Method for quickly reproducing miscanthus plant miscanthus and triarrhena hybrid NO.9 somatic embryo by tissue culture
A plant and hybrid technology, applied in botany equipment and methods, plant regeneration, horticultural methods, etc., can solve the problems of different callus rate and differentiation rate, no embryogenic callus, no embryogenicity, etc., to achieve The effect of high callus reproduction rate, stable proliferation and high efficiency
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Embodiment 1
[0024] A method for rapid propagation by tissue culture of somatic embryos of Miscanth genus Miscanthus hybrid No. 9, the steps of which are:
[0025] 1. Selection of young panicles: Select the young panicles of Mangdi Hybrid No. 9 that are in the formation stage of the spikelet primordium. The seeds in the young panicles have not yet formed, the central axis is relatively soft, and the basic branches have not yet formed.
[0026] 2. First-generation induction (induction first-generation medium): cut it into 2 or 3 cm segments, first disinfect with 75% (volume ratio) alcohol for 25-35s, and then soak in 0.1% (mass volume ratio) mercuric chloride for 5 minutes , and then washed three times with sterile water, and inoculated it on the primary induction medium of young ears. After 30 days of primary induction, embryogenic callus was obtained. The culture conditions were 25°C, dark culture. The primary induction medium is: A: MS medium supplemented with kinetin KT1-2mg / L, 2,4-di...
Embodiment 2
[0031] A method for rapid propagation by tissue culture of somatic embryos of Miscanth genus Miscanthus hybrid No. 9, the steps of which are:
[0032] 1. Selection of young panicles: Select the young panicles of Mangdi Hybrid No. 9 that are in the formation stage of the spikelet primordium. The seeds in the young panicles have not yet formed, the central axis is relatively soft, and the basic branches have not yet formed.
[0033] 2. First-generation induction (induction first-generation medium): cut it into 2 or 3 cm segments, first disinfect with 75% (volume ratio) alcohol for 25-35s, and then soak in 0.1% (mass volume ratio) mercuric chloride for 5 minutes , and then washed three times with sterile water, and inoculated it on the primary induction medium of young ears. After 30 days of primary induction, embryogenic callus was obtained. The culture conditions were 25°C, dark culture. The primary induction medium is: B: MS medium plus kinetin KT3-4mg / L, 2,4-dichlorophenoxyac...
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