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a niger atcc 20611  (ATCC)


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    ATCC a niger atcc 20611
    A Niger Atcc 20611, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 38 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/aspergillus+niger+atcc+20611/Aspergillus+Fijiensis%3B+Ace-2-1/10__1007_slash_s12633___026___03666___8-202-14-16
    Average 96 stars, based on 38 article reviews
    a niger atcc 20611 - by Bioz Stars, 2026-10
    96/100 stars

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    Expressing:

    Article Title: Molecular engineering and biotechnological advancements in β-glucosidase for industrial impact: A review.
    Article Snippet: Cellulases are essential in various industrial processes, particularly for converting cellulosic biomass into valuable biochemicals, contributing to sustainable and eco-friendly technologies.. Despite their significance, cellulases; especially β-glucosidase (BGL), which catalyzes the final step in cellulose hydrolysis, face challenges such as low catalytic efficiency, narrow substrate specificity, and sensitivity to operational conditions, limiting largescale application.. Enhancing these enzymatic properties is vital to improving the economic and environmental performance of bioconversion processes.

    Article Title: High-Level Expression of β-Glucosidase in Aspergillus niger ATCC 20611 Using the Trichoderma reesei Promoter Pcdna1 to Enhance Cellulose Degradation
    Article Snippet: These results demonstrate that the promoters in filamentous fungi could be employed across species in A. niger ATCC 20611 and further facilitated the efficient expression of β-glucosidase to optimize cellulases for efficient cellulose transformation. .. Citation: Chang, J.; Wang, J.; Li, Z.; Wang, L.; Lu, P.; Zhong, Y.; Liu, H. High-Level Expression of β-Glucosidase in Aspergillus niger ATCC 20611 Using the Trichoderma reesei Promoter Pcdna1 to Enhance Cellulose Degradation. ..

    Article Title: High-Level Expression of β-Glucosidase in Aspergillus niger ATCC 20611 Using the Trichoderma reesei Promoter Pcdna1 to Enhance Cellulose Degradation
    Article Snippet: .. Aspergillus niger ATCC 20611 has the potential for efficient protein expression because of its ability to secret enzymes for the industrial production of fructooligosaccharides, but it lacks robust promoters for high-level protein expression. .. Here, the development of A. niger 20611 as a powerful protein expression system exploited the conserved constitutive promoter Pgpd1 of the glyceraldehyde-3-phosphate dehydrogenase-encoding gene from Trichoerma reesei to drive the expression of the enhanced green fluorescent protein in A. niger ATCC 20611.

    Activity Assay:

    Article Title: Molecular engineering and biotechnological advancements in β-glucosidase for industrial impact: A review.
    Article Snippet: Cellulases are essential in various industrial processes, particularly for converting cellulosic biomass into valuable biochemicals, contributing to sustainable and eco-friendly technologies.. Despite their significance, cellulases; especially β-glucosidase (BGL), which catalyzes the final step in cellulose hydrolysis, face challenges such as low catalytic efficiency, narrow substrate specificity, and sensitivity to operational conditions, limiting largescale application.. Enhancing these enzymatic properties is vital to improving the economic and environmental performance of bioconversion processes.

    Article Title: Production of invertase from Penicillium spp. under solid state fermentation and its immobilization on magnetic nanoparticles
    Article Snippet: .. Commercially, invertase is biosynthesized by chiefly by yeast strains of Saccharomyces cerevisiae (Mahendran et al., 2022). some of the fungi reported as invertase producers are the following: Aspergillus niger ATCC 20611, A. niger strain AN 166, Aspergillus foetidus, Aspergillus oryzae CFR 202, Aspergillus awamori GHRTS, and Penicillium chrysogenum (Yun, 1996). some of these fungal strains have the capacity to produce two types of invertase, but the enzymatic activity is different because it depends on the carbon source and type of microorganisms (Mahendran et al., 2022). ..

    other:

    Article Title: Comparative Studies of Structure and Regulatory Genes Controlling Pectinase Expression in Soft Rot Pectobacterium carotovorum NM-NRC;-Multistep Mutagenesis, Purification and Molecular Docking Studies For the Over-Production of Pectinase
    Article Snippet: In this study, the pectinase activity investigated and assessed of 50 bacterial strains isolated from various rotting fruits and vegetables.. Isolate No. 10, which measured 52.42 U/ml had the highest activity, was identified molecularly using the 16Sr DNA gene as Pectobacteriumcarotovorum subsp. carotovorum NM-NRC and deposited in the NCBI database with accession number OQ256290.. Successive mutagenesis was performed utilizing ultraviolet, ethyl methansulfonate, and ethidium bromide for Pectobacteriumcarotovorum NM-NRC.

    Article Title: Optimized Biomass Production of Probiotic Bacterium Pediococcus acidilactici TMAB26 Using Pineapple Peel: A Response Surface Methodology Approach
    Article Snippet: Effect of C/N ratio and media optimization through response surface methodology on simultaneous productions of intra-and extracellular inulinase and invertase from Aspergillus niger ATCC 20611.



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    industrial fungus aspergillus niger atcc 20611  (ATCC)
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    Fig. 2 Recombinant extracellular production of lcc9 in A. niger. A Genomic loci-specific integration diagram of lcc9 expression cassette. B Schematic structure of the plasmid pCGgg-lcc9. C <t>A.niger</t> MA70.15 and AnGggL laccase activity detection based on plates containing ABTS. D SDS-PAGE analysis of A.niger MA70.15 and AnGggL fermentation supernatant. M: protein molecular weight marker; Lane 0: fermentation supernatant samples from MA70.15 shake flasks cultured for 6 d; Lanes 1–6: fermentation supernatant samples from AnGggL shake flasks cultured for 1–6 d, respectively
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    Fig. 2 Recombinant extracellular production of lcc9 in A. niger. A Genomic loci-specific integration diagram of lcc9 expression cassette. B Schematic structure of the plasmid pCGgg-lcc9. C A.niger MA70.15 and AnGggL laccase activity detection based on plates containing ABTS. D SDS-PAGE analysis of A.niger MA70.15 and AnGggL fermentation supernatant. M: protein molecular weight marker; Lane 0: fermentation supernatant samples from MA70.15 shake flasks cultured for 6 d; Lanes 1–6: fermentation supernatant samples from AnGggL shake flasks cultured for 1–6 d, respectively

    Journal: BMC biotechnology

    Article Title: Enhanced extracellular production of Coprinopsis cinerea laccase Lcc9 in Aspergillus niger by gene expression cassette and bioprocess optimization.

    doi: 10.1186/s12896-024-00924-8

    Figure Lengend Snippet: Fig. 2 Recombinant extracellular production of lcc9 in A. niger. A Genomic loci-specific integration diagram of lcc9 expression cassette. B Schematic structure of the plasmid pCGgg-lcc9. C A.niger MA70.15 and AnGggL laccase activity detection based on plates containing ABTS. D SDS-PAGE analysis of A.niger MA70.15 and AnGggL fermentation supernatant. M: protein molecular weight marker; Lane 0: fermentation supernatant samples from MA70.15 shake flasks cultured for 6 d; Lanes 1–6: fermentation supernatant samples from AnGggL shake flasks cultured for 1–6 d, respectively

    Article Snippet: Enhancing fructooligosaccharides production by genetic improvement of the industrial fungus Aspergillus niger ATCC 20611.

    Techniques: Recombinant, Expressing, Plasmid Preparation, Activity Assay, SDS Page, Molecular Weight, Marker, Cell Culture

    Fig. 3 A.niger MA70.15 protoplast preparation system optimization. A Protoplast production with different enzymatic combinations. 1: 2% cellulase; 2: 2% cellulase + 1% snailase; 3: 2% cellulase + 1% lyticase; 4: 2% cellulase + 1% snailase + 1% lyticase; 5: 2% cellulase + 1% snailase + 1% lyticase + 0.5% lysozyme. B Protoplast production with different incubation times. C Protoplast production with different incubation temperatures. D Protoplast production with different mycelial ages. Error bars represent the standard deviation

    Journal: BMC biotechnology

    Article Title: Enhanced extracellular production of Coprinopsis cinerea laccase Lcc9 in Aspergillus niger by gene expression cassette and bioprocess optimization.

    doi: 10.1186/s12896-024-00924-8

    Figure Lengend Snippet: Fig. 3 A.niger MA70.15 protoplast preparation system optimization. A Protoplast production with different enzymatic combinations. 1: 2% cellulase; 2: 2% cellulase + 1% snailase; 3: 2% cellulase + 1% lyticase; 4: 2% cellulase + 1% snailase + 1% lyticase; 5: 2% cellulase + 1% snailase + 1% lyticase + 0.5% lysozyme. B Protoplast production with different incubation times. C Protoplast production with different incubation temperatures. D Protoplast production with different mycelial ages. Error bars represent the standard deviation

    Article Snippet: Enhancing fructooligosaccharides production by genetic improvement of the industrial fungus Aspergillus niger ATCC 20611.

    Techniques: Incubation, Standard Deviation

    Fig. 4 Effect of promoter optimization on the extracellular Lcc9 production. A Native-PAGE analysis of AnGcgL fermentation supernatant. Lanes 1–5: supernatant samples of AnGcgL at 2, 3, 4, 5, and 6 d, respectively. B Relative transcription levels of lcc9 in A.niger strains. Error bars represent the standard deviation

    Journal: BMC biotechnology

    Article Title: Enhanced extracellular production of Coprinopsis cinerea laccase Lcc9 in Aspergillus niger by gene expression cassette and bioprocess optimization.

    doi: 10.1186/s12896-024-00924-8

    Figure Lengend Snippet: Fig. 4 Effect of promoter optimization on the extracellular Lcc9 production. A Native-PAGE analysis of AnGcgL fermentation supernatant. Lanes 1–5: supernatant samples of AnGcgL at 2, 3, 4, 5, and 6 d, respectively. B Relative transcription levels of lcc9 in A.niger strains. Error bars represent the standard deviation

    Article Snippet: Enhancing fructooligosaccharides production by genetic improvement of the industrial fungus Aspergillus niger ATCC 20611.

    Techniques: Clear Native PAGE, Standard Deviation

    Fig. 6 Effect of microparticle optimization on the extracellular Lcc9 production. A Effect of different microparticle types. B Effect of varying the CaCO3 concentration. C Effect of varying the MgSiO3 concentration. D Effect of varying the Al2O3 concentration. E Effect of microparticles on A. niger mycelial morphology in shake flask fermentation. Error bars represent the standard deviation

    Journal: BMC biotechnology

    Article Title: Enhanced extracellular production of Coprinopsis cinerea laccase Lcc9 in Aspergillus niger by gene expression cassette and bioprocess optimization.

    doi: 10.1186/s12896-024-00924-8

    Figure Lengend Snippet: Fig. 6 Effect of microparticle optimization on the extracellular Lcc9 production. A Effect of different microparticle types. B Effect of varying the CaCO3 concentration. C Effect of varying the MgSiO3 concentration. D Effect of varying the Al2O3 concentration. E Effect of microparticles on A. niger mycelial morphology in shake flask fermentation. Error bars represent the standard deviation

    Article Snippet: Enhancing fructooligosaccharides production by genetic improvement of the industrial fungus Aspergillus niger ATCC 20611.

    Techniques: Concentration Assay, Standard Deviation