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Image Search Results
Journal: Scientific Reports
Article Title: Metabolite-enabled mutualistic interaction between Shewanella oneidensis and Escherichia coli in a co-culture using an electrode as electron acceptor
doi: 10.1038/srep11222
Figure Lengend Snippet: ( a ) CFU counts and relative proportion (%) of E. coli and S. oneidensis strains in anode media. ( b ) CFU counts and relative proportion (%) of E. coli and S. oneidensis strains on the anode electrode.
Article Snippet:
Techniques:
Journal: Scientific Reports
Article Title: Metabolite-enabled mutualistic interaction between Shewanella oneidensis and Escherichia coli in a co-culture using an electrode as electron acceptor
doi: 10.1038/srep11222
Figure Lengend Snippet: Selected gene expression changes in E. coli induced by S. oneidensis for energy metabolism.
Article Snippet:
Techniques: Gene Expression
Journal: Scientific Reports
Article Title: Metabolite-enabled mutualistic interaction between Shewanella oneidensis and Escherichia coli in a co-culture using an electrode as electron acceptor
doi: 10.1038/srep11222
Figure Lengend Snippet: Glucose is fermented by E. coli to yield metabolites such as formate, which is taken up by S. oneidensis as electron donor. Flavin mediator molecules are secreted to facilitate electron movement to the external charge collecting electrode to derive energy in MFCs. Flavins can also be taken up by E. coli to facilitate its respiration on electrodes as E. coli does not secrete flavins.
Article Snippet:
Techniques:
Journal: Scientific Reports
Article Title: Metabolite-enabled mutualistic interaction between Shewanella oneidensis and Escherichia coli in a co-culture using an electrode as electron acceptor
doi: 10.1038/srep11222
Figure Lengend Snippet: Bacterial strains used in this study.
Article Snippet:
Techniques:
Journal: Scientific Reports
Article Title: Metabolite-enabled mutualistic interaction between Shewanella oneidensis and Escherichia coli in a co-culture using an electrode as electron acceptor
doi: 10.1038/srep11222
Figure Lengend Snippet: ( a ) Photograph of MFC setup. ( b ) Graphic of mutualistic interactions between E. coli and S. oneidensis in MFC setup.
Article Snippet:
Techniques:
Journal: Bioorganic chemistry
Article Title: Dimeric peptoids as antibacterial agents.
doi: 10.1016/j.bioorg.2024.107334
Figure Lengend Snippet: Fig. 11. S. aureus 38 (A, B and C) and E. coli k12 (D, E, F) membrane permeabilization by peptoid 10 k at their 2XMIC determined by flow cytometry using SYTO9 (membrane permeable) and Propidium iodide (membrane impermeable) stains.
Article Snippet: The efficacy of dimer peptoids was examined against Staphylococcus aureus 38 (originally isolated from an ocular infection) and the
Techniques: Membrane, Flow Cytometry
Journal:
Article Title: Detection and Quantification of Methyl tert -Butyl Ether-Degrading Strain PM1 by Real-Time TaqMan PCR
doi: 10.1128/AEM.67.11.5154-5160.2001
Figure Lengend Snippet: Bacterial strains used to test the specificity of the PM1 TaqMan assay
Article Snippet: Genomic DNA was extracted with standard methods ( 2 ) and quantified using a Lambda 10 UV/Vis spectrometer (PE Applied Biosystems). table ft1 table-wrap mode="anchored" t5 TABLE 1 caption a7 Bacterial strain a
Techniques:
Journal:
Article Title: Detection and Quantification of Methyl tert -Butyl Ether-Degrading Strain PM1 by Real-Time TaqMan PCR
doi: 10.1128/AEM.67.11.5154-5160.2001
Figure Lengend Snippet: TaqMan PM1 detection in spiked sediment or groundwater microcosms
Article Snippet: Genomic DNA was extracted with standard methods ( 2 ) and quantified using a Lambda 10 UV/Vis spectrometer (PE Applied Biosystems). table ft1 table-wrap mode="anchored" t5 TABLE 1 caption a7 Bacterial strain a
Techniques: Standard Deviation, Control
Journal:
Article Title: Detection and Quantification of Methyl tert -Butyl Ether-Degrading Strain PM1 by Real-Time TaqMan PCR
doi: 10.1128/AEM.67.11.5154-5160.2001
Figure Lengend Snippet: PM1 detection in groundwater DNA samples collected from an MTBE-contaminated plume at Port Hueneme, California
Article Snippet: Genomic DNA was extracted with standard methods ( 2 ) and quantified using a Lambda 10 UV/Vis spectrometer (PE Applied Biosystems). table ft1 table-wrap mode="anchored" t5 TABLE 1 caption a7 Bacterial strain a
Techniques: Standard Deviation
Journal:
Article Title: Detection and Quantification of Methyl tert -Butyl Ether-Degrading Strain PM1 by Real-Time TaqMan PCR
doi: 10.1128/AEM.67.11.5154-5160.2001
Figure Lengend Snippet: PM1 standard curve. Real-time analysis of serial 10-fold dilutions of PM1 DNA (A) or PM1 cells (B). The CT values are plotted against the corresponding PM1 cell numbers in the PCR. Template DNA was extracted from 1.8 × 107 CFU of PM1 corresponding to 3 × 106 CFU/PCR and was diluted 10-fold (A). For the second curve (B) DNA was extracted from serial dilutions of PM1 cells mixed with E. coli cells until 108 total CFU/ml was reached.
Article Snippet: Genomic DNA was extracted with standard methods ( 2 ) and quantified using a Lambda 10 UV/Vis spectrometer (PE Applied Biosystems). table ft1 table-wrap mode="anchored" t5 TABLE 1 caption a7 Bacterial strain a
Techniques:
Journal:
Article Title: Detection and Quantification of Methyl tert -Butyl Ether-Degrading Strain PM1 by Real-Time TaqMan PCR
doi: 10.1128/AEM.67.11.5154-5160.2001
Figure Lengend Snippet: TaqMan-estimated PM1 cell density and aerobic MTBE biodegradation in mineral media, inoculated groundwater, and groundwater collected from the bioaugmentation study at Port Hueneme. Biodegradation of MTBE in microcosms of mineral media (A) or groundwater from Port Hueneme (well CBC61CS located upstream from the field plots [B] or well B32D from the field test plot [C]), with or without addition of 106 CFU of PM1 per ml. Ave, average.
Article Snippet: Genomic DNA was extracted with standard methods ( 2 ) and quantified using a Lambda 10 UV/Vis spectrometer (PE Applied Biosystems). table ft1 table-wrap mode="anchored" t5 TABLE 1 caption a7 Bacterial strain a
Techniques: