A compound soil remediation agent and its application in greenhouse soil remediation

A soil remediation and greenhouse technology, applied in the restoration of contaminated soil, methods based on microorganisms, fungi, etc., can solve problems that have not been reported

Active Publication Date: 2018-09-28
新疆惠森生物技术有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although there are many reports on the study of the effects of organic materials on soil properties and crop yields in the field, the isolation and screening of strains that can improve greenhouse soil from greenhouse soil, and the use of self-selection to screen domesticated subtilis spores Bacillus, Geotrichum candidum, Streptomyces flavinus and other strains have not been reported in the preparation of soil remediation agents based on the compatibility, applicability and safety of the strains and the characteristics of the strains to improve the soil in greenhouses.

Method used

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  • A compound soil remediation agent and its application in greenhouse soil remediation
  • A compound soil remediation agent and its application in greenhouse soil remediation
  • A compound soil remediation agent and its application in greenhouse soil remediation

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] Example 1: Molecular level of Bacillus Subtilis (Bacillus Subtilis) XHS0035Kc CGMCC NO.9434

[0036] 1. PCR amplification of the 16S rDNA sequence of Bacillus subtilis and its sequencing

[0037] 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.

[0038] Determination of 16S rDNA gene sequence and construction of phylogenetic tree: Extract the total DNA of the strain according to conventional methods, dilute the universal primer with deionized water, and perform PCR amplification. The primer design is as follows:

[0039] 27f:AGAGTTTGATCCTGGCTCAG

[0040] 1492r:TACGGCTACCTTGTTACGACTT

[0041] Determination of 16S rRNA gene sequence and construction of phylogenetic tree: extract the total DNA of bacterial strains...

Embodiment 2

[0044] Example 2: Molecular level of Geotrichum Candidum XHS0030B CGMCC NO.9435

[0045] 1. PCR amplification of the ITS rDNA sequence of Geotrichum candidum and its sequencing

[0046] Pick a small amount of single colonies of the XHS0030B 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.

[0047] ITS rDNA gene sequence determination and the construction of phylogenetic tree thereof: extract the total DNA of bacterial strain according to routine method, carry out the PCR amplification of ITS rDNA segment with deionized water with the dilution universal primer ITS1 and ITS4, primer design is as follows:

[0048] ITS1(F): 5'-TCCGTAGGTGAACCTGCGG-3'

[0049] ITS4(R): 5'-TCCTCCGCTTATTGATATGC-3'

[0050] The 50 μl reaction system contains: 5 μl of 10×PCR buffer, 20 pmol of each ...

Embodiment 3

[0053] Example 3: Molecular level of Streptomyces microflavus XHS0032Xh CGMCC NO.9432

[0054] 1. PCR amplification of the 16S rDNA sequence of Streptomyces flavinus and its sequencing

[0055] Pick a small amount of single colonies of the XHS0032Xh 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.

[0056] Determination of 16S rDNA gene sequence and construction of phylogenetic tree: Extract the total DNA of the strain according to conventional methods, dilute the universal primer with deionized water, and perform PCR amplification. The primer design is as follows:

[0057] 27f:AGAGTTTGATCCTGGCTCAG

[0058] 1492r:TACGGCTACCTTGTTACGACTT

[0059] Determination of 16S rRNA gene sequence and construction of phylogenetic tree: extract the total DNA of the strain according to co...

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PUM

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Abstract

The invention discloses a complex soil remediation agent and application thereof to remedying greenhouse soil. Bacillus subtillis XHS0035Kc with a number of CGMCC NO.9434, geotrichum candidum XHS0030B with a number of CGMCC NO.9435 and streptomyces microflavus XHSOO32Xh with a number of CGMCC NO.9432 are obtained by means of separating and screening and are mixed with 20%-25% of rhodopseudomonas palustris according to proportions of 20%-25%, 15%-20% and 30%-35%, and strain mixed liquid is sufficiently adsorbed in carriers and is mixed with accessories, so that the complex soil remediation agent can be prepared by means of fermentation. The complex soil remediation agent and the application have the advantage that outstanding technical effects can be realized by the complex soil remediation agent for remedying the greenhouse soil.

Description

technical field [0001] The invention relates to the technical field of application of agricultural microorganisms, in particular to the technical field of self-selected and screened strains to prepare composite soil remediation agents and their application in greenhouse soil remediation. Background technique [0002] With the continuous development of facility agriculture, more and more chemical fertilizers, pesticides and other chemical substances are accumulated in the farmland, resulting in soil compaction and many diseases that directly affect the yield and quality of agricultural products. This problem has become an urgent problem for the planting industry to overcome. . At present, some domestic companies that deal with polluted soil mostly use physical and chemical methods for treatment. Among them, physical methods mostly use incineration and landfill to deal with pollutants, which are easy to damage the soil structure, and the treatment process is cumbersome and cos...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N1/20C12N1/14B09C1/10C12R1/125C12R1/645C12R1/465C12R1/01
Inventor 王心歌张松林韩友青苏玲
Owner 新疆惠森生物技术有限公司
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