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0Nogueira et al. BMC Microbiology (2015) 15:195 DOI 10.1186/s12866-015-0536-z
^BMC Microbiology
RESEARCH ARTICLE
Open Access
Evidence of cAMP involvement in cellobiohydrolase expression and secretion by Trichoderma reesei in presence of the inducer sophorose
Karoline Maria Vieira Nogueira1, Mariana do Nascimento Costa1, Renato Graciano de Paula1, Flavia Costa Mendonga-Natividade2, Rafael Ricci-Azevedo2 and Roberto Nascimento Silva1*
CrossMark
Abstract
Background: The signaling second messenger cyclic AMP (cAMP) regulates many aspects of cellular function in all organisms. Previous studies have suggested a role for cAMP in the regulation of gene expression of cellulolytic enzymes in Trichoderma reesei (anamorph of Hypocrea jecorina).
Methods: The effects of cAMP in T. reesei were analyzed through both activity and expression of cellulase, intracellular cAMP level measurement, western blotting, indirect immunofluorescence and confocal microscopy. Results: To elucidate the involvement of cAMP in the cellulase expression, we analyzed the growth of the mutant strain Nacyi and its parental strain QM9414 in the presence of the inducers cellulose, cellobiose, lactose, or sophorose, and the repressor glucose. Our results indicated that cAMP regulates the expression of cellulase in a carbon source-dependent manner. The expression cel7a, and cel6a genes was higher in the presence of sophorose than in the presence of cellulose, lactose, cellobiose, or glucose. Moreover, intracellular levels of cAMP were up to four times higher in the presence of sophorose compared to other carbon sources. Concomitantly, our immunofluorescence microscopy and western blot data suggest that in the presence of sophorose, cAMP may regulate secretion of cellulolytic enzymes in T. reesei.
Conclusions: These results allow us to better understand the role of cAMP and expand our knowledge on the signal transduction pathways involved in the regulation of cellulase expression in T. reesei. Finally, our data may help develop new strategies to improve the expression of cel7a and cel6a genes, and therefore, favor their application in several biotechnology fields.
Keywords: Carbon source, Cellulases, Saprophytic fungus, Secondary messenger, Signaling pathways
Background
Trichoderma reesei (anamorph of Hypocrea jecorina) is a saprophytic fungus that has an efficient secretion system of cellulolytic proteins involved in the degradation of cell wall polysaccharides of plants. This fungus has an enormous ability to both produce and secrete cellulases. This makes it the most important industrial fungus for the production of these enzymes, which are used for several purposes including the production of bioethanol in the biofuel industry [1].
* Correspondence: rsilva@fmrp.usp.br
department of Biochemistry and Immunology, Ribeirâo Preto Medical School, University of Sao Paulo, 14049-900 Ribeirâo Preto, SP, Brazil Full list of author information is available at the end of the article
Bio Med Central
The cellulolytic system of this fungus consists of at least three different types of enzymes—i.e., exoglucanases (cello-biohydrolases EC 3.2.1.91), endoglucanases (EC 3.2.1.4), and P-glucosidases (EC 3.2.1.21) [2]—that act synergistically and are coordinately expressed in specific growing conditions [3, 4, 5].
In general, fungi belonging to the Trichoderma genus have adaptive abilities to colonize different environments. Their survival is ensured through efficient ways to detect cellulose in the environment and secrete various cellulases responsible for the degradation of insoluble substrates, transportation of soluble products via the cytoplasmic membrane, and assimilation of sugars. Furthermore, this
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fungus has the flexibility to respond to changes in the nutritional composition of the environment, and thus, is able to compete with other microorganisms [6]. Therefore, correct interpretation of environmental stimuli, using the available resources, ensures the success of this fungus in nature [7].
In response to an extracellular signal captured by a receptor, a signaling cascade is initiated, and this signal is transmitted via secondary messengers such as cyclic AMP (cAMP). The cAMP signaling pathway is a cascade that has crucial functions in all organisms and is highly conserved in fungi [7]. In fungi, this messenger is involved in stress response, sporulation, growth, virulence, mycoparasitism, carbon and lipid metabolism as well as other functions in response to extracellular signals [8-12]. It has been suggested that induction of cellulases in T. reesei is related to a signaling pathway involving a cAMP-dependent protein kinase, and that, in certain circumstances the presence of this second messenger can cause an overproduction of some cellulases [7, 13]. However, the biosynthesis of these cellulases is not only induced by cellulose, but also by cellobiose, 1,5-5-lactone celobiono (an analog of cellobiose), lactose and sophorose. On the other hand, readily metabolizable carbon sources such as glucose, fructose, or glycerol repress expression of cellulases [14].
The regulation of transcription of cellulolytic complexes has been extensively studied, and some transcription factors involved in this process have already been identified [15]. However, little is known about how signals are transmitted to these transcription factors. True inductors, receptors, and pathways involved in the transduction of these signals to specific transcription factors have not been identified yet [16]. Many of these factors are induced under the conditions for which they are necessary, and they are degraded once they have done their function. Therefore, it is reasonable to assume that the activity of these transcription factors is also regulated by modifications that occur in response to changes in fungal culture conditions [7].
This study aimed to elucidate the involvement of cAMP in the expression of cellulase genes cel7a and cel6a in T. reesei using different inducers (i.e., cellulose, sophorose, lactose, and cellobiose), and a repressor (i.e., glucose). Our results suggest that cAMP controls the expression of cellobiohydrolases only in the presence of the inducer sophorose and is potentially involved in the secretion process of cellulases.
Methods
Strains and growth conditions
T. reesei QM9414 (ATCC 26921) and mutant Aacyl [17] strains were obtained from the Institute of Molecular Biotechnology, Vienna, Austria. Strains were maintained in MEX medium [malt extract 3 % (w/v) and agar-agar 2 % (w/v)] at 4 °C. QM9414 and Aacyl were grown in
MEX medium at 28 °C for seven to 10 days to complete sporulation. For gene expression assays and cellulase activity measurements in QM9414, a suspension containing approximately 108 spores/mL was inoculated in 200 mL Mandels-Andreotti medium [18] containing 1 % (w/v) cellulose (Avicel, Sigma, St. Louis, Missouri, EUA), or 1 % (w/v) lactose (Sigma, St. Louis, Missouri, EUA), or 1 % (w/v) cellobiose (Serva, Heidelberg, Germany), or 2 % (w/v) glucose (Sigma, St. Louis, Missouri, EUA), or in 20 mL of the same medium containing 1 mM sophor-ose (Serva, Heidelberg, Germany) as the sole carbon source. For gene expression assays in Aacyl, a suspension containing approximately 108 spores/mL was inoculated in 200 mL Mandels-Andreotti medium containing 1 % (w/v) cellulose (Avicel), or in 20 mL of the same medium containing 1 mM sophorose as the sole carbon source, with or without 1 mM dibutyryl-cAMP (dbcAMP - Sigma, St. Louis, Missouri, EUA). Cultures were incubated on an orbital shaker (200 rpm) at 28 °C for 24, 48, and 72 h using cellulose, lactose, or cellobiose; for 24 and 48 h using glucose; and 2, 4 and 6 h, or 6, 12 and 18 h using sophorose. For the latter, the mycelium was previously grown in 1 % (w/v) glycerol (Sigma, St. Louis, Missouri, EUA) for 24 h. After incubation, the mycelia were washed with Mandels-Andreotti medium without peptone, and transferred to 20 mL of Mandels-Andreotti medium without peptone containing 1 mM sophorose. All experiments were performed in three biological replicates. The resulting mycelia and supernatants were collected by filtration, frozen and stored at -80 °C until RNA and protein extraction, as well as cellulose activity measurements were performed.
Determination of cellulase activity
Determination of cellulase activity was performed using Cellulose Azure® (Sigma, St. Louis, Missouri, EUA) as the substrate. This methodology involves the release of a blue color when cellulases are present. In these experiments, the reaction mixture consisted of Cellulose Azure, 100 mM sodium citrate buffer pH 5.0, and samples from culture supernatants. Reactions were performed at 55 °C for 30 min. After this, the alcohol precipitation reagent (APR) was added according to the manufacturer instructions, and samples were centrifuged. Supernatant was collected, and samples were measured using a spectrophotometer (Spectrophotometer xMark™ Micro, Bio-Rad, San Francisco, CA, USA) at 575 nm. A calibration curve was created using varying concentrations of the substrate incubated at 50 °C for 4 h in 100 mM sodium citrate buffer pH 5.0 and 15 U/mL cellulase purified from Trichoderma reesei in the Microbiology Laboratory of Cell Biology at the Biology Department (Faculty of Philosophy, Sciences, and Letters of Ribeirao Preto, University of Sao Paulo, Brazil). Activity was expressed
as the ratio between change in growth factor absorbance and the absorbance obtained in the standard curve, per min, and per amount of enzyme added to the reaction.
RNA extraction
Total RNA was extracted from mycelia of each sample using TRIzol® RNA kit (Invitrogen Life Technologies, Carlsbad, CA, USA), according to the manufacturer instructions. RNA concentration was determined using spectrophotometric optical density at 260/280 nm, and RNA integrity was verified by electrophoresis in 1 % agarose gels.
Quantitative real time-PCR analysis
Approximately 1 ^g RNA was treated with DNAsel (Fermentas, Waltham, Massachusetts, USA) and reverse-transcribed to cDNA using the First Strand cDNA kit Maxima™ Synthesis (Thermo Scientific, Waltham, Massachusetts, USA) according to manufacturer instructions. cDNA was diluted 1:50 for real-time PCR analysis in a Bio-Rad CFX96™ System (Bio-Rad, San Francisco, CA, USA), using SsoFast™ EvaGreen® Supermix (Bio-Rad, San Francisco, CA, USA) for signal detection, in accordance with the manufacturer instructions. Primers used in this study are listed in Table 1. The gene encoding actin was used as a constitutive expression control [19]. The following amplification reaction was used: 95 °C for 10 min followed by 39 cycles at 95 °C for 10 s, 60 °C for 30 s followed by a dissociation curve at 60 to 95 °C with an increment of 0.5 °C every 10 s. Gene expression values were calculated according to the 2-AACT method, using the QM9414 strain grown in glucose as the reference sample [19]. Data analysis was performed using GraphPad Prism v5.1 software.
Extraction and measurement of cAMP
After fungal growth in Mandels-Andreotti medium, my-celia were collected and frozen in liquid nitrogen. For measurement of cAMP, mycelia were macerated, and samples were transferred to polypropylene tubes and weighed. Then, 10 volumes of 0.1 M HCl were added, and the tubes were centrifuged at 6,000 x g for 10 min at 4 °C. The supernatant was used directly for measurement of cAMP levels using the "Direct cAMP Enzyme
Table 1 Primers used in this study
No. Code Protein ID
1 Cel6a F 72567 ACA AGA ATG CAT CGT CTC CG
2 Cel6a R TGT TCC ACC CGT TGT AGT TG
3 Cel7a F 123989 CCG AGC TTG GTA GTT ACT CTG
4 Cel7a R GGT AGC CTT CTT GAC TGA GT
5 Actin F 44504 TGA GAG CGG TGG TAT CCA CG
6 Actin R GGT ACC ACC AGA CAT GAC AAT GTT
Immunoassay" kit (Sigma, St. Louis, Missouri, EUA) according to the manufacturer instructions. The content of intracellular cAMP was relative to protein concentration in the same sample.
Protein extraction and western blot
Secreted proteins from QM9414 and Aacyî strains were precipitated using 10 % tricarboxylic acid (TCA) in acetone, and allowed to stand at -20 °C overnight. Samples were centrifuged at 10,000 x g for 10 min at 4 °C, and the supernatant was removed. |3-mercaptoethanol (0.07 %) in acetone was added, and samples were centrifuged at 10,000 x g for 10 min at 4 °C. This process was repeated three times, discarding the supernatant after each centrifugation. Then, samples were resuspended in buffer (25 mM Tris pH 6.8, 12.5 % SDS, 50 % glycerol and 0.05 % bromophenol blue) and heated for 5 min at 100 °C. For intracellular protein extraction [20], mycelia grown in sophorose were used as the source [21]. Total protein concentration was determined according to the Bradford method using the Coomassie Plus Protein Assay Reagent (Thermo Scientific, Waltham, Massachusetts, USA) at 595 nm, in a spectrophotometer (Spectro-photometer xMark™ Micro, Bio-Rad). Subsequently, 12 ^g of protein samples (secreted and intracellular proteins) were subjected to electrophoresis on 10 % polyacrylamide gels. After electrophoresis, proteins were transferred to nitrocellulose membranes (GE Healthcare) for 40 min using a humid system (Trans-Aid ™ Blot®Turbo transfer system, Bio-Rad) with transfer buffer (25 mM Tris, 197 mM glycine, 20 % methanol). Membranes were blocked for 1 h at room temperature in tris-buffered saline (TBS) containing 0.05 % Tween (TBS-Tween) and 5 % skimmed milk. Membranes were then incubated overnight at 4 °C with a rabbit polyclonal anti-Trichoderma viride cellulase (CEL7A) antibody (MyBioSource) diluted 1:1000. Membranes were then washed three times 10 min each with TBS-Tween and incubated for 1 h with the corresponding peroxidase-conjugated anti-rabbit secondary antibody (Invitrogen). Membranes were again washed three times 10 min each with TBS-Tween and developed using Enhanced Chemiluminescence reagent (ECL, GE Healthcare) according to the manufacturer instructions. Finally, ECL membranes were photographed using ChemiDoc™ XRS+ (BioRad) photo-documentation system.
Indirect immunofluorescence and confocal microscopy
Aliquots withdrawn from Aacyî at 6, 12, and 18 h during culture were centrifuged at 6,000 x g and washed with 0.1 M phosphate buffered saline (PBS) at pH 7.4. After washing, mycelia were immersed in 2 % paraformaldehyde in PBS at room temperature and embedded in optimal cutting temperature (OCT) compound (Tissue Tek, Sakura Finetec, Torrence CA) in a suitable tissue mold for
freezing. Subsequently the inclusion, mycelia were sectioned on a cryostat (10 ^m thick), and sections were mounted on silanized slides kept under vacuum for 12 h to affix the sections. Slides were then stored at -20 °C. For confocal microscopy, slides were washed with PBS and incubated with a 3 % bovine serum albumin (BSA) solution for 1 h at room temperature to block non-specific binding. Then, slides were incubated for 1 h at room temperature with a rabbit polyclonal anti-Trichoderma viride cellulase (CEL7A) antibody (MyBioSource) diluted 1:1000 in 3 % BSA solution in PBS. Slides were then incubated with an Alexa Fluor 488-conjugated secondary antibody (Molecular Probes, Life Technologies) diluted 1:5000 in PBS with 3 % BSA at room temperature. Slides were washed with PBS between steps and images were acquired using a Leica TCS SP5 confocal microscope.
Analytical methods
Biomass was determined by gravimetric analysis for gly-cerol culture. After 24 h of culture, mycelia was filtrated on filter paper and incubated at 70 °C for 3 h and then weighed. For cellulose culture, biomass was indirectly measured by the amount of intracellular protein quantified by the Quick Start Bradford protein assay kit (Bio-Rad) with bovine serum albumin (BSA) as a standard.
Results
Analysis of the expression of the cellobiohydrolases cel7a and cel6a and cellulase activity using different carbon sources
To guarantee comparisons between strains, we first examined the growth pattern of strains on cellulose and glycerol. No significant difference in growth between Aacyl mutant strain and the parental QM9414 as in cellulose as in glycerol was observed [see Additional file 1]. Expression of the two most expressed cellulase genes in T. reesei (cel7a and cel6a) was analyzed after growing the QM9414 strain in different carbon sources, as described in the Methods section. As shown in Fig. 1, cel7a and cel6a expression increased when the fungus was grown in cellulose, sophorose, or lactose. Using cellulose, cel7a expression increased 10-fold at 48 and 72 h (Fig. 1a). Regarding sophorose and lactose, the highest cel7a expression (30-fold) was observed after 6 and 48 h, respectively. The expression profile of cellobiohydrolase cel6a was similar to that of cel7a, with the highest expression levels in sophorose at 6 h (80-fold) and lactose at 48 h (90-fold) (Fig. 1b). As expected, neither cel7a nor cel6a showed detectable expression levels in glucose. Interestingly, no expression of cel7a and cel6a was observed in cellobiose.
Similar to qPCR-RT results, the QM9414 strain exhibited higher cellulolytic activity in cultures with cellulose, sophorose, and lactose (Fig. 2). However, different to
Fig. 1 Gene expression levels of ce/7a (a) and ce/6a (b). T. reesei QM9414 strain was grown in cellulose, lactose, or cellobiose for 24, 48, and 72 h, in glucose for 24, and 48 h, and in sophorose for 2, 4, and 6 h. The absolute expression of the genes was calculated using actin gene as an endogenous control
what was observed in the expression analysis, which showed an increase of cel7a and cel6a expression after 6 h, cellulolytic activity in sophorose increased mainly at 2 h in culture (24.5 U/mL). A similar pattern was observed growing QM9414 in lactose, where cellulolytic activity reached high levels at 72 h (22.5 U/mL). Cellulo-lytic activity in cellulose was higher at 48 and 72 h (24.5 U/mL and 20.7 U/mL, respectively). On the contrary, hydrolytic activity in glucose was lower than in other carbon sources, being 6, 5, and 4.8 times lower than in cellulose, sophorose, lactose and cellobiose, respectively. Interestingly, our results showed no correlation between the expression profile and cellulolytic activity in cellobi-ose. The cellulolytic activity showed a steady increase from 24 h and a maximum at 72 h (19.8 U/mL) (Fig. 2). This result may be explained from the fact that the azure-Cellulose® method detects total cellulolytic activity without distinguishing specific cellulases.
Fig. 2 Totalcellulolytic activity in different carbon sources. T. reesei QM9414 strain was grown in cellulose, lactose, or cellobiose for 24, 48, and 72 h, in glucose for 24, and 48 h, and in sophorose for 2, 4, and 6 h. Activity was measured using the azure-Cellulose method and is expressed as the ratio between growth factor and the absorbance obtained in the standard curve equation, per minute, and per amount of enzyme added to the reaction
Intracellular cAMP levels are regulated according to the carbon source
We found that cellobiohydrolase gene expression and cellulolytic activity profile varied depending on the carbon source used in the experiments of induction. Previous studies have suggested that intracellular levels of cAMP may regulate both expression of cellulase genes and activity of the enzyme. To address this, we measured intracellular levels of cAMP in mycelia from the QM9414 strain grown in cellulose, sophorose, lactose, cellobiose, and glucose.
Our results showed that intracellular levels of cAMP were modulated in a carbon source-dependent manner. As shown in Fig. 3, cAMP concentration (229.8 pmol/mg) at 4 h was at least 4 times higher in the presence of sophorose than in the presence of other carbon sources. In cellulose, the highest cAMP concentration was quantified after 24 h cultivation (61.7 pmol/mg). This value was 3 times higher than the maximum levels found in glucose
Cellulose Glucose Sophorose Lactose Cellobiose
Fig. 3 Intracellular cAMP content. T. reesei QM9414 strain was grown in cellulose, lactose, or cellobiose for 24, 48, and 72 h, in glucose for 24, and 48 h, and in sophorose for 2, 4, and 6 h
(19.13 pmol/mg) at 48 h and 2.5 times higher than with cellobiose (22.5 pmol/mg) at 24 h (Fig. 3). Concomitantly, lower levels of cAMP were detected in lactose and cellulose at 48 and 72 h, and cellobiose at 48 and 72 h. Altogether, our findings showed that in a similar manner to cellobiohydrolase expression and cellulolytic activity, intracellular levels of cAMP are also dependent on the in-ducer. This suggests a regulatory role of cAMP in the control of cellulase expression only in the presence of sophorose, since expression levels of cel7a and cel6a were increased in both lactose and cellulose. On the other hand, intracellular concentration of cAMP did not exhibit the same profile regarding carbon sources.
Analysis cel7a and cel6a expression in the Aacyl mutant strain
The expression profile of the two most abundant cello-biohydrolases in the parental lineage QM9414 was directly regulated in response to four different inducers. Here we showed that the increased expression of cel7a and cel6a correlates with high intracellular levels of cAMP in the presence of sophorose. Then, we wanted to assess how cAMP regulates cellulase expression in T. reesei, and whether the effects of this secondary messenger are determined by the carbon source. To assess this, we used the Aacyl mutant strain, which features a deletion in the adenylate cyclase gene, and dbcAMP (dibu-tyryl-cAMP) in the induction medium. Growth of the Aacyl mutant strain was assessed in cellulose and sophorose at 72 and 6 h, respectively, which were the time points and carbon sources that showed the highest expression of cellobiohydrolases.
Figure 4 shows that in the presence of sophorose and dbcAMP, expression of the cellobiohydrolases cel7a (Fig. 4a) and cel6a (Fig. 4b) was significantly increased relative to cellulose, either in the presence or absence of dbcAMP. Interestingly, dbcAMP effects were mainly evident in the presence of the most potent inducer of cellu-lase expression (i.e., sophorose) than in cellulose at the same concentration. As a result of the abolition of adenyl-ate cyclase expression in the Aacyl mutant strain, the only source of cAMP in the induction medium was dbcAMP. Therefore, supplementation with exogenous cAMP enhanced the expression of cellobiohydrolases in the Aacyl strain, suggesting an essential effect of cAMP in the regulation of cellulase gene expression in T. reesei.
Detection of total cellulase in mycelia and secretome of Aacyl and QM9414
The cAMP signal transduction pathway controls a wide variety of processes in fungi. In the Aacyl mutant strain processes such as carbon metabolism, conidiation, mating, phototropism, and synthesis and secretion of proteins may be disturbed because of adenylate cyclase
Sophorose 6h
Fig. 4 Gene expression levels of ce/7a (a) and ce/6a (b). Aacyl mutant strain was grown in cellulose for 72 h, and in sophorose for 6 h. The absolute expression is shown, with the actin gene used as an endogenous control. Gene expression was analyzed with or without addition of 1 mM dibutyryl-cAMP (dbcAMP)
deletion. Using western blot and indirect immunofluor-escence microscopy approaches we assessed cellulase content in the mycelia (intracellular protein) and in the secretome of QM9414 and Aacyl strains.
Our immunofluorescence results revealed that dbcAMP strongly influenced cellulase expression in the Aacyl mutant strain (Fig. 5). Addition of dbcAMP promoted an increase in cellulase expression at 6 h in induction medium with sophorose. Similar results were also observed at 12 and 18 h (Data not shown), with the same increase in cellulase expression. We observed an accumulation of cellulases in the hyphal tip (Fig. 5, dashed squares), when dbcAMP was added. These results, together with the qRT-PCR and activity analyses, suggest that dbcAMP directly controls expression and secretion of cellulase in T. reesei.
We found no correlation between expression level of cellobiohydrolases and activity in at 6 h of incubation in the presence of sophorose. On the other hand, the im-munofluorescence analysis showed that at 6 h in the presence of dbcAMP there are increased of cellulase expression. So, we asked if occurs a retention of cellulases in the mycelium. Our western blotting results showed a detection of an approximately band of 59-68 kDa (relative to CEL7A), and we observed a lower content of CEL7A in the secretome of Aacyl strain in the absence of dbcAMP (Fig. 6a, upper panel). The addition of dbcAMPC increased the content of CEL7A in the secretome. The differences were more evident at 12 h and 18 h, being the higher expression of CEL7A reached always in the presence of dbcAMP. The detection of CEL7A in the mycelium of Aacyl (Fig. 6b, upper panel) revealed an elevated content of this cellulase at 6 h in the absence of dbcAMP, justifying the lower detection in
the secretome. In the same way, the addition of dbcAMP at 6 h induced a high secretion of CEL7A as demonstrated by the decreased of protein in the mycelium (Fig. 6b, upper panel). In addition, we observed that the content of CEL7A in the mycelium at 12 h and 18 h were higher than at 6 h, but the content of protein in the secretome remain increased at 12 h and 18 h relative to mycelium. In the Aacyl strain the expression of cellu-lase was higher after 6 h of cultivation, being the content of CEL7A maximum at 18 h. Oppositely, in the secretome of QM9414, the maximum content of CEL7A was detectable at 12 h in the absence of dbcAMP (Fig. 6a, lower panel). Moreover, we demonstrated a lower content of cellulase in the mycelium of QM9414 at 6 h, 12 h and 18 h compare to Aacyl mutant strain (Fig. 6b). So, the analysis of secretome and mycelium protein content revealed that addition of dbcAMP alters the pattern of CEL7A secretion in T. reesei. The content of CEL7A in the presence of dbcAMP had no change in the secretome, but comparing the protein content in the mycelium in the absence and in the presence of dbcAMP, we observed the accumulation of protein in the mycelium after addition of dbcAMP mainly at 6 h and 12 h (Fig. 6b, lower panel). Our findings suggest that cAMP may regulate the expression, and secretion of cellobiohydrolases in T. reesei in the presence of the inducer sophorose.
Discussion
In T. reesei, it is well established that expression of cellulases is carbon source-dependent [12]. Our group has described the influence of different carbon sources in the regulation of cellulase gene expression [22, 4]. Although various studies have discussed that cellulase genes are dependent on induction, little is
dbcAMP + dbcAMP
Fig. 5 Cellulase detection using indirect immunofluorescence in the Aacyl mutant strain. The fungus was grown in sophorose for 6 h in the presence or absence of dibutyryl-cAMP (dbcAMP). To detect cellulase in the mycelia we used a rabbit polyclonal anti-Tr/'choderma viride cellulose (CEL7A) antibody diluted 1:1000, and an Alexa Fluor 488-conjgated secondary antibody diluted 1:5000. Furthermore, the fluorochrome DAPIwas used to detect cellnuclei. Images were acquired on a Leica TCS SP5 confocalmicroscope. Lens 40x, and zoom 3.8
known about the nature of the inducer, and the signaling pathways controlling cellulase gene expression in this fungus [16].
In T. reesei the only well characterized signal transduc-tion cascades are: a light-modulated cellulase production (G protein-mediated, Gna1 and Gna3), a PAS/LOV domain protein ENVOY and cAMP-dependent protein kinase A signaling [7, 17, 18, 23], regulation of sexual development [24], and cellulose- and cAMP-independent modulation of cellulase production mediated by Ras GTPase [25]. Recently, Wang et al. [26, 27] described the role of MAPK signaling in the regulation of both expression and activity of cellulases in T. reesei.
The cyclic AMP (cAMP) pathway is a central signaling cascade with crucial functions in all organisms. In Sac-charomyces cerevisiae, nutrient sensing and pseudohy-phal differentiation in response to nitrogen-limiting conditions is controlled by this pathway [28-30]. In the fission yeast, Schizosaccharomyces pombe, cAMP mediates the effect of glucose and gluconeogenesis in spore germination, and regulates mating in response to either glucose or nitrogen deprivation [31, 32]. In filamentous fungi such as Neurospora crassa and Aspergillus species, cAMP controls hyphal growth polarity and morphogenesis, conidiation, and spore germination [33-36]. Furthermore, as a secondary messenger, cAMP is involved
Fig. 6 Analysis of cellulase expression in Aacyl and QM9414 strains. Fungi were grown in sophorose for 6, 12, and 18 h in the presence or absence of dibutyryl-cAMP (dbcAMP). a Expression of CEL7A in the secretome of the Aacyl mutant strain (upper panel) and QM9414 parental strain (lower panel) in the presence or absence of dbcAMP. b Expression of CEL7A in the mycelium of the Aacyl mutant strain (upper panel) and QM9414 parentalstrain (lower panel) in the presence or absence of dbcAMP
in stress response, carbon and lipid metabolism, sporulation, development, virulence, mating, mycoparasitism, and other responses to extracellular signals [8-12, 37].
Previous studies in T. reesei have suggested that cAMP signaling regulates cellulase gene expression [13]. Sestak and Farkas (1993) [13] showed that addition of cAMP can double the efficacy of sophorose in the induction of endoglucanase formation. In another filamentous fungus, Cryptococcus albidus, cAMP was shown to be important for xylanase production [38]. According to Tisch and Schmoll [7], the most important role of cAMP is to activate cAMP-dependent protein kinase A (PKA), which in turn initiates a phosphorylation cascade and activates/inactivates further target genes. Schuster et al. (2012) [17] showed that both adenylate cyclase (ACY1) and PKA (catalytic subunit, PKAC1) were important factors in cellulase gene expression in T. reesei. However, the mechanisms related to the impact on cellulase gene expression remain unclear.
In the present study, we showed that the effect of cAMP in the regulation of cellulase gene expression in T. reesei was carbon source-dependent and that the role of this secondary messenger is more evident in the presence of sophorose. This sugar is formed by transglycosy-lation of cellobiose during cellulose hydrolysis [39], and it is thought to be the natural inducer of cellulase formation, being its presence in culture fluids of T. reesei commonly described [40-42]. Moreover, this disaccharide has a dual role in T. reesei in |3-glucosidase repression and cellulase induction [16]. The efficiency of sophorose and other disaccharides such as lactose in the induction of cellulase has also been observed in Trichoderma viride, Pseudomonas fluorescens var. cellulosa, Acremonium cellulolyticus, Penicillium echinulatum [41, 43-45]. Interestingly, our results showed a low expression of cellu-lase genes in the presence of cellobiose. This may be explained by the fast hydrolysis of this sugar by |3-glucosidase activity, which converts cellobiose to glucose, a carbon source repressor of cellulase synthesis [46, 47]. Altogether,
our results suggest an intriguing mechanism by which the fungus identifies the available carbon source in the culture medium and controls the full transcription machinery of genes responsible for carbon source metabolism. In addition, our results highlight the role of cAMP as a sophorose sensor.
Our qRT-PCR results showed that expression of cello-biohydrolases cel7a and cel6a increased in the presence of cellulose, sophorose, and lactose. However, in the presence of sophorose, addition of dbcAMP induced an increase of 5- and 7.8-fold in the expression of cel7a and cel6a, respectively. As observed, the expression of cel6a was more sensitive to intracellular levels of cAMP than cel7a. Interestingly, the high expression levels of cel7a and cel6a correlated with high intracellular cAMP levels. The influence of cAMP in the regulation of cellulase expression has been shown in important fungi such as Trichoderma, Penicillium, and Aspergillus spp., which have biotechnological interest [41, 45]. Furthermore, Hu et al. [48], in a study in Penicillium decumbens, showed the effect of PGA3, a group III G-protein a subunit, on the expression of amylases and cellulases. Deletion of pga3 resulted in impaired amylase production, and significantly decreased transcription of the major amylase gene amy15A. Moreover, supplementation with exogenous cAMP or its analog dbcAMP restored amylase production in the Apga3 strain, suggesting an essential role for PGA3 in amylase synthesis by controlling cAMP levels. Conversely, transcription of the cellulase gene cel7A-2 increased in the Apga3 strain, although cellulase activity in the medium was not affected. Dong et al. [49] showed that exogenous cAMP could increase cellulase synthesis under derepression conditions. Nevertheless, cAMP has an ambiguous role in the regulation of cellulase expression because at lower concentrations increases cellulolytic activity, while high levels of cAMP repress cellulase synthesis. Interestingly, Herrera-Herrera et al. [50] showed that in Cellulomonas flavigena, an actinobacteria with special interest for its ability to degrade cellulose and
hemicellulose, addition of exogenous cAMP in repres-sor culture medium decreased catabolite repression, while supplementation enhanced cellobiohydrolase production. Similarly, Rizzati et al. [51] showed in As-pergillus phoenicis that repression of xylanase expression by glucose was partially reversed by addition of cAMP or dbcAMP.
In our experiments using cellulose, we showed that expression of cel7a and cel6a in the Aacy1 strain were 6- and 7.3-fold higher with addition of dbcAMP. This increase may be explained because degradation of cellulose releases inducer disaccharides such as sophorose, which in turn may active the expression of cellulolytic enzymes. This result corroborates our hypothesis that cAMP affects the expression of cellobiohydrolase, and that this regulation seems to be dependent on the type of carbon source, since changes in transcription of related genes were observed in both cellulose and sophor-ose, using the same concentration of dbcAMP. Hu et al. [48] described a different regulation in P. decumbens, in which expression of amylases and cellulases seemed to be independent of the carbon source. Taken together, our results suggest that the signaling pathway in response to sophorose involves a cAMP-dependent protein kinase that may control the expression of cellulolytic enzymes in the presence of easily metabolizable disaccharides, and that is also involved in the early stage of carbon sensing.
Our results revealed that the Aacyl mutant strain showed a high expression of cellobiohydrolases in the presence of both cellulose and sophorose. As discussed above, this expression increased with supplementation of exogenous cAMP. This finding suggests that cAMP is not essential for cellulase expression, and that alternative pathways may interact with cAMP-dependent signaling to control expression of cellulolytic enzymes. In this regard, Schmoll et al. [18] showed that in T. reesei intra-cellular cAMP levels were positively correlated with cellulase expression in the presence of light. Furthermore, sensing of environmental signals mediated by G-protein coupled receptors (GNA1 and GNA3) modulates considerably cellulase transcript levels, and the extent of this adjustment is dependent on light status. The critical light regulator ENVOY in T. reesei [52], is a small protein that contains a single PAS/LOV domain. The expression of the envl gene is very low in darkness, but upon illumination the abundance of its transcript increases up to 500-fold. Recently, Tisch et al. [7] reported that ENVOY is involved in signal transduction via G-proteins, acting positively in the feedback of gnal and in the cAMP/protein kinase A pathway, controlling the function of the corresponding phosphodiesterase, although the mechanism is still unclear. In T. atroviride, a GPCR (GPR-1) that activates heterotrimeric G-proteins senses different carbon sources, and the Ga proteins
(tga1 or tga3) can activate adenylate cyclase that in turn may control intracellular levels of cAMP [53]. Thus, our results obtained in the Aacy1 strain provide evidence of the existence of a cAMP-independent pathway that controls cellulase expression, and may involve a receptor that senses different carbon sources; the effects of this sensing are more evident in the presence of disaccha-rides such as sophorose. These results are also in agreement with other studies [13, 54, 55], which showed that cAMP may be an important signal for the regulation of cellulase formation, but not the only one.
The effect of cAMP on the regulation of cellulase expression in T. reesei was also revealed in our comparative analysis of immunofluorescence and western blot. Immunofluorescence data clearly showed that supplementation with exogenous cAMP controls expression of cel7a in sophorose induction. In addition, we observed that in the Aacy1 mutant strain there is a delay in the secretion of cellobiohydrolase CEL7A compared to the parental QM9414. Kinetic studies have shown that secretion is not faster in T. reesei than in other species. However, a good secretion capability depends on the capacity of the secretion machinery [56]. Altogether, our results suggest an involvement of intracellular cAMP levels in the regulation of cellulase secretion.
Filamentous fungi such as T. reesei and A. niger, produce large amounts of extracellular cellulolytic enzymes, while some strains mostly produce them in a multienzyme complex called cellulosome, which is associated with the degrading cell wall [57-61]. Usually, a typical secretory pathway in a cell is composed of at least two components, endoplasmic reticulum and Golgi apparatus, and two endomembrane systems, one for incoming, and another for outgoing traffic [62]. On the other hand, secretion of cellulase suggests the existence of three different mechanisms based on their subcellular location: a specific secretory pathway independent of cellulose, a secretory pathway, which is induced by cellulose, and a process that occurs irrespective of the carbon source [63].
Cellulase secretion needs to be induced, and this process involves the synthesis of new proteins for constructing secretory pathways. In A. niger, de Oliveira et al. [64] described the induction of 254 different predicted proteins related to the secretory pathway. Interestingly, the induction of proteins seemed to be carbon source-dependent. Similarly, studies in Clostridium ther-mocellum showed that endoglucanase activity was regulated by carbon source [65-68]. In A. nidulans, non-essential protein kinases and phosphatases were involved in the sensing of carbon and/or energetic status, and in the regulation of hydrolytic enzyme production [69]. As discussed above, cAMP controls a wide range of processes in the cell, including activity of kinase proteins.
The Aacyl strain exhibited an increase in the cellobiohy-drolase expression. Interestingly, upregulation of cel7a and cel6a was more evident and the intracellular cAMP content was higher in the presence of sophorose than in the presence of other carbon sources tested. Furthermore, secretion of CEL7A was altered compared to the QM9414 parental strain. These results suggest that sophorose may be sensed by a different signaling pathway in the Aacyl mutant strain, and that mutation of the acyl gene may alter the pattern of cellulases secretion in this strain. However, additional studies will be needed to identify potential kinase proteins involved in this process in T. reesei.
Conclusions
The present study contributes to a better understanding of the role of cAMP signaling pathway in the regulation of cellulase expression in T. reesei. Our results showed that cAMP effects are carbon source-dependent, with regulation of cellobiohydrolases more evidently affected in the presence of sophorose. Interestingly, cellulase secretion was altered in the Aacyl mutant strain, in which cAMP synthesis is disrupted. Moreover, our study is the first report discussing a potential role for cAMP in the regulation of cellulase secretion in T. reesei. These results suggest that cAMP is an important signaling pathway involved in cellulase expression in T. reesei, but only in the presence of sophorose. These findings contribute to the understanding of the molecular mechanisms involved in the regulation of the processes of cellulolytic enzyme synthesis and secretion.
Additional file
Additional file 1: Figure S1. Growth profiles of T. reesei QM9414 and Aacy1 strains in cellulose (A) and glycerol (B) as carbon source. Error bars are represented from three biological replicates. No significant difference was showed in growth between Aacyl mutant strain and the parental QM9414 (PDF 117 kb)
Abbreviations
ACY1: Adenylate cyclase; BSA: Bovine serum albumin; cAMP: Cyclic AMP; APR: Alcohol precipitation reagent; dbcAMP: Dibutyryl-cAMP; ECL: Enhanced chemiluminescence; MEX: malt extract; PBS: Phosphate buffered saline; PKA: Protein kinase A; qRT-PCR: Quantitative real time-PCR; SDS: Sodium dodecyl sulfate; TCA: Trichloroacetic acid; TTBS: Tris-buffered saline.
Competing interests
The authors declare that they have no competing interests. Authors' contributions
KMVN performed the experimental design, laboratory experiments, and drafted the manuscript. MNC performed experimental design, and laboratory experiments. RGP drafted the manuscript. FCMN and RRA performed the experimental design, and laboratory experiments of the indirect immunofluorescence and confocal microscopy. 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.
Authors' information
Not applicable.
Acknowledgments
This work was supported by the Fundagao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) (Processes FAPESP 2013/03681-9; 2014/23653-2). We are grateful to Dr. Monika Schmoll (AIT Austrian Institute of Technology GmbH) for providing the Aacyl strain, Professor Maria Cristina Roque Antunes Barreira for providing laboratory infrastructure for the preparation of samples for indirect immunofluorescence and confocal microscopy. In addition, we are grateful to Elizabete Rosa and Vani Maria Alves for their technical assistance.
Author details
department of Biochemistry and Immunology, Ribeirao Preto Medical School, University of Sao Paulo, 14049-900 Ribeirao Preto, SP, Brazil. 2Department of Cell Biology and Molecular and Pathogenic Bioagents, Ribeirao Preto Medical School, University of Sao Paulo, 14049-900 Ribeirao Preto, SP, Brazil.
Received: 30 July 2015 Accepted: 25 September 2015 Published online: 30 September 2015
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