L-Rhamnose induction of Aspergillus nidulans α-L-rhamnosidase genes is glucose repressed via a CreA-independent mechanism acting at the level of inducer uptake
- Juan A Tamayo-Ramos†1, 2,
- Michel Flipphi†1,
- Ester Pardo1,
- Paloma Manzanares1 and
- Margarita Orejas1Email author
© Tamayo-Ramos et al; BioMed Central Ltd. 2012
Received: 30 September 2011
Accepted: 21 February 2012
Published: 21 February 2012
Little is known about the structure and regulation of fungal α-L-rhamnosidase genes despite increasing interest in the biotechnological potential of the enzymes that they encode. Whilst the paradigmatic filamentous fungus Aspergillus nidulans growing on L-rhamnose produces an α-L-rhamnosidase suitable for oenological applications, at least eight genes encoding putative α-L-rhamnosidases have been found in its genome. In the current work we have identified the gene (rhaE) encoding the former activity, and characterization of its expression has revealed a novel regulatory mechanism. A shared pattern of expression has also been observed for a second α-L-rhamnosidase gene, (AN10277/rhaA).
Amino acid sequence data for the oenological α-L-rhamnosidase were determined using MALDI-TOF mass spectrometry and correspond to the amino acid sequence deduced from AN7151 (rhaE). The cDNA of rhaE was expressed in Saccharomyces cerevisiae and yielded p NP-rhamnohydrolase activity. Phylogenetic analysis has revealed this eukaryotic α-L-rhamnosidase to be the first such enzyme found to be more closely related to bacterial rhamnosidases than other α-L-rhamnosidases of fungal origin. Northern analyses of diverse A. nidulans strains cultivated under different growth conditions indicate that rhaA and rhaE are induced by L-rhamnose and repressed by D-glucose as well as other carbon sources, some of which are considered to be non-repressive growth substrates. Interestingly, the transcriptional repression is independent of the wide domain carbon catabolite repressor CreA. Gene induction and glucose repression of these rha genes correlate with the uptake, or lack of it, of the inducing carbon source L-rhamnose, suggesting a prominent role for inducer exclusion in repression.
The A. nidulans rhaE gene encodes an α-L-rhamnosidase phylogenetically distant to those described in filamentous fungi, and its expression is regulated by a novel CreA-independent mechanism. The identification of rhaE and the characterization of its regulation will facilitate the design of strategies to overproduce the encoded enzyme - or homologs from other fungi - for industrial applications. Moreover, A. nidulans α-L-rhamnosidase encoding genes could serve as prototypes for fungal genes coding for plant cell wall degrading enzymes regulated by a novel mechanism of CCR.
KeywordsAspergillus nidulans Carbon catabolite repression CreA-independent Inducer exclusion α-L-rhamnosidase Transcriptional regulation
The degradation of plant cell wall polysaccharides (i.e. cellulose, hemicellulose and pectins), and the subsequent utilization of their components as carbon sources is a key and highly regulated event when filamentous fungi grow on these substrates or infect plants. A number of those plant-derived substrates contain the neutral sugar L-rhamnose (6-deoxy-L-mannose) which is a component of the plant cell wall pectic polysaccharides rhamnogalacturonan I and rhamnogalacturonan II  and diverse secondary metabolites, including anthocyanins, flavonoids and triterpenoids (see reviews [2, 3], and references therein). In addition, L-rhamnose (hereafter rhamnose) is present in animal tissues and in viruses, and is also a component of bacterial polysaccharides where it plays an important role in pathogenicity. The utilization, transformation or detoxification of these rhamnose-containing compounds involves different α-L-rhamnosidases (EC 220.127.116.11), which catalyze the hydrolysis of terminal non-reducing rhamnose residues in polysaccharides and α-L-rhamnosides including the artificial substrate p- nitrophenyl-α-L-rhamnopyranoside (p NPR) that is widely used to evaluate their activity. α-L-Rhamnosidases have been found in some plant and animal tissues as well as in a plethora of microorganisms including filamentous fungi (see reviews [2, 3] and references therein). Based on primary sequence similarities these enzymes are classified within the Carbohydrate-Active Enzymes (CAZy) database  (http://www.cazy.org/) into three glycosyl hydrolase (GH) families. Whereas bacterial α-L-rhamnosidases are classified into either GH78 or GH106, fungal α-L-rhamnosidases (with the possible exception of the Aspergillus niger rhamnogalacturonan α-L-rhamnopyranohydrolase B [RgxB; EC 18.104.22.168] which is assigned to family GH28) belong to GH78.
α-L-Rhamnosidases are of considerable interest given their suitability in various applications within the food (e.g. citrus juice debittering, liberation of aromas and bioactive compounds), pharmaceutical (e.g. biotransformation of antibiotics and steroids), agro-/forestry (e.g. detoxification of rhamnose-conjugated plant secondary metabolites) and chemical industries (e.g. to produce rhamnose) ( and references therein). The biotechnological potentiality of these enzymes has led to the characterization of fourteen microbial α-L-rhamnosidase (GH78 family) encoding genes within the last decade (Additional file 1: Table S1). Of these only four were isolated from filamentous fungi: the genes encoding RhaA and RhaB of Aspergillus aculeatus, that encoding AkRha78 of Aspergillus kawachii and the gene encoding the Aspergillus nidulans AN10277 protein , hereafter named rhaA.
In the presence of rhamnose as the sole carbon source, A. nidulans secretes at least one α-L-rhamnosidase of molecular mass ~102 kDa. Its biochemical properties make it suitable for oenological applications [8, 9] as well as for improvement of the bioavailability of plant rhamnose-containing bioactive compounds. While this enzyme is active against naringin and hesperidin (major rhamnosylated flavonoids in citrus juices in which the rhamnose molecule is bound to glucose by α-(1,2) or α-(1,6) linkages respectively) and also the synthetic substrate p NPR (in which the aglycon is directly linked to the C1 position of rhamnose) [8, 9], recombinant AN10277-His6/RhaA-His6 was not , strongly suggesting that these are two distinct enzymes. At least eight loci putatively encoding α-L-rhamnosidases have been annotated in the A. nidulans genome the products of which range from 62 to 169 kDa [10, 11]. The locus encoding the α-L-rhamnosidase of oenological interest is however unknown.
The regulation of α-L-rhamnosidase genes is less well documented than that of many other genes encoding glycosyl hydrolases. It has been reported  that the Lactobacillus plantarum ram1 and ram2 genes are induced by rhamnose and repressed by D-glucose (hereafter glucose). However, the regulatory circuits controlling fungal α-L-rhamnosidase gene expression are unknown. In filamentous fungi it has been shown that the synthesis of a number of plant cell wall-degrading enzymes is regulated at the level of transcription i.e. induced when the plant polysaccharide or its degradation products are present and repressed by glucose (see reviews [13, 14]). Glucose repression is a well-studied regulatory circuit in A. nidulans (reviewed in [15, 16]), and the role of the wide-domain transcriptional repressor CreA in the expression of a number of genes encoding plant cell wall degrading enzymes has been widely characterized. Our previous studies  have shown that α-L-rhamnosidase activity in A. nidulans is induced by rhamnose and repressed by glucose. However, unlike other glycosyl hydrolase systems, relief of repression by glucose either by cultivation in the presence of the inducer and a so-called non-repressing carbon source (e.g. D-lactose or L-arabinose) or by the use of the creA d 30 derepressed strain  was not sufficient for α-L-rhamnosidase production to be totally derepressed. It was therefore suggested that carbon catabolite repression (CCR) of A. nidulans α-L-rhamnosidase genes could involve a CreA-independent mechanism .
Here we show that rhamnose and glucose regulate α-L-rhamnosidase production at the transcriptional level in the model filamentous fungus A. nidulans. We have identified the A. nidulans gene encoding the previously characterized α-L-rhamnosidase [8, 9] and confirmed that glucose repression of its expression, as well as that of the gene coding for the α-L-rhamnosidase AN10277/RhaA (rhaA), occurs by means of a CreA-independent mechanism. The data suggest that glucose prevents the entry of the inducing carbon source rhamnose into the cell and that this phenomenon does not involve CreA function. We thus hypothesize the existence of an inducer exclusion mechanism by which fungal α-L-rhamnosidase genes are controlled. In this regard, the lack of protection against the toxicity of the non-metabolizable glucose analogue 2-deoxy-D-glucose by a range of rhamnose concentrations suggesting that inducer exclusion is not due to competition for uptake of the inducer. Moreover, α-L-rhamnosidase gene expression was found to be repressed by sugars previously considered non-repressive as well as by some non-sugar carbon sources (e.g. ethanol). In contrast to glucose, ethanol did not prevent the uptake of rhamnose. Hence, these findings provide evidence for the existence of novel molecular mechanisms for exerting CCR on genes encoding plant cell wall degrading enzymes in filamentous fungi which could be of utility in modulating α-L-rhamnosidase production.
Results and discussion
The A. nidulans locus AN7151 encodes an α-L-rhamnosidase of potential oenological relevance
Gene structure of A. nidulans rhaE
Using RT-PCR a full-length cDNA corresponding to the ORF of the A. nidulans rhaE gene was generated and sequenced. Comparison of the cDNA sequence with the genomic sequence (Additional file 2: Figure S1) revealed the presence of two introns of 59 and 51 nucleotides which followed the canonical GT-AG splicing rule (E357/V358 and N504/Y505 within the bacterial alpha-L-rhamnosidase domain - Pfam PF05592 - of the A. nidulans predicted protein). The second intron is in-frame which explains its absence in automatic annotation of the gene. Glycosyl hydrolase genes are frequently found to be subjected to CCR and have CreA consensus motifs upstream of the ORF. Sequence analysis of the 1 kb sequence upstream of the proposed translational start site revealed the presence of 8 CreA (5'-SYGGRG-3') consensus target sites [18–20], 6 of them being located within the first 360 bp, suggesting that the transcription of rhaE could be directly repressed by CreA. However, it has previously been shown that the production of this α-L-rhamnosidase is repressed predominantly via a CreA-independent mechanism  which would indicate that the putative CreA targets in rhaE are not functional. Such a circumstance would not be without precedent for genes encoding plant cell wall degrading enzymes .
The polypeptide encoded by rhaE is 861 amino acids (aa) long and has a calculated molecular mass of 95205 Da. This value is in excellent agreement with the estimated molecular mass of the deglycosylated form of the purified α-L-rhamnosidase. The glycosylated form had a molecular mass of 102 kDa of which 7% was contributed by carbohydrates . Intriguingly, while the A. nidulans α-L-rhamnosidase activity was detected and purified from the culture medium, the predicted RhaE protein appears to lack an N-terminal signal peptide (SignalP probability 0.081), suggesting that secretion of this enzyme may occur through a non-classical pathway . In this regard, subcellular localization prediction using the SecretomeP program supports (NN/SecP score 0.608) this possibility.
The crystal structure of Bacillus sp. GL1 α-L-rhamnosidase RhaB has been resolved, and mutational studies have shown that four acidic residues (D567, E572, D579 and E841) are crucial for catalysis and/or substrate binding . All four residues (D458, E464, D471 and E737) are conserved in the A. nidulans RhaE protein (Additional file 3: Figure S2) and are hence candidates for roles of functional importance.
Phylogenetic relationships between the A. nidulans RhaE and class A bacterial α-L-rhamnosidases
Conservation of RhaE among fungi
Selected fungal homologs of the A. nidulans AN7151/RhaE rhamnosidase
% Identity/% Similarity/
Aligned amino acids
Functional expression of A. nidulans RhaE α-L-rhamnosidase in S. cerevisiae
Location of RhaE rhamnosidase activity in recombinant S. cerevisiae
Total activity (U ml-1)
% Cell wall
15.1 ± 0.4
0.6 ± 0.02
90.9 ± 0.5
6.0 ± 0.3
3.1 ± 0.2
22.9 ± 0.1
1.2 ± 0.1
82.9 ± 1.9
11.2 ± 1.2
5.9 ± 0.7
23.0 ± 0.4
1.4 ± 0.3
82.9 ± 2.3
10.7 ± 1.5
6.4 ± 0.9
Rhamnose induction of A. nidulans α-L-rhamnosidase gene expression is subject to carbon catabolite repression independent of CreA
In the derepressed creA d 30 strain (Figure 4A) induction of rhaE and rhaA likewise occurred within 1 h of transfer but transcript accumulation was considerably greater than in the wild-type. Contrary to the wild-type, the level of rhaE remained stable for at least 6 h after transfer. Interestingly, under inducing-repressing conditions (i.e. 1% w/v rhamnose + 1% w/v glucose), expression of rhaE was totally repressed, whilst a low transient expression of rhaA was observed 1 h after transfer. That glucose repressed the expression of rhaE and rhaA in both creA+ and creA d 30 genetic backgrounds indicate the lack of a role for CreA in glucose repression of these genes. Moreover, the creA d 30 mutation did not override the need for rhamnose for induction since transcripts were not observed in mycelia grown in 0.1% w/v D-fructose. Interestingly, in the creA derepressed mutant the transcript levels of rhaE and rhaA under inducing (1% w/v rhamnose) conditions were considerably greater than those seen in the wild-type indicating that some derepression occurs when functional CreA is absent and hence suggesting a role for CreA in rhaE and rhaA expression under inducing conditions. The presence of putative CreA binding sites in the rhaA and rhaE promoters suggesting direct repression by CreA under certain growth conditions.
To confirm the results with the creA d 30 mutant, we also studied the expression of rhaA in a creA null mutant (strain creA Δ4). Figure 4B shows that glucose repression of rhaA expression was not relieved by the creA Δ4 mutation, strongly indicating the absence of second-site mutations that could have contributed to the repressed phenotype of the creA d 30 strain, and thus leads weight to the hypothesis of glucose repression of the rha genes by a CreA-independent mechanism.
In filamentous fungi numerous genes encoding plant cell wall degrading enzymes have been shown to be subjected to CCR regulated by CreA/Cre1 ( and references therein) whereas there are few indications for the existence of CreA-independent mechanisms. Comparison of the levels of expression of reporter constructs in both creA+ and creA d 30 backgrounds suggested the existence of both CreA-dependent and CreA-independent mechanisms of CCR regulating A. nidulans xylanolytic genes [21, 28]. The occurrence in A. nidulans of a CCR mechanism independent of CreA has also been suggested for the pectinolytic gene pelA. The regulation of the rhaA and rhaE genes shows similarities to that seen for pelA in a derepressed strain (creA204) in that the transcripts accumulated to higher levels than in the wild-type when grown under inducing conditions (1% w/v polygalacturonic acid) while glucose repression was not relieved by the loss-of-function creA204 mutation. It is possible that the same CreA-independent mechanism regulates these different systems.
Effect of other carbon sources on α-L-rhamnosidase gene induction
Our previous results studying α-L-rhamnosidase production  coincide with the current data from northern analyses (Figures 4 and 5) and clearly show that CreA is not solely responsible for CCR of rhaE and rhaA gene expression, implying that α-L-rhamnosidase genes could be regulated via another repressor(s). It is possible for such a regulator to act directly on α-L-rhamnosidase gene promoters and/or indirectly by repression of the gene(s) encoding rhamnose permeases, rhamnose catabolic enzymes and/or rhamnose pathway specific activator(s). In S. cerevisiae it has been shown that glucose repression is mediated in part by the CreA related protein Mig1 and by two homologs (Mig2 and Mig3) which share almost identical zinc fingers and bind similar sites with different affinities [32, 33]. In A. nidulans and other filamentous fungi only one carbon catabolite repressor CreA has been identified. BLASTP searches using the CreA protein sequence or the sequence of its two zinc fingers failed to find any clear alternative candidate within the zinc-finger family.
Glucose repression of rhaA and rhaE correlates with the lack of uptake of rhamnose
In the mixed sugar cultures glucose was consumed preferentially compared to rhamnose in the wild-type strain and no α-L-rhamnosidase activity was detected (Figure 6C). Hence, a key event in the repression of α-L-rhamnosidase synthesis appears to be the lack of uptake of rhamnose. In concordance with the northern results (see above), CreA does not play a major role in this mechanism of repression since the uptake of rhamnose in the creA d 30 strain was blocked by the presence of glucose, rhamnose only being taken up after the exhaustion of glucose, only after which α-L-rhamnosidase activity could be detected (Figure 6D).
Taken together, these results provide strong indications for the existence of a CreA-independent mechanism of 'inducer exclusion' by which the expression of α-L-rhamnosidase genes, and possibly other genes induced by rhamnose, is regulated. Whether rhamnose permeases are repressed by glucose at the transcriptional level by a factor other than CreA, or controlled post-transcriptionally (e.g. catabolite inactivation of the proteins effecting rhamnose uptake) or whether the rhamnose transport system(s) are competed by glucose - and possibly other carbon sources - is not known at present.
By way of antecedents, glucose repression of the A. nidulans proline catabolic cluster genes prnD and prnC is known to result from inducer exclusion since only the transcription of the proline permease gene (prnB) is directly repressed by CreA . CreA-independent mechanisms of inducer exclusion have also been documented, an example of which is the phenylacetic acid (PhAc) uptake system: in the presence of glucose and PhAc, the PhAc transport system is absent in the wild-type as well as in the creA d 30 mutant . Finally, inducer exclusion arising from competitive inhibition of D-xylose uptake by the structurally related sugar glucose has also been suggested to explain at least part of the glucose repression of the xylanolytic gene xlnA[28, 36]. With regard to the later however, two pieces of data cast doubt on competitive inhibition of inducer uptake as the means of effecting inducer exclusion of rhamnose. Firstly, α-L-rhamnosidase expression was completely repressed by both D-sorbitol and ethanol (Figure 5), carbon sources that are structurally distinct and unrelated to rhamnose. Secondly, the transient rhaA response to a mixture of glucose and rhamnose (Figure 4A) suggests that some rhamnose is taken up by the creA d 30 mycelia immediately after medium transfer despite the presence of equimolar amounts of glucose; in the alc system the response to induction has been shown to be much faster than the establishment of CCR .
Repression by ethanol does not result from the lack of rhamnose transport
Using A. nidulans as a model system, we show for the first time that the production of α-L-rhamnosidases in eukaryotes is controlled at the transcriptional level by the carbon source (i.e. induction by L-rhamnose, and repression by glucose and other carbon sources). Interestingly, two loss-of-function mutations in the creA gene, which encodes the carbon catabolite repression (CCR) factor CreA, resulted in overproduction of rhaA and rhaE mRNAs by cells grown in medium containing L-rhamnose as sole carbon source, but had little or no effect on rhaA and rhaE mRNA levels in cells grown with glucose plus L-rhamnose as carbon source. We also show that the CreA-independent mechanism of glucose repression correlates with the absence of L-rhamnose uptake. A. nidulans α-L-rhamnosidase encoding genes could thus serve as a prototype for fungal genes regulated by a novel inducer exclusion, CreA-independent, mechanism of CCR.
We have also identified the gene (rhaE) coding for an α-L-rhamnosidase of oenological relevance that we characterized previously. Phylogenetic analysis shows that this enzyme is the first eukaryotic α-L-rhamnosidase found to be closely related to bacterial rhamnosidases of class A (i.e. Thermomicrobia sp. RhmA, Bacillus sp. RhaA, Clostridium stecolarium RamA and Lactobacillus acidophilus RamA) rather than α-L-rhamnosidases from other fungi. The identification of rhaE and characterization of its regulation make it possible to design strategies to overproduce the encoded enzyme for industrial applications, as well as identify homologs in other fungi.
Strains and growth conditions
Escherichia coli strain DH5α [endA1, hsdR17, gyrA96, thi-1, relA1, supE44, recA1, ΔlacU169 (Φ80 lacZΔM15)]  was used as the recipient strain for cloning experiments and plasmid amplification. The S. cerevisiae wine strain T73-4 (ura3::470/ura3::470)  was used for functional expression of plasmids bearing the TDH3p::rha::PGK1t expression cassettes. The A. nidulans wild-type (biA1; Glasgow GO51), creA d 30 and ΔcreA (creA-Δ4, pantoB100. N.B. offspring of an outcross of the original mutant described by Shroff et al. ; M. Flipphi, unpublished data) strains were used.
E. coli was grown in LB medium (1% w/v tryptone, 0.5% w/v yeast extract, 1% w/v NaCl) with or without 100 μg ml-1 ampicillin. S. cerevisiae strains were grown in YPD-rich medium (1% w/v yeast extract, 2% w/v bacteriological peptone, 2% w/v glucose) or SD-minimal medium (0.17% w/v yeast nitrogen base without amino acids [Difco Laboratories, Detroit, USA], 2% w/v glucose, 0.5% w/v ammonium sulphate, with or without 20 mg l-1 uracil). All media used for A. nidulans strains were based on appropriately supplemented medium [40, 42] containing 1% w/v of carbon source, unless otherwise specified. For creA mutants phosphate was included in the sporulation plates . For solid media 1.5% w/v agar was added.
For transfer experiments mycelial biomass was generated from spores inoculated in minimal medium (MM) supplemented with 5 mM urea as nitrogen source, to which 0.1% w/v D-fructose was added as the sole carbon source. After ~18 h grown at 37°C with orbital shaking at 200 rpm, mycelia were harvested, washed with MM without carbon source and transferred. Induction medium was prepared by substituting D-fructose with rhamnose at 1% w/v, and induction-repression medium by substituting D-fructose with rhamnose plus glucose (1% w/v each). Other carbon sources were added instead of glucose at equimolar amounts.
Sensitivity to 2-DOG was tested by spotting the same number of spores (105 in 3 μl) on plates containing 5 mM urea as nitrogen source, 50 μg ml-1 of the toxic glucose analogue 2-DOG and different concentrations of glucose or rhamnose. Growth was monitored after incubation for 3 days at 37°C.
Production of α-L-rhamnosidase in S. cerevisiae was determined under the following growth conditions: the selected transformants were precultured overnight in SD medium lacking uracil, and cells were then used to inoculate (106 cells ml-1) 50-ml of complete (YPD) medium in 250-ml flasks. Yeast cultures were grown with continuous shaking (200 rpm) at 30°C. Recombinant α-L-rhamnosidase cellular location was determined as described .
DNA manipulations and transformations
E. coli plasmid isolation and general DNA manipulations were performed following standard protocols . Transformation of the T73 strains was done using lithium acetate to permeabilize the cells as previously described [40, 45]. Transformants were selected and maintained on SD plates without uracil. Restriction enzymes, Expand High Fidelity system, and T4 DNA ligase were purchased from Roche Diagnostics and used as recommended by the manufacturer. DNA and cDNA sequencing was carried out using the BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, USA) and the ABI PRISM 310 Genetic Analyzer (Applied Biosystems, USA) at the DNA Sequencing Service of the University of Valencia. Chromatograms were analysed using the program Chromas LITE 2.01. Oligonucleotides used in the present study are listed in Additional file 1: Table S2.
RNA isolation, northern blot analysis and RT-PCR
Total RNA was isolated from powdered mycelia using RNA Plus (Qbiogene, USA) following the manufacturer's instructions. Northern gels were loaded with 15 μg of glyoxylated total RNA per track essentially as described [36, 39]. Membranes (Hybond-N, Amersham Biosciences) were stained with 0.03% w/v methylene blue as a loading control. Gene specific fragments corresponding to rhaE, rhaA and gpdA (350 bp, 385 bp and 610 bp, respectively) were generated by PCR (oligonucleotide pairs: Rha122Ndir_Rha122Nrev; Rha35Ndir_Rha35STOP; gpdAu_gpdAd) and used as templates to generate 32P-dCTP radiolabeled probes using the High Prime system (Roche).
Reverse transcription was performed using 1 μg of total RNA, an oligo (dT)18 anchor primer and the M-MLV reverse transcriptase (USB). Total RNA was previously treated with RNase-free DNase (Roche) for 30 min at 37°C and the DNase was heat-inactivated afterwards. Amplification of the target cDNA by PCR was performed using internal primers (see below).
Heterologous expression of the A. nidulans rhaE gene
To demonstrate the presence of a full-length α-L-rhamnosidase structural gene, the S. cerevisiae wine yeast T73-4 was used for its heterologous expression. The open reading frame (ORF) of rhaE (GenBank accession no. FR873475) was amplified by PCR from A. nidulans cDNA using the primers Rha122dir and Rha122rev and subcloned into pGEM-T-Easy generating pGEM-Rha122. The resulting fragment was ligated between the S. cerevisiae glyceraldehyde-3-phosphate dehydrogenase gene promoter (TDH3p) and the phosphoglycerate kinase terminator (PGK1t) in the high-copy-number shuttle vector YEplac195  in two subcloning steps. First, a 434 bp Pst I-Sal I fragment from pGEM-Rha122 was ligated into the Pst I-Sal I restriction sites of YEp195T that contains the phosphoglycerate kinase terminator and polyadenylation signals (PGK1t) (isolated from pG-1; ); oligonucleotides PGKt-1 and PGKt-2 and the selectable URA3 gene, yielding YEp195T-R122. To complete the expression cassette, the TDH3pHin dIII-Afl III fragment (isolated from pR31; ) and the rest of the rha122 ORF (as a 2154 bp BspH I-Pst I fragment recovered from pGEM-Rha122) were cloned into Hin dIII-Pst I restricted YEp195T-R122 to generate YEplac195-Rha122. Fragments obtained by PCR were checked by sequencing to ensure the absence of PCR-induced mutations. Transformants were selected at 30°C on uracil-deficient media. Three of the resultant colonies (YR150-YR153) were randomly picked and selected for further studies.
α-L-Rhamnosidase activity was measured using an assay based on the hydrolysis of p-nitrophenyl α-L-rhamnopyranoside (p NPR). Release of p-nitrophenol was measured spectrophotometrically at 400 nm. The assay was performed for 15 min at 50°C in a final volume of 250 μl using 1.4 mM substrate in 250 mM McIlvaine buffer (citrate-phosphate buffer) pH 4.0, essentially as described . One unit (U) of enzyme activity was defined as the amount of enzyme that releases 1 μmol of p-nitrophenol (from p NPR) per minute in the same conditions. Protein concentrations were determined by the Bradford assay  using BSA as standard. SD or agar plates supplemented with 40 μM MUR and 1 mM McIlvaine buffer pH 4.0 were used for plate assays of α-L-rhamnosidase activities. After incubation, hydrolysis of MUR was assessed under uv light. Chloroform permeabilization of yeast cells was carried out following the method of Herman and Halvorson .
Protein production, purification and sequence
Protein purification was carried out following a similar protocol to that previously described . Polypeptides remaining in the α-L-rhamnosidase active pool after the final purification step were resolved by SDS-PAGE, manually excised and stored at 4°C in ultrapure water. Protein sequence analyses were performed at the Centro Nacional de Investigaciones Cardiovasculares (CNIC), CSIC, Madrid, Spain. Polypeptides were digested automatically using a Proteineer DP protein digestion station (Bruker-Daltonics, Bremen, Germany) following the protocol described by Schevchenko et al.  with minor variations. For peptide mass fingerprinting and LIFT-TOF/TOF spectra acquisition  an aliquot of α-cyano-4 hydroxycinnamic acid in 33% v/v aqueous acetonitrile and 0.1% v/v trifluoroacetic acid was mixed with an aliquot of the above digestion solution and the mixture was deposited onto an AnchorChip MALDI probe (Bruker-Daltonics). MALDI-mass spectra were generated using an Ultraflex MALDI TOF/TOF system (Bruker-Daltonics). MALDI-MS and MS/MS data were combined using the BioTools program (Bruker-Daltonics) to search the NCBInr (nonredundant) and SwissProt databases using Mascot software (Matrix Science).
Sugars present in the A. nidulans culture filtrates were quantified by high-performance anion-exchange chromatography (HPAEC) using a Dionex (DX500 or ICS 3000) system (Sunnyvale, CA, USA) equipped with a CarboPac PA-1 column and a pulse electrochemical detection unit in the pulsed amperometric detection mode. Separation was performed by isocratic elution with 16 mM NaOH at a flow rate of 1 ml min-1 and the data were analyzed using the Peaknet or the Chromeleon software packages (Dionex). Calibration curves were made using standard solutions of sugars of final concentrations of 0, 1, 2, 5, 10 and 25 mg l-1. Ethanol concentrations were measured by an enzymatic method using a kit (Roche).
Protein sequences were obtained using BLAST programs  at NCBI (http://www.ncbi.nlm.nih.gov/sutils/genom_table.cgi). Retrieved sequences were subsequently used in additional searches against the A. nidulans database at the Broad Institute of MIT and Harvard (http://www.broad.mit.edu/annotation/fgi/). Other bioinformatic tools and software packages were provided by the ExPASy Proteomics Server (http://www.expasy.org/): DNA alignments were done using ClustalW ; protein localization was predicted using SignalP 4.0 (http://www.cbs.dtu.dk/services/SignalP/; ) or SecretomeP 2.0 (http://www.cbs.dtu.dk/services/SecretomeP/; ) using eukaryote or mammalian networks respectively.
Nucleotide sequence accession number
The A. nidulans AN7151 (rhaE) cDNA/mRNA sequence has been deposited in the EMBL database under the accession number FR873475.
Carbon catabolite repression
Matrix-assisted laser desorption/ionization time-of-flight
- p NPR p:
Open reading frame
Reverse transcription-polymerase chain reaction
Sodium dodecyl sulfate-polyacrylamide gel electrophoresis.
This work was supported by the Spanish Ministerio de Ciencia e Innovación/FEDER [grant numbers AGL2002-01906, BIO2008-00228 and CSD2007-0063/Consolider-Ingenio]. J.A.T., M.F. and E.P. were the recipients of a FPI predoctoral fellowship from the Comisión Interministerial de Ciencia y Tecnología, a Ramón y Cajal contract [RYC2004-003005] and a Juan de la Cierva [JCI2007-123/733] contract respectively. The group also participates in the EC COST Action FA0907_BIOFLAVOUR.
We wish to thank Pilar Miró and Claudia Palotti for preliminary RT-PCR experiments, Emilio Camafeita for performing MALDI-TOF assays, Julia Marín for assistance with the Dionex ICS 3000 system, Andrew MacCabe for critical revision of the manuscript prior to submission and to an anonymous referee for helpful suggestions.
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