Beauveria bassiana XNBb-04 strain and culture method thereof
A technology of Beauveria bassiana and its culture method, applied in the field of Beauveria bassiana XNBb-04 strain and its cultivation, can solve the problem of green dairy industry, alfalfa root nodule larvae are difficult to work, and no Beauveria bassiana has been found Bacterial strains and other issues, to achieve the effect of environmental protection
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Embodiment 1
[0019] Example 1, the Beauveria bassiana XNBb-04 strain was deposited in the Type Culture Collection Center on March 6, 2014, and the preservation number is CCTCCM2014075.
Embodiment 2
[0020] Example 2, the morphological characteristics of the Beauveria bassiana XNBb-04 strain are as follows: the colony is white velveteen at the beginning, and then becomes milky yellow powder, and under the potato agar glucose medium culture conditions, the back of the colony is colorless or Yellow; conidiophores are short, colorless, without septa, the top extends in a zigzag shape, solitary or aggregated into spore bundles, the wall is smooth and transparent, the base of the phialide is spherical or quasi-elliptic and enlarged, the upper part is slender, the size is 96 μm to 142 μm × 4.9 μm to 7.3 μm, with an average size of 120 μm × 5.8 μm; conidia are spherical, oval, elliptical, colorless, single cell, with a size of 2.47 μm to 5.21 μm × 1.95 μm to 3.63 μm, The average size is 3.16 μm × 2.65 μm, without chlamydospores. as attached figure 1 shown.
[0021] Specifically, the isolation and acquisition method of Beauveria bassiana XNBb-04 bacterial strain of the pres...
Embodiment 3
[0062] Embodiment 3, the cultivation method of this Beauveria bassiana XNBb-04 bacterial strain, carries out according to the following steps:
[0063] The first step is to expand the cultivation of the first-level strains: put the XNBb-04 strain of Beauveria bassiana into a test tube equipped with PDA slant medium, put it into an incubator, and place it at a temperature of 24°C to 28°C and a relative humidity of Cultivate under the condition of 70% to 85%, and obtain the first-class strain culture after the hyphae cover the slope and produce spores;
[0064] The second step, secondary bacterial strain expansion cultivation: under aseptic conditions, scrape off the strain spore powder of the cultivated primary bacterial strain culture, and prepare a concentration of 5 × 10 with sterile water. 7 spore / mL suspension, suck 1mL and insert it into a 250mL Erlenmeyer flask filled with 50mL PDB culture solution, so that the spore concentration in the culture solution is 10 ...
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