New bacterial strain of pholiota squarrosoides and sporocarp culture method thereof
A cultivation method and fruiting body technology, which are applied in the field of new strains of C. chinensis and their fruiting bodies, can solve the problems of few and no domesticated cultivation of C. The effect of short time and fast speed when the silk bag is full
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Embodiment 1
[0042] Example 1. Isolation and Identification of Pholiota squarrosoides HS4
[0043]The wild fruiting body of the strain of the present invention (referred to as HS4) is collected from a persimmon tree in Changping, Beijing, and identified as Pholiota squarrosoides by Mr. Mao Xiaolan, Institute of Microbiology, Chinese Academy of Sciences. Further, through the observation of the morphological characteristics of its fruiting body and mycelium, and the sequencing of the intergenic sequence (ITS), the biological taxonomy of the strain was determined.
[0044] 1. Morphological characteristics
[0045] 1. Morphological characteristics of fruiting bodies
[0046] Bacterial strain HS4 fruiting bodies of the present invention are generally medium and large ( figure 1 ). Cap diameter 3-12cm, hemispherical to oblate hemispherical, finally flat, sometimes slightly convex in the middle, dry surface, yellowish brown or earthy brown with pink, scales pyramid-like, spiny, darker in color...
Embodiment 2
[0052] Example 2. Artificial cultivation of fruiting bodies of Pholiota squarrosoides HS4CGMCC No.6062
[0053] 1. Preparation of strains
[0054] (1) Mother seed preparation: inoculate the Pholiota squarrosoides HS4CGMCC No.6062 obtained in Example 1 on the mother seed medium, and culture it in the dark at 24°C-28°C for 7-10d to obtain The mycelium is used as the mother seed; if the obtained mother seed is not used in time, it can be stored at 4°C.
[0055] (2) Original seed preparation: transfer the mother seed obtained in step (1) to the original seed medium, cultivate at a temperature of 23°C-25°C, and a relative air humidity of 50%-60%, well ventilated and protected from light Until the mycelia cover the container, the original species is obtained. The storage period of the original species at room temperature generally does not exceed 15 days, and the storage period at low temperature does not exceed 20 days. Expired strains cannot be used.
[0056] (3) Preparation of...
Embodiment 3
[0065] Example 3. Detection of Mycelia Growth Rate, Yield and Nutrient Components of Pholiota squarrosoides HS4CGMCC No.6062
[0066] In this example, Pholiota adipose No. 1 was used as a control (currently there is no report on the cultivation of Pholiota squarrosoides, and only its close relative species Pholiota squarrosoides can be used as a control) to detect Pholiota squarrosoides Mycelium growth rate, yield and nutrient composition of HS4CGMCC No.6062.
[0067] 1. Determination of mycelium growth rate
[0068] 1. Experimental materials
[0069] The mother species, original species and cultivars of Pholiota squarrosoides HS4CGMCC No.6062 and Pholiota adipose No. 1 strain, the preparation method of which is the same as step 1 of Example 2.
[0070] 2. Experimental method
[0071] Determination of the average growth rate of the mycelium of the mother species: the mother species of the two strains were inoculated in the center of the medium surface of the mother species,...
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