]. Due to their abundance in protein, certain minerals, vitamins, and calories, pulse crops are considered nutritional crops for the consumption of human beings, and mung bean can be eaten in a variety of ways boiled, fried, sprouted, and in powdered form, and most nutrient dense form of mung bean is mung bean sprout, which has greater than 200% more protein than other consumable forms. 100-gram mung bean sprouts have a nutritional content of 7 g of protein, 18 g of carbohydrate portion, 0.026 g of sodium, 24 gram of fat, 0.0029gram of calcium, and 103.5 calories and other significant vitamins [8]. Mung bean is the 2nd largest cultivated crop in Pakistan after chickpea. It is planted as a cash crop in summer and spring season. Mung bean cultivated on 0.25 million hectares of land with the annual production of 178 tones and averaged yield of this crop is around 515 kg/ha [9].

Inoculating plants with Azospirillum, which principally stimulates plant root development, may help to boost and stabilize crop yield. Although they have been carried out on various crops and in various regions, evaluations of Azospirillum’s effectiveness under current cultivation practices and at typical environmental conditions are rare [10]. Under field conditions, Azospirillum brasilense can colonize hundreds of plant species and significantly enhance their growth, development, and efficiency. The most researched observed the mechanism for Azospirillum to promote plant growth in inoculated plants, in addition to nitrogen fixation, has been linked to its capacity to produce a number of phytohormones, primarily auxins and particularly indole-3-acetic acid [11], abscisic acid (ABA), polyamines, ethylene, and nitric oxide [12]. Under controlled agronomic conditions, Azospirillum brasilense can colonize the soil rhizosphere and in the internal tissues of many plants that directly enhancing their proliferation, development, and yield. Azospirillum has both direct and indirect effects on plant development. Increases in the bioavailability of nutrients for plants (such as nitrogen, phosphorus, iron, and potassium) or the creation of enzymes and plant growth regulators (phytohormones) are examples of direct methods. Plant resistance to infections and tolerance to abiotic stress are two examples of indirect processes [13]. Under abiotic stress conditions, SA’s ability to restore growth is correlated with its impact on physiological aspects of the plant, including water content, nutrient uptake, synthesis of chlorophyll pigments, growth, stomatal regulation, suppression of ethylene biosynthesis, hormonal profile regulation, and protein kinas synthesis [14]. In extremely modest amounts, SA is an endogenous growth regulator that occurs naturally in plants [15]. There is a need to assess the impact of metals such chromium on the crop production and the impact on important cash crops of Pakistan. The impact of chromium on the mung bean’s germination and growth efficiency is poorly understood. The current study planned to evaluate the impact of differing chromium concentrations on seed germination and plant growth performance. We hypothesized that the combine application of A. brasilense and SA might have the positive impact on mung bean under Cr toxicity and can improve the plant growth. This study explores a novel approach to enhance plant tolerance to heavy metal stress by using combine application of A. brasilense and a natural plant hormone (CA), providing valuable insights into sustainable agricultural practices for managing metal-contaminated soils.

Materials and methods

Experimental design

An approved mung bean variety “PRI Mung-2018” seeds were obtained from the Pulses Research Institute, Faisalabad for research. Six mung bean seeds were planted in a clay pot at a depth of 10 cm, containing 2 kg of that soil that had been carefully rinsed and dried to examine the effects of Azospirillum brasilense and salicylic acid on mung bean plants under chromium-contaminated soil. To create the chromium toxicity, Soil was contaminated with the chromium compound {potassium dichromate (K2Cr2O7)} @200, 300, and 400 mg/kg of the soil as per the treatments. Cr was applied in the soil 5 days before the sowing and uniformly mixed in each pot. Soil sampling and analysis are represented in Table 1. Azospirillum brasilense (FCBP-SB0025) (B3) pure culture was obtained from the Fungal Culture Bank of Pakistan (FCBP) at the Faculty of Agriculture Sciences, University of Punjab, Lahore. A total of 39 plastic pots were arranged in three replications of 13 treatment combinations using randomized block design (RBD) in a greenhouse at the Botanical Garden, Government College, University of Lahore. The greenhouse environment includes controlled temperature (often 20–30 °C), relative humidity (commonly 50–70%), photoperiod (12–16 h of light), and additional lighting to promote optimal plant growth, producing a space suited for study and experimentation. The pot trial was performed from March 28 to April 27, 2022, in a greenhouse.

Table 1 Characteristics of sandy loam soil used in pot experiment
Full size table

Parameters studied

Plant height, shoot root length, fresh and dry weight

Measuring the vertical plant height from the base to the tallest shoot tip is the first step in gathering information on “Plant height, shoot root length, fresh and dry weight” in mung bean plants. Measure the longest root and main stem, respectively, to determine the length of the shoot. Immediately weigh the entire uprooted plant to determine its fresh weight. Dry the plant in an oven to determine dry weight, and then weigh it once it has reached a steady weight. The plant dry weight was determined by drying the 3 tallest plants from each replicate for each concentration, were dried in a hot air oven at 60 °C for 48 h. Repeat the procedure for numerous plants in each treatment, using averages to improve data accuracy. All the relevant data was collected after 1 month of the seed germination.

Crop growth rate (CGR)

Crop growth rate was noticed by the following formula as reported by Karimi and Siddique [16].

$$\mathrm{CGR}\;\;=\;\left({\mathrm W}_2\;-\;{\mathrm W}_1\;\right)\;/\;\left({\mathrm t}_2\;-\;{\mathrm t}_1\;\right)$$

Where:

W2: Final dry weight of the crop (grams per square meter)

W1: Initial dry weight of the crop (grams per square meter)

t2: Final time (days)

t1: Initial time (days)

Chlorophyll contents and relative water contents

Chlorophyll contents (a, b, and total) were also estimated by using the procedure described by Arnon [17]. Relative water content in the leaf was noticed by Barrand Weatherley’s equation [18] as follows,

$$\mathrm{RWC}\;(\%)\;=\;\lbrack(\mathrm{FW}\;-\;\mathrm{DW})\;/\;(\mathrm{TW}\;-\;\mathrm{DW})\rbrack\;\times\;100.$$

5 g of fresh leaves were acquired, and they were mashed in a pestle and mortar with 80% acetone to detect the chlorophyll a and b. After being ground, each sample was boosted in volume by 10 mL using acetone before being centrifuged for five minutes at 4000 rpm. This sample’s absorbance was determined using a UV/visible spectrophotometer (Spectro scan 80D, Kyoto, Japan) at 663 and 645 nm. The following formulas were used to determine the concentrations of chlorophyll a, chlorophyll b, and total chlorophyll as reported by Du et al. [19]:

$$\mathrm{The}\;\mathrm{formula}\;\mathrm{for}\;\mathrm{chlorophyll}\;\mathrm a\;(\mathrm{Chl}\;\mathrm a)\;\mathrm{is}\;\mathrm{Chl}\;\mathrm a\;(\mathrm{mg}/\mathrm{ml})\;=\;12.7\;\ast\;(\mathrm A665)\;-\;2.69\;\ast\;(\mathrm A652).$$
$$\mathrm{The}\;\mathrm{formula}\;\mathrm{for}\;\mathrm{chlorophyll}\;\mathrm b\;(\mathrm{Chl}\;\mathrm b)\;\mathrm{is}\;\mathrm{Chl}\;\mathrm b\;(\mathrm{mg}/\mathrm{ml})\;=\;22.9\;\ast\;(\mathrm A652)\;-\;4.68\;\ast\;(\mathrm A665).$$
$$\mathrm{Total}\;\mathrm{Chlorophyll}\;(\mathrm{Mg}/\mathrm{ml})\;=\;\mathrm{Total}\;\mathrm{Chl}\;(\mathrm{mg}/\mathrm{ml})\;+\;\mathrm{Total}\;\mathrm{Chl}\;(\mathrm{Mg}/\mathrm{ml})$$

Where A665 and A652 are the absorbance figures discovered through spectrophotometric analysis at the appropriate wavelengths.

Enzymatic activities

Harvesting plant tissue and making a homogenised extract in a cold buffer solution are the first steps in measuring the activity of various enzymes in mung bean plants, such as catalase (CAT), ascorbate peroxidase (APX), peroxidase (POD), and superoxide dismutase (SOD). 240 nm hydrogen peroxide (H2O2) breakdowns should be observed for catalase, and enzyme activity should be calculated based on the change in absorbance. By detecting the ascorbate’s reduction by H2O2 at 290 nm, one can measure the activity of ascorbate peroxidase. Track the oxidation of the substrate (such as guaiacol) in the presence of H2O2 to determine the activity of the peroxidase. Determine the superoxide dismutase’s ability to prevent the photoreduction of nitro blue tetrazolium (NBT) at 560 nm and express activity in accordance with that finding. Ensuring correct reporting of enzyme activity per gramme of fresh or dry plant tissue weight. Ascorbate peroxidase (APX), catalase (CAT), Peroxidase (POD), and superoxide dismutase (SOD) activities were noticed according to the Nakano and Asada [20], Vanacker et al. [21], Ghanati et al. [22], and Beyer and Fridovich [23], respectively. All local, national or international guidelines and legislation were adhered to for the use of plants in this study.

Statistical analysis

All data was analyzed at a 95% probability level by using Fisher’s test, and least significant difference (LSD) with the use of Statistix 8.1 computer software.

Results

Effect of Azospirillum brasilense and salicylic acid on growth related parameters of mung bean under chromium toxicity

Chromium (Cr) toxicity showed the significant negative effect on the mung bean seedlings Highest plant height, shoot length, root length, shoot fresh weight, root fresh weight, shoot dry weight and root dry weight was noticed in T1 under control condition when no Cr stress was applied having no soil amendment. Highest plant height (32.22 cm), shoot length (21.07 cm), root length (11.05 cm), shoot fresh weight (16.64 g), root fresh weight (1.01 g), shoot dry weight (9.82 g) and root dry weight (0.65 g) was noticed in T1 under control condition when no Cr stress was applied having no soil amendment followed by T5 (plant height: 30.18 cm, shoot length: 19.43 cm, root length: 9.02 cm, shoot fresh weight: 13.41 g, root fresh weight: 0.96 g, shoot dry weight: 8.43 g and root dry weight: 0.60 g, respectively) when Cr toxicity was 200 mg/kg of soil having seed inoculation of A. brasilense and foliar application of SA. Lowest results were noticed in T10 (plant height: 20.25 cm, shoot length: 11.13 cm, root length: 3.11 cm, shoot fresh weight: 6.12 g, root fresh weight: 0.68 g, shoot dry weight: 3.02 g and root dry weight: 0.13 g, respectively) when Cr toxicity was 400 mg/kg soil having no amendment (Table 2).

Table 2 Effect of salicylic acid (SA) and A. brasilense on plant height, shoot and root length, root shoot dry and fresh weight and chlorophyll content of mung bean plant under Cromium (Cr) toxicity
Full size table

Effect of Azospirillum brasilense and salicylic acid on chlorophyll contents of mung bean under chromium toxicity

Data regarding the chlorophyll contents shows that all studied treatments significantly effected on the chlorophyll contents (Table 2). Highest chlorophyll a (2.15 mg/ml), b (1.16 mg/ml) and total chlorophyll contents (3.31 mg/ml) were noticed in T1 under control conditions having no toxicity followed by T5 (chlorophyll a: 2.09 mg/ml, chlorophyll b:1.12 mg/ml and total chlorophyll: 3.21 mg/ml, respectively) when Cr toxicity was @200 mg/kg of soil with the combine application of A. brasilense and SA. Lowest results (chlorophyll a: 0.81 mg/ml, chlorophyll b: 061 mg/ml and total chlorophyll: 1.42 mg/ml, respectively) were noticed in T10 when Cr toxicity was @ 400 mg/kg of soil having no amendment.

Effect of Azospirillum brasilense and salicylic acid on enzymatic activities of mung bean under chromium toxicity

Enzymatic activities of mung bean were significantly affected by the application of Azospirillum brasilense and salicylic acid under chromium toxicity (Table 3). Higher negative effects were noticed with the increase of Cr toxicity and combine application of A. brasilense and SA is effective to control their negative effect. Highest CAT (Catalase), APX (Ascorbate peroxidase), POD (peroxidase) and SOD (superoxide dismutase) activities was noticed in T1 (CAT: 1.32 units/mg of protein, APX: 4.52 units/mg of protein, POD: 0.82 units/mg of protein, SOD: 4.01 units/mg of protein) followed by T5 (CAT: 1.21 units/mg of protein, APX: 4.20 units/mg of protein, POD: 0.71 units/mg of protein, SOD: 3.81 units/mg of protein) and lowest results were seen in T10 (CAT: 0.68 units/mg of protein, APX: 1.22 units/mg of protein, POD: 0.08 units/mg of protein, SOD: 2.62 units/mg of protein).

Table 3 Effect of salicylic acid (SA) and A. brasilense on catalase (CAT), ascorbate peroxidase, (APX), peroxidase (POD) and superoxide dismutase (SOD) of mung bean plant under Cromium (Cr) toxicity
Full size table

Enzymatic activities of mung bean were significantly affected by the application of Azospirillum brasilense and salicylic acid under chromium toxicity (Table 3). Higher negative effects were noticed with the increase of Cr toxicity and combine application of A. brasilense and SA is effective to control their negative effect. Highest CAT (Catalase), APX (Ascorbate peroxidase), POD (peroxidase) and SOD (superoxide dismutase) activities was noticed in T1 (CAT: 1.32 units/mg of protein, APX: 4.52 units/mg of protein, POD: 0.82 units/mg of protein, SOD: 4.01 units/mg of protein) followed by T5 (CAT: 1.21 units/mg of protein, APX: 4.20 units/mg of protein, POD: 0.71 units/mg of protein, SOD: 3.81 units/mg of protein) and lowest results were seen in T10 (CAT: 0.68 units/mg of protein, APX: 1.22 units/mg of protein, POD: 0.08 units/mg of protein, SOD: 2.62 units/mg of protein).

Effect of Azospirillum brasilense and salicylic acid on relative water content (RWC) and crop growth rate (CGR) of mung bean under chromium toxicity

Relative water content (RWC) significantly affected by all studied treatments (Fig. 1). Highest RWC was noticed in T1 (75.15%) under control condition followed by T5 (69.57%) when Cr toxicity was @200 mg/kg of soil with A. brasilense and SA. Lowest RWC were noticed in T10 (27.64) when Cr toxicity was @ 400 mg/kg of soil having no soil amendment. Crop growth rate (CGR) also affected by the application of A. brasilense and SA under Cr toxicity (Fig. 2). Highest CGR was noticed in T1 (8.12 g m−2 day−1) followed by T5 (7.52 g m−2 day−1) and lowest CGR was observed in T10 (1.43 g m−2 day−1).

Fig. 1
figure 1

Effect of salicylic acid and Azospirillum brasilense on relative water content (RWC) of leaf of mung bean plant under Cadmium stress. Different letters are significantly different in each columns ( P  ≤ 0.05)

Full size image
Fig. 2
figure 2

Effect of salicylic acid and Azospirillum brasilense on crop growth rate of mung bean plant under Cadmium stress. Different letters are significantly different in each columns ( P  ≤ 0.05)

Full size image

Discussion

Variety of growth parameters in mung bean plants were examined in our study, including plant height, shoot and root length, root-shoot dry and fresh weights, chlorophyll content, enzymatic activities, relative water content (RWC), and crop growth rate. Salicylic acid (SA) and Azospirillum brasilense have the significant impact on all studied treatments and can improve the growth under Chromium (Cr) toxicity. Environmental conditions severally effect on the growth and development of the plants [3, 46]. As a result of Azospirillum brasilense promotion of root growth, plants are better able to reach water in deeper soil layers, which improves overall water intake and leads to enhanced RWC [31]. Plants are able to better utilize water resources for growth and stress adaption thanks to the increased nutrient availability brought on by Azospirillum inoculation, thus boosting RWC and CGR. SA and A. brasilense work together to maximize water use, improving both RWC and CGR and enabling mung bean plants [28, 29].

Conclusion

Chromium stress has a negative effect on growth and productivity of mung bean but seed inoculation of Azospirillum brasilense and foliar application of salicylic acid together mitigate the adverse effect of Cr stress. Higher Cr toxicity has the higher negative effect. Sole application of A. brasilense and SA is effective to improve the mung bean growth but it is not enough to control negative effect of Cr toxicity. Combine application of A. brasilense and SA is more effective to mitigate the negative effect of Cr toxicity. Use of A. brasilense and SA is very effective for sustainable crop production even under adverse environmental conditions. In future, there is need to investigate and make an approach with the use of A. brasilense and SA by which farmers can get fully control on Cr toxicity.