Method for rapidly identifying fruiting potential of edible fungus strains
A technology for edible mushrooms and strains, applied in the directions of botanical equipment and methods, applications, mushroom cultivation, etc., can solve the problems that mushroom bags cannot fruit normally, heavy workload, and complicated operation, so as to promote the production and development of edible mushrooms. , Improve work efficiency and simple operation
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Example Embodiment
[0018] Example 1 Identification of fruiting potential of Lentinus edodes hybrid strain
[0019] 1) Weigh 200g of sawdust and 50g of bran in 1L of tap water, boil for 20min, filter, add water to the filtrate and dilute to 1L as a culture medium;
[0020] 2) Pack the culture medium into a 250mL conical flask in an amount of 150mL, and place a heat-resistant sponge with a size of 4cm×4cm×2cm in the bottle, seal it with 8 layers of gauze, and sterilize it in an autoclave at 121°C for 20min. ;
[0021] 3) After the medium is cooled, cut 2 pieces of 1cm×1cm from the slant of the activated Lentinus edodes hybrid strain, one of which is inoculated into the medium to make it grow in large quantities, and the other is inoculated in the center of the surface of the sponge position, as a support point for the formation of primordia or fruiting bodies;
[0022] 4) Incubate the inoculation bottle at 28°C and 160r / min for 5d on a shaker;
[0023] 5) After culturing in a shaker, place the...
Example Embodiment
[0025] Embodiment 2 The fruiting potential identification of a certain wild woody fungus isolated strain
[0026] 1) Weigh 200g of sawdust and 50g of bran in 1L of tap water, boil for 20min, filter, add water to the filtrate and dilute to 1L as a culture medium;
[0027] 2) Pack the culture medium into a 500mL wide-mouth bottle in an amount of 150mL, and place a heat-resistant sponge with a size of 4cm×4cm×2cm in the bottle, seal it with 8 layers of gauze, and sterilize it in an autoclave at 121°C. bacteria 20min;
[0028] 3) After the medium is cooled, cut 2 strain blocks with a size of 1cm × 1cm from the slant of the activated wild woody bacteria isolate, one of which is inoculated into the medium to make it grow in large quantities, and the other inoculated in The center position of the sponge surface, as the support point for the formation of primordium or fruiting body;
[0029] 4) Incubate the inoculated bottle at 28°C and 160r / min for 7d on a shaker;
[0030] 5) Af...
Example Embodiment
[0032] Example 3 Identification of fruiting potential of Pleurotus chinensis introduced species
[0033] 1) Weigh 200g of sawdust and 50g of bran in 1L of tap water, boil for 20min, filter, add water to the filtrate and dilute to 1L as a culture medium;
[0034] 2) Pack the culture medium into a 500mL wide-mouth bottle in an amount of 150mL, and place a heat-resistant sponge with a size of 4cm×4cm×2cm in the bottle, seal it with 8 layers of gauze, and sterilize it in an autoclave at 121°C. bacteria 20min;
[0035] 3) After the medium is cooled, cut two 1cm × 1cm strain blocks from the slanted surface of the activated Pleurotus chinensis, one of which is inoculated into the medium to make it grow in large quantities, and the other is inoculated on the surface of the sponge The central position of , as the support point for the formation of primordia or fruiting bodies;
[0036] 4) Incubate the inoculation bottle at 28°C and 160r / min for 5d on a shaker;
[0037] 5) After cu...
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