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data ribosome em reconstruction  (ATCC)


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    ATCC data ribosome em reconstruction
    Data Ribosome Em Reconstruction, supplied by ATCC, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/data ribosome em reconstruction/product/ATCC
    Average 90 stars, based on 1 article reviews
    data ribosome em reconstruction - by Bioz Stars, 2025-07
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    Actinobacterial strains for biocontrol testing.

    Journal: Frontiers in Plant Science

    Article Title: Presence of the Weakly Pathogenic Fusarium poae in the Fusarium Head Blight Disease Complex Hampers Biocontrol and Chemical Control of the Virulent Fusarium graminearum Pathogen

    doi: 10.3389/fpls.2021.641890

    Figure Lengend Snippet: Actinobacterial strains for biocontrol testing.

    Article Snippet: 20 , S. rimosus subsp. rimosus LMG 19352 , 1984, National Collection of Industrial, Food and Marine Bacteria, Ltd. (NCIMB) < - 1951, M. Lumb.

    Techniques:

    Biocontrol capacity of Streptomyces and Rhodococcus strains against F. graminearum as the main causal agent of FHB. Strains were co-applied with GFP tagged F. graminearum PH-1 in a detached leaf assay. (A) % Fv/Fm (percentage increase/decrease in efficiency of photosystem II) compared to mock-inoculated control plants; values represent symptom development based on the efficiency of photosystem II. Strains with significant positive biocontrol capacities are indicated in green. (B) Assessment of the relative active fungal biomass based on the GFP signal of the mock infected control plants. (C) Picture of R-43120 and LMG 19352 treatment based on the efficiency of photosystem II. (D) Picture of R-43120 and LMG 19352 treatment based on the GFP signal. Significant differences (positive or negative, based on the P -values) are indicated by the colors of the boxes. Boxplots indicate the median (horizontal lines), 25th and 75th percentile range (boxes) and up to 1.5 × IQR (Interquartile Range) (whiskers).

    Journal: Frontiers in Plant Science

    Article Title: Presence of the Weakly Pathogenic Fusarium poae in the Fusarium Head Blight Disease Complex Hampers Biocontrol and Chemical Control of the Virulent Fusarium graminearum Pathogen

    doi: 10.3389/fpls.2021.641890

    Figure Lengend Snippet: Biocontrol capacity of Streptomyces and Rhodococcus strains against F. graminearum as the main causal agent of FHB. Strains were co-applied with GFP tagged F. graminearum PH-1 in a detached leaf assay. (A) % Fv/Fm (percentage increase/decrease in efficiency of photosystem II) compared to mock-inoculated control plants; values represent symptom development based on the efficiency of photosystem II. Strains with significant positive biocontrol capacities are indicated in green. (B) Assessment of the relative active fungal biomass based on the GFP signal of the mock infected control plants. (C) Picture of R-43120 and LMG 19352 treatment based on the efficiency of photosystem II. (D) Picture of R-43120 and LMG 19352 treatment based on the GFP signal. Significant differences (positive or negative, based on the P -values) are indicated by the colors of the boxes. Boxplots indicate the median (horizontal lines), 25th and 75th percentile range (boxes) and up to 1.5 × IQR (Interquartile Range) (whiskers).

    Article Snippet: 20 , S. rimosus subsp. rimosus LMG 19352 , 1984, National Collection of Industrial, Food and Marine Bacteria, Ltd. (NCIMB) < - 1951, M. Lumb.

    Techniques: Infection

    Effect of Streptomyces rimosus strain LMG 19352 (b1) and Rhodococcus sp . R-43120 (b2) on the growth of F. graminearum PH-1 and F. poae 2516 on TSA plates. Treatments: p + w (Inoculation with F. poae and water); p + b1 (Inoculation with F. poae and LMG 19352); p + b2 (Inoculation with F. poae and R-43120); g + w (Inoculation with F. graminearum and water); g + b1 (Inoculation with F. graminearum and LMG 19352); g + b2 (Inoculation with F. graminearum and R-43120). (A) Images taken from day 1 till day 5. (B) F. poae growth from day 1 till day 5, n = 5 (five biological reps per time point). (C) F. graminearum growth from day 1 till day 5, n = 5 (five biological reps per time point).

    Journal: Frontiers in Plant Science

    Article Title: Presence of the Weakly Pathogenic Fusarium poae in the Fusarium Head Blight Disease Complex Hampers Biocontrol and Chemical Control of the Virulent Fusarium graminearum Pathogen

    doi: 10.3389/fpls.2021.641890

    Figure Lengend Snippet: Effect of Streptomyces rimosus strain LMG 19352 (b1) and Rhodococcus sp . R-43120 (b2) on the growth of F. graminearum PH-1 and F. poae 2516 on TSA plates. Treatments: p + w (Inoculation with F. poae and water); p + b1 (Inoculation with F. poae and LMG 19352); p + b2 (Inoculation with F. poae and R-43120); g + w (Inoculation with F. graminearum and water); g + b1 (Inoculation with F. graminearum and LMG 19352); g + b2 (Inoculation with F. graminearum and R-43120). (A) Images taken from day 1 till day 5. (B) F. poae growth from day 1 till day 5, n = 5 (five biological reps per time point). (C) F. graminearum growth from day 1 till day 5, n = 5 (five biological reps per time point).

    Article Snippet: 20 , S. rimosus subsp. rimosus LMG 19352 , 1984, National Collection of Industrial, Food and Marine Bacteria, Ltd. (NCIMB) < - 1951, M. Lumb.

    Techniques:

    (A) Visual symptoms on wheat ears after infection by F. graminearum PH-1 (g), F. poae 2516 (p) or a combination of both pathogens (pg) and treated with water (+w), with S. rimosus LMG 19352 (+b1), with Rhodococcus sp . R-43120 (+b2) or with the fungicides prothioconazole + spiroxamine (f) at 7 dai. (B) Results of quantitation of the Fv/Fm (efficiency of photosystem II) signal at 4 and 7 dai, n = 6 (six biological reps per treatment and per pathogen combination). (C) Results of quantitation of the cGFP (corrected GFP value) signal (background signal) at 4 and 7 dai, n = 6 (six biological reps per treatment and per pathogen combination). Boxplots indicate the median (horizontal lines), 25th and 75th percentile range (boxes) and up to 1.5 × IQR (Interquartile Range) (whiskers). Different letters indicate significant differences ( P < 0.05) between treatments for each time point within the same pathogen combination. The experiment was repeated twice in time.

    Journal: Frontiers in Plant Science

    Article Title: Presence of the Weakly Pathogenic Fusarium poae in the Fusarium Head Blight Disease Complex Hampers Biocontrol and Chemical Control of the Virulent Fusarium graminearum Pathogen

    doi: 10.3389/fpls.2021.641890

    Figure Lengend Snippet: (A) Visual symptoms on wheat ears after infection by F. graminearum PH-1 (g), F. poae 2516 (p) or a combination of both pathogens (pg) and treated with water (+w), with S. rimosus LMG 19352 (+b1), with Rhodococcus sp . R-43120 (+b2) or with the fungicides prothioconazole + spiroxamine (f) at 7 dai. (B) Results of quantitation of the Fv/Fm (efficiency of photosystem II) signal at 4 and 7 dai, n = 6 (six biological reps per treatment and per pathogen combination). (C) Results of quantitation of the cGFP (corrected GFP value) signal (background signal) at 4 and 7 dai, n = 6 (six biological reps per treatment and per pathogen combination). Boxplots indicate the median (horizontal lines), 25th and 75th percentile range (boxes) and up to 1.5 × IQR (Interquartile Range) (whiskers). Different letters indicate significant differences ( P < 0.05) between treatments for each time point within the same pathogen combination. The experiment was repeated twice in time.

    Article Snippet: 20 , S. rimosus subsp. rimosus LMG 19352 , 1984, National Collection of Industrial, Food and Marine Bacteria, Ltd. (NCIMB) < - 1951, M. Lumb.

    Techniques: Infection, Quantitation Assay

    (A) DON, (B) 3ADON, and (C) 15ADON concentrations in wheat ears after infection by F. graminearum PH-1 (g), F. poae 2516 (p) or a combination of both pathogens (pg) and treated with water (+w), with S. rimosus LMG 19352 (+b1), with Rhodococcus sp . R-43120 (+b2) or with the fungicides prothioconazole + spiroxamine (f). Boxplots indicate the median (horizontal lines), 25th and 75th percentile range (boxes) and up to 1.5 × IQR (Interquartile Range) (whiskers). Different letters indicate significant differences ( P < 0.05) between treatments for each time point within the same pathogen combination. The experiment was repeated twice in time.

    Journal: Frontiers in Plant Science

    Article Title: Presence of the Weakly Pathogenic Fusarium poae in the Fusarium Head Blight Disease Complex Hampers Biocontrol and Chemical Control of the Virulent Fusarium graminearum Pathogen

    doi: 10.3389/fpls.2021.641890

    Figure Lengend Snippet: (A) DON, (B) 3ADON, and (C) 15ADON concentrations in wheat ears after infection by F. graminearum PH-1 (g), F. poae 2516 (p) or a combination of both pathogens (pg) and treated with water (+w), with S. rimosus LMG 19352 (+b1), with Rhodococcus sp . R-43120 (+b2) or with the fungicides prothioconazole + spiroxamine (f). Boxplots indicate the median (horizontal lines), 25th and 75th percentile range (boxes) and up to 1.5 × IQR (Interquartile Range) (whiskers). Different letters indicate significant differences ( P < 0.05) between treatments for each time point within the same pathogen combination. The experiment was repeated twice in time.

    Article Snippet: 20 , S. rimosus subsp. rimosus LMG 19352 , 1984, National Collection of Industrial, Food and Marine Bacteria, Ltd. (NCIMB) < - 1951, M. Lumb.

    Techniques: Infection

    (A) DON-3G and (B) percentage of DON being glycosylated in wheat ears after infection by F. graminearum PH-1 (g), F. poae 2516 (p) or a combination of both pathogens (pg) and treated with water (+ w), with S. rimosus LMG 19352 (+b1), with Rhodococcus sp . R-43120 (+b2) or with the fungicides prothioconazole + spiroxamine (f). Boxplots indicate the median (horizontal lines), 25th and 75th percentile range (boxes) and up to 1.5 × IQR (Interquartile Range) (whiskers). Different letters indicate significant differences ( P < 0.05) between treatments for each time point within the same pathogen combination. The experiment was repeated twice in time.

    Journal: Frontiers in Plant Science

    Article Title: Presence of the Weakly Pathogenic Fusarium poae in the Fusarium Head Blight Disease Complex Hampers Biocontrol and Chemical Control of the Virulent Fusarium graminearum Pathogen

    doi: 10.3389/fpls.2021.641890

    Figure Lengend Snippet: (A) DON-3G and (B) percentage of DON being glycosylated in wheat ears after infection by F. graminearum PH-1 (g), F. poae 2516 (p) or a combination of both pathogens (pg) and treated with water (+ w), with S. rimosus LMG 19352 (+b1), with Rhodococcus sp . R-43120 (+b2) or with the fungicides prothioconazole + spiroxamine (f). Boxplots indicate the median (horizontal lines), 25th and 75th percentile range (boxes) and up to 1.5 × IQR (Interquartile Range) (whiskers). Different letters indicate significant differences ( P < 0.05) between treatments for each time point within the same pathogen combination. The experiment was repeated twice in time.

    Article Snippet: 20 , S. rimosus subsp. rimosus LMG 19352 , 1984, National Collection of Industrial, Food and Marine Bacteria, Ltd. (NCIMB) < - 1951, M. Lumb.

    Techniques: Infection

    Expression profile of isochorismate synthase (ICS) at 4 and 7 dai by F. graminearum PH-1 (g), F. poae 2516 (p) or a combination of both pathogens (pg) and treated with water (+w), with S. rimosus LMG 19352 (+b1), with Rhodococcus sp . R-43120 (+b2) or with the fungicides prothioconazole + spiroxamine (f). Bars represent log 2 -transformed means of four biological replicates; error bars indicate ± 1 standard error. Different letters indicate significant differences ( P < 0.05) between treatments for each time point within the same pathogen combination. Fold change was calculated by dividing the CNRQ values (calibrated normalized relative quantities) of the treated ears by values of the control ears. Normalization of defense genes was performed by using the cell division control protein gene (Ta54227) in wheat as reference. Missing bars for the F. graminearum (g), the F. poae (p) and the combined infection (pg) point to an ICS expression level (and Ct value) below the limit of detection. The experiment was repeated twice in time.

    Journal: Frontiers in Plant Science

    Article Title: Presence of the Weakly Pathogenic Fusarium poae in the Fusarium Head Blight Disease Complex Hampers Biocontrol and Chemical Control of the Virulent Fusarium graminearum Pathogen

    doi: 10.3389/fpls.2021.641890

    Figure Lengend Snippet: Expression profile of isochorismate synthase (ICS) at 4 and 7 dai by F. graminearum PH-1 (g), F. poae 2516 (p) or a combination of both pathogens (pg) and treated with water (+w), with S. rimosus LMG 19352 (+b1), with Rhodococcus sp . R-43120 (+b2) or with the fungicides prothioconazole + spiroxamine (f). Bars represent log 2 -transformed means of four biological replicates; error bars indicate ± 1 standard error. Different letters indicate significant differences ( P < 0.05) between treatments for each time point within the same pathogen combination. Fold change was calculated by dividing the CNRQ values (calibrated normalized relative quantities) of the treated ears by values of the control ears. Normalization of defense genes was performed by using the cell division control protein gene (Ta54227) in wheat as reference. Missing bars for the F. graminearum (g), the F. poae (p) and the combined infection (pg) point to an ICS expression level (and Ct value) below the limit of detection. The experiment was repeated twice in time.

    Article Snippet: 20 , S. rimosus subsp. rimosus LMG 19352 , 1984, National Collection of Industrial, Food and Marine Bacteria, Ltd. (NCIMB) < - 1951, M. Lumb.

    Techniques: Expressing, Transformation Assay, Infection

    Expression profile of Lipoxygenase 1 (A) and Lipoxygenase 2 (B) (LOX1 and LOX2) at 4 and 7 dai by F. graminearum PH-1 (g), F. poae 2516 (p) or a combination of both pathogens (pg) and treated with water (+w), with S. rimosus LMG 19352 (+b1), with Rhodococcus sp. R-43120 (+b2) or with the fungicides prothioconazole + spiroxamine (f). Bars represent log 2 -transformed means of four biological replicates; error bars indicate ± 1 standard error. Different letters indicate significant differences ( P < 0.05) between treatments for each time point within the same pathogen combination. Fold change was calculated by dividing the CNRQ values (calibrated normalized relative quantities) of the treated ears to the control ears. Normalization of defense genes was performed by using the cell division control protein gene (Ta54227) in wheat as reference. The experiment was repeated twice in time.

    Journal: Frontiers in Plant Science

    Article Title: Presence of the Weakly Pathogenic Fusarium poae in the Fusarium Head Blight Disease Complex Hampers Biocontrol and Chemical Control of the Virulent Fusarium graminearum Pathogen

    doi: 10.3389/fpls.2021.641890

    Figure Lengend Snippet: Expression profile of Lipoxygenase 1 (A) and Lipoxygenase 2 (B) (LOX1 and LOX2) at 4 and 7 dai by F. graminearum PH-1 (g), F. poae 2516 (p) or a combination of both pathogens (pg) and treated with water (+w), with S. rimosus LMG 19352 (+b1), with Rhodococcus sp. R-43120 (+b2) or with the fungicides prothioconazole + spiroxamine (f). Bars represent log 2 -transformed means of four biological replicates; error bars indicate ± 1 standard error. Different letters indicate significant differences ( P < 0.05) between treatments for each time point within the same pathogen combination. Fold change was calculated by dividing the CNRQ values (calibrated normalized relative quantities) of the treated ears to the control ears. Normalization of defense genes was performed by using the cell division control protein gene (Ta54227) in wheat as reference. The experiment was repeated twice in time.

    Article Snippet: 20 , S. rimosus subsp. rimosus LMG 19352 , 1984, National Collection of Industrial, Food and Marine Bacteria, Ltd. (NCIMB) < - 1951, M. Lumb.

    Techniques: Expressing, Transformation Assay