A kind of in vitro rapid propagation method of Cymbidium cymbidium
A fast, in vitro technology, applied in the field of artificial propagation and cultivation of plants, can solve problems such as inability to increase nutritious endosperm and other tissues, incomplete embryo development, and decline of orchid varieties, so as to relieve healing and infection, shorten The effect of growth cycle and space saving
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Embodiment 1
[0029] The invention provides a method for in vitro rapid propagation of Cymbidium, comprising the following steps:
[0030] S1, selection and preparation of explants: under the condition of temperature of 15°C and air humidity of 45%, young shoots with full axillary buds and not yet germinated were cut, leaves were removed, and then the shoots were cut into small sections of 1 cm. section with at least one pair of axillary buds;
[0031] S2, disinfection of explants: wash 3 times with sterilized water, blot dry with filter paper, soak in 65% alcohol for 30 seconds, soak in 0.5% sodium hypochlorite for 5 minutes, and soak in 0.5% sodium hypochlorite for 5 minutes. Soak in 0.1% mercuric chloride for 10 minutes, soak in 10% bleaching powder for 5 minutes, rinse with sterilized water for 5 times, and blot dry with filter paper;
[0032] S3, Axillary Bud Induction: Cut the sterilized Cymbidium cymbidium stem into 0.5 cm bud-bearing segments, inoculate them into medium 1, and keep...
Embodiment 2
[0038] The invention provides a method for in vitro rapid propagation of Cymbidium, comprising the following steps:
[0039] S1, selection and preparation of explants: under the condition of temperature of 22°C and air humidity of 50%, young shoots with full axillary buds and not yet germinated were cut, leaves were removed, and then the shoots were cut into small sections of 2 cm. section with at least one pair of axillary buds;
[0040] S2, explant disinfection: wash 4 times with sterilized water, blot dry with filter paper, soak in 70% alcohol by mass percentage for 45 seconds, soak in 1% sodium hypochlorite for 10 min, and soak in 1% by mass concentration of sodium hypochlorite for 10 min. Soak in mercuric chloride with a concentration of 0.3% for 12 minutes, soak in bleaching powder with a concentration of 15% by mass for 8 minutes, rinse with sterilized water for 8 times, and blot dry with filter paper;
[0041] S3, axillary bud induction: Cut the sterilized Cymbidium c...
Embodiment 3
[0047] The invention provides a method for in vitro rapid propagation of Cymbidium, comprising the following steps:
[0048] S1, selection and preparation of explants: cut shoots with full axillary buds and not yet germinated at a temperature of 25°C and an air humidity of 60%, remove the leaves, and then cut the shoots into small sections of 3 cm. section with at least one pair of axillary buds;
[0049] S2, disinfection of explants: wash 3-5 times with sterilized water, blot dry with filter paper, soak in 75% alcohol for 60 seconds, soak in 1.5% sodium hypochlorite for 15 minutes, and Soak in 0.5% mercuric chloride by mass for 15 minutes, soak in 20% by mass bleach for 10 minutes, rinse with sterilized water 10 times, and blot dry with filter paper;
[0050] S3, axillary bud induction: cut the sterilized Cymbidium cymbidium stem into 1.5 cm bud-bearing segments, and inoculate them into medium 1, at a temperature of 25°C, light intensity of 3500 lx, light time of 12 hours, a...
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