@article{MTMT:33891585,
	title = {Productivity of Aspergillus niger InaCC F57 Isolate as Cellulase Agent in OPEFB Hydrolysis for Glucose High Yield},
	url = {https://m2.mtmt.hu/api/publication/33891585},
	author = {Nurdin, Muhammad and Mulkiyan, La Ode Muhammad Zuhdi and Sugiwati, Sri and Abimayu, Haznan and Arifin, Zaenal Syam and Muryanto, Muryanto and Maulidiyah, Maulidiyah and Arham, Zul and Salim, La Ode Agus and Irwan, Irwan and Umar, Akrajas Ali},
	doi = {10.1007/s12668-023-01066-5},
	journal-iso = {BIONANOSCI},
	journal = {BIONANOSCIENCE},
	volume = {13},
	unique-id = {33891585},
	issn = {2191-1630},
	abstract = {This study aims to obtain the results of the optimization of biological hydrolysis of oil palm empty fruit bunches (OPEFB) using Aspergillus niger (A. niger) InaCC F57. The optimized hydrolysis parameters include incubation temperature, substrate pH, incubation time, and additional parameters in the form of substrate concentration and the addition of nutrient salt solution (NSS) in alkaline pretreatment and non-pretreatment OPEFB. Pretreatment of OPEFB is alkaline generated from the delignification process with 10% NaOH at a temperature of 150 degrees C and given a pressure of 5 kg/cm(2) for 30 min in a chemical explosive reactor (CHIMEX), and then the NREL method is carried out where the OPEFB is chemically hydrolyzed using H2SO4 72% then followed by HPLC analysis and UV spectrophotometric analysis to determine the content of cellulose, hemicellulose, and lignin. These results indicate that the performance of A. niger InaCC F57 in the hydrolysis process is influenced by the pretreatment stage. Optimization of hydrolysis was carried out by inoculation of OPEFB samples using 10% A. niger isolate under sterile conditions. A. niger InaCC F57 isolate was obtained by regenerating cultures grown on sterile agar media at 28 degrees C for 5 days and followed by inserting 10 mL of sterile distilled water into culture tubes and then scraping them off to separate them from the media. The optimum conditions for the enzymatic hydrolysis of OPEFB based on A. niger InaCC F5 were at a temperature of 40 degrees C, pH 5, incubation time of 48 h (2 days), 10% substrate concentration, and the addition of nutrient salt solution (NSS). The alkaline pretreatment OPEFB hydrolysis yielded 1.40 mg/mL reducing sugar, 14.20% hydrolysis percent, and 0.56 U/mL cellulase activity, while non-pretreated OPEFB produced 1.90 mg/mL reducing sugar, 17.10% hydrolysis percent, and 0.76 U/mL cellulase activity. Based on the results obtained indicate the potential for biological hydrolysis between OPEFB and A. niger InaCC F57 as an important part of the OPEFB pretreatment in the future.},
	keywords = {Aspergillus niger; Bioethanol; reducing sugar; OPEFB; Biological hydrolysis},
	year = {2023},
	eissn = {2191-1649},
	pages = {114-127}
}

@article{MTMT:33002965,
	title = {Microbiome-based screening and co-fermentation of rhizospheric microorganisms for highly ginsenoside Rg(3) production},
	url = {https://m2.mtmt.hu/api/publication/33002965},
	author = {Qi, Geyuan and Ji, Baoyu and Zhang, Yanan and Huang, Luqi and Wang, Juan and Gao, Wenyuan},
	doi = {10.1016/j.micres.2022.127054},
	journal-iso = {MICROBIOL RES},
	journal = {MICROBIOLOGICAL RESEARCH},
	volume = {261},
	unique-id = {33002965},
	issn = {0944-5013},
	abstract = {Ginsenoside Rg3 has a wide range of pharmacological activities and application value while the content of Rg3 in Panax plants is extremely low. The interaction between medicinal plants and microorganisms will be beneficial to produce active compounds by biotechnology. In this study, the rhizosphere soil samples from different P. notoginseng producing areas (Asanlong, Huilong, Demonstration garden) were collected to analyze the soil microflora characteristics by Illumina MiSeq sequencing technology. Based on the highest contents of ginsenosides in Huilong, the first, second, and the specificity dominant strains were predicted and the database was established. Besides, a total of 6 strains of bacteria and 3 strains of fungi were isolated from the soil of P. notoginseng. Among them, F24 was identified as Chaetomium sp, which was not only consistent with the second dominant strain of P. notoginseng predicted in the database, but also had a high level of Rg3. It also indicated that the method of screening the dominant strains in soil was reasonable and the database was reliable. Through the optimization of fermentation conditions, the highest yield of Rg3 was obtained when F24 was cultured in the medium supplemented with 8 mg/L glucose and 5 mg/L methyl jasmonate (MeJA) for 7 days. On this basis, the yield of ginsenoside Rg3 in shake flask reached 108.95 mg/L (4.93 mg/g, ~4.2-fold higher than cultivated P. notoginseng plants) by the co-fermentation with A. niger in a concentration ratio of 2:1. The increase of Rg3 yield mainly came from the conversion of other 20S-protopanaxdiol saponins into Rg3 by beta-glucosidase in A. niger. In addition, the expression levels of ginsenoside biosynthesis genes in different strains were compared, it was found that the expression of key genes was significantly increased after co-fermentation. This research provided certain theoretical and technical support for the large-scale industrial production of ginsenoside Rg3 by microbiology.},
	keywords = {Biotransformation; illumina miseq sequencing; Co-fermentation; ginsenoside Rg 3; Fermentation parameters},
	year = {2022},
	eissn = {1618-0623}
}

@article{MTMT:32391491,
	title = {UTILIZATION OF PAPER WASTES FOR CELLULOLYTIC ENZYME PRODUCTION BY ASPERGILLUS NIGER STRAIN 13A AND USING THE BIOORGANIC MATERIALS IN THE BIOCONTROL OF FUSARIUM WILT OF CUCUMBER (CUCUMIS SATIVUS L.)},
	url = {https://m2.mtmt.hu/api/publication/32391491},
	author = {Belal, E. B. and Shalaby, M. E. and El-Said, R. A. R. and Abdelrazek, M. A. S. and Ebrahim, A. E. E. and Gad, W. A.},
	doi = {10.15666/aeer/1902_12331246},
	journal-iso = {APPL ECOL ENV RES},
	journal = {APPLIED ECOLOGY AND ENVIRONMENTAL RESEARCH},
	volume = {19},
	unique-id = {32391491},
	issn = {1589-1623},
	abstract = {The main purpose of this study is maximizing the utilization of paper waste material and decrease its harmful effect. Eleven fungal isolates were selected and tested to assess their cellulolytic potential. The isolates13A which were isolated from immature compost showed the highest Cellulolytic Index values 0.47 mm. According to the morphological characteristics and the 18S rRNA gene sequence, the isolate13A was identified as Aspergillus niger strain13A. The effect of pH and temperature on growth of Aspergillus niger strain13A and its production of cellulase were investigated, the optimal culture conditions was recorded at pH 6.0 after 6 days of incubation at 35 ?C. Under optimal conditions various paper waste materials were used for enzyme production under submerged and solid-state fermentation. Maximum production of cellulase by Aspergillus niger strain13A was shown using kraft brown bags and cardboard under solid state fermentation. Aspergillus niger strain13A exhibited also good degradability for a mixture of kraft, cardboard, foolscap and printout paper, under solid state fermentation resulting in the production of bioorganic material. Results of this study showed that treatment of soil with bioorganic materials demnstrarting high effectiveness in controlling Fusarium wilt of cucumber (Cucumis sativus L.) could be considered as promising alternative to chemical fungicides.},
	keywords = {Aspergillus niger; Cellulase; biological control; SOLID-STATE FERMENTATION; Waste paper},
	year = {2021},
	eissn = {1785-0037},
	pages = {1233-1246}
}

@article{MTMT:32391492,
	title = {Optimization of extracellular ethanol-tolerant beta-glucosidase production from a newly isolated Aspergillus sp. DHE7 via solid state fermentation using jojoba meal as substrate: purification and biochemical characterization for biofuel preparation},
	url = {https://m2.mtmt.hu/api/publication/32391492},
	author = {El-Ghonemy, Dina H.},
	doi = {10.1186/s43141-021-00144-z},
	journal-iso = {J GENET ENG BIOTECH},
	journal = {JOURNAL OF GENETIC ENGINEERING AND BIOTECHNOLOGY},
	volume = {19},
	unique-id = {32391492},
	issn = {1687-157X},
	abstract = {Background: The increasing demand and the continuous depletion in fossil fuels have persuaded researchers to investigate new sources of renewable energy. Bioethanol produced from cellulose could be a cost-effective and a viable alternative to petroleum. It is worth note that beta-glucosidase plays a key role in the hydrolysis of cellulose and therefore in the production of bioethanol. This study aims to investigate a simple and standardized method for maximization of extracellular beta-glucosidase production from a novel fungal isolate under solid-state fermentation using agro-industrial residues as the sole source of carbon and nitrogen. Furthermore, purification and characterization of beta-glucosidase were performed to determine the conditions under which the enzyme displayed the highest performance.Results: A fungus identified genetically as a new Aspergillus sp. DHE7 was found to exhibit the highest extracellular beta-glucosidase production among the sixty fungal isolates tested. Optimization of culture conditions improved the enzyme biosynthesis by 2.1-fold (174.6 +/- 5.8 U/g of dry substrate) when the fungus grown for 72 h at 35 degrees C on jojoba meal with 60% of initial substrate moisture, pH 6.0, and an inoculum size of 2.54 x 10(7) spores/mL The enzyme was purified to homogeneity through a multi-step purification process. The purified beta-glucosidase is monomeric with a molecular mass of 135 kDa as revealed by the SDS-PAGE analysis. Optimum activity was observed at 60 degrees C and pH of 6.0, with a remarkable pH and thermal stability. The enzyme retained about 79% and 53% of its activity, after 1 h at 70 degrees C and 80 degrees C, respectively. The purified beta-glucosidase hydrolysed a wide range of substrates but displaying its greater activity on p-nitrophenyl-beta-D-glucopyranoside and cellobiose. The values of K-m and V-max on p-nitrophenyl beta-D-glucopyranoside were 0.4 mM and 232.6 U/mL, respectively. Purified beta-glucosidase displayed high catalytic activity (improved by 25%) in solutions contained ethanol up to 15%.Conclusion: beta-glucosidase characteristics associated with its ability to hydrolyse cellobiose, underscore its utilization in improving the quality of food and beverages. In addition, taking into consideration that the final concentration of ethanol produced by the conventional methods is about 10%, suggests its use in ethanol-containing industrial processes and in the saccharification processes for bioethanol production.},
	year = {2021},
	eissn = {2090-5920}
}

@article{MTMT:31439110,
	title = {Valorization of Waste Biomass in Fermentative Production of Cellulases: A Review},
	url = {https://m2.mtmt.hu/api/publication/31439110},
	author = {Verma, Nitin and Kumar, Vivek and Bansal, M. C.},
	doi = {10.1007/s12649-020-01048-8},
	journal-iso = {WASTE BIOMASS VALORI},
	journal = {WASTE AND BIOMASS VALORIZATION},
	volume = {12},
	unique-id = {31439110},
	issn = {1877-2641},
	abstract = {The most promising way to achieve the smooth, flexible and sustainable bioeconomy is the utilization of renewable lignocellulosic biomass as a feedstock for the production of fuels, chemicals, enzymes and high-valued products. Cellulolytic enzymes are indispensable for the maintenance of global carbon cycle, since they catalyze the degradation of cellulose. Therefore for solving the forthcoming waste management and energy issues of mankind, cellulase production technology plays significant and vital role. Cellulases are industrial enzymes and have extensive application in various process industries. Its relatively high cost of production has hindered the wider industrial application. Significant cost reduction is required to enhance the commercial viability of cellulase production technology. Utilization of novel and cheap lignocellulosic renewable resources as substrate for enzyme fermentation process is a promising way of efficient and low cost cellulases production. The present paper reveals, a review on cellulase production through various microorganisms employing economical, abundantly available renewable lignocellulosic biomass as carbon source. It also deals with the recent approaches used at microbial as well as feedstock level, making more efficient, flexible and cost effective fermentation process.},
	keywords = {FERMENTATION; beta-Glucosidase; Cellulases; Waste biomass; FPase; CMcase},
	year = {2021},
	eissn = {1877-265X},
	pages = {613-640}
}

@article{MTMT:31447293,
	title = {Assessment of the ptxD gene as a growth and selective marker in Trichoderma atroviride using Pccg6, a novel constitutive promoter},
	url = {https://m2.mtmt.hu/api/publication/31447293},
	author = {Carreras-Villasenor, Nohemi and Rico-Ruiz, Jose Guillermo and Montes, Ricardo A. Chavez and Yong-Villalobos, Lenin and Lopez-Hernandez, Jose Fabricio and Martinez-Hernandez, Pedro and Herrera-Estrella, Luis and Herrera-Estrella, Alfredo and Lopez-Arredondo, Damar},
	doi = {10.1186/s12934-020-01326-z},
	journal-iso = {MICROB CELL FACT},
	journal = {MICROBIAL CELL FACTORIES},
	volume = {19},
	unique-id = {31447293},
	issn = {1475-2859},
	abstract = {Background Trichoderma species are among the most effective cell factories to produce recombinant proteins, whose productivity relies on the molecular toolkit and promoters available for the expression of the target protein. Although inducible promoter systems have been developed for producing recombinant proteins in Trichoderma, constitutive promoters are often a desirable alternative. Constitutive promoters are simple to use, do not require external stimuli or chemical inducers to be activated, and lead to purer enzyme preparations. Moreover, most of the promoters for homologous and heterologous expression reported in Trichoderma have been commonly evaluated by directly assessing production of industrial enzymes, requiring optimization of laborious protocols. Results Here we report the identification of Pccg6, a novel Trichoderma atroviride constitutive promoter, that has similar transcriptional strength as that of the commonly used pki1 promoter. Pccg6 displayed conserved arrangements of transcription factor binding sites between promoter sequences of Trichoderma ccg6 orthologues genes, potentially involved in their regulatory properties. The predicted ccg6-encoded protein potentially belongs to the SPE1/SPI1 protein family and shares high identity with CCG6 orthologue sequences from other fungal species including Trichoderma reesei, Trichoderma virens, Trichoderma asperellum, and to a lesser extent to that of Neurospora crassa. We also report the use of the Pccg6 promoter to drive the expression of PTXD, a phosphite oxidoreductase of bacterial origin, which allowed T. atroviride to utilize phosphite as a sole source of phosphorus. We propose ptxD as a growth reporter gene that allows real-time comparison of the functionality of different promoters by monitoring growth of Trichoderma transgenic lines and enzymatic activity of PTXD. Finally, we show that constitutive expression of ptxD provided T. atroviride a competitive advantage to outgrow bacterial contaminants when supplied with phosphite as a sole source of phosphorus. Conclusions A new constitutive promoter, ccg6, for expression of homologous and heterologous proteins has been identified and tested in T. atroviride to express PTXD, which resulted in an effective and visible phenotype to evaluate transcriptional activity of sequence promoters. Use of PTXD as a growth marker holds great potential for assessing activity of other promoters and for biotechnological applications as a contamination control system.},
	keywords = {phosphite; Contamination control; ccg6 promoter; Phosphite oxidoreductase (PTXD); Growth marker},
	year = {2020},
	eissn = {1475-2859},
	orcid-numbers = {Herrera-Estrella, Luis/0000-0001-7936-3856; Herrera-Estrella, Alfredo/0000-0002-4589-6870}
}

@article{MTMT:30564952,
	title = {Isolation and characterization of non-cellulolytic Aspergillus flavus EGYPTA5 exhibiting selective ligninolytic potential},
	url = {https://m2.mtmt.hu/api/publication/30564952},
	author = {Hasanin, Mohamed S. and Darwesh, Osama M. and Matter, Ibrahim A. and El-Saied, Houssni},
	doi = {10.1016/j.bcab.2018.11.012},
	journal-iso = {BIOCAT AGRICULT BIOTECH},
	journal = {BIOCATALYSIS AND AGRICULTURAL BIOTECHNOLOGY},
	volume = {17},
	unique-id = {30564952},
	abstract = {Environmental applications of selective lignin-degrading fungi and enzymes are of great interest as alternate technologies for paper industry (biopulping), biofuels, organic fertilizers, animal feeds. For this reason, the current study aimed to isolate selective delignifying fungi to convert the abundant lignocellulosic agricultural wastes into value-added products. From five lignocellulolytic fungi isolated from agricultural soil rich with partial decayed wooden trimmings, one isolate was selected due to its selectivity towards lignin degradation. The selected non-cellulolytic fungus isolate was identified according to morphological and molecular techniques as Aspergillus flavus EGYPTA5 with accession number MH425453. This fungal strain has been proven to cause an efficient and selective degradation of lignin in agricultural lignocellulosic wastes without affecting cellulose content. Lignin peroxidases, laccase, polyphenol oxidase, nitrate reductase and cellulase enzymes from investigating strain were assayed in the current research. All the tested enzymes except cellulase were produced with various activity degrees. Lignin peroxidases were the most active enzyme produced under experimental conditions (reached to 2.45 U/ml). Physical and chemical analysis of lignocellulosic agricultural wastes as well as FTIR analysis confirmed that A. flavus EGYPTA5 could be used as an alternative technology for biotreatment of lignin-rich cellulosic wastes to degrade lignin without affecting cellulose fibers. The isolated fungus and/or its specific-lignolytic enzymes could be applied in various environmental and industrial applications.},
	keywords = {biotechnology; Molecular identification; Agriculture wastes; Lignocelluloses; Non-cellulolytic lignolytic enzymes},
	year = {2019},
	eissn = {1878-8181},
	pages = {160-167}
}

@article{MTMT:27567133,
	title = {An ascomycota coculture in batch bioreactor is better than polycultures for cellulase production},
	url = {https://m2.mtmt.hu/api/publication/27567133},
	author = {Hernandez, Christian and Milagres, Adriane M F and Vazquez-Marrufo, Gerardo and Maria, Munoz-Paez Karla and Antonio, Garcia-Perez Jose and Alarcon, Enrique},
	doi = {10.1007/s12223-018-0588-1},
	journal-iso = {FOLIA MICROBIOL},
	journal = {FOLIA MICROBIOLOGICA},
	volume = {63},
	unique-id = {27567133},
	issn = {0015-5632},
	year = {2018},
	eissn = {1874-9356},
	pages = {467-478}
}

@article{MTMT:30564953,
	title = {Isolation, Cellulase Activity Test and Molecular Identification of Selected Cellulolytic Bacteria Indigenous Rice Bran},
	url = {https://m2.mtmt.hu/api/publication/30564953},
	author = {Jannah, Akyunul and Aulanni'am and Ardyati, Tri and Suharjono},
	doi = {10.22146/ijc.26783},
	journal-iso = {INDONESIAN J CHEM},
	journal = {INDONESIAN JOURNAL OF CHEMISTRY},
	volume = {18},
	unique-id = {30564953},
	issn = {1411-9420},
	abstract = {Rice bran is the waste product of rice milling which is abundant in Indonesia, it can be used as a raw material for the manufacture of bioethanol by fermentation. Before being fermented, rice bran must be hydrolyzed into glucose by biomass degrading. This study was aimed to isolate indigenous cellulolytic bacteria from rice bran as producer of cellulolytic enzymes and resulted in 22 bacterial isolates that demonstrated cellulolytic activity being identified. Among them, BE 8 and BE 14 isolates showed the highest endoglucanase activity at 2.16 and 1.31 U/mL respectively. Identification of the 16S rDNA showed that BE 8 belongs to Bacillus subtilis and BE 14 in Bacillus cereus.},
	keywords = {Bacillus cereus; Cellulase enzyme; rice bran; 16S rDNA method; Bacillus subtillis},
	year = {2018},
	eissn = {2460-1578},
	pages = {514-521}
}

@article{MTMT:27567134,
	title = {Bioethanol Production From Banana Stem By Using Simultaneous Saccharification and Fermentation (SSF)},
	url = {https://m2.mtmt.hu/api/publication/27567134},
	author = {Kusmiyati and Mustofa, A and Jumarmi},
	doi = {10.1088/1757-899X/358/1/012004},
	journal-iso = {IOP CONF SER MATER SCI ENG},
	journal = {IOP CONFERENCE SERIES: MATERIALS SCIENCE AND ENGINEERING},
	volume = {358},
	unique-id = {27567134},
	issn = {1757-8981},
	year = {2018},
	eissn = {1757-899X}
}

@article{MTMT:30564955,
	title = {Growth, substrate consumption, and product formation kinetics of Phanerochaete chrysosporium and Schizophyllum commune mixed culture under solid-state fermentation of fruit peels},
	url = {https://m2.mtmt.hu/api/publication/30564955},
	author = {Olorunnisola, Kola Saheed and Jamal, Parveen and Alam, Md. Zahangir},
	doi = {10.1007/s13205-018-1452-3},
	journal-iso = {3 BIOTECH},
	journal = {3 BIOTECH},
	volume = {8},
	unique-id = {30564955},
	issn = {2190-572X},
	abstract = {Kinetic analysis of solid-state fermentation (SSF) of fruit peels with Phanerochaete chrysosporium and Schizophyllum commune mixed culture was studied in flask and 7 kg capacity reactor. Modified Monod kinetic model suggested by Haldane sufficiently described microbial growth with co-efficient of determination (R-2) reaching 0.908 at increased substrate concentration than the classical Monod model (R-2 = 0.932). Leudeking-Piret model adequately described product synthesis in non-growth-dependent manner (R-2 = 0.989), while substrate consumption by P. chrysosporium and S. commune fungal mixed culture was growth-dependent (R-2 = 0.938). Hanes-Woolf model sufficiently represented a-amylase and cellulase enzymes synthesis (R-2 =0.911 and 0.988); alpha-amylase had enzyme maximum velocity (V-max) of 25.19 IU/gds/day and rate constant (K-m) of 11.55 IU/gds/day, while cellulase enzyme had V-max of 3.05 IU/gds/day and K-m of 57.47 IU/gds/day. Product yield in the reactor increased to 32.65 mg/g/day compared with 28.15 mg/g/day in shake flask. 2.5 cm media thickness was adequate for product formation within a 6 day SSF in the tray reactor.},
	keywords = {KINETICS; growth rate; FERMENTATION; Leudekin-Piret; Monod model},
	year = {2018},
	eissn = {2190-5738}
}

@article{MTMT:30487640,
	title = {A review of bioreactor technology used for enzymatic hydrolysis of cellulosic materials},
	url = {https://m2.mtmt.hu/api/publication/30487640},
	author = {Shokrkar, Hanieh and Ebrahimi, Sirous and Zamani, Mehdi},
	doi = {10.1007/s10570-018-2028-4},
	journal-iso = {CELLULOSE},
	journal = {CELLULOSE},
	volume = {25},
	unique-id = {30487640},
	issn = {0969-0239},
	abstract = {Cellulases are costly, a principal challenge of enzymatic hydrolysis of cellulosic materials for bioethanol production. For an efficient cellulase production, fungi are preferred over bacteria due to their permeation capability and versatile substrate consumption. Some limitations in the enzymatic hydrolysis step prevent the process to be economically feasible. Different strategies have been investigated to overcome these limitations, including genetic engineering, enzyme recycling, high solid loadings, pretreatment technologies, supplementation of cellulases with additives and application of nanomaterials for improving the thermal and pH stability of cellulases. Several studies have been performed in various bioreactors with the target to procure higher yields of glucose in the enzymatic hydrolysis step. The key factors for designing a bioreactor include efficient mixing, sufficient mass transfer, low shear stress, low foaming problems and low consumption of water and energy. In this scenario, different bioreactor configurations, including stirred tank bioreactor, horizontal rotating tubular bioreactor, airlift bioreactor, membrane bioreactor, reciprocating plate bioreactor, solid-state fermentation bioreactors have been reviewed for cellulase production with the aim to investigate main factors for designing a bioreactor.},
	keywords = {enzymatic hydrolysis; Bioethanol; Cellulase; Bioreactor design; Yields of glucose},
	year = {2018},
	eissn = {1572-882X},
	pages = {6279-6304}
}

@article{MTMT:26565098,
	title = {Ethanol production by a cellulolytic fungus Aspergillus terreus NCFT 4269.10 using agro-waste as a substrate},
	url = {https://m2.mtmt.hu/api/publication/26565098},
	author = {Sethi, Bijay Kumar and Das, Ashutosh S and Satpathy, Amrita and Behera, Bikash Chandra},
	doi = {10.1080/17597269.2016.1221296},
	journal-iso = {BIOFUELS-UK},
	journal = {BIOFUELS},
	volume = {8},
	unique-id = {26565098},
	issn = {1759-7269},
	year = {2017},
	eissn = {1759-7277},
	pages = {207-213}
}

@article{MTMT:25360460,
	title = {Study of the rice straw biodegradation in mixed culture of Trichoderma viride and Aspergillus niger by GC-MS and FTIR},
	url = {https://m2.mtmt.hu/api/publication/25360460},
	author = {Chen, Yaoning and Huang, Jingxia and Li, Yuanping and Zeng, Guangming and Zhang, Jiachao and Huang, Aizhi and Zhang, Jie and Ma, Shuang and Tan, Xuebin and Xu, Wei and Zhou, Wei},
	doi = {10.1007/s11356-015-4149-8},
	journal-iso = {ENVIRON SCI POLLUT R},
	journal = {ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH},
	volume = {22},
	unique-id = {25360460},
	issn = {0944-1344},
	year = {2015},
	eissn = {1614-7499},
	pages = {9807-9815}
}

@article{MTMT:25360461,
	title = {Consolidated bioprocess for bioethanol production with alkali-pretreated sugarcane bagasse},
	url = {https://m2.mtmt.hu/api/publication/25360461},
	author = {Liu, Yunyun and Zhang, Yu and Xu, Jingliang and Sun, Yongming and Yuan, Zhenhong and Xie, Jun},
	doi = {10.1016/j.apenergy.2015.05.004},
	journal-iso = {APPL ENERG},
	journal = {APPLIED ENERGY},
	volume = {157},
	unique-id = {25360461},
	issn = {0306-2619},
	year = {2015},
	eissn = {1872-9118},
	pages = {517-522}
}

@article{MTMT:24901438,
	title = {Direct fungal fermentation of lignocellulosic biomass into itaconic, fumaric, and malic acids: current and future prospects},
	url = {https://m2.mtmt.hu/api/publication/24901438},
	author = {Mondala, Andro H},
	doi = {10.1007/s10295-014-1575-4},
	journal-iso = {J IND MICROBIOL BIOT},
	journal = {JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY},
	volume = {42},
	unique-id = {24901438},
	issn = {1367-5435},
	year = {2015},
	eissn = {1476-5535},
	pages = {487-506}
}

@article{MTMT:24902704,
	title = {Cellulolytic and Xylanolytic Potential of High beta-Glucosidase-Producing Trichoderma from Decaying Biomass},
	url = {https://m2.mtmt.hu/api/publication/24902704},
	author = {Okeke, Benedict C},
	doi = {10.1007/s12010-014-1121-x},
	journal-iso = {APPL BIOCHEM BIOTECH},
	journal = {APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY},
	volume = {174},
	unique-id = {24902704},
	issn = {0273-2289},
	year = {2014},
	eissn = {1559-0291},
	pages = {1581-1598}
}

@article{MTMT:24901440,
	title = {Addendum to Issue 1-ENZITEC 2012 Simultaneous biosynthesis of biomass-degrading enzymes using co-cultivation of Aspergillus niger and Trichoderma reesei},
	url = {https://m2.mtmt.hu/api/publication/24901440},
	author = {Rabello, Gabriela Crestana and Perpetua, Buzon Pirota Rosangela Donizete and Figueiredo, Barros Georgia Oliveira and Farinas, Cristiane Sanchez},
	doi = {10.3109/10242422.2014.934362},
	journal-iso = {BIOCATAL BIOTRANSFOR},
	journal = {BIOCATALYSIS AND BIOTRANSFORMATION},
	volume = {32},
	unique-id = {24901440},
	issn = {1024-2422},
	year = {2014},
	eissn = {1029-2446},
	pages = {236-243}
}

@article{MTMT:24004340,
	title = {Enhanced cellulolytic enzyme production by the synergism between Trichoderma reesei RUT-C30 and Aspergillus niger NL02 and by the addition of surfactants},
	url = {https://m2.mtmt.hu/api/publication/24004340},
	author = {Fang, H and Zhao, C and Song, XY and Chen, M and Chang, Z and Chu, J},
	doi = {10.1007/s12257-012-0562-8},
	journal-iso = {BIOTECHNOL BIOPROC E},
	journal = {BIOTECHNOLOGY AND BIOPROCESS ENGINEERING},
	volume = {18},
	unique-id = {24004340},
	issn = {1226-8372},
	year = {2013},
	eissn = {1976-3816},
	pages = {390-398}
}

@article{MTMT:23975309,
	title = {Response surface optimization for the production of marine eubacterial protease and its application},
	url = {https://m2.mtmt.hu/api/publication/23975309},
	author = {Richa, K and Bose, H and Singh, K and Karthik, L and Kumar, G and Rao, KVB},
	journal-iso = {RES J BIOTECHNOL},
	journal = {RESEARCH JOURNAL OF BIOTECHNOLOGY},
	volume = {8},
	unique-id = {23975309},
	issn = {0973-6263},
	year = {2013},
	eissn = {2278-4535},
	pages = {78-85}
}

@article{MTMT:22814831,
	title = {Quantitative proteomic analysis of secretome of microbial consortium during saw dust utilization},
	url = {https://m2.mtmt.hu/api/publication/22814831},
	author = {Adav, SS and Ravindran, A and Cheow, ESH and Sze, SK},
	doi = {10.1016/j.jprot.2012.08.011},
	journal-iso = {J PROTEOMICS},
	journal = {JOURNAL OF PROTEOMICS},
	volume = {75},
	unique-id = {22814831},
	issn = {1874-3919},
	year = {2012},
	eissn = {1876-7737},
	pages = {5590-5603}
}

@article{MTMT:23975306,
	title = {Production of cellulases from Aspergillus niger NS-2 in solid state fermentation on agricultural and kitchen waste residues},
	url = {https://m2.mtmt.hu/api/publication/23975306},
	author = {Bansal, N and Tewari, R and Soni, R and Soni, SK},
	doi = {10.1016/j.wasman.2012.03.006},
	journal-iso = {WASTE MANAGE},
	journal = {WASTE MANAGEMENT},
	volume = {32},
	unique-id = {23975306},
	issn = {0956-053X},
	year = {2012},
	eissn = {1879-2456},
	pages = {1341-1346}
}

@article{MTMT:23975549,
	title = {Simultaneous saccharification and fermentation of paper sludge without pretreatment using cellulase from Acremonium cellulolyticus and thermotolerant Saccharomyces cerevisiae},
	url = {https://m2.mtmt.hu/api/publication/23975549},
	author = {Dwiarti, L and Boonchird, C and Harashima, S and Park, EY},
	doi = {10.1016/j.biombioe.2012.02.019},
	journal-iso = {BIOMASS BIOENERGY},
	journal = {BIOMASS & BIOENERGY},
	volume = {42},
	unique-id = {23975549},
	issn = {0961-9534},
	year = {2012},
	eissn = {1873-2909},
	pages = {114-122}
}

@article{MTMT:23975310,
	title = {EFFECT OF ACID HYDROLYSIS AND FUNGAL BIOTREATMENT ON AGRO-INDUSTRIAL WASTES FOR OBTAINMENT OF FREE SUGARS FOR BIOETHANOL PRODUCTION},
	url = {https://m2.mtmt.hu/api/publication/23975310},
	author = {El-Tayeb, TS and Abdelhafez, AA and Ali, SH and Ramadan, EM},
	doi = {10.1590/s1517-83822012000400037},
	journal-iso = {BRAZ J MICROBIOL},
	journal = {BRAZILIAN JOURNAL OF MICROBIOLOGY},
	volume = {43},
	unique-id = {23975310},
	issn = {1517-8382},
	year = {2012},
	eissn = {1678-4405},
	pages = {1523-1535}
}

@article{MTMT:23975305,
	title = {High Production of beta-Glucosidase by Aspergillus niger on Corncob},
	url = {https://m2.mtmt.hu/api/publication/23975305},
	author = {Wang, CL and Wu, GH and Chen, C and Chen, SL},
	doi = {10.1007/s12010-011-9323-y},
	journal-iso = {APPL BIOCHEM BIOTECH},
	journal = {APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY},
	volume = {168},
	unique-id = {23975305},
	issn = {0273-2289},
	year = {2012},
	eissn = {1559-0291},
	pages = {58-67}
}

@article{MTMT:23975304,
	title = {Purification and some kinetic properties of beta-glucosidase from Aspergillus terreus NRRL 265},
	url = {https://m2.mtmt.hu/api/publication/23975304},
	author = {Elshafei, AM and Hassan, MM and Morsi, NM and Elghonamy, DH},
	doi = {10.5897/AJB10.2617},
	journal-iso = {AFR J BIOTECHNOL},
	journal = {AFRICAN JOURNAL OF BIOTECHNOLOGY},
	volume = {10},
	unique-id = {23975304},
	issn = {1684-5315},
	year = {2011},
	pages = {19556-19569}
}

@article{MTMT:24030538,
	title = {Characterization of a Defined Cellulolytic and Xylanolytic Bacterial Consortium for Bioprocessing of Cellulose and Hemicelluloses RID E-7718-2011},
	url = {https://m2.mtmt.hu/api/publication/24030538},
	author = {Okeke, BC and Lu, J},
	doi = {10.1007/s12010-010-9091-0},
	journal-iso = {APPL BIOCHEM BIOTECH},
	journal = {APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY},
	volume = {163},
	unique-id = {24030538},
	issn = {0273-2289},
	year = {2011},
	eissn = {1559-0291},
	pages = {869-881}
}

@article{MTMT:23975301,
	title = {Production of Cellulases through Solid State Fermentation Using Kinnow Pulp as a Major Substrate},
	url = {https://m2.mtmt.hu/api/publication/23975301},
	author = {Oberoi, HS and Chavan, Y and Bansal, S and Dhillon, GS},
	doi = {10.1007/s11947-008-0092-8},
	journal-iso = {FOOD BIOPROCESS TECH},
	journal = {FOOD AND BIOPROCESS TECHNOLOGY},
	volume = {3},
	unique-id = {23975301},
	issn = {1935-5130},
	year = {2010},
	eissn = {1935-5149},
	pages = {528-536}
}

@article{MTMT:21783314,
	title = {Fungal Bioconversion of Lignocellulosic Residues; Opportunities & Perspectives},
	url = {https://m2.mtmt.hu/api/publication/21783314},
	author = {Dashtban, M and Schraft, H and Qin, WS},
	doi = {10.7150/ijbs.5.578},
	journal-iso = {INT J BIOL SCI},
	journal = {INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES},
	volume = {5},
	unique-id = {21783314},
	issn = {1449-2288},
	year = {2009},
	eissn = {1449-2288},
	pages = {578-595}
}

@article{MTMT:23975340,
	title = {Culture-based strategies to enhance cellulase enzyme production from Trichoderma reesei RUT-C30 in bioreactor culture conditions},
	url = {https://m2.mtmt.hu/api/publication/23975340},
	author = {Ahamed, A and Vermette, P},
	doi = {10.1016/j.bej.2007.11.030},
	journal-iso = {BIOCHEM ENG J},
	journal = {BIOCHEMICAL ENGINEERING JOURNAL},
	volume = {40},
	unique-id = {23975340},
	issn = {1369-703X},
	year = {2008},
	eissn = {1873-295X},
	pages = {399-407}
}

@article{MTMT:23975295,
	title = {Enhanced enzyme production from mixed cultures of Trichoderma reesei RUT-C30 and Aspergillus niger LMA grown as fed batch in a stirred tank bioreactor},
	url = {https://m2.mtmt.hu/api/publication/23975295},
	author = {Ahamed, A and Vermette, P},
	doi = {10.1016/j.bej.2008.05.007},
	journal-iso = {BIOCHEM ENG J},
	journal = {BIOCHEMICAL ENGINEERING JOURNAL},
	volume = {42},
	unique-id = {23975295},
	issn = {1369-703X},
	year = {2008},
	eissn = {1873-295X},
	pages = {41-46}
}

@article{MTMT:23974972,
	title = {Partitioning of beta-glucosidase from Trichoderma reesei in poly(ethylene glycol) and potassium phosphate aqueous two-phase systems: Influence of pH and temperature},
	url = {https://m2.mtmt.hu/api/publication/23974972},
	author = {Gautam, S and Simon, L},
	doi = {10.1016/j.bej.2006.02.010},
	journal-iso = {BIOCHEM ENG J},
	journal = {BIOCHEMICAL ENGINEERING JOURNAL},
	volume = {30},
	unique-id = {23974972},
	issn = {1369-703X},
	year = {2006},
	eissn = {1873-295X},
	pages = {104-108}
}

@CONFERENCE{MTMT:23975298,
	title = {Optimization of inocula for cellulases biosynthesis by Trichoderma harzinum UM-11 under shaking culture},
	url = {https://m2.mtmt.hu/api/publication/23975298},
	author = {Hameed, U and Ali, S and Javed, M and Ikram-Ul-Haq},
	booktitle = {Proceedings Second National Conference of Biology},
	unique-id = {23975298},
	year = {2004},
	pages = {1-6}
}

@article{MTMT:1003073,
	title = {In vitro water activity and pH dependence of mycelial growth and extracellular enzyme activities of Trichoderma strains with biocontrol potential},
	url = {https://m2.mtmt.hu/api/publication/1003073},
	author = {Kredics, László and Manczinger, László and Antal, Zsuzsanna and Pénzes, Zsolt and Szekeres, András and Kevei, F and Nagy, Erzsébet},
	doi = {10.1111/j.1365-2672.2004.02167.x},
	journal-iso = {J APPL MICROBIOL},
	journal = {JOURNAL OF APPLIED MICROBIOLOGY},
	volume = {96},
	unique-id = {1003073},
	issn = {1364-5072},
	year = {2004},
	eissn = {1365-2672},
	pages = {491-498},
	orcid-numbers = {Kredics, László/0000-0002-8837-3973; Manczinger, László/0000-0003-1031-7522; Pénzes, Zsolt/0000-0003-0447-5997; Szekeres, András/0000-0003-1651-4623}
}

@article{MTMT:1003074,
	title = {Influence of environmental parameters on Trichoderma strains with biocontrol potential},
	url = {https://m2.mtmt.hu/api/publication/1003074},
	author = {Kredics, László and Antal, Zsuzsanna and Manczinger, László and Szekeres, András and Kevei, F and Nagy, Erzsébet},
	journal-iso = {FOOD TECHNOL BIOTECH},
	journal = {FOOD TECHNOLOGY AND BIOTECHNOLOGY},
	volume = {41},
	unique-id = {1003074},
	issn = {1330-9862},
	year = {2003},
	eissn = {1334-2606},
	pages = {37-42},
	orcid-numbers = {Kredics, László/0000-0002-8837-3973; Manczinger, László/0000-0003-1031-7522; Szekeres, András/0000-0003-1651-4623}
}