Characterization of a novel sugar transporter involved in sugarcane bagasse degradation in Trichoderma reesei
Trichoderma reesei is a saprophytic fungus implicated in the degradation of polysaccharides present in the cell wall of plants. T. reesei has been recognized as the most important industrial fungus that secretes and produces cellulase enzymes that are employed in the production of second generation bioethanol. A few of the molecular mechanisms involved in the process of biomass deconstruction by T. reesei; in particular, the effect of sugar transporters and induction of xylanases and cellulases expression are yet to be known.
In our study, we characterized a novel sugar transporter, which was previously identified by our group through in silico analysis of RNA-seq data. The novel T. reesei 69957-sugar transport system (Tr69957) is capable of transporting xylose, mannose, and cellobiose using a T. reesei 69957-sugar transport system in Saccharomyces cerevisiae. The deletion of Tr69957 in T. reesei affected the fungal growth and biomass accumulation, and the sugar uptake in the presence of mannose, cellobiose, and xylose. Molecular docking studies revealed that Tr69957 shows reduced protein–ligand binding energy for interactions towards disaccharides in comparison with monosaccharides. Furthermore, the deletion of Tr69957 affected the gene expression of cellobiohydrolases (cel7a and cel6a), β-glucosidases (cel3a and cel1a), and xylanases (xyn1 and xyn2) in the cultures of parental and mutant strains in the presence of cellobiose and sugarcane bagasse (SCB).
The transporter Tr69957 of T. reesei can transport cellobiose, xylose, and mannose, and can affect the expression of a few genes encoding enzymes, such as cellulases and xylanases, in the presence of SCB. We showed for the first time that a filamentous fungus (T. reesei) contains a potential mannose transporter that may be involved in the degradation of cellulose.
KeywordsTrichoderma reesei Sugarcane bagasse Cellulase Sugar transporter Docking Saccharomyces cerevisiae Biofuel
The fungus Trichoderma reesei is one of the most studied microorganisms and is known for its ability to degrade lignocellulose . T. reesei has an efficient degradation system for major polysaccharides present in the plant cell wall, and thus, it is commercially exploited for its effective production and secretion of a wide range of cellulases, hemicellulases, and other Carbohydrate-Active Enzymes (CAZymes) [1, 2]. The expression of CAZymes-encoding genes occurs in a carbon-source-dependent manner and may be regulated by several transcription factors and small molecules that mediate the control of gene expression . Moreover, a wide diversity of mono- and disaccharides is naturally found during biomass hydrolysis, being able to act as regulatory molecules [1, 4]. Accordingly, a complex carbon source such as sugarcane bagasse (SCB), which is the major residue form the Brazilian agroindustry and constituted by cellulose (40–50%), hemicellulose (25–35%), and lignin (15–20%), can be efficiently degraded by fungal enzymes to release key regulatory molecules that might in turn activate the expression of genes to improve the sensing of different carbon sources and secretion of cellulolytic enzymes [5, 6].
The access to sugars released from the complex polysaccharides is dependent on the ability of this fungus to secrete high amounts of a complex mix of hydrolytic enzymes, and also the presence of a large array of sugar transporters that are capable of effectively transporting the constituent sugars into the cell . Therefore, the transporters are essential in the utilization of lignocellulose by the fungus, promoting the transport of molecules that signal environmental changes to the cell and, consequently, controlling the CAZymes-encoding gene expression . One of the most relevant sugar transporters families in filamentous fungi is the Major Facilitator Superfamily (MFS) . In the T. reesei genome, approximately 164 predicted MFS transporters have been annotated . However, the involvement of these transporters in sugar uptake is still unclear, and only a few sugar transporters have been functionally characterized in filamentous fungi. Interestingly, the available data show that MFS transporters can recognize and transport more than one type of sugar such as xylose and cellobiose into the cell . For instance, T. reesei STP1 is involved in glucose and cellobiose uptake . Moreover, the A. nidulans transporter XtrD was shown to be able to transport several other monosaccharides, in addition to xylose and glucose . After the uptake, these sugars have been shown to play an important role in metabolic signaling in the presence of cellulose . Despite the progress made in studies related to cellulases production, the influence of these transporters on cellulose degradation from various carbon sources remains unknown.
Our group has demonstrated new components involved in cellulose degradation including some transporters. A few of them that were identified in the transcriptome analysis were specifically induced by cellulose, sophorose, and glucose, whereas the MFS family was overrepresented in our analysis in the presence of different carbon sources . Therefore, the aim of this study was to characterize one of the T. reesei transporters that was initially identified by RNA-seq and in silico analysis, and to understand its involvement in SCB degradation. We have characterized a T. reesei transporter with potential role in the transport of monosaccharides and disaccharides. The characterization of MFS Tr69957 showed that this transporter can better enhance the efficiency of cellobiose, xylose, and mannose transport as compared to that by T. reesei mutant strain. In addition, with respect to the cellulases production, it was observed that the deletion of MFS Tr69957 leads to decreased expression of cellulase and xylanase genes as compared to that in the parental strain when both the strains were grown on SCB. Furthermore, for the first time, our results showed that T. reesei possesses a potential mannose transporter, which may be involved in the degradation of cellulose.
Materials and methods
Fungal strains, media, and culture methods
The fungal strains used in this study are listed in Additional file 1. The S. cerevisiae strain EBY.VW4000  is a hexose-null mutant and it was used for the initial functional analysis of the Tr69957 transporter. The EBY.VW4000 and its mutants (EBY.VW4000 +pRH195m +pRH274 and Tr69957::GFP EBY.VW4000) were grown at 30 °C in broth or on solid yeast nitrogen base (YNB) medium (which contained 20 g/L agar, 7 g/L YNB without amino acids and supplemented with 0.05 g/L histidine, 0.1 g/L leucine, 0.1 g/L tryptophan, and 0.1 g/L uracil). Selection of transformants was done on the YNB medium lacking tryptophan and uracil. All the reagents were obtained from Sigma Aldrich (St. Louis, MO, USA). The yeast S. cerevisiae SC9721 strain (MATα his3-Δ200 URA3-52 leu2Δ1 lys2Δ202 trp1Δ63) (Fungal Genetic Stock Center—www.fgsc.net) was used to generate the deletion cassette by homologous recombination. This strain was grown at 30 °C in broth or on solid YNB medium (which contains 20 g/L agar, 7 g/L YNB without amino acids and supplemented with 0.05 g/L histidine, 0.1 g/L lysine, 0.1 g/L leucine, 0.1 g/L tryptophan, 0.1 g/L uridine, and 0.1 g/L uracil), along with 2% (w/v) glucose. The strain QM6a∆tmus53∆Pyr4  was used as a parental strain to construct the ∆69957 T. reesei mutant strain. This strain was obtained from the Institute of Chemical Engineering & Technical Biosciences of Vienna University of Technology, TU Vienna, Austria. The strain was maintained at 4 °C on MEX medium [3% (w/v) malt extract and 2% (w/v) agar–agar], which was supplemented with 5 mM uridine in the case of the pyr4 deletion strain. To perform gene expression assays, 106 cells/mL of each specific strain was inoculated into 25 mL of Mandels–Andreotti medium  (MAM) or Minimal Medium (MM) which contains 1% (w/v) of the selected sugar as the sole carbon source.
Conditions for maintenance of cultures
Trichoderma reesei strains QM6a∆tmus53∆Pyr4  and ∆69957 were grown in MEX medium at 28 °C for a period of 7 days. In all the experiments with SCB, the parental and Δ69957 mutant strains were initially grown in 1% (w/v) glycerol for 24 and 48 h, respectively, and then transferred to a medium containing SCB. For this purpose, 106 cells/mL of each specific strain was inoculated into 25 mL of MAM  containing 1% glycerol, and after 24 h (parental strain), the mycelium was transferred into 25 mL of MAM containing 1% of exploded sugarcane bagasse (ESB). Concerning the Δ69957 mutant strain, the mycelium was initially grown in 1% (w/v) glycerol for 48 h to achieve an initial mycelial biomass similar to the parental strain, and then, the mycelium was transferred into 25 mL of MAM containing 1% ESB. The ESB was prepared as described previously in the corresponding Ref. . Briefly, SCB in natura was treated with 14 kg/cm2 water steam, thoroughly washed with distilled water until the reducing sugars were not detected by dinitrosalicylic acid (DNS) , and dried at 40 °C for several days. SCB was kindly donated by Nardini Agroindustrial Ltd, Vista Alegre do Alto, São Paulo, Brazil.
The fungal cultures were incubated at 28 °C for 6, 24, and 48 h in an orbital shaker (200 rpm) for all the SCB experiments. All experiments were performed in three biological replicates. The resultant mycelia were collected by filtration, frozen in liquid nitrogen, and stored at − 80 °C for RNA extraction.
Construction of the ∆69957 mutant strain
The deletion of Tr69957 gene in T. reesei was performed as described previously by Schuster et al. . To construct the deletion cassette, the orotidine-5′-phosphate decarboxylase gene of Aspergillus niger (pyrG) was used as a selection marker. The flanking sequences of Tr69957 were obtained from the T. reesei genome database (http://genome.jgi.doe.gov/Trire2/Trire2.home.html). The marker gene and its respective 5′ and 3′ flanking sequences were amplified using the primers as described in Additional file 2. The primers were designed and analyzed with the help of OligoAnalyzer tool (https://eu.idtdna.com/calc/analyzer). To enable yeast-mediated recombination of the deletion cassette, we used the external 5′-UTR forward and 3′-UTR reverse primers containing cohesive ends with the vector pRS426 [19, 20] and the internal 5′-UTR reverse and 3′-UTR forward primers containing cohesive ends with the 5′ and 3′ sequence of the pyrG gene (Additional file 2). The 50-μL reaction mixture contained 1 U Platinum Taq DNA Polymerase High Fidelity (Thermo Scientific), 1 × High Fidelity PCR Buffer, 0.2 mM dNTPs, 0.3 µM forward and reverse primers, 1 µL T. reesei QM9414 and A. niger genomic DNA (150 ng/µL) as a template, and nuclease-free water. The PCR fragments were purified using a QIAquick PCR Purification Kit (Qiagen).
To perform yeast-mediated recombination, we used the yeast shuttle vector pRS426 (ampR lacZ URA3) [19, 20], which was digested with EcoRI and XhoI (Thermo Scientific), and purified with the QIAquick PCR Purification Kit (Qiagen). Yeast transformation was performed as described previously in the corresponding Ref. [21, 22, 23]. We prepared an overnight culture (200 rpm, 30 °C) of the yeast S. cerevisiae SC9721 strain (MATα his3-Δ200 URA3-52 leu2Δ1 lys2Δ202 trp1Δ63) obtained from Fungal Genetic Stock Center. Then, 1 mL of this overnight culture was added to 50 mL of fresh YPD medium (1% yeast extract, 2% peptone, 1% glucose: all of them were obtained from Sigma Aldrich) and incubated at 30 °C until the attainment of OD600 = 1. Thereafter, the cells were centrifuged and re-suspended in 100 mM lithium acetate for transformation. To this purpose, equimolar quantities of 5′ and 3′ flanking regions of pyrG gene and the digested pRS426 product were mixed and used for yeast transformation by the lithium acetate method . S. cerevisiae SC9721 transformants were selected for their ability to grow on YPD medium supplemented with lysine, histidine, leucine, and tryptophan, without uracil. S. cerevisiae genomic DNA was extracted using a previously described protocol [25, 26]. The deletion cassette of Tr69957 was PCR amplified using TaKaRa Ex Taq DNA Polymerase (Clontech) using Tr69957_pRS426_5 forward and Tr69957_pRS426_3 reverse primer (Additional file 2).
The selected transformants were analyzed by Southern hybridization using a previously described method , to demonstrate that the transformation cassettes had homologously integrated at the targeted T. reesei QM6aΔtmus53Δpyr4 loci (Additional file 3). To perform this analysis, 25 µg of total genomic DNA from the parental and mutant strains were digested with EcoRV (Fermentas) overnight, and then, this digested DNA was transferred onto GE Healthcare Amersham Hybond-N + membranes (GE). The probe was generated from the PCR-amplified fragment using Tr69957_pRS426_5fw and Tr69957_pyrG_5rv (Additional file 2) and labeled using a digoxigenin (DIG) DNA labeling kit (Roche, Mannheim, Germany) by following the manufacturer’s instructions. Labeling, hybridization, and immunological detection were performed using a non-radioactive labeling and immunological detection kit with CDP-Star as the chemiluminescent substrate (Roche, Mannheim, Germany), by following the methods that were previously described .
Measurement of dry weight
A total of 106 cells/mL of T. reesei parental or Δ69957 mutant strains were inoculated into 25 mL of MAM supplemented with 1% (w/v) glycerol. After 24 h, the parental strain mycelium was transferred into 25 mL of MAM containing 1% (w/v) xylose, cellobiose, or mannose. The mutant strain was grown for 48 h in MAM containing 1% (w/v) glycerol to achieve an initial mycelial biomass similar to the parental strain. After 6, 24, and 48 h, mycelia were harvested by filtration, dried by incubation at 70 °C for 3 h and subsequently weighed. The experiments were conducted in triplicates for each sample.
Determination of the extracellular sugar concentrations
The uptake of sugars was measured by HPLC analyses. A total of 106 cells/mL T. reesei parental and Δ69957 mutant strains were inoculated into 25 mL of MAM supplemented with 1% (w/v) glycerol. After 24 h, the parental strain mycelium was transferred into 25 mL of MAM containing 1% (w/v) or 30 mM of xylose, cellobiose, or mannose in the same culture, at 30 °C 200 rpm for 6, 24, and 48 h. The mutant strain was grown for 48 h in MAM containing 1% (w/v) glycerol to achieve an initial mycelial mass similar to that of the parental strain. S. cerevisiae Tr69957::GFP EBY.VW400 strain and EBY.VW4000 + pRH195m + pRH274 + pGH1 (control) were inoculated in 100 mL of YNB medium supplemented with 2% (w/v) maltose until they reached the exponential growth phase. Yeast cells were pelleted by centrifugation at 4000 rpm for 5 min, washed three times with 50-mL water, and re-suspended in water. Next, this cell suspension was inoculated (initial OD600 = 0.5) in 50-mL YNB-Trp-Ura-Leu medium without carbon source and then incubated at 30 °C for 3 h. Finally, this medium was supplemented with 1% (w/v) xylose, cellobiose, or mannose at 30 °C, 150 rpm for 144 h. At each timepoint, 2 mL of the culture were collected, centrifuged, and the supernatants were stored at − 80 °C. The amount of sugar in the supernatant at each timepoint was determined by ion chromatography (HPLC-Thermo Fisher-U3000), coupled with refractive index detector) Suplecogel C611 column (eluted with 5 mM H2SO4, at flow rate 0.5 mL/min and column temperature 60 °C) and Aminex HPX-87P column (eluted with H2O, at flow rate 0.5 mL/min and column temperature 85 °C).
Analysis of the effect of Tr69957 deletion on T. reesei growth in various carbon sources
To analyze the effect of the Tr69957 deletion on the growth of T. reesei in various carbon sources, phenotypic assays for the parental and mutant strains were performed by inoculating of 106 cells/mL on minimal media (MM) and potato dextrose agar (PDA) plates containing 1% of one of the following carbon sources: mannose, xylose, glucose, galactose, arabinose, raffinose, cellobiose, sophorose, lactose, xylitol, glycerol, fructose, or maltose . The experiment was performed in triplicates for each carbon source. The diameters of colonies were measured after 6 days.
Quantitative real-time PCR analysis
Trichoderma reesei mycelia were macerated and total RNA was extracted from each sample using TRIzol® RNA kit (Invitrogen Life Technologies, Carlsbad, CA, USA), according to the manufacturer’s instructions. RNA concentration was determined using a spectrophotometer at an optical density ratio of 260/280 nm, and RNA integrity was verified by electrophoresis in 1% agarose gels. To perform the expression analysis, initially, the total RNA (1 µg) from each sample was digested with DNase I (Fermentas) to remove genomic DNA. Then, cDNA synthesis was carried out using the RevertAid H Minus First Strand cDNA Synthesis kit (Waltham, Massachusetts, USA) according to the manufacturer’s instructions. Synthesized cDNA was diluted at 1:50 and used as a template for real-time PCR. Reactions were performed in the Bio-Rad CFX96™ using SsoFast™ EvaGreen® Supermix (Bio-Rad) for detection according to the manufacturer’s instructions. Each reaction mixture (10 µL) contained 5 µL SsoFast™ EvaGreen® Supermix (Bio-Rad), forward and reverse primers (500 nm each; Additional file 4), cDNA template, and nuclease-free water. PCR cycling conditions: 10 min at 95 °C (1 cycle), 10 s at 95 °C followed by 30 s at 60 °C (40 cycles), and a melting curve of 60–95 °C with an increment of 0.5 °C/10 s to check for primer dimers and nonspecific amplification. The transcript of the sar gene (encodes Sar1 GTPase from T. reesei) was used as an internal reference to normalize the amount of total RNA present in each reaction . To perform gene expression analysis in strains grown on SCB, cellobiose, mannose, and xylose, the expression levels of genes were calculated from the threshold cycle according to the 2−ΔCT method  relative to transcription levels of sar. The experiment was repeated three times for each sample. The results were analyzed using MeV v.4.6.1. Software and heat maps were constructed to assess the variety in the expression of genes among the strains under each indicated condition.
Construction of S. cerevisiae strain expressing T. reesei Tr69957
The construction of S. cerevisiae strain that expresses T. reesei Tr69957 was performed as described by dos Reis et al.  using the EBY.VW4000 yeast strain (Additional file 1). Briefly, the T. reesei Tr69957 ORF was PCR-amplified using cDNA obtained from the wild-type (WT) strain QM6A (Additional file 1) using specific primers 69957-F and 69957-R. To perform in vivo recombination, the plasmid pRH195 was linearized by double digestion with SpeI and SalI, originating the pRH195m (pRH195 without XKS1 gene). The GFP gene was PCR amplified from pCMC17apx plasmid using primers pRH195 GFP_CS_F-yeast and spacerGFP 5´R_pRH195-yeast. Furthermore, the linearized plasmid was co-transformed with the PCR-amplified sugar transporter and GFP fragments into the S. cerevisiae EBY.VW4000 strain, which already contained the pRH27412 and pGH1x plasmids. The pRH274 plasmid contains the xylulose kinase (XK), xylose reductase (XR), and xylose dehydrogenase (XDH) genes which encode enzymes of the xylose metabolic pathway while the pGH1 plasmid contains the β-glucosidase-encoding gene (gh1-1) from Neurospora crassa . The yeast transformation was performed using the lithium acetate method . Transformants were selected for tryptophan, leucine, and uridine prototrophy, and the yeast candidates were confirmed by PCR using the primers 69957-F and 69957-R. A list of all the primers used in this study can be accessed in Additional file 5.
Growth of S. cerevisiae strain on solid medium
Saccharomyces cerevisiae strains were inoculated in 50 mL YNB medium supplemented with 2% (w/v) maltose for 48 h at 30 °C, 200 rpm. Yeast cells were centrifuged at 4000 rpm for 5 min, washed three times with water, and re-suspended in water to a final concentration of 1.0 at OD600nm. A serial dilution of 1:10 of the yeast cells was done, and 5 μL of the cell suspensions were spotted on plates containing 1% (w/v) of specific carbon source. Plates were incubated at 30 °C for 120 h.
Saccharomyces cerevisiae EBY.VW400 strain containing the Tr69957 gene tagged with GFP was grown for 48 h in 0.5 mL of liquid YNB-Trp-Ura-Leu medium supplemented with 2% (w/v) maltose for 24 h at 30 °C in a well of 24-wells plate. Cells were washed with PBS and observed under a Carl Zeiss (Jena, Germany) microscope using the 100 × magnification oil immersion objective lens (EC Plan-Neofluar, NA 1.3) equipped with a 100-W HBO mercury lamp epifluorescence module. Phase contrast bright-field and fluorescent images were acquired with an AxioCam camera (Carl Zeiss), and images were processed using the AxioVision software version 3.1 and saved as TIFF files.
3-D structure prediction and molecular docking
The 3D model for Tr69957 was built using the I-TASSER online platform from the Yang Zhang’s Research Group (https://zhanglab.ccmb.med.umich.edu/I-TASSER/). To this purpose, an FASTA file containing the amino-acid sequence for the referred protein was obtained from the UniProt database (gene: TRIREDRAFT_69957) and submitted to the I-TASSER online server. The structure modeling approach used by this software is based on the sequence alignment to a protein template, which is identified by LOMETS, a method that selects the top ten alignments in a PDB library. The unaligned regions of the sequence are built through ab initio folding, by considering the lowest free energy states and minimized sterical clashes that are identified by SPICKER and TM-align, respectively, and the final models are built at an atomic level by REMO which optimizes the hydrogen-bonding profile. In addition, the I-TASSER online software also allows the prediction of protein biological functions, as it compares the designed models to different libraries of proteins with previously identified functions [34, 35].
The docking analysis was performed using the software iGEMDOCK v. 2.1, a Generic Evolutionary Method for molecular DOCKing, developed by Jinn-Moon Yang (http://gemdock.life.nctu.edu.tw/dock/igemdock.php). It computes the interaction between one or more ligands with the active site of the target protein through empirical scoring function and an evolutionary approach algorithm. It also provides post-analysis tools by k-means and hierarchical clustering methods from the docked poses and the protein–ligand properties, such as atom composition and energy function [36, 37, 38].
To perform the docking analysis, structure of all the ligands was downloaded from the PubChem database (https://www.ncbi.nlm.nih.gov/pccompound) in MOL2 format. [lactose (CID 6134), maltose (CID 6255), mannose (CID 18950), xylose (CID 644160), cellobiose (CID 10712), and fructose (CID 5984)]. The PDB file for the model was uploaded to the iGEMDOCK software along with all the ligands, and the docking was performed using standard settings, with a population size of 200 and a total of 70 generations. The post-docking parameters were analyzed and the best docked pose for each ligand was visualized by The PyMOL Molecular Graphics System, Version 188.8.131.52 Schrödinger, LLC (https://pymol.org/2/).
Structural characterization of the transporter Tr69957
Tr69957 allows the growth of S. cerevisiae on various carbon sources
In contrast, the expression of Tr69957 completely restored the consumption of cellobiose, xylose, and mannose after 24 h (mannose) and 36 h (cellobiose and xylose) of growth (Fig. 2c–e). Altogether, these results suggest that Tr69957 can act as a monosaccharide as well as a disaccharide transporter in the yeast S. cerevisiae.
Disruption of Tr69957 impairs the growth of T. reesei in the presence of monosaccharides and disaccharides
Trichoderma reesei Δ69957 strain was constructed by homologous recombination using QM6aΔtmus53Δpyr4 as the parental strain, whose non-homologous end joining pathway was disrupted . Southern blot analysis of EcoRV-digested chromosomal DNA (Additional file 3) using the terminator region of Tr69957 gene as a probe resulted in expected results in parental (3391 bp) as well as Δ69957 (6698 bp) mutant strains, respectively (Additional file 3).
Tr69957 presents lower protein–ligand free energy in interactions involving disaccharides than that in the monosaccharides
To understand the preference of sugars transported by Tr69957, we performed a docking analysis. The selection of the most adequate model relies on the confidence scores: C-score and TM-score. The C-score estimates the quality of the prediction, for which the higher the value, the higher is the confidence. The TM-score latter measures the structural similarity between the predicted model and the template used for its construction. The values > 0.5 demonstrate a correct topology, whereas values < 0.17 demonstrate a random similarity. RMSD also represents the similarity of the predicted structure to the template, although it may show a very high value due to local errors, even if the model is adequate. The three scores are highly correlated to one another.
Considering all the parameters provided by the I-TASSER platform, the chosen model for the Tr69957 was predicted based on the template 4ZWB.A [human glucose transporter GLUT3 (N45T mutant) with bound d-glucose, outward-occluded conformation], determined by Deng et al. . The predicted structure was considered adequate, since it presented a C-score of − 0.80, TM-score of 0.61 ± 0.14, and an RMSD of 9.3 ± 4.3.
Tr_69957 interactions with different sugars analyzed by docking based on the total free energy, the Van der Waals, hydrogen, and electrostatic interaction for each ligand
These results show that the Tr69957 sugar transporter is able to transport several types of carbohydrates, preferentially disaccharides, such as lactose, cellobiose, and maltose in which the molecules showed the lowest free energies, and thus, the highest binding affinity to the protein (Table 1). With respect to the monosaccharides, fructose (Fig. 4b), mannose (Fig. 4e), and xylose (Fig. 4f), even though these exhibited higher free energy than the disaccharides, they still possess adequate binding affinity, suggesting that the conformational changes the protein may suffer are adaptive to the distinct carbon sources in the environment (Table 1).
Disruption of Tr69957 Impairs the Fungal Biomass Accumulation and the Sugar Uptake
The early gene expression experiments performed to characterize the Tr69957 sugar transporter were done using SCB, a complex lignocellulosic biomass. Similar to other plant cell walls, SCB is mainly formed by two carbohydrate fractions (cellulose and hemicellulose) embedded in a lignin matrix. The hydrolysis of SCB releases a range of sugars, such as mannose, xylose, cellobiose, and fructose that can be used by the fungus for energy production. As demonstrated in Fig. 3a, b, the Δ69957 mutant strain showed an impaired growth in the presence of all these sugars released from SCB hydrolysis. In this way, for the next set of experiments for characterization of Tr69957, we selected three out of the four sugars that presented significant variations during the growth conditions of the mutant strain.
Tr69957 affects cellulolytic and hemicellulolytic gene expression in T. reesei
After 48 h of growth, the highest expression of Tr69957 was achieved in the presence of cellobiose. Under similar conditions, deletion of Tr69957 resulted in a drastic decrease in the expression of cel7a, cel6a, and cel3a in the mutant strain, whereas cel1a and xyn2 were less expressed in the parental QM6a (Fig. 7). In the presence of mannose and xylose, the transporter Tr69957 was less expressed in comparison with that in the other conditions. In both carbon sources, the cel1a was the most affected gene with the Tr69957 deletion, being more expressed in the parental QM6a when compared to the mutant strain after 24 h of cultivation (Fig. 7).
The growth in SCB showed the highest expression of Tr69957 among all the tested conditions, with maximum expression at 6 h of growth. In SCB, the expression of cel7a and cel6a was decreased in the mutant Δ69957 in comparison with the parental strain in the first few hours of growth. Interestingly, after 48 h, the deletion of Tr69957 resulted in increased expression of all the cellulolytic and hemicellulolytic genes analyzed in the mutant strain (Fig. 7). Figure 7 shows that cel1a and cel3a were significantly induced in ∆69957 in the presence of sugarcane bagasse after 24 and 48 h when compared to the WT strain in the same conditions. This result is in accordance with the assumption that the absence of Tr69957 promotes faster consumption of cellobiose due to the increased hydrolysis by β-glucosidases in the presence of mixture of carbon sources like mannose, cellobiose, and xylose, which also compose the sugarcane bagasse.
The fungus T. reesei, in the absence of simple sugars as carbon sources, secretes extracellular lignocellulolytic enzymes, which can degrade biomass through a natural process [1, 40]. Thereafter, the degraded simple sugars can be assimilated for cell metabolism. In this process, transporters are the key role players in T. reesei to sense and utilize sugars [7, 29]. Most transporters encoded by filamentous fungi have not yet been characterized. Therefore, studying the function of transporters will provide new insights to understand the sensing mechanism in T. reesei. This study will enable us to better understand the gene expression pattern of cellulolytic enzymes produced by this fungus, which can contribute to the performance of it in the bioethanol industry. In this study, we characterized a putative sugar transporter Tr69957 that was previously identified by our group using RNA-seq data, which is important for xylose, cellobiose, and mannose utilization in T. reesei. To the best of our knowledge, this is the first report of a potential mannose transporter and its involvement in the degradation process of cellulose in the filamentous fungus T. reesei.
For better demonstration of the phenomenon that Tr69957 is able to transport specific sugars, the S. cerevisiae strain EBY.VW4000  was used. The S. cerevisiae strain (EBY.VW4000) lacks the hexose transport activity due to the deletion of 20 hexose transporter genes and is unable to grow on glucose, fructose, mannose, or galactose as the sole carbon source. The hexose transport-deficient S. cerevisiae strain (EBY.VW4000) has been an important tool for characterizing new hexose transporters of other fungi, such as HXTB  and RhtA  from A. niger, and the TBHXT1  transporter from the ascomycete Tuber borchii. Using this S. cerevisiae strain, we can prevent interference from other sugar transporters that were already described in T. reesei. The yeast experiments suggest that Tr69957 has the capability of transporting a few sugars, including cellobiose, mannose, and xylose. Therefore, Tr69957 can transport more than one sugar, which is not surprising because the filamentous fungi are able to internalize a wide variety of mono- and oligosaccharides and it has already been shown that transporters expressed by them can often transport more than one type of sugar .
Our data showed that Tr69957 probably participated in the transport of cellobiose, mannose, xylose, lactose, galactose, and fructose in T. reesei, as △Tr69957 strain displayed growth defects on these carbon sources. However, the docking results showed that Tr69957 exhibits lower protein-binding energy in interactions involving disaccharides compared to the monosaccharides, suggesting a better orientation and affinity between these molecules.
The absence of transporter specificity can be explained by the similarity in the structures of some of the sugar molecules. Furthermore, some of these proteins can act as transporters as well as nutrient sensors . Substrate transport requires binding and subsequent conformational change. After binding of the substrate, MFS transporters go through a series of conformational changes . Many residues in MFS transport structures are involved in substrate uptake . Besides substrate binding and specific conformational changes, the transporter domains function as gates that influence the substrate specificity . Structurally, similar substrates can bind to the transporter; however, they cannot induce the conformational change, leading to inhibition of transport; for example, d-glucose can competitively inhibit d-xylose transporters as they share similarity in their structures . However, interesting exceptions have been discovered in few A. niger sugar transporters, which suggest that if the binding occurs without subsequent conformational change, then the alternative substrate will be transported across the membrane .
Conversely, the absence of specificity can be advantageous when fungi encounters complex lignocellulosic material, which contains multiple hexoses and pentoses . The fungi can exhibit differences and similarities in response to different lignocellulosic substrates [1, 50, 51].
Concomitantly, in a second instance, in response to early signaling, Tr69957-mediated cellulase expression and secretion of CAZymes could act by cleaving cellulose to release disaccharides, such as cellobiose, that in turn might get internalized promoting a late signaling response, increasing the expression of cellulases in the presence of cellulose (Fig. 8—red arrows). Furthermore, as observed in Fig. 7, in the presence of mannose, the expression of β-glucosidase is higher than that of other cellulases, indicating that mannose present in the environment might signal the expression of these enzymes, which act in the conversion of cellobiose to sophorose , thereby increasing the cellulase expression during the late signaling of Tr69957.
In this study, we characterized a cellobiose, mannose, and xylose transporter involved in SCB degradation in T. reesei. The study also suggests that the transporter is associated with early and late signaling in the presence of lignocellulosic biomass. Taken together, these data contribute to the studies addressing the mechanism of action by which T. reesei senses the cellulose signal. The present study explores the mechanism of sensing and transportation of sugars in T. reesei, which are important and relevant during the application of this fungus in bioethanol production.
The present study aimed to improve our understanding of the sugar transport systems, through characterization of a novel sugar transporter involved in the degradation of lignocellulosic biomass in T. reesei. In addition, this study will aid in understanding the influence of this transporter on metabolic signaling and induction of the cellulase genes, which will subsequently have effect on lignocellulose degradation.
Our results showed that the transporter Tr69957 of T. reesei can transport cellobiose, xylose, and mannose, and can affect the expression of a few genes encoding enzymes, such as cellulases and xylanases, in the presence of SCB. Moreover, our study is the first report that shows a potential role for a mannose transporter in the regulation of cellulase genes in T. reesei in the presence of SCB. These results suggest that Tr69957 can be important during the signaling of cellulase gene expression. These findings contribute to the understanding of the molecular mechanisms involved in the regulation of the processes of cellulolytic enzyme synthesis and signaling.
KMVN performed the experimental design, laboratory experiments, and drafted the manuscript. RGP, ACCA, and TF dos Reis performed laboratory experiments and drafted the manuscript. CBC performed 3D structure prediction and molecular docking, and drafted the manuscript. ACS and MSB performed laboratory experiments. FBRA performed 3D structure prediction. CGVR performed the experimental design with HPLC experiments. GHG performed the experimental design. RNS designed the project, supervised the research study, prepared/drafted the manuscript, and approved the final version to be published. All authors have read and approved the final manuscript.
We would like to thank the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) (Processes FAPESP 2015/09553-8) for supported this work. Dr. Eckardt Boles for providing the EBY.VW4000 yeast strain. We are grateful to the laboratory techniques Luciana Angolo Faria Rocha, Zuleica Aparecida Soares de Moraes and Silvia Helena Castrechini Brito.
The authors declare that they have no competing interests.
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This study needed no ethical approval and had no experimental research on humans.
This work was supported by the Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) (Processes FAPESP 2015/09553-8).
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