- Open Access
A versatile toolkit for high throughput functional genomics with Trichoderma reesei
© Schuster et al; licensee BioMed Central Ltd. 2012
- Received: 20 September 2011
- Accepted: 2 January 2012
- Published: 2 January 2012
The ascomycete fungus, Trichoderma reesei (anamorph of Hypocrea jecorina), represents a biotechnological workhorse and is currently one of the most proficient cellulase producers. While strain improvement was traditionally accomplished by random mutagenesis, a detailed understanding of cellulase regulation can only be gained using recombinant technologies.
Aiming at high efficiency and high throughput methods, we present here a construction kit for gene knock out in T. reesei. We provide a primer database for gene deletion using the pyr4, amdS and hph selection markers. For high throughput generation of gene knock outs, we constructed vectors using yeast mediated recombination and then transformed a T. reesei strain deficient in non-homologous end joining (NHEJ) by spore electroporation. This NHEJ-defect was subsequently removed by crossing of mutants with a sexually competent strain derived from the parental strain, QM9414.
Using this strategy and the materials provided, high throughput gene deletion in T. reesei becomes feasible. Moreover, with the application of sexual development, the NHEJ-defect can be removed efficiently and without the need for additional selection markers. The same advantages apply for the construction of multiple mutants by crossing of strains with different gene deletions, which is now possible with considerably less hands-on time and minimal screening effort compared to a transformation approach. Consequently this toolkit can considerably boost research towards efficient exploitation of the resources of T. reesei for cellulase expression and hence second generation biofuel production.
- Trichoderma reesei; Hypocrea jecorina
- vector construction
- gene knock-out library
- sexual crossing
The increasing awareness of the limited availability of fossil fuels along with the environmental problems caused by their application initiated considerable research efforts towards clean and sustainable biofuels [1–3]. Thereby, the cellulases required to degrade cellulosic plant materials into small building blocks, which can be metabolized by yeast or other microbes to ethanol or hydrocarbon biofuel precursors, respectively, are one major focus of investigation . Trichoderma reesei (Hypocrea jecorina) is currently the most efficient producer of enzyme mixtures for degradation of plant materials . The cellulases produced by this fungus are utilized for diverse industrial processes, from biobleaching of textiles, paper recycling to juice extraction and even as additives in animal feeds [6–8].
The long-standing use of cellulase production by T. reesei is paralleled by a thorough investigation of the cellulolytic enzyme system of this fungus and its regulation [9, 10]. With publication of the genomic sequence of T. reesei , the progress in understanding the mechanisms of cellulase regulation was accelerated. Analysis of the genome indicated, that despite its production efficiency, T. reesei has the lowest amount of cellulolytic enzymes among Sordariomycetes at its disposal.
In order to gain an understanding of gene regulation, manipulation of the genome of T. reesei is indispensible. A transformation system for this fungus has been available for decades with amdS , pyr4  and hph  being the most frequently used selection marker systems. Also pyrithiamine resistence , benomyl resistence  and hexokinase  have proven useful for transformation of T. reesei. Additionally, vector systems enabling excision of the marker gene cassette has facilitated multiple sequential genome modifications despite the limited availability of marker systems [18, 19]. Nevertheless, the typical efficiency of homologous integration is less than 10% using these methods.
One of the most important advancements in recent years, for improving the performance of research with T. reesei was the development of strains deficient in non-homologous endjoining (NHEJ) [19, 20]. These strains strongly enhance the probability of homologous integration of DNA constructs for deletion or modification of genes. Up to 95% of transformants were the result of homologous integration events . While in most fungi little discernible phenotype is reported for this mutation, the respective strains are more sensitive to DNA damage , the HOG-MAPkinase pathway is up-regulated  and effects on genes involved in carbohydrate transport  have been observed in some organisms. The major drawbacks of using strains deficient in non-homologous end joining, however, is that this mutation causes telomere shortening and defects in DNA repair , both of which negatively influence genome stability and fitness of the respective strains.
Recently, a further tool for work with T. reesei became available: After decades of research leading to the conclusion that T. reesei is a clonal, asexual derivative of a previously sexual species , the capability of this fungus for sexual development was discovered . Besides the physiological relevance, this finding also opens up a wide array of new possibilities for research with T. reesei. Crossing can now be used for strain improvement and classical genetics. However, the fact that the parental strain of all T. reesei strains used in research and industry, QM6a, is female sterile , necessitates the use of a sexually competent wildtype isolate for crossing. Consequently, the genetic background introduced by this closely related but also phenotypically different isolate represents a serious drawback for use of sexual crossing in research.
Genome sequencing and high throughput analysis methods for transcriptomics, proteomics and metabolomics have had considerable impact on how research with fungi progresses . Despite considerable improvements in transformation techniques, the recent increase in available genomic sequences of fungi also caused the need to efficiently use these resources. However, despite the wealth of data created, in depth functional analysis of genes often lags behind and consequently many fungal genome databases still remain with their most precious treasures undiscovered. Mostly, this is due to the enormous effort necessary for creation of a gene knock out library, which necessitates thousands of experiments and subsequent screenings. Therefore the respective methods need to be streamlined and automated as much as possible. For the model organism, Neurospora crassa, a community-wide effort recently led to the completion of a whole genome knock-out library . This resource is especially important for evaluation of transcriptome data, because screening of a large number of mutant strains considerably increases the knowledge and understanding to be gained from these studies [28, 29]. Additionally, the possibility to study a group of functionally related genes, such as transcription factors can provide intriguing insights into previously unexplored physiological processes [30, 31].
While elaborate molecular biological tools are available for other fungi, especially N. crassa, tools for efficient systematic analysis of gene function are relatively under-developed in T. reesei. Despite its widespread use in industry, no comprehensive gene knock out library is available for this fungus, nor are there currently efforts to start such an initiative. We therefore aimed to provide a dependable and easy to handle toolkit as a first step towards creation of larger sets of gene knock out strains in T. reesei.
In this study we explored strategies to enable high throughput gene-knockout along with efficient construction of multiple mutants. We applied yeast based recombination mediated vector construction, transformation by electroporation and subsequently removal of the NHEJ-deficient background by crossing with a sexually competent T. reesei strain derived from QM9414. Genome wide primer libraries for knock out vector construction using different marker systems complete this toolkit. These methods can serve as a basis for construction of large scale libraries of knock out strains for systematic functional genomic studies with T. reesei.
Vector construction by yeast mediated recombination
Overview about selected T. reesei genes.
ORF length [bp]
protein size [aa]
successful transformation method
protein kinase C
g-protein alpha subunit two
hypothetical cyclic AMP phosphodiesterase, class II
g-protein alpha subunit three
nonribosomal peptide synthetase (NRPS)
hypothetical GPCR, family 2
G-protein coupled receptor
DNA methylase, required for RIP (GenBank Accession number: JN227866)
Zn2Cys6 transcription factor
basic leucine zipper transcription factor
Zn2Cys6 transcription factor
hypothetical GPCR, family 2,
G-protein coupled receptor
putative E3 ubiquitin ligase
hypothetical transmembrane protein, transport protein
hypothetical F-Box/WD40 repeat protein
Zn2Cys6 transcription factor
G-protein coupled receptor
non-ribosomal peptide synthetase
Construction of deletion mutants in an NHEJ-deficient background
For high throughput gene deletion a high efficiency of homologous recombination is indispensable. Previous deletion of the tku70 gene in T. reesei TU-6, a uridine auxotrophic derivative of QM9414 , resulted in a strain deficient in non homologous endjoining resulting in a homologous integration efficiency which is higher than 95% . For transformation we used both conventional protoplasting  and spore electroporation, as indicated with the respective genes (Table 1). Electroporation was found to be less time consuming and easier to handle,
From the resulting transformants we chose five colonies per gene, which considering the high recombination frequency should result in identification of a positive mutant. For screening we used a PCR based mutant screening. For each gene we designed a specific primer which binds outside from the deletion cassette in the flanking regions of the gene (Additional file 1 Figure 1B). In combination with a specific primer which binds inside of the selectable marker (pyr4) and the primer which binds outside from the cassette we were able to very efficiently screen the mutant strains by PCR. An integration of the deletion cassette at the homologous locus results in a specific amplicon with a size between 1400 to 2000 bp (data not shown) depending on the exact location of the outside primer.
The PCR screening method showed that we were able to generate 18 out of 20 deletion mutant strains. We failed with generation of mutant strains of the following genes: tr_123806, and tr_72004. The frequency of homologous integration was between 33 and 100%.
Phenotype of Trichoderma reesei mutant strains
The mutant lacking NCU00478.5, the homologue of the T. reesei phosphodiesterase gene pde2 (tr_102655), is white due to lack of pigment and no conidia are formed in slants on minimal medium at 25°C. Similarly, the respective T. reesei deletion strain Δpde2 shows reduced growth and white pigmentation. Also the Δfwd1 (tr_79756) strain shows reduced and white pigmentation which was also described for its N. crassa ortholog (NCU04540.5). Deletion of gpr2 (tr_28731) and hpo1 (tr_109088) in T. reesei leads to a reduced growth on rich medium but no phenotype was described for the orthologous genes (NCU04626.5 and NCU04017.5) strain in N. crassa. Deletion of gna3 (tr_21505) leads to a higher sporulation on malt extract plates, a phenomenon which was also shown for mutants of this gene in the closely related Trichoderma atroviride .
This pilot study showed that using vector construction by yeast mediated recombination, amplification of transformation cassettes and electroporation can significantly reduce hands-on time and considerably enhance efficiency of deletion mutant construction. We therefore went on to design an automated approach for construction of deletion primers for all T. reesei genes. This automated approach yielded a full set of primers for 8661 of the 9143 genes in T. reesei v2.0, as well as a partial set of primers for 488 of the genes for use with the pyr4 selection marker system in the NHEJ-deficient background of T. reesei Δtku70 (Additional file 2).
Rescue of non homologous end joining by crossing
Since the deficiency in NHEJ not only brings the advantage of a higher probability of positive transformants, but also the problem of increased sensitivity to DNA damage, decreased genome stability and some changes in gene expression in some fungi [21–23], rescue of wild-type NHEJ is advisable.
All mutant strains created in the course of this study are still able to mate with CBS999.97 and also with QF1 despite their deletions. As a proof of principle we selected three deletion strains for the crossing approach aimed at removal of the tku70 deletion: Δgna2, Δgna3 and Δrid1. While Δgna2 does not show a discernible phenotype, sporulation is increased in Δgna3 and Δrid1 is of particular interest, because in this mutant the mechanism of repeat induced point mutation (RIP) is likely to be perturbed. Deletion of the homologue of rid1 (RIP-deficient-1) in N. crassa abolishes RIP . In T. reesei this phenomenon has not yet been demonstrated, nevertheless the low frequency of gene duplications in the genome of this fungus could be due to the operation of RIP .
Mating assays were performed on malt extract medium . Crosses of these three strains were successful, albeit for Δgna3 lower fertility in sexual crosses was expected . After three weeks the resulting ascospores were isolated randomly and the colonies were grown on selective medium and analyzed. Growth on hygromycin containing medium indicated that the tku70 deletion was retained, and strains not able to grow in the presence of hygromycin were selected for further analysis. Growth on malt extract medium indicated presence of the initial gene deletion i. e. presence of the functional pyr4 marker gene. Strains growing on malt extract medium without uridine as supplement were checked for presence of the genes of interest. PCR screening confirmed restoration of the wild type tku70 and showed that the desired gene deletion was retained.
While this method provides a significant improvement compared to retransformation, because no additional marker genes are needed and the hands on time to achieve rescue of the deletion is decreased there are certain issues to be considered. Due to the number of backcrosses, QF1 is estimated to contain approximately 96 - 97% of the QM9414 genome including the same percentage of QM9414 specific mutations . Thus, QF1 can also be assumed to contain 3 - 4% of the differences that distinguish QM9414 from CBS999.97.
Interestingly, a recent survey on classical mutations and genome polymorphisms in N. crassa  revealed significant genomic variation in classical mutant strains in this fungus. Nevertheless, these strains represent the basis for decades of research with N. crassa and the estimated level of difference between QF1 and QM9414 is well within the range used historically for Neurospora genetic studies.
The major difference between QF1 and QM9414 is likely to be found in the gene(s) involved in female fertility (and the genes located nearby in the genome), which is functional in QF1 and enables this strain to undergo sexual development with female sterile QM6a and its derivatives including QM9414. The nature of the responsible gene(s) is currently unknown as is its function. Additionally, QF1 has mating type MAT1-1 and hence certain differences in gene expression related to the mating type cannot be excluded . We therefore recommend use of MAT1-2 progeny for further analysis and comparison with QM9414 data.
Although mating is a very efficient means of strain improvement and construction of multiple mutants, the fact that sexual development may introduce alterations in the genome has to be considered. In case of QF1, this includes the unlikely but possible interference of the small portion of the CBS999.97 genome retained in this strain. Therefore, segregation of the observed phenotype of a mutant with the selection marker has to be evaluated for several progeny. Additionally, as required with conventional transformations, different mutant strains have to be checked to confirm the effect of the mutation.
Increasing utility of the system by additional selection markers
Since the mutation causing uridine-auxotrophy of Δtku70 is not a complete deletion of the pyr4 gene , the preconditions for the operation of RIP (homologous sequences longer than 400 bps) would be fulfilled . Use of alternative selection markers will likely prove to be beneficial. We consequently modified the full genome primer set described above for use with the amdS marker system , which can also be used with the NHEJ deficient strain Δtku70  (Additional file 3). Additionally, we provide this primer set for use with the hph-marker cassette (Additional file 4) used in the N. crassa high throughput gene knock out program  appropriate for transformation of the NJEH deficient strain QM6aΔtmus53 . These marker systems do not involve the use of homologous sequences of T. reesei and thus circumvent possible problems with RIP. Alternatively, Δrid1 could be used for these constructions, which however would require subsequent removal of this background in order to avoid side effects by this mutation.
The study presented here is intended to serve as a basis for fast and efficient analysis of gene function in T. reesei. Recent studies on genomes of early industrial mutants of T. reesei revealed several interesting mutations in these strains [35, 39, 40], but nevertheless, in many cases the specific genes responsible for the effect on cellulase gene expression as well as possible synergistic effects in these mutant strains, remain to be elucidated. Regulation of cellulase gene expression has been a focus of research with T. reesei for decades and hence a considerable number of transcriptome studies are available [41, 42]. Since the availability of the genome sequence of T. reesei  several approaches using genome-wide microarrays have been reported [43, 44]. These studies provide intriguing insights into various aspects of cellulase gene expression, from transcription factors to secretion pathways. Investigation of the target genes identified to be involved in cellulase regulation by analysis of gene knock out strains largely covering the involved pathways would be a logical further step towards elucidation of the mechanisms triggering induction, transcription, processing and secretion of cellulolytic enzymes.
The high relevance of T. reesei for the production of economically feasible second generation biofuels from cellulosic agricultural waste instead of food crops still requires considerable improvement of the efficiency of the cellulase mixture secreted . Moreover, the use of T. reesei as a host for heterologous protein production necessitates a more detailed understanding of the physiology of this fungus. Our streamlined system for knockout-construction along with the convenient and easy to use method to create multiple mutants by crossing can serve as a starting point for large scale functional analysis studies aimed to uncover the hidden treasures of the biotechnological workhorse T. reesei.
Strains and plasmids
T. reesei Δtku70, which is defective in the non-homologous end-joining pathway  was used in the present study and was maintained on potato dextrose agar (PDA, Difico, Detroit, USA) which was supplemented with 5 mM uridine (Sigma Aldrich, St. Louis, USA) in order to complement the auxotrophy of strain TU-6, a derivative of QM9414 . Parental strain QM9414 (ATCC 26921; [35, 46]) and strains derived from it were maintained on 3% (w/v) malt extract with 2% (w/v) agar 28°C. Mating experiments were performed as described previously . Briefly, strains were grown on 3% (w/v) malt extract medium with 2% (w/v) agar. Plates were incubated at 20-25°C in daylight for 10 - 14 days until formation of fruiting bodies and ascospore discharge. For yeast transformation the shuttle vector pRS426  and the yeast strain WW-YH10 (ATCC number: 208405) were used.
Vector construction for gene deletion
For construction of deletion vectors for the selected genes (Table 1) the orotidine-5'-phosphate decarboxylase gene of T. reesei (pyr4, TR_74020) was used as selectable marker. The marker gene was amplified using primers pyr4F and pyr4R (supplementary file 1). The 50 μl reaction mixture contained 1.25 U Takara Ex Taq™ (Takara Bio, Madison, Wisconsin), 1 × Ex Taq™ Buffer, 0.2 mM dNTP, 0.1 μM forward and reverse primer, 1 μl T. reesei QM9414 genomic DNA (90 ng/μl) as template and nuclease free water. The selectable marker PCR fragment was purified using the E.Z.N.A. Gel Extraction Kit (Omega Bio-Tek, Inc., Norcross, USA).
For generation of the respective 5' and 3' flanking sequences, primers (Table 1) were designed with the OligoExplorer software (version 1.1.2; http://www.genelink.com/tools/gl-oe.asp). In order to enable yeast-mediated recombination of the deletion cassette, linker sequences were added to the primers for amplification of the 5' and 3' flanking region (supplementary file 1; Figure 1). Sequences were obtained from: T. reesei genome database (JGI webpage: http://genome.jgi-psf.org/).
The PCR mixture contained 1.25 U Takara Ex Taq™ (Takara Bio, Madison, Wisconsin), 1 × Ex Taq™ Buffer, 0.2 mM dNTP, 0.1 μM forward and reverse primer, 1 μl T. reesei wild-type genomic DNA (90 ng/μl) as template and nuclease free water.
A genome-wide database of primers for the 5' and 3' fragments for construction of the deletion cassette by yeast mediated recombination was generated using a Python script (provided by Peter Andrews of the Neurospora Genome Project) that serialized the function of the Primer3 core primer design program . A masked genome sequence file and a gene annotation file for T. reesei v2.0 were downloaded from the Joint Genome Institute (JGI; http://genome.jgi-psf.org/Trire2/Trire2.download.html) and converted into a format suitable for input into the Python script. The default parameters which were used for Primer3 were the predefined 29 nucleotide sequences attached to the primers (supplementary file 1) and the following settings: optimal primer length = 20 bp, minimum primer length = 19 bp, flanking region length = 1500 bp, primer product size = min: 1000 bp and max.: 1300 bp, maximal size of GC clamp in primer = 2, primer optimal temperature = 56°C, primer GC content = min: 50% and max: 65%, monovalent catio salt concentration = 50 mM and concentration of annealing DNA oligo = 200 nM.
Vector construction and yeast mediated recombination
The yeast shuttle vector pRS426 was digested with EcoRI and XhoI (restriction enzymes were purchased from New England Biolabs, Ontario, Canada) and purified with the E.Z.N.A. Gel Extraction Kit (Omega Bio-Tek, Inc., Norcross, USA). Yeast transformation and preparation was performed essentially as described previously [30, 49, 50].
An overnight culture (200 rpm, 30°C) of the yeast strain WW-YH10 was prepared. 1 ml of the overnight culture was added to 50 ml of fresh YPD (1% yeast extract, 2% peptone, 1% glucose (all chemicals from Sigma Aldrich, St. Louis, USA unless noted otherwise)) medium and incubated at 30°C until O.D.600 = 1. The cells were centrifuged at 14.000 rpm for 3 min. The supernatant was discarded and the pellet was washed with 25 ml of sterile water and centrifuged again for 3 min. The supernatant was discarded and the pellet was resuspended in 400 μl of 100 mM lithium acetate (Sigma Aldrich). 50 μl of yeast cell suspension was centrifuged for 20 sec and 240 μl 50% PEG 3550, 36 μl 1 M lithium acetate, 50 μl sheared salmon sperm DNA (2 mg/ml) (Sigma Aldrich) and 34 μl sterile water was added to the pelleted cells. Thereafter, 200 ng of 5' DNA fragment, 200 ng of 3' DNA fragment, 100 ng of digested pRS426 and 100 ng of selectable marker fragment was added and mixed. After the heat shock for 30 min at 42°C the mixture was centrifuged for 15 sec at 14.000 g and the supernatant was discarded. 1 ml of sterile water was added, and after thorough mixing centrifuged for 15 sec again. 800 μl of supernatant was discarded and the rest was spread onto SC-URA (1.54 g/l BSM-Iso-Ura Powder, 1.71 g/l yeast nitrogen base (Sunrise Science Products, San Diego, USA), 5 g/l ammonium sulfate, 20 g/l glucose and 20 g/l agar (Sigma Aldrich, St. Louis, USA)) plates and incubated for 3-4 days at 30°C. The resulting colonies were resuspended in 2 ml of sterile water and transferred into a new reaction tube. The sample was centrifuged for 15 sec at 14.000 g and the supernatant was discarded. 400 μl of smash-and-grab lysis buffer (2% Triton X-100, 1% SDS, 100 mM NaCl, 10 mM Tris pH 8.0, 1 mM EDTA), 500 μl phenol (pH = 7.8), 500 μl chloroform/isoamylalcohol (48:2) and 0.3 g of glass beads were added and mixed well. After centrifugation for 10 min at 14.000 g the supernatant was transferred to a new reaction tube and 500 μl of chloroform was added and mixed. The supernatant, after centrifugation for 10 min at 14.000 g, was transferred to a new reaction tube and 0.3 M sodium acetate (pH 5.2) and 2.5 volumes of ethanol (96%) were added. After precipitation and centrifugation for 10 min at 14.000 g, the pellet was washed with 400 μl 70% ethanol and resuspended in 50 μl of sterile water. The final linear deletion cassette was amplified from this solution by PCR. The mixture contained 1.25 U Takara Ex Taq™ (Takara-Bio, Madison, USA) appropriate buffer as described in the application manual, 0.2 mM dNTP, 0.1 μM forward (5F) and reverse primer (3R), 2 μl of isolated yeast DNA (approx. 100 ng) and nuclease free water. The protocol was: 94°C 3:00 min followed by 3 cycles of 94°C, 30 sec; 65°C, 30 s; 72°C, 2:00 min; followed by 2 cycles of 94°C, 30 sec; 63°C, 30 s; 72°C, 2:00 min; followed by 30 cycles of 94°C, 30 sec; 60°C, 30 s; 72°C, 2:00 min; and a final extension of 72°C, 10:00 min. The final linear deletion cassette was purified using the E.Z.N.A. Gel Extraction Kit (Omega Bio-Tek, Inc., Norcross, USA).
Transformation of T. reesei
The T. reesei Δtku70 strain  was used for transformation in order to achieve a high efficiency in homologous integration of the deletion cassettes. The protoplast transformation was carried out as previously described . For transformation 2.5 μg of purified deletion cassette fragment was used. Transformants were grown on selective minimal medium (1 g/liter MgSO4*7H2O, 10 g/liter 1% KH2PO4, 6 g/liter (NH4)2SO4, 3 g/liter trisodium citrate*2H2O, 10 g/liter glucose, 20 ml/liter 50x trace elements solution (0.25 g/liter FeSO4*7H2O, 0.07 g/liter ZnSO4*2H2O, 0.1 g/liter CoCl2*6H2O, 0.085 g/liter MnSO4*H2O), 2% (wt/vol) agar; all chemicals were from Sigma Aldrich, St. Louis, USA).
The protocol for electroporation of T. reesei was adapted from patent application US2010/0304468. Spores of T. reesei Δtku70 were harvested from a freshly sporulated 90 mm malt extract agar plate and suspended in 1.1 M sorbitol. Spores were washed twice, resuspended in 100 μl 1.1 M sorbitol and cooled on ice. 75 μl of cold spore suspension was mixed with 10 μg of vector of interest. For electroporation we used an Electroporation System ECM® 630 (BTX Instrument Division Harvard Apparatus, Holliston, USA). 1.8 kV, 800 Ω and 25 μF were used as setting for the ECM® 630 device. Thereafter one volume of the reaction mixture (consisting of spore suspension plus deletion cassette) of YEPD (1% (w/v) yeast extract, 2% (w/v) peptone, 1% (w/v) glucose) and four reaction volumes 1.1 M sorbitol were added and mixed. For regeneration the whole mixture was incubated over night at room temperature. Thereafter, spores were streaked out on plates containing selection medium.
Compared to the classical protoplast transformation technique  transformation by electroporation is less time consuming, easier to perform and the efficiency of this method was comparable to that of protoplast transformation.
Putative deletion strains were tested for integration of the construct by PCR using primer pyr4Sc (inside in the selectable marker gene pyr4) and the gene-specific primer, geneSc (outside from the transformation cassette) (supplementary file 1). Successful homologous integration results in a specific amplicon (1400 - 2000 bp's, depending on the gene) (supplementary file 1) and no amplification was possible with T. reesei Δtku70 genomic DNA (data not shown).
Construction of a sexually competent derivative of QM9414
The female sterile wild type strain QM9414 (MAT 1-2) and the sexually competent wild-type strain CBS999.97 (MAT1-1)  were inoculated on 3% (w/v) malt extract medium with 2% (w/v) agar for two to three weeks at 28°C until ascospore discharge. The ascospores were isolated from the lid with sterile water. This solution was spread out on a 3% (w/v) malt extract medium with 2% (w/v) agar plate and incubated at 28°C for two days until single colonies could be observed. The resulting colonies were screened for the mating type and again crossed to QM9414. The number of sexually competent strains decreased after each round of crossing, indicating a small region of the genomic to be relevant for this process. After five rounds of backcrossing, sexually competent strains with mating type MAT1-1 were tested for their phenotype upon growth on plates and a strain with characteristics largely indistinguishable from QM9414 was selected for further analysis.
For comparison of cellulase production, the parental strain QM9414 and QF1 were grown in 200 ml of liquid Mandels-Andreotti minimal medium with 1% (w/v) microcrystalline cellulose (No. 14204; Serva, Heidelberg, Germany) as carbon source at 200 rpm and 28°C in a rotary shaker. After 5 days of cultivation, samples were harvested and biomass formation and cellulase activity were measured as described previously .
Crossing of the deletion mutant strains against QF1
The deletion strains were crossed with QF1 as described previously . Ascopores were isolated and colonies were grown on selective medium in order to obtain progeny carrying the desired gene deletion, but not the Δtku70 background. The resulting strains were tested for restoration of the tku70 locus using primers tku70ORFF and tku70ORFR. DNA was isolated with standard protocols. Successful restoration results in a specific band (480 bp's) for tku70 whereas no amplification was possible in the Δtku70 background. Screening of mutants for propagation of the desired deletion was performed by PCR as described above.
We want to thank Kulwant Kandra for technical assistance with selected analyses. Work of AS and MS was supported by grants from the Austrian Science Fund (FWF; P20004 and V152-B20) to MS. The T. reesei genome sequencing project was done at the Joint Genome Institute (JGI) funded by the US Department of Energy.
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