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f nucleatum atcc 10953  (ATCC)


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    ATCC f nucleatum atcc 10953
    F Nucleatum Atcc 10953, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 900 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fusobacterium+nucleatum+atcc+10953/Fusobacterium+nucleatum+subsp%2E+polymorphum+(Knorr)+Dzink+et+al/pm41071528-363-22-24
    Average 97 stars, based on 900 article reviews
    f nucleatum atcc 10953 - by Bioz Stars, 2026-10
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    other:

    Article Title: Stillbirth with a false-positive lung float test result - an unusual case report.
    Article Snippet: Aspects of the growth and metabolism of Fusobacterium nucleatum ATCC 10953 in continuous culture.

    Hybridization:

    Article Title: Potential Pharmacological Properties of Triterpene Derivatives of Ursolic Acid
    Article Snippet: 43 , UA was reacted with acetic anhydride (Ac 2 O) in pyridine at room temperature for 24 h to yield compound 54 , K. pneumoniae (ATCC 10031) Shigella flexneri (ATCC 12022) E. coli (ATCC 25922) , Enhanced antibacterial activity against Shigella flexneri and E. coli , a multidrug-resistant clinical isolate from sputum , [ ] . .. 44 , Hybridization of UA with hydrazide and 1,3,4-oxadiazole groups , S. mutans ATCC 25175, Fusobacterium nucleatum ATCC 10953 , Showed significant antibacterial activity against S. mutans , [ ] . .. 45 , The commercial anhydride was added to UA in pyridine (CH 2 Cl 2 , 2 mL) to form an ester derivative , E. faecalis , S. epidermidis and S. aureus , An antibiofilm activity against S. aureus without any effect on mammalian cells. , [ ] .

    Activity Assay:

    Article Title: Potential Pharmacological Properties of Triterpene Derivatives of Ursolic Acid
    Article Snippet: 43 , UA was reacted with acetic anhydride (Ac 2 O) in pyridine at room temperature for 24 h to yield compound 54 , K. pneumoniae (ATCC 10031) Shigella flexneri (ATCC 12022) E. coli (ATCC 25922) , Enhanced antibacterial activity against Shigella flexneri and E. coli , a multidrug-resistant clinical isolate from sputum , [ ] . .. 44 , Hybridization of UA with hydrazide and 1,3,4-oxadiazole groups , S. mutans ATCC 25175, Fusobacterium nucleatum ATCC 10953 , Showed significant antibacterial activity against S. mutans , [ ] . .. 45 , The commercial anhydride was added to UA in pyridine (CH 2 Cl 2 , 2 mL) to form an ester derivative , E. faecalis , S. epidermidis and S. aureus , An antibiofilm activity against S. aureus without any effect on mammalian cells. , [ ] .

    Sterility:

    Article Title: Quantifying synthetic bacterial community composition with flow cytometry: efficacy in mock communities and challenges in co-cultures
    Article Snippet: .. Aggregatibacter actinomycetemcomitans ATCC 43718, Actinomyces naeslundii ATCC 51655, Actinomyces viscosus ATCC 15987, Fusobacterium nucleatum ATCC 10953, Porphyromonas gingivalis ATCC 33277, Prevotella intermedia ATCC 25611, and Veillonella parvula DSM 2007 were maintained on blood agar base No. 2 (Oxoid, Hampshire, UK) supplemented with menadione (1 mg/L) (Sigma-Aldrich, Diegem, Belgium), hemin (5 mg/L) (Sigma-Aldrich, Diegem, Belgium), and 5% sterile defibrinated horse blood (Oxoid, Hampshire, UK) under anaerobic conditions (90% N 2 , 10% CO 2 ) at 37°C. .. All strains maintained on blood agar as well as frozen stocks of Streptococcus gordonii ATCC 49818, Streptococcus mitis ATCC 49456, Streptococcus mutans ATCC 25175, Streptococcus oralis ATCC 35037, Streptococcus salivarius TOVE-R, Streptococcus sanguinis LMG 14657, and Streptococcus sobrinus ATCC 33478 were incubated in triplicate in Brain Heart Infusion broth 2 (BHI-2) ( ) under anaerobic conditions (90% N 2 , 10% CO 2 ) at 37°C for 24 h. All bacterial strains were grown in triplicate.

    Isolation:

    Article Title: Effect of rubusoside, a natural sucrose substitute, on the metabolism of Scardovia wiggsiae: a novel potential cariogenic pathogen.
    Article Snippet: .. Skår CK, Krüger PG, Bakken V. Characterisation and subcellular localisation of the GroEL-like and DnaK-like proteins isolated from Fusobacterium nucleatum ATCC 10953. ..

    Control:

    Article Title: Association between dental diseases and stroke
    Article Snippet: .. Nishi, H., et al. (2020). , 534 , 71.1 ± 12.4 , Case control , Fusobacterium nucleatum ATCC 10953 , Unfavorable outcome following stroke , NA , OR 3.12 [1.55–6.29]. ..



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    https://www.bioz.com/product/fusobacterium+nucleatum+atcc+10953/Fusobacterium+nucleatum+subsp%2E+polymorphum+(Knorr)+Dzink+et+al/pm41071528-363-22-24
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    (A) Phylogenetic relationship of representative F. nucleatum strains used in this study, grouped by subspecies—subsp. nucleatum (FNN; ATCC 25586, ATCC 23726, CTI-2), subsp. vincentii (FNV; 3_1_27, ATCC 49256, ATCC 51190), subsp. animalis (FNA; 7_1, F0401, ATCC 51191), and subsp. polymorphum (FNP; ATCC 10953, 12230). The phylogenetic tree was constructed based on znpA gene using the maximum-likelihood method implemented in DNAMAN Version 10 (Lynnon Biosoft). Fusobacterium periodonticum ATCC 33693 (FP) was included as an outgroup. (B) Schematic of the chromosomal region between uraA and pepF showing subspecies-specific presence of luxS . luxS is absent from FNN and FNV at this locus, present as an intact gene in FNA (between uraA and pepF ), and disrupted in FNP by insertion of an IS200-family element. The corresponding region from F. periodonticum is shown for comparison. Arrows indicate gene orientation; uraA (gray), pepF (black), luxS (blue), IS200 insertion (magenta), and the adjacent gene ( ddpA , orange) are indicated. (C) AI-2 activity in cell-free culture supernatants was measured using the Vibrio harveyi BB170 bioluminescence reporter assay. Supernatants from FNN, FNV, and FNP strains showed signals at or near background levels, whereas all tested FNA strains and F. periodonticum generated robust reporter induction. E. coli wild type (WT) and its Δ luxS mutant served as positive and negative controls, respectively. Data are presented as relative fluorescence units (RFU; mean ± SD) from three independent experiments (each assayed in technical triplicate); the y-axis includes a break to display both low- and high-signal samples.
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    (A) Phylogenetic relationship of representative F. nucleatum strains used in this study, grouped by subspecies—subsp. nucleatum (FNN; ATCC 25586, ATCC 23726, CTI-2), subsp. vincentii (FNV; 3_1_27, ATCC 49256, ATCC 51190), subsp. animalis (FNA; 7_1, F0401, ATCC 51191), and subsp. polymorphum (FNP; ATCC 10953, 12230). The phylogenetic tree was constructed based on znpA gene using the maximum-likelihood method implemented in DNAMAN Version 10 (Lynnon Biosoft). Fusobacterium periodonticum ATCC 33693 (FP) was included as an outgroup. (B) Schematic of the chromosomal region between uraA and pepF showing subspecies-specific presence of luxS . luxS is absent from FNN and FNV at this locus, present as an intact gene in FNA (between uraA and pepF ), and disrupted in FNP by insertion of an IS200-family element. The corresponding region from F. periodonticum is shown for comparison. Arrows indicate gene orientation; uraA (gray), pepF (black), luxS (blue), IS200 insertion (magenta), and the adjacent gene ( ddpA , orange) are indicated. (C) AI-2 activity in cell-free culture supernatants was measured using the Vibrio harveyi BB170 bioluminescence reporter assay. Supernatants from FNN, FNV, and FNP strains showed signals at or near background levels, whereas all tested FNA strains and F. periodonticum generated robust reporter induction. E. coli wild type (WT) and its Δ luxS mutant served as positive and negative controls, respectively. Data are presented as relative fluorescence units (RFU; mean ± SD) from three independent experiments (each assayed in technical triplicate); the y-axis includes a break to display both low- and high-signal samples.
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    (A) Phylogenetic relationship of representative F. nucleatum strains used in this study, grouped by subspecies—subsp. nucleatum (FNN; ATCC 25586, ATCC 23726, CTI-2), subsp. vincentii (FNV; 3_1_27, ATCC 49256, ATCC 51190), subsp. animalis (FNA; 7_1, F0401, ATCC 51191), and subsp. polymorphum (FNP; ATCC 10953, 12230). The phylogenetic tree was constructed based on znpA gene using the maximum-likelihood method implemented in DNAMAN Version 10 (Lynnon Biosoft). Fusobacterium periodonticum ATCC 33693 (FP) was included as an outgroup. (B) Schematic of the chromosomal region between uraA and pepF showing subspecies-specific presence of luxS . luxS is absent from FNN and FNV at this locus, present as an intact gene in FNA (between uraA and pepF ), and disrupted in FNP by insertion of an IS200-family element. The corresponding region from F. periodonticum is shown for comparison. Arrows indicate gene orientation; uraA (gray), pepF (black), luxS (blue), IS200 insertion (magenta), and the adjacent gene ( ddpA , orange) are indicated. (C) AI-2 activity in cell-free culture supernatants was measured using the Vibrio harveyi BB170 bioluminescence reporter assay. Supernatants from FNN, FNV, and FNP strains showed signals at or near background levels, whereas all tested FNA strains and F. periodonticum generated robust reporter induction. E. coli wild type (WT) and its Δ luxS mutant served as positive and negative controls, respectively. Data are presented as relative fluorescence units (RFU; mean ± SD) from three independent experiments (each assayed in technical triplicate); the y-axis includes a break to display both low- and high-signal samples.
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    fpo atcc 10953  (ATCC)
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    (A) Phylogenetic relationship of representative F. nucleatum strains used in this study, grouped by subspecies—subsp. nucleatum (FNN; ATCC 25586, ATCC 23726, CTI-2), subsp. vincentii (FNV; 3_1_27, ATCC 49256, ATCC 51190), subsp. animalis (FNA; 7_1, F0401, ATCC 51191), and subsp. polymorphum (FNP; ATCC 10953, 12230). The phylogenetic tree was constructed based on znpA gene using the maximum-likelihood method implemented in DNAMAN Version 10 (Lynnon Biosoft). Fusobacterium periodonticum ATCC 33693 (FP) was included as an outgroup. (B) Schematic of the chromosomal region between uraA and pepF showing subspecies-specific presence of luxS . luxS is absent from FNN and FNV at this locus, present as an intact gene in FNA (between uraA and pepF ), and disrupted in FNP by insertion of an IS200-family element. The corresponding region from F. periodonticum is shown for comparison. Arrows indicate gene orientation; uraA (gray), pepF (black), luxS (blue), IS200 insertion (magenta), and the adjacent gene ( ddpA , orange) are indicated. (C) AI-2 activity in cell-free culture supernatants was measured using the Vibrio harveyi BB170 bioluminescence reporter assay. Supernatants from FNN, FNV, and FNP strains showed signals at or near background levels, whereas all tested FNA strains and F. periodonticum generated robust reporter induction. E. coli wild type (WT) and its Δ luxS mutant served as positive and negative controls, respectively. Data are presented as relative fluorescence units (RFU; mean ± SD) from three independent experiments (each assayed in technical triplicate); the y-axis includes a break to display both low- and high-signal samples.
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    strains atcc 10953  (ATCC)
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    ATCC strains atcc 10953
    (A) Phylogenetic relationship of representative F. nucleatum strains used in this study, grouped by subspecies—subsp. nucleatum (FNN; ATCC 25586, ATCC 23726, CTI-2), subsp. vincentii (FNV; 3_1_27, ATCC 49256, ATCC 51190), subsp. animalis (FNA; 7_1, F0401, ATCC 51191), and subsp. polymorphum (FNP; ATCC 10953, 12230). The phylogenetic tree was constructed based on znpA gene using the maximum-likelihood method implemented in DNAMAN Version 10 (Lynnon Biosoft). Fusobacterium periodonticum ATCC 33693 (FP) was included as an outgroup. (B) Schematic of the chromosomal region between uraA and pepF showing subspecies-specific presence of luxS . luxS is absent from FNN and FNV at this locus, present as an intact gene in FNA (between uraA and pepF ), and disrupted in FNP by insertion of an IS200-family element. The corresponding region from F. periodonticum is shown for comparison. Arrows indicate gene orientation; uraA (gray), pepF (black), luxS (blue), IS200 insertion (magenta), and the adjacent gene ( ddpA , orange) are indicated. (C) AI-2 activity in cell-free culture supernatants was measured using the Vibrio harveyi BB170 bioluminescence reporter assay. Supernatants from FNN, FNV, and FNP strains showed signals at or near background levels, whereas all tested FNA strains and F. periodonticum generated robust reporter induction. E. coli wild type (WT) and its Δ luxS mutant served as positive and negative controls, respectively. Data are presented as relative fluorescence units (RFU; mean ± SD) from three independent experiments (each assayed in technical triplicate); the y-axis includes a break to display both low- and high-signal samples.
    Strains Atcc 10953, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    strain fpo atcc 10953  (ATCC)
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    ATCC strain fpo atcc 10953
    (A) Phylogenetic relationship of representative F. nucleatum strains used in this study, grouped by subspecies—subsp. nucleatum (FNN; ATCC 25586, ATCC 23726, CTI-2), subsp. vincentii (FNV; 3_1_27, ATCC 49256, ATCC 51190), subsp. animalis (FNA; 7_1, F0401, ATCC 51191), and subsp. polymorphum (FNP; ATCC 10953, 12230). The phylogenetic tree was constructed based on znpA gene using the maximum-likelihood method implemented in DNAMAN Version 10 (Lynnon Biosoft). Fusobacterium periodonticum ATCC 33693 (FP) was included as an outgroup. (B) Schematic of the chromosomal region between uraA and pepF showing subspecies-specific presence of luxS . luxS is absent from FNN and FNV at this locus, present as an intact gene in FNA (between uraA and pepF ), and disrupted in FNP by insertion of an IS200-family element. The corresponding region from F. periodonticum is shown for comparison. Arrows indicate gene orientation; uraA (gray), pepF (black), luxS (blue), IS200 insertion (magenta), and the adjacent gene ( ddpA , orange) are indicated. (C) AI-2 activity in cell-free culture supernatants was measured using the Vibrio harveyi BB170 bioluminescence reporter assay. Supernatants from FNN, FNV, and FNP strains showed signals at or near background levels, whereas all tested FNA strains and F. periodonticum generated robust reporter induction. E. coli wild type (WT) and its Δ luxS mutant served as positive and negative controls, respectively. Data are presented as relative fluorescence units (RFU; mean ± SD) from three independent experiments (each assayed in technical triplicate); the y-axis includes a break to display both low- and high-signal samples.
    Strain Fpo Atcc 10953, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    (A) Phylogenetic relationship of representative F. nucleatum strains used in this study, grouped by subspecies—subsp. nucleatum (FNN; ATCC 25586, ATCC 23726, CTI-2), subsp. vincentii (FNV; 3_1_27, ATCC 49256, ATCC 51190), subsp. animalis (FNA; 7_1, F0401, ATCC 51191), and subsp. polymorphum (FNP; ATCC 10953, 12230). The phylogenetic tree was constructed based on znpA gene using the maximum-likelihood method implemented in DNAMAN Version 10 (Lynnon Biosoft). Fusobacterium periodonticum ATCC 33693 (FP) was included as an outgroup. (B) Schematic of the chromosomal region between uraA and pepF showing subspecies-specific presence of luxS . luxS is absent from FNN and FNV at this locus, present as an intact gene in FNA (between uraA and pepF ), and disrupted in FNP by insertion of an IS200-family element. The corresponding region from F. periodonticum is shown for comparison. Arrows indicate gene orientation; uraA (gray), pepF (black), luxS (blue), IS200 insertion (magenta), and the adjacent gene ( ddpA , orange) are indicated. (C) AI-2 activity in cell-free culture supernatants was measured using the Vibrio harveyi BB170 bioluminescence reporter assay. Supernatants from FNN, FNV, and FNP strains showed signals at or near background levels, whereas all tested FNA strains and F. periodonticum generated robust reporter induction. E. coli wild type (WT) and its Δ luxS mutant served as positive and negative controls, respectively. Data are presented as relative fluorescence units (RFU; mean ± SD) from three independent experiments (each assayed in technical triplicate); the y-axis includes a break to display both low- and high-signal samples.

    Journal: bioRxiv

    Article Title: AI-2 Production in Fusobacterium nucleatum Is Subspecies-Specific and Uncoupled from Quorum Sensing

    doi: 10.64898/2026.03.02.709096

    Figure Lengend Snippet: (A) Phylogenetic relationship of representative F. nucleatum strains used in this study, grouped by subspecies—subsp. nucleatum (FNN; ATCC 25586, ATCC 23726, CTI-2), subsp. vincentii (FNV; 3_1_27, ATCC 49256, ATCC 51190), subsp. animalis (FNA; 7_1, F0401, ATCC 51191), and subsp. polymorphum (FNP; ATCC 10953, 12230). The phylogenetic tree was constructed based on znpA gene using the maximum-likelihood method implemented in DNAMAN Version 10 (Lynnon Biosoft). Fusobacterium periodonticum ATCC 33693 (FP) was included as an outgroup. (B) Schematic of the chromosomal region between uraA and pepF showing subspecies-specific presence of luxS . luxS is absent from FNN and FNV at this locus, present as an intact gene in FNA (between uraA and pepF ), and disrupted in FNP by insertion of an IS200-family element. The corresponding region from F. periodonticum is shown for comparison. Arrows indicate gene orientation; uraA (gray), pepF (black), luxS (blue), IS200 insertion (magenta), and the adjacent gene ( ddpA , orange) are indicated. (C) AI-2 activity in cell-free culture supernatants was measured using the Vibrio harveyi BB170 bioluminescence reporter assay. Supernatants from FNN, FNV, and FNP strains showed signals at or near background levels, whereas all tested FNA strains and F. periodonticum generated robust reporter induction. E. coli wild type (WT) and its Δ luxS mutant served as positive and negative controls, respectively. Data are presented as relative fluorescence units (RFU; mean ± SD) from three independent experiments (each assayed in technical triplicate); the y-axis includes a break to display both low- and high-signal samples.

    Article Snippet: In our experiments, the signal levels previously reported for ATCC 10953 were comparable to background readings( ).

    Techniques: Construct, Comparison, Activity Assay, Reporter Assay, Generated, Mutagenesis, Fluorescence