Culture medium and culture method for inducing morphological transformation of Paecilomyces hepiali strain SH-1, and strain
A technology based on Paecilomyces bat moth and SH-1, which is applied in the direction of microorganism-based methods, biochemical equipment and methods, fungi, etc., can solve the problems of difficult selection and low recognition degree, and achieve high recognition degree and practical High performance and easy to use
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Embodiment 1
[0061] The culture medium for inducing the morphological transformation of Paecilomyces hematalis strain SH-1 provided by the present embodiment is mainly made of the following raw materials, and every 100ml of liquid culture medium includes,
[0062]
[0063] This embodiment also provides a method for inducing morphological transformation of the Paecilomyces hematalis strain SH-1, comprising culturing the Paecilomyces hematalis strain SH-1 on a medium.
[0064] This embodiment also provides the bacterial strain obtained by cultivating the above-mentioned medium using the above-mentioned method.
Embodiment 2
[0066] The culture medium for inducing the morphological transformation of Paecilomyces hematalis strain SH-1 provided by the present embodiment is mainly made of the following raw materials, and every 100ml of liquid culture medium includes,
[0067]
[0068] This embodiment also provides a method for inducing the morphological transformation of the Paecilomyces hematalis strain SH-1, comprising culturing the Paecilomyces hematalis strain SH-1 on a medium, wherein the ambient temperature is 20°C.
[0069] This embodiment also provides the bacterial strain obtained by cultivating the above-mentioned medium using the above-mentioned method.
Embodiment 3
[0071] This example provides a method for inducing the morphological transformation of Paecilomyces hematalis strain SH-1, comprising culturing the Paecilomyces hematalis strain SH-1 on a medium.
[0072] Among them, the culture conditions are: the amount of liquid in a 500mL glass culture bottle is 200mL (medium), the inoculum size is 10%, the flask is shaken on a shaker at 160r / min for 10min, and the temperature is placed in a culture room at 20°C for cultivation After 60 days, the pH was 5.8.
[0073] The formula for calculating the transition probability is:
[0074]
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