Mixed bacteria for promoting nodulation and nitrogen fixation of Robinia pseudoacacia and application thereof

Abstract

A mixed bacteria for promoting nodulation and nitrogen fixation of Robinia pseudoacacia and their application are provided. The mixed bacteria includes Kocuria sp. X-22, Microbacterium sp. X-26, and Bacillus sp. X-28, all of which have been preserved in China Center for Type Culture Collection, and the preservation numbers respectively are: CCTCC No: M 2019237; CCTCC No: M 2019238; CCTCC No: M 2019239. The mixed bacteria are watered directly around the seedlings of Robinia pseudoacacia. Compared with the single bacteria control group and the sterile control group, the disclosure can produce synergistic superimposing effects, significantly improve the nodulation rate and symbiotic nitrogen fixation of the Robinia pseudoacacia, and promote the photosynthesis of the Robinia pseudoacacia.

Claims

1. A method for promoting nodulation and nitrogen fixation of Robinia pseudoacacia Robinia pseudoacacia comprising a step of adding a mixed bacteria to a Robinia pseudoacacia seedling, wherein the mixed bacteria comprises Kocuria sp. X-22, Microbacterium sp. X-26, and Bacillus sp. X-28; and wherein the Kocuria sp. X-22 is preserved in China Center for Type Culture Collection with a preservation date of Apr. 8, 2019 and a preservation number of CCTCC No: M 2019237; the preservation address is Wuhan University, Wuhan, China; the Microbacterium sp. X-26 is preserved in China Center for Type Culture Collection with a preservation date of Apr. 8, 2019 and a preservation number of CCTCC No: M 2019238; the preservation address is Wuhan University, Wuhan, China; and the Bacillus sp. X-28 is preserved in China Center for Type Culture Collection with a preservation date of Apr. 8, 2019 and the preservation number of CCTCC No: M 2019239; the preservation address is Wuhan University, Wuhan, China.

2. The method according to claim 1, wherein the mixed bacteria are respectively prepared into fermentation broths, and the respective fermentation broths are diluted and mixed and directly watered on the rhizosphere soil of Robinia pseudoacacia seedlings.

3. The method according to claim 2, wherein a preparation method of the fermentation broth comprises: A) preparing strains of Kocuria sp. X-22, Microbacterium sp. X-26, and Bacillus sp. X-28, and activating the prepared strains on a nutrient agar solid medium at 35? C. for 24 hours; B) picking up a loop of bacterial paste of the activated Microbacterium sp. X-26 and Bacillus sp. X-28 strains with an inoculation loop, adding the bacterial paste to an Luria-Bertani (LB) liquid medium respectively, inoculating Kocuria sp. X-22 into a Nutrient Agar (NA) liquid medium, and shaking the medium under a constant temperature of 35? C. with a frequency of 200_r/min for 24 hours to prepare a seed solution; C) taking the seed solution with 3% of the inoculum amount, inoculating the taken seed solution into liquid medium, and culturing with shaking under a temperature of 35? C. with a frequency of 200 r/min for 36 hours to obtain the fermentation broth; and D) diluting the fermentation broth obtained in step C with sterile water and then mixing in an equal volume for use.

4. The method according to application of claim 3, wherein the liquid medium in step C consists of 10 g peptone, 3 g yeast powder, 5 g sodium chloride, and 1000 mL sterile water, with a pH of 5.6.

5. A method for promoting growth of Robinia pseudoacacia comprising a step of adding a mixed bacteria to a Robinia pseudoacacia seedling, wherein the mixed bacteria comprises Kocuria sp. X-22, Microbocterium sp. X-26, and Bacillus sp. X-28; wherein the Kocuria sp. X-22 is preserved in China Center for Type Culture Collection with a preservation date of Apr. 8, 2019 and a preservation number of CCTCC No: M 2019237; the preservation address is Wuhan University, Wuhan, China; the Microbacterium sp. X-26 is preserved in China Center for Type Culture Collection with a preservation date of Apr. 8, 2019 and a preservation number of CCTCC No: M 2019238; the preservation address is Wuhan University, Wuhan, China; and the Bacillus sp. X-28 is preserved in China Center for Type Culture Collection with a preservation date of Apr. 8, 2019 and the preservation number of CCTCC No: M 2019239; the preservation address is Wuhan University, Wuhan, China.

6. The method according to claim 5, wherein the mixed bacteria are respectively prepared into fermentation broths, and the respective fermentation broths are diluted and mixed and directly watered on the rhizosphere soil of Robinia pseudoacacia seedlings.

7. The method according to claim 6, wherein a preparation method of fermentation broth comprises: A) preparing strains of Kocuria sp. X-22, Microbacterium sp. X-26, and Bacillus sp. X-28, and activating the prepared strains on a nutrient agar solid medium at 35? C. for 24 hours; B) picking up a loop of bacterial paste of the activated Microbacterium sp. X-26 and Bacillus sp. X-28 strains with an inoculation loop, adding the bacterial paste to an Luria-Bertani (LB) liquid medium respectively, inoculating the Kocuria sp. X-22 into a Nutrient Agar (NA) liquid medium, and shaking the medium under a constant temperature of 35? C. with a frequency of 200 r/min, for 24 hours to prepare a seed solution; C) taking the seed solution with 3% of the inoculum amount, inoculating the seed solution into liquid medium, and culturing with shaking under a temperature of 35? C. with a frequency of 200 r/min, for 36 hours to obtain the fermentation broth; and D) diluting the fermentation broth obtained in step C with sterile water, and then mixing in an equal volume for use.

8. The method according to application of claim 7, wherein the liquid medium in step C consists of 10 g peptone, 3 g yeast powder, 5 g sodium chloride, and 1000 mL sterile water, with a pH of 5.6.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a diagram of the colonies of Kocuria sp. X-22, Microbacterium sp. X-26, and Bacillus sp. X-28 on a nutrient agar solid medium; in the figure, A: Kocuria sp. X-22; B: Microbacterium sp. X-26; C: Bacillus sp. X-28.

DETAILED DESCRIPTION OF EMBODIMENTS

(2) The present disclosure will be further described below in conjunction with specific embodiments, but these embodiments are not used to limit the present disclosure. The methods used in the following embodiments are conventional methods unless otherwise specified.

Embodiment 1

(3) 1) Acquisition and Identification of Strain

(4) Soil samples were collected from the 5 cm rhizosphere soil on the slopes on both sides of Yueyang Avenue in Yueyang City. The dilution coating plate method is adopted. In a 35? C. incubator, it was cultured on a nutrient agar solid medium (NA medium: peptone 10 g; beef powder 3 g; sodium chloride 5 g; agar 15 g; sterile water 1000 mL) for 2 to 3 days. Different colonies were picked out by naked eye observation, and several different species of single colonies were obtained through repeated streaking and purification.

(5) A single colony was selected and made into a plate, and was sent to Shanghai Jinyu Medical Laboratory for sequencing, and the 16S rDNA gene sequence was obtained, as shown in SEQ ID NO. 1. The detected 16S rDNA gene sequence was BLAST aligned with the sequence in the GenBank database. The results showed that the similarity between this strain and Kocuria polaris was 99.32%. The morphological characteristics and 16S rDNA gene sequence were combined and analyzed, and it was identified as Kocuria sp. X-22.

(6) Another single colony was selected and made into a plate, and was sent to Shanghai Jinyu Medical Laboratory for sequencing, and the 16S rDNA gene sequence was obtained, as shown in SEQ ID NO. 2. The detected 16S rDNA gene sequence was BLAST aligned with the sequence in the GenBank database. The results showed that the similarity between this strain and Microbacterium arabinogalactanolyticum was 98.91%. The morphological characteristics and 16S rDNA gene sequence were combined and analyzed, and it was identified as Microbacterium sp. X-26.

(7) Still another single colony was selected and made into a plate, and was sent to Shanghai Jinyu Medical Laboratory for sequencing, and the 16S rDNA gene sequence was obtained, as shown in SEQ ID NO. 3. The detected 16S rDNA gene sequence was BLAST aligned with the sequence in the GenBank database. The results showed that the similarity between this strain and Bacillus megaterium was 99.70%. The morphological characteristics and 16S rDNA gene sequence were combined and analyzed, and it was identified as Bacillus sp. X-28.

(8) 2) The physiological and biochemical results of Kocuria sp. X-22, Microbacterium sp. X-26, and Bacillus sp. X-28 are shown in Table 1, and the colony diagram is shown in FIG. 1.

(9) TABLE-US-00001 TABLE 1 Physiological and biochemical results of strains X-22 X-26 X-28 Glucose fermentation + No bubbles + No bubbles + No bubbles Lactose fermentation + No bubbles ? No bubbles + No bubbles Starch hydrolysis ? ? + Indole test ? ? + Methyl red (MR) test + + + V.P. test ? ? ? Citrate test + ? ? Hydrogen sulfide test ? ? ? Gram stain + + + Colony morphology coccus bacillus bacillus

Embodiment 2

(10) 1. Cultivation of Robinia pseudoacacia

(11) The cultivation of the Robinia pseudoacacia seedlings was carried out in a greenhouse at the Baima Teaching Base of Nanjing Forestry University, with an air humidity of 65%, a CO.sub.2 concentration of 450 ppm and a maximum photosynthetic active radiation of 1850 ?mol/(m.sup.2.Math.s). The light intensity and time for each potted plant are ensured to be consistent every day. In order to prevent the roots of Robinia pseudoacacia from being rotted due to too frequent watering, the weighing method is used to add water every time to ensure that the soil water content of each pot reaches 100% of the field water holding capacity. 1) Seed soaking: The sieved black locust seeds were soaked in hot water at 60? C. (seed: water=1:3), and after natural cooling for 24 hours, the expanded seeds were selected for germination, and the remaining seeds were soaked in hot water at 80? C. The ratio is the same as above. After natural cooling for 24 hours, the expanded seeds were selected for germination. Soaking seeds in batches by successively increasing the temperature could save seeds and ensure the neat emergence of seedlings. When soaking the seeds, the cold water was changed every 12 hours to remove impurities in the water. 2) Germination: The stratification method of germination was adopted. The expanded seeds were mixed with 3 times the wet sand (being disperse once the hands are loose). To ensure the humidity of the sand, the surface of the sand was covered with a plastic wrap with some holes, and a thermometer was inserted into the sand. The sand was placed in a dark place. Germination lasted for 3?4 days, and the temperature was kept at about 20? C. 3) Into pot and thinning: The treated substrate was mixed into a pot, and seedlings with a bud length of 1 cm or more were planted. Five plants were planted in each pot, and 3 parallel treatments were set up for each treatment. After 4 weeks of growth, the seedlings were thinned, leaving 3 seedlings of the same growth in each pot.
2. Preparation of Fermentation Broth: 1) Strains of Kocuria sp. X-22, Microbacterium sp. X-26, and Bacillus sp. X-28 were taken, and the taken strains were activated on a nutrient agar solid medium at 35? C. for 24 hours; 2) A loop of bacterial paste of the activated Microbacterium sp. X-26 and Bacillus sp. X-28 strains was picked up with an inoculation loop and added to the LB liquid medium respectively, and Kocuria sp. X-22 was inoculated into NA liquid medium. The mediums were shaken at a constant temperature of 35? C., at a frequency of 200 r/min, for 24 hours to prepare a seed solution; 3) The seed solution was taken with 3% of the inoculum amount and was inoculated into liquid medium (10 g peptone, 3 g yeast powder, 5 g sodium chloride, and 1000 mL sterile water, pH 5.6). The seed solution was cultured with shaking at a temperature of 35? C., at a frequency of 200 r/min, until the OD.sub.560 was 0.8-1.2 hours (about for 36 hours) to obtain the fermentation broth; 4) Before use, the fermentation broth obtained in step 3) was diluted with sterile water by 100 times, and then mixed in an equal volume for use.
3. Pot Experiment

(12) Single bacteria control group (the fermentation broth dilutions of X-22, X-26, and X-28 were taken 60 mL respectively), blank control group (sterile liquid fermentation medium) and mixed bacteria group (a total of 60 mL of bacteria liquid was taken from the three fermentation bacteria broth dilutions, each 20 mL) is set. By irrigating the rhizosphere soil, the five groups were respectively added around the planted Robinia pseudoacacia seedlings (the first 1-4 weeks was the thinning period when no bacteria were applied, and the next 5-16 weeks is the bacteria cultivation observation period).

(13) Three parallels were set for each treatment.

(14) Potted plants were observed and counted for one quarter. At the 8th week, the plants were carefully dug out, the soil at the roots of the Robinia pseudoacacia was simply cleaned up, and the number of nodules was recorded, and then the plants were replanted into the pots. At the 16th week, the nodules were counted for the last time, and the number and weight of nodules were counted and record. The results are shown in Table 2.

(15) TABLE-US-00002 TABLE 2 Results of Nodule Number, Nodule Weight and Root Dry Weight Nodule Number (Pcs/plant) Processing 8th 12th 16th Nodule Weight Root Dry method week week week (g/Pcs) Weight (g) Mixed 0 3 7 0.0076 ? 0.001 0.57 ? 0.14 bacteria X-22 0 0 0 0.30 ? 0.11 X-26 0 0 0 0.29 ? 0.07 X-28 0 1 2 0.0061 ? 0.001 0.35 ? 0.10 CK 0 0 0 0.23 ? 0.05

(16) It can be seen from Table 2 that the nodules formed first in the mixed bacteria group, about between the 8th week and the 12th week, and 7 nodules had been formed by the last sampling, with a large number. Compared with the blank control group, nodule number and nodule weight of Robinia pseudoacacia were significantly increased after the mixture of three bacteria was applied, and the root dry weight of Robinia pseudoacacia treated with it also increased significantly, with an average increase of 147.83% relative to the blank control group. It can be seen that the mixed bacteria can promote the nodulation and nitrogen fixation of Robinia pseudoacacia and accelerate the growth and development of its roots. It is a very promising model for the configuration of promoting strains for Robinia pseudoacacia.

(17) 4. Promoting Experiment

(18) According to the above method, the activated bacteria liquid is mixed and added to the surrounding of the planted Robinia pseudoacacia seedlings. After the first thinning, the ground diameter of the Robinia pseudoacacia seedlings was measured every 30 days using a vernier caliper. The seedling height of the seedlings was measured using a tape measure. On the termination day, a total of 10 upper, middle and lower leaves were selected from each pot, and the leaf areas were measured with a root scanner. The results are shown in Table 3.

(19) TABLE-US-00003 TABLE 3 Promoting results ground seedling Processing diameter height leaf area method (mm) (cm) (cm.sup.2) Mixed 6.50 ? 0.89 51.93 ? 3.74 52.98 ? 2.69 bacteria X-22 4.63 ? 0.34 44.70 ? 5.30 40.42 ? 3.23 X-26 4.81 ? 0.33 40.57 ? 4.44 45.86 ? 3.54 X-28 5.17 ? 0.43 41.13 ? 4.97 41.50 ? 2.58 CK 4.75 ? 0.38 40.04 ? 5.76 43.53 ? 2.21

(20) The ground diameter is used to indicate the size of the trees, and the growing plants generally have a larger ground diameter. It can be seen from Table 3 that the ground diameter of the Robinia pseudoacacia seedlings treated with X-22 was lower than that of the sterile seedlings, and the ground diameter of other treatments were all higher than that of the sterile seedlings. The ground diameter of seedlings treated with mixed bacteria was significantly higher than that of sterile seedlings, increasing by 36.84% (P<0.05).

(21) Seedling height is one of the most basic indicators of plant morphology, which can directly reflect the growth status of vegetation. In general, the seedling height of plants that grow well is relatively high. It can be seen from Table 3 that the height of the seedlings treated with various soil bacteria was higher than that of the sterile seedlings, the average seedling height was 44.58 cm, and the average increase was 11.34%. The height of the seedlings treated with the mixed bacteria was significantly higher than that of sterile seedlings, increasing by 29.7% (P<0.05).

(22) Leaf area is one of the indicators most closely related to yield. The increase in plant yield can be directly reflected by leaf area. In general, a proper size of leaf area can make full use of light conditions without affecting photosynthesis. It can be seen from Table 3 that the leaf areas of the seedlings treated with X-22 and X-28 were lower than that of the sterile seedlings. The average leaf area is 45.19 mm2, and the average increase is 3.81%. The leaf area of seedlings treated with the mixed bacteria was significantly higher than that of sterile seedlings, increasing by 21.71% (P<0.05).