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Academic literature on the topic 'Trichoderma reesei'

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Published: 4 June 2021
Last updated: 31 July 2024

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Journal articles on the topic "Trichoderma reesei"

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Schmoll, Monika. "Trichoderma reesei." Trends in Microbiology 30, no. 4 (April 2022): 403–4. http://dx.doi.org/10.1016/j.tim.2021.12.008.

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Jasim Mahi, Aymen, and Yasir Naser Alhamiri. "First record of Fusarium brachygibbosum as a causal agent of seed decay and damping-off disease on cotton in Iraq and Control using some bioagents." Bionatura 8, no. 4 (December 15, 2023): 1–15. http://dx.doi.org/10.21931/rb/2023.08.04.63.

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The results of the isolation and identification of pathogens accompanying the symptomatic seeds and seedlings of cotton showed that the most common fungus was Fusarium brachygibbosum. Molecular identification of the studied fungus was performed using the universal primers: the results of the genetic analysis revealed the identities of the fungus as follows: a 100% identity for F. brachygibbosum that was deposited at the GenBank under accession number ON738702.1. This fungus has shown high pathogenicity against cotton seeds and seedlings by severely reducing their Germination and growth and treating cotton seeds with the biological factors of Trichoderma spp. It revealed a high efficiency in reducing disease incidence and increasing cotton germination percentage. Trichoderma viride showed the highest ability to increase seed germination to 94.44%. In comparison, the lowest ability reached 77.77 % in Trichoderma pseudokoningii and Trichoderma reesei—the results of extracting toxins from the filters of Trichoderma spp. The study's use of trichodermin and Gliotoxin showed the presence of trichodermin and Gliotoxin in large quantities. The percentage of toxin inhibition was significant against the growth of pathogenic fungi. The highest percentage of inhibition was 86.1% for the isolate Trichoderma koningiopsis, and the lowest percentage was 66.65% for the isolate Trichoderma reesei. As for the effect of isolates of resistant fungus on the Pathogen in the field, the highest germination rate was 100%, and the inhibition rate was 0.00% when using the biological preparation prepared from the isolates (T. viride, T. pseudokoningii, T. koningiopsis and T. reesei). Keywords: Fusarium brachygibbosum; Trichoderma spp.; Trichodermin; gliotoxin; Biological control.
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Jasim Mahdi, Aymen, and Yasir Naser Alhamiri. "Evaluation of the Efficacy of Trichoderma species and their Fungal Toxins in the Eradication of Alternaria alternata Causing Seeds Decay and Damping-off Disease on Cotton in Iraq." Bionatura 8, no. 4 (December 15, 2023): 1–14. http://dx.doi.org/10.21931/rb/2023.08.04.64.

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This study aimed to isolate and identify the pathogens accompanying the rotting and death of cotton seeds and seedlings. Also, some Trichoderma spp. were assessed against the fungal pathogen associated with the disease. The results showed that one of the essential isolated fungi, Alternaria alternata, has demonstrated high virulence in attacking cotton seeds and seedlings and reducing germination and growth. This fungus was identified based on its morphological and molecular characteristics. The Trichoderma species applied have shown high efficiency in reducing infection rates and increasing cotton germination percentage. Every isolate of Trichoderma showed a high efficiency against the fungus A. alternata by providing the highest antagonistic ability, reaching 93.75%. The highest percentage of inhibition growth of the pathogen (86.11%) was achieved by Trichoderma koningiopsis, while the lowest percentage of inhibition growth of the pathogen was 66.65 % for Trichoderma reesei. However, the biological formula prepared from species Trichoderma viride, Trichoderma pseudokoningii, Trichoderma koningiopsis and Trichoderma reesei displayed the highest percentage of inhibition of 100% against the fungus A. alternata. Keywords. Alternaria alternata; Trichoderma spp.; Trichodermin; gliotoxin; Biological control.
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Febrianti, Nurul Husnah. "(The Interactive Effect between Fermentation with Trichoderma reesei on Ammoniation on Fiber Component of Sugar Palm Pulp." Bulletin of Applied Animal Research 2, no. 2 (September 30, 2020): 56–60. http://dx.doi.org/10.36423/baar.v2i2.468.

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The purpose of this research was to examine the combination effect of fermentation time by Trichoderma reesei and ammoniation on fiber component of sugar palm pulp. The research used sugar palm pulp from Boyolali which was sun-dried. Sugar palm pulp fermentation with Trichoderma reesei requires nitrogen for microbial growth. Ammoniation process could loose lignocellulosic bonds and provides the nitrogen supply for Trichoderma reesei, therefore these treatments could optimize Trichoderma reesei in the fermentation process. Samples were fermented for 0, 3 and 6 days with 1,5% Trichoderma reesei. The research treatments were allocated according to a completely randomize design with pattern of 2x3 factorial. First factor was ammoniation treatment and second factor was variation of fermentation time. The parameters observedd were NDF, ADF, hemicellulose, cellulose and lignin. Research result showed that there is was no interactive effect between treatments on reducing levels of NDF and ADF, but interaction treatments decreased (P<0.05) levels of, cellulose and lignin. In conclusion, the interactive effet between fermentation time with Trichoderma reesei and ammoniation reduce levels of hemicellulose, cellulose and lignin in sugar palm pulp.
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Peterbauer, Clemens K., Erich Heidenreich, Ralph T. Baker, and Christian P. Kubicek. "Effect of benomyl and benomyl resistance on cellulase formation by Trichoderma reesei and Trichoderma harzianum." Canadian Journal of Microbiology 38, no. 12 (December 1, 1992): 1292–97. http://dx.doi.org/10.1139/m92-213.

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To investigate the possible relationship between resistance to benomyl and the production of cellulases by Trichoderma spp., we investigated the effect of benomyl on growth and cellulase formation in Trichoderma reesei, Trichoderma harzianum, and the benomyl-resistant mutant T. harzianum T95. While T. reesei produced the highest and T. harzianum the lowest cellulase amounts, growth of both strains was equally inhibited by 2 μg/mL benomyl. However, sublethal doses of benomyl (0.2–0.5 μg/mL) promoted growth, stimulated cellulase production, and produced a highly branched, crippled morphology. The same phenomenon was observed with T. harzianum T-95, albeit at higher (5–10 μg/mL) benomyl concentrations. Introduction of the Neurospora crassa ben gene, coding for a benomyl-resistant β-tubulin, into a T. reesei by transformation yielded a series of transformants, which exhibited increased growth, increased cellulase formation, and highly branched, crippled morphology. Key words: Trichoderma harzianum, Trichoderma reesei, benomyl, rhizosphere competence, cellulase.
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BHIKHABHAI, RAMAGAURI, GUNNAR JOHANSSON, and GÖRAN PETTERSSON. "Cellobiohydrolase from Trichoderma reesei." International Journal of Peptide and Protein Research 25, no. 4 (January 12, 2009): 368–74. http://dx.doi.org/10.1111/j.1399-3011.1985.tb02187.x.

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Kumakura, Minoru, Setsuko Kanno, and Kazutoshi Nisizawa. "Cellulase production in Trichoderma reesei immobilized with polymeric fibrous carriers." Canadian Journal of Microbiology 35, no. 10 (October 1, 1989): 968–71. http://dx.doi.org/10.1139/m89-159.

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Trichoderma reesei mycelia were immobilized on polymeric fibrous carriers covered with various polymers, using a radiation polymerization technique. The mycelia were firmly attached to the surface of the fibril of the carrier covered with hydrophobic polymers. Cellulase production was in some cases higher by immobilized mycelia than by free mycelia and was affected by the chain structure of the polymer.Key words: Trichoderma reesei, immobilization, radiation, cellulase, fibril.
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Brown, D. E., and A. J. Thornton. "Chitinous Material in Trichoderma reesei." Biotechnology Letters 20, no. 8 (August 1998): 777–79. http://dx.doi.org/10.1023/b:bile.0000015921.68046.d2.

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MURKOVIC, M., W. STEINER, and H. ESTERBAUER. "Electrofusion of Trichoderma reesei protoplasts." Letters in Applied Microbiology 5, no. 6 (December 1987): 107–9. http://dx.doi.org/10.1111/j.1472-765x.1987.tb01625.x.

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Shobha, Balagangadharaswamy, Thimappa Ramachandrappa Lakshmeesha, Mohammad Azam Ansari, Ahmad Almatroudi, Mohammad A. Alzohairy, Sumanth Basavaraju, Ramesha Alurappa, Siddapura Ramachandrappa Niranjana, and Srinivas Chowdappa. "Mycosynthesis of ZnO Nanoparticles Using Trichoderma spp. Isolated from Rhizosphere Soils and Its Synergistic Antibacterial Effect against Xanthomonas oryzae pv. oryzae." Journal of Fungi 6, no. 3 (September 20, 2020): 181. http://dx.doi.org/10.3390/jof6030181.

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The Plant Growth Promoting Fungi (PGPF) is used as a source of biofertilizers due to their production of secondary metabolites and beneficial effects on plants. The present work is focused on the co-cultivation of Trichoderma spp. (T. harzianum (PGT4), T. reesei (PGT5) and T. reesei (PGT13)) and the production of secondary metabolites from mono and co-culture and mycosynthesis of zinc oxide nanoparticles (ZnO NPs), which were characterized by a UV visible spectrophotometer, Powder X-ray Diffraction (PXRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron Microscopy (SEM) with Energy Dispersive Spectroscopy (EDAX) and Transmission Electron Microscope (TEM) and Selected Area (Electron) Diffraction (SAED) patterns. The fungal secondary metabolite crude was extracted from the mono and co-culture of Trichoderma spp. And were analyzed by GC-MS, which was further subjected for antibacterial activity against Xanthomonas oryzae pv. Oryzae, the causative organism for Bacterial Leaf Blight (BLB) in rice. Our results showed that the maximum zone of inhibition was recorded from the co-culture of Trichoderma spp. rather than mono cultures, which indicates that co-cultivation of beneficial fungi can stimulate the synthesis of novel secondary metabolites better than in monocultures. ZnO NPs were synthesized from fungal secondary metabolites of mono cultures of Trichoderma harzianum (PGT4), Trichoderma reesei (PGT5), Trichoderma reesei (PGT13) and co-culture (PGT4 + PGT5 + PGT13). These ZnO NPs were checked for antibacterial activity against Xoo, which was found to be of a dose-dependent manner. In summary, the biosynthesized ZnO NPs and secondary metabolites from co-culture of Trichoderma spp. are ecofriendly and can be used as an alternative for chemical fertilizers in agriculture.
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Dissertations / Theses on the topic "Trichoderma reesei"

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Lajoie, Denis. "Lactose hydrolases de Trichoderma reesei MCG-80." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp04/mq26227.pdf.

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Zhang, Qin. "COLLECTION OF TRICHODERMA REESEI CELLULASE BY FOAMING." University of Akron / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=akron1195069754.

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Heikinheimo, Lea. "Trichoderma reesei cellulases in processing of cotton /." Espoo : Technical Research Centre of Finland, 2002. http://www.vtt.fi/inf/pdf/publications/2002/P483.pdf.

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Chahal, Parminder Singh. "Cellulase production from lignocellulosic materials by Trichoderma reesei." Thesis, University of Ottawa (Canada), 1987. http://hdl.handle.net/10393/5536.

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Cochet-Giraud, Nelly. "Les Cellulases de Trichoderma reesei production et application /." Grenoble 2 : ANRT, 1987. http://catalogue.bnf.fr/ark:/12148/cb37604010n.

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Curach, Natalie Claire. "An investigation into the hex1 gene and gene promoter for the enhancement of protein production in Trichoderma reesei." Phd thesis, Australia : Macquarie University, 2005. http://hdl.handle.net/1959.14/71199.

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Supplementary material to figures contained on DVD only available with manuscript.
Thesis (PhD)--Macquarie University, Division of Environmental & Life Sciences, Dept. of Biological Sciences, 2005.
Bibliography: p. 221-244.
Introduction -- Materials and methods -- Isolation of the hex1 gene from Trichoderma reesei and Ophiostoma floccosum -- Expression of DsRed under the cbh1 promoter and the hex1 promoter with random integration -- Modified expression vectors containing a fusion to a portion of hex1 gene sequence -- Expression of DsRed from the hex1 locus and the phenotypic characteristics of a hex1 deletion mutant -- Summary and concluding discussion.
For Trichoderma reesei to be developed as an effiecient producer of a large variety of proteins, the expression system requires diversification. In particular, the choice of promoters available needs to be broadened to include promoters which are active in conditions other than those conducive to induction of cellulase expression. Using proteomics, the HEX1 protein was identified as an abundant protein of the cell envelope of T. reesei when grown on a range of carbon sources, suggesting that a strong constitutive promoter drives the expression of this physiologically important protein. This thesis is an exploration into the hex1 gene promoter and the role of hex1 in the maintenance of mycelium integrity in T. reesei with consideration for the application of this gene in the further development of filamentous fungi as protein expression systems. -- The single copy hex1 gene and flanking regions were isolated from T. reesei and another biotechnologically important fungus, Ophiostoma floccosum. The fluorescent reporter protein DsRed1-E5 was expressed under the T. reesei hex1 promoter and promoter activity was monitored by fluorescence CLSM and RNA analysis. During the rapid growth phase of a culture, the hex1 promoter was active in a range of carbon sources and three transcipt types with alternative tsp and splicing sites were discovered for the hex1 gene. The distribution of fluorescence throughout the mycelium suggested spatial regulation of the hex1 promoter as well as temporal regulation. The promoter was continually active in the absence of a functional hex1 gene product suggesting that the hex1 promoter is regulated in part, by negative feedback from the endogenous gene product. Interruption of the hex1 gene produced hyphae that leaked excessive volumes of cytoplasm when physically damaged which may be advantageous for the externalisation of selected protein products. The results indicate that the regulation of the hex1 hene promoter is complex and that the hex1 gene is integral to the maintenance of the integrity of the fungal mycelium.
Mode of access: World Wide Web.
xv, 244 p. ill
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Poggi-Parodi, Dante. "Une approche de biologie systémique pour développer des souches industrielles performantes de Trichoderma reesei." Electronic Thesis or Diss., Paris 6, 2014. http://www.theses.fr/2014PA066721.

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La compréhension de la régulation de la synthèse et sécrétion de cellulases dans le champignon Trichoderma reesei a fortement évolué ces dernières années. Cependant, le coût de production de cellulases reste encore un des principaux problèmes pour la production de bioéthanol à partir de lignocellulose. C’est dans ce contexte que mon projet de thèse s’inscrit, dans l’amélioration de la production de cellulases de T. reesei et son adaptation aux conditions industrielles. D’abord, nous avons réalisé une analyse du transcriptome sur une lignée de souches améliorées dans des conditions proches du procède industrielle avec lactose comme inducteur. Cette étude nous a permis de trouver des gènes spécifiquement régulés dans la souche plus performante, probablement impliqués dans sa grande capacité de production de cellulases. Dans un deuxième temps, nous avons identifié parmi les gènes régulés du transcriptome lesquels impliquées dans la production de cellulases. A cet effet, des souches mutées ont été construites et leur phénotype évalué. Trois de ces gènes mutés ont affecté la production de cellulase et leur fonction ont dévoilé des nouvelles mécanismes régules. Finalement, nous avons exploré les différences d’expression lorsque nous utilisons un hydrolysat de lignocellulose comme inducteur de cellulases à la place du lactose. Une étude du transcriptome dans ces conditions, nous a permis de caractériser les différences de régulation des gènes entre ces inducteurs. En outre, nous avons identifié un groupe des gènes probablement impliqué dans la détoxification qui peuvent être utilisés dans le futur pour développer une souche résistante aux inhibiteurs
A lot of progress had been done in recent years to understand the regulation of synthesis and secretion of cellulases in the fungus Trichoderma reesei. However, the production cost of cellulases still remains one of the most important limiting steps in the production of bioethanol from lignocellulose. It is in this context that my PhD project has been developed: to genetic engineering T. reesei strains to increase its cellulase production and its adaptation to industrial conditions. First, we conducted a transcriptome analysis to an improved lineage of industrial strains during cellulase production following conditions close to the industrial process (lactose as inducer and fed-batch culture in bioreactor). We found specifically regulated genes for the most performant strain, possibly involved in its high cellulase production capacity. Then, we identified which regulated genes from transcriptome were involved in cellulase production. For this purpose mutated strains for highly regulated genes were constructed and their phenotype assessed. Three mutated genes showed to impact cellulase production and their function gave us an insight into new mechanisms being regulated. Finally, we explored the expression differences when we used a lignocellulose hydrolysate as cellulases inducer instead of lactose. A transcriptomic study of cellulases production on lignocellulose hydrolysates and lactose, allowed us to characterize the differences in regulated genes between these inducers. In addition, a group of genes probably related to detoxification was identified and could be used in the future to develop an inhibitor resistant strain
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Askolin, Sanna. "Characterization of the Trichoderma reesei hydrophobins HFBI and HFBII /." [Espoo, Finland] : VTT Technical Research Centre of Finland, 2006. http://www.vtt.fi/inf/pdf/publications/2006/P601.pdf.

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Belshaw, N. J. "The nuclear matrix and gene expression in Trichoderma reesei." Thesis, University of East Anglia, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296346.

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Chan, Ho Tong Laetitia. "Amélioration du champignon cellulolytique Trichoderma reesei par reproduction sexuée." Thesis, Paris, Institut agronomique, vétérinaire et forestier de France, 2017. http://www.theses.fr/2017IAVF0017.

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Dans le cadre de la production de bioéthanol de deuxième génération, l’ingénierie génétique de Trichoderma reesei est une des solutions envisagées pour diminuer le coût de l’étape d’hydrolyse enzymatique. Elle permet d’améliorer les performances de sécrétion de ce champignon filamenteux producteur de cellulases et les propriétés de ces enzymes. Comme de nombreux champignons industriels, T. reesei a longtemps été considéré comme possédant exclusivement un cycle asexuel. La mise en évidence récente d’un cycle de reproduction sexuée chez ce champignon filamenteux ouvre de nouvelles perspectives d’amélioration des souches utilisées en biotechnologie. Cependant, comme toutes les souches industrielles de T. reesei dérivent de l’isolat sauvage QM6a, elles sont toutes de type sexuel MAT1-2 et stériles en tant que femelles. L’objectif de ce travail de thèse est de mettre en place la reproduction sexuée comme outil génétique et d’amélioration des performances des souches industrielles. Son utilisation en complément des outils d’ingénierie génétique permet de combiner des caractères intéressants ou d’en générer de nouveaux, de stabiliser les souches industrielles en éliminant les mutations non désirées, de s’affranchir des marqueurs de sélection et d’identifier les gènes et mutations responsables d’un caractère d’intérêt. La première partie de ce travail a été consacré à l’optimisation de la reproduction sexuée puis à l’étude des étapes et des mécanismes de la reproduction sexuée entre souches sauvages et hyperproductrices. Dans un deuxième temps, nous avons mis en place la reproduction sexuée entre des souches hyperproductrices femelles stériles, à l’aide de la stratégie originale de la « souche assistante », qui a abouti au rétablissement partiel de leur reproduction sexuée. Afin de compléter ce rétablissement, une étude de l’étape de fécondation que nous supposons être l’étape problématique dans notre stratégie a été initiée. Parallèlement, l’exploitation de la reproduction sexuée entre souches sauvage et hyperproductrices a permis de générer une souche hyperproductrice de cellulases, de type sexuel MAT1-1 donc compatible avec toutes les souches industrielles, femelle fertile et possédant une activité β-glucosidase améliorée. Enfin, la reproduction sexuée associée à la génétique classique (« Bulk Segregant Analysis ») et aux techniques de séquençage haut débit a été mise en oeuvre pour permettre l’identification de mutations impliquées dans des phénotypes d’intérêt
Genetic engineering of Trichoderma reesei is one of the solutions considered to reduce the cost of the enzymatic hydrolysis step in second-generation ethanol production processes. It allows the improvement of the secretory performances of this cellulase producer fungus and the properties of its enzymes. Like many industrial fungi, T. reesei has long been considered to possess exclusively an asexual cycle. The recent discovery of a sexual reproduction cycle in this filamentous fungus opens up new prospects of improvement for strains used in biotechnology. However, all industrial strains of T. reesei are derived from the wild isolate QM6a and therefore possess the MAT1-2 mating type and are female sterile.The aim of this work was to develop sexual reproduction as a genetic tool and to improve the performance of the industrial strains. In combination with the genetic engineering tools, it would enable combination of interesting traits or generation of new ones, improve strains stability by purging deleterious mutations, selection markers elimination and identification of genes and mutations responsible of interesting characteristics.The first part of this work was dedicated to the optimization of sexual reproduction and to the study of the steps and mechanisms of sexual reproduction between wild-type and hyperproducer strains. In a second step, we set up sexual reproduction between female sterile hyperproducer strains, using the original "assistant strain" strategy, which resulted in the partial restoration of their sexual reproduction. A study of the fertilization step was also initiated, as we suspect it to be the blocking point in our strategy. In a second part, we took advantage of sexual reproduction between wild-type and hyperproducer strains for (i) the generation of a MAT1-1 mating-type strain compatible with all industrial strains, female fertile and possessing improved β-glucosidase activity and (ii) the implementation of a bulk segregation analysis associated with high-throughput sequencing techniques to identify mutations involved in phenotypes of interest
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Books on the topic "Trichoderma reesei"

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Mach-Aigner, Astrid R., and Roland Martzy, eds. Trichoderma reesei. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1048-0.

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Nakari-Setälä, Tiina. Highly expressed Trichoderma reesei genes: Cloning, characterization and use in protein production on glucose-containing media. Espoo: Technical Research Centre of Finland, 1995.

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Heikinheimo, Lea. Trichoderma reesei cellulases in processing of cotton. Espoo [Finland]: VTT Technical Research Centre of Finland, 2002.

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Marc, Claeyssens, Nerinckx Wim, Piens Kathleen, and Royal Society of Chemistry (Great Britain), eds. Carbohydrates from Trichoderma Reesei and other microorganisms: Structures, biochemistry, genetics and applications. Cambridge: Royal Society of Chemistry, 1998.

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Askolin, Sanna. Characterization of the Trichoderma reesei hydrophobins HFBI and HFBII. [Espoo, Finland]: VTT Technical Research Centre of Finland, 2006.

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P, Kubicek C., and Royal Society of Chemistry (Great Britain), eds. Trichoderma reesei cellulases: Biochemistry, genetics, physiology and application. Cambridge [England]: Royal Society of Chemistry, 1990.

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TRICEL Symposium on Trichoderma Reesei Cellulases and Other Hydrolases (2nd 1993 Espoo, Finland). Trichoderma reesei cellulases and other hydrolases: Enzyme structures, biochemistry, genetics, and applications : proceedings of the TRICEL93 Symposium, June 2-5, 1993, Espoo, Finland. Helsinki, Finland: Foundation for Biotechnical and Industrial Fermentation Research, 1993.

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Miettinen-Oinonen, Arja. Trichoderma reesei strains for production of cellulases for the textile industry. [Espoo, Finland]: VTT Technical Research Centre of Finland, 2004.

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Salovuori, Irma. Biosynthesis of an inducible glycosylated secretory enzyme (CBH I) of Trichoderma reesei. Espoo: Technical Research Centre of Finland, 1987.

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Vasara, Tuija. Functional analysis of the RHOIII and 14-3-3 proteins of Trichoderma reesei. Espoo [Finland]: Technical Research Centre of Finland, 2002.

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Book chapters on the topic "Trichoderma reesei"

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Chenthamara, Komal, Irina S. Druzhinina, Mohammad J. Rahimi, Marica Grujic, and Feng Cai. "Ecological Genomics and Evolution of Trichoderma reesei." In Trichoderma reesei, 1–21. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-1048-0_1.

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Jovanović, Birgit. "Batch Cultivation of Trichoderma reesei." In Trichoderma reesei, 113–18. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-1048-0_10.

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Hardy, Nicolas, Maxime Moreaud, and Fadhel Ben Chaabane. "Image Analysis Method for the Characterization of Trichoderma reesei During Fermentations." In Trichoderma reesei, 119–33. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-1048-0_11.

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Meng, Qing-Shan, Fei Zhang, Chen-Guang Liu, Feng-Wu Bai, and Xin-Qing Zhao. "Measurement of Cellulase and Xylanase Activities in Trichoderma reesei." In Trichoderma reesei, 135–46. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-1048-0_12.

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Steiger, Matthias G. "Flow Cytometry for Filamentous Fungi." In Trichoderma reesei, 147–55. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-1048-0_13.

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Rahimi, Mohammad J., Feng Cai, Marica Grujic, Komal Chenthamara, and Irina S. Druzhinina. "Molecular Identification of Trichoderma reesei." In Trichoderma reesei, 157–75. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-1048-0_14.

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Rassinger, Alice. "In Vivo Footprinting Analysis in Trichoderma reesei." In Trichoderma reesei, 177–89. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-1048-0_15.

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Till, Petra. "RNA Characterization in Trichoderma reesei." In Trichoderma reesei, 191–235. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-1048-0_16.

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Ngan, So Fong Cam, and Siu Kwan Sze. "Proteomic Profiling of the Secretome of Trichoderma reesei." In Trichoderma reesei, 237–49. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-1048-0_17.

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Antonieto, Amanda C. C., and Roberto N. Silva. "Transcriptomics in Trichoderma reesei." In Trichoderma reesei, 251–69. New York, NY: Springer US, 2020. http://dx.doi.org/10.1007/978-1-0716-1048-0_18.

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Conference papers on the topic "Trichoderma reesei"

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Mao, Jianing, Xiang Nong, Yaojun Yang, and Zi Liang. "Trichoderma reesei utilized tea residue to production cellulase." In 2015 International Conference on Mechatronics, Electronic, Industrial and Control Engineering. Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/meic-15.2015.379.

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Yang, Yanling, Lihua Liu, Miao Diao, Zhiwei Lin, Wunian Guo, and Shihua Wang. "Cloning and Bioinformatics Analysis of an Endoglucanase 2 from Trichoderma reesei." In 2009 WRI World Congress on Software Engineering. IEEE, 2009. http://dx.doi.org/10.1109/wcse.2009.175.

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Cañas, J. A., S. Higuera, V. Cuevas, A. Portillo, G. Lopez, A. Bañares-Hidalgo, and P. Estrada. "Adsorption of xylanase II from Trichoderma reesei QM 9414 on several polymers." In MICROBES IN APPLIED RESEARCH - Current Advances and Challenges. WORLD SCIENTIFIC, 2012. http://dx.doi.org/10.1142/9789814405041_0132.

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BONFIM, K. S. do, R. K. P. da SILVA, E. J. F. CHAVES, L. C. T. de CARVALHO, D. A. M. de ARAÚJO, and S. F. de M. SANTOS. "COMPARAÇÃO DA SÍNTESE DE CELULASES PELOS FUNGOS Trichoderma reesei E O FSDE15." In XX Congresso Brasileiro de Engenharia Química. São Paulo: Editora Edgard Blücher, 2015. http://dx.doi.org/10.5151/chemeng-cobeq2014-0210-26519-179588.

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Anindyawati, Trisanti, Raditya Putra, Yuliawati, Kartika Sari Dewi, Asrul Muhamad Fuad, and Yanni Sudiyani. "Heterologous expression of Trichoderma reesei exoglucanase (Cel6A) in Pichia pastoris under the control of GAP promoter." In PROCEEDINGS OF THE 2ND INTERNATIONAL CONFERENCE ON BIOSCIENCES AND MEDICAL ENGINEERING (ICBME2019): Towards innovative research and cross-disciplinary collaborations. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5125548.

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Kittanan, Thammaratchai, Lexpet Nareerat, Kaisaard Sawwanit, and Chysirichote Teerin. "Uses of Copra Waste and Wheat Bran for Cellulase Production by Trichoderma reesei in Solid State Fermentation." In the 2018 8th International Conference. New York, New York, USA: ACM Press, 2018. http://dx.doi.org/10.1145/3180382.3180392.

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Frédéric, Augier, Roque Tamiris, Ben Fadhel, Nienow Alvin, and Béal Catherine. "Impact of Mixing on Cellulase Production by the Filamentous Fungi Trichoderma Reesei: Scale-Down Experiments and Modelling." In 17th European Conference on Mixing. Porto, Portugal: MIXING17 - 17th European Conference On Mixing, 2024. http://dx.doi.org/10.52202/074122-0009.

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Riadi, Lieke, Yuana Elly Agustin, Leony Dita Kusuma, Paulina Filiana Sutrisno, and Titie Prapti Utami. "Reutealis trisperma press cake induced production of xylanase by Trichoderma reesei: Effect of C/N ratio and initial pH." In THE 11TH REGIONAL CONFERENCE ON CHEMICAL ENGINEERING (RCChE 2018). Author(s), 2019. http://dx.doi.org/10.1063/1.5094992.

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ASTOLFI, V., A. L. ASTOLFI, C. E. V. BUSTAMANTE, L. H. CULAU, J. A. do NASCIMENTO, E. RIGO, M. DI LUCCIO, and H. TREICHEL. "SACARIFICAÇÃO DE DIFERENTES RESÍDUOS AGROINDUSTRIAIS PELO EXTRATO ENZIMÁTICO BRUTO PRODUZIDO POR Trichoderma reesei NRRL 3652 EM CASCA DE SOJA." In XI Congresso Brasileiro de Engenharia Química em Iniciação Científica. São Paulo: Editora Edgard Blücher, 2015. http://dx.doi.org/10.5151/chemeng-cobeqic2015-178-32692-248839.

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Casciatori, Priscila Aparecida, Fernanda Casciatori, Joao Claudio Thomeo, and Roberto da Silva. "HIDRÓLISE DE BAGAÇO DE CANA IN NATURA E PRÉ-TRATADO EMPREGANDO CELULASES PRODUZIDAS POR TRICHODERMA REESEI EM CULTIVO SÓLIDO." In Simpósio Nacional de Bioprocessos e Simpósio de Hidrólise Enzimática de Biomassa. Campinas - SP, Brazil: Galoá, 2015. http://dx.doi.org/10.17648/sinaferm-2015-32806.

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