A strain hb161398 with nitrogen-fixing activity and its application
A technology of HB161398 and nitrogen fixation, applied in the field of genetic engineering, can solve the problems of weak non-symbiotic nitrogen-fixing microorganisms, and achieve the effect of wide application range and good nitrogen fixation activity
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Embodiment 1
[0014] The isolation of embodiment 1 bacterial strain HB161398
[0015] Mix the collected mangrove bottom mud (mangrove bottom mud at Qinglan Port, Wenchang, Hainan Province) and weigh 10g in a 100mL container. Put it in a Erlenmeyer flask with nitrogen-free medium and place it on a shaker to vibrate at 200r / min for 30min to fully disperse the soil sample. Take out the sample and let it stand for enrichment for 5 days, then take the upper layer liquid for gradient dilution, take 10 -3 -10 -6 Dilution applied to On nitrogen-free medium plates, 2 replicates per gradient. Inverted culture at 28°C for 5-7d. The strains with large colonies and transparent viscous shape were picked and purified by streaking on the plate. After purification, the 16s rDNA and nifH (nitrogen fixation) gene sequences were amplified and identified, and the strains were numbered and stored on a slant at 4°C and a glycerol tube at -80°C. Strain morphology such as figure 1 As shown, the cells are o...
Embodiment 2
[0031] The cultivation of embodiment 2 bacterial strain HB161398
[0032] The strain HB161398 can be preserved or temporarily stored by slant culture, and the strain HB161398 can be activated or transferred by plate culture, as follows:
[0033] (1) Slope culture: From the purified plate, pick a single colony of the strain and culture it for 3-5 days. Medium: 10g of peptone, 3g of beef extract, 1000mL of 50% old sea water, pH7.2, and store it at 4 ℃ refrigerator storage;
[0034] (2) Plate culture: From the purified plate, pick a single colony of the strain and culture it for 3-5 days. Medium: 10g of peptone, 3g of beef extract, 1000mL of 50% old sea water, pH7.2, and store it at 4 ℃ refrigerator storage.
Embodiment 3
[0035] Example 3 Detection of Nitrogen Fixation Activity of Bacterial Strain HB161398
[0036] Inoculate 10 mL of the Dobereiner nitrogen-free liquid medium with the pure bacterial strains preserved on the slant in Example 2, culture in a shaking table at 30°C for 72 hours, measure the OD600, and make uniform adjustments. Take 1 mL of the bacteria in sterilized 5 mL vials and cover with rubber stoppers. . The rim of the cap is sealed with paraffin. Inject 1 mL of acetylene with a syringe and incubate for 24 hours under the same conditions, then take 40 μL of the reacted gas, and use gas chromatography to measure the acetylene reducing activity (Acetylene reducing activity, ARA) of nitrogen-fixing bacteria.
[0037] The calculation method of acetylene reduction activity is as follows, wherein the ratio of the acetylene amount of acetylene reduction and fixed nitrogen adopts: C 2 h 4 :N 2 =4:1 for conversion):
[0038] ARA[nmol / (mL·h)]=Vst×Cst×Asa×Vtu / Vsa / Ast / h / 22.4
[003...
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