Skip to main content
Browse Subject Areas

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Enhancement of osmotic stress tolerance in soybean seed germination by bacterial bioactive extracts

  • Sang Tae Kim,

    Roles Formal analysis, Investigation, Methodology, Visualization, Writing – original draft

    Affiliations Division of Agricultural Microbiology, National Institute of Agricultural Sciences, Rural Development Administration, Wanju, Republic of Korea, Department of Applied Bioscience, Dong-A University, Busan, Republic of Korea

  • Mee Kyung Sang

    Roles Conceptualization, Supervision, Writing – review & editing

    Affiliation Division of Agricultural Microbiology, National Institute of Agricultural Sciences, Rural Development Administration, Wanju, Republic of Korea


Soybean (Glycine max (L.) Merr.) is important to the global food industry; however, its productivity is affected by abiotic stresses such as osmosis, flooding, heat, and cold. Here, we evaluated the bioactive extracts of two biostimulant bacterial strains, Bacillus butanolivorans KJ40 and B. siamensis H30-3, for their ability to convey tolerance to osmotic stress in soybean seeds during germination. Soybean seeds were dip-treated in extracts of KJ40 (KJ40E) or H30-3 (H30-3E) and incubated with either 0% or 20% polyethylene glycol 6000 (PEG), simulating drought-induced osmotic stress. We measured malondialdehyde content as a marker for lipid peroxidation, as well as the activity of antioxidant enzymes, including catalase, glutathione peroxidase, and glutathione reductase, together with changes in sugars content. We also monitored the expression of genes involved in the gibberellic acid (GA)-biosynthesis pathway, and abscisic acid (ABA) signaling. Following osmotic stress in the extract-treated seeds, malondialdehyde content decreased, while antioxidant enzyme activity increased. Similarly, the expression of GA-synthesis genes, including GmGA2ox1 and GmGA3 were upregulated in KJ40E-dipped seeds at 12 or 6 h after treatment, respectively. The ABA signaling genes GmABI4 and GmDREB1 were upregulated in H30-3E- and KJ40E-treated seeds at 0 and 12 h after treatment under osmotic stress; however, GmABI5, GmABI4, and GmDREB1 levels were also elevated in the dip-treated seeds in baseline conditions. The GA/ABA ratio increased only in KJ40E-treated seeds undergoing osmotic stress, while glucose content significantly decreased in H30-3E-treated seeds at 24 h after treatment. Collectively, our findings indicated that dip-treatment of soybean seeds in KJ40E and H30-3E can enhance the seeds’ resistance to osmotic stress during germination, and ameliorate cellular damage caused by secondary oxidative stress. This seed treatment can be used agriculturally to promote germination under drought stress and lead to increase crop yield and quality.


Soybeans (Glycine max (L.) Merr.) are major crops owing to their versatility, nutritional value, and use in several industrial applications, and are grown in various countries around the world [1, 2]. Soybean cultivation depends on region and crop variety, and generally begins in the spring between early April and late May, with a maturation stage lasting from 100 to 150 days after sowing, and a harvest season during fall [3]. The production of soybeans can be affected by abiotic factors, including drought, salt, and flooding, as well as biotic factors, such as plant pathogens and pests, that collectively determine the final crop yield and its quality [4, 5]. Therefore, to prevent infection by plant pathogens and insects after planting, soybeans require regular disease and insect management, which can be achieved through a variety of fungicides and pesticides, mechanical cultivation, the use of cover crops, and disease-resistant cultivars [6, 7]. Moreover, previous studies have investigated physiological, biochemical, and molecular aspects [811] in an attempt to comprehend mechanisms of abiotic stress tolerance and identify potential applications in soybean [12, 13].

Soybeans are highly sensitive to water stress, and it can severely impact their growth and production. Drought damage can occur at several stages of soybean development, especially during the early stages of growth, which can lead to a decrease in germination rate and sprout emergence, as well as growth delay or stunting [14, 15]. This can result in smaller and less vigorous plants with fewer branches and leaves [16, 17]. Seed germination is influenced by environmental conditions such as water, light, and temperature, though moisture has a significant impact on seed germination, which is divided into three phases (phase I: imbibition, phase II: lag phase, phase III: radical emergence) [18, 19]. Phytohormones also play a role, including abscisic acid, which is related to seed dormancy, and gibberellic acid (GA), which is involved in seed germination and development [19]. For example, the overexpression of ABA response genes, ABI4 and ABI5, showed minimal germination than wild-type, and in the case of the GA2ox mutant, which deactivate bioactive GA, a reduction in seed dormancy was observed [2024]. During the plant’s maturation, drought stress also causes wilting, leaf yellowing, premature leaf drop, and accumulated abscisic acid (ABA) owing to increased water loss through transpiration, stomatal conductance in response to elevated temperatures [25]. If drought stress persists, this can negatively impact flower and pod production as well as seed quality, which may be seen in the reduced seed size and weight, and the dropping of premature pods [26, 27]. To alleviate drought stress, a range of soybean crop management strategies have been developed, including planting drought-tolerant cultivars, managing irrigation, and employing alternatives such as trehalose, and biostimulants using microorganisms [12, 13, 2830].

Biostimulants refer to microorganisms or microorganism-derived compounds, that can enhance plant growth, development, and stress tolerance [31]. These can be applied to alleviate drought stress by increasing the ability of plants to absorb and retain water [32]. Biostimulants can improve the soil structure and increase plant root development, allowing plants to absorb water more efficiently and increase their water-holding capacity, in addition to enhancing plant antioxidant and osmotic adjustment capacities, which together allow for the development of a level of tolerance to drought-induced stress [33, 34]. Drought stress may cause secondary oxidative stress in plant cells, leading to cell death and reduced growth [35]. In this context, biostimulants can increase the production of antioxidants and protect plants from oxidative damage [36]. Moreover, they facilitate plant adjustment to osmotic stress by upregulating osmoprotectants production, such as proline, which can help toward maintaining water balance and prevent cell damage [37]. Biostimulants may finally improve plant nutrient uptake and metabolism, which can enhance stress resistance and enable the more efficient utilization of available nutrients [38]. Together, these qualities make biostimulants attractive tools for conferring osmotic stress tolerance to crops, and thereby mitigate the more adverse effects of drought in plants grown in drought-prone environments.

In our previous study, we identified three bacterial strains, Bacillus aryabhattai H26-2, B. siamensis H30-3, and Peribacillus butanolivorans KJ40, as biostimulant candidates for alleviating plant abiotic stresses, including heat and drought [39, 40]. Strains H26-2 and H30-3 could promote plant growth, decrease leaf wilting, and enhance recovery after rewatering against heat and drought stress in Chinese cabbage, by regulating leaf abscisic acid (ABA) content and stomatal opening [39]. In particular, strain H30-3 produces exopolysaccharides that play a pivotal role in the mitigation of heat and drought stress in plants [39]. Strain KJ40 modulates antioxidant activities, such as peroxidase and glutathione peroxidase, allocated polyphenol contents, including flavonoids, of pepper plants that were impacted by drought, and could influence the development of stress tolerance in plants [40].

Recently, soybean cultivation and production in Korea, has increased from 50,638 ha cultivation area and 177 kg production per 10 a in 2018, to 63,956 ha and 203 kg per 10 a in 2022 [41], however, cumulative precipitation during the six months from December 2021 to May 2022 was 167.9 mm, which is 49.1% of the standard normal precipitation from 1991 to 2020, soybean crops could have been stressed by a lack of rainfall after sowing in the field. Given the importance of a robust stress tolerance against drought, the objectives of this study were: (1) to identify bacterial bioactive extracts resistant to osmotic stress, in soybean seeds, that could maintain efficient germination under stress-inducing conditions, and (2) to explore seed physiological changes, including those related to lipid peroxidation, antioxidant activities, osmotic and germination-related hormone gene expression, and reducing sugar content in the selected bioactive extracts, under osmotic stress conditions during germination.

Materials and methods

Extract preparation of drought-tolerant inducing bacteria

Bacillus butanolivorans KJ40, B. siamensis H30-3, and B. aryabhathai H26-2 were used as drought tolerance-inducing bacteria as described in our previous studies [39, 40]. The strains were cultured in 1 L of tryptic soy broth (TSB, Difco, USA) at 28°C, for three days, and then the cultures were centrifuged at 6,000 × g for 30 min. The supernatants were collected and filtered through a 0.45 μm vacuum filter. The filtrates were serially fractionated with organic solvents (1:1, v/v) including hexane, dichloromethane, ethyl acetate, and n-butanol, according to polarity, by using a funnel on a shaker at 120 rpm overnight. Each separated extract was vacuum-evaporation (KJ40 extract was hexane: 110 mg, dichloromethane: 80 mg, ethyl acetate: 93 mg, n-butanol: 320 mg; H30-3 was hexane: 50 mg, dichloromethane 130 mg, ethyl acetate: 73 mg, n-butanol: 230 mg; H26-2 was hexane: 90 mg, dichloromethane: 110 mg, ethyl acetate: 180 mg, n-butanol: 220 mg) and dissolved in methanol. The concentrated extracts were diluted in water.

Screening for drought tolerance -inducing bacterial extracts on soybean seeds

Glycine max ‘Daewon’ was surface-sterilized in 2% sodium hypochlorite, and then soaked in different concentrations of bacterial extracts (1, 10, and 100 μg/mL) for 1 h at 25°C and 100 rpm, before blotting onto sterile filter papers to remove excess solution. To examine the drought-tolerance-inducing activity of the extracts, 20 mL of 20% polyethylene glycol (PEG) 6000 (81260, Sigma, USA) (-0.49MPa) [42] with a half-diluted Hoagland solution was placed in a Petri dish (diameter 90 mm) with two-layered filter papers (No. 2, Whatman, England), and soaking-treated seeds were placed on a plate. Ten soybean seeds were used for selection of bioactive fractions, and then 25 seeds were tested for determination of the effective concentration of each fraction. Seven days after incubation at 25°C and 16 h light/8 h dark, we evaluated the final germination percentage (FGP, %), median germination time (T50, day), and mean germination time (MGT, day). The calculations were as follows: FGP (%) = final day of germination seeds/total seeds × 100; T50 = ti + [(N/2-ni) (ti-tj)]/ni-nj (where N = final number of germinated seeds; ni, nj = accumulative number of seeds germinated by adjacent counts at times ti and tj, respectively [ni < N/2 < nj]); MGT = ∑(nxd)/N, n = number of germinated seeds on each day (where d = number of days from the beginning of the experiment; and N = total number of germinated seeds at the end of the test) [43].

Malondialdehyde, glutathione, and antioxidant enzyme activity

Seeds were sampled at 0, 3, 6, 9, 12, 24, 48, and 72 h after PEG treatment. For the seed physiological assay, three seeds were pooled and grounded using a mortar and pestle, prior to collection. The malondialdehyde (MDA) content was determined as described by Dhindsa et al. [44]. Ground seeds (100 mg) were homogenized in 500 μL of 0.1% trichloroacetic acid (TCA) (w/v) and centrifuged for 10 min at 13,000 × g at 4°C. The supernatant (200 μL) was mixed with 600 μL of 20% TCA amended with 0.5% 2-thiobarbituric acid (TBA); incubated at 90°C for 30 min. The reaction was inhibited on ice for 5 min., and the absorbance at 450, 532, and 600 nm were measured by a spectrophotometer (Infinite M200 PRO, TECAN, Switzerland). The MDA content was calculated according to Bao et al. [45]. Glutathione (GSH, 703002; Cayman, USA) and antioxidant enzyme activities, including those of superoxide dismutase (SOD, 706002; Cayman, USA), catalase (CAT, 707002; Cayman, USA), glutathione peroxidase (GPX, 703102; Cayman, USA), and glutathione reductase (GR, 703202; Cayman, USA), were detected according to the manufacturer’s instructions.

Seed RNA extraction and qRT-PCR

Seeds were sampled and grounded as already described. Total RNA from the seeds was extracted using the TRIzol™ reagent (Invitrogen, USA), and RNA concentration in our samples was measured in Nanodrop (ND-1000, Thermo Scientific, USA). Total RNA was synthesized into cDNA using TOPscriptTM RT DryMIX (dT18) (Cat. No. RT200; Enzynomics) and diluted to 1:10. For quantitative real-time (qRT) PCR, we used a CFX96 Real-time PCR Detection system (Bio-Rad), together with specific primers for the studied genes (Table 1). The qRT-PCR was performed as follows: 95°C for 10 min (initial denaturation); 45 cycles of 95°C for 15 s (denaturation), 58°C for 60 s (annealing), and 72°C for 45 s (extension). To normalize Glycine max gene expression, GAActin11 was used as a reference gene, and the relative expression level was determined using the 2-△△Ct method [50].

Table 1. Primers of soybean genes used in the real-time PCR analysis.

Abscisic acid, gibberellic acid, and sugars contents

Abscisic acid content was measured as described by Lim et al [51]. Crushed seed (0.1 g) was extracted in 2ml of methanol containing 500 mg/L citric acid monohydrate and 100 mg/L butylated hydroxyl toluene, at 4°C overnight on a rotary shaker. The mixture was centrifuged at 2000 × g for 10 min, and the supernatant was transferred and dried using a speed vac (CVE-2000, EYELA). Samples were quantified using a Phytodetek-ABA kit (Agdia Inc., USA) according to the manufacturer’s instructions. Gibberellic acid (GA, MBS9310617, MyBioSource) and sugars (K-SUFRG, Megazyme, Ireland), including sucrose, D-fructose, D-glucose, were evaluated according to the manufacturer’s protocol.

Statistical analysis

All data were analyzed using the Statistical Analysis System (SAS) (version 9.4, SAS Institute Inc., Cary, NC, USA). Fraction and concentration selections were conducted with six and eight replications (fraction selection: 10 seeds/replication, concentration selection: 25 seeds/replication) from two experiments, while MDA, antioxidant enzyme activities, and sugars (sucrose, glucose, and fructose) analyses were conducted with nine replicates, obtained from three experiments. Gene expression was performed with six replicates from two experiments. Each replicate was randomly combined with three seeds. Data from repeated experiments were pooled after confirming the homogeneity of variance using Levene’s test. After the ANOVA, the least significant difference (LSD) or Tukey’s test was conducted for statistical comparisons between groups.


Selection of bacterial bioactive extracts promoting seed germination under osmotic stress conditions

Final seed germination was reduced under drought stress conditions (KJ40; F value = 27.01, P <0.0001, H30-3; F value = 39.56, P <0.0001; H26-2; F value = 39.49, P <0.0001) (S1 Table). The seed dipping treatment in selected bacterial extracts (100 μg/ml) promoted the development of resistance to drought-induced stress and ameliorated the decrease of seed germination (KJ40; F value =2.43, P = 0.0767, H30-3; F value =9.26, P = 0.0005, and H26-2, F value =0.69, P = 0.6044) (S1 Fig). The strain KJ40 and H30-3-extracts by ethyl acetate significantly increased soybean seed FGP compared to control under PEG 20% conditions (S1 Fig). By contrast, the effect of strain H26-2 extract was less pronounced and not significantly different compared to the control, as such it was excluded from further study in this work (S1 Fig).

After dipping treatment of various concentration (1, 10, 100 μg/mL) of the extracts by ethyl acetate of strains KJ40 and H30-3, we observed that treatment had a significant effect on FGP (F value = 6.18, P <0.0001). The 100 μg/mL of H30-3 and 1 μg/mL of KJ40 extracts effectively increased FGP compared to control under PEG 20% conditions. The FGP of seeds dipped-treated with 100 μg/mL of H30-3 and 1 μg/mL of KJ40 extracts were 89.3 ± 2.2%, and 85.3 ± 1.3, respectively; that of control was 64.5 ± 5.5 (Table 2). However, T50 and MGT values were similar to those of the control group (Table 2). Therefore, 100 μg/mL of H30-3 extract (H30-3E) and 1 μg/mL of KJ40 extract (KJ40E), isolated in ethyl acetate, were selected for further study.

Table 2. Soybean seed final germination percentage, median germination time, and mean germination time.

Changes in seed MDA and antioxidant enzyme activities during germination under osmotic stress

Osmotic stress caused by PEG 20% treatment during seed germination triggered secondary oxidative stress, as indicated by the increased production of the oxidative stress marker MDA, compared to the control PEG 0% treatment (3 h after treatment; F value = 10.52, P value = 0.0022, 6 h after treatment; F value = 1.59, P value = 0.2137, 9 h after treatment; F value = 4.76, P value = 0.0342, 12 h after treatment; F value = 0.03, P value = 0.872, 18 h after treatment; F value = 5.61, P value = 0.0221, 24 h after treatment; F value = 5.83, P value = 0.02, 48 h after treatment; F value = 2.74, P value = 0.1045, 72 h after treatment; F value = 6.36, P value = 0.0151) (Fig 1). Under non-stressed conditions, MDA content in soybean seeds was not affected by dipping treatments with H30E and KJ40E, except at 9 and 48 h after treatment (Fig 1A). However, H30-3E and KJ40E significantly reduced the MDA content compared to the control, from 12 to 72h after treatment under osmotic stress conditions (Fig 1B).

Fig 1. Changes in malondialdehyde content in soybean seeds dip-treated with control, H30-3 extract (H30-3E), and KJ40 extract (KJ40E) under 0 and 20% of PEG conditions.

The MDA content was measured at 3, 6, 9, 12, 18, 24, 48, and 72 hours after PEG-treatment (HAT). (A) 0% PEG; (B) 20% PEG. Data presented as means ± standard error (n=9, statistical significance assessed by the LSD test, *P < 0.05).

To scavenge reactive oxidative stress at the early germination stage, we measured several antioxidant enzyme activities, including catalase at 3 and 6 h after treatment, and glutathione peroxidase at 12 h after treatment for H30-3E-dipped seeds. For KJ40E-dipped seeds, we examined activity of catalase at 6 and 12 h after treatment, glutathione peroxidase at 9 h after treatment, and glutathione reductase at 12 h after treatment. All measured antioxidant enzyme activities were significantly increased in the treatment groups compared to controls (Fig 2B). However, superoxide dismutase activity did not differ between the treatments, regardless of PEG conditions (Fig 2).

Fig 2. Antioxidant enzyme activities, including catalase, glutathione peroxidase, glutathione reductase, and superoxide dismutase, in soybean seeds dip-treated with control, H30-3 extract (H30-3E), and KJ40 extract (KJ40E), and incubated in 0 or 20% PEG.

The enzyme activities were evaluated at 3, 6, 9, 12, 18, and 24 hours after PEG-treatment (HAT). (A) 0% PEG; (B) 20% PEG. Data presented as means ± standard error (n=9, statistical significance assessed by the LSD test, *P < 0.05).

Gibberellin and ABA-related genes expression

Gibberellic acid (GA) biosynthesis and ABA signaling genes were evaluated using qRT-PCR. Under non-stressed conditions, relative expression of GA biosynthesis-related genes in H30-3E-dipped seeds, including GmGA20ox1 and GmGA3ox1 levels at 12 h after treatment, and GmGA2ox1 at 0, 6, and 12 h after treatment, were upregulated (At 12 h after treatment: GmGA20ox1; 7.37-fold increase, GmGA3ox1; 8.53-fold increase, GmGA2ox1 increase in expression at 0 h after treatment; 1.52-fold, at 6 h after treatment; 3.27-fold, and 12 h after treatment; 13.13-fold, all relative to control). However, expression of GmGA3 at 6 h after treatment decreased (0.55-fold). In contrast, in KJ40E-dipped seeds, relative expression levels of GA synthesizing genes, including GmGA20ox1 and GmGA3ox1 at 0h after treatment, and GmGA3 at 0 and 6 h after treatment, were downregulated compared to control (GmGA20ox1; 0.35-fold decrease, GmGA3ox1; 0.46-fold decrease, and GmGA3-0 h after treatment; 0.43-fold decrease, GmGA3—6 h after treatment; 0.48-fold decrease). However, we observed increased expression for GmGA3ox1 (9.30-fold), GmGA2ox1 (15.16-fold), and GmGA3 (6.34-fold) at 12 h after treatment, in relation to the control (Fig 3A). Under PEG 20%-induced osmotic stress conditions, the relative expression of GA biosynthesis-related genes was not significantly affected by H30-3E-dipping treatment, except for GmGA3ox1 at 6 h after treatment and GmGA2ox1 at 0 h after treatment (GmGA3ox1; 0.40-fold decrease, and GmGA2ox1; 2.09-fold increase, relative to the corresponding control) (Fig 3B). In the case of KJ40E-dipped seeds, GA biosynthetic genes were downregulated at 0 h after treatment relative to controls (GmGA20ox1; 0.29-fold, GmGA3ox1; 0.32-fold, GmGA2ox1; 0.71-fold, and GmGA3; 0.49-fold); however, the expression of GmGA2ox1 at 12 h after treatment and GmGA3 at 6 h after treatment was significantly higher than that of the reference group (GmGA2ox1; 2.49-fold and GmGA3; 2.04-fold) (Fig 3B).

Fig 3. The relative expression of gibberellin-synthesis genes, including GmGA20ox1, GmGA3ox1, GmGA2ox1, and GmGa3, in soybean seeds dip-treated with control, H30-3 extract (H30-3E), and KJ40 extract (KJ40E), and incubated with 0 or 20% PEG.

Gene expression was measured at 0, 6, 12, and 24 hours after PEG-treatment (HAT). (A) 0% PEG; (B) 20% PEG. Data presented as means ± standard error (n=6, statistical significance assessed by the Tukey test, *P < 0.05).

The relative expression of ABA-signaling genes transiently increased at 12 h after treatment in H30-3E- and KJ40E-dipped seeds. Under baseline conditions, we observed an increase in levels of GmABI5 at 0 (2.66-fold) and 12 h after treatment (9.11-fold) in H30-3E-dipped seeds, and of GmDREB1 at 12 h after treatment (3.93-fold) in KJ40-dipped seeds (Fig 4A). Following osmotic stress induction, in H30-3E-dipped seeds the GmABI4 and GmDREB1 levels at 12 h after treatment were significantly upregulated (GmABI4; 5.19-fold and GmDREB1; 2.43-fold), as were the levels of GmABI4 at 12 h after treatment (4.41-fold) in KJ40E-dipped seeds, in comparison to the control (Fig 4B). Evaluation of GA and ABA content in soybean seeds at 24 h after treatment showed that ABA content was not significantly different between baseline and osmotic stress conditions; however, the GA content and GA/ABA ratios in KJ40E-dipped seeds were higher than those in the control following osmotic stress (GA; F = 5.69, P = 0.0098, GA/ABA; F = 4.22, P = 0.103) (Fig 5).

Fig 4. The relative expression of abscisic acid-related genes, including GmABI5, GmABI4, and GmDREB1 in soybean seeds dip-treated with control, H30-3 extract (H30-3E), and KJ40 extract (KJ40E), and incubated with 0 or 20% PEG.

Gene expression was measured at 0, 6, 12, and 24 hours after PEG-treatment (HAT). (A) 0% PEG; (B) 20% PEG. Data presented as means ± standard error (n=6, statistical significance assessed by the Tukey test, *P < 0.05).

Fig 5.

Contents of abscisic acid (A) and gibberellic acid (B), and the GA/ABA ratio (C) in soybean seeds at 24 hours after PEG-treatment (HAT). Left column, 0% PEG; Right column, 20% PEG. Data presented as means ± standard error (n=9, statistical significance assessed by the LSD test, *P < 0.05).

Changes in sucrose, glucose, and fructose contents

Glucose levels significantly decreased at 24 h after treatment in H30-3E-treated seeds under drought-simulating stress (F = 2.77, P = 0.0868), however, sucrose and fructose levels did not significantly differ between conditions. Sugars showed a decreasing pattern, but glucose showed a trend for increase in the control under osmotic stress conditions (Fig 6).

Fig 6. Changes in the contents of sucrose, glucose, and fructose, in soybean seeds during germination.

(A) 0% PEG; (B) 20% PEG. Data presented as means ± standard error (n=9, statistical significance assessed by the LSD test, *P < 0.05).


In our previous studies, two bacterial strains, Bacillus siamensis H30-3 and B. butanolivorans KJ40, were shown to ameliorate the more adverse effects related to heat and drought stress in Chinese cabbage, as well as drought stress in pepper plants [39, 40]. These mitigative activities result from indirect effects on the plants through tolerance development, including the regulation of stomatal opening and production of antioxidant and phenolic compounds. To more efficiently protect plants from being affected by unfavorable environmental conditions, alternative application strategies related to plant cultivation must be explored. As such, here we investigated whether the bacterial extract of H30-3 and KJ40 could decrease the impact of osmotic stress on soybean seeds during the germination stage, and indirectly promote the development of resistance to osmotic stress through induction of physiological changes in seeds. Our results demonstrated that the two bacterial extracts alleviated osmotic stress in soybean seeds and increased germination via different mechanisms.

Seed germination is the most important and sensitive stage in the plant life cycle. However, osmotic stress can cause secondary oxidative stress, low germination rates, and delayed germination times [52, 53]. In seeds dip-treated with the extracts of H30-3 at 100 μg/mL and KJ40 at 1 μg/mL, the measured FGP was higher than that of the un-treated control; however, MGT and T50 did not differ between treatments. This implies that the H30-3 and KJ40 extracts did not affect the rate of germination under osmotic stress conditions induced by 20% PEG treatment. To investigate the pathways related to the observed increase in FGP in the bacterial extract-treated seeds, we measured MDA levels as a readout for assessing secondary oxidative stress and lipid peroxidation state, as well as examined antioxidant enzyme activity. The MDA is used as an oxidative stress indicator, and the germination percentage increases with a decrease in oxidative stress. Our findings indicated that MDA content was higher in seeds subjected to osmotic stress relative to the reference group. Goharrizi et al. [54] have reported that the MDA content positively correlates with PEG concentration. In our study, MDA generally decreased in H30-3E- or KJ40E-dipped seeds from 12 hours after PEG treatment, suggesting that the two extracts could contribute to the mitigation of secondary oxidative stress effects during germination of soybean seeds under osmotic stress conditions. In addition, in the early stages of germination, catalase, and glutathione peroxidase activities were significantly higher in the two extract-dipped seed groups than in the un-treated controls. In the case of KJ40E-dipped seeds, glutathione reductase was also increased compared to control. Exogenous osmotic stress has been found to induce the overproduction of reactive oxygen species, which can cause membrane lipid peroxidation [55]. To mitigate this, plants have developed defensive mechanisms for scavenging reactive oxygen species; these mechanisms involve the production of enzymatic antioxidants such as ascorbate peroxidase, catalase, glutathione peroxidase, glutathione reductase, glutathione S-transferase, NADPH oxidase, and superoxide dismutase, as well as non-enzymatic antioxidants, including ascorbate, glutathione, and phenolic compounds [56]. Sheteiwy et al. [57] demonstrated that GABA-treated rice seeds exhibit increased germination percentage under osmotic stress conditions, with MDA and hydroperoxide decreasing in activity, while that of other antioxidant enzymes increased. Similarly, melatonin-soaked soybean seeds showed an increased germination rate under 6% PEG conditions, with a reduction in MDA, hydroperoxide, and superoxide anion levels; and a concomitant increase in the production of antioxidant enzymes, including catalase, peroxidase, and ascorbate peroxidase [58]. Therefore, the increase in catalase, glutathione peroxidase, and glutathione reductase activities which we also observed in our present work, indicated that H30-3E and KJ40E decreased membrane lipid peroxidation by increasing enzymatic antioxidant activities.

Breaking seed dormancy and germination are regulated by light, moisture, and temperature as well as by modulating expression of the plant hormones GA and ABA [59, 60]. The GA stimulates seed germination, plant growth, and development by promoting hydrolytic enzyme production, which induces softening of the seed cover [61]. Gibberellins are synthesized through the terpenoid pathway: within plastids, geranylgeranyl diphosphate is transformed to ent-kaurene through the actions of ent-copalyl diphosphate synthase and ent-kaurene synthase. Following this, ent-kaurene is further processed into GA12 through ent-kaurene oxidase and ent-kaurenoic acid oxidase. Finally, GA12 is transformed to bioactive GA4 through the activities of the GA 20-oxidase (GA20ox) and GA 3-oxidase (GA3ox) in the cytoplasm [62]. In this pathway, GA3 encodes for ent-kaurene oxidase [63] that converts GA12 within the plastids, while the respective enzymes encoded by GA20ox1 and GA3ox1 convert bioactive GA4 in the cytoplasm, which is fundamental for GA biosynthesis [64, 65]. Our qRT-PCR results showed that relative gene expression under drought conditions was upregulated for GmGA3 at 6 h after treatment, and it could lead to a subsequent marked accumulation of GA content in KJ40E-dipped seeds. Increased or excessively active GA correlated with a significantly enhanced expression of GmGA2ox1, which is involved in the inhibition of the GA biosynthesis pathway, at 12 h after treatment [66]. The ABA is one of non-hydraulic root-sourced signals (nHRS) accumulated by plants when drought stress occurs and is known to induce tolerance by stomata closure in plants [6769]. However, in seed, it is associated with the maintenance of seed dormancy, and ABI4, ABI5, and DERB1 are known to be important genes for ABA signaling. The ABI4 and ABI5 positively regulate ABA signaling [70, 71]. The expression of DERB1 gene is controlled by abiotic stresses such as drought, salt concentration, cold, and heat. Additionally, DERB1 affects the expression of abscisic acid-responsive element (ABRE) -related genes via an ABA-independent pathway [49, 72, 73]. We observed that GmABI4 expression in H30-3E- or KJ40E-dipped seeds was upregulated at 12 h after treatment, with a similar increase also noted for GmDREB1 at 12 h after treatment regardless of treatment. The ABA content was not affected by the treatment. The ratio of GA to ABA was significantly increased only in KJ40E-dipped seeds compared to the control, suggesting that KJ40E could be involved in the modulation of the biosynthesis of plant hormones, such as GA, during the germination stage, which can lead to a decrease in seed germination by osmotic stress.

Seeds require energy from stored sucrose and the raffinose family oligosaccharides (RFOs) during germination process [74]. Free sugars, including sucrose, stachyose, fructose, glucose, raffinose, and galactose, are reduced during germination [75] and used as an energy source. Our findings showed that the sucrose, glucose, and fructose contents tended to decrease regardless of PEG conditions and treatment; however, the time-dependent changes seemed to be different. Sucrose content drastically decreased in 20% PEG, with slope values of 0.0699 for the control, 0.0978 for H30-3E, and 0.756 for KJ40E, which were higher than 0.0278, 0.0439, and 0.0236, respectively, in the 0% PEG reference condition. The glucose content in the KJ40E-dipped seeds, and the fructose content in H30-3E-dipped seeds, also steeply decreased in 20% relative to 0% PEG. These results suggest that osmotic stress tended to promote the rapid degradation of sucrose to glucose and fructose, and that glucose and fructose could be effectively used as energy sources in the germination stage in KJ40E- or H30-3E-dipped seeds, which could be associated with the increased gemination rates observed in the extract-dipped seeds under 20% PEG conditions.

In conclusion, our study’s findings suggest that the bacterial extracts of H30-3E and KJ40E could indirectly alleviate the decrease in soybean germination under osmotic stress caused by 20% PEG treatment. This alleviation is likely achieved through the regulation of secondary oxidative stress responses, accomplished by enhancing the activities of antioxidant enzymes (CAT, GPX, and GR). In terms of gene expression, KJ40E-treated seeds exhibited regulated GA biosynthesis genes and ABA response genes, whereas H30-3E-treated seeds displayed upregulated ABA response genes. Consequently, KJ40E-treated seeds showed a significant accumulation of GA, leading to an increased GA-to-ABA ratio. In both H30-3E and KJ40E-treated seeds, glucose and fructose were likely utilized as energy sources to adapt to osmotic conditions. Overall, KJ40E and H30-3E had the potential for enhancing tolerance to osmotic stress during soybean seed germination by inducing physiological changes in the seeds, which could ultimately contribute to improved crop yield and quality under challenging environmental conditions.

Supporting information

S1 Fig. Selection of bioactive extracts.

Final germination percentage of KJ40 (A), H30-3 (B), and H26-2 (C) under 0% or 20% PEG. Data presented as means + standard error; small letters on the bar mean significant difference (n=6, statistical significance assessed by the LSD test).


S1 Table. One-way anova analysis of the final germination percentage between conditions.



  1. 1. Sheteiwy MS, Abd Elgawad H, Xiong Y, Macovei A, Brestic M, Skalicky M, et al. Inoculation with Bacillus amyloliquefaciens and mycorrhiza confers tolerance to drought stress and improve seed yield and quality of soybean plant. Physiol Plant. 2021;172: 2153–2169. pmid:33964177
  2. 2. FAO. 2022. World food and Agriculture-Statistical Yearbook 2022. Rome.
  3. 3. Egli DB. Soybean yield physiology: principles and processes of yield production. In: The soybean: botany, production and uses. CABI Wallingford UK; 2010. pp. 113–141.
  4. 4. Verslues PE, Agarwal M, Katiyar‐Agarwal S, Zhu J, Zhu J. Methods and concepts in quantifying resistance to drought, salt and freezing, abiotic stresses that affect plant water status. Plant J. 2006;45: 523–539. pmid:16441347
  5. 5. Suzuki N, Rivero RM, Shulaev V, Blumwald E, Mittler R. Abiotic and biotic stress combinations. New Phytol. 2014;203: 32–43. pmid:24720847
  6. 6. Hartman GL, West ED, Herman TK. Crops that feed the World 2. Soybean—worldwide production, use, and constraints caused by pathogens and pests. Food Secur. 2011;3: 5–17.
  7. 7. Roth MG, Webster RW, Mueller DS, Chilvers MI, Faske TR, Mathew FM, et al. Integrated management of important soybean pathogens of the United States in changing climate. J Integr Pest Manag. 2020;11: 17.
  8. 8. Manavalan LP, Guttikonda SK, Phan Tran L, Nguyen HT. Physiological and molecular approaches to improve drought resistance in soybean. Plant Cell Physiol. 2009;50: 1260–1276. pmid:19546148
  9. 9. Katam R, Shokri S, Murthy N, Singh SK, Suravajhala P, Khan MN, et al. Proteomics, physiological, and biochemical analysis of cross tolerance mechanisms in response to heat and water stresses in soybean. PLoS One. 2020;15: e0233905. pmid:32502194
  10. 10. Mutava RN, Prince SJK, Syed NH, Song L, Valliyodan B, Chen W, et al. Understanding abiotic stress tolerance mechanisms in soybean: A comparative evaluation of soybean response to drought and flooding stress. Plant Physiol Biochem. 2015;86: 109–120. pmid:25438143
  11. 11. Yahoueian SH, Bihamta MR, Babaei HR, Bazargani MM. Proteomic analysis of drought stress response mechanism in soybean (Glycine max L.) leaves. Food Sci Nutr. 2021;9: 2010–2020. pmid:33841819
  12. 12. Cao L, Qin B, Zhang YX. Exogenous application of melatonin may contribute to enhancement of soybean drought tolerance via its effects on glucose metabolism. Biotechnol Biotechnol Equip. 2021;35: 964–976.
  13. 13. Bakhshandeh E, Gholamhosseini M, Yaghoubian Y, Pirdashti H. Plant growth promoting microorganisms can improve germination, seedling growth and potassium uptake of soybean under drought and salt stress. Plant Growth Regul. 2020;90: 123–136.
  14. 14. Desclaux D, Roumet P. Impact of drought stress on the phenology of two soybean (Glycine max L. Merr) cultivars. Field Crops Res. 1996;46: 61–70.
  15. 15. Dubey A, Kumar A, Abd_Allah EF, Hashem A, Khan ML. Growing more with less: breeding and developing drought resilient soybean to improve food security. Ecol Indic. 2019;105: 425–437.
  16. 16. Hoogenboom G, Peterson CM, Huck MG. Shoot growth rate of soybean as affected by drought stress1. Agron J. 1987;79: 598–607.
  17. 17. Poudel S, Vennam RR, Shrestha A, Reddy KR, Wijewardane NK, Reddy KN, et al. Resilience of soybean cultivars to drought stress during flowering and early-seed setting stages. Sci Rep. 2023;13: 1277. pmid:36690693
  18. 18. Holdsworth MJ, Finch-Savage WE, Grappin P, Job D. Post-genomics dissection of seed dormancy and germination. Trends Plant Sci. 2008;13: 7–13. pmid:18160329
  19. 19. Finch‐Savage WE, Leubner‐Metzger G. Seed dormancy and the control of germination. New Phytol. 2006;171: 501–523. pmid:16866955
  20. 20. Shu K, Meng YJ, Shuai HW, Liu WG, Du JB, Liu J, et al. Dormancy and germination: How does the crop seed decide? Plant Biol. 2015;17: 1104–1112. pmid:26095078
  21. 21. Shu K, Zhang H, Wang S, Chen M, Wu Y, Tang S, et al. ABI4 regulates primary seed dormancy by regulating the biogenesis of abscisic acid and gibberellins in Arabidopsis. PLoS Genet. 2013;9: e1003577. pmid:23818868
  22. 22. Piskurewicz U, Jikumaru Y, Kinoshita N, Nambara E, Kamiya Y, Lopez-Molina L. The gibberellic acid signaling repressor RGL2 inhibits Arabidopsis seed germination by stimulating abscisic acid synthesis and ABI5 activity. Plant Cell. 2008;20: 2729–2745. pmid:18941053
  23. 23. Hu Y, Han X, Yang M, Zhang M, Pan J, Yu D. The transcription factor INDUCER OF CBF EXPRESSION1 interacts with ABSCISIC ACID INSENSITIVE5 and DELLA proteins to fine-tune abscisic acid signaling during seed germination in Arabidopsis. Plant Cell. 2019;31: 1520–1538. pmid:31123050
  24. 24. Yamauchi Y, Takeda-Kamiya N, Hanada A, Ogawa M, Kuwahara A, Seo M, et al. Contribution of gibberellin deactivation by AtGA2ox2 to the suppression of germination of dark-imbibed Arabidopsis thaliana seeds. Plant Cell Physiol. 2007;48: 555–561. pmid:17289793
  25. 25. Jumrani K, Bhatia VS. Interactive effect of temperature and water stress on physiological and biochemical processes in soybean. Physiol Mol Biol Plants. 2019;25: 667–681. pmid:31168231
  26. 26. Ohashi Y, Nakayama N, Saneoka H, Mohapatra PK, Fujita K. Differences in the responses of stem diameter and pod thickness to drought stress during the grain filling stage in soybean plants. Acta Physiol Plant. 2009;31: 271–277.
  27. 27. Arya H, Singh MB, Bhalla PL. Towards developing drought-smart soybeans. Front Plant Sci. 2021;12: 750664. pmid:34691128
  28. 28. Zhang T, Lin X, Sassenrath GF. Current irrigation practices in the central United States reduce drought and extreme heat impacts for maize and soybean, but not for wheat. Sci Total Environ. 2015;508: 331–342. pmid:25497355
  29. 29. Asaf S, Khan AL, Khan MA, Imran QM, Yun B, Lee I. Osmoprotective functions conferred to soybean plants via inoculation with Sphingomonas sp. LK11 and exogenous trehalose. Microbiol Res. 2017;205: 135–145. pmid:28942839
  30. 30. Yan C, Song S, Wang W, Wang C, Li H, Wang F, et al. Screening diverse soybean genotypes for drought tolerance by membership function value based on multiple traits and drought-tolerant coefficient of yield. BMC Plant Biol. 2020;20: 1–15. pmid:32640999
  31. 31. Van Oosten MJ, Pepe O, De Pascale S, Silletti S, Maggio A. The role of biostimulants and bioeffectors as alleviators of abiotic stress in crop plants. Chem Biol Technol Agric. 2017;4: 1–12.
  32. 32. Del Buono D. Can biostimulants be used to mitigate the effect of anthropogenic climate change on agriculture? It is time to respond. Sci Total Environ. 2021;751: 141763. pmid:32889471
  33. 33. Vurukonda SSKP, Vardharajula S, Shrivastava M, SkZ A. Enhancement of drought stress tolerance in crops by plant growth promoting rhizobacteria. Microbiol Res. 2016;184: 13–24. pmid:26856449
  34. 34. Rouphael Y, Colla G. Biostimulants in agriculture. Front Plant Sci. 2020;11: 40. pmid:32117379
  35. 35. Dumanović J, Nepovimova E, Natić M, Kuča K, Jaćević V. The significance of reactive oxygen species and antioxidant defense system in plants: A concise overview. Front Plant Sci. 2021;11: 552969. pmid:33488637
  36. 36. Ana Carolina Feitosa dV. Amelioration of Drought Stress on Plants under Biostimulant Sources. In: Hossain Akbar, editor. Plant Stress Physiology. Rijeka: IntechOpen; 2020. p. Ch. 18.
  37. 37. Hasanuzzaman M, Parvin K, Bardhan K, Nahar K, Anee TI, Masud AAC, et al. Biostimulants for the regulation of reactive oxygen species metabolism in plants under abiotic stress. Cells. 2021;10: 2537. pmid:34685517
  38. 38. Calvo P, Nelson L, Kloepper JW. Agricultural uses of plant biostimulants. Plant Soil. 2014;383: 3–41.
  39. 39. Shin DJ, Yoo S, Hong JK, Weon H, Song J, Sang MK. Effect of Bacillus aryabhattai H26-2 and B. siamensis H30-3 on growth promotion and alleviation of heat and drought stresses in Chinese cabbage. Plant Pathol J. 2019;35: 178. pmid:31007648
  40. 40. Kim ST, Yoo S, Weon H, Song J, Sang MK. Bacillus butanolivorans KJ40 contributes alleviation of drought stress in pepper plants by modulating antioxidant and polyphenolic compounds. Sci Hortic. 2022;301: 111111.
  41. 41. KOSIS (Korea statistical information service). 2022.
  42. 42. Michel BE, Kaufmann MR. The Osmotic Potential of Polyethylene Glycol 6000. Plant Physiol. 1973;51: 914–916. pmid:16658439
  43. 43. Farooq M, Basra S, Ahmad N, Hafeez K. Thermal hardening: a new seed vigor enhancement tool in rice. J Integr Plant Biol. 2005;47: 187–193.
  44. 44. Dhindsa RS, Plumb-Dhindsa P, Thorpe TA. Leaf senescence: correlated with increased levels of membrane permeability and lipid peroxidation, and decreased levels of superoxide dismutase and catalase. J Exp Bot. 1981;32: 93–101.
  45. 45. Bao A, Wang S, Wu G, Xi J, Zhang J, Wang C. Overexpression of the Arabidopsis H+ -PPase enhanced resistance to salt and drought stress in transgenic alfalfa (Medicago sativa L.). Plant Sci. 2009;176: 232–240.
  46. 46. Jiang H, Shui Z, Xu L, Yang Y, Li Y, Yuan X, et al. Gibberellins modulate shade-induced soybean hypocotyl elongation downstream of the mutual promotion of auxin and brassinosteroids. Plant Physiol Biochem. 2020;150: 209–221. pmid:32155449
  47. 47. Meng Y, Chen F, Shuai H, Luo X, Ding J, Tang S, et al. Karrikins delay soybean seed germination by mediating abscisic acid and gibberellin biogenesis under shaded conditions. Sci Rep. 2016;6: 22073. pmid:26902640
  48. 48. Chen F, Zhou W, Yin H, Luo X, Chen W, Liu X, et al. Shading of the mother plant during seed development promotes subsequent seed germination in soybean. J Exp Bot. 2020;71: 2072–2084. pmid:31925954
  49. 49. Wang T, Yu T, Fu J, Su H, Chen J, Zhou Y, et al. Genome-wide analysis of the GRAS gene family and functional identification of GmGRAS37 in drought and salt tolerance. Front Plant Sci. 2020;11: 604690. pmid:33424904
  50. 50. Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods. 2001;25: 402–408. pmid:11846609
  51. 51. Lim CW, Park C, Kim J, Joo H, Hong E, Lee SC. Pepper CaREL1, a ubiquitin E3 ligase, regulates drought tolerance via the ABA-signalling pathway. Sci Rep. 2017;7: 1–12. pmid:28352121
  52. 52. Wijewardana C, Alsajri FA, Reddy KR. Soybean seed germination response to in vitro osmotic stress. Seed Technol. 2018: 143–154.
  53. 53. Wijewardana C, Reddy KR, Krutz LJ, Gao W, Bellaloui N. Drought stress has transgenerational effects on soybean seed germination and seedling vigor. PloS One. 2019;14: e0214977. pmid:31498795
  54. 54. Jamshidi Goharrizi K, Moosavi SS, Amirmahani F, Salehi F, Nazari M. Assessment of changes in growth traits, oxidative stress parameters, and enzymatic and non-enzymatic antioxidant defense mechanisms in Lepidium draba plant under osmotic stress induced by polyethylene glycol. Protoplasma. 2020;257: 459–473. pmid:31776775
  55. 55. Upadhyaya H, Sahoo L, Panda SK. Molecular Physiology of Osmotic Stress in Plants. In: Rout GR, Das AB, editors. Molecular Stress Physiology of Plants. India: Springer India; 2013. pp. 179–192.
  56. 56. Ahmad P, Sarwat M, Sharma S. Reactive oxygen species, antioxidants and signaling in plants. J Plant Biol. 2008;51: 167–173.
  57. 57. Sheteiwy MS, Shao H, Qi W, Hamoud YA, Shaghaleh H, Khan NU, et al. GABA-alleviated oxidative injury induced by salinity, osmotic stress and their combination by regulating cellular and molecular signals in rice. Int J Mol Sci. 2019;20: 5709. pmid:31739540
  58. 58. Zhang M, He S, Qin B, Jin X, Wang M, Ren C, et al. Exogenous melatonin reduces the inhibitory effect of osmotic stress on antioxidant properties and cell ultrastructure at germination stage of soybean. PLoS One. 2020;15: e0243537. pmid:33320882
  59. 59. Oracz K, Karpiński S. Phytohormones signaling pathways and ROS involvement in seed germination. Front Plant Sci. 2016;7: 864. pmid:27379144
  60. 60. Skubacz A, Agata Daszkowska‐Golec. Seed Dormancy: The Complex Process Regulated by Abscisic Acid, Gibberellins, and Other Phytohormones that Makes Seed Germination Work. In: Mohamed El-Esawi, editor. Phytohormones. Rijeka: IntechOpen; 2017. pp. 77–100.
  61. 61. Ali AS, Elozeiri AA. Metabolic Processes During Seed Germination. In: Jose C. Jimenez-Lopez , editor. Seed Biology. Rijeka: IntechOpen; 2017. pp. 141–166.
  62. 62. Gupta R, Chakrabarty SK. Gibberellic acid in plant: still a mystery unresolved. Plant signal Behav. 2013;8: e25504. pmid:23857350
  63. 63. Yamaguchi S, Kamiya Y. Gibberellin biosynthesis: its regulation by endogenous and environmental signals. Plant and cell physiology. 2000;41: 251–257. pmid:10805587
  64. 64. Bawa G, Feng L, Chen G, Chen H, Hu Y, Pu T, et al. Gibberellins and auxin regulate soybean hypocotyl elongation under low light and high‐temperature interaction. Physiol Plant. 2020;170: 345–356. pmid:32588443
  65. 65. Chen S, Wang X, Tan G, Zhou W, Wang G. Gibberellin and the plant growth retardant Paclobutrazol altered fruit shape and ripening in tomato. Protoplasma. 2020;257: 853–861. pmid:31863170
  66. 66. Chen S, Wang X, Zhang L, Lin S, Liu D, Wang Q, et al. Identification and characterization of tomato gibberellin 2-oxidases (GA2oxs) and effects of fruit-specific SlGA2ox1 overexpression on fruit and seed growth and development. Hortic Res. 2016;3: 16059. pmid:28018605
  67. 67. Batool A, Cheng Z, Akram NA, Lv G, Xiong J, Zhu Y, et al. Partial and full root-zone drought stresses account for differentiate root-sourced signal and yield formation in primitive wheat. Plant Methods. 2019;15: 1–14. pmid:31338115
  68. 68. Lv G, Cheng Z, Li F, Akram NA, Xiong Y. Comparative response to drought in primitive and modern wheat: a cue on domestication. Planta. 2019;250: 629–642. pmid:31139926
  69. 69. Gui Y, Sheteiwy MS, Zhu S, Batool A, Xiong Y. Differentiate effects of non-hydraulic and hydraulic root signaling on yield and water use efficiency in diploid and tetraploid wheat under drought stress. Environ Exp Bot. 2021;181: 104287.
  70. 70. Feng C, Chen Y, Wang C, Kong Y, Wu W, Chen Y. Arabidopsis RAV 1 transcription factor, phosphorylated by S n RK 2 kinases, regulates the expression of ABI3, ABI4, and ABI5 during seed germination and early seedling development. Plant J. 2014;80: 654–668. pmid:25231920
  71. 71. Zhou H, Huang J, Willems P, Van Breusegem F, Xie Y. Cysteine thiol–based post-translational modification: What do we know about transcription factors? Trends Plant Sci. 2023;28: 415–428. pmid:36494303
  72. 72. Kidokoro S, Watanabe K, Ohori T, Moriwaki T, Maruyama K, Mizoi J, et al. Soybean DREB 1/CBF-type transcription factors function in heat and drought as well as cold stress-responsive gene expression. Plant J. 2015;81: 505–518. pmid:25495120
  73. 73. Zhou Y, Chen M, Guo J, Wang Y, Min D, Jiang Q, et al. Overexpression of soybean DREB1 enhances drought stress tolerance of transgenic wheat in the field. J Exp Bot. 2020;71: 1842–1857. pmid:31875914
  74. 74. Bellieny-Rabelo D, De Oliveira EAG, Ribeiro EdS, Costa EP, Oliveira AEA, Venancio TM. Transcriptome analysis uncovers key regulatory and metabolic aspects of soybean embryonic axes during germination. Sci Rep. 2016;6: 36009. pmid:27824062
  75. 75. Kim S, Lee J, Kwon Y, Kim W, Jung G, Kim D, et al. Introduction and nutritional evaluation of germinated soy germ. Food Chem. 2013;136: 491–500. pmid:23122089