Plant regeneration via callus-mediated organogenesis in commercial variety of Chuanbeichai No. 1 in Bupleurum chinense DC.

Bupleurum chinense DC is an important medicinal plant with many active ingredients that are used for the treatment of different types of diseases and valued in pharmaceutical markets. In vitro shoot regeneration can efficiently contribute to the improvement of B. chinense. In the present study, we investigated the effects of the explant type and plant growth regulators (PGRs) on embryogenic callus induction and plant regeneration in B. chinense. Our investigation demonstrated that 2 mg/L 2,4-dichlorophenoxyacetic acid (2,4-D) combined with 1 mg/L thidiazuron (TDZ) played a major role in promoting callus induction from leaf, hypocotyl and stem 2 explants, whereas the most effective treatment for stem 1 callus formation was Murashige and Skoog (MS) medium supplemented with 1 mg/L 2,4-D, 0.5 mg/L 6-benzyladenine (BA) and 0.5 mg/L kinetin (Kin). The highest shoot regeneration rate (57.14%) was obtained from hypocotyl-induced calli in MS medium with 0.5 mg/L Kin after 12 weeks of cultivation. This regeneration protocol can be used in large-scale cultivation and may be useful for future genetic modifications of B. chinense . © Korean Society for Plant Biotechnology 2022.

Introduction

Bupleurum is a genus of the family Umbelliferae (Apiaceae), represented by 200 species, which are widely distributed in the Northern Hemisphere, Eurasia and North Africa. This genus was first recorded under the name Chai Hu (saiko in Japanese and shiho in Korean) more than 2000 years ago in Shen-Nong’s Herbal (Shen Nong Ben Cao Jing), and the earliest professional pharmaceutical book described the properties, flavor, efficacy and clinical applications of Bupleurum in detail (Yang et al. 2017). In addition, the latest research shows that a lung cleansing and detoxifying decoction (Qing Fei Pai Du Tang), composed of 21 kinds of traditional Chinese medicines, such as Bupleuri Radix, Ephedra sinica and Pogostemon cablin, exerts obvious curative effects on mild COVID-19 (Cao et al. 2020; Zhong et al. 2020).

As early as the beginning of 2000, the annual consumption of Radix Bupleuri in China reached 8000 tons, and the gross proceeds of prescription medicines containing saiko reached 27 billion yen in Japan. The demand for Chinese herbal medicine resources is still increasing worldwide (Cao et al. 2021; Pan 2006). Although 20 species of Bupleurum can be made into Chinese herbal medicines, only the dry roots of B. chinense and B. scorzonerifolium are the official botanical origins of Bupleuri Radix specified in the Chinese Pharmacopoeia (Chinese Pharmacopoeia Commission 2020). Furthermore, due to years of excessive and indiscriminate digging and inappropriate use to meet the raw material demands for Bupleuri Radix, natural populations of these plants have declined sharply. Sichuan Province, China, has a long history of cultivating Bupleurum. Currently, the cultivation area of Bupleurum is approximately 47,500 acres (data unpublished), but excellent cultivars for industrialized planting are still lacking. A commercial variety of B. chinense “Zhong Chai No. 2” with high yield and good quality was introduced to Sichuan. However, this genotype is intolerant to the soil waterlogging resulting from the very rainy weather during summer in Southwest China. Although the improved variety Chuanbeichai No. 1 showed moderate waterlogging tolerance after years of rigorous selection from the population originating from Zhong Chai No. 2, its flowering and seed setting are still negatively affected by the summer rainy season, resulting in poor seed production, which has greatly hindered its popularization (Gao et al. 2020; Xu et al. 2018). Therefore, with the typical introduction and domestication processes of traditional breeding, combined with modern biotechnology to improve the existing medicinal Bupleurum varieties, enhancing the stress resistance and environmental adaptability of these plants for their further development is a future breeding goal. A stable and efficient plant regeneration system is not only useful in the micropropagation and conservation of endangered Bupleurum varieties but also opens up alternative ways of introducing novel traits via genetic transformation.

There are several previous reports of in vitro studies on B. chinense (Hao et al. 2008; Xu et al. 2013; Yang et al. 2011). However, in previous reports on the induction of calli of Chuanbeichai No. 1, the induction rate was very low, and the callus browned easily. Furthermore, the regeneration efficiency of calli largely depends on genotype and explant type. Thus, a protocol that is suitable for one cultivar may not be applicable for other cultivars. Hence, there is a need to develop an in vitro tissue regeneration system for “Chuanbeichai No. 1” to meet the demands for planting material for cultivation and to improve this species through trait-specific genetic manipulation. Therefore, we focused on developing a more efficient regeneration protocol for mass multiplication and commercial cultivation of B. chinense.

Materials and methods

Plant material

The seeds of “Chuanbeichai No. 1” used in this study were chosen from a new variety of Bupleurum chinense. DC, which was jointly bred by Sichuan Agricultural University, Southwest University of Science and Technology, Institute of Medicinal Plant Development & Chinese Academy of Medical Sciences and Sichuan De Pei Yuan Traditional Chinese Medicine Science & Technology Development Co., Ltd. from farm-holding populations through systemic and purification selection methods.

In early 2019, stem segments were collected from B. chinense “Chuan Bei Chai No 1” plants at the jointing stage grown in the Chai Hu Demonstration Base of College of Life Science and Engineering, Southwest University of Science and Technology.

Explant sterilization

Seed sterilization and germination

The seeds were maintained in water (at 24 ± 1 °C) that was changed every 4 h for 24 h. Then, seeds were rinsed with flowing water for 2 h, placed in 75% ethanol for 30 s and washed with sterilized water three times, followed by 10% (w/v) NaClO for 15 min and 0.1% HgCl2 for 5 min. After the surface sterilization process, the seeds were washed with sterile distilled water to remove any trace of the sterilization agents. The seeds were then planted on MS (Murashige and Skoog 2006) seed germination medium supplemented with 3.0% (w/v) sucrose, 0.4% (w/v) plant gel, 1.5 mg/L 6-benzylaminopurine (BA) and 1.0 mg/L indole-3-acetic acid (IAA) (pH 5.8). All culture plates were kept in darkness at 24 ± 1 °C in an incubator for 14 days. When the seeds germinated, the culture conditions were changed to a 16-h light/8-h dark cycle at 23 ± 1 °C, and the light intensity was 2000 lx (25 μmolm−2 s−1). From 25 to 60 days, we collected hypocotyls and leaves and used them as explants.

Stem sterilization

After removing leaves, the fresh stems were rinsed with flowing water for 2 h, and then the stems were placed in 75% ethanol for 30 s and washed with distilled water. After that, the stems were sterilized with 0.1% (w/v) HgCl2 for 7 min and washed 5 ~ 6 times with distilled water. Surface-sterilized stems were cut into 3–5 cm segments, inoculated on MS medium and maintained at 24 ± 1 °C in the dark. The basic medium used in this study was MS medium containing 3.0% (w/v) sucrose and 0.4% (w/v) plant gel (pH 5.8).

Embryogenic callus induction

Leaf callus induction

Fully expanded green leaves were excised from the in vitro shoots (30 days old) and scratched with a surgical blade perpendicular to the vein at an interval of 0.5 cm. The treated leaves were soaked in 0.6% (w/v) polyvinylpyrrolidone for 10 min to remove the phenolic substances secreted from the wound and reduce browning and blotted with sterilized filter paper. Each treatment had 30 explants and was repeated three times. The cultures were kept in the dark for two weeks and then transferred to the light conditions described above. The callus induction rate and mortality were determined after four weeks.

Previous studies showed that the induction of Bupleurum callus is mainly accomplished with plant growth regulators (PGRs), such as 2,4-dichlorophenoxyacetic acid (2,4-D), BA, thidiazuron (TDZ), α-naphthaleneacetic acid (NAA) and kinetin (Kin) (Hao et al. 2008; Park et al. 1994; Yang et al. 2011; Zhao and Xi 1993). Therefore, according to tissue culture studies of Bupleurum plants and preliminary experiments, different hormone combinations were designed with leaves as explants, and induction formulas for embryogenic calli of B. chinense were preliminarily screened. The callus induction MS medium included 6 different concentrations and combinations of PGRs (Table 1).

Table 1

Composition of plant growth regulators used for callus induction of B. chinense

Medium	Plant grows regulators (mg/L)
	2,4-D	KT	BA	IAA	TDZ	NAA
A	1	0.5	0.5
B	1					1
C	2				1
D	3		0.5
E	5		0.5
F			0.5	0.5

Hypocotyl and stem segment callus induction

Hypocotyls were obtained from 15-day-old seedlings in vitro under sterile conditions; the cotyledons and roots were cut off, and 3–5 mm hypocotyls were reserved and soaked in 0.6% (w/v) polyvinylpyrrolidone for 10 min. The stems, which were cut into 1–2-cm segments, were sterilized and pre-cultured for seven days, and those without browning or contamination were soaked in 0.6% (w/v) polyvinylpyrrolidone for 10 min. The stems were then divided into two parts based on their maturity: the slightly younger part was Stem 1, and the slightly lignified part was Stem 2. All the explants were transferred to three different types of MS media, including different types and combinations of PGRs (1 mg/L2,4-D + 0.5 mg/L BA + 0.5 mg/L Kin, 2 mg/L 2,4-D + 1 mg/L TDZ or 0.5 mg/L BA + IAA 0.5 mg/L). The explants were subjected to darkness for 14 days of callus incubation at 24 ± 1 °C and then cultured under a 16 h photoperiod and 2000 lx light intensity. The induction rate and callus growth status were recorded 4 weeks after the inoculation of explants.

Shoot induction

Stem explants were taken from B. chinense planted in the field at the jointing stage. The acquisition of materials was limited by the growth cycle of the plant. Therefore, we only selected the hypocotyl calli and leaf calli of sterile seedlings as differentiation materials. Calli cultured for more than eight weeks were transferred to 9 different MS media with 3 different PGRs, zeatin (ZEA), Kin and abscisic acid (ABA), and each had three different concentrations (0.5, 1.0, and 1.5 mg/L ZEA; 0.5, 1.0, and 1.5 mg/L Kin; and 0.5, 1.0, and 1.5 mg/L ABA). All flasks were cultured at 24 ± 1 °C under a 16 h photoperiod and 2000 lx light intensity. The regeneration efficiency was calculated by counting the shoots or roots that formed from at least one out of the total number of shoots and roots cultivated on MS media after 4 weeks.

Rooting and plantlet acclimatization

In reference to our previous study (Li et al. 2018), the in vitro regenerated shoots of B. chinense (3 – 4 cm) were transferred to MS medium supplemented with indole-3-butyric acid (IBA) 0.5 mg/L for rooting. All the shoots for rooting were held at 22 ± 1 °C with a 12 h photoperiod and 1800 lx light intensity.

After 30 days of culture, the bottles with tube-rooted plantlets were opened under natural light for 5 ~ 7 days, the root medium was washed off, and the plants were planted into seedling substrate. The bottles were prepared by mixing peat soil and sandy loam soil at a ratio of 2:1.

Statistical analysis

The effects of different media on callus induction rate of different explants were modeled via the PROC MIXED procedure in SASv.9.2. (SAS Institute Inc., Cary, NC), similar to an analysis of variance for repeated measures, referring to the studies by Wiklund et al. (2012) and Ranganathan et al. (2014). The callus differentiation data are expressed as the means ± standard errors of the mean (SE) and were subjected to analysis of variance (ANOVA), and significant differences were selected by Duncan’s multiple range test with SPSS v.23 (SPSS Inc., Chicago, IL, USA) (Denis 2018). The histograms were plotted with GraphPad Prism v.8.0 (GraphPad Software Inc., La Jolla, CA, USA) (Motulsky 2007).

Results

Callus induction

Initially, we drew lessons from previous reports on Bupleurum plants, and six induction media were used for callus induction of B. chinense leaves for the first round of screening. Since whole leaves were the easiest and most abundant to obtain, they were cultured on the six media to test the induction rate. In contrast to other media, media C (MS + 2 mg/L 2,4-D + 1 mg/L TDZ) and F (MS + 0.5 mg/L IAA + 0.5 mg/L BA) showed good callus induction and a low death rate (P < 0.05), with callus induction rates of 66.43% and 65.30%, respectively (Fig. 1). It was observed that the callus in medium F grew only at the wound and was small and easily browned, while medium C could induce the whole leaf into callus with a compact texture and strong proliferation ability. A previous study showed that medium A can result in a high induction rate of calli of different explants, particularly floral buds (Hao et al. 2008), but in this study, the callus ratio from young leaves was not high (only 8.63%). This different result may be caused by the different genotypes. Therefore, other explants, such as stems and hypocotyls, should be used for further screening.

Fig. 1

Effects of different medium on leaf callus induction. Bars represent the mean ± SE. Bars marked with different letters indicate statistically different values between the different medium on leaf callus induction according to Duncan’s test (P < 0.05)

The mortality results showed a significant difference (P < 0.05) between the six media. The mortality of medium B was the highest (61.29%), whereas that of medium F and C was lower than 14%. Although the mortality under treatments D and E was significantly lower than that under the other treatments, they did not induce callus formation.

According to the results of the first round of tests, we chose the three media (C, F, A) with the highest leaf callus induction abilities to carry out the second-round screening on different organs of B. chinense; the explants were from hypocotyls, leaves and stems. As shown in Fig. 2, there were significant differences in the callus rate among different explants in the same medium (P < 0.05), and the percentage of explants producing calli was in the range of 8.64 – 83.95%. To further compare the difference in callus formation among different explants in different media, the mixed model was employed for the following analysis. The fixed effect test showed that a single factor of explant type or medium had no significant effect on the induction of callus, but the interaction between explant and medium was statistically significant (Table 2, P < 0.05). To compare the differences among the 12 interactions (Explant * Medium), we performed a t test using the least square mean of interactions to check whether the difference was significant (Table 3). A total of 66 groups of interactions were compared in pairs, and 17 of these groups exhibited significant differences (P < 0.05). From the comparisons, hypocotyls were found to be the most suitable explants for callus induction, and the highest induction rate (83.97%) was achieved in C medium supplemented with TDZ (1 mg/L) and 2,4-D (2 mg/L).

Fig. 2

Effects of different medium on callus induction rate of different explants. Bars represent the mean ± SE, * indicate significant differences in callus induction rate among different explants in the same medium subjected to two-way ANOVA (P < 0.05) using GraphPad Prism v8.0

Table 2

The fixed effect test of explant and medium type on callus formation of B. chinense

Effect	Num DF	Den DF	F value	P > F
Explant	3	28	1.59	0.2131
Medium	2	28	3.04	0.0639
Explant * Medium	6	28	4.59	0.0023 *

Num DF, the numerator degrees of freedom for the F test for a fixed effect term. Den DF, the denominator degrees of freedom for the F test for a fixed effect term. Num DF and Den DF equal the number of parameters for the fixed effect term, * means the fixed factor term significantly affects the callus formation (P < 0.01)

Table 3

The differences of Least Squares Means between interaction effects of Explant and Medium

Effect 1(Explant * Medium)	LS means of effect 1	Effect 2 (Explant * Medium)	LS means of effect 2	Differences	Standard error	t value	P
Stem 2*A	33.30	Leaf*C	66.30	−33	15.89	−2.08	0.0471
Stem 2*A	33.30	Stem 1*A	78.75	−45.45	19.81	−2.29	0.0295
Stem 2*A	33.30	Hypocotyl*C	83.95	−50.65	19.81	−2.56	0.0163
Stem 2*F	43.13	Leaf*A	8.64	34.49	14.47	2.38	0.0242
Stem 2*F	43.13	Hypocotyl*C	83.95	−40.82	18.09	−2.26	0.032
Stem 2*C	47.20	Leaf*A	8.64	38.56	16.58	2.33	0.0275
Leaf*A	8.64	Leaf*F	65.06	−56.42	11.6	−4.86	< .0001
Leaf*A	8.64	Leaf*C	66.30	−57.66	11.6	−4.97	< .0001
Leaf*A	8.64	Stem 1*A	78.75	−70.11	16.58	−4.23	0.0002
Leaf*A	8.64	Stem 1*C	58.05	−49.41	16.58	−2.98	0.0059
Leaf*A	8.64	Hypocotyl*A	52.65	−44.01	16.58	−2.65	0.0129
Leaf*A	8.64	Hypocotyl*F	47.47	−38.83	14.47	−2.68	0.0121
Leaf*A	8.64	Hypocotyl*C	83.95	−75.31	16.58	−4.54	< .0001
Leaf*F	65.06	Stem 1*F	32.50	32.56	13.67	2.38	0.0243
Leaf*C	66.30	Stem 1*F	32.50	33.8	13.67	2.47	0.0198
Stem 1*A	78.75	Stem1*F	32.50	46.25	18.09	2.56	0.0163
Stem 1*F	32.50	Hypocotyl*C	83.95	−51.45	18.09	−2.84	0.0082

LS means, Least Squares Means. Effect of “Explant * Medium” represents the interaction effect of Explant and Medium. Difference, difference between LS means of Effect 1 and LS means of Effect 2. The t test was used to check the significance of difference, and only significant differences listed in the table (P < 0.05)

The calli were inoculated with individual cytokinin (ZEA, Kin) and ABA in MS media and tested for shoot regeneration. After 10 days of cultivation, the hypocotyl calli were first to initiate differentiation to produce cluster shoots and roots. Roots were formed in leaf calli after approximately 15 days, but after 4 weeks, they still failed to produce regenerated shoots. Therefore, we extended the induction time and recorded data every 4 weeks (Table 4). When leaf calli were cultured on MS media supplemented with different concentrations of PGRs, new purple or yellow soft and fragile calli were formed on the surface of compact green calli, white growth spots appeared in the cells of these purple calli, and they gradually developed into adventitious roots. In the three investigation stages, the highest root differentiation rate of leaf calli was in MS medium supplemented with 0.5 mg/L Kin (Table 5). While the hypocotyl callus was softer than the leaf callus, white globular embryogenic calli and dense green globular calli were incubated on protocalli during induced differentiation. The white spheroids can be transformed into somatic embryo structures and produced a green separate bud from each structure loosely attached to the parental tissue (Fig. 3a). These independent buds further developed radicles and hypocotyls in the basal callus and became complete plants (Fig. 3b, c). After another 20 days of culture, the plant height of the regenerated seedlings reached approximately 8 cm (Fig. 3d). The dense green granular callus gradually transformed into spherical embryos, heart-shaped embryos and torpedo embryos, differentiated into leaf primordia and finally developed into a new shoot (Fig. 4a-d). Furthermore, these regenerated shoots were densely distributed on the surface of the callus, and this effect was accompanied by the emergence of adventitious roots, as shown in Fig. 4e. After eight weeks of culture, the callus still maintained high differentiation ability and became a chimera containing dense cluster buds and adventitious roots (Fig. 4f). To avoid affecting the next cycle of data investigation and the further differentiation of calli, we did not destructively count the number of adventitious buds per callus. Instead, the hypocotyl calli that produced new shoots were graded and counted (Tables 6, 7, 8). We divided the differentiated calli into three grades: calli with fewer than 5 regenerated buds were defined as level-1 differentiated calli (Fig. 5a), calli with 5–10 regenerated buds were defined as level-2 differentiated calli (Fig. 5b), and calli with more than 10 regenerated buds were defined as level-3 differentiated calli (Fig. 5c). Among the PGRs, Kin more efficiently promoted hypocotyl callus differentiation. ANOVA revealed that different kinds and contents of PGRs in the medium had significant effects (P < 0.05) on the induction of regeneration shoots from calli of B. chinense. (Table 4) at the 4th and 12th week. At the 4th and 8th week, the hypocotyl callus was best induced in MS medium containing 1 mg/L Kin, and the adventitious shoot regeneration rates were 28.57% and 35.71%, respectively. After 12 weeks of culture, the highest regeneration rate was observed in hypocotyl calli cultivated on medium supplemented with 0.5 mg L−1 Kin, and the adventitious bud and root regeneration rates were 57.12% and 97.92%, respectively.

Table 4

Effect of plant growth regulators on hypocotyl callus differentiation of B. chinense

PGRs	Concentration(mgl−1)	Mean differentiation rate of hypocotyl calli (%)
		4 weeks		8 weeks		12 weeks
		Shoot	Root	Shoot	Root	Shoot	Root
ZEA	0.5	17.2 ± 3.92ab	10.23 ± 4.90ab	26.15 ± 6.39ab	21.63 ± 5.00a	31.14 ± 4.55ab	90.37 ± 4.59 cd
	1	16.91 ± 1.87ab	1.56 ± 1.46a	26.17 ± 6.67ab	9.16 ± 2.99a	31.48 ± 4.50ab	67.99 ± 6.19a
	1.5	25.27 ± 5.62b	3.87 ± 2.38ab	25.86 ± 6.10ab	27.29 ± 7.59a	34.85 ± 4.09ab	72.35 ± 5.67a
Kin	0.5	25.93 ± 4.91b	8.73 ± 4.11ab	33.29 ± 5.56ab	16.88 ± 5.65a	57.14 ± 4.98c	97.92 ± 1.95d
	1	28.57 ± 3.77b	3.70 ± 2.19ab	35.71 ± 5.86b	27.78 ± 8.47a	47.86 ± 6.12bc	88.57 ± 3.35bcd
	1.5	22.31 ± 4.68ab	9.26 ± 3.27ab	28.13 ± 7.02ab	30.51 ± 5.20a	39.95 ± 4.68ab	75.93 ± 5.30abc
ABA	0.5	8.71 ± 3.48a	14.96 ± 5.55b	17.86 ± 4.99ab	25.69 ± 8.48a	26.35 ± 7.97a	70.16 ± 6.52a
	1	8.04 ± 4.10a	5.65 ± 3.62ab	13.10 ± 3.15a	24.76 ± 5.93a	28.71 ± 4.28a	73.36 ± 4.97ab
	1.5	13.99 ± 4.63ab	7.22 ± 3.61ab	20.65 ± 5.55ab	24.70 ± 9.95a	32.07 ± 2.74ab	79.89 ± 2.87abc

Values are mean ± SE of 9 independent experiments, each experiment contains at least 6 explants. Means within each column followed by the same letter are not significantly different at P < 0.05 using Duncan’s Multiple Range Test

Table 5

Effect of plant growth regulators on rooting of callus from in B. chinense leaves

PGRs	Concentration (mgl−1)	The root formation rate of leaf callus
		4 weeks	8 weeks	12 weeks
ZEA	0.5	18.89 ± 8.83ab	20.83 ± 7.45abc	30.00 ± 4.47ab
	1	9.00 ± 4.10a	16.11 ± 6.11ab	17.98 ± 7.58b
	1.5	3.33 ± 2.98a	6.67 ± 5.96a	11.67 ± 6.50a
Kin	0.5	42.86 ± 6.39b	49.61 ± 10.07c	75.49 ± 7.71c
	1	25.67 ± 7.33ab	32.33 ± 8.27abc	64.90 ± 5.85bc
	1.5	18.93 ± 8.14ab	23.69 ± 10.24abc	46.95 ± 5.67c
ABA	0.5	12.86 ± 0.194a	25.83 ± 9.38abc	44.44 ± 9.56bc
	1	26.21 ± 8.09ab	44.90 ± 11.01bc	63.98 ± 9.50c
	1.5	10.22 ± 6.93a	25.67 ± 7.3abc	64.73 ± 7.61c

Values are mean ± SE of 9 independent experiments, each experiment contains at least 5 explants. Means within each column followed by same letter are not significantly different at P < 0.05 using Duncan’s Multiple Range Test

Fig. 3

The differentiation process of white globular embryogenic callus obtained from hypocotyl explant. a Shoot initiation from globular embryogenic callus (Scale bar indicates 2 mm). b Hypocotyl and radicle produced from globular embryogenic callus (Scale bar indicates 2 mm). c Embryoids develop into complete plants (Scale bar indicates 2 mm). d Plant produced by embryoids elongate further (Scale bar indicates 1 cm)

Fig. 4

The differentiation process of green embryogenic calli obtained from hypocotyl explant. a-d Embryogenic callus at globular, heart-shaped, torpedo, and cotyledonary stages (Scale bar indicates 500 μm). e General view of green embryogenic callus obtained on differentiation medium (Scale bar indicates 1 mm). f Shoots induced from hypocotyl callus 8 weeks after initiating differentiation, the shoots and root elongated further (Scale bar indicates 1 cm)

Table 6

Effects of plant growth regulators on regeneration of shoots from hypocotyl callus after 4 weeks of culture

PGRs	Concentration(mgl−1)	Total calli	Number of calli that differentiated shoots	Number of level-1 differentiated calli	Number of level-2 differentiated calli	Number of level-3 differentiated calli
		n	n	n	n	n
ZEA	0.5	58	10	4	4	2
	1	59	9	5	2	2
	1.5	55	14	5	5	4
Kin	0.5	58	17	8	6	3
	1	62	16	6	5	4
	1.5	67	15	6	6	3
ABA	0.5	57	5	3	1	1
	1	53	4	2	1	1
	1.5	53	8	4	2	2

Calli with fewer than 5 regenerated buds were defined as level-1 differentiated calli (length > 3 mm), calli with 5–10 regenerated buds were defined as level-2 differentiated calli (length > 3 mm), and calli with more than 10 regenerated buds were defined as level-3 differentiated calli (length > 3 mm)

Table 7

Effects of plant growth regulators on regeneration of shoots from hypocotyl callus after 8 weeks of culture

PGRs	Concentration(mgl−1)	Total calli	Number of calli that differentiated shoots	Number of level-1 differentiated calli	Number of level-2 differentiated calli	Number of level-3 differentiated calli
		n	n	n	n	n
ZEA	0.5	69	18	4	7	7
	1	57	14	4	5	5
	1.5	58	16	3	7	6
Kin	0.5	70	23	6	7	10
	1	52	19	5	6	8
	1.5	62	18	4	6	8
ABA	0.5	63	12	3	4	5
	1	61	8	2	3	3
	1.5	55	11	3	4	4

Calli with fewer than 5 regenerated buds were defined as level-1 differentiated calli (length > 3 mm), calli with 5–10 regenerated buds were defined as level-2 differentiated calli (length > 3 mm), and calli with more than 10 regenerated buds were defined as level-3 differentiated calli (length > 3 mm)

Table 8

Effects of plant growth regulators on regeneration of shoots from hypocotyl callus after 12 weeks of culture

PGRs	Concentration (mgl−1)	Total calli	Number of calli that differentiated shoots	Number of level-1 differentiated calli	Number of level-2 differentiated calli	Number of level-3 differentiated calli
		n	n	n	n	n
ZEA	0.5	89	27	7	9	11
	1	60	19	4	7	8
	1.5	62	21	5	7	9
Kin	0.5	67	37	8	10	19
	1	61	29	7	8	14
	1.5	70	26	8	6	12
ABA	0.5	61	18	3	7	8
	1	65	18	4	6	8
	1.5	62	20	5	6	9

Calli with fewer than 5 regenerated buds were defined as level-1 differentiated calli (length > 3 mm), calli with 5–10 regenerated buds were defined as level-2 differentiated calli (length > 3 mm), and calli with more than 10 regenerated buds were defined as level-3 differentiated calli (length > 3 mm)

Fig. 5

Example of calli grading standard. a One-level differentiation calli (calli with fewer than 5 regenerated buds). b Two-level differentiation calli (calli with 5–10 regenerated buds). c Three-level differentiation calli (calli with more than 10 regenerated buds. a-c, Scale bar indicates 1 cm)

Discussion

Adjusting PGRs in culture media is one of the most common approaches used in developing regeneration protocols, such as somatic embryogenesis and shoot proliferation. Previous studies mostly explored the synergistic effect of 2,4-D with auxins or cytokinins on the induction of calli. These studies demonstrated that 2,4-D in combination with other PGRs could modify the frequency of embryogenic callus induction and growth. This kind of PGR combination has also been widely used in regeneration systems of some other Bupleurum plants, such as Bupleurum scorzonerifolium and Bupleurum latissimum (Bae 2015; Cheng et al. 2015; Xia et al. 1992). Therefore, according to previous reports, we designed 5 PGR combinations containing 2,4-D to induce calli of B. chinense. In addition, we also found that the adventitious bud proliferation medium (MS + IAA 0.5 mg/L + BA 0.5 mg/L) could induce calli in the roots of tube plantlets; hence, we also tried to use other explants to induce calli on this medium.

In the present study, different explants showed different states in the process of callus formation. After 14 days of dark culture, the whole hypocotyl dedifferentiated into soft white calli, the stem explants formed green granular calli at both ends of the wound, while the dedifferentiation of whole leaves into tender green calli took 20 days. Initial calli grew slowly from all explants. However, once stable callus growth had been established, the growth rate increased. The results showed that the calli of B. chinense were induced successfully from aseptic leaf, hypocotyl and stem explants. The best PGR combination for inducing calli varied according to the type of explant, and the hypocotyl had the highest rate of callus induction. The callus induced by different explants varied in texture, color and size.

During the process of callus differentiation, cytokinins are key regulators used to induce somatic embryogenesis and play very important roles in the success of plant regeneration (Bidabadi and Jain 2020; Jiménez 2005). Among the protocols in which cytokinins were used as the sole PGR for the induction of somatic embryogenesis, Kin and ZEA were the most frequently used cytokinins (Phillips and Garda 2019). In addition, ABA can induce somatic embryogenesis and regulate somatic embryo development in certain cases (Lü et al. 2013; Liu et al. 2021; Nishiwaki et al. 2000; Su and Zhang 2014). Therefore, we utilized ABA, ZEA and Kin to test their effects on the differentiation of leaf and hypocotyl calli of B. chinense. We also set up a blank control group, and some calli could also produce cluster buds, but a large number of calli gradually browned and died after 2 weeks. On the medium containing cytokinin and ABA, the callus showed active proliferation ability, the volume of the callus increased rapidly, and the differentiation rate also increased. This finding indicates that the medium without PGRs is not conducive to the survival and proliferation of B. chinense calli. Among the three PGRs, Kin showed the best differentiation-inducing ability, so the hypocotyl callus could differentiate more shoots and roots, and their elongation rate was faster. However, regardless of the type of PGR, the leaf callus could not produce regenerated shoots, and only roots could be produced. To further dissect this cause, we tried to induce leaf callus differentiation with BA/IAA, three concentration gradients (0.5, 1.0, 1.5 mg/L BA and 0.05, 0.1, 0.15 mg/L IAA) were set up. However, the effect was not satisfactory, and the leaf callus still could not differentiate into shoots. A similar result was reported by Hao et al. (2008), they used high levels of cytokinin/auxin to induce calli differentiation, but most leaf calli died of browning during culture and that a few continued to divide and proliferate but never differentiated. And there is no report of other genus Bupleurum plants successfully utilizing leaf regeneration. These results showed that leaf calli from B. chinense may not have the ability to differentiate regenerated shoots.

The present study is also an important part of our team’s systematic research on B. chinense. By analyzing the transcriptome data of B. chinense, we found some genes that may play an important role in the development of lateral roots and saponin synthesis (Yu et al. 2021; 2020). Transgenic transformation based on regeneration systems is in progress, and manipulation of these genes may improve the yield of saikosaponins.

Conclusion

The hypocotyls of B. chinense were used as explants to establish an indirect somatic embryogenesis system through calli. The hypocotyl callus proliferated and differentiated into shoots. Compared with previous methods, we obtained a higher hypocotyl embryogenic callus induction rate and produced a higher de novo shoot regeneration rate and differentiation rate. Moreover, most of the shoots produced by hypocotyl calli were dense cluster shoots. Thus, our results demonstrate that hypocotyl explants of B. chinense offer great potential for large-scale in vitro multiplication of this popular medicinal plant species. Furthermore, this improved regeneration of B. chinense can be used in genetic transformation studies to improve its qualitative traits.