阅读说明：本技术 一种柔毛淫羊藿无菌体系的建立及快速增殖的方法 (Method for establishing and rapidly proliferating Epimedium pubescens sterile system ) 是由 林良科 王旭东 于 2021-08-02 设计创作，主要内容包括：本发明属于药用植物组织培养技术领域,尤其涉及一种柔毛淫羊藿无菌体系的建立及快速增殖的方法,包括如下步骤：1)采集淫羊藿幼嫩根状茎,去掉叶片,用洗衣粉饱和溶液浸泡30min,并用刷子轻轻刷表面,再用流水冲洗2h后,置于超净工作台上,消毒,用无菌手术剪剪掉根状茎两端各2mm,得到带完整芽点的无菌茎段,备用；2)将步骤1)获得的无菌茎段垂直接种到诱导培养基上培养,诱导出芽；3)将步骤2)获得的萌蘖芽切为单个芽点,垂直接种到增殖培养基上培养,得到淫羊藿丛生芽；本发明方法可获得淫羊藿快速增殖的方法,可为淫羊藿人工繁育提供优质种苗,解决了淫羊藿因种子采集困难、发芽率低而育苗困难的难题。(The invention belongs to the technical field of medicinal plant tissue culture, and particularly relates to a method for establishing and rapidly proliferating a epimedium dauricum sterile system, which comprises the following steps: 1) collecting young and tender rhizome of herba Epimedii, removing leaves, soaking in washing powder saturated solution for 30min, brushing the surface with a brush, washing with flowing water for 2 hr, placing on a clean bench, sterilizing, and shearing off 2mm of each end of the rhizome with sterile surgical scissors to obtain sterile stem segment with complete bud point; 2) vertically inoculating the sterile stem section obtained in the step 1) to an induction culture medium for culture, and inducing germination; 3) cutting the shoot buds obtained in the step 2) into single shoot points, vertically inoculating the shoot points to a proliferation culture medium, and culturing to obtain epimedium clustered buds; the method can obtain the method for quickly proliferating the epimedium, can provide high-quality seedlings for the artificial breeding of the epimedium, and solves the problem of difficult seedling culture of the epimedium due to difficult seed collection and low germination rate.)

1. A method for establishing and rapidly proliferating an Epimedium pubescens sterile system is characterized by comprising the following steps:

1) collecting young and tender rhizome of herba Epimedii, removing leaves, soaking in washing powder saturated solution for 30min, brushing the surface with brush, washing with flowing water for 2h, placing on a clean bench, sterilizing with 75% alcohol for 30s, washing with sterile water for 3 times, sterilizing, and shearing off 2mm each of two ends of the rhizome with sterile surgical scissors to obtain sterile stem segment with complete bud point;

2) vertically inoculating the sterile stem section obtained in the step 1) to an induction culture medium for culture, and inducing germination; the induction culture medium is MS +0.5-2.0mg/L6-BA +0.3-1.1mg/L IBA +40-70mg/L PVP +80-140mg/L streptomycin +5.8g/L agar +30g/L sucrose;

3) cutting the shoot buds obtained in the step 2) into single bud points, vertically inoculating the shoot points to a multiplication culture medium for culture, and culturing for 28 days under the conditions that the temperature is 25 ℃, the illumination intensity is 2300-; the proliferation culture medium is MS +1.5-2.5mg/L6-BA +0.3-0.9mg/L NAA +60mg/L PVP +5.8g/L agar +30g/L sucrose.

2. The method for establishing and rapidly propagating epimedium dauricum sterile system according to claim 1, wherein in the step 1), the re-sterilization method comprises the following steps: sterilizing with 0.1% mercuric chloride for 4min, washing with sterile water for 5 times, sterilizing with 0.1% mercuric chloride for 2.5min, and washing with sterile water for 5 times.

3. The method as claimed in claim 1, wherein in step 2), the culture condition is dark culture at 25 ℃ for 7d, and then the culture medium is turned to 25 ℃ and the illumination intensity is 2300-.

4. The method for establishing and rapidly propagating epimedium dauricum sterile system according to claim 1, wherein in the step 2), the induction medium is MS +1.5mg/L6-BA +0.8mg/L IBA +60mg/L PVP +120mg/L streptomycin +5.8g/L agar +30g/L sucrose, and the pH is adjusted to 5.8.

5. The method for establishing and rapidly proliferating the epimedium dauricum sterile system according to claim 1, wherein in the step 3), the proliferation medium is MS +2.0 mg/L6-BA +0.5mg/L NAA +60mg/L PVP +5.8g/L agar +30g/L sucrose, and the pH is adjusted to 5.8.

Technical Field

The invention belongs to the technical field of medicinal plant tissue culture, and particularly relates to a method for establishing and rapidly proliferating a epimedium hirsutum sterile system.

Background

Epimedium pubescens is one of the original plants of Epimedium pubescens collected in the pharmacopoeia of the people's republic of China (2020 edition), is a traditional Chinese medicinal material in China, mainly has the effects of tonifying kidney yang, strengthening tendons and bones and dispelling wind-damp, and has more than 2000 years of application history in China. Modern researchers find various physiologically active chemical components such as general flavone, polysaccharide, alkaloid and the like in bodies of the modern researchers, and the modern researchers are widely applied to traditional medicine and modern medicine at present. The current market demand of epimedium is about 5000 tons/year, and the main acquisition mode is still for excavating wild resources, and along with the increase of the excavation amount and the unordered excavation of people, the wild epimedium resources are continuously reduced, so that the regeneration and the sustainable utilization of the resources are not very facilitated. Therefore, the artificial introduction and cultivation of epimedium is urgent.

Under natural conditions, due to the natural dormancy and the after-ripening of seed embryos, the seed germination rate of epimedium dauricum seeds is extremely low, the germination period is long, and the method is very not beneficial to the large-scale planting of epimedium. At present, the artificial planting of epimedium basically adopts a way of plant division propagation, long-term asexual propagation easily causes variety degradation, and the yield and the quality of medicinal materials are reduced.

Disclosure of Invention

The method can obtain an epimedium sterile system and a rapid propagation method, can provide high-quality seedlings for artificial breeding of the epimedium, and solves the problem of difficult seedling culture of the epimedium due to difficult seed collection and low germination rate.

The invention provides a method for establishing and rapidly proliferating an epimedium dauricum sterile system, which comprises the following steps:

1) collecting young and tender rhizome of herba Epimedii, removing leaves, soaking in washing powder saturated solution for 30min, brushing the surface with brush, washing with flowing water for 2h, placing on a clean bench, sterilizing with 75% alcohol for 30s, washing with sterile water for 3 times, sterilizing, and shearing off 2mm each of two ends of the rhizome with sterile surgical scissors to obtain sterile stem segment with complete bud point;

2) vertically inoculating the sterile stem section obtained in the step 1) to an induction culture medium for culture, and inducing germination; the induction culture medium is MS +0.5-2.0mg/L6-BA +0.3-1.1mg/L IBA +40-70mg/L PVP +80-140mg/L streptomycin +5.8g/L agar +30g/L sucrose;

3) cutting the shoot buds obtained in the step 2) into single bud points, vertically inoculating the shoot points to a multiplication culture medium for culture, and culturing for 28 days under the conditions that the temperature is 25 ℃, the illumination intensity is 2300-; the proliferation culture medium is MS +1.5-2.5mg/L6-BA +0.3-0.9mg/L NAA +60mg/L PVP +5.8g/L agar +30g/L sucrose.

Further, in step 1), the method for re-sterilization is: sterilizing with 0.1% mercuric chloride for 4min, washing with sterile water for 5 times, sterilizing with 0.1% mercuric chloride for 2.5min, and washing with sterile water for 5 times.

Further, in step 2), the culture conditions are dark culture at 25 ℃ for 7d, and then the culture medium is transferred to 25 ℃ and the illumination intensity is 2300-.

Further, in step 2), the induction medium is: MS +1.5mg/L6-BA +0.8mg/L IBA +60mg/L PVP +120mg/L streptomycin +5.8g/L agar +30g/L sucrose, pH was adjusted to 5.8.

Further, in step 3), the proliferation medium is: MS +2.0 mg/L6-BA +0.5mg/L NAA +60mg/L PVP +5.8g/L agar +30g/L sucrose, pH was adjusted to 5.8.

The invention has the beneficial effects that: the invention adopts the buds of epimedium as explants, and establishes a rapid proliferation sterile system of the epimedium dauricum through a cluster bud approach; the rapid propagation sterile system of the epimedium dauricum is established by combining disinfection, induction culture and propagation culture, so that the pollution rate is reduced, and the yield and the quality of the epimedium are improved; the method has the advantages of simple flow and short propagation period, provides technical guidance for herba epimedii seedling breeding and large-scale propagation, solves the problem of difficult seedling culture caused by low germination rate and long germination period of herba epimedii seeds, reduces the herba epimedii seedling breeding cost, and provides high-quality seedlings for artificial propagation of herba epimedii.

Drawings

FIG. 1 is a line graph showing the effect of a mercuric chloride disinfectant composition of the present invention on explant disinfection.

Detailed Description

The principles and features of this invention are described below in conjunction with examples which are set forth to illustrate, but are not to be construed to limit the scope of the invention.

Unless otherwise specifically stated, various raw materials, reagents, instruments, equipment and the like used in the present invention are commercially available or can be prepared by existing methods.

The invention provides a method for establishing and rapidly proliferating an epimedium dauricum sterile system, which comprises the following steps:

1) collecting young and tender rhizome of herba Epimedii, removing leaves, soaking in washing powder saturated solution for 30min, brushing the surface with brush, washing with flowing water for 2h, placing on a clean bench, sterilizing with 75% alcohol for 30s, washing with sterile water for 3 times, sterilizing, and shearing off 2mm each of two ends of the rhizome with sterile surgical scissors to obtain sterile stem segment with complete bud point;

2) vertically inoculating the sterile stem section obtained in the step 1) to an induction culture medium for culture, and inducing germination; the induction culture medium is MS +0.5-2.0mg/L6-BA +0.3-1.1mg/L IBA +40-70mg/L PVP +80-140mg/L streptomycin +5.8g/L agar +30g/L sucrose;

3) cutting the shoot buds obtained in the step 2) into single bud points, vertically inoculating the shoot points to a multiplication culture medium for culture, and culturing for 28 days under the conditions that the temperature is 25 ℃, the illumination intensity is 2300-; the proliferation culture medium is MS +1.5-2.5mg/L6-BA +0.3-0.9mg/L NAA +60mg/L PVP +5.8g/L agar +30g/L sucrose.

The effect of cutting off 2mm of each of the two ends of the rhizome by using the sterile surgical scissors is to cut off the part seriously stimulated by the disinfectant, so as to ensure the subsequent normal culture of the sterile stem section;

wherein, MS culture medium is a common basic culture medium formula in plant tissue culture technology, the content composition is fixed, and the formula is shown in table 1:

TABLE 1MS media composition Table

In addition, 6-BA (6-benzylamino adenine) is one of plant cytokinins, can promote plant cell division and elongation in stem tip or bud culture, can break apical dominance and promote the generation and proliferation of lateral buds and multiple buds;

IBA (indolebutyric acid) is one of auxin and can promote the regeneration and proliferation of plant seedling buds;

PVP (polyvinylpyrrolidone K30) has an inhibiting effect on explant browning, the action mechanism is that PVP is a specific adsorbent of phenolic substances, CO-N in PVP has strong ability of complexing polyphenol compounds, and the PVP can enable the polyphenol compounds not to be substrates of polyphenol oxidase, so that browning is inhibited;

streptomycin and 72% streptomycin sulfate have an inhibiting effect on bacteria, and streptomycin with a proper concentration is added into an induction culture medium to inhibit the endophyte pollution of explants, so that the pollution rate is reduced, and the induction rate is improved;

NAA (naphthylacetic acid) is one of auxin, can promote plant cell differentiation, and can promote seedling bud regeneration and proliferation by combining with cytokinin under proper concentration;

6-BA, IBA, PVP and streptomycin in the induction culture medium are cooperatively matched to improve the bud induction rate of the Epimedium dauricum explant, and simultaneously reduce the pollution rate and browning rate of the explant;

6-BA, NAA and PVP in the multiplication culture medium cooperate to improve the multiplication times of the hairy epimedium clustered shoots and reduce the browning rate of the clustered shoots at the same time.

Further, in step 1), the method for re-sterilization is: sterilizing with 0.1% mercuric chloride for 4min, washing with sterile water for 5 times, sterilizing with 0.1% mercuric chloride for 2.5min, and washing with sterile water for 5 times.

Further, in step 2), the culture conditions are dark culture at 25 ℃ for 7d, and then the culture medium is transferred to 25 ℃ and the illumination intensity is 2300-.

Further, in step 2), the induction medium is: MS +1.5mg/L6-BA +0.8mg/L IBA +60mg/L PVP +120mg/L streptomycin +5.8g/L agar +30g/L sucrose, pH was adjusted to 5.8.

Further, in step 3), the proliferation medium is: MS +2.0 mg/L6-BA +0.5mg/L NAA +60mg/L PVP +5.8g/L agar +30g/L sucrose, pH was adjusted to 5.8.

The method for establishing and rapidly propagating epimedium dauricum sterile system of the present application will be described in detail below with reference to examples and experimental data.

Example 1

1) Collecting young and tender rhizome of epimedium, removing leaves, soaking for 30min by using a washing powder saturated solution, slightly brushing the surface by using a brush, washing for 2h by using running water, placing on a super-clean workbench, disinfecting for 30s by using 75% alcohol by volume fraction, washing for 3 times by using sterile water, disinfecting by using 0.1% mercury bichloride according to a disinfection combination shown in table 2, washing for 5 times by using the sterile water, washing for more than 90s each time, and shearing two ends of the rhizome by using a sterile surgical scissors to obtain sterile stem sections with complete bud points for later use, wherein the two ends of the rhizome are 2mm respectively;

TABLE 2 Mercury-mercurial-sterilizing combined experimental design table

2) Vertically inoculating the sterile stem section obtained in the step 1) to an induction culture medium (MS +1.5mg/L6-BA +0.8mg/L IBA +60mg/L PVP +120mg/L streptomycin +5.8g/L agar +30g/L sucrose, pH is 5.8) for culture, inoculating 10 bottles in each group, and inoculating 1 explant in each bottle; culturing the inoculated induction culture medium in the dark at 25 ℃ for 7d, and then culturing the culture medium at 25 ℃ under the conditions of 2300 illumination intensity and 2500lx and 12h/d illumination time;

3) the number of the polluted explants and the number of the explants which are disinfected by mercury bichloride for too long to damage and die are observed and counted in 1-10d of culture, and the pollution after 10d of culture is not considered as the pollution caused by incomplete disinfection of the explants.

The results are shown in Table 3:

TABLE 3 Mercury mercurial disinfection combination test results table

The explant contamination rate and explant sterilization mortality rate were plotted and the results are shown in FIG. 1.

FIG. 1 is a line chart showing the effect of mercuric chloride disinfection combination on explant disinfection, and as can be seen from FIG. 1 and Table 3, only one disinfection (combinations 1-4) is adopted, so that the explant pollution rate is continuously reduced and the explant disinfection death rate is continuously increased with the increase of disinfection time; adopting subsection secondary disinfection (combination 5-10), along with the increase of the secondary disinfection time, the contamination rate of the explant is changed from high to low, and the disinfection death rate of the explant is gradually increased; the explant loss rate of the disinfection combination 7 and the disinfection combination 9 is the lowest and is 30%, the disinfection time of the disinfection combination 7 is shorter, so the combination 7 is adopted as the most suitable disinfection time, namely the explant is disinfected for 4min by using mercury bichloride with the mass fraction of 0.1%, the explant is washed by sterile water for 5 times, the explant is disinfected for 2.5min by using mercury bichloride with the mass fraction of 0.1% again, the sterile water is washed by the sterile water for 5 times, the explant pollution rate is low, the disinfection death rate is low, the disinfection time is shorter, and the economic benefit is favorably realized.

Example 2

1) Collecting young and tender rhizome of epimedium, removing leaves, soaking for 30min by using a washing powder saturated solution, slightly brushing the surface by using a brush, washing for 2h by using running water, then placing on a super-clean workbench, disinfecting for 30s by using 75% alcohol by volume fraction, washing for 3 times by using sterile water, disinfecting for 4min by using 0.1% mercury bichloride, washing for 5 times by using the sterile water, disinfecting for 2.5min by using 0.1% mercury bicide again, washing for 5 times by using the sterile water, and shearing two ends of the rhizome by using a sterile operation for 2mm respectively to obtain a sterile stem section with a complete bud point for later use;

2) vertically inoculating the sterile stem sections obtained in the step 1) to a single-hormone culture medium shown in a table 4, inoculating 10 bottles in each group, inoculating 1 explant in each bottle, and setting 2 groups for repeated experiments; culturing in dark at 25 deg.C for 7d, and culturing at 25 deg.C under illumination intensity 2300-;

TABLE 4 Single hormone Medium design Table

3) And (4) counting the budding rate of the explant and the growth vigor of buds. The growth vigor of the buds is respectively shown as poor to good by +, + + +, and + + +.

The results are shown in Table 5:

TABLE 5 test results on Single hormone Medium

As can be seen from Table 5, the effect of 6-BA when cytokinin was used alone was better than that of 6-KT, and the growth of shoots was better when the concentration of 6-BA was 1.5 mg/L; when the auxin is used alone, the IBA effect is better than that of NAA, and the growth vigor of buds is better when the IBA concentration is 0.9mg/L, so that the Epimedium dauricum explant is sensitive to hormones 6-BA and IBA, and the bud induction effect is better.

Example 3

1) Collecting young and tender rhizome of epimedium, removing leaves, soaking for 30min by using a washing powder saturated solution, slightly brushing the surface by using a brush, washing for 2h by using running water, then placing on a super-clean workbench, disinfecting for 30s by using 75% alcohol by volume fraction, washing for 3 times by using sterile water, disinfecting for 4min by using 0.1% mercury bichloride, washing for 5 times by using the sterile water, disinfecting for 2.5min by using 0.1% mercury bicide again, washing for 5 times by using the sterile water, and shearing two ends of the rhizome by using a sterile operation for 2mm respectively to obtain a sterile stem section with a complete bud point for later use;

2) vertically inoculating the sterile stem sections obtained in the step 1) to induction culture media with different concentrations of hormone combinations as shown in table 6 for culture, inoculating 10 bottles in each group, inoculating 1 explant in each bottle, and setting 2 groups of repeated experiments; culturing in dark at 25 deg.C for 7d, and culturing at 25 deg.C with illumination intensity of 2300-;

TABLE 6 Induction Medium design Table for different concentrations of hormone combinations

Serial number	6-BA(mg/L)	IBA(mg/L)
			1	1.3	0.7
2	1.5	0.8
			3	1.7	0.9
4	--	1.0
			5	--	1.1

3) And (4) counting the budding rate of the explant and the growth vigor of buds. The growth vigor of the buds is respectively shown as poor to good by +, + + +, and + + +.

The results are shown in Table 7:

TABLE 7 Induction Medium test results for different concentrations of hormone combinations

Combination of	6-BA(mg/L)	IBA(mg/L)	Rate of induction	Growth vigor of buds
					1	13	07	45％	+
2	13	08	50％	++
					3	13	09	55％	++
4	13	10	50％	++
					5	13	11	4％	+
6	15	07	50％	++
					7	15	08	70％	+++
8	15	09	65％	+++
					9	15	10	50％	+++
10	1.5	1.1	45％	++
					11	1.7	0.7	35％	+
12	1.7	0.8	50％	++
					13	17	09	50％	++
14	17	10	45％	+
					15	17	11	40％	+

As is clear from Table 7, in combination 7, i.e., 6-BA at 1.5mg/L, IBA at 0.8mg/L, the highest explant induction was 70%, and the best shoot growth was observed. The hormone combination 7 is proved to have the best effect on the induction of the epimedium dauricum explants.

Example 4

1) Collecting young and tender rhizome of epimedium, removing leaves, soaking for 30min by using a washing powder saturated solution, slightly brushing the surface by using a brush, washing for 2h by using running water, then placing on a super-clean workbench, disinfecting for 30s by using 75% alcohol by volume fraction, washing for 3 times by using sterile water, disinfecting for 4min by using 0.1% mercury bichloride, washing for 5 times by using the sterile water, disinfecting for 2.5min by using 0.1% mercury bicide again, washing for 5 times by using the sterile water, and shearing two ends of the rhizome by using a sterile operation for 2mm respectively to obtain a sterile stem section with a complete bud point for later use;

2) vertically inoculating the sterile stem segments obtained in the step 1) to induction culture media (MS +1.5mg/L6-BA +0.8mg/L IBA +5.8g/L agar +30g/L sucrose, pH 5.8) which are respectively added with PVP with different concentrations and streptomycin with different concentrations and are shown in a table 8 for culture, inoculating 10 bottles in each group, inoculating 1 explant in each bottle, and setting 2 groups for repeated experiments; culturing in dark at 25 deg.C for 7d, and culturing at 25 deg.C with illumination intensity of 2300-;

TABLE 8 concentration design Table for PVP and streptomycin

Serial number	PVP(mg/L)	Streptomycin (mg/L)
			1	40	80
2	50	100
			3	60	120
4	70	140

3) Observing and counting the browning quantity and the browning rate of the explant, and the pollution quantity and the pollution rate of endophytes of the explant.

The results are shown in Table 9:

TABLE 9 test results of different concentrations of PVP and streptomycin

As can be seen from Table 9, the PVP concentration is 60mg/L, the explant browning rate is the lowest, and although the browning rate is 10% when the PVP concentration is 70mg/L, the growth vigor of the buds is obviously inferior to that when the PVP concentration is 60mg/L, and the inhibition effect on the growth of the bud points probably can be achieved when the PVP concentration is too high; the contamination rate is lowest when the streptomycin concentration is 140 and 160mg/L, but the bud growth is inhibited, so that the streptomycin concentration of 120mg/L is most beneficial to the growth of the Epimedium dauricum explants.

Example 5

1) Collecting young and tender rhizome of epimedium, removing leaves, soaking for 30min by using a washing powder saturated solution, slightly brushing the surface by using a brush, washing for 2h by using running water, then placing on a super-clean workbench, disinfecting for 30s by using 75% alcohol by volume fraction, washing for 3 times by using sterile water, disinfecting for 4min by using 0.1% mercury bichloride, washing for 5 times by using the sterile water, disinfecting for 2.5min by using 0.1% mercury bicide again, washing for 5 times by using the sterile water, and shearing two ends of the rhizome by using a sterile operation for 2mm respectively to obtain a sterile stem section with a complete bud point for later use;

2) vertically inoculating the sterile stem section obtained in the step 1) to an induction culture medium (MS +1.5mg/L6-BA +0.8mg/L IBA +60mg/L PVP +120mg/L streptomycin +5.8g/L agar +30g/L sucrose, pH is 5.8) for culture, carrying out dark culture at the temperature of 25 ℃ for 7d, then transferring the culture medium to the conditions of 25 ℃, the illumination intensity of 2300 and 2500lx, and the illumination duration of 12h/d for culture for 18d, and inducing germination;

(3) cutting the bud of the sprout obtained in the step 2) into single bud points, vertically inoculating the bud points to enrichment culture media with different hormone combinations shown in a table 10 for culture, inoculating 10 bottles in each group, inoculating 1 explant in each bottle, setting 2 groups of repeated experiments, culturing for 28d under the conditions of 25 ℃, illumination intensity 2300 and illumination duration of 2500lx and illumination duration of 12h/d, observing and counting multiplication times and growth vigor of the epimedium clustered buds, wherein the plant height and the bud coarseness are used as indexes of the clustered bud growth vigor, and the indexes of + the growth, the + show that the bud growth vigor is from poor to good.

TABLE 10 proliferation medium design table for different hormone combinations

The results are shown in Table 11:

TABLE 11 proliferation medium test results for different hormone combinations

As can be seen from Table 11, when the NAA concentration is 0.5mg/L, the multiplication times of the clustered shoots of Epimedium hirsutum are generally higher and the growth vigor of the clustered shoots is better; when the concentration of 6-BA is increased from 1.5mg/L to 2.0mg/L, the multiplication times are gradually increased, the growth vigor of the cluster buds is gradually improved, the multiplication times are reduced along with the continuous increase of the concentration of 6-BA, the concentration of 6-BA is probably higher, and the differentiation of the cluster buds is inhibited, so the hormone combination with the optimal multiplication is that the concentration of 6-BA is 2.0mg/L, the concentration of NAA is 0.5mg/L, the maximum multiplication times is 3.9, and the growth vigor of the cluster buds is also best.

In conclusion, the optimal re-disinfection method of the invention is to disinfect by using 0.1 percent by mass of mercury bichloride for 4min, wash by using sterile water for 5 times, disinfect by using 0.1 percent by mass of mercury bichloride for 2.5min again, and wash by using sterile water for 5 times; the most suitable induction medium is MS +1.5mg/L6-BA +0.8mg/L IBA +60mg/L PVP +120mg/L streptomycin +5.8g/L agar +30g/L sucrose, and the pH is 5.8; the most suitable proliferation medium is MS +2.0 mg/L6-BA +0.5mg/L NAA +60mg/L PVP +5.8g/L agar +30g/L sucrose, and the pH is 5.8; the invention has simple flow and short propagation period, the multiplication rate reaches 3.9, provides technical guidance for the herba epimedii seedling propagation and large-scale propagation, solves the problems of low germination rate of herba epimedii seeds and difficult seedling propagation caused by long germination period, reduces the herba epimedii seedling propagation cost and provides high-quality seedlings for the artificial propagation of herba epimedii.

The above description is only for the purpose of illustrating the preferred embodiments of the present invention and is not to be construed as limiting the invention, and any modifications, equivalents, improvements and the like that fall within the spirit and principle of the present invention are intended to be included therein.