Biological function of Klebsiella variicola and its effect on the rhizosphere soil of maize seedlings

Bacterial strain, soil, and plant material

K. variicola (CGMCC1. 15640) was acquired from the China General Microbial Species Preservation and Management Center. Natural saline-alkali soil (pH 9.2, Na⁺ content: 0.906 g kg⁻¹) was obtained from Daqing City, Heilongjiang Province. Neutral soil (pH 7.4, Na⁺ content: 0.628 g kg⁻¹) was obtained from Zhaodong County, Heilongjiang Province. Corn seed was Xianyu 335, and was purchased from Heilongjiang Fuzun Agricultural Integrated Service Chain Co. Ltd.

Instruments

Autoclavous steam sterilizer (Hitachi, Japan), super clean workbench (Boke, Beijing), constant temperature oscillating culture shaker (Zhicheng, Shanghai), light incubator (Shanghai Boxun, Shanghai), high speed frozen centrifuge (Kecheng Hunan).

Main drugs

Sucrose, NaCl, K₂HPO₄ ⋅ 3H₂O, CaCO₃, MgSO₄ ⋅7H₂O, Agar, naphthol, creatine, acetoin, toluene, benzenedisodium phosphate, 4-aminoantiimidoline, potassium ferricyanide, purchased from Daqing City Salto District Yineng Materials Sales Office

Induction and colonization of rifampicin (Rif) resistant strains

The colonization of K. variicola was determined using the antibiotic labelling method (Gao et al., 2020). Rifampicin resistance was induced in the bacterial strain by increasing the concentration of rifampicin to 300 µg mL⁻¹, using a concentration gradient set up at 50, 100, 150, 200, 250, and 300 µg mL⁻¹. The strain was allowed to grow normally in LB medium containing the lowest concentration of rifampicin, and then transferred to the next higher concentration for induction, until the strain was able grow normally at a concentration of 300 µg mL⁻¹ rifampicin.

Determination of genetic stability of rifampicin resistance: Following rifampicin resistance induction, the genetic stability of the antibiotic resistance was determined by transferring rifampicin resistant strains to LB plates without rifampicin for 5 generations. The strains were then transferred back to LB plates containing 300 µg mL⁻¹ rifampicin to detect its genetic stability. Normal growing bacteria were identified as positive, and vice versa.

Determination of strain colonization: K. variicola was inoculated using the root irrigation method, whereby each pot was inoculated with 100 mL of Rif-resistant bacterial suspension (with the concentration of K. variicola at 1 × 10⁸ cfu mL⁻¹), and pot culture was carried out. At 0, 3, 6, 9, 12, and 15 d after inoculation, 1 g of soil was collected from the rhizosphere of plant seedlings and diluted with sterile water. Tenfold gradient dilution was carried out, and the diluted bacterial suspension was coated on LB solid plate with colony counting method. After 48 h, the bacterial colonies on the plate were counted. The colony number of labelled strains per gram of soil was determined. Rifampicin-resistant strains were isolated using LB selective medium, prepared by adding 300 µg mL⁻¹ of rifampicin solution to LB medium.

Preparation of bacterial suspension

K. variicola was inoculated in LB liquid medium, then the culture flasks were put in a shaker incubator and incubated at 30 °C and 180 rpm for 24 h. The bacterial suspension was then centrifuged at 6,000 × g for 15 min, and the supernatant was discarded. The precipitate was washed with aseptic distilled water and re-suspended. This process was repeated three times. It was then diluted to 1 × 10² cfu mL⁻¹, 1 × 10⁴ cfu mL⁻¹, and 1 × 10⁶ cfu mL⁻¹, according to the requirements of the experiment.

Maize sprouting treatment

Xianyu 335 corn seeds of similar size and showing no damage on the surface were selected, soaked, and disinfected for 10 min using a 10% sodium hypochlorite solution. Seeds were then washed with sterile water more than five times until there was no obvious trace of sodium hypochlorite. The sterilized seeds were soaked in sterile water and transferred to an incubator maintained at 25 °C for 6 h, before discarding the sterile water. A piece of filter paper was spread across the bottom of the germination box and sterile water was evenly added until the filter paper was slightly soaked. Imbibed seeds were spread out evenly in the germination box, with 20 seeds in each box, and a piece of filter paper evenly coated with 3 mL sterile water was spread across the seeds. The germination box was covered with a lid and placed in a 25 °C incubator for 24 h, in order to accelerate germination in darkness.

Pot-based experiment

Potted soil was thoroughly air-dried and passed through a 2-mm sieve. Each pot (10 cm length × 10 cm width × 12 cm height) was loaded with 200 g of soil. Corn seeds with bud lengths of approximately 1 cm (0. 9 cm –1. 1 cm) were planted in pots filled with soil. Five seeds were evenly sown in each pot, which was then topped with 100 g more of soil. Bacterial suspensions (100 mL) at different concentrations (1 × 10² cfu/ml, 1 × 10⁴ cfu/ml, 1 × 10⁶ cfu/ml, 1 × 10⁸ cfu/ml) were poured into each pot. The pots were cultured in a light incubator for 15 d, and 10 mL of sterile water was added to each pot every 48 h, for the duration of the culture period. The control group was set up without the addition of a bacterial suspension. The culture conditions were as follows: the day and night temperatures were set at 25 °C and 20 °C, respectively, light was set at a 12:12 h light:dark cycle, and the humidity was at 60%–80%.

Determination of the biological function of K. variicola

Nitrogen fixation ability was determined by inoculating activated K. variicola colonies on a nitrogen-free solid medium [sucrose (10 g), NaCl (0.12 g), K₂HPO₄ ⋅3H₂O (0.5 g), CaCO₃ (1 g), MgSO₄ ⋅7H₂O (0.2 g), Agar (20 g), distilled water (1,000 ml), pH 7.2]. The presence or absence of K. variicola growth was observed to determine whether the bacteria possessed the ability to fix nitrogen. (Singh et al. 2015)

K. variicola was inoculated into 250-mL flasks containing nitrogen-free liquid medium, and a no inoculation (CK) condition was set up as the control. Each treatment was repeated 3 times at 30 °C, and 180 rpm, and flasks were cultured for 7 d. The culture medium was then divided into two parts, one of which was centrifuged at 6,000 × g for 15 min, and the supernatant was collected. The centrifuged supernatant and corresponding uncentrifuged sample were diluted 10x with ammonia-free water. Determination of soluble nitrogen concentration in the fermentation broth was by potassium persulfate oxidation-UV spectrophotometry (corresponding to determination of total nitrogen in water; GB-11894-89).

Determination of phosphorus solubilizing ability: K. variicola was inoculated on inorganic phosphorus and organophosphorus plates. Inorganic phosphorus medium (Ji, Gururani & Chun, 2014) consisted of glucose (10 g), Ca₃(PO₄)₂ (5 g), MgCl₂ ⋅6H₂O (5 g), MgSO₄ ⋅7H₂O (0.25 g), KCl (0.2 g), (NH₄)₂SO₄ (0.1 g), Agar (20 g), distilled water (1,000 mL), at pH 7.0. Among these chemicals, Ca₃(PO₄)₂ was sterilized separately, and then mixed with other components in the medium once the temperature had reduced to 70 °C. Organophosphorus medium (Wang, 2010) contained glucose (10 g), (NH₄)₂SO₄ (0.5 g), NaCl (0.3 g), FeSO₄ ⋅7H₂O (0.03 g), MnSO₄ ⋅4H₂O (0.03 g), CaCO₃ (5 g), yeast extract (0.4 g), Agar (20 g), lecithin (0.2 g), distilled water (1,000 mL), at pH 7.0. Following bacterial culture at 30 °C for 7 d, the occurrence of a transparent phosphorus solubilizing circle on either the inorganic or organic phosphorus medium was interpreted as the bacteria having the capability of dissolving inorganic or organic phosphorus, respectively. The ability to dissolve phosphorus was gauged according to the ratio of the radius of the phosphorus dissolving circle to the radius of the colony (Ke et al., 2015; Zeng, Wen & Wu, 2016). Dissolved inorganic phosphorus by K. variicola was quantitatively detected using the molybdenum-antimony colorimetric method (Lang, 2014).

Determination of potassium dissolving ability

The soluble potassium content in the K. variicola fermentation broth was determined using sodium tetraphenylborate (Ran, Ma & Meng, 2009). The standard curve was drawn according to the absorbance value and the content of potassium in solution at 420 nm. The soluble potassium content in the K. variicola fermentation broth was determined from the standard curve.

Determination of ammonia production capacity

Activated K. variicola was inoculated into a test tube containing 10 mL of protein water, according to the method described Singh, Jha & Jha (2015). Following incubation at 30 °C for 48 h, 0.5 mL of reagent was added to each test tube, and uninoculated medium was used as a blank control. If the strain appeared to be brown to yellow in colour, following the addition of Nessler’s reagent, it was considered able to produce ammonia. Ammonia production by K. variicola was quantitatively detected using Nessler’s reagent colorimetric method (Zheng, 2006).

The ability of K. variicola to produce indole acetic acid was determined according to the method described by Wang, Yuan & Zhao (2010). L-tryptophan, the precursor of indole-acetic acid, was added to the nitrogen-containing medium, which was inoculated with K. variicola and cultured at 180 rpm at 30 °C for 3 d. The fermentation broth containing K. variicola was centrifuged at 6,000 × g for 15 min, and the collected supernatant was mixed with 50 µL of 10 mM phosphoric acid, followed by the addition of 2 mL of Salkowski chromogenic solution (0. 5 M FeCl₃ ⋅6H₂O and 98 mL of 35% HClO₄, mixed evenly). The colour changes were observed after incubation for 30 min in the dark, at 30 °C. The quantitative determination of indole acetic acid production by K. variicola was deduced from the absorbance value of discoloration solution at 530 nm. The concentration of indole acetic acid produced by K. variicola was calculated from the standard curve of indole acetic acid.

Determination of the ability to produce acetoin

K. variicola was cultured for 24 h in V-P selective medium [glucose (5 g), peptone (5 g), K₂HPO₄ (5 g), distilled water (1,000 mL)], and 1 mL of the supernatant was added to creatine chromogenic solution (0.6 mL of 5% α-naphthol, 0.6 mL of 0.5% creatine, and 0.2 mL of 40% KOH). If the solution turned red, the strain produced acetoin. A standard curve was drawn from colour reaction with a range of concentrations of acetoin solution, and the concentration of acetoin produced by K. variicola was quantitatively detected (Liu, 2018).

Determination of soil nutrients and enzyme activities

To determine alkaline phosphatase activity, 5 g of soil and 0.5 mL toluene was added. The components were allowed to mix for 15 min, and 20 mL of 0.5% disodium benzene phosphate solution was added. The components were mixed well and placed in an incubator maintained at 37 °C for 2 h. After the culture period, 5 mL of filtrate was transferred into a 50-mL volumetric flask, followed by 0.25 mL of buffer solution, 0.5 mL of 4-aminoantipyrine solution, and 0.5 mL of potassium ferricyanide solution. Once the colour was stable (after approximately 15 min), the optical density was measured at a wavelength of 510 nm (Guan, 1986; Zhou et al., 2016).

Determination of urease activity

A soil sample (5 g) was treated with 1 mL toluene for 15 min. A 10% urea solution (10 ml; pH 6.7) and citrate buffer (20 mL) was added to the flask, and the mixture was incubated at 37 °C for 24 h. The collected filtrate (3 mL) was then mixed with an addition 20 mL of distilled water, 4 mL of phenol sodium solution, and 3 mL of sodium hypochlorite solution. Colour developed after 20 min, and the volume was adjusted. The spectrophotometer was used, within 1 h, to compare the absorbance at a wavelength of 578 nm (Bao, 2000).

Determination of catalase activity

A soil sample (2 g) with the addition of 40 mL of distilled water and 5 mL of 0.3% H₂O₂. The flask placed in an oscillator (120 rpm) was maintained at 30 °C constant temperature, for 20 min. Immediately after, 1 mL of saturated aluminium potassium alum was added to the flask, and the contents were immediately filtered into a triangular flask containing 5 mL of 1.5 mol L⁻¹ sulfuric acid solution. The filter was dried, and absorbance of the filtrate was determined directly at 240 nm using a 1-cm quartz colorimetric plate. The test results were expressed as the difference between the control and the test (Yang et al., 2011).

Determination of sucrase activity

A soil sample (2 g) injected with 15 mL of 8% sucrose solution, 5 mL of phosphate buffer solution (pH 5.5), and 0.25 mL of toluene. The mixture was incubated at 37 °C for 24 h. The filtrate (1 mL) and 3 mL of 3, 5-dinitrosalicylic acid were mixed. The mixture was heated in a boiling water bath for 5 min and subjected to colorimetric analysis at 508 nm wavelength on a spectrophotometer (Li, Wang & Hong, 2010).

Determination of organic matter content

A sample of air-dried soil (0.3 g) was weighed. A standard solution of 0.8 mol L⁻¹ K₂Cr₂O₇ (5 mL) was added, followed by injection with 5 mL of concentrated sulfuric acid. The test tube was heated in an oil bath, with the temperature controlled at 170 °C–−180 °C. The mixture was heated for 5 min. The test tube was then removed Three drops of o-phenanthroline indicator was added to the bottle, and the mixture was titrated with a 0.2 mol L⁻¹ FeSO₄ solution. The end point occurred when the solution colour changed from green to brownish red (Lu, 1999).

Determination of alkali-hydrolysable nitrogen content

An air-dried soil sample (2 g) was weighed and spread evenly in the outer chamber of a diffusion dish. A 2% boric acid mixed indicator solution (2 mL) was added to the diffusion dish chamber. A 1.8 mol L⁻¹ sodium hydroxide solution (10 mL) was added to the diffusion dish outer chamber, and the side of the cover glass slide was immediately tightly pushed back. The diffusion dish was transferred to an oven maintained at 40 °C, for 24 h, to allow alkaline hydrolysis and diffusion to take place. The amount of ammonia absorbed by indoor boric acid was titrated with 0.01 mol L⁻¹ hydrochloric acid, with a colour change from blue to reddish (Shi et al., 2017).

Determination of available phosphorus content

An air-dried soil sample (2.5 g) and 50 mL of 0.5 mol L⁻¹ NaHCO₃ solution was added. The mixture was shaken for 30 min. The filtrate (10 mL) was then absorbed in a 25-mL capacity flask, and 5 mL of molybdenum and antimony antichromogenic agent was added. The mixture was incubated at 37 °C for 30 min, before being subjected to colorimetric analysis at 880 nm (Xiao et al., 2012).

Determination of available potassium content

An air-dried soil sample (2 g) was placed in a 150-mL flask, and 20 mL of 1 mol L⁻¹ NH₄OAc solution was added. The mixture was shaken at 25 °C for 30 min, filtered, and the filtrate was analysed on a flame photometer at 766.5 nm (Meng et al., 2014).

Statistical analysis

One-way analysis of variance tests were conducted with SPSS 21.0 software (SPSS Inc., Chicago, IL, USA). Duncan’s test method was employed for multiple comparisons and analysis of the differences; significance was set as P < 0.05. All data in the tables are average values of triplicate or more repetitions.

Biological function of K. variicola

Nitrogen fixation capacity of K. variicola

Following culture on a nitrogen-free solid medium for 72 h, K. variicola grew well, as shown in Fig. 1A, indicating the bacteria’s ability to perform nitrogen fixation. Following bacterial culture in nitrogen-free liquid medium for 15 d, the concentration of soluble nitrogen in the fermentation broth was determined by potassium persulfate oxidation-UV spectrophotometry. The results showed that the concentration of soluble nitrogen in fermentation broth treated with K. variicola was 6.5 mg L⁻¹, and that the amount of nitrogen fixed by the bacteria in each litre of culture medium was 9.2 mg, with the total amount of nitrogen obtained via fixation being 15.7 mg L⁻¹. This indicated that K. variicola possessed the ability to effectively fix nitrogen.

Colonization of K. variicola in soil

The colonization of K. variicola in both saline-alkaline and neutral soils produced an initial decrease, followed by an increase in cfu number. The lowest level of colonization in saline-alkali soil was at 7.35 × 10⁶ cfu g⁻¹, when the treatment was applied for 3 d. The process appeared to stabilize after 12 d, and the colonization reached 4.68 × 10⁸ cfu g⁻¹ (Fig. 2). This may be owing to the competition from other microorganisms present in the saline-alkali soil and to additional feeding by protozoa, which resulted in a decrease in the number of K. variicola colonies formed in the early stages of treatment. As time progressed, the colonization K. variicola gradually increased, and the number of bacterial colonies appeared to reach an equilibrium with the external environment after 12 d. Application of the bacteria in neutral soil for 6 d produced the lowest level of colonization at 4.27 × 10⁵ cfu g⁻¹. The level of colonization subsequently gradually increased and reached 1.78 × 10⁹ cfu g⁻¹ on the 15th day. The types of species, as well as number of microorganisms and protozoa present in neutral soil, were more than those present in saline-alkali soil. This created a more intense competition and supplementary feeding effect of K. variicola in neutral soil than in saline-alkali soil, causing the colonization number to be reduced to 4.27 × 10⁵ cfu g⁻¹ in the early stages of application. As the nutrient content in neutral soil was more abundant than that in saline-alkali soil, which is beneficial to the reproduction of K. variicola, the colonization number of K. variicola increased rapidly after 6 d, and the final level of colonization exceeded that obtained in saline-alkali soil.

Effects of K. variicola on the rhizosphere soil of maize seedlings

Effects of K. variicola on organic matter content

The content of soil organic matter is closely related to soil fertility and is also the main source of soil nitrogen and phosphorus, which provides energy for crop growth and soil microbial life activities. The organic matter content in saline-alkali and neutral soils increased with increasing K. variicola concentration. As shown in Fig. 3A, while saline-alkali stress (CK) significantly decreased (P < 0.05) the organic matter content in the rhizosphere of maize seedlings, no significant change was observed in the organic matter content of the rhizosphere of seedlings treated with low concentrations of K. variicola (A1 and A2). Organic matter content increased significantly when high concentrations of K. variicola (A3 and A4) were applied (P < 0.05) and was 64.22% higher in A4 compared to that in CK. In neutral soil, the organic matter content in A1 was lower than that in CK, and significantly increased with the increase in K. variicola concentration (P < 0.05). The A4 treatment produced the most significant result, which was 49.12% higher than the CK treatment. Owing to the variety of growth-promoting characteristics and products of K. variicola, the microbial community structure in the soil was improved, thereby increasing the soil organic matter content. The rate of increase of organic matter content in saline-alkali soil was higher than that observed in neutral soil, possibly owing to poor soil nutrition in, and greater stress on, the rhizosphere microbial community in saline-alkali soils. The effect of saline-alkali stress on the rhizosphere microenvironment of maize seedlings was alleviated by applying K. variicola, and the rate of increase of organic matter content in the rhizosphere soil was higher in saline-alkali soil. The results showed that K. variicola significantly increased (P < 0.05) organic matter content in the rhizosphere soil of maize seedlings, especially in saline-alkali soil, and played an effective role in promoting the growth of maize seedlings in a saline-alkali environment.

Effects of K. variicola on the growth of maize seedlings

The results of the pot-based experiment showed that K. variicola could promote the growth of maize seedlings in neutral soil, as well as improve the saline-alkali tolerance of maize seedlings under saline-alkali stress conditions. In saline-alkaline soil environments, the plant height, root length, as well as aboveground and underground dry weights of maize seedlings were increased by 17.57%, 28.59%, 25%, and 31.48%, respectively, in saline-alkaline soil environments, and by 8.64%, 8.44%, 14.16% and 15.28%, respectively, in neutral soil environments (Table 1). K. variicola can therefore effectively promote the growth of maize seedlings, especially under saline-alkali stress conditions (Fig. 4).

Biological function of K. variicola

K. variicola can produce indole acetic acid, acetoin, ammonia, phosphorus, and potassium, as well as perform nitrogen fixation, indicating its potential as a type of plant growth-promoting bacteria. This study showed that K. variicola can produce indole acetic acid. Following the inoculation of K. variicola in liquid medium containing L-tryptophan for 3 d, the concentration of IAA reached 399.43 ± 11.56 mg L⁻¹. Related studies have shown that indole acetic acid is one of the important hormones that regulate growth and development processes in plant cells, such as cell enlargement and differentiation, organogenesis, and directional movement (Toscano et al., 2019; Ji, Gururani & Chun, 2014; Timmusk et al., 2014). During the interactions between plants and bacteria, indole acetic acid not only regulates the interaction between bacteria and plants (Duca et al., 2014), it increases plant resistance, and IAA signalling has also been reported to adjust to stomatal opening. Many phytopathogens use open stomata as gateways to enter into the plant, thus by limiting stomatal opening, pathogen entry is also encumbered (Duca et al., 2014). Also, plants with mutations in the IAA biosynthesis pathways have defects in lateral root, root hair and vascular tissue development. Many soil pathogens infect the plant through root tips and lateral root initials. Therefore, changes in plant root architecture or vascular tissue could restrict pathogen entry into the roots and colonization within the plant (Kazan & Manners, 2009; Tsavkelova, Cherdyntseva & Netrusov, 2005), IAA also can be used as a signal molecule improving the balance of indoleacetic indole-acetic acid in host plants by regulating the indoleacetic acid synthesis pathway (Mathesius, 2008; Than et al., 2019). With regards to the bacteria adapting to environmental stress, indole acetic acid can allow the bacteria to better adapt to external stress conditions (150 mmol NaCl) (Bianco et al., 2006; Spaepen, Vanderleyden & Remans, 2007). The ipdC gene in Pa. agglomerans pv. gypsophilae is strongly induced during plant colonization and it allows bacterial cells to colonize in the plant rhizosphere for a long time, in order to alleviate the harm caused by saline-alkali stress to crops. K. variicola was cultured in V-P selective medium for 48 h and then mixed with creatine chromogenic solution. The results showed that K. variicola produced 152.88 ± 13.56 mg L⁻¹ of acetoin. Acetoin is a recognized elicitor and has been proven to not only promote the growth of crops, but also to stimulate plant-induced resistance to infection by Pseudomonas aeruginosa in tomato. The research results show that, exogenous application of the B. subtilis derived elicitor, acetoin (3-hydroxy-2-butanone), was found to trigger induced systemic resistance (IsR) and protect plants against DC3000 pathogenesis (Rudrappa et al., 2010). In addition, K. variicola can produce large amounts of ammonia. Ammonia played an important role in inhibiting populations of the soybean cyst nematode and southern root-knot nematode. The results showed that ammonia induced the upregulation of 93 disease-resistant genes in soybean and increased the soybean yield by 9.62% (Mi, Marilyn & Ye, 2012). K. variicola grew well on nitrogen-free medium, confirming that K. variicola displayed nitrogen-fixing activity. The concentration of soluble nitrogen in the fermentation broth was determined by potassium persulfate oxidation-UV spectrophotometry. The results showed that the total amount of fixed nitrogen reached 15.7 mg L⁻¹ in the culture medium, and that nitrogen played an important role in the synthesis of DNA, RNA, protein, and chlorophyll in plants. However, the utilization rate of nitrogen in the agroecosystem was very low. The interaction between non-symbiotic nitrogen-fixing bacteria and plants can provide the latter with available nitrogen as nutrition, and thus, increase plant vegetative growth and increase yield (Elkoca, Kantar & Sahin, 2007; Hayat et al., 2010). Phosphorus is also one of a large number of elements needed for plant growth. K. variicola can degrade inorganic phosphorus and convert insoluble phosphorus in soil, such as phosphate bound with calcium, into a useable form to supply host plants. As for the mechanism of phosphorolysis, there are mainly the following statements. The polysaccharides produced by phosphodiophores and small molecular organic acids can produce acid hydrolysis and complexation to minerals to release phosphate. The secondary metabolites can lead to the change of the microenvironment around mineral particles. Phosphorolytic bacteria can also break the dynamic balance of mineral dissolution and crystallization through the active absorption of K+, thus promoting the release of P and K surrounded by the lattice (Wang, Yuan & Zhao, 2010). Studies have shown that K. variicola possesses a variety of biological functions to promote crop growth and is able to extensively colonize the rhizosphere soil of maize seedlings.

Effect of K. variicola on soil nutrient content in the rhizosphere of Maize seedlings

Soil organic matter is an important component of the soil, as well as the main source of various nutrient elements in the soil. It can also adsorb cations in the soil, so that the soil has a certain buffer (Xiang et al., 2020). The content of available nutrients in soil can reflect the short-term supply and release efficiency of soil nutrients. The present study found that the application of K. variicola in saline-alkali and neutral soils effectively improved soil nutrition, especially in saline-alkali soil, where the rate of increase was significantly higher than that in neutral soil. Following the application of K. variicola in saline-alkali environments, the organic matter, alkali-hydrolysable nitrogen, available phosphorus, and available potassium increased by 64.22%, 117.39%, 175.64%, and 28.63%, respectively. There was a notable increase in alkali-hydrolysable nitrogen and available phosphorus after the application of K. variicola, which was consistent with the results of nitrogen fixation and phosphorus dissolution assays with K. variicola. The main mechanism of phosphorus-soluble microorganisms is to dissolve insoluble phosphate in soil (Peix, Rivas & Santaregina, 2004). Phosphorus-soluble microorganisms can secrete a lot of organic acids, reduce the pH of their culture medium or soil, and then dissolve phosphate. The results of 4 strains of lysophotic bacteria screened from soybean rhizome showed that strains WJ1, WJ3, WJ5 and WJ6 could secrete a variety of acid substances during their fermentation, among which strains WJ1, WJ3 and WJ6 could produce large amounts of secondary product-ketoglutaric acid (Yang, Wang & Wu, 2016).

Effect of K. variicola on soil enzyme activity in rhizosphere of Maize seedlings

In addition, the results showed that soil enzyme activity in the rhizosphere was significantly altered following the application of K. variicola, and that soil enzyme activity played a major role in the transformation and cycling of soil nutrients (Hiradate et al., 2005; Jin et al., 2015). They have important effects on energy transfer, environmental quality, and crop yield (Dick, 1994; Tabatabai, 1994). Soil enzyme activity is greatly influenced by soil organic matter content, which is often used as an indicator to characterize microbial activity and soil fertility (Dick & Tabatabai, 1992; Kumar, Manigundan & Amaresan, 1992). Previous studies have also shown that inoculation of plant growth-promoting bacteria could improve the soil enzyme activity. Some research results showed that inoculation of GM bacteria significantly increased the urease and sucrase activities in upland rice rhizosphere soil (Luo et al., 2015). Other research results show that inoculation strains Glomus Mosseae and Glomus Etunicatum increased the polyphenol oxidase activity of clover rhizosphere soil by 19.6%∼72.0% and 29.7%∼90.6%, respectively, and catalase activity by 3.3%∼12.2% and 7.8%∼34.7%, respectively, indicating an overall increasing trend of acid phosphatase activity (Xiao et al., 2009). The results of this study indicate that saline-alkali stress significantly inhibited the activities of four enzymes in soil; however, these activities gradually increased with increasing concentrations of applied K. variicola. The optimum application concentration of K. variicola varied for different types of enzymes. At the optimum application rate, alkaline phosphatase activity, sucrase activity, urease activity, and catalase activity increased by 146.08%, 76.77%, 86.60%, and 45.29%, respectively and effectively improved the enzyme activity of maize seedling rhizosphere soil under saline-alkali stress.

Outlook

In this study, the three-leaf single heart stage, which is the most sensitive to saline-alkali stress in the growth cycle of maize, was taken as the research object. In the future, we will continue to study the effects of K. variicola on maize rhizosphere soil at other growth stages. In the future, in-depth studies will be carried out at the molecular level, and combined with transcriptome and metabonomic data, and the effects of Klebsiella variicola on maize root metabolism genes and root exudates will be analysed and studied comprehensively on the microenvironment of maize root, root gene expression and interaction mechanisms of root exudates. In addition, this study takes the untreated bacterial liquid as the experimental material, which has higher requirements for the storage conditions of bacteria in agricultural production. In future studies, we intend to develop a protective agent suitable for this strain, to enhance the feasibility of application and distribution.