Establishing method for indoor symbiotic relationship of amanita flavipes and cyclobalanopsis glaucoides as symbiotic plant
A technology of symbiotic relationship and establishment method, applied in the biological field, can solve problems such as difficulty in development and utilization, incapability of artificial cultivation, etc., and achieve the effect of fast growth
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example 1
[0017] Pick mature fruiting bodies with good growth, no pests, unopened or incompletely opened umbrellas, thick stipe, and thick caps in the field; bring the fruiting bodies back to the laboratory, use alcohol cotton balls on the ultra-clean table, lightly Wipe the surface of the cap and the stipe and other parts, remove the surface sand or soil, divide the fruit body into four parts from the middle of the cap, use a scalpel to take the internal tissue block at the junction of the stipe and the cap, and cut it into about 0.08~ 0.16cm 2 small pieces; gently embed the above cut small tissue pieces into the test tube slant induction medium (potato 200.00g / L, glucose 20.00g / L, NH 4 NO 3 0.30g / L, glutamic acid 0.32 g / L, V B1 0.10mg / L, wort juice 150 ml / L, agar 11.00g / L, control the pH value to about 5.4) on the surface, culture temperature is 22~23℃, dark culture for 14 days, very few white bacteria began to germinate around the bacteria block Silk, 60 days, the tissue blocks ...
example 2
[0021] Pick mature fruiting bodies with good growth, no pests, unopened or incompletely opened umbrellas, thick stipe, and thick caps in the field; bring the fruiting bodies back to the laboratory, use alcohol cotton balls on the ultra-clean table, lightly Wipe the surface of the cap and the stipe and other parts, remove the surface sand or soil, divide the fruit body into four parts from the middle of the cap, use a scalpel to take the internal tissue block at the junction of the stipe and the cap, and cut it into about 0.08~ 0.16cm 2 small pieces; gently embed the above cut small tissue pieces into the test tube slant induction medium (potato 200.00g / L, glucose 20.00g / L, NH 4 NO 3 0.30g / L, glutamic acid 0.32 g / L, V B1 0.10mg / L, wort juice 150 ml / L, agar 11.00g / L, control the pH value to about 5.4) on the surface, culture temperature is 22~23℃, dark culture for 14 days, very few white bacteria began to germinate around the bacteria block Silk, 60 days, the tissue blocks ...
example 3
[0025] Pick mature fruiting bodies with good growth, no pests, unopened or incompletely opened umbrellas, thick stipe, and thick caps in the field; bring the fruiting bodies back to the laboratory, use alcohol cotton balls on the ultra-clean table, lightly Wipe the surface of the cap and the stipe and other parts, remove the surface sand or soil, divide the fruit body into four parts from the middle of the cap, use a scalpel to take the internal tissue block at the junction of the stipe and the cap, and cut it into about 0.08~ 0.16cm 2 small pieces; gently embed the above cut small tissue pieces into the test tube slant induction medium (potato 200.00g / L, glucose 20.00g / L, NH 4 NO 3 0.40g / L, glutamic acid 0.28 g / L, V B1 0.10mg / L, wort juice 150 ml / L, agar 11.00g / L, control the pH value to be about 5.4) on the surface, culture temperature is 22~23℃, dark culture for 16 days, very few white bacteria began to germinate around the bacteria block Filament, 55 days, the tissue ...
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