Cytochromes P450 in the biosynthesis of glucosinolates and indole alkaloids

Characteristic of cruciferous plants is the synthesis of nitrogen- and sulfur-rich compounds, such as glucosinolates and indole alkaloids. The intact glucosinolates have limited biological activity, but give rise to an array of bio-active breakdown products when hydrolysed by endogenous β-thioglucosidases (myrosinases) upon tissue disruption. Both glucosinolates and indole alkaloids constitute an important part of the defence of plants against herbivores and pathogens, with the difference that a basal level of glucosinolates is ever-present in the plant whereas indole alkaloids are true phytoalexins that are de novo synthesised upon pathogen attack. With the completion of the genome sequence of the model plant, Arabidopsis thaliana, which is a crucifer, many genes involved in the biosynthesis of glucosinolates and indole alkaloids have been identified and cytochromes P450 are key players in these pathways. In the present review, we will focus on the cytochromes P450 in the biosynthesis of both groups of compounds. Their functional roles and regulation will be discussed.     

Elucidating the Role of Transport Processes in Leaf Glucosinolate Distribution

In Arabidopsis (Arabidopsis thaliana), a strategy to defend its leaves against herbivores is to accumulate glucosinolates along the midrib and at the margin. Although it is generally assumed that glucosinolates are synthesized along the vasculature in an Arabidopsis leaf, thereby suggesting that the margin accumulation is established through transport, little is known about these transport processes. Here, we show through leaf apoplastic fluid analysis and glucosinolate feeding experiments that two glucosinolate transporters, GTR1 and GTR2, essential for long-distance transport of glucosinolates in Arabidopsis, also play key roles in glucosinolate allocation within a mature leaf by effectively importing apoplastically localized glucosinolates into appropriate cells. Detection of glucosinolates in root xylem sap unambiguously shows that this transport route is involved in root-to-shoot glucosinolate allocation. Detailed leaf dissections show that in the absence of GTR1 and GTR2 transport activity, glucosinolates accumulate predominantly in leaf margins and leaf tips. Furthermore, we show that glucosinolates accumulate in the leaf abaxial epidermis in a GTR-independent manner. Based on our results, we propose a model for how glucosinolates accumulate in the leaf margin and epidermis, which includes symplasmic movement through plasmodesmata, coupled with the activity of putative vacuolar glucosinolate importers in these peripheral cell layers.Feeding behavior of herbivorous insects and distribution of defense compounds in plants have been suggested to be a result of an arms race between plants and insects that has spanned millions of years (Ehrlich and Raven, 1964). Whether insects adapted first to plants or the other way around is an ongoing debate in this research field (Schoonhoven et al., 2005; Ali and Agrawal, 2012). Leaf margin accumulation of defense compounds has been demonstrated in various plant species (Gutterman and Chauser-Volfson, 2000; Chauser-Volfson et al., 2002; Kester et al., 2002; Cooney et al., 2012). In the model plant Arabidopsis (Arabidopsis thaliana), higher concentration of glucosinolates, which constitute a major part of the chemical defense system in this plant (Kliebenstein et al., 2001a; Halkier and Gershenzon, 2006), was found at the leaf midrib and margins compared with the leaf lamina (Shroff et al., 2008; Sønderby et al., 2010). This nonuniform leaf distribution of glucosinolates appeared to explain the feeding pattern of a generalist herbivore (Helicoverpa armigera), as it avoided feeding at the leaf margin and midrib (Shroff et al., 2008). A similar feeding pattern on Arabidopsis was observed for a different generalist herbivore, Spodoptera littoralis (Schweizer et al., 2013). Interestingly, S. littoralis was shown to favor feeding from Arabidopsis leaf margins in glucosinolate-deficient mutants (Schweizer et al., 2013), which could indicate an inherent preference for margin feeding and that Arabidopsis adapted to such behavior by accumulating defense compounds here. A damaged leaf margin may be more critical for leaf stability than damage to inner leaf parts (Shroff et al., 2008), further motivating protection of this tissue. The margin-feeding preference of S. littoralis might be explained by better nutritional value of the leaf margin cells (Schweizer et al., 2013), which has been shown to consist of specialized elongated cell files (Koroleva et al., 2010; Nakata and Okada, 2013).Other distribution patterns have been reported for glucosinolates in an Arabidopsis leaf. A study investigating spatiotemporal metabolic shifts during senescence in Arabidopsis reported that fully expanded mature leaves exhibited a glucosinolate gradient from base to tip, with highest level of glucosinolates at the leaf base (Watanabe et al., 2013). In contrast to the horizontal plane, less has been reported on distribution of glucosinolates in the vertical plane of a leaf. A localization study of cyanogenic glucosides, defense molecules related to glucosinolates (Halkier and Gershenzon, 2006), determined that these compounds primarily were located in the epidermis of sorghum (Sorghum bicolor; Kojima et al., 1979). Whereas epidermis-derived trichomes in Arabidopsis were recently demonstrated to contain glucosinolates and to express glucosinolate biosynthetic genes (Frerigmann et al., 2012), no studies have investigated glucosinolates in the epidermal cell layer.Based on promoter-GUS studies, biosynthesis of glucosinolates in leaves of Arabidopsis has been associated with primarily major and minor veins in leaves and silique walls (Mikkelsen et al., 2000; Reintanz et al., 2001; Tantikanjana et al., 2001; Chen et al., 2003; Grubb et al., 2004; Schuster et al., 2006; Gigolashvili et al., 2007; Li et al., 2011; Redovniković et al., 2012). The discrepancy between vasculature-associated glucosinolate biosynthesis and margin accumulation of glucosinolates suggests that transport processes must be involved in establishing the distribution pattern of glucosinolates within a leaf.Plant transport systems include the apoplastic xylem, the symplastic phloem, and plasmodesmata. Xylem transport is mainly driven by an upward pull generated by transpiration from aerial plant organs, thereby directing transport to sites of rapid evaporation (such as leaf margins; Sattelmacher, 2001). Phloem flow is facilitated by an osmosis-regulated hydrostatic pressure difference between source and sink tissue, primarily generated by Suc bulk flow (Lucas et al., 2013). Plasmodesmata are intercellular channels that establish symplasmic pathways between neighboring cells, and most cell types in a plant are symplastically connected via plasmodesmata (Roberts and Oparka, 2003). Translocation of small molecules in these channels is driven by diffusion and is regulated developmentally as well as spatially to form symplastically connected domains (Roberts and Oparka, 2003; Christensen et al., 2009). To what extent any of these transport processes are involved in establishing specific distribution patterns of glucosinolates within leaves is not known.Recently, two plasma membrane-localized, glucosinolate-specific importers, GLUCOSINOLATE TRANSPORTER1 (GTR1) and GTR2, were identified in Arabidopsis (Nour-Eldin et al., 2012). In leaf, their expression patterns were shown to be in leaf veins (GTR1 and GTR2) and surrounding mesophyll cells (GTR1; Nour-Eldin et al., 2012). Absence of aliphatic and indole glucosinolates in seeds of the gtr1gtr2 double knockout (dKO) mutant (gtr1gtr2 dKO) demonstrated that these transporters are essential for long-distance glucosinolate transport to the seeds and indicates a role in phloem loading (Nour-Eldin et al., 2012). Another study investigating long-distance transport of glucosinolates in the 3-week-old wild type and gtr1gtr2 dKO indicated that GTR1 and GTR2 were involved in bidirectional transport of aliphatic glucosinolates between root and shoot via both phloem and xylem pathways (Andersen et al., 2013). The authors suggested a role for GTR1 and GTR2 in the retention of long-chained aliphatic glucosinolates in roots by removing the compounds from the xylem (Andersen et al., 2013).Identification of the glucosinolate transporters GTR1 and GTR2 has provided a molecular tool to investigate the role of transport processes in establishing leaf glucosinolate distribution. In this study, we have performed a detailed spatial investigation of the distribution of an exogenously fed glucosinolate (sinigrin) and endogenous glucosinolates within mature wild-type and gtr1gtr2 dKO Arabidopsis leaves, achieved by collecting and analyzing leaf parts at the horizontal (y axis: petiole, base, and tip; x axis: midrib, lamina, and margin) as well as at the vertical leaf plane (z axis: abaxial epidermis). Furthermore, we analyze wild-type and gtr1gtr2 dKO root xylem sap and leaf apoplastic fluids for glucosinolates. Based on our results, we propose a model where GTR1 and GTR2 import glucosinolates from the apoplast to the symplast and where the glucosinolate distribution pattern within an Arabidopsis leaf is established via symplasmic movement of glucosinolates through plasmodesmata, coupled with the activity of putative vacuolar glucosinolate importers in peripheral cell layers.     

Focus on Metabolism: Alteration of Plant Primary Metabolism in Response to Insect Herbivory

Plants in nature, which are continuously challenged by diverse insect herbivores, produce constitutive and inducible defenses to reduce insect damage and preserve their own fitness. In addition to inducing pathways that are directly responsible for the production of toxic and deterrent compounds, insect herbivory causes numerous changes in plant primary metabolism. Whereas the functions of defensive metabolites such as alkaloids, terpenes, and glucosinolates have been studied extensively, the fitness benefits of changes in photosynthesis, carbon transport, and nitrogen allocation remain less well understood. Adding to the complexity of the observed responses, the feeding habits of different insect herbivores can significantly influence the induced changes in plant primary metabolism. In this review, we summarize experimental data addressing the significance of insect feeding habits, as related to herbivore-induced changes in plant primary metabolism. Where possible, we link these physiological changes with current understanding of their underlying molecular mechanisms. Finally, we discuss the potential fitness benefits that host plants receive from altering their primary metabolism in response to insect herbivory.Plants in nature are subject to attack by a wide variety of phytophagous insects. Nevertheless, the world is green, and most plants are resistant to most individual species of insect herbivores. To a large extent, this resistance is due to an array of toxic and deterrent small molecules and proteins that can prevent nonadapted insects from feeding. Although many plant defenses are produced constitutively, others are inducible (i.e. defense-related metabolites and proteins that are normally present at low levels become more abundant in response to insect feeding). Inducible defense systems, which allow more energy to be directed toward growth and reproduction in the absence of insect herbivory, represent a form of resource conservation. Well-studied examples of inducible plant defenses include the production of nicotine in tobacco (Nicotiana tabacum; Baldwin et al., 1998), protease inhibitors in tomato (Solanum lycopersicum; Ryan, 2000), benzoxazinoids in maize (Zea mays; Oikawa et al., 2004), and glucosinolates in Arabidopsis (Arabidopsis thaliana; Mewis et al., 2005). Additionally, herbivore-induced plant responses can include the production of physical defenses such as trichomes or thickened cell walls that can make insect feeding more difficult. Some plant defensive metabolites are highly abundant, suggesting that their biosynthesis can have a significant effect on overall plant metabolism. For instance, benzoxazinoids can constitute 1% to 2% of the total dry matter of some Poaceae (Zúñiga et al., 1983), and up to 6% of the nitrogen in herbivore-induced Nicotiana attenuata can be devoted to nicotine production (Baldwin et al., 1998).In addition to the herbivore-induced production of physical and chemical defenses, numerous changes in plant primary metabolism occur in response to insect herbivory. Among other observed effects, these can include either elevated or suppressed photosynthetic efficiency, remobilization of carbon and nitrogen resources, and altered plant growth rate. However, although the defensive value of induced toxins such as nicotine, terpenes, benzoxazinoids, and glucosinolates is clear, it is sometimes more difficult to elucidate the function of herbivore-induced changes in plant primary metabolism. Insects may also manipulate plant primary metabolism for their own benefit, making it challenging to determine whether the observed changes are actually a plant defensive response.Here, we describe commonly observed changes in plant primary metabolism, focusing on carbohydrates and nitrogen, and discuss their possible functions in plant defense against insect herbivory. There are large differences among published studies involving different plant-herbivore combinations, and no universal patterns in the herbivory-induced changes in plant primary metabolism. Therefore, we also discuss how the potential benefits can depend on the tissue that is being attacked, the extent of the tissue damage, and the type of insect herbivore that is involved in the interaction.     

Indole Glucosinolates and Camalexin do not Influence the Development of the Clubroot Disease in Arabidopsis thaliana

Root galls of Brassicaceae caused by Plasmodiophora brassicae are dependent on increased auxin and cytokinin formation. In this study we investigated whether indole glucosinolates are involved in indole‐3‐acetic acid (IAA) biosynthesis in root galls, by using a genetic approach. The cytochrome P450 enzymes, CYP79B2 and CYP79B3, convert tryptophan to indole‐3‐acetaldoxime (IAOx), which is a precursor for indole glucosinolates and the phytoalexin camalexin in Arabidopsis thaliana. Root galls of the Arabidopsis ecotypes Wassilewskija (WS) and Columbia (Col) accumulated camalexin, WS at levels up to 320 μg/g dry weight. By contrast, camalexin was absent in root galls of cyp79b2/b3 double mutants. Infection rate and disease index as a measure of club development in mutant and wild‐type plants of the two ecotypes were investigated and no differences were found in gall formation. This demonstrates that camalexin is an ineffective inhibitor of P. brassicae and indole glucosinolates are not the source of elevated levels of IAA in galls, because free IAA levels in mutant galls were comparable with those in wild type.     

Identification of Defense Compounds in Barbarea vulgaris against the Herbivore Phyllotreta nemorum by an Ecometabolomic Approach

Winter cress (Barbarea vulgaris) is resistant to a range of insect species. Some B. vulgaris genotypes are resistant, whereas others are susceptible, to herbivory by flea beetle larvae (Phyllotreta nemorum). Metabolites involved in resistance to herbivory by flea beetles were identified using an ecometabolomic approach. An F2 population representing the whole range from full susceptibility to full resistance to flea beetle larvae was generated by a cross between a susceptible and a resistant B. vulgaris plant. This F2 offspring was evaluated with a bioassay measuring the ability of susceptible flea beetle larvae to survive on each plant. Metabolites that correlated negatively with larvae survival were identified through correlation, cluster, and principal component analyses. Two main clusters of metabolites that correlate negatively with larvae survival were identified. Principal component analysis grouped resistant and susceptible plants as well as correlated metabolites. Known saponins, such as hederagenin cellobioside and oleanolic acid cellobioside, as well as two other saponins correlated significantly with plant resistance. This study shows the potential of metabolomics to identify bioactive compounds involved in plant defense.Plants are sessile organisms that have developed various strategies to adapt to or counteract abiotic and biotic stress. The ability to accumulate low-molecular-weight bioactive compounds, often referred to as allelochemicals, secondary metabolites, or bioactive natural products, provides a chemical defense against herbivorous insects used by plants. As a result of natural selection, insects often develop mechanisms to adapt to such compounds and eventually manage to break the resistance.The interaction between Barbarea vulgaris (Brassicaceae) and the flea beetle Phyllotreta nemorum (Coleoptera: Chrysomelidae) is a unique model system to study chemical defenses in plants and counteradaptations in insects (Nielsen, 1997a; de Jong et al., 2000; Agerbirk et al., 2001, 2003b; Nielsen and de Jong, 2005). B. vulgaris, a biennial or short-lived perennial wild crucifer (MacDonald and Cavers, 1991), is polymorphic with respect to insect resistance: the pubescent P-type is susceptible to all known flea beetle genotypes, whereas the glabrous G-type is resistant to most common genotypes of the insect (Nielsen, 1997a, 1997b; Agerbirk et al., 2003a). In contrast, P. nemorum is polymorphic with respect to plant defenses (Breuker et al., 2005; Nielsen and de Jong, 2005).B. vulgaris has a potential as an oil crop for use at northern latitudes (Börjesdotter, 1999) and is considered to be an important genetic resource for food and agriculture (International Treaty on Plant Genetic Resources for Food and Agriculture; ftp://ftp.fao.org/ag/cgrfa/it/ITPGRe.pdf). It has been used for salads and garnishes as well as a medicinal plant (Senatore et al., 2000). B. vulgaris has a wide native distribution area (Eurasia) and is furthermore naturalized in North America, Africa, Australia, New Zealand, and Japan as a weed (Hegi, 1958; MacDonald and Cavers, 1991; Tachibana et al., 2002). The subspecies arcuata is by far the most common Barbarea taxon in Denmark and comprises two morphologically, biochemically, and cytologically deviating genotypes, P and G, which differ by glucosinolate profiles, flea beetle resistance, and leaf pubescence (Agerbirk et al., 2003b; Fig. 1). B. vulgaris is a diploid; the G-type has 2n = 16 chromosomes, while the P-type has 2n = 16 or 2n = 18 chromosomes (Ørgaard and Linde-Laursen, 2008). B. vulgaris is phylogenetically positioned between Arabidopsis (Arabidopsis thaliana) and allopolyploid oil seed rape (Brassica napus; Bailey et al., 2006). Accordingly, research on plant-insect interaction in B. vulgaris may be applied to B. napus.Open in a separate windowFigure 1.Rosette leaves of P- and G-types of B. vulgaris subspecies arcuata. The P-type has hairs, while the G-type does not.Glucosinolates constitute a group of defense compounds present in crucifers and play a key role in host selection by crucifer specialists (Renwick, 2002). These compounds are feeding and oviposition stimulants for a number of specialist insects, which have become adapted to such compounds as an outcome of long-standing coevolutionary interactions with host plants containing them (Renwick, 2002; Thompson, 2005). Therefore, glucosinolates no longer offer efficient protection against many specialist insects, and the relationship between glucosinolate profiles of plants and their suitability as food for insects is not simple (Nielsen et al., 2001; Poelman et al., 2008; van Leur et al., 2008). The P-type B. vulgaris contains the R-isomer of 2-hydroxy-2-phenylethylglucosinolate, whereas the G-type contains the S-isomer. However, the differences in glucosinolate profiles between the P- and G-types are not related to resistance to flea beetles (Agerbirk et al., 2003b).As a putative response to renewed selection pressure from herbivorous insects, a number of crucifers have evolved a second generation of defense secondary compounds (e.g. cucurbitacins in Iberis species, cardenolides in Cheirantus and Erysimum species, and saponins in B. vulgaris). These compounds are feeding deterrents for a number of insect species (Nielsen, 1978; Renwick, 2002; Shinoda et al., 2002; Agerbirk et al., 2003a). Until now, Barbarea is the only crucifer known to contain saponins. Two saponins, oleanolic acid cellobioside (3-O-β-cellobiosyloleanolic acid) and hederagenin cellobioside (3-O-β-cellobiosylhederagenin), have been identified in B. vulgaris (Shinoda et al., 2002; Agerbirk et al., 2003a). The restricted distribution of such saponins in crucifers suggests that they originated later than the glucosinolates, which have a much wider distribution in the family.Saponins are triterpenoid glycosides widely distributed in higher plants (Hostettmann and Marston, 1995; Sparg et al., 2004; Vincken et al., 2007). They are constituents of many plant drugs and folk medicines and possess a wide range of biological activities, including antifungal, antibacterial, molluscicidal, and insecticidal activities (Hostettmann and Marston, 1995; Sparg et al., 2004; Chwalek et al., 2006; Güçlü-Ustündağ and Mazza, 2007; Gauthier et al., 2009). The toxicity of saponins to fungi and insects is thought to be a result of their ability to form complexes with sterols in the plasma membrane, thus destroying the cellular semipermeability and leading to cell death. Although saponins are toxic to cold-blooded animals, their oral toxicity to mammals is low (for review, see Hostettmann and Marston, 1995; Sparg et al., 2004; Güçlü-Ustündağ and Mazza, 2007).Hederagenin cellobioside has been identified as an active defense compound of B. vulgaris against the world-wide pest diamondback moth (Shinoda et al., 2002), which has become resistant to most insecticides. Oleanolic acid cellobioside concentration has been shown to correlate with resistance of B. vulgaris to the diamondback moth (Agerbirk et al., 2003a). This compound is present in the resistant G-type plant, and its concentration declines in autumn at the same time as the decline in resistance toward diamondback moth (Agerbirk et al., 2001, 2003b). The impact of the two saponins on defense against flea beetles, a major pest in oil seed rape, has not been reported previously.The objective of this study was to develop an unbiased strategy to identify metabolites that correlate with resistance to flea beetle larvae in B. vulgaris and to provide knowledge that may facilitate more efficient and sustainable breeding for resistance toward insect pests. The results presented in this study are significant for understanding chemical plant defense against insects and may be utilized in future crop protection breeding by screening for the presence of similar bioactive compounds, biosynthetic enzymes, and genetic markers or transfer of resistance components to crop plants.     

Biosynthèse des glucosinolates indoliques et rôle écologique de leurs modifications secondaires

Indole glucosinolates are plant secondary metabolites derived from the amino acid tryptophan. They are part of a large group of sulfur-containing molecules almost exclusively found among Brassicales, which include the mustard family (Brassicaceae) with many edible plant species of major nutritional importance. These compounds mediate numerous interactions between these plants and their natural enemies and are therefore of major biological and economical interest. This literature review aims at taking stock of recent advances of our knowledge about the biosynthetic pathways of indole glucosinolates, but also about the defense strategies and ecological processes involving these metabolites.     

Identification of indole glucosinolate breakdown products with antifeedant effects on Myzus persicae (green peach aphid)

The cleavage of glucosinolates by myrosinase to produce toxic breakdown products is a characteristic insect defense of cruciferous plants. Although green peach aphids ( Myzus persicae ) are able to avoid most contact with myrosinase when feeding from the phloem of Arabidopsis thaliana , indole glucosinolates are nevertheless degraded during passage through the insects. A defensive role for indole glucosinolates is suggested by the observation that atr1D mutant plants, which overproduce indole glucosinolates, are more resistant to M. persicae , whereas cyp79B2 cyp79B3 double mutants, which lack indole glucosinolates, succumb to M. persicae more rapidly. Indole glucosinolate breakdown products, including conjugates formed with ascorbate, glutathione and amino acids, are elevated in the honeydew of M. persicae feeding from atr1D mutant plants, but are absent when the aphids are feeding on cyp79B2 cyp79B3 double mutants. M. persicae feeding from wild-type plants and myrosinase-deficient tgg1 tgg2 double mutants excrete a similar profile of indole glucosinolate-derived metabolites, indicating that the breakdown is independent of these foliar myrosinases. Artificial diet experiments show that the reaction of indole-3-carbinol, a breakdown product of indol-3-ylmethylglucosinolate, with ascorbate, glutathione and cysteine produces diindolylmethylcysteines and other conjugates that have antifeedant effects on M. persicae . Therefore, the post-ingestive breakdown of indole glucosinolates provides a defense against herbivores such as aphids that can avoid glucosinolate activation by plant myrosinases.     

Jasmonate-dependent induction of indole glucosinolates in Arabidopsis by culture filtrates of the nonspecific pathogen Erwinia carotovora

Elicitors from the plant pathogen Erwinia carotovora trigger coordinate induction of the tryptophan (Trp) biosynthesis pathway and Trp oxidizing genes in Arabidopsis. To elucidate the biological role of such pathogen-induced activation we characterized the production of secondary defense metabolites such as camalexin and indole glucosinolates derived from precursors of this pathway. Elicitor induction was followed by a specific increase in 3-indolylmethylglucosinolate (IGS) content, but only a barely detectable accumulation of the indole-derived phytoalexin camalexin. The response is mediated by jasmonic acid as shown by lack of IGS induction in the jasmonate-insensitive mutant coi1-1. In accordance with this, methyl jasmonate was able to trigger IGS accumulation in Arabidopsis. In contrast, ethylene and salicylic acid seem to play a minor role in the response. They did not trigger alterations in IGS levels, and methyl jasmonate- or elicitor-induced IGS accumulation in NahG and ethylene-insensitive ein2-1 mutant plants was similar as in the wild type. The breakdown products of IGS and other glucosinolates were able to inhibit growth of E. carotovora. The results suggest that IGS is of importance in the defense against bacterial pathogens.     

Transient Transcriptional Regulation of the CYS-C1 Gene and Cyanide Accumulation upon Pathogen Infection in the Plant Immune Response

Cyanide is produced concomitantly with ethylene biosynthesis. Arabidopsis (Arabidopsis thaliana) detoxifies cyanide primarily through the enzyme β-cyanoalanine synthase, mainly by the mitochondrial CYS-C1. CYS-C1 loss of function is not toxic for the plant and leads to an increased level of cyanide in cys-c1 mutants as well as a root hairless phenotype. The classification of genes differentially expressed in cys-c1 and wild-type plants reveals that the high endogenous cyanide content of the cys-c1 mutant is correlated with the biotic stress response. Cyanide accumulation and CYS-C1 gene expression are negatively correlated during compatible and incompatible plant-bacteria interactions. In addition, cys-c1 plants present an increased susceptibility to the necrotrophic fungus Botrytis cinerea and an increased tolerance to the biotrophic Pseudomonas syringae pv tomato DC3000 bacterium and Beet curly top virus. The cys-c1 mutation produces a reduction in respiration rate in leaves, an accumulation of reactive oxygen species, and an induction of the alternative oxidase AOX1a and pathogenesis-related PR1 expression. We hypothesize that cyanide, which is transiently accumulated during avirulent bacterial infection and constitutively accumulated in the cys-c1 mutant, uncouples the respiratory electron chain dependent on the cytochrome c oxidase, and this uncoupling induces the alternative oxidase activity and the accumulation of reactive oxygen species, which act by stimulating the salicylic acid-dependent signaling pathway of the plant immune system.The gaseous hormone ethylene is known to regulate multiple physiological and developmental processes in plants, such as seedling emergence, leaf and flower senescence, climacteric fruit ripening, and organ abscission. Ethylene is also involved in the response of plants to abiotic and biotic stresses (Wang et al., 2002; Broekaert et al., 2006; van Loon et al., 2006). Enhanced ethylene production is an early, active response of plants to the perception of pathogen attack and is associated with the induction of defense reactions. During ethylene biosynthesis, S-adenosyl-l-Met is converted to 1-aminocyclopropane-1-carboxylic acid (ACC) by ACC synthase. ACC is finally oxidized by ACC oxidase to form ethylene, carbon dioxide, and cyanide (Hartley et al., 1998; Wang et al., 2002). Hydrogen cyanide is a colorless and highly volatile liquid. The anion cyanide is toxic and renders the cells of an organism unable to use oxygen, primarily through the chelation of divalent and trivalent metal ions in the prosthetic groups of several metalloenzymes, including copper/zinc superoxide dismutase, catalase, nitrate and nitrite reductase, nitrogenase, peroxidases, and the mitochondrial cytochrome c oxidase (Isom and Way, 1984; Donato et al., 2007).Cyanide must be rapidly detoxified and metabolized by the plant to keep the concentration below toxic levels. Plants detoxify cyanide primarily through the enzyme β-cyanoalanine synthase (CAS), for which considerable levels of activity are constitutively found in many plant species. Rhodanese and mercaptopyruvate sulfurtransferase activities also make minor contributions to the cyanide detoxification process (Miller and Conn, 1980). CAS is a pyridoxal phosphate-dependent enzyme that converts Cys and cyanide to hydrogen sulfide and β-cyanoalanine, which is later converted to Asn, Asp, and ammonia by NIT4 class nitrilases (Piotrowski, 2008). Arabidopsis (Arabidopsis thaliana) plants carry the mitochondrial CAS CYS-C1 (At3g61440; Watanabe et al., 2008), which belongs to the family of β-substituted Ala synthase enzymes. The family also includes the three major O-acetyl-serine(thiol)lyase enzymes OAS-A1 (At4g14880), OAS-B (At2g43750), and OAS-C (At3g59760; Watanabe et al., 2008), the l-Cys desulfhydrase DES1 (At5g28030; Álvarez et al., 2010), the S-sulfocysteine synthase CS26 (At3g03630; Bermúdez et al., 2010), and the functionally unknown cytosolic isoforms CYS-D1 (At3g04940) and CYS-D2 (At5g28020). Mutations in CYS-C1 result in plants that accumulate cyanide and that display abnormal root hair (García et al., 2010), suggesting that cyanide has a signaling role in root development. The lack of the mitochondrial O-acetyl-serine(thiol)lyase isoform OAS-C, which is necessary to detoxify the sulfide released by the CAS activity, causes an accumulation of sulfide and cyanide and a root phenotype similar to the cys-c1 loss-of-function mutant (Álvarez et al., 2012b).Several authors have suggested that cyanide could act as a regulator of other metabolic processes in addition to performing the described role in plant root development (Siegien and Bogatek, 2006). It has been observed that this molecule is released during seed germination and that exogenously applied hydrogen cyanide breaks seed dormancy in several plants (Cohn and Hughes, 1986; Fol et al., 1989; Bogatek et al., 1991; Bethke et al., 2006). The role of cyanide as a regulatory molecule is not restricted to plants, and it has been demonstrated that cyanide is generated in leukocytes from Gly via a peroxidase (Stelmaszyńska, 1986) as well as in the central nervous system, where it has been hypothesized to act as a neuromodulator (Gunasekar et al., 2000; Cipollone and Visca, 2007). Cyanide production can be stimulated by opiates and decreased by treatment with muscarinic receptor agonists (Borowitz et al., 1997; Gunasekar et al., 2004).Despite the variety of known functions for cyanide in different organisms, the role of cyanide production in plants seems to have been unevaluated to date. In cyanogenic plants, cyanide is produced during the degradation of cyanogenic lipids and from the catabolism of cyanogenic glycosides (Poulton, 1990). Cyanide and cyanogenic compounds play an important role in plant defense against herbivores (Zagrobelny et al., 2008). In noncyanogenic plants, cyanide is a coproduct of ethylene biosynthesis. The molecule is also produced during the biosynthesis of camalexin, a phytoalexin formed in Arabidopsis plants upon infection by a large variety of microorganisms, including bacteria, fungi, and oomycetes (Glawischnig, 2007). During camalexin biosynthesis, the Trp-derived intermediate indole-3-acetonitrile is conjugated with Cys and serves as a substrate for the cytochrome P450 enzyme CYP71B15. This enzyme catalyzes the formation of the thiazoline ring as well as the release of cyanide and subsequent oxidative decarboxylation of dihydrocamalexic acid to camalexin (Glawischnig, 2007; Böttcher et al., 2009). Since both cyanide sources, camalexin and ethylene, are produced after pathogen attack, cyanide should be produced at significant levels during the plant response to pathogens. It has been shown that exogenous cyanide can enhance the resistance of tobacco (Nicotiana tabacum) and Arabidopsis leaves to Tobacco mosaic virus and Turnip vein clearing virus, respectively (Chivasa and Carr, 1998; Wong et al., 2002). Recently, it has been demonstrated that exogenously applied cyanide increases the resistance of young rice (Oryza sativa) plants to blast fungus infection, suggesting that cyanide rather than ethylene contributes to plant resistance (Seo et al., 2011).This work aims to further investigate the role of endogenously produced cyanide in the plant immune response by analyzing the behavior of Arabidopsis knockout mutants of the mitochondrial CAS CYS-C1 and the regulation of CYS-C1 in response to pathogen attack.     

Co-regulation of indole glucosinolates and camalexin biosynthesis by CPK5/CPK6 and MPK3/MPK6 signaling pathways

Secondary plant metabolites, represented by indole glucosinolates (IGS) and camalexin, play important roles in Arabidopsis immunity. Previously, we demonstrated the importance of MPK3 and MPK6, two closely related MAPKs, in regulating Botrytis cinerea (Bc)‐induced IGS and camalexin biosynthesis. Here we report that CPK5 and CPK6, two redundant calcium‐dependent protein kinases (CPKs), are also involved in regulating the biosynthesis of these secondary metabolites. The loss‐of‐function of both CPK5 and CPK6 compromises plant resistance to Bc. Expression profiling of CPK5‐VK transgenic plants, in which a truncated constitutively active CPK5 is driven by a steroid‐inducible promoter, revealed that biosynthetic genes of both IGS and camalexin pathways are coordinately upregulated after the induction of CPK5‐VK, leading to high‐level accumulation of camalexin and 4‐methoxyindole‐3‐yl‐methylglucosinolate (4MI3G). Induction of camalexin and 4MI3G, as well as the genes in their biosynthesis pathways, is greatly compromised in cpk5 cpk6 mutant in response to Bc. In a conditional cpk5 cpk6 mpk3 mpk6 quadruple mutant, Bc resistance and induction of IGS and camalexin are further reduced in comparison to either cpk5 cpk6 or conditional mpk3 mpk6 double mutant, suggesting that both CPK5/CPK6 and MPK3/MPK6 signaling pathways contribute to promote the biosynthesis of 4MI3G and camalexin in defense against Bc.     

The biosynthesis and genetic engineering of bioactive indole alkaloids in plants

Indole alkaloids are widely distributed secondary metabolites that exhibit a broad range of pharmacological activities. They are synthesized through plant biosynthetic pathways involving complex enzyme activities and regulatory strategies. Since many compounds of indole alkaloids are structurally too complex to be manufactured economically by chemical synthesis, they have to be isolated from naturally grown or cultivated plants. Therefore, the biotechnological production of high-value plant secondary metabolites in cultivated cells or transgenic plants is potentially an attractive alternative. The present review describes the regulation of indole alkaloids biosynthesis, as well as their pharmacological functions in plants such as anti-microbes, anti-inflammatory and anti-tumor. Furthermore, it discusses different strategies by which the genetic engineering of indole alkaloids biosynthesis through the reconstruction of the pathway achieves high production of specific compounds.