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A plant growth-promoting strain xn-k13 and its application

A plant pathogenic bacteria, a technology for promoting plant growth, applied in the directions of plant growth regulators, plant growth regulators, applications, etc., can solve problems such as reduced utilization rate, and achieve the effects of promoting growth and development, increasing the content of available potassium, and promoting plant growth

Active Publication Date: 2022-05-10
GUANGXI UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] Chemical fertilizers play a huge role in modern agricultural production, but with the increase in the use of chemical fertilizers, their utilization rate decreases year by year

Method used

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  • A plant growth-promoting strain xn-k13 and its application
  • A plant growth-promoting strain xn-k13 and its application
  • A plant growth-promoting strain xn-k13 and its application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] Isolation and identification of plant growth promoting strain xn-k13

[0038] 1.1 isolation of plant growth promoting strain xn-k13

[0039] The separation of plant growth promoting strain xn-k13 includes three steps: sampling, enrichment, preliminary screening and re screening, as follows:

[0040] 1.1.1 sampling

[0041] Take samples from the soil of Guangxi Medicinal Botanical Garden (E108 ° 19 ', N22 ° 51'), put them into clean sampling bags, mark them, and store them in a 4 ℃ refrigerator as rhizosphere soil samples.

[0042] Primary screening and enrichment

[0043] Weigh 1.0g rhizosphere soil sample, put it into a test tube containing 9ml sterile deionized water, fully shake and mix, 37 ℃, 200R / min, shake and culture for 30min, and dilute it according to ten step gradient to obtain the diluent; In order to isolate salt tolerant bacteria, 10g / L NaCl was added as salt stress, 100ul diluent was absorbed and coated on beef extract peptone solid medium containing 10g ...

Embodiment 2

[0062] Accurate characterization of potassium hydrolysis by plant growth promoting strain xn-k13:

[0063] The solubilization ability of Enterobacter ludwigii xn-k13 to insoluble potassium was preliminarily evaluated through the improved potassium solubilizing bacteria selection medium: the strain isolated and purified from 1.1.3 was pricked in the center of the improved potassium solubilizing bacteria selection medium containing potassium feldspar as insoluble potassium source with a sterile toothpick, and cultured in a 37 ℃ incubator for 5 days, with three repetitions in each group, Observe the occurrence of potassium dissolving circle, measure the diameter of colony (d) and potassium dissolving circle (d), and the results are shown in Table 2. Calculate the ratio of potassium dissolving circle to colony diameter( Figure 4 ); From table 2 and Figure 4 It can be concluded that the ratio of potassium dissolving circle to colony diameter of environmental stress resistant strain xn-...

Embodiment 3

[0067] Quantitative analysis of potassium hydrolysis of plant growth promoting strain xn-k13:

[0068] Potassium standard solution: accurately weigh 1.9068g of dried (dried at 105 ℃ for 4-6 hours) analytical pure KCl, dissolve it in 200ml deionized water, fix the volume to 1L, shake well to obtain 1000mg / L potassium, suck the above solution into a 25ml to 250ml volumetric flask, fix the volume and shake well to obtain 100mg / L potassium standard solution.

[0069] 3% sodium tetraphenylborate solution: weigh 3G sodium tetraphenylborate and dissolve it in 100ml deionized water. Add 10 drops of 0.2mol / l sodium hydroxide solution to adjust the pH to 8-9. After standing overnight, filter it with dense filter paper and store it in a brown bottle.

[0070] 0.05mol / l borax solution: weigh 19.07g borax and dissolve it in 1000ml deionized water.

[0071] Formaldehyde EDTA solution: weigh 2.5G disodium EDTA salt and dissolve it in 20ml 0.05mol / l borax solution, add 80ml 37% formaldehyde, ...

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Abstract

The invention discloses a plant growth-promoting bacterial strain XN-K13, which is classified as Enterobacter ludwigil XN-K13, and was preserved in the China Type Culture Collection Center on May 25, 2020, with an address of China Luojia Mountain, Wuchang, Wuhan City, Hubei Province, the preservation number is CCTCC NO: M 2020145. The plant growth-promoting bacterial strain XN-K13 provided by the present invention can synthesize plant growth hormone indole acetic acid (IAA) as a precursor by tryptophan, because it is adsorbed on the surface of seeds and roots, it can be directly used by plants, and it may also be used by plants The endogenous IAAs work together to stimulate the growth and proliferation of plant cells, thereby promoting the growth and development of plant roots, effectively absorbing water and nutrients in the soil, and participating in the regulation of other life activities in plants.

Description

technical field [0001] The invention belongs to the technical field of plant growth promoting bacteria, in particular to a plant growth promoting strain xn-k13 for dissolving insoluble potassium and its application. Background technology [0002] Chemical fertilizer plays a great role in modern agricultural production, but with the increase of chemical fertilizer use, its utilization rate decreases year by year. Pesticide and chemical fertilizer residues release a large number of harmful substances to the environment, pollute soil, water and food, and pose a great threat to human health and living environment. The voice for protecting the ecological environment and producing safe food is becoming stronger and stronger. Therefore, it is urgent to develop and utilize new fertilizer sources instead of chemical fertilizers to meet the needs of developing green agriculture and green food. Microbial fertilizer can make the ineffective nutrition in the soil effective, prevent and contro...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12N1/20A01N63/20A01P21/00C05G3/00C05G3/40C05G3/80C12R1/01
CPCA01N63/20C05G3/00C05G3/40C05G3/80C12R2001/01C12N1/205
Inventor 李有志樊宪伟黄巧
Owner GUANGXI UNIV