A kind of rhizobia yzm0144 and its application
A rhizobia, M2018217 technology, applied to rhizobia YZM0144 and its application fields, to achieve strong nitrogen fixation ability, increase total nitrogen content, and high nodulation rate
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Embodiment 1
[0022] Example 1 Isolation and purification of rhizobia YZM0144
[0023] (1) During the flowering period of normal peanut growth, take fresh whole peanut roots, take fresh, mature and large nodules of peanuts from the roots, rinse them with water, and dry the surface water with filter paper.
[0024] (2) Put it into ethanol with a volume fraction of 95% for 3 to 5 minutes, take it out and wash it with sterile water for 5 to 6 times, and then put it in 1g / L HgCl 2 Sterilize for 3-5 minutes, take it out and rinse with sterile water 5-6 times.
[0025] (3) Cut in half on a flame-sterilized glass slide, hold half of the tumor with sterile tweezers, make the incision face the surface of YMA (Table 1) culture medium, and incubate at 28°C after inversion.
[0026] (4) After the bacteria grow, use a sterilized toothpick to scrape a small amount of rhizobia colonies from the plate, dilute them with sterile water, and culture them on the plate again. Observe the colonies after 3 days ...
Embodiment 2
[0033] Example 2 of Rhizobium YZM0144 16s rDNA sequence sequencing
[0034] Perform PCR specific amplification on rhizobia monoclonal liquid, primers are V3-V4-F and V4-V5-R respectively, forward primer V3-V4-F is 5′-GWATTACCGCGGCKGCTG-3′; reverse primer V4 -V5-R is 5′-CCGTCAATTCMTTTRAGTTT-3′, and the enzyme is 2×star Mix. The PCR amplification products were detected by electrophoresis imaging technology to observe whether they had bands, and the remaining PCR amplification products were used for sequence determination. The sequencing result is shown in SEQ ID NO:1. Its PCR reaction system is as follows:
[0035] Table 2 16s rDNA 2×starMix enzyme reaction system
[0036]
[0037] The sequences of 12 reference strains were obtained from the NCBI (GenBank) database, and the sequences of the isolated strains and reference strains were analyzed using the software BioEdit and MEGA6. 16s The rDNA partial sequence was analyzed, and the phylogenetic tree of the isolated str...
Embodiment 3
[0038] Example 3 Tieback test
[0039] 1. Strain cultivation: Transfer the test strains stored at -80°C to YMA liquid culture, and cultivate to logarithmic phase. The growth of the strains is detected by a nucleic acid protein analyzer, and the OD value is used to calculate the bacterial content; among them, YMA ( Yeast MannnitolAgar) liquid medium composition is: take by weighing mannitol 10 g, MgSO 4 ∙7H 2 O 0.2g, NaCl 0.1g, yeast powder 3g, K 2 HPO 4 0.25 g, KH 2 PO 4 0.25 g, CaCO 3 3 g (added during storage), 15 g of agar was dissolved in 1 L of pure water.
[0040] 2. Sterilization treatment: Wrap the 2.5L plastic bucket, beaker, tweezers, Petri dish, filter paper, and glass rod required for the test, pack the vermiculite in a fresh-keeping bag, and sterilize at 121°C for 30 minutes. Pack YMA liquid medium and distilled water in bottles, and sterilize at 121°C for 20 minutes.
[0041] Put peanut seeds in 1g / L HgCl 2 Sterilize the epidermis for 3 minutes, rinse ...
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