Nutrient solution and method for applying nutrient solution to stem tissue-cultured seedling of dendrobium officinale
A technology of Dendrobium officinale and nutrient solution, applied in the directions of application, horticultural methods, botanical equipment and methods, etc., can solve the problems of uneven quality of seedlings, separation and degradation, and speed up reproduction, and achieve excellent effects, speed up process, and improve reproduction speed. Effect
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Embodiment 1
[0023] Example 1 Protocorm induction and selection of proliferation medium
[0024] After preliminary experiments, the induction rate of the middle part of the stem section was higher than that of the lower and upper part of the stem section. In order to avoid the error between the induction materials, the middle part of the stem section of the same biennial Dendrobium officinale species was selected for the experiment. Firstly, the leaves and leaf sheaths are peeled off, and after being rinsed with clean water, the surface is disinfected with 75% alcohol and 0.1% mercuric chloride solution successively, rinsed with sterile water, and blotted dry with sterile filter paper. Take out the stem section below the bud point by oblique cutting, and inoculate it on protocorm induction and proliferation medium A-E, and inoculate 150 stem sections in each medium:
[0025] Medium A: 1 / 2 MS basic medium, 30% sucrose, 8g / L agar.
[0026] Medium B: 1 / 2 MS basic medium, 0.5mg / L naphthalenea...
Embodiment 2
[0033] Example 2 Cutting method selection
[0034] In order to explore the effects of different cutting methods on the induction of protocorms by stem segments, the middle part of the stem segments of the same biennial Dendrobium officinale species was collected for cutting induction in this experiment. The media for protocorm induction and proliferation were: 1 / 2MS basic medium, 0.5mg / L naphthaleneacetic acid, 1.5mg / L phenylthiadiazolyl urea, 10% taro juice, 30% sucrose and 8g / L agar. Choose the cutting method of A-D as follows to carry out the experiment, and inoculate 150 stem segments in each medium:
[0035] Cutting method A: Carefully scratch the axillary buds of the stem section to stimulate.
[0036]Cutting method B: Take out the lower portion of the adventitious buds and the stem section by longitudinal cutting.
[0037] Cutting method C: Take out the lower portion of the adventitious buds together with the stem section by oblique cutting.
[0038] Table 2 is a tab...
Embodiment 3
[0041] Example 3 Selection of physical stimulation methods
[0042] Collect the middle part of the stem section of the same biennial Dendrobium officinale species for cutting induction, protocorm induction and proliferation medium are: 1 / 2MS basic medium, 0.5mg / L naphthaleneacetic acid, 1.5mg / L phenylthiadiazolyl Urea, 10% taro juice, 30% sucrose and 8g / L agar. Take out the stem section under the adventitious bud by oblique cutting, inoculate 150 stem sections in each medium, and choose the following physical methods A-D for stimulation:
[0043] Stimulation method A: irradiate under ultraviolet light for 1h.
[0044] Stimulation method B: ultrasonic treatment for 15min, 500W.
[0045] Stimulation method C: placed in -8°C environment, cultured in the dark for 5 hours, then transferred to 25°C environment, cultured under light intensity of 2000Lx.
[0046] Stimulation method D: placed in an environment of 4°C, cultured in the dark for 3 hours, microwaved for 2 minutes, power...
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