A strain of algae scsio X and its application
A technology of SCSIOX and mat algae, applied in the direction of organic fertilizers, microorganisms, bacteria, etc., to achieve high value, promote germination, and broad application prospects
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Embodiment 1
[0020] Example 1: Isolation, purification and identification of Phormidium sp. SCSIO X
[0021] 1. Separation and purification of Phormidium sp. SCSIO X
[0022] Collect the seaweed Thalias spp. collected from Sanya Bay, Hainan Province, China, add seawater to scrub, and filter to obtain the cyanobacteria liquid. Pick cyanobacteria hyphae and culture them in marine cyanobacteria medium ATCC Medium 957, nitrogen-fixing cyanobacteria medium ATCC Medium 819, marine nitrogen-fixing cyanobacteria medium ATCC Medium 1077 and BG-11Medium, and the continuous light intensity is 150μE / m 2 / s, the light cycle is 12:12h (light: dark cycle), the temperature is 23-27°C, in the light incubator (the model is LRH-250-GH microcomputer-controlled light incubator), every two weeks into fresh medium until the microscopic examination shows a single mycelium. The cyanobacteria SCSIO X was obtained by separation and purification.
[0023] 2. Identification of Phormidium sp. SCSIO X
[0024] 1) Mo...
Embodiment 2
[0037] The mensuration of embodiment 2 cyanobacteria indole acetic acid production
[0038] The salkowski colorimetric method was used to determine the ability of the isolate to produce plant growth hormone substances, and the standard curve was prepared using pure 3-IAA (3-indole acetic acid). Inoculate the cyanobacteria SCSIO X in 100mL selective liquid nitrogen-free liquid improved medium (formulation is the same as in Example 1), and the continuous light intensity is 150 μE / m 2 / s, the light cycle is 12:12h (light: dark cycle), the temperature is 25-28°C, cultivate for 120h, take 5mL of the cyanobacteria culture supernatant every 24h, centrifuge at 10000r / min for 10min, take the supernatant and add colorimetric The solution was left to stand in the dark for 0.5h, taken out, and measured immediately with a spectrophotometer at a wavelength of 530nm (Glickmann and Dessaux Y.A).
[0039] Indole acetic acid content in the sample (μg / mg) = (A × V1) / (W × V2) × 1000
[0040] ...
Embodiment 3
[0045] 16SRNA and nitrogen fixation gene amplification of the strain of embodiment 3
[0046] Select the pure bacterial strain cyanobacteria SCSIO X obtained by separation and purification in Example 1 to carry out DNA extraction and purification, the extraction and purification of DNA in this embodiment, its operation method refers to Dong Xiuzhu's "Common Bacteria System Identification Manual" P 409 . 1SF / 16SR (Weisenburg et al., 1991, 16S ribosomal DNA amplification forphylogenetic study., Journal of bacteriology, 1991, 173(2): 697-703) and ITS amplification primer 23S30R / 27F1 (Taton et al. ., 2003, Cyanobacterial diversity in natural and artificial microbial mats of Lake Fryxell (McMurdo Dry Valleys, Antarctica): amorphological and molecular approach. Appl Environ Microb, 2003, 69:5157–5169) and nifH gene general primer PolF / PolR (reference Poly et al., 2001, Comparison of nifH Gene Poolsin Soils and Soil Microenvironments with Contrasting Properties, Applied and Environm...
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