Burkholderia multivorans WS FJ9 and application thereof to growth promotion of pine
A polyphagic Burkholderia and Holderia technology, applied in the field of microorganisms, to achieve the effect of promoting growth and development, significant differences, and excellent strain resources
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0025] The phosphorus solubilizing ability test of embodiment 1WS-FJ9 bacterial strain:
[0026] Phosphate Solubilizing Medium A: Glucose 10g, Ca 3 (PO 4 ) 2 5g, MgCl 2 5g, KCl 0.2g, MgSO 4 .7H 2 O0.25g, (NH 4 ) 2 SO 4 0.1g, distilled water 1000mL, pH 7.0.
[0027] Phospholytic medium B: with AlPO 4 Instead of Ca in phosphate-dissolving medium A 3 (PO 4 ) 2 , the other components and contents are the same.
[0028] Montkina organophosphate medium, used for the liquid culture of organophosphate-decomposing bacteria for the determination of phosphorus-dissolving ability: glucose 10g, (NH 4 ) 2 SO 4 0.5g, NaCl 0.3g, KCl 0.3g, CaCO 3 5g, MgSO 4 ·7H 2 O 0.3g, FeSO 4 ·7H 2 O 0.03g, MnSO 4 4H 2 O 0.03g, lecithin 0.2g, distilled water 1000mL, pH7.0~7.5.
[0029] Inoculate the activated WS-FJ9 strain into NB medium (3g of beef extract, 10g of peptone, 5g of sodium chloride, 1000mL of distilled water, pH 7.2-7.4), shake culture at 30°C for 18-24h to make seed...
Embodiment 2
[0032]Example 2 WS-FJ9 bacterial strain optimum phosphorus solubilizing condition test:
[0033] After WS-FJ9 is activated, inoculate into NB medium (3g of beef extract, 10g of peptone, 5g of sodium chloride, 1000mL of distilled water, pH 7.2-7.4), shake culture at 30°C for 18-24h to make seed liquid, and take 0.5mL of seed solution were respectively inoculated in 100mL Erlenmeyer flasks equipped with 50mL of NBRIP (Phosphate Growth Medium of the International Botanical Research Institute, formulated with phosphate-dissolving medium A) as the basic medium, and the carbon source of the NBRIP medium was respectively set to sucrose, fructose , maltose, lactose, and mannitol; the nitrogen source was set to peptone, beef extract, potassium nitrate, ammonium nitrate, and calcium nitrate, respectively, and the phosphorus-solubilizing medium connected with the same volume of blank seed solution was used as the control (CK), and each treatment had 3 Repeat, 30°C, 180r / min shaking cultu...
Embodiment 3
[0034] Embodiment 3WS-FJ9 bacterial strain greenhouse pot test:
[0035] After WS-FJ9 was activated, a small amount of bacterial cells were picked with an inoculation loop and inoculated into a 100 mL Erlenmeyer flask containing 50 mL of NB medium (the formula is the same as that in Example 1), and cultured at 29°C and 180 r / min for 72 hours with shaking. Centrifuge the fermentation broth (4°C, 6000r / min) for 5min, rinse the bacteria with sterile normal saline for 2 to 3 times, then adjust the bacterial suspension with sterile normal saline (7~8×10 8 cfu / mL) to make WS-FJ9 bacterial agent. Pine slash seedlings (120 days old) were inoculated, and the same amount of sterile saline was used as the control (CK), and the inoculation volume was 15 mL / plant. 20 replicates per treatment were placed in the greenhouse for unified management, the light was 12h / d, and watering was timely.
[0036] The growth situation of slash pine seedlings inoculated 180d, the results are shown in Tab...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com