Method for promoting polysaccharide accumulation of hairy roots of beautiful millettia roots
A hairy root and Niu Dali technology, which is applied in the field of Niu Dali tissue culture, can solve problems such as taking a long time, degeneration, and slow development speed, and achieve the effects of facilitating development and utilization, enhancing synthesis ability, and accelerating growth speed
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Embodiment 1
[0026] A method for promoting the accumulation of polysaccharides in bovine vigorous hairy roots, inoculating bovine vigorous hairy roots into a liquid medium and placing it on a constant temperature shaker for proliferation and culture for at least 30 days, and the liquid medium contains 100 μmol / L jasmonate formazan ester.
[0027] Wherein, the formula of the liquid medium also contains: 1 / 2MS, 0.5mg / L indolebutyric acid and 30g / L sucrose.
[0028] Wherein, the conditions for the proliferation culture are: light intensity 1500Lx, light time 10h / d.
[0029] Wherein, the rotation speed of the constant temperature shaker was 90 rpm, and the proliferation culture temperature was set at 24°C.
Embodiment 2
[0031] A method for promoting the accumulation of polysaccharides in bovine vigorous hairy roots, inoculating bovine vigorous hairy roots into a liquid medium and placing it on a constant temperature shaker for proliferation and culture for at least 30 days, and the liquid medium contains 300 μmol / L jasmonate formazan ester.
[0032] Wherein, the formula of the liquid medium also contains: 1 / 2MS, 1.0mg / L indolebutyric acid and 30g / L sucrose.
[0033] Wherein, the conditions of the proliferation culture are: light intensity 2000Lx, light time 10h / d.
[0034] Wherein, the rotation speed of the constant temperature shaker was 150 rpm, and the proliferation culture temperature was set at 28°C.
Embodiment 3
[0036] A method for promoting the accumulation of polysaccharides in bovine villous roots, inoculating bovine villous roots into a liquid medium and placing them on a constant temperature shaker for proliferation and culture for 30 days, and the liquid medium contains 220 μmol / L methyl jasmonate .
[0037] Wherein, the formula of the liquid medium also contains: 1 / 2MS, 0.8mg / L indolebutyric acid and 30g / L sucrose.
[0038] Wherein, the conditions for the proliferation culture are: light intensity 18000Lx, light time 10h / d.
[0039] Wherein, the rotation speed of the constant temperature shaker was 120rmp, and the proliferation culture temperature was set at 26°C.
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