Next Article in Journal
Novel Steroidal Glycosides from the Bulbs of Lilium pumilum
Previous Article in Journal
Synthesis, Biological Evaluation and Molecular Docking Studies of Piperidinylpiperidines and Spirochromanones Possessing Quinoline Moieties as Acetyl-CoA Carboxylase Inhibitors
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 20
Issue 9
10.3390/molecules200916235
molecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

The Biosynthetic Pathways of Tanshinones and Phenolic Acids in Salvia miltiorrhiza

by
Xiao-Hui Ma
1,2,†,
Ying Ma
2,3,†,
Jin-Fu Tang
2,
Ya-Li He
2,
Yu-Chen Liu
2,4,
Xiao-Jing Ma
2,
Ye Shen
2,
Guang-Hong Cui
2,
Hui-Xin Lin
2,
Qi-Xian Rong
2,
Juan Guo
2,* and
Lu-Qi Huang
2,*
1
Pharmacy College, Chengdu University of Traditional Chinese Medicine, Chengdu 611137, China
2
State Key Laboratory Breeding Base of Dao-Di Herbs, National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China
3
Beijing Key Laboratory of Protection and Application of Chinese Medicinal Resources, Beijing Normal University, Beijing 100875, China
4
Pharmaceutical College, Guiyang College of Traditional Chinese Medicine, Guiyang 550002, China
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Molecules 2015, 20(9), 16235-16254; https://doi.org/10.3390/molecules200916235
Submission received: 19 July 2015 / Accepted: 24 August 2015 / Published: 8 September 2015
(This article belongs to the Section Metabolites)
Browse Figures
Versions Notes

Abstract

Secondary metabolites from plants play key roles in human medicine and chemical industries. Due to limited accumulation of secondary metabolites in plants and their important roles, characterization of key enzymes involved in biosynthetic pathway will enable metabolic engineering or synthetic biology to improve or produce the compounds in plants or microorganisms, which provides an alternative for production of these valuable compounds. Salvia miltiorrhiza, containing tanshinones and phenolic acids as its active compounds, has been widely used for the treatment of cardiovascular and cerebrovascular diseases. The biosynthetic analysis of secondary metabolites in S. miltiorrhiza has made great progress due to the successful genetic transformation system, simplified hairy roots system, and high-throughput sequencing. The cloned genes in S. miltiorrhiza had provided references for functional characterization of the post-modification steps involved in biosynthesis of tanshinones and phenolic acids, and further utilization of these steps in metabolic engineering. The strategies used in these studies could provide solid foundation for elucidation of biosynthetic pathways of diterpenoids and phenolic acids in other species. The present review systematically summarizes recent advances in biosynthetic pathway analysis of tanshinones and phenolic acids as well as synthetic biology and metabolic engineering applications of the rate-limiting genes involved in the secondary metabolism in S. miltiorrhiza.

1. Introduction

Plant secondary metabolites including terpenes, phenolic compounds, and nitrogen-containing compounds, which are served as signaling or defense molecules, are not only important to plant development and adaptation, but also have significant economic value as resources in human medicine and chemical industries. Many secondary metabolites from plants have been used in the clinical treatment of diseases, such as taxol in the treatment of refractory ovarian cancer and metastatic breast cancer [1], and ginkgolides in the treatment of cardiovascular diseases and diabetic vascular complications [2]. Secondary metabolites are always accumulated at low levels in plants with long growth periods. Moreover, chemical synthesis is challenging and has little practical value for those compounds with complicated structures. Scientists have turned to biotechnology and genetic engineering to produce or improve these compounds in plants or microorgnisms.
Elucidation of the biosynthetic pathways of secondary metabolites in plants enabled the exploration of metabolic engineering or synthetic biology as potentially effective approaches for producing specific metabolites, which provide alternative for the production of the valuable compounds. Metabolic engineering can be optimized by enhancing the rate-limiting steps or blocking competitive pathways to improve production. Overexpression of genes that encode the rate-limiting enzymes involved in scopolamine biosynthesis has resulted in greater accumulation of scopolamine in hairy roots of transgenic Hyoscyamus niger compared to the wild-type [3]. Contents of oleanane-type ginsenoside (ginsenoside Ro) in Panax ginseng plant were highly increased by overexpression of CYP716A52v2, and the amount of ginsenoside Ro declined in an RNA interference transgenic line targeting this gene [4]. Alternatively, synthetic biology can be used to construct engineered strains for the high-yield production of bioactive secondary metabolites. Paddon et al. used synthetic biology to develop strains of Saccharomyces cerevisiae for the high-yield biological production of artemisinic acid, which led to the heterologous production of 25 g/L of this compound by baker’s yeast after multiple steps of optimization [5].
The root and rhizome of S. miltiorrhiza with diterpenoid tanshinones and phenolic acids as its active compounds is a traditional Chinese medicine (usually called danshen in China) has been widely used for the treatment of cardiovascular and cerebrovascular diseases. The Fufang Danshen Dripping Pill with danshen as its main material has been extensively used for treatment of cardiovascular diseases in China and some other countries, and has been approved for phase III clinical trials in the USA (ClinicalTrials.gov Identifier: NCT01659580). The two typical secondary metabolites made S. miltiorrhiza as a model for analyzing plant secondary metabolism pathways. Tanshinones including tanshinone I, tanshinone IIA, cryptotanshinone, and dihydrotanshinone I are lipophilic compounds, which are widely accumulated in Salvia (Labiaceae) [6,7]. More than 40 tanshinones have been isolated from danshen. It possesses significant antioxidant, anti-inflammatory, and antineoplastic activities and has been shown to have potent anticancer activities both in vitro and in vivo [8,9]. The anti-inflammatory activity of tanshinone IIA is especially outstanding, as this compound blocks pro-inflammatory signals in vivo and these effects are conserved in human neutrophils [10]. In addition, the sulfotanshinone sodium injection constituted with sodium tanshinone IIA sulfate, which significantly improves the intestinal absorption of it, has been widely used for treatment of coronary disease, angina pectoris, and myocardial infarction in China [11]. Tanshinones also have significant anti-aging activity. For instance, cryptotanshinone can greatly extend the chronological lifespan of budding yeast S. cerevisiae [12]. Phenolic acids are widely distributed in the plant kingdom, especially in the Boraginaceae and Labiaceae families [13]. These compounds include caffeic acid monomers as well as oligomers of danshensu, caffeic acid, salvianolic acids, rosmarinic acid (RA), and lithospermic acids [14]. Among more than 20 phenolic acids isolated from danshen, salvianolic acid B (SAB) is the major water-soluble constituent with particular activity, and the content of SAB in S. miltiorrhiza is more abundant than in other Labiaceae species [15]. Phenolic acids from danshen were prominent with its antioxidant, anticoagulant, and cell protection activities [14]. The main effective ingredients of Danhong Injection (China food and drug administration: Z20026866) are the water-soluble constituents, which have been used for treatment of various kinds of ischemic disease in China.
Due to the medicinal and economic value of these secondary metabolites in danshen, it is important to enhance the production of these compounds through metabolic engineering or synthetic biology. Elucidating the biosynthesis of these compounds and identifying the exact genes that catalyze their synthesis are critical for improving the production of these compounds. Fortunately, advances in sequencing and comparative transcriptome analysis have provided efficient candidates for biosynthetic pathway analysis. The successful hairy root transformation and generation system in S. miltiorrhiza have provided a simple system for studying the biochemical properties and gene functions [16,17,18]. Though the downstream biosynthetic pathway analysis of tanshinones and phenolic acids is still ongoing, it has made great progress in elucidating the biosynthesis of these secondary metabolites which could provide a solid foundation for other compounds. In this article, we systematically reviewed the recent progresses in biosynthetic pathway analysis of tanshinones and phenolic acids as well as synthetic biology and metabolic engineering applications of the rate-limiting genes involved in the secondary metabolism in S. miltiorrhiza from year 2005 to year 2015, and further discussed the analysis and utilization of the metabolic pathways.

2. Comparative Transcriptome Provides Informative Data in Biosynthetic Pathway Analysis

Advances in sequencing and bioinformatics analysis could provide a large amount of candidate genes for the biosynthetic pathway responsible for the secondary metabolites. S. miltiorrhiza hairy root could be generated by infecting leaf explants with Agrobacterium rhizogenes strains in S. miltiorrhiza [19,20] and exhibits a similar protective activity against hypoxia and reoxygenation injury in rat cardiac myocytes to danshen [21]. In addition, the secondary metabolites in hairy roots could be stimulated by elicitors within several days, which provide a simplified system to identity new candidate genes by different expression or comparative transcriptome analysis. The first cDNA microarray analysis for different stages of S. miltiorrhiza hairy root cultures revealed 203 differentially expressed genes from 4354 cDNA clones, including seven genes (especially two important terpenoid synthases) involved in tanshinone biosynthesis [22]. However, the information in cDNA microarray is limited, a large amount of candidates related to the post-modification progress in biosynthesis of secondary metabolites are to be investigated.
Deep sequencing could provide high-throughput data for the discovery of candidate genes involved in the biosynthesis of natural products, especially in non-model species. Furthermore, comparative transcriptome analyses of different tissues with and without active ingredients could provide a comprehensive insight into the biosynthesis and regulation of these compounds. In the transcriptome over the entire growth cycle, including the seedling stage, vegetable stage, and different tissues in the reproductive stage, a total of 47 unigenes encoding more than 24 enzymes and 200 unigenes related to 32 enzymes were identified, which are potentially involved in the biosynthesis of rosmarinic acids and terpenoids, respectively [23]. In a more recent study, Yang et al. further conducted transcriptomic profiling of the S. miltiorrhiza root and leaf tissues by using 454 GS-FLX pyrosequencing platform to identify genes and transcriptional regulators involved in the biosynthesis of tanshinones. 168 unigenes involved in the biosynthesis of the terpenoid backbone and 2863 unigenes that are highly expressed in roots were identified, including those genes involved in the biosynthesis of tanshinones, such as copalyl diphosphate synthase (SmCPS1), kaurene synthase-like (SmKSL1) and CYP76AH1 [24].
The transcriptome among different tissues including different expression genes related to plant development resulted in too many candidates for further characterization, while the comparative transcriptome from different elicitation processes could significantly narrow the candidates for functional characterization. The transcriptional profiles of MJ elicitated S. miltiorrhiza leaves yielded 37647 unique sequences. Almost all of the known genes involved in tanshinone and phenolic acid biosynthesis in S. miltiorrhiza were expressed differentially between the untreated and treated samples. Three and four candidate P450s that could be involved in the biosynthesis of tanshinones and phenolic acids, respectively, were selected from the RNA-seq data based on the co-expression analyses with SmCPS1/SmKSL1 or SmRAS [25]. Metabolomics could further provide an instantaneous snapshot of the entire physiology of an organism by comparing the relative differences between biological samples based on their metabolite profiles. Gao et al. combined metabolomics and deep sequencing to investigate the inducible biosynthesis of tanshinones. The comprehensive transcriptome comprised 20972 non-redundant genes, of which 39 CYPs exhibited up-regulation at all time points following induction. Eight cytochrome P450s (P450s) were co-regulated with known genes involved in tanshinones biosynthesis, providing targets for future investigations [26]. This study provided reference for combining metabolomics and deep sequencing to investigate new targets for future secondary metabolic pathway analysis in S. miltiorrhiza.
P450s have been demonstrated to play key role in post-modification of tanshinones biosynthesis [27]. Using RNA-Seq technology, Chen et al. systematically studied the P450 genes in S. miltiorrhiza, and identified 116 full-length and 135 partial-length P450 genes by combining their data with previously identified P450 sequences and scanning the data with the P450 model from Pfam [28]. Through a comparison with the KEGG database, ten of these P450 genes were speculated to be related to diterpenoid biosynthesis, three genes were predicted to be potentially involved in terpenoid biosynthesis. The database set up in this study provided a centralized resource for P450 exploration in secondary metabolism analysis in S. miltiorrhiza. More recently, combination of next-generation sequencing (NGS) and single-molecule real-time (SMRT) sequencing was applied to various root tissues to generate a much more complete transcriptome of S. miltiorrhiza, particularly including the periderm, where the biosynthesis and accumulation of tanshinones occurred. Combining this transcriptome data with qRT-PCR to analyze these genes expression pattern, 15 CYPs, one 2-oxo-glutarate dependent di-oxygenase (2ODD) and five short-chain alcohol dehydrogenases (SDRs) which co-expressed with SmCPS1, SmKSL1, and CYP76AH1 were predicted to play roles in tanshinones biosynthesis [29]. These databases provide valuable resource and full-length candidate genes for further investigation of secondary metabolites biosynthesis in S. miltiorrhiza.

3. Biosynthesis of Tanshinones in S. miltiorrhiza

Tanshinones are a group of abietane-type norditerpenoid quinone natural products that primarily accumulate in the roots of S. miltiorrhiza. The biosynthetic pathway of tanshinones could be divided into three steps: the formation of precursors for all terpenoids; the construction of skeletons of tanshinones; and the post-modification of the skeleton, such as oxidation, methylation, decarboxylation or cyclization to produce the various tanshinones. This pathway has been explored for more than two decades, and most genes involved in tanshinone biosynthesis have been cloned (Table 1 and Figure 1) [6,26,27].
Figure 1. Biosynthethsis of tanshinones in S. miltiorrhiza. Solid arrows indicate the established relationships, and dashed arrows indicate hypothetical relationships. G3P: glyceraldehyde-3-phosphate, IPP: isopentenyl pyrophosphate, DMAPP: dimethylallyl pyrophosphate, IPI: IPP isomerase, GPP: geranyl diphosphate, GPPS: GPP synthase, FPP: farnesyl diphosphate, FPPS: FPP synthase, GGPP: geranylgeranyl diphosphate, GGPPS: GGPP synthase, CPP: copalyl diphosphate, SmCPS: CPP synthase, SmKSL: kaurene synthase-like cyclase.
Figure 1. Biosynthethsis of tanshinones in S. miltiorrhiza. Solid arrows indicate the established relationships, and dashed arrows indicate hypothetical relationships. G3P: glyceraldehyde-3-phosphate, IPP: isopentenyl pyrophosphate, DMAPP: dimethylallyl pyrophosphate, IPI: IPP isomerase, GPP: geranyl diphosphate, GPPS: GPP synthase, FPP: farnesyl diphosphate, FPPS: FPP synthase, GGPP: geranylgeranyl diphosphate, GGPPS: GGPP synthase, CPP: copalyl diphosphate, SmCPS: CPP synthase, SmKSL: kaurene synthase-like cyclase.
Table 1. The genes involved in isoprenoids metabolic pathway in S. miltiorrhiza.
Table 1. The genes involved in isoprenoids metabolic pathway in S. miltiorrhiza.
Gene (Genbank No.)Highest Expression SitesElicitorReference
SmAACT1 (EF635969)rootYE, Ag+[30]
SmAACT2 (AEZ55671)stem [31]
SmHMGS (FJ785326)leafSA, MJ, YE[32]
SmHMGR1 (EU680958 GU367911)flower and rootSA, JA, MJ, PEG, ABA[31,33,34]
SmHMGR2 (FJ747636)leaf, stem, rootMJ, Ag+[22,31,35,36]
SmHMGR3 (JN831102)leafMJ[31,37]
SmHMGR4 (JN831103)flower [31]
SmMK (JN831104)stemMJ[31]
SmPMK (JN831095)stem and rootMJ[31]
SmMDC (JN831105)stem and rootMJ[31]
SmDXS1 (EU670744)leafAg+[31,35]
SmDXS2 (FJ643618)root and leafMJ, PEG, ABA, MJ Act12, Ag+[17,31,34,35,38]
SmDXS3 (JN831116)leaf, stem, root cortex, and root steleMJ[31]
SmDXS4 (JN831117)ubiquitous [31]
SmDXS5 (JN831118)leaf and stem [31]
SmDXR (FJ768959, FJ476255, DQ991431)leafSA,YE, Hypertonic stress, Act12 PEG, ABA and MJ, Ag+[34,35,38,39,40]
SmCMT (JN831096)leaf [31]
SmCMK (EF534309)leafMJ[31,41]
SmMCS (JX233816)leaf and stemAg+[31,42]
SmHDS1 (JN831098)leaf [31,43]
SmHDS2 (KJ746807) [44]
SmHDR1 (JX233817 JN831099)leafMJ, Ag+[31]
SmHDR2 (JN831100)leaf [31]
SmHDR (JX516088)leafMJ, SA[45]
SmIPI1 (JN831106)rootMJ, fungal elicitor[22,46]
SmIPI2 (JN831106)stemMJ[31]
SmGPPS (JN831107) [31]
SmGPPS.LSU (JN831111)stem and flowerMJ[31]
SmGPPS.SSUI (JN831108)leafMJ[31]
SmGPPS.SSUII.1 (JN831109)leaf and root cortex [31]
SmGPPS.SSUII.2 (JN831110)stem [31]
SmFPPS (EF635968 HQ687768)stemMJ[22,31,47]
SmGGPPS1 (FJ643617 FJ178784)leafNaCl, wounding, high temperature, darkness, pathogen, MJ, ABA, SA and GA, Act12, Ag+[17,35,38,48,49,50]
SmGGPPS2 (JN831112)root stele [31]
SmGGPPS3 (JN831113)ubiquitous [31]
SmCPS1 (EU003997)root cortexAg+, MJ, YE[35,51,52]
SmCPS2 (JN831114)leaf [31,53]
SmCPS3 (JN831115)stem [31,53]
SmCPS4 (JN831120)sepal [31,53]
SmCPS5 (JN831121)stemMJ[31,53]
SmKSL1 (EF635966)rootAg+, MJ[35,51,53]
SmKSL2 (JN831119)root xylem [31,53]
CYP76AH1 (JX422213)rootAg+[27,35]
CYP76s (KR140168) (KR140169)rootAg+[54]
SmCPR1(FR693803) [27,55]
SmCPR2(JX848592) [27]
Isopentenyl diphosphate (IPP) and its isomer dimethylallyl diphosphate (DMAPP) are the precursors of all terpenoids. In plants, two biosynthetic pathways are involved in the production of the universal isoprene precursors IPP and DMAPP: the mevalonate (MVA) pathway in the cytosol, and the methylerythritol phosphate (MEP) pathway in the plastids. The MEP pathway was identified through labeling experiments in bacteria and plants [56,57]. In plants, the MEP pathway is mainly responsible for production of monoterpenoids, diterpenoids, carotenoids, and the side chains of chlorophylls and plastoquinone [58]. Glyceraldehyde 3-phosphate (G3P) and pyruvate have been identified as the direct precursors of IPP and DMAPP. Most genes in the MEP pathway have been identified in S. miltiorrhiza. 1-Deoxy-d-xylulose-5-phosphate synthase (DXS) is the key enzymes of the MEP pathway and is involved in the important rate-limiting reaction. There are five DXSs in the draft genome of S. miltiorrhiza, and the expression level of SmDXS2 in S. miltiorrhiza roots was highest compared with the other SmDXSs [31]. It was also reported that the overexpression of SmDXS2 could increase the accumulation of tanshinones in S. miltiorrhiza hairy root [17], indicating that SmDXS2 might be closely related to the accumulation of tanshinones.
The MVA pathway, which has been studied for decades, is maily involved in the biosynthesis of sesquiterpenoids, polyisoprenoids and sterols [59]. In S. miltiorrhiza, it was considered that tanshinones are mainly synthesized by the MEP pathway, while the MVA pathway could be better explained as being involved in cell growth. However, both cell growth and tanshinone production could partially depend on the crosstalk between the two pathways [60,61]. In the MVA pathway, IPP is synthesized from two acetyl-CoA molecules. The 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR) converts 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) to MVA with two NADPH as the rate-limiting step of the MVA pathway [36]. There are four HMGRs in the draft genome of S. miltiorrhiza [31]. SmHMGR1, SmHMGR2, SmHMGR3 are considered to play more important roles in tanshinone biosynthesis [31]. Actually, overexpression of SmHMGR1 [17,62] and SmHMGR2 [36] in S. miltiorrhiza hairy root cultures both could significantly increase the tanshinone content, indicating that SmHMGR1 and SmHMGR2 from MVA pathway might also contribute to the biosynthesis of tanshinones.
The conversion of IPP and DMAPP could be catalyzed by IPP isomerase (IPI). DMAPP and IPP are further condensed by geranyl diphosphate synthase (GPPS), farnesyl diphosphate synthase (FPPS), geranylgeranyl diphosphate synthase (GGPPS) to form GGPP [6]. GGPP is the universal precursor of all diterpenoids and can be catalyzed by different terpenoid synthases to form various diterpenoid skeletons. Terpenoid synthases are the key enzymes for the biosynthesis of the tanshinone skeletons. 12 SmCPS and nine SmKSL homologs have been reported in S. miltiorrhiza [29]. The functions of four SmCPSs and two SmKSLs were identified through the expression of the protein in Escherichia coli and enzymatic catalysis in vitro combined with GC-MS measurements, which characterized the role of SmCPS1, SmCPS2, and SmKSL1 in tanshinone biosynthesis to form the skeleton miltiradiene [51,53], and kenetic analysis showed that SmCPS1 had both higher affinity and activity with GGPP than SmCPS2. RNA interference was employed to down-regulate the expression of SmCPS1, which resulted in a decrease in the accumulation of tanshinones, further verified the key role of SmCPS1 in tanshinone biosynthesis [16,53].
According to the structure of tanshinones, the genes involved in the downstream pathway involved in tanshinone biosynthesis are P450s, dehydrogenases, demethylases, and other structural modifying enzymes, which always begin with P450s [27,63]. Guo et al. [27] used comparative transcriptome analysis to identify six candidate P450s genes that were co-regulated with the diterpenoid synthase genes in both the root and S. miltiorrhiza hairy roots. CYP76AH1 was identified to catalyze miltiradiene to produce ferruginol both in vitro and in vivo. Recently, based on co-expression analysis, the authors further identified two new P450s which can work sequentially to catalyze ferruginol into the metabolic intermediate, which with two keto in C11 and C12 is more close to the tanshinones [54]. Now, the post-modification from ferruginol to tanshinones is still ongoing. The identified enzymes involved in biosynthetic pathway could provide reference genes for post-modification characterization.

4. Biosynthesis of Phenolic Acids in S. miltiorrhiza

There are more than 20 phenolic acids in S. miltiorrhiza, with RA and SAB as the typical water-soluble constituents which contribute to the effects in the treatment of cardiovascular disease. RA was a dominant phenolic acid distributing in Lamiaceae. The biosynthetic pathway of RA in Coleus blumei has been characterized [13]. In Lamiaceae including S. miltiorrhiza, two biosynthetic pathways are involved in the biosynthesis of the processor of phenolic acid: the phenylpropanoid pathway and the tyrosine-derived pathway. In the phenylpropanoid pathway, phenylalanine is transformed into 4-coumaroyl-CoA by phenylalanine ammonia-lyase (PAL), cinnamic acid 4-hydroxylase (C4H) and 4-coumarate: CoA ligase (4CL). In the tyrosine-derived pathway, tyrosine is metabolized to 4-hydroxyphenyllactate through tyrosine aminotransferase (TAT) and 4-hydroxyphenylpyruvate reductase (HPPR), finally forming 3,4-dihydroxyphenyllactic acid (DHPL, also known as salvianic acid A or danshensu). It was reported that the expression of enzymes involved in the tyrosine-derived pathway were more correlated to rosmarinic and salvianolic acid B biosynthesis after elicited with MJ, hyphal extracts or other elicitors, which indicated that the tyrosine-derived pathway might be the rate-limiting step in biosynthesis of phenolic acid [64,65]. 4-coumaroyl-CoA and DHPL were further coupled by the ester-forming enzyme rosmarinic acid synthase (RAS) to form 4-coumaroyl-3′4′-dihydroxyphenyllactic acid (4C-DHPL). 4C-DHPL is oxidized by CYP98A14, which introduces the 3-hydroxyl group to form RA.
RA was believed to be the processor of SAB. Di et al. [15] employed isotopic labeling experiments in vivo using [ring-13C]-phenylalanine to trace the metabolic origin of phenolic acids in S. miltiorrhiza. It was speculated that RA might be transformed into a phenoxyl radical by oxidation, and two phenoxyl radicals unite spontaneously to form SAB [15]. In S. miltiorrhiza, 4C-DHPL was considered as the main intermediate for RA biosynthesis, and DHPL was involved in this pathway as a principal intermediate. However, the pathway from RA to LAB remains to be elucidated (Figure 2).
The majority of genes involved in phenolic acid biosynthesis have been cloned in S. miltiorrhiza, including SmPAL, SmC4H, Sm4CL, SmTAT, SmHPPR, SmRAS and CYP98A14 (Table 2). Three SmPALs were identified in the working draft of the S. miltiorrhiza genome. Coexpression analyses with the accumulation of phenolic acids revealed that SmPAL1 and SmPAL3 were more abundant in the root which indicated that they might be more important in the biosynthesis of rosmarinic acids [66]. The function of SmPAL1 was further verified by in vivo and in vitro analyses, which revealed that SmPAL1 exhibited high catalyzation activity using L-Phe as substrate [67]. Otherwise, when the expression of SmPAL1 was suppressed in S. miltiorrhiza, the rosmarinic acid and salvianolic acid B content was significantly decreased which proved the key role of SmPAL1 in biosynthesis of phenolic acids [68]. Several Sm4CLs have been identified in S. miltiorrhiza. The enzyme activity analyses and expression analyses of Sm4CL2 and Sm4CL3 indicated that these two genes are more likely to be involved in the biosynthesis of water-soluble phenolic compounds [69,70,71]. In addition to PAL and 4CL, the function of SmC4H1, SmTAT1, and SmHPPR1 were also confirmed in vivo. Overexpression in the hairy roots of S. miltiorrhiza could increase the accumulation of RA and SAB [18]. The functional characterization genes involved in the biosynthesis of phenolic acids could be used as targets in metabolic engineering to accelerate the production of these compounds.
Figure 2. Biosynthethsis of phenolic acids in S. miltiorrhiza [15]. Solid arrows indicate the established relationships, and dashed arrows indicate hypothetical relationships. RA is mainly biosynthesized from the pathway showed with black arrows in S. miltiorrhiza, and part is from the pathway showed with green arrows. PAL: phenylalanine ammonialyase, C4H: cinnamic acid 4-hydroxylase, 4CL: 4-coumaroyl: CoA ligase, TAT: tyrosine aminotransferase, HPPR: 4-hydroxyphenylpyruvate reductase, RAS: rosmarinic acid synthase.
Figure 2. Biosynthethsis of phenolic acids in S. miltiorrhiza [15]. Solid arrows indicate the established relationships, and dashed arrows indicate hypothetical relationships. RA is mainly biosynthesized from the pathway showed with black arrows in S. miltiorrhiza, and part is from the pathway showed with green arrows. PAL: phenylalanine ammonialyase, C4H: cinnamic acid 4-hydroxylase, 4CL: 4-coumaroyl: CoA ligase, TAT: tyrosine aminotransferase, HPPR: 4-hydroxyphenylpyruvate reductase, RAS: rosmarinic acid synthase.
Table 2. The genes involved in phenolic acids biosynthesis in S. miltiorrhiza.
Table 2. The genes involved in phenolic acids biosynthesis in S. miltiorrhiza.
Gene (Genbank No.)Highest Expression SitesElicitorReference
SmPAL1 (EF462460)root, leafABA, wounding and dehydration, PEG, MJ, SA, Ca2+, GA, ethylene[66,67,68,71,72,73,74,75]
SmPAL2 (GQ249111)stem, flowerPEG and MJ[66,68,71]
SmPAL3 (KF220569)rootleafPEG and MJ[66,71]
SmC4H1 (EF377337 DQ355979)root, stemMJ, ABA, UV-B, Ag+[35,71,76,77]
SmC4H2 (KF220564)stem, root [71]
Sm4CL1 (AY237163)leafMJ, YE[69,70]
Sm4CL2 (AY237164)rootMJ, YE, Ag+[35,69,70,71]
Sm4CL3 (KF220556)rootMJ[71]
Sm4CL-like1 (KF220557)rootMJ[71]
Sm4CL-like2 (KF220558) MJ[71]
Sm4CL-like3 (KF220559) [71]
Sm4CL-like4 (KF220560)root [71]
Sm4CL-like5 (KF220561) [71]
Sm4CL-like6 (KF220562) MJ[71]
Sm4CL-like7 (KF220563) [71]
SmTAT1 (DQ334606 EF192320)stemMJ, ABA, SA, UV-B, GA, ethylene, Ag+, YE[35,65,72,74,78]
SmTAT2 (KF220575)flowerMJ[71]
SmTAT3 (KF220555)Stem, root [71]
SmHPPR1 (DQ099741 DQ266514 EF458148)stemflowerMJ, SA, GA3, ABA, UV-B, Ag+[35,71,79]
SmHPPR2 (KF220565)Stem,leaf [71]
SmHPPR3 (KF220566)stem [71]
SmHPPR4 (KF220567) [80]
SmRAS-Like (GU647199)stemPseudomonas lachrymans, MJ, light, and SA[81]
SmRAS1 (FJ906696)rootMJ, Ag+[15,35]
SmHCT1 (KF220570)root [71]
SmHCT2 (KF220571)stem [71]
SmHCT3 (KF220572)stemMJ[71]
SmHCT4 (KF220573)stemMJ[71]
SmHCT5 (KF220574)stemMJ[71]
CYP98A14 (HQ316179)rootMJ, Ag+[15,35]

5. Biotechnological Applications

Natural plant products are often produced in relatively low amounts and are difficult to chemically synthesize. Biotechnology is one of the most important ways to improve the active compounds of plants. Elucidating the secondary metabolites biosynthetic pathway is helpful for further revealing the mechanisms that produce bioactive components. Based on the biosynthetic pathway analyses, synthetic biology and metabolic engineering have been used to produce or improve the production of tanshinone and phenolic acid in both microorganisms and S. miltiorrhiza or its hairy roots (Figure 3).
Figure 3. Biotechnogical applications in Salvia miltiorrhiza.
Figure 3. Biotechnogical applications in Salvia miltiorrhiza.
The advances in recombinant DNA technology offered the opportunity of using synthetic biology to produce tanshinones and phenolic acid-related compounds in microorganisms. Zhou et al. applied a modular pathway engineering (MOPE) strategy for the rapid assembly of synthetic miltiradiene pathways in S. cerevisiae, using a fusion of the diterpene synthases SmCPS1 and SmKSL1 as well as the fusion of BTS1 (GGPPS) and ERG20 (farnesyl diphosphate synthase, FPPS). This approach led to a significant improvement in the production of miltiradiene and a reduction of byproduct accumulation. The miltiradiene yield of the most prolific strain reached 365 mg/L in a 15-L bioreactor culture [82]. Further study revealed that simultaneous overexpression of tHMGR-upc2.1 and ERG20-BTS1-SaGGPS genes had a synergetic effect on the miltiradiene production in yeast strains, and 488 mg/L miltiradiene was produced in fed-batch fermentation [83]. Based on the establishment of miltiradiene production in S. cerevisiae, Guo et al. engineered the yeast by incorporating modules expressing CYP76AH1 as well as a P450 reductase gene (SmCPR1) into this efficient pathway, leading to the heterologous production of ferruginol at 10.5 mg/L under flask shaking conditions without process optimization [27]. As the biosynthetic pathway of tanshinones remains unsolved and most of the metabolic intermediates could rarely accumulate in plants, the engineered yeast strain provided a basis strain to identify additional enzymes.
The production of RA in microorganisms has also been realized. Bloch et al. [84] designed a biosynthetic pathway tailored for the production of RA and isorinic acid (IA) in Escherichia coli through the overexpression of a six-enzyme chimeric bacterial and plant pathway. They compared three plant RAS orthologues from Coleus blumei (CbRAS), Lavandula angustifolia (LaRAS) and Melissa officinalis (MoRAS). The strains with different plant RAS genes produced different levels of RA and IA but in the same ratios, and the amount of RA and IA produced could also be increased by the optimization of another pathway. In S. miltiorrhiza, the analysis of phenolic acid biosynthesis could provide more candidate modules for pathway optimization. This work provided a microbial platform for the production of RA and IA that uses a modular biosynthetic approach to produce these compounds.
The metabolic engineering of S. miltiorrhiza or its hairy roots provides an alternative method for accelerating the production of tanshinones and phenolic acids by overexpression the key enzymes or suppression the competition pathway. SmGGPPS, SmHMGR, and SmDXS were key enzymes involved in the biosynthesis of tanshinone precursors [17,38,48,49,50]. To increase the supply of precursors in S. miltiorrhiza, SmGGPPS1, SmHMGR1, and SmDXS2 were overexpressed in transgenic hairy root lines. It was revealed that the co-expression of SmHMGR1 and SmGGPPS1 resulted in the highest production of tanshinones (approximately 2.727 mg/g dw), which was approximately 4.74-fold higher than the production in the control (0.475 mg/g dw) [17]. The simultaneous overexpression of SmHMGR and SmDXR in S. miltiorrhiza hairy roots also significantly increased the production of tanshinones, especially with elicitor-mediated induction [62].
The production of RA and SAB in S. miltiorrhiza hairy root cultures could be greatly increased by overexpression of SmC4H, SmTAT, and SmHPPR or by co-expression of SmTAT and SmHPPR. Co-expressing SmTAT1/SmHPPR1 produced the most abundant RA (906 mg/liter) and LAB (992 mg/L) in S. miltiorrhiza hairy root cultures, which were 4.3- and 3.2-fold more than in wild-type, respectively [18]. To enrich the precursors available for SAB biosynthesis, Zhang et al. simultaneously expressed an Arabidopsis Production of Anthocyanin Pigment 1 transcription factor (AtPAP1) and co-suppressed cinnamoyl-CoA reductase (SmCCR) and caffeic acid O-methyltransferase (SmCOMT), two endogenous key enzyme genes, in S. miltiorrhiza plants. The accumulation of SAB was up to three-fold higher in these plants than in the control. This was the first study to describe the production of valuable end products through combinational genetic manipulation in S. miltiorrhiza plants [85]. The suppression of competing pathways is also an alternative approach for accelerating the conversion of a substrate into the target compound. The suppression of 4-hydroxyphenylpyruvate dioxygenase (SmHPPD), which was reported to compete with the biosynthesis of rosmarinic acid, was shown to inhibit the substrate competition from a bypassing pathway, thereby increasing the accumulation of phenolic acids [18].

6. Perspectives

Most genes involved in the biosynthesis of tanshinones and phenolic acids in S. miltiorrhiza have been cloned either through a homology cloning strategy or by tissue-specific and induced-expression patterns. These genes have been functionally characterized in vitro or in vivo through enzymatic assays, RNAi, overexpression or isotopic labeling, which provide a basis for investigating the downstream pathways involved in tanshinone and phenolic acid biosynthesis. Firstly, co-expression analysis with the known functional genes could be employed as reference to narrow down the candidate genes obtained from various transcriptomes. In addition, comparative transcriptomes, such as those from different tissues, different development stages, and different induction times, as well as more efficient screening methods, should be applied to offer more information about the candidate genes involved in the biosynthetic pathway. Secondly, obtaining metabolic intermediates involved in biosynthetic pathways is extremely important for the analysis of downstream biosynthesis pathways, and given that the metabolic intermediates are always unstable and accumulated with low level, synthetic biology seems to be an increasingly important approach for analyzing biosynthetic pathways [63]. The functional genes could be incorporated into microorganisms through the MOPE strategy, thereby producing sufficient compounds for use in in vitro enzymatic assays. In addition to synthetic biology, the chemical synthesis and exploration of intermediates from plants belonging to the same species are also effective approaches.
The studies on the biosynthetic pathway of tanshinones and phenolic acids in S. miltiorrhiza have made significant progress. Tanshinones are widely extant in Salvia [7], due to the various biological activities, biosynthetic pathway analysis of tanshinones in Salvia will receive increasing attention. 13C tracer and precursor feeding experiments revealed that RA is likely to be the precursor of SAB [15]. The biosynthesis of RA has been well studied in Coleus blumei (Lamiaceae) as well as in S. miltiorrhiza (Lamiaceae), and the enzymes involved in the biosynthesis of RA have also been elucidated in Melissa officinalis (Lamiaceae), Anchusa officinalis (Boraginaceae), and Lithospermum erythrorhizon (Boraginaceae) [13]. The existing research results for the biosynthesis of tanshinones and RA in S. miltiorrhiza have laid a foundation for the analysis of downstream biosynthetic processes, providing more modules for synthetic biology and references for the analysis of the biosynthetic pathways involved in producing phenolic acids and diterpenoids in both S. miltiorrhiza and other species.

Acknowledgments

This work was supported by National Natural Science Foundation of China Grants (81130070, 81325023, 81573532, 81202871 and 81403049), the National High Technology Research and Development Program (2012AA02A704 and SS2014AA022201), the Open Research Fund of State Key Laboratory Breeding Base of Systematic Research, Development and Utilization of Chinese Medicine Resources, and National Science and Technology major projects (2013ZX09201020).

Author Contributions

X.-H.M. and Y.M.: conception, data collection, and manuscript preparation; J.-F.T. and Y.-L.H.: review of the manuscript; Y.-C.L., X.-J.M., Y.S., G.-H.C., H.-X.L. and Q.-X.R.: data collection; J.G. and L.-Q.H.: manuscript preparation and review of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Croteau, R.; Ketchum, R.B.; Long, R.; Kaspera, R.; Wildung, M. Taxol biosynthesis and molecular genetics. Phytochem. Rev. 2006, 5, 75–97. [Google Scholar] [CrossRef] [PubMed]
  2. Zhao, Q.; Gao, C.; Cui, Z. Ginkgolide a reduces inflammatory response in high-glucose-stimulated human umbilical vein endothelial cells through STAT3-mediated pathway. Int. Immunopharmacol. 2015, 25, 242–248. [Google Scholar] [CrossRef] [PubMed]
  3. Zhang, L.; Ding, R.; Chai, Y.; Bonfill, M.; Moyano, E.; Oksman-Caldentey, K.M.; Xu, T.; Pi, Y.; Wang, Z.; Zhang, H.; et al. Engineering tropane biosynthetic pathway in Hyoscyamus niger hairy root cultures. Proc. Natl. Acad. Sci. USA 2004, 101, 6786–6791. [Google Scholar] [CrossRef] [PubMed]
  4. Han, J.Y.; Kim, M.J.; Ban, Y.W.; Hwang, H.S.; Choi, Y.E. The involvement of β-Amyrin 28-oxidase (CYP716A52v2) in oleanane-type ginsenoside biosynthesis in Panax ginseng. Plant Cell Physiol. 2013, 54, 2034–2046. [Google Scholar] [CrossRef] [PubMed]
  5. Paddon, C.J.; Westfall, P.J.; Pitera, D.J.; Benjamin, K.; Fisher, K.; McPhee, D.; Leavell, M.D.; Tai, A.; Main, A.; Eng, D.; et al. High-level semi-synthetic production of the potent antimalarial artemisinin. Nature 2013, 496, 528–532. [Google Scholar] [CrossRef] [PubMed]
  6. Dong, Y.; Morris-Natschke, S.L.; Lee, K.-H. Biosynthesis, total syntheses, and antitumor activity of tanshinones and their analogs as potential therapeutic agents. Nat. Prod. Rep. 2011, 28, 529–542. [Google Scholar] [CrossRef] [PubMed]
  7. Li, M.H.; Peng, Y.; Xiao, P.G. Distribution of tanshinones in the genus Salvia (family Lamiaceae) from China and its systematic significance. J. Syst. Evol. 2010, 48, 118–122. [Google Scholar] [CrossRef]
  8. Zhang, Y.; Jiang, P.; Ye, M.; Kim, S.H.; Jiang, C.; Lu, J. Tanshinones: Sources, pharmacokinetics and anti-cancer activities. Int. J. Mol. Sci. 2012, 13, 13621–13666. [Google Scholar] [CrossRef] [PubMed]
  9. Chen, X.; Guo, J.; Bao, J.; Lu, J.; Wang, Y. The anticancer properties of Salvia miltiorrhiza Bunge (Danshen): A systematic review. Med. Res. Rev. 2014, 34, 768–794. [Google Scholar] [CrossRef] [PubMed]
  10. Robertson, A.L.; Holmes, G.R.; Bojarczuk, A.N.; Burgon, J.; Loynes, C.A.; Chimen, M.; Sawtell, A.K.; Hamza, B.; Willson, J.; Walmsley, S.R.; et al. A zebrafish compound screen reveals modulation of neutrophil reverse migration as an anti-inflammatory mechanism. Sci. Transl. Med. 2014, 6. [Google Scholar] [CrossRef] [PubMed]
  11. Wu, T.W.; Zeng, L.H.; Fung, K.P.; Wu, J.; Pang, H.; Grey, A.A.; Weisel, R.D.; Wang, J.Y. Effect of sodium tanshinone IIA sulfonate in the rabbit myocardium and on human cardiomyocytes and vascular endothelial cells. Biochem. Pharmacol. 1993, 46, 2327–2332. [Google Scholar] [CrossRef]
  12. Wu, Z.; Song, L.; Liu, S.; Huang, D. Tanshinones extend chronological lifespan in budding yeast Sacchraromyces cerevisiae. Appl. Microbiol. Biotechnol. 2014, 98, 8617–8628. [Google Scholar] [CrossRef] [PubMed]
  13. Petersen, M. Rosmarinic acid: New aspects. Phytochem. Rev. 2013, 12, 207–227. [Google Scholar] [CrossRef]
  14. Wang, X.; Morris-Natschke, S.L.; Lee, K.-H. New developments in the chemistry and biology of the bioactive constituents of tanshen. Med. Res. Rev. 2007, 27, 133–148. [Google Scholar] [CrossRef] [PubMed]
  15. Di, P.; Zhang, L.; Chen, J.; Tan, H.; Xiao, Y.; Dong, X.; Zhou, X.; Chen, W. 13C Tracer reveals phenolic acids biosynthesis in hairy root cultures of Salvia miltiorrhiza. ACS Chem. Biol. 2013, 8, 1537–1548. [Google Scholar] [CrossRef] [PubMed]
  16. Cheng, Q.; Su, P.; Hu, Y.; He, Y.; Gao, W.; Huang, L. RNA interference-mediated repression of SmCPS (copalyldiphosphate synthase) expression in hairy roots of Salvia miltiorrhiza causes a decrease of tanshinones and sheds light on the functional role of SmCPS. Biotechnol. Lett. 2014, 36, 363–369. [Google Scholar] [CrossRef] [PubMed]
  17. Kai, G.; Xu, H.; Zhou, C.; Liao, P.; Xiao, J.; Luo, X.; You, L.; Zhang, L. Metabolic engineering tanshinone biosynthetic pathway in Salvia miltiorrhiza hairy root cultures. Metab. Eng. 2011, 13, 319–327. [Google Scholar] [CrossRef] [PubMed]
  18. Xiao, Y.; Zhang, L.; Gao, S.; Saechao, S.; Di, P.; Chen, J.; Chen, W. The c4h, tat, hppr and hppd genes prompted engineering of rosmarinic acid biosynthetic pathway in salvia miltiorrhiza hairy root cultures. PLoS ONE 2011, 6, e29713. [Google Scholar] [CrossRef] [PubMed]
  19. Chen, H.; Chen, F.; Zhang, Y.L.; Song, J.Y. Production of lithospermic acid B and rosmarinic acid in hairy root cultures of Salvia miltiorrhiza. J. Ind. Microbiol. Biotechnol. 1999, 22, 133–138. [Google Scholar] [CrossRef]
  20. Hu, Z.; Alfermann, A.W. Diterpenoid production in hairy root cultures of Salvia miltiorrhiza. Phytochemistry 1993, 32, 699–703. [Google Scholar]
  21. Yuan, Y.; liu, Y.; Lu, D.; Huang, L.; Liang, R.; Yang, Z.; Chen, S. Genetic stability, active constituent, and pharmacoactivity of Salvia miltiorrhiza hairy roots and wild plant. Z. Naturforsch. C. 2009, 64, 557–563. [Google Scholar] [CrossRef] [PubMed]
  22. Cui, G.; Huang, L.; Tang, X.; Zhao, J. Candidate genes involved in tanshinone biosynthesis in hairy roots of Salvia miltiorrhiza revealed by cDNA microarray. Mol. Biol. Rep. 2011, 38, 2471–2478. [Google Scholar] [CrossRef] [PubMed]
  23. Hua, W.; Zhang, Y.; Song, J.; Zhao, L.; Wang, Z. De novo transcriptome sequencing in Salvia miltiorrhiza to identify genes involved in the biosynthesis of active ingredients. Genomics 2011, 98, 272–279. [Google Scholar]
  24. Yang, L.; Ding, G.; Lin, H.; Cheng, H.; Kong, Y.; Wei, Y.; Fang, X.; Liu, R.; Wang, L.; Chen, X.; et al. Transcriptome analysis of medicinal plant Salvia miltiorrhiza and identification of genes related to tanshinone biosynthesis. PLoS ONE 2013, 8, e80464. [Google Scholar] [CrossRef] [PubMed]
  25. Luo, H.; Zhu, Y.; Song, J.; Xu, L.; Sun, C.; Zhang, X.; Xu, Y.; He, L.; Sun, W.; Xu, H.; et al. Transcriptional data mining of Salvia miltiorrhiza in response to methyl jasmonate to examine the mechanism of bioactive compound biosynthesis and regulation. Physiol. Plant. 2014, 152, 241–255. [Google Scholar] [CrossRef] [PubMed]
  26. Gao, W.; Sun, H.-X.; Xiao, H.; Cui, G.; Hillwig, M.; Jackson, A.; Wang, X.; Shen, Y.; Zhao, N.; Zhang, L.; et al. Combining metabolomics and transcriptomics to characterize tanshinone biosynthesis in Salvia miltiorrhiza. BMC Genomics 2014, 15. [Google Scholar] [CrossRef] [PubMed]
  27. Guo, J.; Zhou, Y.J.; Hillwig, M.L.; Shen, Y.; Yang, L.; Wang, Y.; Zhang, X.; Liu, W.; Peters, R.J.; Chen, X.; et al. CYP76AH1 catalyzes turnover of miltiradiene in tanshinones biosynthesis and enables heterologous production of ferruginol in yeasts. Proc. Natl. Acad. Sci. USA 2013, 110, 12108–12113. [Google Scholar] [CrossRef] [PubMed]
  28. Chen, H.; Wu, B.; Nelson, D.R.; Wu, K.; Liu, C. Computational identification and systematic classification of novel cytochrome P450 genes in Salvia miltiorrhiza. PLoS ONE 2015, 10, e0120063. [Google Scholar] [CrossRef] [PubMed]
  29. Xu, Z.; Peters, R.J.; Weirather, J.; Luo, H.; Liao, B.; Zhang, X.; Zhu, Y.; Ji, A.; Zhang, B.; Hu, S.; et al. Full-length transcriptome sequences and splice variants obtained by a combination of sequencing platforms applied to different root tissues of Salvia miltiorrhiza and tanshinone biosynthesis. Plant. J. 2015, 82, 951–961. [Google Scholar] [CrossRef] [PubMed]
  30. Cui, G.H.; Wang, X.Y.; Feng, H.; Zhao, J.X.; Huang, L.Q. Molecular cloning and SNP analysis of a acetyl-CoA C-acetyltransferase gene (SmAACT) from Salvia miltiorrhiza. Acta Pharm. Sin. 2010, 45, 785–790. [Google Scholar]
  31. Ma, Y.; Yuan, L.; Wu, B.; Li, X.; Chen, S.; Lu, S. Genome-wide identification and characterization of novel genes involved in terpenoid biosynthesis in Salvia miltiorrhiza. J. Exp. Bot. 2012, 63, 2809–2823. [Google Scholar] [CrossRef] [PubMed]
  32. Zhang, L.; Yan, X.; Wang, J.; Li, S.; Liao, P.; Kai, G. Molecular cloning and expression analysis of a new putative gene encoding 3-hydroxy-3-methylglutaryl-CoA synthase from Salvia miltiorrhiza. Acta Physiol. Plant. 2011, 33, 953–961. [Google Scholar] [CrossRef]
  33. Liao, P.; Zhou, W.; Zhang, L.; Wang, J.; Yan, X.; Zhang, Y.; Zhang, R.; Li, L.; Zhou, G.; Kai, G. Molecular cloning, characterization and expression analysis of a new gene encoding 3-hydroxy-3-methylglutaryl coenzyme A reductase from Salvia miltiorrhiza. Acta Physiol. Plant. 2009, 31, 565–572. [Google Scholar] [CrossRef]
  34. Yang, D.; Ma, P.; Liang, X.; Wei, Z.; Liang, Z.; Liu, Y.; Liu, F. PEG and ABA trigger methyl jasmonate accumulation to induce the MEP pathway and increase tanshinone production in Salvia miltiorrhiza hairy roots. Physiol. Plant. 2012, 146, 173–183. [Google Scholar] [CrossRef] [PubMed]
  35. Xing, B.; Yang, D.; Guo, W.; Liang, Z.; Yan, X.; Zhu, Y.; Liu, Y. Ag+ as a more effective elicitor for production of tanshinones than phenolic acids in Salvia miltiorrhiza hairy roots. Molecules 2014, 20, 309–324. [Google Scholar] [CrossRef] [PubMed]
  36. Dai, Z.; Cui, G.; Zhou, S.-F.; Zhang, X.; Huang, L. Cloning and characterization of a novel 3-hydroxy-3-methylglutaryl coenzyme A reductase gene from Salvia miltiorrhiza involved in diterpenoid tanshinone accumulation. J. Plant Physiol. 2011, 168, 148–157. [Google Scholar] [CrossRef] [PubMed]
  37. Zhang, X.; Guo, J.; Shen, Y.; Huang, L. Cloning and expression analysis of a new 3-hydroxy-3-methylglutaryl coenzyme A reductase gene from Salvia miltiorrhiza (SmHMGR3). China J. Chin. Mater. Med. 2012, 37, 2378–2382. [Google Scholar]
  38. Yan, Y.; Zhang, S.; Yang, D.; Zhang, J.; Liang, Z. Effects of Streptomyces pactum Act12 on Salvia miltiorrhiza hairy root growth and tanshinone synthesis and its mechanisms. Appl. Biochem. Biotechnol. 2014, 173, 883–893. [Google Scholar] [CrossRef] [PubMed]
  39. Wu, S.J.; Shi, M.; Wu, J.Y. Cloning and characterization of the 1-deoxy-d-xylulose 5-phosphate reductoisomerase gene for diterpenoid tanshinone biosynthesis in Salvia miltiorrhiza (Chinese sage) hairy roots. Biotechnol. Appl. Biochem. 2009, 52, 89. [Google Scholar] [CrossRef] [PubMed]
  40. Yan, X.; Zhang, L.; Wang, J.; Liao, P.; Zhang, Y.; Zhang, R.; Kai, G. Molecular characterization and expression of 1-deoxy-d-xylulose 5-phosphate reductoisomerase (DXR) gene from Salvia miltiorrhiza. Acta Physiol. Plant. 2009, 31, 1015–1022. [Google Scholar] [CrossRef]
  41. Wang, X.Y.; Cui, G.H.; Huang, L.Q.; Gao, W.; Yuan, Y. A full length cDNA of 4-(cytidine 5′-diphospho)-2-C-methyl-d-erythritol kinase cloning and analysis of introduced gene expression in Salvia miltiorrhiza. Acta Pharm. Sin. 2008, 43, 1251–1257. [Google Scholar]
  42. Gao, W.; Cheng, Q.; Ma, X.; He, Y.; Jiang, C.; Yuan, Y.; Huang, L. Cloning and bioinformatics analysis of 2-C-methyl-d-erythritol 2,4-cyclodiphosphate synthase gene in Salvia miltiorrhiza. China J. Chin. Mater. Med. 2012, 37, 3365–3370. [Google Scholar]
  43. Cheng, Q.Q.; He, Y.F.; Li, G.; Jiang, C.; Yuan, Y.; Gao, W.; Huang, L.Q. Cloning and induced expression analysis of 4-hydroxy-3-methyl-but-2-enyl diphosphate reductase gene (SmHDR) of Salvia miltiorrhiza. Acta Pharm. Sin. 2013, 48, 236–242. [Google Scholar]
  44. Jiang, D.; Rong, Q.; Yuan, Q.; Zhang, W.; Zhang, Y.; Huang, L. Cloning and prokaryotic expression analysis of HDS from Salvia miltiorrhiza bge.f.alba. Acta Pharm. Sin. 2014, 49, 1614–1620. [Google Scholar]
  45. Hao, G.; Shi, R.; Tao, R.; Fang, Q.; Jiang, X.; Ji, H.; Feng, L.; Huang, L. Cloning, molecular characterization and functional analysis of 1-hydroxy-2-methyl-2-(E)-butenyl-4-diphosphate reductase (HDR) gene for diterpenoid tanshinone biosynthesis in Salvia miltiorrhiza Bge. f. alba. Plant Physiol. Biochem. 2013, 70, 21–32. [Google Scholar] [CrossRef] [PubMed]
  46. Yang, Y.; Zhou, L.; Hua, W.; Wang, Z.; Li, C. Bioinformatics and expression analysis of isopentenyl diphosphate isomerase (SmIPI) from Salvia militiorrhiza Bunge. Plant Phisiol. J. 2011, 47, 1086–1090. [Google Scholar]
  47. Zhou, L.; Hua, W.; Yang, Y.; Wang, Z.; Li, C. Expression pattern of farnesyl diphosphate synthese (SmFPPS1) from Salvia Miltiorrhiza Bunge. J. Shaanxi Norm. Univ. (Nat. Sci. Ed.) 2013, 41, 70–75. [Google Scholar]
  48. Hua, W.; Song, J.; Li, C.; Wang, Z. Molecular cloning and characterization of the promoter of SmGGPPs and its expression pattern in Salvia miltiorrhiza. Mol. Biol. Rep. 2012, 39, 5775–5783. [Google Scholar] [CrossRef] [PubMed]
  49. Kai, G.; Liao, P.; Zhang, T.; Zhou, W.; Wang, J.; Xu, H.; Liu, Y.; Zhang, L. Characterization, expression profiling, and functional identification of a gene encoding geranylgeranyl diphosphate synthase from Salvia miltiorrhiza. Biotechnol. Bioprocess Eng. 2010, 15, 236–245. [Google Scholar] [CrossRef]
  50. Zhang, L.; Dai, Z.; Cui, G.; Cheng, Y.; Qi, X.; Gao, Z. Cloning and characterization of geranylgeranyl diphosphate synthase gene of Salvia miltiorrhia. China J. Chin. Mater. Med. 2009, 34, 2704–2708. [Google Scholar]
  51. Gao, W.; Hillwig, M.L.; Huang, L.; Cui, G.; Wang, X.; Kong, J.; Yang, B.; Peters, R.J. A functional genomics approach to tanshinone biosynthesis provides stereochemical insights. Org. Lett. 2009, 11, 5170–5173. [Google Scholar] [CrossRef] [PubMed]
  52. Cheng, Q.; He, Y.; Li, G.; Liu, Y.; Gao, W.; Huang, L. Effects of combined elicitors on tanshinone metabolic profiling and SmCPS expression in Salvia miltiorrhiza hairy root cultures. Molecules 2013, 18, 7473–7485. [Google Scholar] [CrossRef] [PubMed]
  53. Cui, G.; Duan, L.; Jin, B.; Qian, J.; Xue, Z.; Shen, G.; Snyder, J.H.; Song, J.; Chen, S.; Huang, L.; et al. Functional divergence of diterpene syntheses in the medicinal plant Salvia miltiorrhiza Bunge. Plant. Physiol. 2015. [Google Scholar] [CrossRef] [PubMed]
  54. Guo, J.; Ma, X.H.; Cai, Y.; Ma, Y.; Zhan, Z.L.; Zhou, Y.J.; Liu, W.J.; Guan, M.X.; Cui, G.H.; Kang, L.P.; et al. Cytochrome P450 Promiscuity Leads to a Bifurcating Pathway in Tanshinone Biosynthesis; National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences: Beijing, China, 2015; Unpublished work. [Google Scholar]
  55. Cai, Y.; Guo, J.; Zhou, Y.; Zhu, Z.; Wu, W.; Huang, L.; Chen, M.; Zhao, Z. Construction of Saccharomyces cerevisiae whole-cell biocatalyst system for conversion miltiradiene. Acta Pharm. Sin. 2013, 48, 1618–1623. [Google Scholar]
  56. Rohmer, M.; Knani, M.; Simonin, P.; Sutter, B.; Sahm, H. Isoprenoid biosynthesis in bacteria: A novel pathway for the early steps leading to isopentenyl diphosphate. Biochem. J. 1993, 295, 517–524. [Google Scholar] [CrossRef] [PubMed]
  57. Schwarz, M.K. Terpen-Biosynthese in Ginkgo biloba: Eine Überraschende Geschichte. Ph.D. Thesis, ETH Zurich, Zurich, Switzerland, 1994. [Google Scholar]
  58. Rodrı́guez-Concepción, M.; Boronat, A. Elucidation of the methylerythritol phosphate pathway for isoprenoid biosynthesis in bacteria and plastids. A metabolic milestone achieved through genomics. Plant Physiol. 2002, 130, 1079–1089. [Google Scholar] [CrossRef] [PubMed]
  59. Miziorko, H.M. Enzymes of the mevalonate pathway of isoprenoid biosynthesis. Arch. Biochem. Biophys. 2011, 505, 131–143. [Google Scholar] [CrossRef] [PubMed]
  60. Ge, X.; Wu, J. Tanshinone production and isoprenoid pathways in Salvia miltiorrhiza hairy roots induced by Ag+ and yeast elicitor. Plant Sci. 2005, 168, 487–491. [Google Scholar] [CrossRef]
  61. Yang, D.; Du, X.; Liang, X.; Han, R.; Liang, Z.; Liu, Y.; Liu, F.; Zhao, J. Different roles of the mevalonate and methylerythritol phosphate pathways in cell growth and tanshinone production of Salvia miltiorrhiza hairy roots. PLoS ONE 2012, 7, e46797. [Google Scholar] [CrossRef] [PubMed]
  62. Shi, M.; Luo, X.; Ju, G.; Yu, X.; Hao, X.; Huang, Q.; Xiao, J.; Cui, L.; Kai, G. Increased accumulation of the cardio-cerebrovascular disease treatment drug tanshinone in Salvia miltiorrhiza hairy roots by the enzymes 3-hydroxy-3-methylglutaryl CoA reductase and 1-deoxy-d-xylulose 5-phosphate reductoisomerase. Funct. Integr. Genomics 2014, 14, 603–615. [Google Scholar] [CrossRef] [PubMed]
  63. Kirby, J.; Keasling, J.D. Biosynthesis of plant isoprenoids: Perspectives for microbial engineering. Annu. Rev. Plant Biol. 2009, 60, 335–355. [Google Scholar] [CrossRef] [PubMed]
  64. Zhang, S.; Yan, Y.; Wang, B.; Liang, Z.; Liu, Y.; Liu, F.; Qi, Z. Selective responses of enzymes in the two parallel pathways of rosmarinic acid biosynthetic pathway to elicitors in Salvia miltiorrhiza hairy root cultures. J. Biosci. Bioeng. 2014, 117, 645–651. [Google Scholar] [CrossRef] [PubMed]
  65. Yan, Q.; Shi, M.; Ng, J.; Wu, J.Y. Elicitor-induced rosmarinic acid accumulation and secondary metabolism enzyme activities in Salvia miltiorrhiza hairy roots. Plant Sci. 2006, 170, 853–858. [Google Scholar] [CrossRef]
  66. Hou, X.; Shao, F.; Ma, Y.; Lu, S. The phenylalanine ammonia-lyase gene family in Salvia miltiorrhiza: Genome-wide characterization, molecular cloning and expression analysis. Mol. Biol. Rep. 2013, 40, 4301–4310. [Google Scholar] [CrossRef] [PubMed]
  67. Song, J.; Wang, Z. Molecular cloning, expression and characterization of a phenylalanine ammonia-lyase gene (SmPAL1) from Salvia miltiorrhiza. Mol. Biol. Rep. 2009, 36, 939–952. [Google Scholar] [CrossRef] [PubMed]
  68. Song, J.; Wang, Z. RNAi-mediated suppression of the phenylalanine ammonia-lyase gene in Salvia miltiorrhiza causes abnormal phenotypes and a reduction in rosmarinic acid biosynthesis. J. Plant Res. 2011, 124, 183–192. [Google Scholar] [CrossRef] [PubMed]
  69. Jin, X.Q.; Chen, Z.W.; Tan, R.H.; Zhao, S.J.; Hu, Z.B. Isolation and functional analysis of 4-coumarate: Coenzyme A ligase gene promoters from Salvia miltiorrhiza. Biol. Plant 2012, 56, 261–268. [Google Scholar] [CrossRef]
  70. Zhao, S.-J.; Hu, Z.-B.; Liu, D.; Leung, F.C.C. Two divergent members of 4-coumarate: Coenzyme A ligase from Salvia miltiorrhiza Bunge: cDNA cloning and functional study. J. Integr. Plant Biol. 2006, 48, 1355–1364. [Google Scholar] [CrossRef]
  71. Wang, B.; Sun, W.; Li, Q.; Li, Y.; Luo, H.; Song, J.; Sun, C.; Qian, J.; Zhu, Y.; Hayward, A.; et al. Genome-wide identification of phenolic acid biosynthetic genes in Salvia miltiorrhiza. Planta 2015, 241, 711–725. [Google Scholar] [CrossRef] [PubMed]
  72. Dong, J.; Wan, G.; Liang, Z. Accumulation of salicylic acid-induced phenolic compounds and raised activities of secondary metabolic and antioxidative enzymes in Salvia miltiorrhiza cell culture. J. Biotechnol. 2010, 148, 99–104. [Google Scholar] [CrossRef] [PubMed]
  73. Liu, L.; Dong, J.; Zhang, J.; Dang, X.; Xing, B.; Yang, X. Effects of calcium on synthesis of rosmarinic acid and related enzymes in suspension cultures of Salvia miltiorrhiza. Sheng Wu Gong Cheng Xue Bao 2012, 28, 1359–1369. [Google Scholar] [PubMed]
  74. Liang, Z.; Ma, Y.; Xu, T.; Cui, B.; Liu, Y.; Guo, Z.; Yang, D. Effects of abscisic acid, gibberellin, ethylene and their interactions on production of phenolic acids in Salvia miltiorrhiza Bunge hairy roots. PLoS ONE 2013, 8, e72806. [Google Scholar] [CrossRef] [PubMed]
  75. Hao, W.F.; Guo, H.B.; Zhang, J.Y.; Hu, G.G.; Yao, Y.Q.; Dong, J.E. Hydrogen peroxide is involved in salicylic acid-elicited rosmarinic acid production in Salvia miltiorrhiza cell cultures. Sci. World J. 2014, 2014. [Google Scholar] [CrossRef] [PubMed]
  76. Huang, B.; Duan, Y.; Yi, B.; Sun, L.; Lu, B.; Yu, X.; Sun, H.; Zhang, H.; Chen, W. Characterization and expression profiling of cinnamate 4-hydroxylase gene from Salvia miltiorrhiza in rosmarinic acid biosynthesis pathway. Russ. J. Plant Physiol. 2008, 55, 390–399. [Google Scholar] [CrossRef]
  77. Xiao, Y.; Gao, S.; Di, P.; Chen, J.; Chen, W.; Zhang, L. Methyl jasmonate dramatically enhances the accumulation of phenolic acids in Salvia miltiorrhiza hairy root cultures. Physiol. Plant. 2009, 137, 1–9. [Google Scholar] [CrossRef] [PubMed]
  78. Huang, B.; Yi, B.; Duan, Y.; Sun, L.; Yu, X.; Guo, J.; Chen, W. Characterization and expression profiling of tyrosine aminotransferase gene from Salvia miltiorrhiza (Dan-shen) in rosmarinic acid biosynthesis pathway. Mol. Biol. Rep. 2008, 35, 601–612. [Google Scholar] [CrossRef] [PubMed]
  79. Yi, B. Molecular Cloning and Regulation Analysis of Important Genes Involved in Tyrosine-branch Pathway of Rosmarinic Acid Metabolism from Salvia miltiorrhza Bunge. Master’s Thesis, Second Military Medical University, Shanghai, China, 2007. [Google Scholar]
  80. Chen, S.L.; Wang, B.; Sun, W.; Xu, H.B. Genome-Wide Identification and Profiling of Novel Genes Involved in Phenolic Acids Biosynthesis Pathway in Salvia miltiorrhiza, Chinese Academy of Medical Sciences, Institute of Medicinal Plant Development (IMPLAD): Beijing, China, 2013; Unpublished Work.
  81. Song, J. Function Analysis of the Genes Involved in Rosmarinic Acid Biosynthesis Pathway in Salvia miltiorrhiza Bunge. Ph.D. Thesis, Shaanxi Normal University, Xi’an, China, 2010. [Google Scholar]
  82. Zhou, Y.J.; Gao, W.; Rong, Q.; Jin, G.; Chu, H.; Liu, W.; Yang, W.; Zhu, Z.; Li, G.; Zhu, G.; et al. Modular pathway engineering of diterpenoid synthases and the mevalonic acid pathway for miltiradiene production. J. Am. Chem. Soc. 2012, 134, 3234–3241. [Google Scholar] [CrossRef] [PubMed]
  83. Dai, Z.; Liu, Y.; Huang, L.; Zhang, X. Production of miltiradiene by metabolically engineered Saccharomyces cerevisiae. Biotechnol. Bioeng. 2012, 109, 2845–2853. [Google Scholar] [CrossRef] [PubMed]
  84. Bloch, S.E.; Schmidt-Dannert, C. Construction of a chimeric biosynthetic pathway for the de novo biosynthesis of rosmarinic acid in Escherichia coli. Chembiochem 2014, 15, 2393–2401. [Google Scholar] [CrossRef] [PubMed]
  85. Zhang, Y.; Yan, Y.-P.; Wu, Y.-C.; Hua, W.-P.; Chen, C.; Ge, Q.; Wang, Z.-Z. Pathway engineering for phenolic acid accumulations in Salvia miltiorrhiza by combinational genetic manipulation. Metab. Eng. 2014, 21, 71–80. [Google Scholar] [CrossRef] [PubMed]
  • Sample Availability: Samples of the compounds are not available from the authors.

Share and Cite

MDPI and ACS Style

Ma, X.-H.; Ma, Y.; Tang, J.-F.; He, Y.-L.; Liu, Y.-C.; Ma, X.-J.; Shen, Y.; Cui, G.-H.; Lin, H.-X.; Rong, Q.-X.; et al. The Biosynthetic Pathways of Tanshinones and Phenolic Acids in Salvia miltiorrhiza. Molecules 2015, 20, 16235-16254. https://doi.org/10.3390/molecules200916235

AMA Style

Ma X-H, Ma Y, Tang J-F, He Y-L, Liu Y-C, Ma X-J, Shen Y, Cui G-H, Lin H-X, Rong Q-X, et al. The Biosynthetic Pathways of Tanshinones and Phenolic Acids in Salvia miltiorrhiza. Molecules. 2015; 20(9):16235-16254. https://doi.org/10.3390/molecules200916235

Chicago/Turabian Style

Ma, Xiao-Hui, Ying Ma, Jin-Fu Tang, Ya-Li He, Yu-Chen Liu, Xiao-Jing Ma, Ye Shen, Guang-Hong Cui, Hui-Xin Lin, Qi-Xian Rong, and et al. 2015. "The Biosynthetic Pathways of Tanshinones and Phenolic Acids in Salvia miltiorrhiza" Molecules 20, no. 9: 16235-16254. https://doi.org/10.3390/molecules200916235

APA Style

Ma, X.-H., Ma, Y., Tang, J.-F., He, Y.-L., Liu, Y.-C., Ma, X.-J., Shen, Y., Cui, G.-H., Lin, H.-X., Rong, Q.-X., Guo, J., & Huang, L.-Q. (2015). The Biosynthetic Pathways of Tanshinones and Phenolic Acids in Salvia miltiorrhiza. Molecules, 20(9), 16235-16254. https://doi.org/10.3390/molecules200916235

Article Metrics

Back to TopTop