Method for high-density culture of endophytic bacteria of psidium guajava leaves
A technology of high-density culture and guava leaves, applied in the direction of biochemical equipment and methods, microorganisms, microorganisms, etc., to achieve the effects of stable product performance, simple cultivation methods, and easy operation
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Embodiment 1
[0033] Such as figure 1 Shown, a kind of method for cultivating guava leaf endophyte at high density comprises the following steps:
[0034] (1) Guava leaf pretreatment: pick fresh guava leaves from the guava tree, dry the guava leaves at 45°C for 12 hours, then grind them into fine powder, add sterile water, and filter through a 220 μm filter membrane Remove other miscellaneous bacteria other than specific endophytes;
[0035] (2) Activation and cultivation of endophytes: Inoculate endophytes isolated and screened from guava leaves that can produce terpenoids on solid microbial culture media for endophyte culture and activation, control the inoculum size and solid microbial culture The ratio of carbon source and nitrogen source in the base is: inoculum amount (10 7 cells): Carbon source (g): Nitrogen source (g) = 1.6:5:1.3, and the culture temperature was controlled at 28°C for 30 hours; wherein, the composition of the solid microbial culture medium included: peptone 6g / L, ...
Embodiment 2
[0041] Such as figure 1 Shown, a kind of method for cultivating guava leaf endophyte at high density comprises the following steps:
[0042] (1) Guava leaf pretreatment: pick fresh guava leaves from the guava tree, dry the guava leaves at 45°C for 18 hours, then grind them into fine powder, add sterile water, and filter through a 220 μm filter membrane Remove other miscellaneous bacteria other than specific endophytes;
[0043] (2) Activation and cultivation of endophytes: Inoculate endophytes isolated and screened from guava leaves that can produce terpenoids on solid microbial culture media for endophyte culture and activation, control the inoculum size and solid microbial culture The ratio of carbon source and nitrogen source in the base is: inoculum amount (10 7cells): Carbon source (g): Nitrogen source (g) = 1.6:5:1.3, and the culture temperature was controlled at 28°C for 24 hours; wherein, the composition of the solid microbial culture medium included: peptone 6g / L, y...
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