Method for converting and synthesizing saponin through adventitious root system culture of Chinese thorowax root
A culture medium formula and the technology of Bupleuri, applied in chemical instruments and methods, horticultural methods, steroids, etc., can solve the problems of high cost, complicated induction process, and long cultivation cycle, and achieve short production cycle and biotransformation system Simple, update-friendly effects
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Embodiment 1
[0029] The cut sections of Bupleurum root taken from Taigu, Shanxi (originally produced in Zuoquan, Shanxi) were used as explants, and the floating soil was washed away by running water, cut into 2cm-3cm long sections, soaked in 75% ethanol for 30s, 0.1 %HgCl 2 Disinfect the aqueous solution for 10 minutes, rinse with sterile water four times, inoculate in B supplemented with 2,4-D 1.0mg / L, KT 0.2mg / L, sucrose 3.0%, agar 0.7%, pH 5.8 5 culture medium (A medium), cultured at 25±2°C in the dark, and obtained callus after 4w (such as figure 1 ). Subculture once every 30 days, and obtain a large amount of light yellow callus after subculturing three times.
[0030] The pale yellow callus was transferred to rooting induction medium (B medium). The composition of the rooting induction medium is: B 5 Medium + 1.0mg / L calcium diphenylurea disulfonate + 3.0% sucrose + 0.7% agar, pH 5.8. After 35 days, adventitious roots (such as figure 2 ).
[0031] After rooting for 40 days, se...
Embodiment 2
[0035] Cut the roots of Bupleurum bupleurum taken from the field of Lingchuan, Shanxi, wash away the floating soil, cut into 2cm-3cm long sections, soak in 75% ethanol for 30s, 0.1% HgCl 2 The aqueous solution was sterilized for 10 min, washed with sterile water four times, inoculated on the B5 medium (A medium) containing 2,4-D 1.0 mg / L, KT 0.2 mg / L, sucrose 3.0%, pH 5.8 (A medium) at 25 Cultured at ±2°C in the dark, the explants dedifferentiated to form callus after 2w-4w, and a large number of callus were obtained after three subcultures.
[0036] Select the compact, light yellow callus and transfer it to the rooting induction medium (B medium) obtained by screening. The composition of B medium is: B 5 Medium + 1.0 mg / L calcium diphenylurea disulfonate + 3.0% sucrose + 0.7% agar, pH 5.8. During the subculture process, adventitious roots continuously differentiated into new roots.
[0037] Every 30d is one generation, and a large amount of adventitious root systems of Bup...
Embodiment 3
[0041] The cut sections of Bupleurum chinensis roots taken from the cultivation site in Ruicheng, Shanxi were sterilized and inoculated into the culture medium to induce callus formation, induce adventitious root differentiation, conduct adventitious root proliferation and adventitious root system formation culture, and conduct biotransformation of active ingredients in adventitious roots synthesis. The culture conditions, culture medium and the extraction and determination of saikosaponin are the same as in Example 1. It is determined that the monthly proliferation rate of adventitious roots reaches 7.212g, the monthly dry weight multiplication multiple reaches 6.67, and the total amount of saikosaponins a and d reaches 0.127%.
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