Endophytic fungi of Sargassum chinensis in Fujian and Zhejiang and methods and applications thereof for producing huperzine A
An endophytic fungus and huperzine A technology, applied in the field of microorganisms, can solve the problems of inability to apply industrialized production, low huperzine A yield, etc., and achieve the effect of solving the bottleneck problem
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Embodiment 1
[0035] 1. Observation of bacterial strain micromorphology: Two kinds of endophytic fungi that produce huperzine A of the present invention are spot-inoculated in the center of the flat plate, and then the sterilized cover glass is inserted obliquely at 45 ° in the flat plate of the inoculated bacteria (2 Slices / plates) were cultivated in a fungal incubator at 28°C. After the strains had grown to a certain extent (6 days), the inserts (in an ultra-clean bench) were taken and observed under a microscope.
[0036] see figure 1 It is the micromorphological figure of the cereus tearing fungus MY183 of the present invention, and the microscopic shape of the tearing cereus spore MY183 is: hyphae without septa, branched, smooth, tubular, with unequal spacing, spores oval, single spore.
[0037] see figure 2 It is the micromorphological figure of the covered carbon group bacteria MY311 of the present invention, and the microscopic morphology of the covered carbon group bacteria MY311 ...
Embodiment 2
[0054] One, the collection of endophytic fungus of Sargassum pine in Fujian and Zhejiang provinces of the present invention
[0055] 1. Separation of endophytic fungi from Sargassum lanceolata collected from Guanzhai Mountain, Liancheng County, Longyan City, Fujian Province according to the separation method of Shi Wei et al. Rinse the collected fresh Chinese fir from Fujian and Zhejiang with tap water, immerse in 75% ethanol (5min), and rinse with sterile water for 5 times; dry it with sterile filter paper and then immerse it in 0.1% mercuric chloride (about 1min). ), rinse again with sterile water, blot dry with sterile filter paper, and finally soak in 75% ethanol for 30 seconds, and blot dry with sterile filter paper. Different plant tissue materials (ie roots, stems, leaves) were divided into approximately 5 mm long size with sterilized scissors. Each sample was then transferred to PDA plates containing 3% streptomycin for the isolation of endophytic fungi. Cultivate fo...
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