l-Arabinose (l-Ara) is a plant-specific sugar accounting for 5–10 % of cell wall saccharides in Arabidopsis (Arabidopsis thaliana) and rice (Oryza sativa). l-Ara occurs in pectic arabinan, rhamnogalacturonan II, arabinoxylan, arabinogalactan-protein (AGP), and extensin in the cell walls, as well as in glycosylated signaling peptides like CLAVATA3 and small glycoconjugates such as quercetin 3-O-arabinoside. This review focuses on recent advances towards understanding the generation of l-Ara and the metabolism of l-Ara-containing molecules in plants.
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l-Arabinose (l-Ara) is a plant saccharide that is not found in animals. Like xylose (Xyl—we omit the D-prefix of sugars belonging to the d-series), l-Ara is a pentose comprising five carbons, not six carbon containing hexose like glucose (Glc) and galactose (Gal) (Fig. 1). Although its content in the cell walls varies depending on the plant species, l-Ara can be considered a major sugar. It accounts for 5–10 % of cell wall sugar, for instance, in Arabidopsis (Arabidopsis thaliana) and rice (Oryza sativa) (Konishi et al. 2011; Zablackis et al. 1995). The fact that l-Ara is widely distributed not only in land plants including liverworts and mosses but also found in several Chlorophycean and Charophycean green algae suggests that the metabolic pathway for the synthesis of l-Ara was acquired early by primitive plants (Domozych et al. 2009, 2012; Konno et al. 2010; Lee et al. 2005; Popper and Fry 2003; Roberts et al. 2012; Thomas 1977). The broad range of l-Ara-containing molecules seen in land plants today is likely due to subsequent diversification of the use of l-Ara during plant evolution.
l-Ara may be useful as a natural pharmaceutical. Monomeric l-Ara inhibits intestinal maltase and sucrase (α-glucosidase hydrolyzing sucrose) activities in vitro (Seri et al. 1996). In rats, dietary sucrose increases the insulin level in blood and triacylglycerol levels in blood plasma and the liver, but feeding l-Ara together with sucrose can significantly reduce the increase in these levels (Osaki et al. 2001; Seri et al. 1996). Recently, the effect of l-Ara on controlling insulin and blood-Glc levels was also observed in humans (Kaats et al. 2011). While its effect in humans is still controversial (Halschou-Jensen et al. 2015), the use of l-Ara for these purposes is receiving attention and becoming more wide-spread.
Several excellent reviews have surveyed nucleotide sugar synthesis and sugar metabolism in land plants (Bar-Peled and O’Neill 2011; Bar-Peled et al. 2012; Lagaert et al. 2014; Reiter 2008; Reiter and Vanzin 2001; Seifert 2004). Here we concentrate on recent progress in our understanding of the generation of l-Ara and the synthesis and degradation of l-Ara-containing molecules in land plants.
l-Ara-containing molecules in plants
l-Ara has two ring forms, called l-arabinopyranose (l-Arap, sugars other than l-Ara are in pyranose form unless stated otherwise) and l-arabinofuranose (l-Araf), respectively (Fig. 1). Free l-Ara exists as l-Arap in solution because the pyranose form is more stable than the furanose, but among cell wall polysaccharides and glycoproteins/proteoglycans, l-Araf residues outnumber the l-Arap residues. Representative l-Ara-containing molecules in plants are listed in Table 1.
Pectin is a complex molecule with many different domains, including homogalacturonan, rhamnogalacturonan I (RG-I), and rhamnogalacturonan II (RG-II) (Mohnen 2008; Tan et al. 2013; Willats et al. 2001). Pectic RG-I is a domain to which α-1,3:1,5-arabinan (pectic arabinan) and type I arabinogalactan (AG) are attached (Table 1, Fig. 2a) (Mohnen 2008). The pectic arabinan consists of α-l-Araf residues and is a major l-Ara-containing molecule in the cell walls in many plants (Levigne et al. 2004). ARABINAN DEFICIENT 1 (ARAD1) and ARAD2 are glycosyltransferases associated with the synthesis of pectic arabinan (Harholt et al. 2012). Based on amino acid sequence and structural similarity, ARADs are categorized into glycosyltransferase family (GTF) 47 (Campbell et al. 1997; Coutinho et al. 2003) (Table 2). The importance of pectic arabinan in the regulation of stomata opening was demonstrated in a study using endo-α-1,5-arabinanase specifically degrading α-1,5-arabinan main chains (Jones et al. 2003). α-l-Araf residues also exist in type I AG, another type of RG-I side chain, where they appear as non-reducing terminal residues (Nakamura et al. 2001) (Table 1). RG-II is the most complicated domain comprising more than ten types of sugars and includes β-l-Araf and α-l-Arap residues (Bar-Peled et al. 2012; O’Neill et al. 2001) (Table 1).
Arabinogalactan-proteins (AGPs) constitute a family of plant extracellular proteoglycans with a large carbohydrate moiety rich in l-Ara and Gal. In order to distinguish it from the type I AG of pectin, the glycan of AGP is called type II AG. The basic structure of type I AG is β-1,4-galactan, whereas that of type II AG is β-1,3:1,6-galactan (main chain, β-1,3-galactan; side chain, β-1,6-galactan) (Shimoda et al. 2014; Tan et al. 2004, 2010; Tsumuraya et al. 1988). In AGP, α-l-Araf residues exist as non-reducing terminal residues of type II AG. AGP sometimes has continuous α-l-Araf residues linked through α-1,5-linkages, thus resembling pectic arabinan (Tan et al. 2004; Tryfona et al. 2012). However, it is still unknown whether ARADs also participate in the synthesis of this structure in AGP. In wheat AGP, the α-l-Araf residues are further substituted with β-l-Arap residues (Tryfona et al. 2010) (Table 1; Fig. 2b). The activity of glycosyltransferase (ArapT) catalyzing the transfer of β-l-Arap from UDP-l-Arap onto α-l-Araf residues was detected in the microsomal fraction of mung bean seedlings (Ishii et al. 2005), but the gene encoding this glycosyltransferase has not been identified (Table 2).
In the vegetative tissues of grasses, including rice (Oryza sativa) and wheat (Triticum aestivum), instead of pectic arabinan, arabinoxylan is a major l-Ara-containing molecule in the cell walls (Table 1). The α-l-Araf residues are attached to the β-1,4-xylan main chain through α-1,2- and/or α-1,3-linkages. The α-1,3-l-Araf residues of arabinoxylan are formed by xylan arabinofuranosyltransferase (XAT), which belongs to GTF 61 (Anders et al. 2012). Interestingly, the α-l-Araf residues can be further substituted with ferulic acid, which forms cross-links between arabinoxylans (Grabber et al. 1995; Saulnier et al. 1999). This cross-link formation is physiologically important, as it is regulated by environmental signals including light and osmotic stress and affects cell wall extensibility, thereby controlling growth and development (Parvez et al. 1997; Tan et al. 1992; Wakabayashi et al. 1997, 2015).
Xyloglucan is a major hemicellulosic polysaccharide in many dicotyledonous plants. This polysaccharide usually consists of β-Glc, α-Xyl, β-Gal, and α-l-fucose (α-l-Fuc), but in several plants such as potato and olive, the β-Gal residues are replaced by α-l-Araf residues (Table 1) (Jia et al. 2003; Vierhuis et al. 2001; Vincken et al. 1996; York et al. 1996). The glycosyltransferases catalyzing the transfer of α-l-Araf residues onto the xylosyl (Xyl) residues, xyloglucan S-side chain transferases (XSTs), have been identified. XSTs are members of GTF 47, which also includes Xyloglucan l-side chain galactosylTransferase 2 (XLT2) and MURUS3 catalyzing the transfer of β-Gal residues onto the Xyl residues (Schultink et al. 2013).
Extensins form a class of cell wall glycoproteins with Hyp-rich core-protein and contain arabino-oligosaccharides consisting of α-l-Araf and β-l-Araf residues (Kieliszewski et al. 1995; Lamport et al. 1973; McNeill et al. 1984) (Fig. 2c; Table 1). Surprisingly, a glycoprotein from Chlamydomonas reinhardtii appears to have similar arabinan chains, that is, the proximal two residues linked to Hyp, β-l-Araf1→2β-l-Araf1→Hyp, are identical to those of extensin (Bollig et al. 2007). This fact suggests that some of Chlorophycean green algae and land plants share the basic mechanism for the synthesis of this arabino-oligosaccharides and points to the possibility that l-arabinofuranosyltransferases and the metabolic pathway for UDP-l-Araf may be conserved.
Extensin-type arabino-oligosaccharides are also attached to glycosylated signaling peptides, the CLAVATA3 (CLV3)/Endosperm surrounding region-related (CLE) peptides (Ohyama et al. 2009; Okamoto et al. 2013; Xu et al. 2015). Using synthetic peptides with or without β-l-Araf1→2β-l-Araf1→2β-l-Araf chain, it has been demonstrated that the arabino-oligosaccharide is necessary for the proper function of CLV3 as a signaling molecule (Ohyama et al. 2009). The transfer of the first β-l-Araf residue onto Hyp is catalyzed by Hyp O-arabinosyltransferases (HPAT) classified into GTF 95 (Table 2). Indeed, loss of function mutations of HPAT genes causes pleiotropic phenotypes in Arabidopsis (Ogawa-Ohnishi et al. 2013). The importance of this arabino-oligosaccharide is further demonstrated by the existence of a tomato inflorescence branching mutant with extra flower and fruit organs, which has defects in a gene encoding GTF77 β-l-arabinofuranosyltransferase that synthesizes the β-l-Araf residues, and can be rescued by treatment with l-arabinofuranosylated CLV3 peptide (Xu et al. 2015).
Most l-Ara-containing polysaccharides, proteoglycans, glycoproteins, and secreted peptides are synthesized in the Golgi apparatus, but small l-Ara-containing glycoconjugates are synthesized in the cytosol. Flavonoids are good examples of small glycoconjugates with l-Araf and l-Arap residues (Table 1). In Arabidopsis, a number of l-arabinopyranosylated flavonols have been found (Tueber and Herrmann 1978; Yonekura-Sakakibara et al. 2008). By transcriptome co-expression network analysis using public databases, an l-arabinosyltransferase, UGT78D3, was identified. This enzyme participates in the synthesis of quercetin 3-O-l-arabinoside in Arabidopsis (Yonekura-Sakakibara et al. 2008) (Table 2). Other l-arabinopyranosylated small glycoconjugates were also found. Floratheasaponin in the tea (Camellia sinensis) plant has an α-l-Arap residue in its carbohydrate moiety (Yoshikawa et al. 2005).
Generation of l -Ara
l-Ara is synthesized as a form of UDP-l-Arap from UDP-Xyl by UDP-Xyl 4-epimerases (UXEs) through C-4 epimerization of UDP-Xyl (Fig. 3). This is the only reaction route known to generate l-Ara in plants so far. It is also possible to synthesize UDP-l-Arap from UDP-galacturonic acid (UDP-GalA) through C-6 decarboxylation. However, no UDP-GalA decarboxylase forming UDP-l-Arap from UDP-GalA has been found in plants so far, although UDP-glucuronic acid (UDP-GlcA) decarboxylase (other name, UDP-Xyl synthase, UXS) forming UDP-Xyl from UDP-GlcA exists in many eukaryotes, including plants (Bar-Peled et al. 2001; Harper and Bar-Peled 2002).
The reaction synthesizing UDP-l-Arap is part of the de novo pathway for UDP-sugars (Fig. 3). The enzymes constituting the de novo pathway are listed in Table 3. In the de novo pathway, UDP-Glc, the starting substrate of this pathway, is first synthesized from sucrose and UDP by sucrose synthase (SUS) (Baud et al. 2004; Cardini et al. 1955) or from Glc 1-phosphate (Glc 1-P) and UTP by UDP-Glc pyrophosphorylase (UGP) (Meng et al. 2009; Park et al. 2010) or UDP-sugar pyrophosphorylase (USP) (Kotake et al. 2004, 2007; Litterer et al. 2006). UDP-Glc undergoes C-6 oxidation, which turns it into UDP-GlcA by UDP-Glc dehydrogenase (UGD) (Reboul et al. 2011), and then undergoes C-6 decarboxylation to form UDP-Xyl by UXS. Plants have Golgi-localized and cytosolic UXSs, implying that the pathway is dual. In Arabidopsis, UXS1, 2, and 4 with a transmembrane domain at the N-terminus produce UDP-Xyl as Golgi-localized enzymes, whereas UXS3, 5, and 6 catalyze the same reaction in the cytosol. Other enzymes, UDP-apiose/UDP-Xyl synthases (AXSs) also participate in this reaction in the cytosol (Mølhøj et al. 2003). Following l-Ara forming reaction, C-4 epimerization of UDP-Xyl to form UDP-l-Arap, also occurs both in the Golgi apparatus and cytosol. In the Golgi apparatus, the formation of UDP-l-Arap is catalyzed by a Golgi-localized UXE, MURUS4 (MUR4) (Burget and Reiter 1999; Burget et al. 2003), but in the cytosol, it is catalyzed by bifunctional UGE1 and UGE3 in Arabidopsis (Fig. 3). Among five UGEs, only UGE1 and UGE3 possess UXE activity beside UDP-Glc 4-epimerase activity in Arabidopsis (Kotake et al. 2009). An Arabidopsis mur4 mutant shows a 50 % reduction in cell wall l-Ara, but a uge1 uge3 double mutant has normal cell walls (Burget and Reiter 1999; Rösti et al. 2007). These observations suggest that, at least in Arabidopsis, the main reaction to generate UDP-l-Arap occurs in the Golgi apparatus. The role of the cytosolic pathway may be clarified in the future via studies on mur4 uge1 uge3 triple mutants.
Conversion from UDP-l -Arap to UDP-l -Araf
The metabolism of UDP-l-Arap turned out to be more complicated than expected, when the subsequent conversion to UDP-l-Araf was investigated. The interconversion between UDP-l-Arap and UDP-l-Araf is catalyzed by a cytosolic enzyme, UDP-l-Arap mutase/reversibly glycosylated protein (UAM/RGP, Drakakaki et al. 2006; Konishi et al. 2007; Konishi et al. 2011). No Golgi-localized enzyme catalyzing this reaction has been found so far. It thus looks very much as if the main reaction to convert UDP-Xyl to UDP-l-Arap occurs in the Golgi apparatus, but the following conversion of UDP-l-Arap to UDP-l-Araf takes place in the cytosol. For this to work, two specific nucleotide sugar transporters (NSTs) would seem to be necessary: one transporter exporting UDP-l-Arap from the Golgi apparatus and one importing UDP-l-Araf into the Golgi apparatus. To efficiently incorporate synthesized UDP-l-Araf back into the Golgi apparatus, the mutase reaction may occur around the Golgi apparatus in the cytosol. Supporting this view, a recent proteomics analysis has revealed that one of the UAM/RGPs, RGP4, is associated with the Golgi apparatus in Arabidopsis (Nikolovski et al. 2012). NSTs are a family of proteins including 40 members in Arabidopsis, which are categorized into six subgroups (Rautengarten et al. 2014). To date, plant-specific NSTs for GDP-sugars, UDP-GalA/UDP-l-rhamnose, and UDP-Xyl are known (Baldwin et al. 2001; Ebert et al. 2015; Rautengarten et al. 2014), but those for UDP-l-Arap and UDP-l-Araf remain to be identified. While l-Ara mainly exists as a form of l-Araf residues in the cell walls, the level of UDP-l-Araf is lower than that of UDP-l-Arap in plant tissues (Ito et al. 2014; Pabst et al. 2010). It may be derived from the instability of UDP-l-Araf under the experimental condition. It is also conceivable that UDP-l-Araf imported by the transporter into the Golgi apparatus is immediately consumed by l-arabinofuranosyltransferases.
Origin of UDP-Xyl 4-epimerase
As described above, l-Ara is synthesized as a form of UDP-l-Arap by Golgi-localized MUR4 and cytosolic UGEs in land plants. These enzymes have similar amino acid sequences and are all categorized into the Rossmann fold superfamily (Rao and Rossman 1973), which also includes other UDP-sugar metabolizing enzymes: AXS, UXS, UDP-GlcA 4-epimerase, and UDP-l-rhamnose synthase (Diet et al. 2006; Gu and Bar-Peled 2004; Harper and Bar-Peled 2002; Mølhøj et al. 2003). In Arabidopsis, both of MUR4 and the bifunctional UGEs possess UXE activity, but the origin of these proteins seems different. It has thus been suggested that the UXE MUR4 is likely older than the bifunctional UGE.
UGE is one of the most highly conserved enzymes and found not only in eukaryotes but also in prokaryotes. In mammals, it is called UDP-Gal 4-epimerase (GalE), as the enzyme catalyzes interconversion between UDP-Glc and UDP-Gal, which constitutes the Leloir pathway for the detoxification of Gal. Phylogenetic relationships suggest that angiosperm UGEs can be grouped into UGE I and II families (Fig. 4). In Arabidopsis, two out of five UGEs, UGE1 and UGE3 belong to the UGE I family and the other three UGEs, UGE2, UGE4, and UGE5 s to the UGE II family. Biochemical characterization using recombinant UGEs expressed in Escherichia coli showed that Arabidopsis UGE1 and UGE3 have UXE activity beside UDP-Glc 4-epimerase activity but UGE2, UGE4, and UGE5 s have none or only weak UXE activity (Kotake et al. 2009). Interestingly, the Norway spruce (Picea sitchensis, gymnosperm) genome includes a gene encoding UGE corresponding to Arabidopsis UGE1 and UGE3, whereas no UGE from Physcomitrella patens (moss) and Selaginella moellendorffii (spikemoss) was grouped into the UGE I family (Fig. 4). These facts lead to the hypothesis that the UGE I family with UXE activity recently evolved from UGE without UXE activity. To support this conjecture, it would be necessary to characterize other UGEs, particularly UGEs in gymnosperm and moss. In fact, only two MUR4-related proteins, Arabidopsis MUR4 and barley (Hordeum vulgare) UXE1 (Zhang et al. 2010), and three bifunctional UGEs, Arabidopsis UGE1 and UGE3 and pea (Pisam sativum) UGE1, have been shown to possess UXE activity so far (Fig. 4).
In sharp contrast with the plant UGE I family, close homologues to Arabidopsis MUR4 can be found not only in gymnosperms, ferns, and mosses, but also in green algae. Although the biochemical properties of MUR4 homologues in green algae have not been determined, the existence of l-Ara-containing glycoprotein and UAM catalyzing subsequent conversion of UDP-l-Arap to UDP-l-Araf strongly suggests their role as UXE (Bollig et al. 2007; Kotani et al. 2013). Together with algal homologues, MUR4 and MUR4 homologues in land plants form a subclade apart from plant the UGE I and II families, suggesting that MUR4 is a highly conserved old enzyme in plants.
Degradation of l-Ara containing molecules
l-Ara-containing molecules undergo hydrolysis by glycoside hydrolases (GHs). The α-l-Araf residues of pectic arabinan, arabinoxylan, and AGP are hydrolyzed by α-l-arabinofuranosidases belonging to the GH family (GHF) 3 and GHF 51 in the cell walls in land plants (Fig. 3). Many plant GHF 3 and GHF 51 α-l-arabinofuranosidases are bifunctional enzymes with β-xylosidase activity (Arsovski et al. 2009; Kotake et al. 2006; Lee et al. 2003; Minic et al. 2004; Tateishi et al. 2005). A native GHF 3 α-l-arabinofuranosidase/β-xylosidase purified from radish, RsAraf1, hydrolyzes pectic arabinan, type I AG, AGP (type II AG), and arabinoxylan showing broad substrate specificity toward α-l-Araf residues (Hata et al. 1992). An Arabidopsis mutant with a defect in a GHF 51 α-l-arabinofuranosidase/β-xylosidase gene, araf1, exhibits accumulation of pectic arabinan in vascular tissues (Chávez Montes et al. 2008).
The enzyme hydrolyzing β-l-Arap residues of AGP has not been identified, but candidate genes exist in land plants. Microbial GHF 27 β-l-arabinopyranosidases acting on β-l-Arap residue of larch (Larix laricina) type II AG have been reported (Ichinose et al. 2009; Salama et al. 2012). Based on the similarity of amino acid sequences, four genes in the genome of Arabidopsis are presumed to encode GHF 27 β-l-arabinopyranosidase or α-galactosidase. As the structure of β-l-Arap resembles that of α-Gal (Fig. 1), it is not surprising that β-l-arabinopyranosidase and α-galactosidase exhibit quite similar three dimensional structures (Ichinose et al. 2009).
The hydrolysis of β-l-Araf residues of arabino-oligosaccharides of extensin and CLE peptides has so far remained elusive. A bacterial β-l-arabinofuranosidase including a domain of unknown function (DUF) 1680 has been identified in Bifidobacterium longum (Fujita et al. 2014). Several proteins of Arabidopsis have this domain, but the similarity of amino acid sequences is low (identity at amino acid level, <15 %). It is necessary to examine whether these proteins act on the β-l-Araf residues. No α-l-arabinopyranosidase acting on α-l-Arap residues of RG-II is known at all. It is conceivable that to some extent, α-l-Arap residues are hydrolyzed by GHF 35 β-galactosidase that widely exists in land plants, because α-l-Arap and β-Gal are structurally similar.
Recycling of free l -Ara released in the degradation
Free l-Ara released during the degradation and metabolism of l-Ara-containing molecules is recycled in the salvage pathway for the generation of nucleotide sugars. The enzymes constituting the salvage pathway are listed in Table 3. l-Arap is first phosphorylated by l-arabinokinase1 (ARA1) and turned into l-Arap 1-P (Fig. 3) (Dolezal and Cobbet 1991; Gy et al. 1998; Sherson et al. 1999). l-Arap 1-P is then converted to UDP-l-Arap by USP in the cytosol (Kotake et al. 2004, 2007; Litterer et al. 2006). This metabolic pathway probably functions as a third pathway for the generation of UDP-l-Arap parallel to the dual de novo pathways occurring in the Golgi apparatus and cytosol (Fig. 3). It is interesting that two plant aldopentoses, l-Ara and Xyl, undergo different metabolism although they are C-4 epimer sugars of each other (Fig. 1). Free Xyl differs from l-Ara in that it is predicted to be converted to xylulose by Xyl isomerase (Maehara et al. 2013) and metabolized in the pentose phosphate pathway. The salvage pathway for free l-Ara is implicated in the detoxification of l-Ara: an Arabidopsis ara1 mutant shows a severe growth defect in the presence of a high concentration of l-Ara (Dolezal and Cobbett 1991). Although no homozygous usp mutant has been analyzed—because USP is necessary for pollen development in Arabidopsis—, Geserick and Tenhaken (2013) have demonstrated the physiological importance of USP in vegetative tissue using USP-knock down (kd-usp) Arabidopsis. The kd-usp plant exhibited dwarf phenotype accumulating much free l-Ara and Xyl.
Physiological importance of the l-Ara salvage pathway in pollen development
Observing the remarkable reduction of cell wall l-Ara in Arabidopsis mur4 mutant (Burget and Reiter 1999; Burget et al. 2003), one is tempted to conclude that UDP-l-Arap is mainly synthesized in the de novo pathway. However, several lines of evidence indicate the physiological importance of the salvage pathway for UDP-l-Arap in developing pollens (Table 4). First, the rice l-arabinokinase named Collapsed Abnormal Pollen 1 (CAP1) has been shown to be necessary for normal development of pollens (Ueda et al. 2013), unfortunately, the effect of Arabidopsis ara1 mutation on pollen development has not been studied. Second, the pollen development also appears to be influenced by lack of USP that catalyzes the subsequent conversion of l-Ara 1-P to UDP-l-Arap as an Arabidopsis heterozygous usp mutant did not give any homozygous usp mutant (Kotake et al. 2007). In addition, collapsed pollens were observed in the anthers of heterozygous usp mutants and kd-usp plants (Geserick and Tenhaken 2013; Schnurr et al. 2006). As is the case in the vegetative tissues, UDP-l-Arap generated in the salvage pathway is probably converted to UDP-l-Araf by the action of UAM/RGPs in developing pollens. UAM/RGP was first identified as a factor necessary for the development of pollen in Arabidopsis (Drakakaki et al. 2006). Consistent with the phenotype of the rice cap1 mutant and the Arabidopsis usp mutant, collapsed pollen grains were also observed in the anthers of homo/hetero rgp1 rgp2 double mutants (rgp1/rgp1 RGP2/rgp2 mutant) (Drakakaki et al. 2006). Furthermore, RNA-interference of the rice UAM3 gene results in the formation of abnormal pollens lacking starch inside (Sumiyoshi et al. 2015). The importance of pectic arabinan for pollen development has been shown in the potato (Cankar et al. 2012), therefore it is highly probable that for pollen development the synthesis of a physiologically important portion of pectic arabinan depends on the salvage pathway.
Conclusion and future prospects
The plant-specific sugar l-Ara is generated as a form of UDP-l-Arap through C-4 epimerization of UDP-Xyl in the de novo pathway. This reaction is catalyzed by MUR4 in the Golgi apparatus and by bifunctional UGE in the cytosol. However, the exact extent of the cytosolic contribution to the synthesis of l-Ara-containing molecules and the physiological role of this alternate pathway are not quite clear. l-Ara appears as α-l-Araf, β-l-Araf, α-l-Arap, and β-l-Arap residues in plants. Various GTs and GHs are involved in the synthesis and degradation of these residues, but many pieces of the puzzle, in particular enzymes dealing with β-l-Araf and α-l-Arap residues, remain to be identified. Reasons for slow progress on this question may include the difficulty in the preparation of l-Ara-containing molecules as substrates. Given the physiological importance of l-Araf, it is not surprising that it is involved in various metabolic pathways. However, it is still unclear what significance in the evolution of plants the diversification of l-Ara use and the later emergence of a new pathway in the cytosol had. It would be of great interest to determine the relationship between other evolutionary events and the diversification of the l-Ara metabolism.
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Kotake, T., Yamanashi, Y., Imaizumi, C. et al. Metabolism of l-arabinose in plants. J Plant Res 129, 781–792 (2016). https://doi.org/10.1007/s10265-016-0834-z