BIOLOGICAL REACTION DEVICE AND CULTURE METHOD FOR ADVENTITIOUS ROOTS OF PANAX GINSENG C. A. MEY

Abstract

The present disclosure discloses a biological reaction device and a culture method for adventitious roots of panax ginseng C. A. MEY. The biological reaction device includes a tank body, wherein the top of the tank body is provided with a cover body which can be opened and closed, and a bottom of the tank body is provided with at least two air inlet devices. The method includes washing and disinfecting mature ginseng, cutting the disinfected ginseng into slices, inoculating the ginseng slices into an induction medium to induce ginseng adventitious roots, re-inoculating the ginseng adventitious roots into an induction medium for subculture and propagation, then inoculating the obtained ginseng adventitious roots into a shake flask containing a liquid medium for dark culture, and then inoculating the obtained ginseng adventitious roots into a biological reaction device containing a liquid medium for culture to obtain ginseng adventitious roots.

Claims

1. (canceled)

2. (canceled)

3. (canceled)

4. (canceled)

5. (canceled)

6. (canceled)

7. A method for culturing adventitious roots of ginseng by using a biological reaction device, said method comprising: (1) washing and disinfecting mature ginseng, cutting the mature ginseng disinfected into ginseng slices, and inoculating the ginseng slices into an induction medium to induce adventitious roots of ginseng; (2) re-inoculating the adventitious roots of ginseng obtained in step (1) into an induction medium for subculture and propagation; (3) inoculating the adventitious roots of ginseng obtained in step (2) into a shake flask containing a liquid medium for dark culture; and then (4) inoculating the adventitious roots of ginseng obtained in step (3) into the biological reaction device containing a liquid medium for culture to obtain adventitious roots of ginseng.

8. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 7, wherein in the steps (1) and (2), the induction medium comprises 1-6 mg/L of naphthylacetic acid, 0.1-0.6 mg/L of kinetin, 0.2-1 mg/L of gibberellin, 0.075-1.5 g/L of citric acid, 0.03-1 g/L of ascorbic acid, 20-60 g/L of sucrose, 1-6 g/L of Phytagel, 1-4 g/L of a B5 medium and 1-2.4 g/L of a WPM medium.

9. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 7, wherein in the steps (3) and (4), the liquid medium includes a basic medium selected one or more one medium from a group containing a B5 medium, a WPM medium and a MS medium, and 4 mg/L of indolebutyric acid, and 30 g/L of sucrose.

10. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 7, wherein in the step (3), a volume of a sterilized liquid medium is 20%-80% of a volume of the biological reaction device.

11. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 9, wherein the liquid medium further comprises 0.1 g/L of citric acid, and 0.05 g/L of ascorbic acid.

12. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 7, wherein the volume of sterilized liquid medium is 30%-70% of a volume of the biological reaction device.

13. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 7, wherein the adventitious roots are inoculated into the liquid medium at an inoculation amount of 0.2%-3%.

14. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 7, wherein the biological reaction device is fed with filtered air by air inlet devices at an air feeding amount of 0.02-0.5 vvm.

15. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 7, wherein the dark culture is conducted at 221 C. for 4-5 weeks in the biological reaction device.

16. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 7, wherein the biological reaction device for cultivation of adventitious roots of ginseng, comprising: a tank body, a cover body, being capable of being open and close and arranged on a top of the tank body; an air discharge device, arranged on the cover body or at the top of the tank body; and at least two air inlet devices, arranged at a bottom of the tank body, and allowing air to enter an inside of the tank body through the at least two air inlet devices.

17. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 16, wherein a discharge opening is arranged at a center of the bottom of the tank body, and the air inlet devices are evenly distributed around the discharge opening at intervals.

18. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 16, wherein a height of a bottom wall of the tank body is gradually decreased from a periphery to a center to form an inverted cone, a diameter of an upper part of the inverted cone is larger than a diameter of a lower part of the inverted cone; and the discharge opening is formed at the lowest position of the center of the bottom of the tank body, and the air inlet devices are evenly distributed around the discharge opening at intervals at the bottom wall of the tank body gradually decreasing from the periphery to the center.

19. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 16, wherein each of the air inlet devices comprises an air inlet, an air inlet pipe and an air filter, the air inlet is located on the bottom wall of the tank body, the air inlet pipe is connected to the air inlet in sealing manner, and the air filter is disposed in the air inlet pipe to filter air passing through the air inlet pipe.

20. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 16, wherein the air discharge device comprises an exhaust port, an exhaust pipe and a filter device, the exhaust port is arranged on the cover body or on the top of the tank body, the exhaust pipe is connected with the exhaust port in sealing manner, and the filter device is disposed in the exhaust pipe.

21. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 20, wherein the filter device is an air filter or a liquid filter.

22. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 16, wherein the tank body is provided with a plurality of viewing windows of transparent for viewing the interior of the tank body.

23. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 22, wherein the viewing windows are arranged on a side wall of a middle part and/or a lower part of the tank body.

24. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 16, wherein the tank body is also provided with a handle.

25. The method for culturing the adventitious roots of ginseng by using the biological reaction device according to claim 24, wherein the tank body is provided with at least two handles.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0081] The drawings serving as one part of the present disclosure are intended to provide a further understanding for the present disclosure. Schematic embodiments of the present disclosure and the descriptions thereof are intended to explain the present disclosure, rather than an improper limitation of the present disclosure. Obviously, the drawings described below are merely some embodiments. On the premise of not paying inventive labor, those of ordinary skill in the art can further obtain other drawings according to these drawings. In the drawings:

[0082] FIG. 1 is a structural schematic diagram of a biological reaction device of the present disclosure;

[0083] FIG. 2 is a schematic diagram of induction of adventitious roots by using an induction medium in Embodiment 1 of the present disclosure; and

[0084] FIG. 3 is a schematic diagram of induction of adventitious roots by using an induction medium in Comparative example 1; [0085] wherein, 1 tank body, 2 cover body, 3 air discharge device, 4 air inlet device, 5 discharge opening, 6 air inlet pipe, 7 air filter, 8 exhaust pipe, 9 filter device, 10 viewing window, 11 handle, and 12 support foot.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0086] To make the objectives, technical solutions, and advantages of embodiments of the present disclosure clearer, the technical solutions in the embodiments will be clearly and completely described below in combination with the accompanying drawings in the embodiments of the present disclosure. The following embodiments are used to describe the present disclosure but not to limit the scope of the present disclosure.

[0087] It should be noted that a preparation method or a detection method, which is not specifically defined in the present disclosure, can be performed by using a method that can be used to achieve its purpose in the prior art of the field.

[0088] As shown in FIG. 1, the present disclosure provides a biological reaction device for cultivation of adventitious roots of ginseng, including a tank body 1, wherein the top of the tank body 1 is provided with a cover body 2 which can be opened and closed, and an air discharge device 3 is arranged on the cover body 2 or at the top of the tank body 1; and the bottom of the tank body 1 is provided with at least two air inlet devices 4, and air enters the tank body 1 through the air inlet devices 4.

[0089] The biological reaction device of the present disclosure is a small bioreactor with a simple structure and easy operation. The biological reaction device can be used to produce ginseng adventitious roots conveniently, and the adventitious roots grow quickly and the growth multiple is high.

[0090] In the present disclosure, the tank body 1 is hollow inside for holding a liquid medium. The biological reaction device can be made of any material suitable for manufacturing a fermenter that can be used for high-temperature sterilization, e.g., glass, stainless steel, high temperature resistant plastic, etc.; preferably, stainless steel, which is durable and has a long service life. The cover body 2 at the top of the tank body 1 can be opened or closed for adding a liquid medium into the tank body, and the cover body 2 is in sealed connection with the tank body 1 after the liquid medium is added. The bottom of the tank body 1 is provided with at least two air inlet devices 4, and sterile air is introduced into the tank body 1 from different positions, so as to ensure that a culture in the tank body can be in full contact with the air and grows evenly, which is conducive to promoting the rapid growth of adventitious roots.

[0091] A center of bottom of the tank body 1 is provided with a discharge opening 5, and the air inlet devices 4 are evenly distributed around the discharge opening 5 at intervals; and preferably, a side wall and a bottom wall of the tank body 1 are in smooth transition, and a height of the bottom wall of the tank body 1 gradually decreases from the periphery to the center to form an inverted cone with a large upper part and a small lower part. And the discharge opening 5 is formed at the lowest position of the center, and the air inlet devices 4 are evenly distributed around the discharge opening 5 at intervals on the bottom wall gradually decreasing from the periphery to the center.

[0092] In the present disclosure, the air inlet devices 4 are arranged on inclined planes of the bottom wall of the tank body 1, the bottom wall of the tank body being of the inverted cone with the large upper part and the small lower part, so that inlet air will not rise vertically. Further, two or more air inlet devices 4 are evenly distributed around the center at intervals, which is conducive to uniform distribution of air in the tank body 1 and uniform growth of adventitious roots in the tank body 1.

[0093] The biological reaction device of the present disclosure further includes a support structure for supporting the tank body 1 to be placed vertically on a plane. In particular, the support structure includes support feet 12 which are connected to or disposed integrally with a lower part of the tank body 1, and the tank body 1 is placed on a plane or platform by means of the support feet 12. Preferably, the conical bottom of the tank body 1 is located within a space enclosed by the support feet 12.

[0094] Each air inlet device 4 includes an air inlet, an air inlet pipe 6 and an air filter 7; the air inlet is located on the bottom wall of the tank body 1, the air inlet pipe 6 is connected to the air inlet in sealing manner, and the air filter 7 is disposed on the air inlet pipe 6 to filter air passing through the air inlet pipe 6.

[0095] The air discharge device 3 includes an exhaust port, an exhaust pipe 8 and a filter device 9, the exhaust port is arranged on the cover body 2 or on the top of the tank body 1, the exhaust pipe 8 is connected with the exhaust port in sealing manner, and a filter device 9 is disposed on the exhaust pipe 8; and preferably, the filter device 9 is the air filter 7 or a liquid filter.

[0096] As one preferred embodiment, the exhaust port is formed in the center of the cover body 2.

[0097] In the above solution, when the filter device 9 disposed on the exhaust pipe 8 is the air filter 7, external air can be prevented from entering the tank body 1 from the top, ensuring a sterile culture environment inside the tank body 1. In addition, liquid can be added from the top when the filter device 9 on the exhaust pipe 8 is replaced with a liquid filter.

[0098] An inoculation port is arranged on the cover body 2 or on the top of the tank body 1 for inoculation.

[0099] The tank body 1 is provided with a plurality of viewing windows 10 of transparent; and the viewing windows 10 are arranged on a side wall of a middle part and/or a lower part of the tank body 1.

[0100] When the tank body 1 is made of opaque stainless steel, the interior of the tank body 1 can be viewed from different angles through the plurality of the viewing windows 10 of transparent arranged at different positions to timely grasp the growth of ginseng adventitious roots inside the tank body 1.

[0101] The tank body 1 is also provided with a handle 11; and preferably, at least two handles 11 are provided.

[0102] The handles 11 arranged on the tank body 1 may be symmetrically arranged, which is convenient for users to conveniently take and move the biological reaction device.

Embodiment 1

(1) Induction of Adventitious Roots

[0103] Rhizomes and adventitious roots on rhizomes were removed from 20-year-old wild ginseng, leaving the taproots. The taproots were washed and sterilized, cut into slices having a width of 0.6 cm, a length of 0.7 cm, and a thickness of 0.3 mm, and inoculated into an induction medium for dark culture at 221 C. for 4-5 weeks to induce wild ginseng adventitious roots; wherein the induction medium includes 4 mg/L of naphthylacetic acid, 0.6 mg/L of gibberellin, 0.4 mg/L of kinetin, 0.1 g/L of citric acid, 0.05 g/L of ascorbic acid, 30 g/L of sucrose, 3 g/L of Phytagel, 1.55 g/L of a B5 medium and 1.21 g/L of a WPM medium, with a pH of 5.8.

(2) Subculture of Adventitious Roots

[0104] the wild ginseng adventitious roots obtained in the step (1) were inoculated into the same induction medium as that in the step (1) for dark culture under the same conditions for 4-5 weeks.

(3) Culture of Adventitious Roots in a Shake Flask

[0105] the ginseng adventitious roots obtained in the step (2) were cut into tissue of about 1 cm in length, and were inoculated into a shake flask containing a liquid medium for dark culture at 110 rpm at 221 C. for 3-4 weeks; wherein the liquid medium contains 4 mg/L of indolebutyric acid, 2.3 g/L of a MS medium and 30 g/L of sucrose, with a pH of 5.8.

(4) Culture of Adventitious Roots in a Biological Reaction Device

[0106] a liquid medium was added into a tank body of the biological reaction device, wherein a volume of the liquid medium in the biological reaction device is 70% of a volume of the biological reaction device; and the liquid medium was sterilized at 121 C. for 20 min for standby application; wherein the liquid medium contains 4 mg/L of indolebutyric acid, 2.3 g/L of a MS medium and 30 g/L of sucrose, with a pH of 5.8.

[0107] The adventitious roots obtained in the step (3) were cut into tissue of about 1 cm in length, and inoculated into the liquid medium of the biological reaction device at an inoculation amount of 0.8%, the biological reaction device being fed with air at an air feeding amount of 0.1 vvm, for dark culture at 221 C. for 3-4 weeks to obtain adventitious roots.

[0108] In this embodiment, the adventitious roots produced on the induction medium in the step (1) are shown in FIG. 2, wherein A is a photograph of 1 week of culture, B is a photograph of 3 weeks of culture, and C is a photograph of 5 weeks of culture. It can be seen that after 5 weeks, adventitious roots were directly induced on the mature wild ginseng slices.

Embodiment 2

(1) Induction of Adventitious Roots

[0109] Rhizomes of 6-year-old garden ginseng were washed and sterilized, cut into slices having a width of 0.5 cm, a length of 0.6 cm, and a thickness of 0.3 mm, and inoculated into an induction medium for dark culture at 221 C. for 4-5 weeks to induce adventitious roots; wherein the induction medium includes 6 mg/L of naphthylacetic acid, 0.2 mg/L of gibberellin, 0.4 mg/L of kinetin, 1.2 g/L of citric acid, 0.1 g/L of ascorbic acid, 20 g/L of sucrose, 5 g/L of Phytagel, 4 g/L of a B5 medium and 1.8 g/L of a WPM medium, with a pH of 5.6.

(2) Subculture of Adventitious Roots

[0110] the adventitious roots obtained in the step (1) were inoculated into the same induction medium as that in the step (1) for dark culture under the same conditions for 4-5 weeks.

(3) Culture of Adventitious Roots in a Shake Flask

[0111] the ginseng adventitious roots obtained in the step (2) were inoculated into a shake flask containing a liquid medium for dark culture at 120 rpm at 221 C. for 3-4 weeks; wherein the liquid medium contains 4 mg/L of indolebutyric acid, 0.1 g/L of citric acid, 0.05 g/L of ascorbic acid, a MS medium and 30 g/L of sucrose, with a pH of 5.6.

(4) Culture of Adventitious Roots in a Biological Reaction Device

[0112] a liquid medium was added into a tank body of the biological reaction device, wherein a volume of the liquid medium in the biological reaction device is 40% of a volume of the biological reaction device; and the liquid medium was sterilized at 121 C. for 20 min for standby application; wherein the liquid medium contains 4 mg/L of indolebutyric acid, 0.1 g/L of citric acid, 0.05 g/L of ascorbic acid, a MS medium and 30 g/L of sucrose, with a pH of 5.6.

[0113] The ginseng adventitious roots obtained in the step (3) were cut into tissue of about 1 cm in length, and inoculated into the liquid medium of the biological reaction device at an inoculation amount of 0.5%, the biological reaction device being fed with air at an air feeding amount of 0.02 vvm, for dark culture at 221 C. for 3-4 weeks to obtain adventitious roots.

Embodiment 3

(1) Induction of Adventitious Roots

[0114] Adventitious roots on rhizomes of 10-year-old ginseng under forest were washed and sterilized, cut into slices having a width of 0.7 cm, a length of 0.7 cm, and a thickness of 0.5 mm, and inoculated into an induction medium for dark culture at 221 C. for 4-5 weeks to induce adventitious roots; wherein the induction medium includes 5 mg/L of naphthylacetic acid, 1 mg/L of gibberellin, 0.1 mg/L of kinetin, 0.075 g/L of citric acid, 0.03 g/L of ascorbic acid, 40 g/L of sucrose, 4 g/L of Phytagel, 2 g/L of a B5 medium and 1 g/L of a WPM medium, with a pH of 6.0.

(2) Subculture of Adventitious Roots

[0115] the adventitious roots obtained in the step (1) were inoculated into the same induction medium as that in the step (1) for dark culture under the same conditions for 4-5 weeks.

(3) Culture of Adventitious Roots in a Shake Flask

[0116] the ginseng adventitious roots obtained in the step (2) were inoculated into a shake flask containing a liquid medium for dark culture at 120 rpm at 221 C. for 3-4 weeks; wherein the liquid medium contains 4 mg/L of indolebutyric acid, 0.1 g/L of citric acid, 0.05 g/L of ascorbic acid, a WPM medium and 30 g/L of sucrose, with a pH of 6.0.

(4) Culture of Adventitious Roots in a Biological Reaction Device

[0117] a liquid medium was added into a tank body of the biological reaction device, wherein a volume of the liquid medium in the biological reaction device is 60% of a volume of the biological reaction device; and the liquid medium was sterilized at 121 C. for 20 min for standby application; wherein the liquid medium contains 4 mg/L of indolebutyric acid, 0.1 g/L of citric acid, 0.05 g/L of ascorbic acid, a WPM medium and 30 g/L of sucrose, with a pH of 6.0.

[0118] The ginseng adventitious roots obtained in the step (3) were cut into tissue of about 2 cm in length, and inoculated into the liquid medium of the biological reaction device at an inoculation amount of 1%, the biological reaction device being fed with air at an air feeding amount of 0.2 vvm, for dark culture at 221 C. for 3-4 weeks to obtain adventitious roots.

Embodiment 4

(1) Induction of Adventitious Roots

[0119] Taproots of 15-year-old transplant wild ginseng were washed and sterilized, cut into slices having a width of 0.5 cm, a length of 0.6 cm, and a thickness of 0.4 mm, and inoculated into an induction medium for dark culture at 221 C. for 4-5 weeks to induce ginseng adventitious roots; wherein the induction medium includes 1 mg/L of naphthylacetic acid, 0.5 mg/L of gibberellin, 0.6 mg/L of kinetin, 1.5 g/L of citric acid, 1 g/L of ascorbic acid, 50 g/L of sucrose, 6 g/L of Phytagel, 1 g/L of a B5 medium and 2.4 g/L of a WPM medium, with a pH of 5.7.

(2) Subculture of Adventitious Roots

[0120] the ginseng adventitious roots obtained in the step (1) were inoculated into the same induction medium as that in the step (1) for dark culture under the same conditions for 4-5 weeks.

(3) Culture of Adventitious Roots in a Shake Flask

[0121] the ginseng adventitious roots obtained in the step (2) were inoculated into a shake flask containing a liquid medium for dark culture at 120 rpm at 221 C. for 3-4 weeks; wherein the liquid medium contains 4 mg/L of indolebutyric acid, 0.1 g/L of citric acid, 0.05 g/L of ascorbic acid, a B5 medium and 30 g/L of sucrose, with a pH of 5.7.

(4) Culture of Adventitious Roots in a Biological Reaction Device

[0122] a liquid medium was added into a tank body of the biological reaction device, wherein a volume of the liquid medium in the biological reaction device is 30% of a volume of the biological reaction device; and the liquid medium was sterilized at 121 C. for 20 min for standby application; wherein the liquid medium contains 4 mg/L of indolebutyric acid, 0.1 g/L of citric acid, 0.05 g/L of ascorbic acid, a B5 medium and 30 g/L of sucrose, with a pH of 5.7.

[0123] The ginseng adventitious roots obtained in the step (3) were cut into tissue of about 1 cm in length, and inoculated into the liquid medium of the biological reaction device at an inoculation amount of 0.2%, the biological reaction device being fed with air at an air feeding amount of 0.05 vvm, for dark culture at 221 C. for 3-4 weeks to obtain adventitious roots.

Embodiment 5

(1) Induction of Adventitious Roots

[0124] Rhizomes and adventitious roots on rhizomes were removed from centennial wild ginseng, taproots were washed and sterilized, cut into slices having a width of 0.6 cm, a length of 0.7 cm, and a thickness of 0.3 mm, and inoculated into an induction medium for dark culture at 221 C. for 4-5 weeks to induce ginseng adventitious roots; wherein the induction medium includes 4 mg/L of naphthylacetic acid, 0.6 mg/L of gibberellin, 0.4 mg/L of kinetin, 0.1 g/L of citric acid, 0.05 g/L of ascorbic acid, 30 g/L of sucrose, 3 g/L of Phytagel, 1.55 g/L of a B5 medium and 1.21 g/L of a WPM medium, with a pH of 5.8.

(2) Subculture of Adventitious Roots

[0125] the ginseng adventitious roots obtained in the step (1) were inoculated into the same induction medium as that in the step (1) for dark culture under the same conditions for 4-5 weeks;

(3) Culture of Adventitious Roots in a Shake Flask

[0126] the ginseng adventitious roots obtained in the step (2) were inoculated into a shake flask containing a liquid medium for dark culture at 120 rpm at 221 C. for 3-4 weeks; wherein the liquid medium contains 4 mg/L of indolebutyric acid, 0.1 g/L of citric acid, 0.05 g/L of ascorbic acid, a MS medium and 30 g/L of sucrose, with a pH of 5.8.

(4) Culture of Adventitious Roots in a Biological Reaction Device

[0127] a liquid medium was added into a tank body of the biological reaction device, wherein a volume of the liquid medium in the biological reaction device is 75% of a volume of the biological reaction device; and the liquid medium was sterilized at 121 C. for 20 min for standby application; wherein the liquid medium contains 4 mg/L of indolebutyric acid, 0.1 g/L of citric acid, 0.05 g/L of ascorbic acid, a MS medium and 30 g/L of sucrose, with a pH of 5.8.

[0128] The ginseng adventitious roots obtained in the step (3) were cut into tissue of about 1 cm in length, and inoculated into the liquid medium of the biological reaction device at an inoculation amount of 3%, the biological reaction device being fed with air at an air feeding amount of 0.5 vvm, for dark culture at 221 C. for 3-4 weeks to obtain adventitious roots.

Comparative Example 1

[0129] This comparative example differed from Embodiment 1 in that the induction medium used was different and the other steps were carried out with reference to Embodiment 1. The induction medium in this comparative example includes: 30 g/L of sucrose, 0.5 mg/L of kinetin, 3 mg/L of indolebutyric acid, 1.5 mg/L of 2,4-dichlorophenoxyacetic acid, a MS medium, and 3 g/L of Phytagel, with a pH of 5.8.

[0130] The adventitious roots produced on the induction medium in the step (1) of this comparative example are shown in FIG. 3, wherein A is a photograph of 1 week of culture, B is a photograph of 3 weeks of culture, and C is a photograph of 5 weeks of culture. It can be seen that after 5 weeks, adventitious roots cannot be directly induced from mature wild ginseng slices by using the medium in Comparative example 1.

Comparative Example 2

[0131] This comparative example differed from Embodiment 1 in that the induction medium used was different and the other steps were carried out with reference to Embodiment 1. The induction medium in this comparative example includes: 30 g/L of sucrose, 0.5 mg/L of kinetin, 3 mg/L of indolebutyric acid, a MS medium, and 3 g/L of Phytagel, with a pH of 5.8.

[0132] As a result, similar to that shown in the picture in Comparative example 1, adventitious roots cannot be directly induced from mature wild ginseng slices.

Comparative Example 3

[0133] This comparative example differed from Embodiment 1 in that the induction medium used was different and the other steps were carried out with reference to Embodiment 1. The induction medium in this comparative example includes: 30 g/L of sucrose, 0.5 mg/L of kinetin, 3 mg/L of indoleacetic acid, WPM, and 3 g/L Phytagel, with a pH of 5.8.

[0134] Results: in the first week, the whole body turned yellow, in the third week, the color deepened, and the middle part began to turn brown, and in the fifth week, all became brown and withered.

Comparative Example 4

[0135] In this comparative example, the difference from Embodiment 1 was that the biological reaction device employed was different in that only one air vent was formed in the center of the bottom of the tank body, one air inlet device was provided, and the bottom wall of the tank body was of a downward concave circular arc; and other conditions were the same as those in Embodiment 1.

[0136] The ginseng adventitious roots were cultured by using the biological reaction device of the present disclosure (i.e., a 5 L fermenter of the present disclosure) and the biological reaction device in this Comparative example 4 (with a volume of 5 L), respectively, and the growth results of the ginseng adventitious roots in the medium are as follows:

TABLE-US-00001 TABLE 1 Adventitious root Experimental group growth multiple Comparative example 4 8 Embodiment 1 14

[0137] Thus, under the same conditions, the weight gain multiple of adventitious roots is higher, and the growth is better by using the biological reaction device of the present disclosure, which is beneficial to improving the efficiency and obtaining higher content of ginsenoside.

Test Example 1 Screening of Liquid Medium

[0138] In order to increase the content of ginsenoside in the ginseng adventitious roots, a liquid medium was further subjected to screening optimization.

[0139] A culture method in this test example refers to the method in Embodiment 1 with the difference that: [0140] 1. the liquid medium in Embodiment 1 was replaced with a plurality of liquid media in this test example described below, and [0141] 2. the step (4) was omitted, and liquid culture in a shake flask was used for examination.

[0142] The content of ginsenoside in the ginseng adventitious roots was then detected.

[0143] A detection method of ginsenoside in the ginseng adventitious roots includes:

(1) Principle

[0144] After pretreatment such as extraction, a sample was separated by a C18 chromatographic column, and detected by a HPLC-UV detector, and the content of ginsenoside components was determined quantitatively by an external standard method.

(2) Reagents

[0145] Methanol (CH.sub.4O): chromatographically pure, and acetonitrile (C.sub.6H.sub.11N): chromatographically pure

[0146] Standard reagent: ginsenosides Re, Rg1, Ra3, Rb1, Rf, Rb2, Rb3, F3, Rg2, Rd, and F1.

(3) Analysis Steps

Preparation of Adventitious Root Test Solution:

[0147] about 6 g (accurate to 0.01 g) of uniformly mixed adventitious roots to be tested was taken, ground in a 150 mL mortar, transferred to a 50 ml centrifuge tube, mixed with 10 ml of water, wall broken on a ultrasonic cell disruptor at 400 W for 3 min, and frozen in a refrigerator at 18 C. for 3 h. The frozen material was lyophilized in a lyophilizer for 48 h until there were no water beads outside a cup.

[0148] The above sample was ground in a mortar, 50 mg of the ground sample was accurately weighed to be placed in a 10 ml centrifuge tube, a 70% methanol solution was added, and vortex was conducted. Ultrasonic treatment was conducted on an ultrasonic oscillator for 10 min, the above operation was conducted repeatedly twice, and filtration was conducted for later use.

Standard Preparation:

[0149] Preparation of stock solution (0.8 mg/ml): 8.00 mg of ginsenosides Re, Rb1, Rg1, Rd, [0150] Rf, F3, Rk2, Rb2, Rb3, Rg2, and F1, which are 11 standards in total, were respectively weighed to be placed in a 10 ml volumetric flask, and the volume was made up to a constant volume with superior pure methanol.

[0151] Preparation of use solution (32 g/ml): 1 ml of the stock solution (0.8 mg/ml) was accurately pipetted into a 25 ml volumetric flask, and made up to a constant volume with superior pure methanol, and filtered through a 0.22 m organic filter membrane for later use.

(4) Instrument Reference Conditions

[0152] A) Chromatographic column: a C18 column with a column length of 150 mm, a column internal diameter of 4.6 mm, and a column packing particle size of 5 m, or equivalent; [0153] B) Mobile phase: a: acetonitrile, and b: water filtered through a 0.45 m microporous filter membrane; [0154] C) Flow rate: 0.7 mL/min; gradient elution procedure: 0-13 min, 23-46% acetonitrile, with a volume flow rate of 0.7 mL/min; 13-33 min, 46-68% acetonitrile, with a volume flow rate of 0.7 mL/min; 33-46.5 min, 68-85% acetonitrile, with a volume flow rate of 0.7 mL/min; [0155] D) Column temperature: 30 C.; [0156] E) Detection wavelength: 203 nm; and [0157] F) Injection volume: 10 L.

(5) Expression of Analysis Results

[0158] The content of ginsenoside components in the sample is calculated according to a formula (1):

[00001]$\begin{array}{cc}X=\frac{A1}{A2}\frac{V}{M}& \left(1\right)\end{array}$ [0159] in the formula: [0160] Xthe content of ginsenoside components in a sample in milligrams per kilogram (mg/kg) or milligrams per liter (mg/L); [0161] A1peak area of ginsenoside components in a sample [0162] A2peak area of ginsenoside components in a standard [0163] pconcentration of ginsenoside components in a standard (g/ml) [0164] Vfinal constant volume of a sample solution in milliliters (mL); [0165] Msample mass in grams (g);

[0166] The content of ginsenoside in the sample is the sum of those detected in the components.

The Growth Multiple is Calculated as Follows:

[0167] Growth multiple=weight of adventitious roots after growth/weight of inoculated adventitious root seeds.

1. Liquid Medium 1

[0168] A liquid medium 1 includes: 15-50 g/L of sucrose, 0.6-2.4 g/L of a WPM medium, 1-2 g/L of a N6 medium, 0-150 mg/L of ascorbic acid (Vc), 0-225 mg/L of citric acid, and 0-7 mg/L of indolebutyric acid (IBA), with a pH of 5.8.

TABLE-US-00002 TABLE 2 N6 WPM Citric Ginsenoside Experimental Sucrose medium medium Vc acid IBA Growth content group (g/l) (g/l) (g/l) (mg/L) (mg/L) (mg/L) multiple (mg/kg) 1 15 2 2.4 150 150 7 4.7 9310.8 2 20 2 2.4 150 0 6 3.2 7999.3 3 25 2 1.8 100 150 5 12.8 9458.8 4 30 2 1.8 100 0 4 8 9923.9 5 35 1 1.2 50 225 3 11.5 16622.1 6 40 1 1.2 50 75 2 12.5 11733.5 7 45 1 0.6 0 225 1 8.4 10453.6 8 50 1 0.6 0 75 0 1.4 9607.3

[0169] As can be seen in Table 2 above, the growth multiple of adventitious roots was higher, and the total amount of ginsenosides detected was higher by using the liquid media 1 with the ratios in Experimental groups 5-7, with a best combination of the growth multiple of adventitious roots and the ginsenosides content in Experimental group 5.

2. Liquid medium 2

[0170] A liquid medium 2 includes: 10-55 g/L of sucrose, 0.3-1.2 g/L of a MS medium, 0.6-1.6 g/L of a B5 medium, 0-5.4 mg/L of indoleacetic acid (IAA), 0-5.4 mg/L of indolebutyric acid (IBA), 0-5.4 mg/L of naphthylacetic acid (NAA), 0-5.4 mg/L of 6-benzylaminoadenine (6BA), and 0-8 mg/L of gibberellin (GA), with a pH of 5.8.

TABLE-US-00003 TABLE 3 B5 Ginsenoside Experimental Sucrose MS medium IAA IBA NAA 6BA GA Growth content group (g/l) (g/l) (g/l) (mg/l) (mg/l) (mg/l) (mg/l) (mg/l) multiple (mg/kg) 1 10 0.405 0.78 3 5.4 4.2 3.6 1.6 2.7 7157.77 2 50 1.005 1.38 2.4 5.4 3.6 1.8 6.4 1.7 9773.01 3 55 0.305 0.68 3.6 1.8 0.6 4.2 4 1.8 7908.18 4 45 0.905 1.28 0.6 0.6 3 4.2 0.8 6.7 15878.75 5 15 0.805 1.18 4.2 0 2.4 2.4 8 1.7 16575 6 45 0.705 1.08 4.8 3.6 1.8 0 0 9.3 10523.13 7 20 1.205 1.58 1.8 2.4 0 1.2 2.4 3.9 6784.19 8 35 0.505 0.88 1.2 1.2 5.4 0.6 4.8 1.5 11589.18 9 30 1.105 1.48 5.4 3 5.4 5.4 3.2 6.3 8850.39 10 25 0.605 0.98 0 4.8 1.2 4.8 5.6 1.9 7516.73

[0171] As can be seen in Table 3 above, the growth multiple of adventitious roots was higher, and the total amount of ginsenosides detected was higher by using the liquid media 2 with the ratios in Experimental groups 4 and 6, with a best combination of the growth multiple of adventitious roots and the ginsenosides content in Experimental group 4.

3. Liquid Medium 3

[0172] A liquid medium 3 includes: 35 g/L of sucrose, 1.35 g/L of a WPM medium, 1 g/L of a N6 medium, 0-1.8 mg/L of indolebutyric acid (IBA), 1-6 mg/L of naphthylacetic acid (NAA), and 0.2-1.2 mg/L of kinetin (KT), with a pH of 5.8.

TABLE-US-00004 TABLE 4 Ginsenoside Experimental Sucrose WPM N6 IBA NAA KT Growth content Culture group (g/l) (g/l) (g/l) (mg/L) (mg/l) (mg/l) multiple (mg/kg) day 1 35 1.35 1 1 2 1.2 6.9 7727.6 33 2 35 1.35 1 0.2 4 1.2 8.2 9123.5 42 3 35 1.35 1 1 6 0.2 9.5 9977.3 33 4 35 1.35 1 0.6 2 0.2 9.7 10045.2 42 5 35 1.35 1 0 4 0.2 7.8 8745.6 33 6 35 1.35 1 0.4 6 0.4 8.8 9576.1 30 7 35 1.35 1 0.8 2 1 10.1 11457.3 30 8 35 1.35 1 0.4 4 1 10.5 11948.1 39 9 35 1.35 1 0.2 6 1.2 8.5 9011.4 30 10 35 1.35 1 1 1 0.8 9.5 11387.5 30 11 35 1.35 1 0.6 3 0.8 12.3 14567.2 39 12 35 1.35 1 0.2 5 1 13.1 15432.7 36 13 35 1.35 1 0 1 0.6 5.4 6741.2 45 14 35 1.35 1 0.8 3 0.6 8.5 8764.1 35 15 35 1.35 1 0.4 5 0.8 11.9 10743.4 45 16 35 1.35 1 1.8 1 0.4 12.0 11547.3 36 17 35 1.35 1 0.8 3 0.4 12.1 12634.1 42 18 35 1.35 1 0.6 5 0.6 12.5 12749.5 45

[0173] As can be seen from Table 4 above, on the basis of determining the amount of sucrose, WPM and N6, the effects of plant hormones IBA, NAA and KT on the yield of adventitious roots and the content of ginsenosides were examined at different addition amounts, so as to select the appropriate plant hormones and their ratios. As can be seen from the table, the growth multiple of adventitious roots and the total ginsenosides content were better under the formulas of Experimental groups 4, 7-8, 10-12 and 15-18, with a best combination of the growth multiple of adventitious roots and the total ginsenosides content according to the conditions in Experimental group 12.

[0174] The inventors further use the liquid medium 1, the liquid medium 2 or the liquid medium 3 to culture the ginseng adventitious roots by using the above biological reaction device, and the growth multiple of the obtained adventitious roots is high.

[0175] The above description is only preferred embodiments of the present disclosure, and is not intended to limit the present disclosure in any form. Although the present disclosure has been disclosed above with the preferred embodiments, it is not intended to limit the present disclosure. Any person familiar with this patent can make some changes or modifications to equivalent embodiments by using the technical contents mentioned above without departing from the scope of the technical solution of the present disclosure. However, any simple changes, equivalent variations and modifications made to the above embodiments according to the technical essence of the present disclosure without departing from the content of the technical solution of the present disclosure are still within the scope of the solution of the present disclosure.