Bacillus subtilis and application thereof in greenhouse soil remediation
A technology of Bacillus subtilis and greenhouses, applied in application, soil conditioning materials, bacteria, etc., can solve problems that have not been reported before, and achieve the effects of strong growth and reproduction, improved soil, improved and activated soil
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Embodiment 1
[0029] Example 1: Isolation, screening and identification of Bacillus Subtilis XHS0035KcCGMCCNO.9434
[0030] 1. Isolation and screening of strains
[0031] (1) Separation
[0032] The Bacillus subtilis used in the present invention is sampled and separated from the typical greenhouse soil with severe salinization, soil desertification or compaction in Korla, southern Xinjiang, and is initially screened out according to the analysis of the antagonism mechanism of the strains to the greenhouse soil. A strain with a certain antagonistic ability to soil problems such as salinization and soil compaction. Use the traditional plate culture method to isolate the microorganisms in the soil layer, purify the strains by the plate streak method, and use different culture temperatures, pH values, and medium as enrichment conditions to screen out a batch of well-growing microbial strains, and select one of them The strain whose serial number is XHS0035Kc.
[0033] Separation steps: acco...
Embodiment 2
[0040] Embodiment 2: the growth factor of Bacillus subtilis (Bacillus Subtilis) XHS0035KcCGMCCNO.9434
[0042] Gram staining generally includes four steps: primary staining, mordant staining, decolorization, and counterstaining. The specific operation method is:
[0043] (1) Slides are fixed. Under sterile operating conditions, use an inoculation loop to pick a small amount of strain XHS0035Kc, spread it evenly on a clean glass slide, and heat it on a flame to kill the bacteria and make it adhere and fix.
[0044] (2) Ammonium oxalate crystal violet staining for 1 minute.
[0045] (3) Rinse with tap water to remove floating color.
[0046] (4) Mordant with iodine-potassium iodide solution for 1 minute, pour off excess solution.
[0047] (5) Decolorize with a neutral decolorizing agent such as ethanol (95%) or pyruvic acid for 30 seconds, the Gram-positive bacteria will not be faded but will be purple, and the Gram-negative bacteria will be colorle...
Embodiment 3
[0084] Example Three: Molecular Level of Bacillus Subtilis XHS0035KcCGMCCNO.9434
[0085] 1. PCR amplification of the 16SrDNA sequence of Bacillus subtilis and its sequencing
[0086] Pick a small amount of single colonies of the XHS0035Kc strain, put them into an EP tube filled with 25 μL of sterile water, boil at 100°C for 8-10 minutes, and then quickly put them into the ice-water mixture for 5 minutes. Centrifuge at 10000r / min for 5min, store at 4°C, and take the supernatant when used.
[0087] Determination of 16SrDNA gene sequence and construction of phylogenetic tree: Extract the total DNA of the strain according to conventional methods, dilute the universal primers with deionized water, and perform PCR amplification. The primers are designed as follows:
[0088] 27f:AGAGTTTGATCCTGGCTCAG
[0089] 1492r:TACGGCTACCTTGTTACGACTT
[0090] Determination of 16SrRNA gene sequence and construction of phylogenetic tree: extract the total DNA of bacterial strains according to co...
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