Method for producing catalpol by using suspension cultured rhizoma rhizome cambium stem cells
A technology of suspension culture and cambium, applied in the field of medical bioengineering, can solve the problems of low catalpol content in dedifferentiated cells of Rehmannia glutinosa and inability to stabilize active secondary metabolites for a long time, so as to overcome changes in physiological and biochemical characteristics and reduce feedback inhibition function, the effect of increasing production
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[0043] The preparation process of the MS liquid medium and the MS solid medium is the same as the preparation process of the above-mentioned WPM liquid medium and WPM solid medium.
[0044] The formula of table 3 anti-browning preservation solution
[0045]
[0046]
[0047] Below we will describe and illustrate the technical solutions of the present invention in detail in the form of specific examples.
Embodiment 1
[0049] In this embodiment, a method for producing catalpol using suspension-cultured rhizoma rhizome cambium stem cells specifically comprises the following steps:
[0050] S1: Obtaining the culture system of rehmannia cambium stem cells
[0051] In the spring morning, collect the newly grown young stems of the three-year-old wild Rehmannia genus Rehmannia piasezkii Maxim, cut them into 3-5 cm sections, rinse them with flowing sterile distilled water for 6 hours, dry the surface moisture, cut into 1 cm of xylem, phloem, and cambium containing vascular bundles 2 Small pieces of as explants;
[0052] Under sterile conditions, rinse the explants with flowing sterile distilled water continuously for 2 hours, then soak them in 70% ethanol solution for 2.0 minutes, transfer them to 0.2% sodium hypochlorite solution for 5 minutes, and then sterilize them with 0.01% mercuric chloride solution. Bacteria treatment for 2 minutes, and finally rinsed with flowing sterilized distilled wat...
Embodiment 2
[0064] In this embodiment, a method for producing catalpol using the stem cells of the rhizome of Rehmannia glutinosa stem cells cultured in suspension, the acquisition of the stem cell culture system of the rhizoma rehmanniae root is the same as in Example 1, the only difference being:
[0065] At the 8th day of culture, 120 mmol / L methyl-β-cyclodextrin and 120 μmol / L methyl jasmonate were added to the bioreactor to stimulate the accumulation of catalpol, and the co-culture time was 16 days. The final obtained catalpol pure product is 16.18g.
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