Academic literature on the topic 'Endo-(1,4)-β-glucanase'
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Journal articles on the topic "Endo-(1,4)-β-glucanase"
Fujiwara, Takaaki, Ayumi Fujishima, Yui Nakamura, Kenji Tajima, and Min Yao. "Structural snapshot of a glycoside hydrolase family 8 endo-β-1,4-glucanase capturing the state after cleavage of the scissile bond." Acta Crystallographica Section D Structural Biology 78, no. 2 (January 24, 2022): 228–37. http://dx.doi.org/10.1107/s2059798321012882.
Full textAllardyce, Benjamin J., and Stuart M. Linton. "Synergistic interaction of an endo-β-1,4-glucanase and a β-glucohydrolase leads to more efficient hydrolysis of cellulose-like polymers in the gecarcinid land crab, Gecarcoidea natalis." Australian Journal of Zoology 60, no. 5 (2012): 299. http://dx.doi.org/10.1071/zo12074.
Full textYa. V., Chabaniuk, Brovko I. S., Melnikova I. O., and Spataru K. V. "SEARCHING ENDO-1,4-β-GLUCANASE ACTIVE PRODUCERS FOR BIODESTRUCTION OF PLANT RESIDUES." Agriciltural microbiology 34 (November 11, 2021): 15–22. http://dx.doi.org/10.35868/1997-3004.34.15-22.
Full textMendu, Lavanya, Gayani Jalathge, Kamalpreet Kaur Dhillon, Nagendra Pratap Singh, Vimal Kumar Balasubramanian, Rebecca Fewou, Dennis C. Gitz, Junping Chen, Zhanguo Xin, and Venugopal Mendu. "Mutation in the Endo-β-1,4-glucanase (KORRIGAN) Is Responsible for Thick Leaf Phenotype in Sorghum." Plants 11, no. 24 (December 15, 2022): 3531. http://dx.doi.org/10.3390/plants11243531.
Full textMwenje, E., and N. Mguni. "Cellulolytic and pectinolytic activities of Capnodium isolates (sooty mould) from Zimbabwe." Canadian Journal of Botany 79, no. 12 (December 1, 2001): 1492–95. http://dx.doi.org/10.1139/b01-126.
Full textZerva, Ioanna, Nikolaos Remmas, and Spyridon Ntougias. "Biocatalyst Potential of Cellulose-Degrading Microorganisms Isolated from Orange Juice Processing Waste." Beverages 5, no. 1 (March 2, 2019): 21. http://dx.doi.org/10.3390/beverages5010021.
Full textAllardyce, Benjamin J., and Stuart M. Linton. "Characterisation of cellulose and hemicellulose digestion in land crabs with special reference to Gecarcoidea natalis." Australian Journal of Zoology 59, no. 6 (2011): 380. http://dx.doi.org/10.1071/zo11054.
Full textHan, Yejun, Dylan Dodd, Charles W. Hespen, Samuel Ohene-Adjei, Charles M. Schroeder, Roderick I. Mackie, and Isaac K. O. Cann. "Comparative Analyses of Two Thermophilic Enzymes Exhibiting both β-1,4 Mannosidic and β-1,4 Glucosidic Cleavage Activities from Caldanaerobius polysaccharolyticus." Journal of Bacteriology 192, no. 16 (June 18, 2010): 4111–21. http://dx.doi.org/10.1128/jb.00257-10.
Full textZheng, Baisong, Wen Yang, Xinyu Zhao, Yuguo Wang, Zhiyong Lou, Zihe Rao, and Yan Feng. "Crystal Structure of Hyperthermophilic Endo-β-1,4-glucanase." Journal of Biological Chemistry 287, no. 11 (November 29, 2011): 8336–46. http://dx.doi.org/10.1074/jbc.m111.266346.
Full textTouzani, Abdellah, and Bernard Donèche. "Production et propriétés du complexe cellulasique du Botrytis cinerea." Canadian Journal of Botany 74, no. 3 (March 1, 1996): 486–91. http://dx.doi.org/10.1139/b96-059.
Full textDissertations / Theses on the topic "Endo-(1,4)-β-glucanase"
Woolley, Lindsey C. "The role of endo-#beta#-1,4-glucanase in strawberry fruit development." Thesis, Open University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340705.
Full textAkiba, Shunichi. "Studies on Protease-Resistant Endo-β-1, 4-glucanase from Aspergillus niger." Kyoto University, 1999. http://hdl.handle.net/2433/181918.
Full textRobert, Stéphanie. "Etude de la protéine KORRIGAN, une endo-β-1,4-glucanase impliquée dans la synthèse de cellulose chez Arabidopsis thaliana et Gossypium hirsutum." Paris 11, 2005. http://www.theses.fr/2005PA112007.
Full textIn order to better understand the molecular mechanisms that govern cellulose synthesis, KORRIGAN1, an endo--1,4-glucanase involved in this process, has been studied. In the first part of my thesis, KOR1 was shown to be present in high molecular weight complexes in Arabidopsis thaliana and cotton fibers. The weight of this complex changes in function of the level of cellulose synthesis, demonstrating that cellulose synthesis and KOR1 function are linked. Different putative protein partners have been identified which suggest a close interaction between KOR1 and the cytoskeleton. It has been suggested that KOR1 may recycle sitosterol primers involved in the initiation of celullose synthesis in cotton fibers. In the second part of my thesis, I tested this hypothesis and the results obtained suggest that this hypothetic function is not real. Finally, I focussed on the subcellular localization of KOR1. Using a variety of methods, we showed that KOR1 was present in intracellular compartments, distinct from the Golgi apparatus and showing some colocalization with endosomal compartments. These compartments were very motile in a microtubules integrity dependent manner, linking KOR1 to the cytoskeleton again. When cellulose synthesis was inhibited, the KOR1 compartments were closer to the plasma membrane and distinct from the endosomal compartments. These results suggest that cellulose synthesis is highly regulated through the control of the localisation and interaction of the enzymes involved in this process
Phan, Minh Thi Tuyet, Viet Quoc Nguyen, Hy Gia Le, Thoa Kim Nguyen, and Man Dinh Tran. "Molecular cloning gene and nucleotide sequence of the gene encoding an endo-1,4-β-glucanase from Bacillus sp VLSH08 strain applying to biomass hydrolysis." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2013. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-99522.
Full textChủng vi khuẩn Bacillus sp VLSH08 được tuyển chọn từ tập hợp chủng vi khuẩn phân lập ở vùng ngập mặn tỉnh Nam Định có khả năng sinh tổng hợp enzyme endo-1,4-beta-glucanase ngoại bào. Kết quả phân loại chủng vi khuẩn Bacillus sp VLSH08 bằng Kit hóa sinh API 50/CHB cũng như trình tự gen mã hóa 16S rRNA cho thấy độ tương đồng của chủng Bacillus sp VLSH08 và chủng Bacillus amyloliquefaciene JN999857 đạt 98%. Dịch lên men của chủng được sử dụng làm nguồn enzyme thô để nghiên cứu hoạt độ tối ưu của enzyme ở pH 5,8 và nhiệt đô 60oC. Hoạt tính enzyme tăng 2,03 lần khi có mặt 5 mM ion Co2+. Đồng thời, gen mã hóa cho enzyme endo-1,4-betaglucanase cũng được tách dòng trong tế bào Escherichia coli sử dụng vector pCR 2.1. Gen mã hóa cho enzyme này có chiều dài 1500 bp, mã hóa cho 500 axit amin, bao gồm 29 axit amin của chuỗi peptid tín hiệu. So sánh cho thấy trình tự gen endo-1,4-beta-glucanase của chủng Bacillus sp VLSH08 có độ tương đồng cao với enzyme này của chủng Bacillus subtilis (EU022560.1) và của chủng Bacillus amyloliquefaciene (EU022559.1). Tất cả các enzyme nhóm này đều thuộc họ cellulase E2. Enzyme của chủng này cũng đã được phối trộn với các enzyme khác tạo thành cocktail để thủy phân sinh khối cho kết quả cellulose bị thủy phân 72,76% sau 48 giờ
Louw, Maureen Elizabeth. "Characterization of an alkalophilic Bacillus brevis isolate with respect to its endo-(1,3-1,4)-β-glucanase gene, protein hyperproduction and the degS-degU operon." Doctoral thesis, University of Cape Town, 1994. http://hdl.handle.net/11427/21696.
Full textBacillus brevis Alk 36 was isolated from soil during a screening programme for the selection of extracellular enzyme producing strains. A gene coding for an endo(1,3- 1,4 )-.8-glucanase (or lichenase) was cloned from B. brevis Alk 36 and expressed in Escherichia coli. The nucleotide sequence of this gene was determined and found to encode a protein of 252 amino acid residues. The amino acid sequence of the B. brevis lichenase gene showed only a 50% similarity to previously published data for Bacillus endo-(1,3-1,4)-β-glucanases. The enzyme exhibited some unique properties. The optimum temperature and pH for enzyme activity were 65-70°C and 8-10, respectively. When held at 75°C for 1 h, 75% residual activity was measured. The molecular mass was estimated to be 29 kDa and the enzyme was found to be resistant to sodium dodecyl sulphate (SDS). B. brevis Alk 36 was evaluated as a potential host strain for the efficient production and secretion of foreign proteins and was found to grow optimally between pH 8.0 and pH 9.5 and between 42°C and 52°C. B. brevis was successfully transformed using vector DNA and was found to produce relatively low levels of protease. In addition, it was evaluated as a possible protein hyper-secreting strain. However, using PCR technology, the highly conserved cell wall protein genes could not be positively identified in B. brevis Alk 36.
Tarrés, Farrés Joaquim Agustí. "Endo-β-1,4-glucanasa para la fabricación de micro/nanocelulosa: propiedades y aplicaciones." Doctoral thesis, Universitat de Girona, 2017. http://hdl.handle.net/10803/456211.
Full textEn els darrers anys, entre la comunitat científica i tecnològica s’ha despertat un gran interès en la producció, caracterització i utilització de nanofibres de cel·lulosa. Aquesta especial atenció es deu, principalment, al seu caràcter biodegradable, el seu origen renovable i la versatilitat que presenten, fent-les aptes per ser utilitzades en multitud d’aplicacions. L’esclat d’aquesta temàtica de recerca va tenir lloc aproximadament deu anys enrere, doncs només cal observar el creixement exponencial de publicacions científiques i patents des d’aleshores. De manera general, la present tesi pretén demostrar que les nanofibres de cel·lulosa obtingudes mitjançant un pretractament d’hidròlisi enzimàtica poden ser produïdes de forma efectiva, de manera que pugin ser aplicades en una gran varietat de camps científics i tecnològics. La seva gran versatilitat, disponibilitat, baix cost i baix impacte mediambiental, justifiquen que en el futur es continuï amb la seva investigació sobre noves aplicacions
Stronach, Morag Shona. "The molecular cell biology of a xyloglucan specific endo 1,4 #beta#-D-glucanase from Tropaeolum majus L. cotyledons." Thesis, University of Stirling, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294012.
Full textSilva, Caio de Oliveira Gorgulho. "Emericella nidulans e bagaço de cana-de-açucar : ferramentas para produção de endo-β-1,4-xilanase." reponame:Repositório Institucional da UnB, 2014. http://repositorio.unb.br/handle/10482/15669.
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O bagaço de cana-de-açúcar é um importante resíduo agroindustrial brasileiro que apresenta grande potencial para ser utilizado como fonte de carbono para produção de holocelulases de interesse industrial por microrganismos. As xilanases, objeto de estudo deste trabalho, são enzimas que apresentam uma série de aplicações biotecnológicas que incluem a produção de etanol de segunda geração, o branqueamento de papel, a produção de sucos e pães e o uso como aditivo em rações animais. O objetivo desta pesquisa foi purificar e caracterizar uma xilanase produzida pelo fungo Emericella nidulans quando cultivado em bagaço de cana, visando o aproveitamento deste resíduo e a avaliação do potencial biotecnológico da enzima. O fungo foi capaz de secretar xilanases a partir do primeiro dia de cultivo sob fermentação submersa utilizando o bagaço. Uma xilanase de 22 kDa foi purificada a partir do extrato bruto obtido no cultivo através de ultrafiltração, precipitação com sulfato de amônio e cromatografias de filtração em gel e troca aniônica. A enzima apresentou alta homologia com endo-β-1,4-xilanase A (XynA) de E. nidulans e desta forma foi chamada. A enzima XynA apresentou maior atividade a 55°C e na faixa de pH 3,0 – 6,5. A enzima se mostrou pouco termoestável, com meiasvidas de 40, 10 e 7 minutos a 28, 50 e 55°C, respectivamente. XynA foi mais ativa sobre a porção solúvel da xilana, com valores de KM e Vmáx 3,39 mg/mL e 0,502 UI/mL, respectivamente. A hidrólise da xilana por XynA gerou xilooligossacarídeos, indicando ação tipo endo. Diferentes compostos fenólicos comumente liberados durante o pré-tratamento de biomassa lignocelulósica causaram efeitos variados sobre XynA. Os ácidos tânico e cinâmico inibiram a enzima, enquanto o ácido 4-hidroxi-benzóico aumentou sua atividade e os ácidos ferúlico, p-cumárico e vanilina não mostraram efeito. O etanol aumentou a atividade, estabilidade e Vmáx da enzima, indicando potencial para aplicação em processos de sacarificação e fermentação simultâneas de biomassa. O ultrafiltrado (uma fração semipurificada de xilanases) foi capaz de hidrolisar polpas de celulose em diferentes etapas do processo Kraft, resultando na liberação de açúcares redutores, cromóforos, pentoses e produtos de hidrólise de xilana sem concomitante liberação de glicose. O extrato bruto se mostrou capaz de degradar bagaço de cana-de-açúcar não-tratado ou sumetido a explosão a vapor, liberando açúcares redutores e produtos de hidrólise de xilana. ______________________________________________________________________________ ABSTRACT
Sugarcane bagasse is a major lignocellulosic agroindustrial residue in Brazil with great potencial for utilization as carbon source for production of industrial holocellulases by microrganisms. Xylanases present several biotechnological applications such as in ethanol production, paper bleaching, juice and bread production and utilization as feed additive. The goal of this reseach was to purify and characterize one xylanase produced by the fungus Emericella nidulans when grown on sugarcane bagasse, aiming the use of this residue and the investigation of biotechnological potencials of the enzyme. E. nidulans secreted xylanases from the first day of growth on liquid media containing bagasse as sole carbon source. One 22 kDa xylanase was purified from crude extract through ultrafiltration, ammonium sulphate precipitation, gelfiltration and anion-exchange chromatographies. The enzyme showed significant homology with endo-β-1,4-xylanase A (XynA) from E. nidulans, and was named that way. XynA was most active at 55°C and pH 3,0 – 6,5. Considering its thermostability, XynA presented half-lives of 40, 10 and 7 minutes at 28, 50 and 55°C, respectively. The enzyme was more active on the soluble portion of xylan, with Km and Vmax values 3,39 mg.mL¯ ¹ and 0,502 UI.mL¯ ¹, respectively. Xylan hydrolysis by XynA produced xylooligossacharides, indicating endo-type action. Phenolic compounds released during pre-treatment of lignocellulosic biomass caused different effects on XynA. Tannic and cinnamic acids inhibited XynA, while 4-hidroxibenzoic acid enhanced its activity and ferulic and p-coumaric acids and vanillin caused no effect. Ethanol increased XynA activity, thermostability and Vmax, suggesting potencial for aplication in simultaneous sacharification and fermentation processes. Ultrafiltrate sample (partialy purified xylanases) was able to hydrolyse celullose pulps obtained from different stages of Kraft process, resulting in release of reducing sugars, chromophores, pentoses and xylans degradation products with apparent no release of glucose. E. nidulans crude extract was able to hydrolyse untreated or steam-explosion pretreated sugarcane bagasses, releasing reducing sugars and xylans degradation products.
Miotto, Lis Schwartz. "Estudos moleculares, estruturais e funcionais da Cel12A de Gloeophyllum trabeum, uma endo-1,4-β-glucanase da família 12 de hidrolases de glicosídeos." Universidade Federal de São Carlos, 2014. https://repositorio.ufscar.br/handle/ufscar/272.
Full textUniversidade Federal de Minas Gerais
The production of second-generation ethanol by enzymatic hydrolysis of biomass is considered a viable and promising alternative to face the global energy crisis and to decrease our dependence on fossil fuels. Therefore, it is necessary to degrade the constituent molecules of the plant cell wall such as lignin, cellulose and hemicellulose to fermentable sugars. However, the use of enzymes for this purpose is still expensive, leading to the increase on studies seeking to make them more feasible economically and technically. The present study aimed the molecular, structural and functional characterization of the endoglucanase Cel12A from the fungus Gloeophyllum trabeum by different techniques. Biochemical data revealed the substrate specificity for the enzyme and showed that β-glucan is the best substrate for its activity (239.2 ± 9.1 U mg-1). Optimal conditions for activity were pH 4.5 and temperature of 50 oC. Thermal stability assay indicated a half-life of 84.6 ± 3.6 hours at 50 oC. The kinetic parameters Km (3.2 ± 0.5 mg mL-1) and Vmax (0,40 ± 0,02 μmol min-1) were determined using β-glucan as substrate. Analysis of scanning electron microscopy of oat spelts and filter paper samples submitted to the hydrolysis by GtCel12A evidenced the degradation effects of these substrates compared to control samples. Moreover, the low-resolution envelope and the crystallographic structure for GtCel12A were determined. The structure revealed a β-sandwich fold with two β-sheets (A and B) and three α-helices, while sheet A showed five strands and sheet B nine strands. The comparative analysis of the amino acid sequence and homologous structures prompted us to identify the catalytic residues, Glu142 and Glu227 in the active site of the enzyme. These results are important for understanding and elucidating the enzyme molecular mechanism of action and other glycoside hydrolase family 12 endoglucanases.
A produção de etanol de segunda geração, a partir da hidrólise enzimática da biomassa vegetal é considerada uma alternativa viável e promissora para enfrentarmos a crise energética mundial e diminuirmos a dependência das fontes fósseis de energia. Para isso, é necessário que ocorra a degradação das moléculas constituintes da parede celular como a lignina, a celulose e a hemicelulose a açúcares fermentescíveis. No entanto, a utilização de enzimas para esse fim ainda apresenta um custo elevado, o que tem desencadeado, cada vez mais, estudos que busquem torná-las mais viáveis econômica e tecnicamente. O presente estudo visou à caracterização molecular, estrutural e funcional da endoglucanase Cel12A do fungo Gloeophyllum trabeum por diferentes técnicas. Os dados bioquímicos revelaram a especificidade por substratos da enzima, sendo que o melhor substrato para a atividade foi o β-glucano (239,2 ± 9,1 U mg-1). As condições ótimas para a atividade foram pH 4,5 e temperatura de 50 oC. Os ensaios de estabilidade térmica indicaram uma meia-vida de 84,6 ± 3,6 horas a 50 oC. Os parâmetros cinéticos Km (3,2 ± 0,5 mg mL-1)) e Vmax (0,40 ± 0,02 μmol min-1) foram determinados utilizando-se β-glucano como substrato. Análises de microscopia eletrônica de varredura de amostras de papel de filtro e aveia submetidos à hidrólise pela GtCel12A evidenciaram os efeitos de degradação dos substratos em relação às amostras controle. Adicionalmente, o envelope de baixa resolução e a estrutura cristalográfica da GtCel12A foram obtidos. O modelo de alta resolução revelou um enovelamento do tipo sanduíche β, com duas folhas β (A e B) e três hélices α, sendo que a folha A apresentou cinco fitas e a B, nove fitas. Por meio de análises comparativas da sequência de aminoácidos e de estruturas homólogas identificamos os resíduos catalíticos Glu142 e Glu227 no sítio ativo da enzima. Tais resultados são importantes para a elucidação e compreensão do mecanismo molecular de atuação dessa enzima e de outras endoglucanases da família GH12.
Menu-Bouaouiche, Laurence. "Relations structure-fonction et propriétés de surface de protéines PR5 "thaumatin-like" de fruits comestibles." Toulouse 3, 2003. http://www.theses.fr/2003TOU30171.
Full textPR-5 or Thaumatin-like proteins (TLP) are structurally and phylogenetically related but their activities in vitro are very diverse: antifungal, antifreeze, glucan affinity and/or hydrolysis. Some of them are induced by biotic or abiotic stresses and could be involved in plant's defense against pathogenic fungi. In contrast, some fruits accumulate similar proteins during their maturation, like these of cherry or apple that are allergenic A better understanding of functional and structural properties of fruit specific's PR-5 proteins could allow new allergy diagnostics elaboration and new orientations' definition, beware of allergy risks, for natural plant defense amelioration. For the definition of TLP structure-function relationships, we have, first, analyzed different members of this family, for their phylogeny, their structure and their surface electrostatics and hydrophobic properties, by sequence analysis and molecular modeling methodologies. Thereafter, cherry, apple and banana's TLP and Thaumatin were compared for their enzymatic and antifungal activities. .
Book chapters on the topic "Endo-(1,4)-β-glucanase"
Brummell, David A., Coralie C. Lashbrook, and Alan B. Bennett. "Plant Endo-1,4-β-D-glucanases." In ACS Symposium Series, 100–129. Washington, DC: American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0566.ch006.
Full textRose, J. K. C., C. Catala, D. A. Brummell, C. C. Lashbrook, C. Gonzalez-Bosch, and A. B. Bennett. "The Tomato Endo-β-1,4-Glucanase Gene Family: Regulation by Both Ethylene and Auxin." In Biology and Biotechnology of the Plant Hormone Ethylene, 197–205. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5546-5_26.
Full textLashbrook, Coralie C., and Alan B. Bennett. "Functional Analysis of Cx-cellulase (Endo-β-1,4-Glucanase) Gene Expression in Transgenic Tomato Fruit." In Cellular and Molecular Aspects of the Plant Hormone Ethylene, 123–28. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-017-1003-9_25.
Full textAnnamalai, Neelamegam, Mayavan Veeramuthu Rajeswari, and Thangavel Balasubramanian. "Endo-1,4-β-glucanases: Role, Applications and Recent Developments." In Biofuel and Biorefinery Technologies, 37–45. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-43679-1_3.
Full textRodrigues, Alexandre Gomes. "Endo-β-1,4-xylanase: An Overview of Recent Developments." In Biofuel and Biorefinery Technologies, 125–49. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-43679-1_6.
Full textTrainotti, L., C. A. Tomasin, and G. Casadoro. "Characterization of caEG2, a Pepper Endo-β-1,4-Glucanase Gene Involved in the Abscission of Leaves and Flowers." In Biology and Biotechnology of the Plant Hormone Ethylene II, 269–70. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4453-7_48.
Full textShani, Ziv, Mara Dekel, Galit Tsabary, Christian Sig Jensen, Tzvi Tzfira, Raphael Goren, Arie Altman, and Oded Shoseyov. "Expression of Arabidopsis Thaliana Endo-1,4-ß-Glucanase (cel1) in Transgenic Poplar Plants." In Plant Biotechnology and In Vitro Biology in the 21st Century, 209–12. Dordrecht: Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4661-6_49.
Full textSpezio, Mike, P. Andrew Karplus, Diana Irwin, and David B. Wilson. "Structure—Function Studies of Endo-l,4-β-D-glucanase E2 fromThermomonospora fusca." In ACS Symposium Series, 66–74. Washington, DC: American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0566.ch003.
Full textTrainotti, L., L. Ferrarese, and G. Casadoro. "Different Endo-β-1,4-Glucanases are Expressed During Abscission and Fruit Ripening in Pepper and Peach Plants." In Biology and Biotechnology of the Plant Hormone Ethylene, 191–96. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-011-5546-5_25.
Full textMcCleary, Barry V., Vincent McKie, and Anna Draga. "Measurement of endo-1,4-β-Glucanase." In Cellulases, 1–17. Elsevier, 2012. http://dx.doi.org/10.1016/b978-0-12-415931-0.00001-x.
Full textConference papers on the topic "Endo-(1,4)-β-glucanase"
AZEVEDO, B., R. A. SILVA, S. S. OLIVEIRA, R. P. VELOSO, S. B. F. SANTOS, and L. S. C. OLIVEIRA. "PRODUÇÃO DE ENDO-Β-1,4-GLUCANASE UTILIZANDO SORGO SACARINO IPA P15." In XXII Congresso Brasileiro de Engenharia Química. São Paulo: Editora Blucher, 2018. http://dx.doi.org/10.5151/cobeq2018-pt.0606.
Full textRibeiro de Assis, Samila, Cristian Lourenço, Camila Telles de Bessa, LUCAS VINÍCIUS TRINDADE, Hamilton Cabral, and Gustavo Orlando Bonilla Rodriguez. "Caracterização da endo-1,4-β-D-xilanase do extrato bruto produzido pelo fungo mesofílico Penicillium corylophilum em cultivo submerso." In Simpósio Nacional de Bioprocessos e Simpósio de Hidrólise Enzimática de Biomassa. Campinas - SP, Brazil: Galoá, 2015. http://dx.doi.org/10.17648/sinaferm-2015-33864.
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