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comamonas testosteroni atcc 11996  (ATCC)


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    ATCC comamonas testosteroni atcc 11996
    Comamonas Testosteroni Atcc 11996, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 168 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 95 stars, based on 168 article reviews
    comamonas testosteroni atcc 11996 - by Bioz Stars, 2026-09
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    other:

    Article Title: From single-cell sorting to metabolic pathways of bisphenol A: Cultivation, genome, and biotransformation products.
    Article Snippet: • Two-step cultivation approach successfully cultured bacterial cells after

    Incubation:

    Article Title: Direct Production of Bio-Recalcitrant Carboxyl-Rich Alicyclic Molecules Evidenced in a Bacterium-Induced Steroid Degradation Experiment.
    Article Snippet: .. Here, a steroid-degrading bacterium, Comamonas testosteroni ATCC 11996, was incubated in a liquid medium supplemented with testosterone (a typical steroid) as the sole carbon source for 90 days. ..

    Article Title: Direct Production of Bio-Recalcitrant Carboxyl-Rich Alicyclic Molecules Evidenced in a Bacterium-Induced Steroid Degradation Experiment
    Article Snippet: .. After the 90-day incubation with Comamonas testosteroni ATCC 11996, a total of 1,775 molecular formulas (MFs) were assigned to the TIM using ultrahigh-resolution FT-ICR MS. ..

    Sequencing:

    Article Title: Enhancing the specific activity of 3α-hydroxysteroid dehydrogenase through cross-regional combinatorial mutagenesis.
    Article Snippet: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record.. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article.. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

    Article Title: Treatment of 2-naphthalene sulfonate by free and immobilized cells of indigenous isolate Comamonas sp. C2 and toxicity evaluation of biotransformed sample
    Article Snippet: An indigenous bacterial strain Comamonas sp. C2, capable of utilizing 2-naphthalene sulfonate (2-NS) as a sole source of carbon, was isolated after enrichment of microbial diversity present in sample collected from sewage treatment plant (STP) receiving untreated or partially treated effluent from textile industries.. The isolate was able to degrade 100 mg/L of 2-NS, when grown in sulfur free minimal salt medium (SFMSM), after an incubation of 8 h. The release of sulfite/sulfate ions during biotransformation, assay of protocatechuate 4, 5-dioxygenase activity and formation of metabolic intermediates like salicylaldehyde, protocatechuate and 2-hydroxy-4-carboxy-muconatesemialdehyde in the biologically treated sample indicated to the meta-cleavage of aromatic ring of 2-NS.. An immobilized-cell plug flow bioreactor (PFR) was developed and evaluated for its efficiency to treat simulated feed supplemented with 100 mg/L of 2-NS.

    DNA Hybridization:

    Article Title: Genomic and taxonomic characterization of the Comamonas sp. nov., a bacterium isolated from Brazilian Cerrado soil.
    Article Snippet: A novel strain identified as Comamonas sp. was isolated from the soil of the Brazilian savanna-like Cerrado biome, a global hotspot for biodiversity.. Phylogenetic analysis based on 16 S rRNA gene sequences showed that this strain is classified as Betaproteobacteria from the family Comamonadaceae.. The digital DNA-DNA hybridization (dDDH) and Average Nucleotide Identity (ANI) results, of respectively 48.6% and < 93%, indicated that Comamonas sp. consists in a new species with Comamonas testosteroni as its closest strain.

    In Vitro:

    Article Title: Genomic and taxonomic characterization of the Comamonas sp. nov., a bacterium isolated from Brazilian Cerrado soil.
    Article Snippet: A novel strain identified as Comamonas sp. was isolated from the soil of the Brazilian savanna-like Cerrado biome, a global hotspot for biodiversity.. Phylogenetic analysis based on 16 S rRNA gene sequences showed that this strain is classified as Betaproteobacteria from the family Comamonadaceae.. The digital DNA-DNA hybridization (dDDH) and Average Nucleotide Identity (ANI) results, of respectively 48.6% and < 93%, indicated that Comamonas sp. consists in a new species with Comamonas testosteroni as its closest strain.

    Comparison:

    Article Title: Treatment of 2-naphthalene sulfonate by free and immobilized cells of indigenous isolate Comamonas sp. C2 and toxicity evaluation of biotransformed sample
    Article Snippet: An indigenous bacterial strain Comamonas sp. C2, capable of utilizing 2-naphthalene sulfonate (2-NS) as a sole source of carbon, was isolated after enrichment of microbial diversity present in sample collected from sewage treatment plant (STP) receiving untreated or partially treated effluent from textile industries.. The isolate was able to degrade 100 mg/L of 2-NS, when grown in sulfur free minimal salt medium (SFMSM), after an incubation of 8 h. The release of sulfite/sulfate ions during biotransformation, assay of protocatechuate 4, 5-dioxygenase activity and formation of metabolic intermediates like salicylaldehyde, protocatechuate and 2-hydroxy-4-carboxy-muconatesemialdehyde in the biologically treated sample indicated to the meta-cleavage of aromatic ring of 2-NS.. An immobilized-cell plug flow bioreactor (PFR) was developed and evaluated for its efficiency to treat simulated feed supplemented with 100 mg/L of 2-NS.



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    ATCC comamonas testosteroni
    (A) Growth curves of Bacillus sp. NRRL B-14911 (dark green), <t>Comamonas</t> <t>testosteroni</t> (light green), Marinobacter sp. NK-1 (light brown), and Microbulbifer sp. SOL66 (dark brown) cultured in Marine Broth at 30 °C. (B) Degradation of PHB by the marine bacteria species was determined by growing bacterial colonies on Marine Broth-agar plates containing PHB powder and measuring the radii of the clear zones of depolymerized PHB formed around the colonies after 7 days (n=8). **** P < 0.0001 by one-way ANOVA statistical analysis To measure the ability of these strains to degrade PHB, cultures of each of the strains were grown on Marine Broth-agar plate containing powdered PHB. A clear zone assay was employed to measure the PHB-depolymerizing activity of these bacterial colonies. Depolymerization of the opaque PHB creates a clear zone within the PHB plate, the radius of which can expand over time at different rates correlating to depolymerization rates . Among the marine bacteria tested, only Marinobacter sp. NK-1 and Bacillus sp. NRRL B-14911 created measurable clear zones of PHB degradation after 7 days, and the clear zones created by the Bacillus sp. NRLL B-14911 colonies were significantly larger than observed for the other strains . Due to its higher rate of PHB degradation on ocean-mimicking media, Bacillus sp. NRLL B-14911 was used throughout the rest of our work.
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    (A) Growth curves of Bacillus sp. NRRL B-14911 (dark green), Comamonas testosteroni (light green), Marinobacter sp. NK-1 (light brown), and Microbulbifer sp. SOL66 (dark brown) cultured in Marine Broth at 30 °C. (B) Degradation of PHB by the marine bacteria species was determined by growing bacterial colonies on Marine Broth-agar plates containing PHB powder and measuring the radii of the clear zones of depolymerized PHB formed around the colonies after 7 days (n=8). **** P < 0.0001 by one-way ANOVA statistical analysis To measure the ability of these strains to degrade PHB, cultures of each of the strains were grown on Marine Broth-agar plate containing powdered PHB. A clear zone assay was employed to measure the PHB-depolymerizing activity of these bacterial colonies. Depolymerization of the opaque PHB creates a clear zone within the PHB plate, the radius of which can expand over time at different rates correlating to depolymerization rates . Among the marine bacteria tested, only Marinobacter sp. NK-1 and Bacillus sp. NRRL B-14911 created measurable clear zones of PHB degradation after 7 days, and the clear zones created by the Bacillus sp. NRLL B-14911 colonies were significantly larger than observed for the other strains . Due to its higher rate of PHB degradation on ocean-mimicking media, Bacillus sp. NRLL B-14911 was used throughout the rest of our work.

    Journal: bioRxiv

    Article Title: 3D-bioprinted marine bacteria for the degradation of bioplastics

    doi: 10.1101/2025.02.05.636490

    Figure Lengend Snippet: (A) Growth curves of Bacillus sp. NRRL B-14911 (dark green), Comamonas testosteroni (light green), Marinobacter sp. NK-1 (light brown), and Microbulbifer sp. SOL66 (dark brown) cultured in Marine Broth at 30 °C. (B) Degradation of PHB by the marine bacteria species was determined by growing bacterial colonies on Marine Broth-agar plates containing PHB powder and measuring the radii of the clear zones of depolymerized PHB formed around the colonies after 7 days (n=8). **** P < 0.0001 by one-way ANOVA statistical analysis To measure the ability of these strains to degrade PHB, cultures of each of the strains were grown on Marine Broth-agar plate containing powdered PHB. A clear zone assay was employed to measure the PHB-depolymerizing activity of these bacterial colonies. Depolymerization of the opaque PHB creates a clear zone within the PHB plate, the radius of which can expand over time at different rates correlating to depolymerization rates . Among the marine bacteria tested, only Marinobacter sp. NK-1 and Bacillus sp. NRRL B-14911 created measurable clear zones of PHB degradation after 7 days, and the clear zones created by the Bacillus sp. NRLL B-14911 colonies were significantly larger than observed for the other strains . Due to its higher rate of PHB degradation on ocean-mimicking media, Bacillus sp. NRLL B-14911 was used throughout the rest of our work.

    Article Snippet: The bacteria strains used in this study are Bacillus sp. NRRL B-14911 [ – ] (Agricultural Research Service Culture Collection, United States Department of Agriculture), Comamonas testosteroni [ ] (ATCC 11996), Marinobacter sp. NK-1 [ ] (ATCC 700491), and Microbulbifer sp. SOL66 [ ] (ATCC 70072).

    Techniques: Cell Culture, Bacteria, Activity Assay