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Stud Mycol. 2011 Jun 30; 69(1): 31–38.
PMCID: PMC3161754

Analysis of regulation of pentose utilisation in Aspergillus niger reveals evolutionary adaptations in Eurotiales


Aspergilli are commonly found in soil and on decaying plant material. D-xylose and L-arabinose are highly abundant components of plant biomass. They are released from polysaccharides by fungi using a set of extracellular enzymes and subsequently converted intracellularly through the pentose catabolic pathway (PCP).

In this study, the L-arabinose responsive transcriptional activator (AraR) is identified in Aspergillus niger and was shown to control the L-arabinose catabolic pathway as well as expression of genes encoding extracellular L-arabinose releasing enzymes. AraR interacts with the D-xylose-responsive transcriptional activator XlnR in the regulation of the pentose catabolic pathway, but not with respect to release of L-arabinose and D-xylose.

AraR was only identified in the Eurotiales, more specifically in the family Trichocomaceae and appears to have originated from a gene duplication event (from XlnR) after this order or family split from the other filamentous ascomycetes. XlnR is present in all filamentous ascomycetes with the exception of members of the Onygenales. Since the Onygenales and Eurotiales are both part of the subclass Eurotiomycetidae, this indicates that strong adaptation of the regulation of pentose utilisation has occurred at this evolutionary node. In Eurotiales a unique two-component regulatory system for pentose release and metabolism has evolved, while the regulatory system was lost in the Onygenales. The observed evolutionary changes (in Eurotiomycetidae) mainly affect the regulatory system as in contrast, homologues for most genes of the L-arabinose/D-xylose catabolic pathway are present in all the filamentous fungi, irrespective of the presence of XlnR and/or AraR.


The order Eurotiales consists of the families Trichocomaceae and Elaphomycetaceae. Most species belonging to the Trichocomaceae are saprobic filamentous ascomycetes, which in nature grow predominantly in soil or on decaying plant material. The Elaphomycetaceae entails a family of underground, saprobic or mycorrhiza-forming fungi. The family Trichocomaceae includes the well-known genera of Penicillium and Aspergillus. Aspergilli are found throughout the world in almost all ecosystems and are well-known for their ability to degrade different complex plant polymers. Despite the fact that some Aspergillus species have evolved additional lifestyles, for example as human or plant pathogens, there seems to be no restriction to a specific niche concerning their saprobic lifestyle.

Decaying plant material consists for a major part of plant cell wall polysaccharides which can be split into three major groups: cellulose, hemicellulose and pectin. L-arabinose and/or D-xylose are the main components of the hemicelluloses arabinoxylan and xyloglucan, and of pectin. Release of these sugars from polysaccharides as well as metabolic conversion of them through the pentose catabolic pathway (PCP) has been studied for many years, particularly in Aspergillus and the genus Trichoderma belonging to the order Hypocreales [reviewed in (de Vries & Visser 2001, de Vries 2003, Stricker et al. 2008)]. The PCP was first described in Aspergillus niger (Witteveen et al. 1989) and shown to consist of a series of reversible reductase/dehydrogenase steps followed by phosphorylation to D-xylulose-5-phosphate, which enters the pentose phosphate pathway (PPP). In A. niger, the gene encoding D-xylose reductase (xyrA) (Hasper et al. 2000), D-xylulokinase (xkiA) (vanKuyk et al. 2001), L-arabitol dehydrogenase (ladA) and xylitol dehydrogenase (xdhA) (Seiboth et al. 2003, de Groot et al. 2007) have been characterised. For Trichoderma reesei, genes encoding L-arabitol dehydrogenase (lad1) (Richard et al. 2001) and xylitol dehydrogenase (xdh1) (Seiboth et al. 2003) have been described. In A. niger, induction of pentose release and the PCP occurs in the presence of L-arabinose and/or D-xylose (Witteveen et al. 1989). In the presence of D-xylose, the xylanolytic transcriptional activator XlnR (van Peij et al. 1998b) regulates the expression of genes encoding extracellular polysaccharide degrading enzymes, as well as the expression of xyrA [reviewed in (de Vries 2003)]. L-arabinose induction of the PCP is not mediated via XlnR. The genes of the L-arabinose catabolic pathway are co-regulated with the genes encoding extracellular arabinanolytic enzymes (α-L-arabinofuranosidase and endoarabinanase) (Flipphi et al. 1994, de Vries et al. 1994) and L-arabitol is most likely the inducer (de Vries et al. 1994, vanKuyk et al. 2001). Analysis of A. niger arabinanolytic regulatory mutants, araA and araB, demonstrated an antagonistic effect between XlnR and the L-arabinose/L-arabitol responsive regulation (de Groot et al. 2003).

In this study, we report the identification and characterisation of the L-arabinose catabolic pathway specific regulator (AraR) in A. niger and demonstrate that this regulator is only present in the order Eurotiales. These fungi have evolved a fine-tuned two-regulator activating system for pentose release and catabolism compared to other filamentous ascomycetes that only contain XlnR or have neither of the regulators.


Strains, media and growth conditions

The A. niger strains used in this study are listed in Table 1 and are all derived from A. niger CBS 120.49. Aspergillus niger strains were grown in Minimal Medium (MM) or Complete Medium (CM) with addition of a carbon source at 30 °C. MM contained (per liter): 6 g NaNO3, 1.5 g KH2PO4, 0.5 g KCL, 0.5 g MgSO4·7 H2O and 200 μl trace elements solution (Vishniac & Santer 1957), pH 6.0. CM = MM supplemented with (/L): 2 g peptone, 1 g casamino acids, 1 g yeast extract and 0.5 g yeast ribonucleic acids, pH 6.0. For growth on solid media, 1.5 % agar was added to the medium. When necessary, the medium was supplemented with 0.2 g/L arginine, 0.2 g/L leucine, 0.2 g/L uridine and/or 1 mg/L nicotinamide.

Table 1.
Strains used in this study.

In transfer experiments, all the strains were pre-grown in CM containing 2 % D-fructose. After 16 h of incubation, the mycelium was harvested without suction over a filter, washed twice with MM without a carbon source and transferred to 50 mL MM containing the appropriate carbon source and supplements. The mycelium was harvested with suction over a filter and culture samples were taken after 2 and 4 h of incubation. The mycelium samples were dried between tissue paper and directly frozen in liquid nitrogen.

Molecular biology methods

Molecular biology methods were performed according to standard procedures (Sambrook et al. 1989), unless stated otherwise. All PCR reactions were performed using Accutaq™ LA DNA Polymerase (Sigma-Aldrich) according to the manufacturer's instruction. The flanking regions of the araR gene were amplified with 5'primers and 3'-primers (see online Supplemental Table 1) by PCR to generate the 5' flank with the HindIII/SphI site and 3' flank with a KpnI/BamHI site, respectively, to enable deletion of the complete coding region of araR by replacing it with the argB selection marker. The functional construct was obtained using PCR with the extreme 5'-end 3'-primers (see online Supplemental Table 1) for complementation of araR. The araR disruption cassette (containing the argB gene for selection for arginine prototrophy) was transformed to the A. niger strain NW249 (pyrA6, leuA1, nicA1, ΔargB). The xlnR gene was amplified with the extreme 5'-primer and 3'-primer by PCR (see online Supplemental Table 1) The PCR fragment was ligated into pGEM-T-easy (Promega) from which the NsiI/PstI restriction sites were removed. The construct was digested with SalI/EcoRI to remove most of the coding region including the DNA binding domain and ligated with the A. oryzae pyrA gene that was digested with BamHI (made blunt with Klenow fragment) and SalI. The xlnR disruption cassette was transformed to A. niger strains NW249 (pyrA6, leuA1, nicA1, ΔargB) and UU-A033.21 (pyrA6, leuA1, nicA1, ΔaraR). All A. niger transformations were carried out as described previously (Kusters-van Someren et al. 1991).

The primers used to generate the probes for Southern and Northern analysis are listed in online Supplemental Table 1. The probes were DIG-labelled using the PCR DIG Probe Syntheses Kit (Roche Applied Science) according to the supplier's instructions. A cDNA library (de Groot et al. 2007) or genomic DNA (obtained from N402) was used as a template in the PCR reactions for synthesis of the probes.

Expression analysis

Total RNA was isolated from mycelium that was ground in a microdismembrator (B Braun) using a standard RNA isolation method with the TRIzol Reagent (Invitrogen). In the Northern analysis, 3 μg total RNA was transferred to a Hybond-N+ membrane (Amersham Biosciences). The Minifold II slot blot apparatus (Schleicher & Schuell) was used for Slot blot analysis. Equal loading was determined by soaking the blot for 5 min in 0.04 % methylene blue, 0.5 M acetate pH 5.2 solution.

Hybridisation of the DIG-labeled probes to the blot was performed according to the DIG user's manual (www.roche-applied-science.com). All the blots were incubated overnight at 50 °C. The blots were exposed for 25 min up to 24 h to a Lumi-Film Chemiluminescent Detection Film (Roche Applied Science). Micro array analysis was performed as described previously (Levin et al. 2007).

Phylogenetic analysis

The amino acid sequences of AraR, XlnR, LadA, XdhA, XyrA and XkiA were used as queries in a local Blast against the protein files of 38 fungal genomes (see online Supplemental Table 2) with a expect value cut-off of 1E-10. The resulting ORFs were aligned using ClustalX and a Maximum Parsimony tree (1 000 bootstraps) was produced using MEGA (v. 4.0).

Enzyme assays

Extracellular enzyme activity was measured using 0.01 % p-nitrophenol linked substrates, 10 μL of the culture samples, 25 mM sodium acetate pH 5.0 in a total volume of 100 μL. Samples were incubated in microtiter plates for 120 min at 30 °C. Reactions were stopped by addition of 100 μL 0.25 M Na2CO3. Absorbance was measured at 405 nm in a microtiter platereader (Biorad Model 550). The extracellular enzyme activity was calculated using a standard curve ranging from 0 to 80 nmol p-nitrophenol per assay volume.

To measure intracellular enzyme activity, cell free extract was prepared by adding 1 mL extraction buffer (50 mM K2HPO4, 5 mM MgCl2, 5 mM 2-mercaptoethanol, 0.5 mM EDTA) to powdered mycelium. The mixtures were centrifuged for 10 min at 12000 RPM at 4 °C. The L-arabitol and xylitol dehydrogenase activities were determined using 100 mM glycine pH 9.6, 0.4 mM NAD+ and 1 M L-arabitol or xylitol, respectively. L-arabinose reductase and D-xylose reductase activities were determined using 50 mM Tris-HCL pH 7.8, 0.2 mM NADPH and 1 M L-arabinose or D-xylose, respectively. L-arabinose reductase (ArdA) and D-xylose reductase (XyrA) both convert D-xylose to xylitol and L-arabinose to L-arabitol, but have a higher activity on their primary substrate (de Groot et al. 2003). As a result, the measured activity is the sum of the two enzymes. To be able to discriminate between the two enzymes, the ratio of the activity on L-arabinose and on D-xylose was calculated that allows us to extrapolate the relative activities of ArdA and XyrA. An increase in the ratio indicates a relative increase in ArdA or decrease in XyrA, while a reduction in the ratio indicates a relative increase in XyrA or decrease in ArdA.

Absorbance changes were measured at 340 nm using a spectrometer (Spectronic Unicam UV1). L-arabinose and D-xylose reductase activity and L-arabitol and D-xylitol dehydrogenase activity was calculated using the molar coefficient for NADPH and NADH (both ε = 6.22 mM-1cm-1) and the following formula:


Abl/min = decrease absorbance per minute before adding substrate. A/min = decrease absorbance per minute after adding substrate. a = sample volume (mL). d = sample dilution. v= total volume cuvet. l = lightpath (cm). Protein concentrations of intracellular and extracellular samples were determined using a BCA protein assay kit (Pierce).


Identification and analysis of araR

Blast analysis of XlnR against the A. niger genome (Pel et al. 2007) revealed 3 homologues with expect values smaller than e-30 (An04g08600, An11g00140, An11g06290). Expression analysis of these genes revealed that the closest xlnR homologue (An04g08600) was specifically induced in the presence of L-arabinose or L-arabitol, while only low constitutive expression was observed for An11g06290 and no expression for An11g00140 (Fig. 1A). In order to study its possible role in L-arabinose utilisation, a disruption strain for An04g08600 (referred to as araR) was constructed and verified by Southern analysis (data not shown). The disruption strain showed poor growth on L-arabitol, whereas complementation with araR restored growth again (Fig. 1B).

Fig. 1. A.
Expression analysis of the three XlnR homologues (An04g08600 (araR), An11g00140 and An11g06290) on D-fructose (1), L-arabinose (2), L-arabitol (3), D-xylose (4) and xylitol (5). B. Growth of the reference (UU-A049.1), ΔaraR (UU-A033.21) and Δ ...

The araR gene consists of 2552 bp interrupted by a single intron of 53 bp. Within the 1000 bp promoter region of araR putative six binding sites for the carbon catabolite repressor protein CreA (Kulmburg et al. 1993) and two binding sites for the xylanolytic regulator XlnR (van Peij et al. 1998b, de Vries et al. 2002) can be found. The AraR protein contains a Zn(2)Cys(6) binuclear cluster domain (amino acids 36-73, Pfam00172) and a Fungal specific transcription factor domain (amino acids 386-532, Pfam04082). An amino acid motif Arg-Arg-Thr-Leu-Trp-Trp is found at position 493 to 498. This motif differs in only one amino acid from a conserved motif of unknown function found in Zn(2)Cys(6) family members (Arg-Arg-Arg-Leu-Trp-Trp), first described in the UaY regulator in Aspergillus nidulans (Suarez et al. 1995). AraR shows 32 % identity to XlnR, with the highest homology in the C-terminal part of the proteins. The sequence between the 2nd and the 3rd Cysteine in the Zn(2)Cys(6) region was previously shown to be important in DNA binding specificity of this class of regulators (Marmorstein et al. 1992, Marmorstein & Harrison 1994), but differs significantly between AraR (C2HSRRVRC3) and XlnR (C2NQLRTKC3). Between the third and the fourth Cysteine, the Proline residue can be found that is essential for correct folding of the DNA binding domain (Marmorstein et al. 1992) and is highly conserved in all the fungal zinc binuclear transcriptional regulators.

The presence of AraR in the genome is restricted to Eurotiales and possibly to Trichocomaceae

BlastP analysis of both AraR and XlnR against 38 fungal genome sequences (see online Supplemental Table 2) identified homologues for both proteins in all 11 analysed species of the family Trichocomaceae of the order Eurotiales (Aspergillus clavatus, A. flavus, A. fumigates, A. nidulans, A. niger, A. oryzae, A. terreus, Neosartorya fischeri, Penicillium chrysogenum, P. marneffei, Talaromyces stipitatus), but neither of them was found in three representatives of Onygenales (Coccidioides immitis, Histoplasma capsulatum, Uncinocarpus reesei) (Fig. 2). XlnR was also found in the genomes of all other filamentous ascomycetes used in this study. No XlnR and AraR homologues were found in ascomycete yeasts, basidiomycetes or zygomycetes.

Fig. 2.
Bootstrapped (1000 bs) Maximum Parsimony tree of of putative homologues of XlnR and AraR in fungi. Homologues of the A. nidulans acetate regulatory protein (FacB) were used as an outgroup.

In addition, a BlastP analysis was performed with the amino acid sequence of four genes of the A. niger pentose catabolic pathway (ladA, xyrA, xdhA and xkiA) against the genomes of the fungal species that contain XlnR and/or AraR as well as the three Onygenales genomes used in this study (see online Supplemental Fig. 1). Phylogenetic analysis showed that all genomes contain homologues of three genes of the pentose catabolic pathway. Homologues for the 4th gene (ladA) were found in all species except for Onygenales.

Influence of AraR and XlnR on growth of A. niger on monomeric and polymeric carbon sources

In addition to the araR disruptant (UU-A033.21), an xlnR disruptant (UU-A062.10) and an araR/xlnR double disruptant (UU-A063.22) were generated, as described in Materials and Methods. The utilisation of several monomeric and polymeric carbon sources was analysed in all strains (including the reference) to determine the effect of the single disruption of the araR gene and the double disruption of araR and xlnR (Fig. 3). Polymeric sugars containing L-arabinose residues (arabinan, Arabic gum, arabinogalactan and apple pectin) and D-xylose residues (birchwood xylan) were included in the analysis. Guar gum was used as a control; it is a galactomannan and contains no L-arabinose or D-xylose residues.

Fig. 3.
Growth of the reference strain (Ref., UU-A049.1), and the ΔaraR (UU-A033.21), ΔxlnR (UU-A062.10) and ΔaraR/ΔxlnR (UU-A063.22) strains on a selection of mono- and polysaccharides. Concentrations of the substrates were 25 ...

Disruption of araR resulted in reduced growth on L-arabinose, xylitol, arabinan, Arabic gum, arabinogalactan and apple pectin and poor growth on L-arabitol (Fig. 3). Disruption of xlnR resulted in reduced growth on birchwood xylan, while growth was unaffected on D-xylose, xylitol and the other carbon sources. Disruption of both regulators resulted in a similar phenotype as disruption of araR for L-arabitol, Arabic gum, arabinan and arabinogalactan and a similar phenotype as disruption of xlnR for birchwood xylan. In contrast to the single disruptants, no growth was observed on D-xylose for the double disruptant, only residual growth on L-arabitol and L-arabinose, and reduced growth on xylitol.

AraR and XlnR control L-arabinose and D-xylose release and catabolism

The reference, ΔaraR, ΔxlnR and ΔaraR/ΔxlnR strains were pre-grown in complete medium containing D-fructose. After 16 h of growth, equal amounts of mycelium were transferred for 2 and 4 h to minimal medium containing 25 mM D-fructose, 25 mM L-arabinose or 25 mM D-xylose. Extracellular α-L-arabinofuranosidase (Abf) and intracellular PCP enzyme activities (Ard, Xyr, Lad, Xdh) were analysed. Activity of α-L-arabinofuranosidase (Abf), L-arabitol dehydrogenase (Lad) and xylitol dehydrogenase (Xdh) was strongly reduced in the ΔaraR and ΔaraR/ΔxlnR strain compared to the reference strain when grown on L-arabinose (Fig. 4A). On D-xylose, Lad and Xdh activity was reduced in ΔaraR and ΔaraR/ ΔxlnR. For L-arabinose reductase (ArdA) and D-xylose reductase (XyrA), the ratio of the activity on L-arabinose and on D-xylose was calculated that allowed extrapolation of the relative activities of ArdA and XyrA (see Materials and Methods). The ratio in the ΔaraR strain became less than 1.0 after 4 h growth in the presence of L-arabinose, while the ratio of the reference strain was around 1.5, which suggests that the ArdA activity was reduced in the ΔaraR strain (Fig. 4A). The Ard/Xyr ratio in the wild type and ΔaraR disruptant grown on D-xylose were both around 1. In the absence of both regulators, no Ard and Xyr activities were detected (data not shown). Xylitol dehydrogenase activity (Xdh) was reduced in the ΔaraR strain on L-arabinose and to a lesser extent on D-xylose compared to the reference strain (Fig. 4). All the measured activities after 2 h of growth on L-arabinose and D-xylose in the ΔxlnR are similar to those published previously (de Groot et al. 2003). After 4 h, the difference in activity between the reference and ΔxlnR is similar to that observed after 2 h of growth, except for Xdh and Abf. Xdh activity in the ΔxlnR became similar to that in the reference strain after 4 h on D-xylose, whereas the Abf activity increased at this point. No activity for any of the enzymes was detected during growth of D-fructose.

Fig. 4.
Comparison of intracellular and extracellular enzyme activities in reference and disruption strains. The reference strains (UU-A049.1), ΔaraR (UU-A033.21), ΔxlnR (UU-A062.10) and ΔaraR/ΔxlnR (UU-A063.22) were transferred ...

In addition, expression levels were determined using micro array analysis for genes involved in release (abfA, abfB) and catabolism (ladA, xdhA, xyrA, xkiA) of L-arabinose and D-xylose. No gene expression was observed for any of the genes discussed in this section during growth on 25 mM D-fructose (data not shown). Expression profiles of all the genes in Table 2, except for araR and xlnR, were confirmed by Northern analysis (see online Supplemental Fig. 1). Expression of araR and xlnR was below detection levels for Northern analysis in these samples. Disruption of araR resulted in 74, 6, 10, 2 and 13-fold reduced expression levels of abfA, abfB, ladA, xdhA and xkiA, respectively, after 2 h of growth on L-arabinose (Table 2). Disruption of xlnR did not significantly reduce expression levels of any of the tested genes, except for xyrA for which expression reduced 2-fold after 2 h of growth on D-xylose. Disruption of araR did not affect xdhA, xkiA and xyrA expression on D-xylose, while none of the genes were affected on L-arabinose by disruption of xlnR (see online Supplemental Fig. 1). None of the tested genes were expressed in the ΔaraR/ΔxlnR strain, except for abfB (see online Supplemental Fig. 1). Expression of xlnR was not affected in the ΔaraR on L-arabinose, whereas araR expression showed a 3-fold increase in the ΔxlnR on D-xylose compared to the reference.

Table 2.
Expression analysis of genes encoding extracellular L-arabinose releasing enzymes and PCP enzymes. abfA, abfB = α-L-arabinofuranosidase A and B, ladA = L-arabitol dehydrogenase, xdhA = xylitol dehydrogenase, xyrA = D-xylose reductase, xkiA = D-xylulose ...


Previously, it has been shown that the pentose catabolic pathway is under control of the D-xylose specific transcriptional activator (XlnR) and a second, unidentified L-arabinose specific transcriptional activator regulator (de Groot et al. 2007). In this study, we identified the gene encoding the L-arabinose responsive regulator, AraR, and confirmed its role in the release and catabolism of L-arabinose and D-xylose. AraR is a member of the Zn(2)Cys(6) family of transcriptional regulators and a close homologue of the xylanolytic transcriptional activator XlnR from A. niger. Functional analysis of AraR and XlnR as described in this study confirm the previously published antagonistic relation of the two regulatory systems involved in pentose catabolism (de Groot et al. 2003).

Expression levels of abfA, abfB, ladA as well as the corresponding enzyme activities (Abf and Lad) were strongly reduced in the ΔaraR strain on L-arabinose, indicating that they are only controlled by AraR. Gene expression levels of xdhA and xkiA are reduced in the ΔaraR strain after 2 h of growth on L-arabinose. On D-xylose, xdhA expression is up-regulated in the ΔxlnR strain compared to the reference strain, which confirms data published previously (de Groot et al. 2007). An increase in xkiA expression was observed in the ΔxlnR strain on L-arabinose. These results indicate that both AraR and XlnR are involved in regulating the expression of xdhA and xkiA. The stronger effect in the ΔaraR strain, suggests that AraR has a larger influence on xdhA and xkiA expression than XlnR.

Expression of the AraR regulated genes on D-xylose and reduction of the expression in the araR disruptant can be explained by the presence of a small amount of L-arabinose in the D-xylose preparation from SIGMA (R.P. de Vries, unpubl. data). This is supported by a reduction in the expression of these genes on D-xylose at 4 h compared to 2 h.

The discrepancies between some of the expression and activity data can be explained by the substrate specificities of the enzymes. The L-arabinose and D-xylose reductases are both active on both pentoses, so under conditions where both are expressed, the measured activity is the result of the combined activity of the two enzymes. Although xylitol dehydrogenase is (almost) not active on L-arabitol, the L-arabitol dehydrogenase is active on xylitol (de Groot et al. 2007), indicating that the measured xylitol dehydrogenase can also consist of two components depending on the condition used.

Previously, it has been shown that the expression of xyrA was only reduced and not absent in the ΔxlnR on D-xylose (de Groot et al. 2003) and it was suggested that in addition to XlnR another unknown inducing factor is involved. Our results confirm this observation. The reason why there is no reduction in growth of the ΔxlnR strain on D-xylose can be explained by the fact that xyrA expression/activity was not absent combined with the compensatory regulation by AraR for xkiA and xdhA expression. No growth was observed for the double disruptant on D-xylose, suggesting both regulators are necessary for growth on D-xylose. The strong growth reduction of the ΔxlnR strain on xylan, similar to growth of the double disruptant, indicates that D-xylose release is mainly dependent on XlnR.

Only residual growth was observed for the double disruptant on L-arabinose and L-arabitol, demonstrating the importance of AraR and XlnR for growth on these substrates. Strongly reduced growth was observed for the ΔaraR strain and the ΔaraRxlnR strain on arabinan, indicating that release of L-arabinose residues depends only on AraR.

The absence of AraR orthologues in fungal genomes except for those of the aspergilli and penicillia and its similarity to XlnR suggests that this regulator has originated by a gene duplication of xlnR after Eurotiales split from the other filamentous ascomycetes. All genomes available from Eurotiales are of the family Trichocomaceae, while currently none are available for the other family of this order, Elaphomycetaceae. At this point we can therefore not determine whether this gene duplication may have occurred even later, when Elaphomycetaceae and Trichocomaceae split into two different families.

The regulatory system controlling pentose release and utilisation in this group of fungi likely evolved to become a highly interactive two-regulator system. Whether this implies that in the other ascomycete fungi XlnR is responsible for L-arabinose and D-xylose induced expression remains to be studied. It suggests there are large evolutionary differences in regulation of the pentose catabolic pathway. Afterthe Onygenales split from Eurotiales it seems to have lost both XlnR and AraR regulators. Homologues for three of the A. niger genes of the pentose catabolic pathway (xdhA, xyrA and xkiA) are present in the other fungal genomes. The L-arabitol dehydrogenase encoding gene (ladA) appears to have been lost in Onygenales, but is present in all species that contain XlnR. This may suggest that loss of L-arabinose utilisation has proceded further in Onygenales than just loss of the regulatory systems.

Data from our study was combined with the previously reported data on XlnR (van Peij et al. 1998a, de Groot et al. 2003) to construct a regulatory model for release and utilisation of L-arabinose and D-xylose in the A. niger (Fig. 5). This model correlates not only well with the expression profiles of the pentose-related genes but also with the growth comparison of the disruptant strains and the reference. It indicates that XlnR and AraR control distinct sets of genes in response to the presence of D-xylose and L-arabinose, respectively. However, in the absence of one of the regulators the other can partially compensate for this loss. Although the data supporting this model comes from A. niger, we postulate that this model applies to all Eurotiales, since we have demonstrated in this study that the presence of AraR is conserved among all species of Eurotiales studied so far.

Fig. 5.
Regulatory model for release and utilisation of D-xylose and L-arabinose in A. niger. ArdA = L-arabinose reductase; LadA = L-arabitol dehydrogenase; LxrA = L-xylulose reductase; XdhA = xylitol dehydrogenase; XyrA = D-xylose reductase; XkiA = D-xylulose ...

Supplementary Material


We were supported by grants of the Dutch Foundation for Applied Science (STW) UGC5683 and 07063.


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