Oxytropis Ehrig cinerea FEL2-OG and separation method and application thereof
A technology of FEL2-OG and separation method, which is applied in the field of separation of the bacteria, Ehrigia spinosa FEL2-OG, can solve the problems of lack of swainsonine source and high price
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Embodiment 1
[0028] Example 1: Isolation of Ehrigia spinosa FEL2-OG
[0029] 1) Wash the whole plant Oxytropis glacialis grown on the alpine meadow in Ngari region of Tibet with deionized water to remove the dust on the surface of Oxytropis glacialis, and separate the leaves, stems and seeds of the plant with sterilized tweezers, and then separate the leaves, The stems and seeds were wrapped with gauze for surface disinfection.
[0030] 2) Use sterilized filter paper to absorb the water on the surface-sterilized plant tissue, then use sterilized scissors to cut leaves, stems, seeds, etc. into 3mm tissue pieces, and then use sterilized forceps Each tissue block was inoculated on the surface of water agar medium, and cultured in an incubator at 18°C.
[0031] 3) When the hyphae grow out from around the tissue block, pick the mycelium at the edge of the colony and inoculate it on the surface of the enrichment medium, and place it in an incubator at 18°C for enrichment culture; collect the ...
Embodiment 2
[0032] Example 2: Identification of Ehrigia spinosa FEL2-OG
[0033] 1. Morphological features
[0034] The colony of the FEL2-OG strain was round, white at first, and gradually changed to light yellow, yellowish brown, dark brown with the prolongation of the culture time, with a slight protrusion in the center ( figure 1 ). The mycelium has a transverse septum without a mediastinum, and some old hyphae give birth to conidiophores, which have branches. Conidia and conidiophores with septum, without mediastinum, the septum of conidia is thicker, the number of septa varies from 1 to 3, the spores are rod-shaped, nearly cylindrical, and the size of conidia is 20-70 μm ×5~10μm( figure 2 ).
[0035] 2) Characteristics of culture
[0036]The strain grows very slowly on PDA, PCA, Czapek and other media, and its growth rate is 0.50, 0.58 and 0.37mm / d respectively. The optimum growth temperature is 18°C, and the growth is inhibited when the temperature is higher than 25°C.
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