Salvia miltiorrhiza is one of the most important traditional Chinese medicinal plants because of its excellent performance in treating coronary heart disease. Phenolic acids mainly including caffeic acid, rosmarinic acid and salvianolic acid B are a group of active ingredients in S. miltiorrhiza. Abscisic acid (ABA), gibberellin (GA) and ethylene are three important phytohormones. In this study, effects of the three phytohormones and their interactions on phenolic production in S. miltiorrhiza hairy roots were investigated. The results showed that ABA, GA and ethylene were all effective to induce production of phenolic acids and increase activities of PAL and TAT in S. miltiorrhiza hairy roots. Effects of phytohormones were reversed by their biosynthetic inhibitors. Antagonistic actions between the three phytohormones played important roles in the biosynthesis of phenolic acids. GA signaling is necessary for ABA and ethylene-induced phenolic production. Yet, ABA and ethylene signaling is probably not necessary for GA3-induced phenolic production. The complex interactions of phytohormones help us reveal regulation mechanism of secondary metabolism and scale-up production of active ingredients in plants.
Citation: Liang Z, Ma Y, Xu T, Cui B, Liu Y, Guo Z, et al. (2013) Effects of Abscisic Acid, Gibberellin, Ethylene and Their Interactions on Production of Phenolic Acids in Salvia miltiorrhiza Bunge Hairy Roots. PLoS ONE8(9): e72806. https://doi.org/10.1371/journal.pone.0072806
Editor: Wei Xu, University of Wisconsin - Madison, United States of America
Received: May 7, 2013; Accepted: June 24, 2013; Published: September 2, 2013
Copyright: © 2013 Liang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This material is based upon work funded by Specialized Research Fund for the Doctoral Program of Higher Education (20110204110028), Science Foundation of Zhejiang Sci-Tech University (ZSTU) under grant numbers 1204806-Y and 1204822-Y, and Zhejiang Provincial Natural Science Foundation of China under grant number LQ13C020003. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: Yan Liu is employed by Tasly Modern TCM Resources Co., Ltd. Zhi-Xin Guo is employed by Tasly Institute. This does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials.
Salvia miltiorrhiza Bunge (Danshen in Chinese) is a very useful traditional Chinese medicine in treatment of myocardial infraction, angina pectoris, heart diseases, stroke, alzheimer’s disease, cardiovascular and cerebrovascular diseases . Demands of Salvia miltiorrhiza in China are more 4, 000, 000 kilograms, which needs 160 km2 cultivated land to produce. Improvement of Salvia miltiorrhiza quality or industrialization of active ingredients production is very important to save cultivated land. There are two major groups of active ingredients in S. miltiorrhiza, tanshinones and phenolic acids. These years, more and more attentions have been paid to phenolic acids in S. miltiorrhiza roots because of their excellent effects on heart disease . Phenolic acids including salvianolic acid B (SAB), rosmarinic acid (RA) and caffeic acid (CA) (Fig. 1) in S. miltiorrhiza are biosynthesized via the phenylpropanoid and the tyrosine-derived pathways. Phenylalanine ammonia-lyase (PAL) and tyrosine aminotransferase (TAT) are two key enzymes involved in the biosynthesis of phenolic acids. Various elicitors have been investigated to stimulate phenolic production in S. miltiorrhiza hairy roots,including yeast extracts, Ag+, methyl jasmonate, salicylic acid and abscisic acid . However, our knowledge about the regulation mechanism of phenolic biosynthesis in S. miltiorrhiza is far from complete.
Phytohormones, a group of crucial signal molecules, not only regulated all aspects of plant growth and development, but also were involved in plant secondary metabolism . Many phytohormones have been used as efficient elicitors to stimulate production of plant secondary metabolites. ABA was defined as a stress plant hormone because of its rapid accumulation in response to stress. We found that accumulations of tanshinones and phenolic acids were significantly improved by ABA treatment , , , . Ethylene was a phytohormone that regulated a wide range of plant processes. It has been reported that ethylene is effective to induce anthocyanin production in strawberry  and phenolic production in carrots . Gibberellin (GA) was also well known as an effective elicitor for production of secondary metabolites. The previous work indicated that tanshinone production in S. miltiorrhiza hairy roots were significantly induced by gibberellic acid 3 (GA3) .
Interactions of phytohormone signalings in regulating plant development and metabolism have been widely reported , . GA was regarded as an antagonist of ABA and ethylene. Effects of ABA on plants could be counteracted by applications of GA and ethylene , , , . The antagonistic action between GA and ABA was an important factor regulating the developmental transition from embryogenesis to seed germination . Ethylene could also partially inhibited the action of GA on seedlings of Alaska pea . Although our previous work has shown that production of phenolic acids in S. miltiorrhiza hairy roots is stimulated by ABA, effects of ethylene and GA on phenolic production are still unknown. Interactions between the three phytohormones are still unclear. The goal of this study is to investigate effects of GA and ethylene on the accumulations of phenolic acids in S. miltiorrhiza hairy roots and reveal interactions between the three phytohormones.
Materials and Methods
Preparation for Phytohormones and Inhibitors
ABA (Wolsen, China), gibberellic acid 3 (GA3, Wolsen, China ), ethephon (Eth, Sigma, USA), and CoCl2 (ethylene biosynthesis inhibitor, Sigma, USA) were dissolved in distilled water. Paclobutrazol (GA biosynthetic inhibitor, Sigma, USA) and fluridone (ABA biosynthesis inhibitor, Augsburg, Germany) were dissolved in 70% ethanol. Finally, all the reagents were sterilized by filtering through a microfilter (0.2 µm) and stored at 4°C in a refrigerator prior to use.
Hairy Root Culture and Treatment
The S. miltiorrhiza hairy roots were derived after the infection of Agrobacterium rhizogenes bacterium (ATCC15834). The 6,7-V medium was chosen as the basal medium with 20 g/L sucrose and pH was adjusted to 5.6–5.8 with NaOH. All experiments in this research were performed in suspension culture of S. miltiorrhiza hairy roots in a liquid medium of 6, 7-v. Hairy roots with 0.2 g fresh roots were cultivated in 250-ml shake flasks containing 50 ml of the hormone-free liquid basal medium on an orbital shaker at 110 rpm and 25°C in the dark.
Treatments of phytohormones and inhibitors were conducted on the 18th day after inoculation of the hairy root cultures. Initially, four concentrations of GA3 (10, 50, 100 and 150 µM) and Eth (50, 100, 200 and 400 µM) were added into the culture medium, respectively. Afterwards, 100 µM GA3 and 50 µM Eth were chosen as the best concentrations. Then, three concentrations of paclobutrazol (26, 52 and 104 µM) and CoCl2 (50, 100 and 150 µM) were applied into the cultures. Concentrations of paclobutrazol at 52 µM and CoCl2 at 100 µM were finally selected. Concentrations of ABA (50 µM) and fluridone (34 µM) were chosen according to our previous study . Finally, the selected concentrations of phytohormones and their inhibitors were employed to study their interactions on production of phenolic acids in S. miltiorrhiza hairy roots. The equal volume of distilled water was added to the hairy root cultures as the control.
Hairy roots were harvested from the culture medium by filtration on the 6th day after treatments, blotted dry with paper towels (yielding the fresh weight, FW), and then dried at 45°C in an oven until constant weight (yielding the dry weight, DW). All treatments were performed in triplicate.
Extraction and HPLC Analysis of Phenolic Acids
The dried hairy roots were comminuted to powder in a mortar and sieved through a 0.45-mm screen. The powder (0.1 g) was extracted ultrasonically with 2 ml methanol-water solution (7∶3) for 45 min. The extracts were centrifuged at 10,000 rpm for 15 min and filtered through a 0.45-µm Millipore filter. Then, contents of phenolic acids with HPLC was measured according to the method established in our lab .
All the data were analyzed using SPSS 16.0 for Windows. The data were initially compared by one way analysis of variance (ANOVA) and difference was detected using the Tukey test. The difference between treatments was considered to be statistically significant when p values ≤0.05. Figures were performed using GraphPad Prism 5 and means ± standard deviation (S.D.) (n = 3) were shown.
Effects of Phytohormones and Inhibitors on Growth of S. miltiorrhiza Bunge Hairy Roots
Four concentrations of ABA, GA3 and Eth were separately added into the cultures to investigate their effects on S. miltiorrhiza hairy roots. Then, the inhibitors in combination with phytohormones were applied into the cultures to elucidate regulation mechanism of phenolic biosynthesis. The growth of S. miltiorrhiza hairy roots on day 6 after treatments was initially measured. Effects of ABA and fluridone on growth of Salvia miltiorrhiza hairy roots have been reported in our previous work . Effects of GA3 on the growth of Salvia miltiorrhiza hairy roots were shown in Fig. 2a. The results showed that the fresh weight and dry weight were almost not affected by 10 µM GA3, while they were significantly increased by 100 µM GA3 (from 3.81 to 4.75 g FW and from 0.27 to 0.33 g DW). The fresh weight was almost not affected by 50 µM GA3, but significantly increased by 150 µM GA3. The dry weight was significantly increased by 50 µM GA3, but almost not affected by 150 µM GA3. A low concentration of paclobutrazol (26 µM) could not affect the growth of GA3-induced hairy roots, while the higher concentrations (52 and 104 µM) led to significant decreases as shown in Fig. 2b.
GA3, pibberellin acid 3; Eth, ethephon. Different letters indicate significant difference at p≤0.05 using Tukey test test. Means ± standard deviation (S.D.) (n = 3) are shown.
Treatments with four concentrations of Eth (50, 100, 200 and 400 µM) resulted in significant increases of the hairy root growth as shown in Fig. 2c. The highest fresh weight and dry weight were observed in 200 µM Eth treatment (to 5.40 g FW and 3.66 g DW, respectively). Treatments with CoCl2 (50, 100 and 150 µM) inhibited the growth of Eth-induced hairy roots (Fig. 2d). The higher the CoCl2 concentration was, the lower the hairy root weight was. When compared to 100 µM Eth treatment, the fresh weight and dry weight in 100 µM Eth +150 µM CoCl2 treatment were decreased by 22.2 and 17.7%.
Effects of Phytohormones on Accumulation of Phenolic Acids in S. miltiorrhiza Hairy Roots
Three phenolic acids including caffeic acid (CA), rosmarinic acid (RA) and salvianolic acid B (SAB) in S. miltiorrhiza hairy roots were determined by HPLC. Effects of ABA at 50, 100, 150 and 200 µM on accumulations of three compounds have been reported in our previous work . Effects of Eth at 50, 100, 200 and 400 µM on accumulations of three compounds were shown in Fig. 3abc. The CA and RA contents were significantly increased by 50 and 100 µM Eth treatments, and SAB content was significantly increased by 50 µM Eth treatment. The highest contents of three compounds reached to 0.90, 23.12 and 25.13 mg/g, respectively, in 50 µM Eth treatment. Fig. 3def showed effects of GA at 10, 50, 100, 150 µM on accumulations of three compounds. The results showed that CA content in the hairy roots was almost not affected by GA. Both RA and SAB accumulations were induced by GA, but differences of four treatments were not significant. Eth treatment was more efficient to enhance phenolic production than GA treatment. Responses of RA and SAB accumulations to three phytohormones were similar.
Effects of Inhibitors on Phytohormone-induced Phenolic Production in S. miltiorrhiza Hairy Roots
To investigate further regulation mechanism of phytohormones on the biosynthesis of phenolic acids in S. miltiorrhiza hairy roots, inhibitors of phytohormone biosynthesis were applied into the hairy root cultures. Concentrations of ABA (50 µM), Eth (50 µM) and GA3 (100 µM) were selected according to the above work. Three phytohormones together with the related inhibitors were respectively added into the cultures.
Fluridone was one of the efficient inhibitor of ABA biosynthesis. Effects of fluridone on ABA-induced phenolic production has been investigated in our work . CoCl2 was an effective inhibitor of Eth biosynthesis in plants. In our experiments, three concentrations of CoCl2 (50, 100 and 150 µM) were separately applied into the cultures together with 50 µM Eth. The results showed that accumulations of three compounds induced by Eth were all significantly inhibited by CoCl2 treatment (Fig. 4a, b, c). The lowest contents of CA, RA and SAB were observed in 150 µM CoCl2 treatment. They were reduced by 75, 83 and 68% when compared to 50 µM Eth treatment. It suggested that phenolic production induced by the exogenous ethylene was probably related to endogenous ethylene. Paclobutrazol was an inhibitor of GA biosynthesis. Three concentrations of paclobutrazol (26, 52 and 104 µM) in combination with 100 µM GA3 were added into the cultures. The results showed that increases of RA and SAB contents induced by GA3 were significantly reversed by paclobutrazol (Fig. 4d, e, f). The lowest content of RA was observed in 52 µM paclobutrazol+100 µM GA3 treatment. It was decreased by 53% when compared to 100 µM GA3 treatment. The lowest SAB content was observed in 26 µM paclobutrazol+100 µM GA3 treatment, and was reduced by 54%. However, CA content was just slightly reduced by paclobutrazol treatment.
Interaction between ABA and Gibberellin on Production of Phenolic Acids in S. miltiorrhiza Hairy Roots
To elucidate interaction between ABA and gibberellin on production of phenolic acids, the combined effects of ABA, GA3, paclobutrazol and fluridone were investigated. Concentrations of 50 µM ABA, 100 µM GA3, 34 µM fluridone and 52 µM paclobutrazol were selected according to the above results. Fig. 5abc showed that contents of CA, RA and SAB were significantly increased from 0.37, 3.66 and 7.39 mg/g to 1.96, 7.45 and 26.3 mg/g by 50 µM ABA treatment. RA and SAB accumulation was also significantly increased to by 100 µM GA3 treatment. However, when ABA and GA3 were applied into the cultures together, RA contents were slightly reduced and SAB content was just slightly increased when compared to the control. Although CA content was significantly increased in ABA+GA3 treatment, the content was less than that in ABA treatment.
Eth, ethephon; GA3, gibberellin acid 3; ABA, abscisic acid. Different letters indicate significant difference at p≤0.05 using Tukey test. Means ± standard deviation (S.D.) (n = 3) are shown.
Treatments with paclobutrazol or fluridone alone almost could not affect contents of CA, RA and SAB in the hairy roots. The ABA-induced CA, RA and SAB production was significantly inhibited by 34 µM fluridone. Simultaneously, the ABA-induced RA and SAB accumulation was completely reversed by 52 µM paclobutrazol. Contents of RA and SAB in ABA+paclobutrazol were just 15% and 31% of the control levels. However, the ABA-induced CA production was almost not affected by paclobutrazol. The results indicated that endogenous GA was probably involved in ABA-induced RA and SAB production. Although increases of RA and SAB contents induced by GA3 were significantly reversed by paclobutrazol, they were almost not affected by fluridone. It suggested that endogenous GA was probably not involved in ABA-induced phenolic production in the hairy roots. Interestingly, CA production in ABA+GA3 treatment was significantly increased by paclobutrazol or fluridone.
Interaction between ABA and Ethylene on Production of Phenolic Acids in S. miltiorrhiza Hairy Root
To study the interaction of ABA and ethylene on production of phenolic acids in S. miltiorrhiza hairy roots, the combined effects of 50 µM ABA, 50 µM Eth, 100 µM CoCl2 and 34 µM fluridone were investigated. Fig. 5def showed that CA content was increased to 13.8 folds of the control levels by ABA treatment and to 4.5 folds by Eth treatment. Although CA content was also significantly induced by ABA+Eth treatment, it was just 9.2 folds of the control levels. RA content in ABA and Eth treatments was increased from 2.5 mg/g to 9.1 and 19.9 mg/g, respectively. However, it was just 13.4 mg/g in ABA+Eth treatment. Significant increases of SAB content were observed in three treatments, but the differences of three treatments were insignificant.
Accumulations of three compounds were almost not affected by CoCl2 treatment alone. The ABA-induced CA production was significantly decreased from 2.8 mg/g to 1.4 mg/g by CoCl2 treatment, and increases of RA and SAB contents induced by ABA were slightly reduced by CoCl2 treatment. RA content in ABA+Eth treatment was significantly reduced by CoCl2 treatment, but CA and SAB production induced by ABA+Eth was almost not affected. The increases of three compounds contents in Eth treatment were significantly inhibited by fluridone.
Interaction between Gibberellin and Ethylene on Production of Phenolic Acids in S. miltiorrhiza Hairy Roots
The combined effects of 50 µM Eth, 100 µM GA3, 100 µM CoCl2 and 52 µM paclobutrazol on production of phenolic acids in S. miltiorrhiza hairy roots were then investigated to reveal interaction between gibberellin and ethylene. Fig. 5ghi showed that contents of three compounds were largely improved by Eth. Although productions of RA and SAB were also induced by GA3, they were much less that those in Eth treatment. The combination of GA3 and Eth had no effect on CA content when compared to the control. RA and SAB contents were largely improved by GA3+Eth, but they were much less than those in Eth treatment. The Eth-induced phenolic production was significantly reversed by paclobutrazol treatment. Contents of CA, RA and SAB in Eth+paclobutrazol treatment were just 33%, 57% and 63% of the levels in Eth treatment. However, RA and SAB contents in Eth+GA3 treatment were just slightly reduced by paclobutrazol. Increases of RA and SAB contents in GA3 treatment were almost not affected by CoCl2, while those in GA3+Eth treatment were just slightly reversed by CoCl2.
Effects of Phytohormones and Inhibitors on PAL and TAT Activities of S. miltiorrhiza Hairy Roots
PAL and TAT were two key enzymes involved the biosynthesis of phenolic acids in S. miltiorrhiza hairy roots. To reveal regulation mechanism of phenolic acids biosynthesis, effects of phytohormones and inhibitors on PAL and TAT activities of S. miltiorrhiza hairy roots were investigated.
Effects of ABA and fluridone on PAL ad TAT activities of S. miltiorrhiza hairy roots have been reported in our previous work . Responses of enzyme activities to GA and ethylene were shown in Fig. 6. The results showed that activities of PAL and TAT were significantly increased by GA3 treatments, and the highest values were observed in 10 µM GA3 treatment. Values of TAT and PAL activities in 10 µM GA3 treatment were increased by 154% and 73% when compared to the control. The GA3-induced TAT activity was completely reversed by 26 and 52 µM paclobutrazol treatments, and GA3-induced PAL activity was completely inhibited by paclobutrazol at three concentrations.
GA3, gibberellin acid 3; Eth, ethephon; PAL, phenylalanine ammonia-lyase, TAT, tyrosine aminotransferase. Different letters indicate significant difference at p≤0.05 using Tukey test test. Means ± standard deviation (S.D.) (n = 3) are shown.
PAL activity was significantly improved by Eth at four treatments, and the highest value were observed in 50 µM Eth treatment (increased by 86% when compared to the control). TAT activity was significantly improved by 50, 150 and 200 µM Eth treatments and the highest value was observed in 150 µM Eth treatment (increased by 59% when compared to the control). However, TAT activity was significantly inhibited by 100 µM Eth, and the value was just 63% of the control level. The Eth-induced PAL activity was completely reversed by 50 µM Cocl2 treatment, while it was significantly enhanced by 100 and 150 µM Cocl2 treatment. Although TAT activity was not stimulated by 100 µM Eth treatment, it was significantly induced by 50 µM Cocl2+100 µM Eth treatment.
Various elicitors have been proved efficient to induce production of secondary metabolites in plant tissue cultures. Phytohormones, the special elicitors and plant growth regulators, have been widely used to stimulate accumulation of some important secondary metabolites in plants. Previous studies showed that accumulations of phenolic acids in plants were affected by ABA, GA3 and ethylene , . ABA treatment could suppress PAL activity and phenolic acids accumulation in soybeans . However, in strawberry, PAL activity and phenolic production were rapidly stimulated by ABA . Our previous work suggested that activities of PAL and TAT as well as accumulations of CA, RA and SAB were significantly improved by ABA treatment . It indicated that the responses of different plants to ABA were diverse and ABA was effective to stimulate the biosynthesis of phenolic acids in S. miltiorrhiza hairy roots. Ethylene was regarded as a plant senescence hormone, and it was effective to improve production of phenolic acids in strawberry  and carrots . In S. miltiorrhiza hairy roots, application of ethephon led to significant increases of RA and LAB contents, but could not affect CA production. It was probably because that CA located on a branch pathway before RA and SAB biosynthesis, and ethephon facilitated metabolic flux to RA and SAB biosynthesis. Like ABA and ethylene, GA3 can also affect production of phenolic acids. Chlorogenic acid accumulation in tobacco callus was induced by high concentration of GA3, but was reduced by the low concentration treatment . We found that CA production was not affected by GA3 treatment, while RA and SAB productions were significantly increased by GA3 at 10–150 µM. Simultaneously, PAL and TAT activities were significantly induced by Eth and GA3 treatments. It demonstrated that increases of phenolic acids contents in S. miltiorrhiza hairy roots induced by the three phytohormones were probably depended on the improvement of PAL and TAT activities.
Increasing evidence showed that effects of exogenous hormones on secondary metabolite accumulations can be arrested by their biosynthetic inhibitors. Our previous work showed that the ABA-induced tanshinone and phenolic productions were probably via the biosynthesis of endogenous ABA , . Paclobutrazol was an inhibitor of GA biosynthesis. The GA3-induced tanshinone production were significantly inhibited by paclobutrazol in S. miltiorrhiza hairy roots . We also observed that increases of RA and SAB contents induced by GA3 were significantly arrested by paclobutrazol. It was inferred that endogenous GA was probably involved in accumulations of RA and SAB under GA3 treatment. CoCl2 was considered to be effective to block the conversion of ACC to ethylene. Effects of ethylene on plants were significantly inhibited by CoCl2 . In the present study, we found that CoCl2 could significantly reduce increases of phenolic production and enzyme activities induced by ethylene. The inhibitory effect of CoCl2 was probably caused by the inhibition of ethylene biosynthesis.
Interaction of phytohormones in regulating plant development and metabolism is a very complex process . GA was regarded as an antagonist of ABA and ABA also acted as a competitive inhibitor of GA . The antagonistic action between GA and ABA is an important factor regulating the developmental transition from embryogenesis to seed germination . The same results were obtained in our experiments. Contents of phenolic acids in GA3+ABA treatment were less than those in GA3 or ABA treatment alone. It demonstrated that the antagonistic action between ABA and GA played an important role in phenolic production. ABA acted through inhibition of GA biosynthesis . We obtained the same results. The increase of RA and SAB induced by ABA was significantly inhibited by paclobutrazol, which suggested that ABA-induced phenolic production probably depended on GA signaling. Yet, GA3-induced phenolic production was almost not affected by the inhibitor of ABA biosynthesis.
It has been suggested that effect of ethylene could be counteracted directly by the application of ABA . In the opposite, effect of ABA could be also counteracted by ethylene . Enhanced levels of ethylene are known to reduce the endogenous ABA concentration in rehydrated Xanthium leaves . ABA can antagonize ethylene-induced hyponastic growth in Arabidopsis . In S. miltiorrhiza hairy roots, we found that ABA-induced CA production was counteracted by ethylene, and ethylene-induced RA production was counteracted by ABA. It demonstrated that the ABA-ethylene antagonistic action was involved in production of phenolic acids in S. miltiorrhiza hairy roots. The previous work suggested that the function of ABA signaling in the root growth requires the cascade of ethylene signaling . ABA treatment led to increase of ethylene production, and application of inhibitors of ethylene biosynthesis reversed the inhibitory effect of ABA on flowering . The inhibitory effect of ethylene on Pharbitisnil flowering may depend on its influence on the ABA level . In tomato, exogenous ABA treatment promoted ethylene synthesis and fruit ripening, and it was proposed that ABA may act at upstream metabolic events of ethylene action/perception . In our experiments, we observed that ABA-induced phenolic production was reversed by CoCl2 and ethylene-induced phenolic production was also inhibited by fluridone. It was suggested that ethylene was probably involved in ABA-induced phenolic production and ABA probably also participated in ethylene-induced response of S. miltiorrhiza hairy roots. It was inferred that the balance between ABA and ethylene levels probably played an important role in the biosynthesis of phenolic acids.
Ethylene and gibberellic acid are antagonistic on growth of seedlings of Alaska pea. Ethylene interfered severely with the action of gibberellic acid but did not completely suppress it . In the other hand, the potential of GA3 to counteract the effects of ethylene has also been reported . Although both GA3 and ethylene could increase RA and SAB content, the ethylene-induced effects were antagonized by GA3 treatment. Notably, the increase of CA content in ethylene treatment was completely suppressed by GA3. It indicated that GA3 acted as a competitive inhibitor of ethylene on the biosynthesis of phenolic acids. However, in deepwater rice, ethylene and GA have a synergistic effect on the growth rate of emerged roots . Ethylene-mediated enhancement of apical hook formation in Arabidopsis thaliana seedlings is gibberellin dependent . Our results showed that ethylene-induced phenolic production was also inhibited by paclobutrazol, which suggested that GA signanling was probably involved in the ethylene-induced biosynthesis of phenolic acids. In lowland rice, gibberellin-dependent early response to submergence is not necessarily mediated by ethylene . This conclusion held true for S. miltiorrhiza. We observed that effects of GA3 on phenolic acid accumulation was not affected CoCl2. Probably, ethylene signaling is not necessary for GA3-induced phenolic production.
In conclusion, phytohornones including ABA, GA3 and Ethylene were effective to improve production of phenolic acids and increase activitives of PAL and TAT in S. miltiorrhiza hairy roots. Antagonistic actions between the three phytohormones played important roles in the biosynthesis of phenolic acids. GA signaling is necessary for ABA and ethylene-induced phenolic production. Yet, ABA and ethylene signaling is not necessary for GA3-induced phenolic production. The complex interactions among phytohormones help us understand regulation mechanism of secondary metabolism and scale-up production of active ingredients in plants.
Conceived and designed the experiments: ZL DY BC. Performed the experiments: DY YM BC. Analyzed the data: DY TX BC. Contributed reagents/materials/analysis tools: ZL YL ZG. Wrote the paper: ZL DY BC.
- 1. Zhou L, Zuo Z, Chow MSS (2005) Danshen: An Overview of Its Chemistry, Pharmacology, Pharmacokinetics, and Clinical Use. Journal of clinical pharmacology 45: 1345–1359.
- 2. Xu LL, Deng YP, Feng LX, Li DF, Chen XY, et al.. (2011) Cardio-Protection of Salvianolic Acid B through Inhibition of Apoptosis Network. PLoS One 6.
- 3. Wang JW, Wu JY (2010) Tanshinone biosynthesis in Salvia miltiorrhiza and production in plant tissue cultures. Appl Microbiol Biotechnol 88: 437–449.
- 4. Zhao J, Davis LC, Verpoorte R (2005) Elicitor signal transduction leading to production of plant secondary metabolites. Biotechnol Adv 23: 283–333.
- 5. Yang D, Ma P, Liang X, Wei Z, Liang Z, et al. (2012) PEG and ABA trigger methyl jasmonate accumulation to induce the MEP pathway and increase tanshinone production in Salvia miltiorrhiza hairy roots. Physiol Plant 146: 173–183.
- 6. Yang D, Sheng D, Duan Q, Liang X, Liang Z, et al. (2012) PEG and ABA Trigger the Burst of Reactive Oxygen Species to Increase Tanshinone Production in Salvia miltiorrhiza Hairy Roots. J Plant Growth Regul 31: 579–587.
- 7. Liang ZS, Yang DF, Liang X, Zhang YJ, Liu Y, et al. (2012) Roles of reactive oxygen species in methyl jasmonate and nitric oxide-induced tanshinone production in Salvia miltiorrhiza hairy roots. Plant Cell Rep 31: 873–883.
- 8. Cui B, Liang Z, Liu Y, Liu F, Zhu J (2012) Effects of ABA and its biosynthetic inhibitor fluridone on accumulation of penolic acids and activity of PAL and TAT in hairy root of Salvia miltiorrhiza. Zhongguo Zhong Yao Za Zhi 37: 754–759.
- 9. McSteen P, Zhao Y (2008) Plant Hormones and Signaling: Common Themes and New Developments. Developmental cell 14: 467–473.
- 10. Heredia JB, Cisneros-Zevallos L (2009) The effect of exogenous ethylene and methyl jasmonate on pal activity, phenolic profiles and antioxidant capacity of carrots (Daucus carota) under different wounding intensities. Postharvest Biology and Technology 51: 242–249.
- 11. YUAN Y, HUANG L, CUI Gh, MAO Y, HE X (2008) Effect of Gibberellins and Its Synthetic Inhibitor on Metabolism of Tanshinones. Chin J ExpTrad Med Form 14: 1–3.
- 12. Jiang Y, Joyce DC (2003) ABA effects on ethylene production, PAL activity, anthocyanin and phenolic contents of strawberry fruit. Plant Growth Regul 39: 171–174.
- 13. Zentella R, Zhang Z-L, Park M, Thomas SG, Endo A, et al. (2007) Global Analysis of DELLA Direct Targets in Early Gibberellin Signaling in Arabidopsis. Plant Cell 19: 3037–3057.
- 14. Gomez-Cadenas A, Zentella R, Walker-Simmons MK, Ho TH (2001) Gibberellin/abscisic acid antagonism in barley aleurone cells: site of action of the protein kinase PKABA1 in relation to gibberellin signaling molecules. Plant Cell 13: 667–679.
- 15. Steffens B, Wang J, Sauter M (2006) Interactions between ethylene, gibberellin and abscisic acid regulate emergence and growth rate of adventitious roots in deepwater rice. Planta 223: 604–612.
- 16. Beaudoin N, Serizet C, Gosti F, Giraudat J (2000) Interactions between Abscisic Acid and Ethylene Signaling Cascades. Plant Cell 12: 1103–1116.
- 17. Linkies A, Muller K, Morris K, Tureckova V, Wenk M, et al. (2009) Ethylene interacts with abscisic acid to regulate endosperm rupture during germination: a comparative approach using Lepidium sativum and Arabidopsis thaliana. Plant Cell 21: 3803–3822.
- 18. Fuchs Y, Lieberman M (1968) Effects of Kinetin, IAA, and Gibberellin on Ethylene Production, and Their Interactions in Growth of Seedlings. Plant Physiol 43: 2029–2036.
- 19. Weiss D, Ori N (2007) Mechanisms of Cross Talk between Gibberellin and Other Hormones. Plant Physiol 144: 1240–1246.
- 20. Li HC, Rice EL, Rohrbaugh LM, Wender SH (1970) Effects of Abscisic Acid on Phenolic Content and Lignin Biosynthesis in Tobacco Tissue Culture. Physiol Plant 23: 928–936.
- 21. Gil-Amado JA, Gomez-Jimenez MC (2012) Regulation of polyamine metabolism and biosynthetic gene expression during olive mature-fruit abscission. Planta 235: 1221–1237.
- 22. Beevers L, Loveys B, Pearson JA, Wareing PF (1970) Phytochrome and hormonal control of expansion and greening of etiolated wheat leaves. Planta 90: 286–294.
- 23. Zeevaart J (1983) Metabolism of Abscisic Acid and Its Regulation in Xanthium Leaves during and after Water Stress. Plant Physiol 71: 477–481.
- 24. Benschop J, Millenaar F, Smeets M, van Zanten M, Voesenek L, et al. (2007) Abscisic acid antagonizes ethylene-induced hyponastic growth in Arabidopsis. Plant Physiol 143: 1013–1023.
- 25. Ghassemian M, Nambara E, Cutler S, Kawaide H, Kamiya Y, et al. (2000) Regulation of Abscisic Acid Signaling by the Ethylene Response Pathway in Arabidopsis. Plant Cell 12: 1117–1126.
- 26. Wilmowicz E, Kesy J, Kopcewicz J (2008) Ethylene and ABA interactions in the regulation of flower induction in Pharbitis nil. J Plant Physiol 165: 1917–1928.
- 27. Zhang M, Yuan B, Leng P (2009) The role of ABA in triggering ethylene biosynthesis and ripening of tomato fruit. J Exp Bot 60: 1579–1588.
- 28. Goldschmidt EE, Aharoni Y, Eilati SK, Riov JW, Monselise SP (1977) Differential counteraction of ethylene effects by gibberellin a(3) and n(6)-benzyladenine in senescing citrus peel. Plant Physiol 59: 193–195.
- 29. Vriezen WH, Achard P, Harberd NP, Van Der Straeten D (2004) Ethylene-mediated enhancement of apical hook formation in etiolated Arabidopsis thaliana seedlings is gibberellin dependent. Plant J 37: 505–516.
- 30. Dubois V, Moritz T, Garcia-Martinez JL (2011) Examination of two lowland rice cultivars reveals that gibberellin-dependent early response to submergence is not necessarily mediated by ethylene. Plant Signal Behav 6: 134–136.