Extraction and fusion method for strawberry protoplast
A technology of protoplasts and fusion methods, applied in biochemical equipment and methods, botany equipment and methods, plant cells, etc., can solve the problems of mixed varieties, poor resistance, and quality decline, and achieve the effect of mild action and easy operation
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Embodiment 1
[0025] The extraction and fusion method of strawberry protoplasts, the steps are as follows:
[0026] 1) Get green-leaf oriental strawberry and rupee strawberry test-tube plants respectively and move into the MS medium that has reduced the sucrose concentration and cultivate for 10 days. The MS medium contains 6-benzyl adenine (6-BA) 1.0mg / L, sucrose 1.5% and agar 0.7%;
[0027] 2) Take the pretreated leaves in step 1) and cut them into 2.0mm×2.0mm sized strips with scissors and remove the veins;
[0028] 3) Mix the material and the enzyme solution according to the volume ratio of 1:10, seal with Parafilm, seal with tinfoil paper, place on a shaker at a constant temperature of 26°C, and perform dark enzymatic hydrolysis at a speed of 60r / min, every hour after 7 hours Observing the enzymatic hydrolysis under a microscope, the composition of the enzyme solution is 1.0% Cellulase Onozuka R-10+0.5% Pectolyase Y-23+0.6mol / L Mannitol+0.1-0.2% 2-(N-morphine Phyloline)ethanesulfonic...
Embodiment 2
[0035] The extraction and fusion method of strawberry protoplasts, the steps are as follows:
[0036] 1) Get green-leaf oriental strawberry and rupee strawberry test-tube plantlets respectively and move into the MS medium that has reduced the sucrose concentration and cultivate for 10 days. The MS medium contains 6-benzyl adenine (6-BA) 1.5mg / L, sucrose 1.5% and agar 0.7%;
[0037] 2) Take the pretreated leaves in step 1) and cut them into 2.0mm×2.0mm sized strips with scissors and remove the veins;
[0038] 3) Mix the material with the enzyme solution at a ratio of 1:10, seal it with Parafilm, seal it with tinfoil paper, place it on a shaker, and carry out dark enzymolysis at a constant temperature and low speed (60r / min) at 26°C, every hour after 7 hours Observing the enzymatic hydrolysis under a microscope, the composition of the enzyme solution is 2.0% Cellulase Onozuka R-10+0.5% Pectolyase Y-23+0.6mol / L Mannitol+0.1-0.2% 2-(N-morphine Phyloline)ethanesulfonic acid MES+0...
Embodiment 3
[0045] The extraction and fusion method of strawberry protoplasts, the steps are as follows:
[0046] 1) Take the test-tube plantlets of green-leaf oriental strawberry and rupee strawberry respectively and culture them in the dark at 26±1°C for one week;
[0047] 2) Take the pretreated leaves in step 1) and cut them into 2.0mm×2.0mm sized strips with scissors and remove the veins;
[0048] 3) Mix the material with the enzyme solution at a ratio of 1:10, seal it with Parafilm, seal it with tinfoil paper, place it on a shaker, and carry out dark enzymolysis at a constant temperature and low speed (60r / min) at 26°C, every hour after 7 hours Observing the enzymatic hydrolysis under a microscope, the composition of the enzyme solution is 1.0% Cellulase Onozuka R-10+1.0% Pectolyase Y-23+0.6mol / L mannitol+0.1-0.2% 2-(N-morphine Phyloline)ethanesulfonic acid MES+0.05mol / L CaCl 2 combination, the enzyme digestion time is 13 hours;
[0049] 4) Filter the two kinds of strawberry mesop...
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