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fibrobacter succinogenes s85  (ATCC)


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    Structured Review

    ATCC fibrobacter succinogenes s85
    Metabolite production and ammonia consumption by F. <t>succinogenes</t> culture and coculture with S. ruminantium on cellulose in the presence or absence of S. cerevisiae . The acetate, succinate and formate concentrations were quantified by enzymatic kits and the propionate concentration was estimated via 1 H NMR. Triplicate cultures were used for the metabolite quantification. Light orange: 48 h-cultures in the absence of S. cerevisiae (SC); dark orange: 63 h-cultures in the absence of SC; light green: 48 h-cultures in the presence of SC; dark green: 63 h-cultures in the presence of SC
    Fibrobacter Succinogenes S85, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 37 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fibrobacter+succinogenes/Fibrobacter+succinogenes/pmc12323243-88-7-10
    Average 93 stars, based on 37 article reviews
    fibrobacter succinogenes s85 - by Bioz Stars, 2026-09
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    1) Product Images from "Transcriptomic analysis of the interactions between Fibrobacter succinogenes S85 , Selenomonas ruminantium PC18 and a live yeast strain used as a ruminant feed additive"

    Article Title: Transcriptomic analysis of the interactions between Fibrobacter succinogenes S85 , Selenomonas ruminantium PC18 and a live yeast strain used as a ruminant feed additive

    Journal: BMC Genomics

    doi: 10.1186/s12864-025-11894-2

    Metabolite production and ammonia consumption by F. succinogenes culture and coculture with S. ruminantium on cellulose in the presence or absence of S. cerevisiae . The acetate, succinate and formate concentrations were quantified by enzymatic kits and the propionate concentration was estimated via 1 H NMR. Triplicate cultures were used for the metabolite quantification. Light orange: 48 h-cultures in the absence of S. cerevisiae (SC); dark orange: 63 h-cultures in the absence of SC; light green: 48 h-cultures in the presence of SC; dark green: 63 h-cultures in the presence of SC
    Figure Legend Snippet: Metabolite production and ammonia consumption by F. succinogenes culture and coculture with S. ruminantium on cellulose in the presence or absence of S. cerevisiae . The acetate, succinate and formate concentrations were quantified by enzymatic kits and the propionate concentration was estimated via 1 H NMR. Triplicate cultures were used for the metabolite quantification. Light orange: 48 h-cultures in the absence of S. cerevisiae (SC); dark orange: 63 h-cultures in the absence of SC; light green: 48 h-cultures in the presence of SC; dark green: 63 h-cultures in the presence of SC

    Techniques Used: Concentration Assay

    Principal component analysis (PCA) plot of the F. succinogenes S85 (FS) and S. ruminantium PC18 (SR) transcriptomes. The data points are coloured by condition, and triplicates within each PCA have the same colour. A triplicate samples of F. succinogenes S85 (FS) grown on cellobiose (circles) or cellulose (triangles). FS alone (blue), FS + SC (yellow), FS + SR (green) and FS + SR + SC (red). B triplicate samples of S. ruminantium PC18 (SR) grown on cellobiose (circles). SR alone (blue), SR + SC (yellow), SR + FS (green) and SR + FS + SC (red). SC: S. cerevisiae
    Figure Legend Snippet: Principal component analysis (PCA) plot of the F. succinogenes S85 (FS) and S. ruminantium PC18 (SR) transcriptomes. The data points are coloured by condition, and triplicates within each PCA have the same colour. A triplicate samples of F. succinogenes S85 (FS) grown on cellobiose (circles) or cellulose (triangles). FS alone (blue), FS + SC (yellow), FS + SR (green) and FS + SR + SC (red). B triplicate samples of S. ruminantium PC18 (SR) grown on cellobiose (circles). SR alone (blue), SR + SC (yellow), SR + FS (green) and SR + FS + SC (red). SC: S. cerevisiae

    Techniques Used:


    Figure Legend Snippet: F. succinogenes CAZyme genes upregulated on cellulose

    Techniques Used:

    Related Articles

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    Article Snippet: The compositions contain concentrated mixtures of novel peptides produced by a new multi-stage fermentation method, in addition to naturally-occurring milk proteins in untreated milk, but lack the deleterious components commonly found in fermented milk products. .. Significantly enhanced nutritional products are also obtained from fermentation of animal feedstock, such as fodder, grass, or grain by-products treated with Przewalski bacteria, particularly with mixtures of one or more Przewalski strains Ruminococcus flavefaciens (ATCC Accession No. 49949), Butyrivibrio fibrisolvens (ATCC Accession No. 19171), Fibrobacter succinogenes (ATCC Accession No. 51216) and Ruminococcus albus (ATCC Accession No. 27211). ..

    Article Title: Nutritional supplements for animal health and development
    Article Snippet: .. The bacteria comprising the “Przewalski culture” as employed herein comprise a mixture of Ruminococcus flavefaciens (ATCC Accession No. 49949), Butyrivibrio fibrisolvens (ATCC Accession No. 19171), Fibrobacter succinogenes (ATCC Accession No. 51216) and Ruminococcus albus (ATCC Accession No. 27211). .. Each of these organisms is available from the American Type Culture Collection (ATCC), or other similar culture collections throughout the world.

    other:

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    Infection:

    Article Title: Gut commensal bacteria influence colorectal cancer development by modulating immune response in AOM/DSS-treated mice.
    Article Snippet: .. Bacterial culture and oral infection Bacterial strains Eubacterium dolichum (ATCC29143), Ruminococcus flavefaciens (ATCC49949), and Fibrobacter succinogenes (ATCC51214) were obtained from American Type Culture Collection (ATCC). .. The strains were cultivated under anaerobic conditions at 37°C using brain heart infusion (BHI) culture medium with oxygen-free mixed gas (95% N2 and 5% CO2) in the anaerobic incubator (DG250, Don Whitley Scientific).



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    Metabolite production and ammonia consumption by F. succinogenes culture and coculture with S. ruminantium on cellulose in the presence or absence of S. cerevisiae . The acetate, succinate and formate concentrations were quantified by enzymatic kits and the propionate concentration was estimated via 1 H NMR. Triplicate cultures were used for the metabolite quantification. Light orange: 48 h-cultures in the absence of S. cerevisiae (SC); dark orange: 63 h-cultures in the absence of SC; light green: 48 h-cultures in the presence of SC; dark green: 63 h-cultures in the presence of SC

    Journal: BMC Genomics

    Article Title: Transcriptomic analysis of the interactions between Fibrobacter succinogenes S85 , Selenomonas ruminantium PC18 and a live yeast strain used as a ruminant feed additive

    doi: 10.1186/s12864-025-11894-2

    Figure Lengend Snippet: Metabolite production and ammonia consumption by F. succinogenes culture and coculture with S. ruminantium on cellulose in the presence or absence of S. cerevisiae . The acetate, succinate and formate concentrations were quantified by enzymatic kits and the propionate concentration was estimated via 1 H NMR. Triplicate cultures were used for the metabolite quantification. Light orange: 48 h-cultures in the absence of S. cerevisiae (SC); dark orange: 63 h-cultures in the absence of SC; light green: 48 h-cultures in the presence of SC; dark green: 63 h-cultures in the presence of SC

    Article Snippet: The strains used in this study were Fibrobacter succinogenes S85 (ATCC 19169), Selenomonas ruminantium subsp. lactilytica PC18 (DSM 2872) and Saccharomyces cerevisiae (CNCM I-1077).

    Techniques: Concentration Assay

    Principal component analysis (PCA) plot of the F. succinogenes S85 (FS) and S. ruminantium PC18 (SR) transcriptomes. The data points are coloured by condition, and triplicates within each PCA have the same colour. A triplicate samples of F. succinogenes S85 (FS) grown on cellobiose (circles) or cellulose (triangles). FS alone (blue), FS + SC (yellow), FS + SR (green) and FS + SR + SC (red). B triplicate samples of S. ruminantium PC18 (SR) grown on cellobiose (circles). SR alone (blue), SR + SC (yellow), SR + FS (green) and SR + FS + SC (red). SC: S. cerevisiae

    Journal: BMC Genomics

    Article Title: Transcriptomic analysis of the interactions between Fibrobacter succinogenes S85 , Selenomonas ruminantium PC18 and a live yeast strain used as a ruminant feed additive

    doi: 10.1186/s12864-025-11894-2

    Figure Lengend Snippet: Principal component analysis (PCA) plot of the F. succinogenes S85 (FS) and S. ruminantium PC18 (SR) transcriptomes. The data points are coloured by condition, and triplicates within each PCA have the same colour. A triplicate samples of F. succinogenes S85 (FS) grown on cellobiose (circles) or cellulose (triangles). FS alone (blue), FS + SC (yellow), FS + SR (green) and FS + SR + SC (red). B triplicate samples of S. ruminantium PC18 (SR) grown on cellobiose (circles). SR alone (blue), SR + SC (yellow), SR + FS (green) and SR + FS + SC (red). SC: S. cerevisiae

    Article Snippet: The strains used in this study were Fibrobacter succinogenes S85 (ATCC 19169), Selenomonas ruminantium subsp. lactilytica PC18 (DSM 2872) and Saccharomyces cerevisiae (CNCM I-1077).

    Techniques:

    Journal: BMC Genomics

    Article Title: Transcriptomic analysis of the interactions between Fibrobacter succinogenes S85 , Selenomonas ruminantium PC18 and a live yeast strain used as a ruminant feed additive

    doi: 10.1186/s12864-025-11894-2

    Figure Lengend Snippet: F. succinogenes CAZyme genes upregulated on cellulose

    Article Snippet: The strains used in this study were Fibrobacter succinogenes S85 (ATCC 19169), Selenomonas ruminantium subsp. lactilytica PC18 (DSM 2872) and Saccharomyces cerevisiae (CNCM I-1077).

    Techniques: