The role of PKAc1 in gene regulation and trichodimerol production in Trichoderma reesei
Trichoderma reesei represents a model system for investigation of plant cell wall degradation and its connection to light response. The cyclic adenosine monophosphate pathway (cAMP pathway) plays an important role in both physiological outputs, being crucial for regulation of photoreceptor function as well as for cellulase regulation on different carbon sources. Phosphorylation of photoreceptors and of the carbon catabolite repressor CRE1 was shown in ascomycetes, indicating a relevance of protein kinase A in regulation of the target genes of these transcription factors as well as an impact on regulation of induction specific genes. Moreover, the cAMP pathway impacts growth and development.
Here, we investigated gene regulation by the catalytic subunit of protein kinase A (PKAc1) upon growth on cellulose. We found distinct gene sets for regulation upon growth in light and darkness with an overlap of only 13 genes. PKAc1 regulates metabolic genes as well as transport and defense functions. The overlap of gene regulation by PKAc1 with the genes representing the cAMP dependent regulatory output of the photoreceptor ENV1 indicates an involvement of PKA in this pathway, which counteracts its effects by contrasting regulation. Moreover, we found considerable overlap with the gene sets regulated under cellulase inducing conditions and by the carbon catabolite repressor CRE1. Our analysis also showed that PKAc1 regulates the genes of the SOR cluster associated with the biosynthesis of sorbicillinoids. The homologue of gin4, encoding a CAMK type kinase, which is regulated by PKAc1, CRE1 and YPR2 showed a moderate impact on trichodimerol production. We isolated trichodimerol as representative sorbicillin compound and established a method for its quantification in large sample sets using high performance thin layer chromatography (HPTLC), which can be broadly applied for secondary metabolite screening of mutants or different growth conditions. Due to the high expression levels of the SOR cluster under conditions of sexual development we crosschecked the relevance of PKAc1 under these conditions. We could show that PKAc1 impacts biosynthesis of trichodimerol in axenic growth and upon mating.
We conclude that PKAc1 is involved in light dependent regulation of plant cell wall degradation, including carbon catabolite repression as well as secondary metabolism and development in T. reesei.
KeywordsTrichoderma reesei Hypocrea jecorina cAMP pathway Cellulase Trichodimerol Secondary metabolism Sexual development
Trichoderma reesei is one of the most prolific enzyme producers in industry worldwide and plays a crucial role in expression of plant cell wall degrading enzymes for second generation biofuel production [1, 2]. Therefore, its enzyme system is studied in detail as are the complex regulation systems supporting high efficiency production of homologous and heterologous proteins . Regulation of plant cell wall degrading enzymes is induced in response to carbon sources such as cellulose, lactose and sophorose, the natural inducer, and genes encoding the major enzymes for this purpose are coregulated [3, 4, 5, 6]. Numerous transcription factors are involved in adjustment of transcript levels of plant cell wall degrading enzymes to environmental conditions, which can act positively or negatively . In T. reesei the most important transcription factors are XYR1  and ACE3 , which are essential for cellulase gene expression, ACE1 , which negatively affects cellulases and CRE1 , the carbon catabolite repressor, which represses cellulase formation in the presence of easily metabolizable carbon sources. Besides regulation at the transcriptional level, recent analyses revealed that cellulase expression is also regulated at a posttranscriptional level in dependence of nutrient sensing via the heterotrimeric G-protein pathway .
In addition to the carbon source, also other environmental cues influence enzyme expression . Especially light was shown to considerably impact cellulase gene expression in T. reesei and the gene set specific for inducing conditions is different in light and darkness [12, 14]. Light response in T. reesei is predominantly mediated by the photoreceptor complex consisting of BLR1 and BLR2 (blue light regulator 1 and 2) as well as by the photoreceptor ENV1 . While BLR1 and BLR2 are GATA-type transcription factors, ENV1 is assumed to act on this complex by protein–protein interaction adjusting its function. All three components impact cellulase gene expression as well as transcript levels of numerous CAZyme encoding genes in T. reesei [16, 17]. The functions of ENV1 in T. reesei further extend to sexual and asexual development, growth and stress response .
Cyclic AMP (cAMP) is a central second messenger in the cellular function of all organisms and highly conserved across the kingdoms of life. The cAMP pathway crucially regulates morphology and nutrient sensing in fungi [18, 19].
The genome of T. reesei harbors an adenylate cyclase gene, an adenylate cyclase associated gene, two genes encoding catalytic subunits of protein kinase A (pkac1 and pkac2), one regulatory subunit encoding gene and two phosphodiesterase genes . Protein kinase A is the main target of cAMP signaling. PKAc1 was found to be the major catalytic subunit of protein kinase A in N. crassa  and plays an important role in circadian rhythmicity as well as stabilization of the photoreceptor complex WCC and the protein FREQUENCY (FRQ1) [21, 22, 23]. For Aspergillus nidulans a function of PkaA was found in biomass formation in complete media and on cellulose, endocellulase activity, expression of xylanases and cellulases . Additionally, CreA is differentially phosphorylated depending on the presence of PkaA, resulting in altered characteristics for import in the nucleus . A positive role of the cAMP pathway as well as the heterotrimeric G-protein pathway on cellulase gene expression and secondary metabolism was further shown in Chaetomium globosum [26, 27]. Besides functions in development, a role of the cAMP pathway in secondary metabolism was shown for Aspergillus fumigatus, Pestalotiopsis microspora and Fusarium graminearum [28, 29, 30].
The light dependent functions of both the G-protein alpha subunits as well as of acy1 and pkac1 in T. reesei indicated a connection of the cAMP pathway to the light response pathway. Indeed, in a mutant lacking the photoreceptor ENV1, cAMP levels are strongly decreased. This phenotype is prevalent, even if GNA1 or GNA3 are constitutively activated in such a strain . Additionally, genes regulated by ENV1 and ACY1, and hence likely reflecting the cAMP dependent output of the ENV1 regulon, show considerable overlap in light upon growth on cellulose . Analysis of transcriptomes from different carbon sources suggests that this cAMP dependent regulatory output of ENV1 may be involved in substrate- or surface sensing . The characteristic phenotype of strains lacking ENV1 (growth defect in light, altered sporulation [42, 43]) is reminiscent of both the perturbed growth of acy1 and pkac1 deletion strains and is hence likely to be cAMP related as well.
In this study we investigated the alterations in the transcriptome in dependence of the catalytic subunit 1 of protein kinase A (pkac1). Evaluation of the regulatory targets of PKAc1 showed functions in enzyme expression in light and darkness as well as modulation of secreted secondary metabolites upon growth on cellulose. Comparison of the PKAc1 regulome with those of known targets of PKA revealed considerable overlapping regulation, implicating the CAMK kinase GIN4 as potential target. Importantly, we also optimized a method for fungal secondary metabolite production by high performance thin layer chromatography (HPTLC) with a focus on large scale screening and metabolite quantification, using trichodimerol as representative compound.
Transcriptome analysis of ∆pkac1
Previous studies showed that the cAMP pathway, including pkac1, is involved in regulation of cellulase gene expression in T. reesei upon growth on the cellulase inducing carbon source lactose . Based on DNA–protein interaction studies and gene regulation analysis of the cellulase regulator xyr1, which is co-regulated with the cellobiohydrolase gene cbh1 under these conditions, it was concluded, that PKAc1 acts on a transcriptional regulator impacting XYR1, rather than on XYR1 itself .
We investigated the transcriptome of ∆pkac1 in comparison the the wildtype QM9414 upon growth on cellulose, which is more closely related to the natural substrate of T. reesei (Additional file 1). Due to the previously reported effect of light on the regulatory output of PKAc1  and the functions of its homologues in N. crassa in regulation of the light response machinery as well as circadian rhythmicity [21, 22], we performed our experiments under controlled light conditions in constant light and constant darkness.
In order to validate the results of the transcriptome data we checked whether transcript levels of the wild-type correspond to known regulation patterns from previous studies . The strongly light regulated genes env1 and hpp1 as well as TR_68924 and TR_123955 show the characteristic decrease in transcript levels in constant light compared to darkness. TR_123865 and TR_44278 show the characteristic increase in transcript abundance in light in the wild-type in our dataset. Hence we consider our transcriptome data valid and reliable.
PKAc1 impacts metabolism and transport functions
Genes regulated by PKAc1 in darkness
Constant darkness represents a condition closely related to the conditions of industrial fermentation and is hence most interesting for studying T. reesei. We found 170 genes to be more than twofold regulated (p-value threshold 0.01) in constant darkness compared to wildtype (Additional file 1). Among the 128 genes downregulated in darkness, we found 6 CAZyme encoding genes including a predicted trehalase as well as eight transcription factor genes, of which TR_122523 was previously shown to positively influence plant cell wall degradation . TR_123881 (SxlR), which is more than threefold downregulated in ∆pkac1, represses xylanase, but not cellulase activity .
Interestingly, under these conditions the recently described SOR cluster, which is responsible for biosynthesis of dihydrotrichotetronine on cellulose  and impacts sorbicilline formation upon growth on glucose , is downregulated as well. The consistently positive effect of PKAc1 on the polyketide synthases (pks) sor1 and sor2, the predicted flavoprotein monooxygenase gene sor5, the transporter sor4 as well as the transcription factor ypr2 (sor3) supports a regulation of this cluster via nutrient dependent phosphorylation. The second transcription factor gene in this cluster, ypr1, is not regulated by PKAc1 on cellulose, but positively regulated by the adenylate cyclase (ACY1) upon growth on cellulose in darkness . For ypr2, the opposite is the case, it is not regulated by ACY1 . Previously it was shown that the transcription factors YPR1 and YPR2 exert their functions in a different way on glucose and cellulose [46, 47]. Accordingly, carbon source dependent regulation of ypr1 and ypr2 is different between inducing and repressing carbon sources .
The 43 genes upregulated in ∆pkac1 in darkness included the small, cellulose specific gene ooc1 , the polyketide synthase pks4g, which was shown to be responsible for the green spore coloration in T. reesei . Additionally, transcript levels the gene represented by the model TR_64125, encoding a protein kinase were increased. Moreover, this gene set comprises the protein phosphatase gene pp1 (TR_120722), which is related to N. crassa histidine phosphatase pph-3 as well as two putative multicopper oxidases (TR_102820 and TR_124079) (Additional file 1). Of the two transcription factor genes upregulated in darkness in ∆pkac1, TR_112524 was screened for a function in plant cell wall degradation, which was however not detected .
Genes regulated by PKAc1 in light
Upon growth in light with cellulose as carbon source, 225 genes were regulated compared to wild-type, 126 showed decreased transcript levels and 99 increased transcript levels in ∆pkac1 (Additional file 1). Among the 126 genes downregulated in light, we found 9 CAZyme encoding genes including gph1 encoding a glycogen phosphorylase regulated by Hog1 under stress conditions in Candida albicans  and the light dependent induction of which is positively regulated by ENV1. Additionally, this gene set comprises the gene encoding the mannitol dehydrogenase lxr1 [52, 53] which resides in a gene cluster regulated by the photoreceptor ENV1 . We also found downregulation of 5 genes associated to secondary metabolism, of them 4 cytochrome P450 encoding genes and 8 transcription factor genes of unknown function. The transcription factor encoding TR_54703 was tested for a positive function on plant cell wall degradation, but no alteration in enzyme expression was found .
Of the 6 transporter encoding genes regulated by PKAc1 in light, there is also ste6, encoding the putative pheromone transporter, which is downregulated in ∆pkac1. This is in agreement with the previously reported positive effect of the cAMP pathway on sexual development .
For 99 genes we detected upregulation in ∆pkac1 in light. This geneset comprised 6 CAZyme including cip2, cel3d and egl5/cel45a, 9 genes involved in sulphur metabolism, among them 5 taurine dioxygenases and 3 methionine permeases. Moreover, we found 2 transcription factor encoding genes including vib1 and TR_3449 as well as 3 transporters including MFS hexose transporter CLP1, which transports cellodextrins in N. crassa .
Interestingly, of the genes regulated by PKAc in light, cip2 and the glycoside hydrolase family 30 xylanase TR_69276, which is assumed to have both endoxylanase and endoglucanase functionality  encode proteins that are listed among the three most important limiting proteins for hydrolysis of pretreated corn stover (PCS), a typical substrate for industrial enzyme production .
Light independent targets of PKAc1
Induction specific genes regulated by PKAc1
Protein kinase A impacts diverse important physiological pathways in fungi (Fig. 1), often by phosphorylation of important transcription factors including photoreceptors  and the carbon catabolite repressor CRE1 . Due to the relevance of PKAc1 in cellulase regulation [24, 36], a more general impact on induction specific genes is also expected. Therefore, we evaluated available transcriptomes from growth of T. reesei on cellulose in light and darkness for overlapping or contrasting regulation indicating functions in the same pathway.
Induction of plant cell wall degrading enzymes and more specifically of cellulases happens in response to distinct carbon sources, mainly representing plant cell wall components . We were therefore interested if the core set of induction specific genes (regulation on the inducing carbon sources cellulose, lactose and sophorose versus glucose and glycerol, in the presence of which no cellulases are induced; ) in light and darkness is subject to regulation by PKAc1.
Of the 170 PKAc targets (indirect) in darkness, 48 overlapped with genes regulated in an induction specific manner , most of which were regulated in the opposite direction in ∆pkac1 (positive vs. negative regulation; contrasting) (Additional file 3) (Fig. 3b). These overlapping genes were enriched in the function of catalase reaction (p-value 8.45e−04), but comprised also genes associated with stress response, metabolism including C-compound and carbohydrate metabolism and transport functions.
Among the 225 genes regulated by PKAc1 in light, 91 genes overlapped with the previously reported genes specifically regulated under inducing conditions  (Fig. 2c). As seen in darkness, in many cases the regulation in ∆pkac1 was contrasting that under inducing conditions (Additional file 3). The function of catalase reaction was also enriched among the genes regulated by PKAc1 in light (p-value 3.12E−03) as were those involved in secondary metabolism (p-value 9.16E−03). Additionally, 37 genes associated with metabolism, particularly with C-compound and carbohydrate metabolism, amino acid metabolism, detoxification and transport functions were detected in this gene set.
The overlap of induction specific genes and those regulated by PKAc1 is limited to only six genes between light and darkness. Consequently, regulation of induction specific genes by PKAc is light dependent with distinct target gene sets. The contrasting regulation both in light and in darkness suggests that particularly induction specific up-regulation under the respective conditions is dependent on the function of PKAc1.
Overlapping targets with CRE1
The carbon catabolite repressor CRE1 shows the potential for cAMP dependent phosphorylation in its protein sequence. Moreover, an influence on phosphorylation of CRE1 was recently shown for PKA in A. nidulans . Therefore we screened the respective dataset for gene regulation by CRE1 in constant light and constant darkness upon growth on cellulose  for overlapping regulation with PKAc1 (Additional file 4).
Of the 225 genes regulated by PKAc in light, 99 were also regulated by CRE1 in light (Fig. 3c). Among these 99 genes, 46 were downregulated in ∆pkac1 and in ∆cre1 in light. Fifty-one genes were upregulated in ∆pkac1 and in ∆cre1 in light. They comprise cip1 and cel3d, several putative permeases and genes involved in sulphur metabolism. However, two genes were upregulated in ∆pkac1 and downregulated in ∆cre1 in light.
In darkness, 48 genes were downregulated in ∆pkac1 and ∆cre1 (Fig. 3d), among them four CAZyme encoding genes, the catalase gene cat2 and the superoxidedismutase gene sod1. Twenty-one genes were upregulated in ∆pkac1 and ∆cre1, which comprise ooc1 and pks4 as well as the putative multicopperoxidase gene TR_124079. Only two genes showed contrasting regulation including the regulator of G-protein signaling (RGS) gene rgs2 (TR_72259). These overlapping regulation patterns (Fig. 3c, d) support the hypothesis of a positive effect of phosphorylation by protein kinase A in the function of CRE1.
Overlapping targets with photoreceptors
In N. crassa, a function for protein kinase A (PKA) in phosphorylation dependent regulation of the photoreceptor complex (white collar complex; WCC) activity was shown and PKA was found to serve as a priming kinase for the casein kinase dependent phosphorylation of the WCC components . The T. reesei homologues of the WC photoreceptor complex, BLR1 and BLR2 , comprise putative cAMP dependent phosphorylation sites (data not shown). Hence, deletion of pkac1 may in part cause similar gene regulation as lack of functionality or deletion of blr1 or blr2.
Comparison of gene regulation by light in ∆pkac1 with that in ∆blr1 and ∆blr2  showed 98 of the 225 genes regulated by PKAc1 in light to be regulated by BLR1 in light as well (Fig. 3e) (Additional file 4). They include 15 CAZyme genes, 10 genes involved in sulfur metabolism, 10 transcription factor encoding genes including vib1, which was recently shown to regulate cellulase gene expression  and 9 genes encoding transporters.
Most of the genes overlapping between BLR1 targets and PKAc1 targets in light were consistently regulated in both mutants, but in some cases also contrasting regulation was observed (Fig. 3e). Of the 76 genes down regulated in ∆blr1, 22 were up-regulated in ∆pkac1. Interestingly, these genes comprise four CAZyme encoding genes including cip2, cel3d and egl5 as well as the hexose transporter gene clp1, which is located next to cel3d in the genome.
Among the 22 genes up regulated in ∆blr1, 7 were down-regulated in ∆pkac1. They include three transcription factors (TR_120975, TR_122523 and TR_105220). TR_122523 was previously shown to positively influence cellulase gene expression and to be co-expressed with many hemicellulase genes .
Many of the genes with regulation in ∆pkac1 and ∆blr1 in light are also regulated in ∆blr2 (Additional file 4). Ninety of the 225 genes were regulated by both. Again 39 of the genes down regulated in ∆blr2 showed contrasting regulation in ∆pkac1, with 7 genes involved in sulphur metabolism. Up-regulated genes in ∆blr2, which are down-regulated in ∆pkac1 comprise the same transcription factor genes showing contrasting regulation with ∆blr1. Protein kinase A was shown to inhibit the activity of the photoreceptor complex by acting as a priming kinase in N. crassa . Hence deletion of protein kinase A would lead to increased photoreceptor activity. Our findings show a complex picture in this respect. Positive regulation of transcription factors by the photoreceptor complex BLR1–BLR2 (up-regulation in the mutants) occurs in the wildtype. Under these conditions, inhibition of the photoreceptor complex (to some extent) by PKA is operative. Deletion of pkac1 should alleviate the negative effect on BLR1 and BLR2 activity and the regulation by the photoreceptor complex should remain or even increase. This is the case for two transcription factor genes (TR_71823 and TR_105980). However, we also saw the opposite effect for three transcription factors (TR_120975, TR_105220 and TR_122523), potentially reflecting an indirect effect of the presence of pkac1 on a downstream component of the regulatory cascade of BLR1 and BLR2.
Functional category analysis of genes with altered transcript levels in ∆pkac1, ∆blr1 and ∆blr2 in light, indicating regulation by an effect of PKAc1 on activity of the photoreceptor complex showed enrichment (p-value threshold < 5e−02) in nitrogen, sulfur and selenium metabolism (p-value 8.48e−3), C-compound and carbohydrate transport (p-value 8.19e−04) and detoxification involving cytochrome P450 (p-value 3.0e−03) (Additional file 2).
The cAMP dependent output of ENV1
Deletion of env1 causes strongly decreased cAMP levels and a severe growth defect in light [40, 43]. Comparison of the transcriptional targets of ENV1 with those of the adenylate cyclase ACY1, revealed an overlap of 31 genes up-regulated in light and 114 genes down regulated in light, which represent the cAMP dependent regulatory targets of the photoreceptor ENV1. No genes with contrasting regulation in the two mutants were found . In part these genes also correlate with genes implicated in surface sensing in T. reesei .
Of the respective gene set down regulated in light in ∆env1 and ∆acy1, 29 of 114 genes were also regulated by PKAc1, but surprisingly all of them were upregulated in ∆pkac1 (Fig. 3f) (Additional file 4). They include the CAZyme encoding genes cip1 and egl5, four genes involved in sulphur metabolism as well as the transcription factor vib1. Also the 8 genes which overlap with the 31 genes up-regulated in ∆acy1 and ∆env1 in light, show contrasting regulation in ∆pkac1. We conclude that part of the cAMP dependent regulatory output of ENV1 in light is mediated by PKAc1, including the important transcription factor gene vib1. The overlapping regulation also with the photoreceptors BLR1 and BLR2 emphasizes the light dependent function of VIB1 in light dependent substrate sensing and cellulase regulation, which remains to be studied in detail.
GIN4 moderately influences trichodimerol levels
Due to the positive influence of PKAc1 on SOR cluster genes, we checked regulated genes overlapping with the CRE1 regulon to select a potential regulator of sorbicillin production. TR_64125, encoding a homologue of the CAMK kinase GIN4 is up-regulated in ∆pkac1 (2.8fold) and in ∆cre1 (20-fold) in darkness. Additionally, transcript abundance of this gene is more than twofold significantly decreased in a strain lacking the SOR-cluster transcription factor YPR2 under the same conditions .
Establishing a method for large scale screening of fungal secondary metabolite patterns
We found that PKAc1 is involved in regulation of the SOR cluster at the transcript level. Previously, genes of this cluster were shown to be among the most strongly transcribed genes under conditions of sexual development, considerably exceeding the transcript levels on cellulose . Therefore, we aimed to cross-check the impact of PKAc1 on production of sorbicillin compounds under mating conditions. Deletion of pkac1 causes delayed fruiting body formation in T. reesei  and N. crassa , indicating a positive effect of the cAMP pathway on sexual development, although it is not essential for mating .
First, we aimed to isolate a representative sorbicillin compound as a reference in our analyses. Then we optimized secondary metabolite extraction and the previously tested method of high performance thin layer chromatography (HPTLC) to establish a method for large scale screening of samples from diverse fungal strains and environmental conditions.
HPTLC allows for analysis of patterns of secreted metabolites of multiple samples (tens to even hundreds within reasonable time), which can be directly visually compared without employing complex and costly metabolomics tools like mass spectrometry. Reliable identification and quantification of individual compounds based on authentic standards is possible [63, 64]. The provided workflow also allows extraction of liquid samples from culture filtrates—ideally related to the produced biomass. Consequently, we consider HPTLC as the optimal system for screening of mutant libraries and the evaluation of diverse conditions for selection of samples for in depth analysis by mass spectrometry.
PKAc1 impacts trichodimerol production
Crossing plates containing the wild-type strains FF1 and FF2 , both sexually fertile, were extracted with a focus on potential sorbicillinoids. After chromatographic purification, NMR analysis confirmed the identity of the sorbicillin derivative trichodimerol, production of which is associated with the SOR cluster . Trichodimerol was produced under conditions of sexual development and therefore reflects chemical communication events between the two (potential) mating partners. Hence, trichodimerol can be used as a reference in high performance thin layer chromatography (HPTLC) analyses for secondary metabolite production during sexual development.
The cAMP pathway represents one of the most important signaling checkpoints in living organisms, with protein kinase A being a central component of the signal transmission machinery. Due to its function in adjustment of the levels of the secondary messenger cAMP, this pathway was postulated to be a coincidence detector  or a means to integrate signals from different sources. The components of this pathway as well as cAMP itself were previously shown to impact cellulase regulation  in a concentration dependent manner . Additionally, considerable light dependent effects in correlation with the cAMP pathway were observed including altered membrane potential, intracellular levels of ATP and cAMP and an increase of oxygen consumption . cAMP dependent protein kinase A is an important output pathway of altered cAMP levels and represents one of the factors mediating the physiological effects of changing cAMP concentrations in the cell.
Besides an influence on regulation of several CAZyme encoding genes, our data showed that PKAc1 also impacts glycogen metabolism. Interestingly, several genes involved in metabolism of energy reserves like glycogen or trehalose are downregulated in ∆pkac1, for example the glycoside hydrolase family 31 encoding TR_82235 and the putative trehalase TR_123456. The glycosylphosphorylase gene gph1, (glycosyltransferase family 35; TR_120198), is down regulated as well in light and darkness in ∆pkac1. This gene is located between the G-protein alpha subunit gene gna3 and the MAPkinase gene tmk3  and is regulated by light and ENV1 in T. reesei . Moreover, growth on glycogen as carbon source is decreased in a mutant lacking ENV1, but not in wildtype in light . The regulatory output of ENV1 is in part mediated by adjustment of cAMP levels [40, 41], particularly in light. Also gene regulation in ∆pkac1 overlaps with the gene set representing the cAMP dependent output of ENV1. Intriguingly, all these genes show contrasting regulation in ∆pkac1 compared to ∆env1 and ∆acy1 (Fig. 2g). Consequently, the cAMP dependent output of ENV1 involves the function of PKAc1 as well. Moreover, the previously reported involvement of the cAMP pathway in energy supply of the cell and adjustment of reserve carbohydrates is in agreement with the function of PKAc1, which positively influences genes involved in degradation of glycogen and trehalose.
Besides the connection of PKAc1 to the photoreceptor ENV1, also the considerable overlap of gene regulation by PKAc1 with the components of the photoreceptor complex BLRC, BLR1 and BLR2, strengthens the importance of PKA in dealing with altered light conditions in T. reesei.
One of the most interesting genes in this PKAc1 mediated, cAMP dependent output of ENV1 is the regulator gene vib1. In N. crassa, VIB1 links glucose signaling to carbon catabolite expression and is required for cellulase gene expression, due to its impact on the transcription factor CLR2 . VIB1 impacts expression of genes involved in metabolism and energy and may hence mediate the effects we saw for PKAc1. Accordingly, VIB1 is a key regulator of cellulase gene expression in T. reesei . However, T. reesei CLR2 does not have a striking function in cellulase regulation in T. reesei , indicating rewiring of the pathway.
Secondary metabolism in T. reesei is known to be modulated in light upon growth on cellulose . We isolated trichodimerol as a representative of sorbicillins, which are enhanced under conditions of sexual development  and demonstrate its regulation by PKAc1. Together with the refined HPTLC method for quantification, we thereby provide a means to screen large numbers of samples for modifications in trichodimerol production, which can also serve as a representative for metabolites associated with the SOR cluster including sorbicillins in general. This method is valuable as a prescreening for in depth analysis of selected samples by mass spectrometry. In addition, the presented method is applicable for extraction of secondary metabolites from supernatants of liquid cultures in relation to the biomass produced by the organism.
The genes associated with secondary metabolism regulated by PKAc1 comprise the particularly interesting secondary metabolite cluster responsible for biosynthesis of sorbicillinoids (SOR cluster). Ypr2, encoding one of the transcription factors regulating the SOR cluster, is regulated by light , by PKAc1 in darkness and by BLR1 and BLR2 in light. Previously we found a positive feedback cycle for regulation of the SOR cluster in darkness, which may involve the function of YPR2 . Since the genes of the SOR cluster are considerably upregulated under mating conditions  and the production of sorbicillins including trichodimerol and dihydrotrichotetronine on cellulose is low, we chose to evaluate the role of PKAc1 in secondary metabolism in combination with sexual development. Therefore we isolated trichodimerol as a representative for the SOR cluster.
Besides a decrease in trichodimerol production and biosynthesis of putative sorbicillinoids in general we also found that in ∆pkac1 communication with a putative mating partner on the plate was altered. Interestingly, the response to a wildtype strain, that was elicited in the fully fertile CBS999.97 strain in a confrontation assay, was not observed with ∆pkac1. In addition to a certain defect in sexual development in ∆pkac1 as shown previously , this signaling alteration represents a further function of PKAc1 in development.
Materials and methods
Strains and culture conditions
QM9414 (ATCC26921) and ∆pkac1  were used for transcriptome analysis. FF1 and FF2  were used for analysis of development and CBS999.97 MAT1-1  was used to study secondary metabolite production and chemical communication. For transcriptome analysis, strains were grown in 200 ml Mandels Andreotti minimal medium  with 1% (w/v) cellulose (Alfa Aesar, Karlsruhe, Germany) as carbon source in constant light (1800 lx) or constant darkness at 28 °C on a rotary shaker (200 rpm) for 72 h. Dark grown cultures were harvested under red safety light (darkroom light, Philips PF712E) to prevent any influence of a light pulse on transcript levels.
For HPTLC analysis, strains were cultivated on 2% malt extract agar medium at 22 °C, LD (12 h light, 12 h darkness) at 1700 lx until harvest after 14 days. Petri dishes were inoculated near the margin with agar slices of 0.5 × 4 cm from fully grown cultures to guarantee an even confrontation line.
For transcriptome analysis, custom arrays were used with the gene expression service as provided by Roche-NimbleGen (Madison, USA). Therefore, total RNA was isolated and quality controlled as described previously [40, 44]. Data of two biological replicates are deposited at NCBI Gene Expression Omnibus (GEO accession number GSE131419). Bioinformatic analysis was done using the PARTEK Genomics Suite 6.6 (St. Louis, USA) applying a threshold of twofold regulation and a p-value of 0.01 (false discovery rate (FDR) corrected; ANOVA statistics). Functional category analysis was done using the FUNGIFUN2 online tool . Genomic clustering was evaluated using the open source software REEF  and adjusted manually.
Construction and analysis of ∆gin4
Deletion of gin4 (TR_64125) was performed as described previously  using yeast mediated recombination for vector construction and protoplast transformation for homologous integration into QM6a∆mus53  and the hygromycin phosphotransferase cassette as selection marker. Successful deletion of gin4 was confirmed by PCR with primers binding within the deleted region. DNA integrity appropriate for PCR amplification of the samples representing gin4 was ensured using standard primers amplifying the tef1 gene. Sexual development was investigated under standard conditions [71, 77]. ∆gin4 was grown on minimal medium with cellulose as carbon source as described above in constant darkness. Trichodimerol production in culture filtrates was analyzed by mass spectrometry using internal standards as described previously [46, 78].
High-performance thin-layer chromatographic (HPTLC) analysis and sample preparation
Detection and quantification of trichodimerol using HPTLC
Trichodimerol was identified in secondary metabolite samples by comparing the Rf-value and UV/vis spectra (200–800 nm; Scanner 3, CAMAG, Muttenz, Switzerland) to those of the isolated reference compound. Trichodimerol was quantified relative to wildtype. A linear calibration based on peak height at 420 nm was obtained from combined wildtype replicates and two dilutions (1:3; n = 3). Significance was evaluated by t-test in RStudio (compare_means, ggpubr).
Isolation of trichodimerol
Well grown FF1 and FF2 plates containing 3% (w/v) malt extract agar were extracted with an excess amount of a mixture of chloroform and acetone (1:1) and sonication for 15 min. The solvent mixture was filtered and further purified by two times liquid–liquid extraction with water. The solvents of the organic phase were evaporated and the crude extract stored at − 20 °C until processing.
Size-exclusion column chromatography of 126 mg crude extract over Sephadex LH-20® [GE Healthcare; 750 mm column length, 12 mm diameter, coupled with C-640 UV detector (Büchi)] eluted isocratically with methanol yielded 16 mg of impure trichodimerol. Final purification of this fraction was accomplished by preparative thin layer chromatography (TLC) using silica gel 60 glass plates (PLC Silica gel 60 F254, 0.5 mm thickness; Merck, Darmstadt, Germany) developed in dichloromethane/methanol (98:2). This step afforded 7.2 mg trichodimerol.
For NMR spectroscopic measurements trichodimerol was dissolved in CD3OD (~ 3.0 mg in 0.7 mL) and transferred into 5 mm high precision NMR sample tubes. All spectra were measured on a Bruker DRX-600 at 600.25 MHz (1H) or 150.94 MHz (13C) and performed using the Topspin 3.5 software (Bruker, Rheinstetten, Germany). Measurement temperature was 298 K ± 0.05 K. 1D spectra were recorded by acquisition of 32 k data points and after zero filling to 64 k data points and Fourier transformation spectra were performed with a range of 7200 Hz (1H) and 32,000 Hz (13C), respectively. To determine the 2D COSY, TOCSY, NOESY, HMQC, and HMBC spectra 128 experiments with 2048 data points each were recorded, zero filled and Fourier transformed to 2D spectra with a range of 6000 Hz (1H) and 24,000 Hz (HSQC) or 32,000 Hz (HMBC) (13C), respectively. Residual CD2HOD was used as internal standard for 1H NMR measurements (δH 3.34) and CD3OD for 13C NMR measurements (δC 49.0).
Mass spectra were measured on a high resolution time-of-flight (hr-TOF) mass spectrometer (maXis, Bruker Daltonics) by direct infusion electrospray ionization (ESI) in positive ionization mode (mass accuracy ± 5 ppm). TOF MS measurements have been performed within the selected mass range of m/z 100–2500. ESI was made by capillary voltage of 4 kV to maintain a (capillary) current between 30 and 50 nA. Nitrogen temperature was maintained at 180 °C using a flow rate of 4.0 l min−1 and the N2 nebulizer gas pressure at 0.3 bar.
We acknowledge NMR Center and MS Center, Faculty of Chemistry, University of Vienna for measuring NMR and MS spectra, respectively. We want to thank Sabrina Beier, Michael Sulyok, Kaja S. Liepert and Bianca Mikulasek for technical assistance.
DT and AS performed experimental work for transcriptome analysis and contributed to bioinformatic analyses. WH contributed to secondary metabolite analysis and to drafting of the manuscript. EÖ extracted and measured secondary metabolites. HB contributed construction and analysis of the deletion strain. StB contributed to secondary metabolite analysis and quantification. WH and StB supervised work of EÖ. JS extracted trichodimerol. LB performed NMR structure elucidation. MS conceived of the study, supervised work of DT, AS, and WH, contributed to bioinformatic analyses and wrote the final version of the manuscript. All authors read and approved the final manuscript.
Work of WH was supported by the NFB (Science Fund of Lower Austria; grant LC16-04 to MS). Work of DT and AS was supported by the Austrian Science Fund (FWF; grant P22511 to MS). Work of HB was supported by the Austrian Science Fund (FWF, grants P24350 and P26935).
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The authors declare that they have no competing interests.
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