Preparation method of Calibrachoa protoplast
A technology of petunia florida and protoplasts, which is applied in the direction of plant cells, can solve the problems of large differences in protoplast separation, long separation time, and low efficiency of petunia floret protoplast separation, achieving high yield and good growth status Effect
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[0031] The present invention relates to a kind of preparation method of petunia florida protoplast, described method comprises the following steps:
[0032] A, under dark conditions, the young leaves of Petunia florida are pretreated;
[0033] B. Use the enzymolysis solution to enzymolyze the leaves treated in step A; the solvent of the enzymolysis solution is 0.25M phosphate solution, and the solute is the following final concentration: 2wt% cellulase, 0.8wt% eluent , 0.2wt% pectinase, 0.11wt% anhydrous calcium chloride, 0.10wt% bovine serum albumin; the pH of the enzymolysis solution is 5.6-5.7;
[0034] C. Add CPW washing solution equal to the volume of the enzymolysis solution to the solution after the enzymolysis in step B, shake the enzyme solution, filter through a 300-mesh cell sieve and centrifuge at 1100r / min for 2min, and suck off the supernatant; The solvent in the CPW lotion is CPW salt solution, the solute is mannitol with a final concentration of 0.25M, and the...
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[0069] This example relates to the preparation of petunia floret mesophyll protoplasts. The variety of petunia florida is Calibrachoahybrid 'lindurayellow' with yellow flower color, purchased from Fides company. Specifically include the following steps:
[0070] 1. Preparation materials: Take the 1st to 2nd young leaves under the terminal buds of Petunia florida, and weigh 0.33g.
[0071] 2. Separation of plasmodium: pretreatment of leaves, under dark conditions, collect young leaves and place them in clear water at 3-5°C for 20-25 hours of pretreatment.
[0072] 3. Enzymatic hydrolysis: Add 5ml of enzymatic hydrolysis solution to a 6cm small petri dish, cut the pretreated leaves into 0.1cm×0.2cm strips and lay them flat in the enzyme solution so that they do not overlap each other. Static hydrolysis at 26±1°C for 5 hours in the dark, during which the culture dish was gently shaken every 1 hour to fully contact the two phases. The enzymolysis solution is 0.25M phosphate solu...
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