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mg1655 atcc 700926  (ATCC)


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    Structured Review

    ATCC mg1655 atcc 700926
    Strains and plasmids used in this study.
    Mg1655 Atcc 700926, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mg1655 atcc 700926/product/ATCC
    Average 99 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    mg1655 atcc 700926 - by Bioz Stars, 2024-10
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    Images

    1) Product Images from "Transcriptomic Analysis of Carboxylic Acid Challenge in Escherichia coli : Beyond Membrane Damage"

    Article Title: Transcriptomic Analysis of Carboxylic Acid Challenge in Escherichia coli : Beyond Membrane Damage

    Journal: PLoS ONE

    doi: 10.1371/journal.pone.0089580

    Strains and plasmids used in this study.
    Figure Legend Snippet: Strains and plasmids used in this study.

    Techniques Used:

    MG1655 was challenged with sufficient octanoic acid to inhibit growth by 23% (10 mM) in MOPS minimal media at pH 7.0, 37°C, 150 rpm. This diagram shows central metabolism and highlights the regulatory effect of regulators with significantly perturbed activity during C8 challenge, as identified by network component analysis. Dashed lines indicate regulatory connections that were proposed in our previous analysis . Mechanisms for changes in transcription factor activity are discussed in the text.
    Figure Legend Snippet: MG1655 was challenged with sufficient octanoic acid to inhibit growth by 23% (10 mM) in MOPS minimal media at pH 7.0, 37°C, 150 rpm. This diagram shows central metabolism and highlights the regulatory effect of regulators with significantly perturbed activity during C8 challenge, as identified by network component analysis. Dashed lines indicate regulatory connections that were proposed in our previous analysis . Mechanisms for changes in transcription factor activity are discussed in the text.

    Techniques Used: Activity Assay

    E. coli MG1655 pJTD1 was grown to midlog in minimal media at pH(HCl). Values are the average of 4 biological replicates, with error bars indicating the standard deviation.
    Figure Legend Snippet: E. coli MG1655 pJTD1 was grown to midlog in minimal media at pH(HCl). Values are the average of 4 biological replicates, with error bars indicating the standard deviation.

    Techniques Used: Standard Deviation

    Measurements of the intracellular pH of E. coli MG1655 pJTD1 during C8 challenge while grown in the presence of supplemental arginine and glutamate. The cells were incubated for 3°C in MOPS media to allow utilization of the amino acid-dependent acid resistance systems. All concentrations are 10 mM.
    Figure Legend Snippet: Measurements of the intracellular pH of E. coli MG1655 pJTD1 during C8 challenge while grown in the presence of supplemental arginine and glutamate. The cells were incubated for 3°C in MOPS media to allow utilization of the amino acid-dependent acid resistance systems. All concentrations are 10 mM.

    Techniques Used: Incubation

    GABA measurements of MG1655 during log phase growth in MOPS with 2% dextrose at 37°C, 150 rpm. All concentrations are 10 mM. GABA: γ-amino butyric acid.
    Figure Legend Snippet: GABA measurements of MG1655 during log phase growth in MOPS with 2% dextrose at 37°C, 150 rpm. All concentrations are 10 mM. GABA: γ-amino butyric acid.

    Techniques Used:

    a: Membrane lipid profile of MG1655 and strains with altered cfa expression. Strains were incubated with 0–30 mM C8, pH = 7.0. Inset: specific growth rate in the log phase of E. coli with varying cfa expression. C16:0- palmitic acid, C16:1- palmitoleic acid, C17cyc- cyclopropane C17:0, C18:1- vaccenic acid, C18:0- stearic acid, C19cyc- cyclopropane C19:0. The complete lipid profiles are shown in of the Supporting Information. Membrane properties are calculated from a to obtain: b: saturated:unsaturated lipid ratio and c: average lipid length.
    Figure Legend Snippet: a: Membrane lipid profile of MG1655 and strains with altered cfa expression. Strains were incubated with 0–30 mM C8, pH = 7.0. Inset: specific growth rate in the log phase of E. coli with varying cfa expression. C16:0- palmitic acid, C16:1- palmitoleic acid, C17cyc- cyclopropane C17:0, C18:1- vaccenic acid, C18:0- stearic acid, C19cyc- cyclopropane C19:0. The complete lipid profiles are shown in of the Supporting Information. Membrane properties are calculated from a to obtain: b: saturated:unsaturated lipid ratio and c: average lipid length.

    Techniques Used: Expressing, Incubation



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    Strains and plasmids used in this study.

    Journal: PLoS ONE

    Article Title: Transcriptomic Analysis of Carboxylic Acid Challenge in Escherichia coli : Beyond Membrane Damage

    doi: 10.1371/journal.pone.0089580

    Figure Lengend Snippet: Strains and plasmids used in this study.

    Article Snippet: MG1655 ATCC#700926 , F- lambda- ilvG- rfb-50 rph-1 , Wildtype.

    Techniques:

    MG1655 was challenged with sufficient octanoic acid to inhibit growth by 23% (10 mM) in MOPS minimal media at pH 7.0, 37°C, 150 rpm. This diagram shows central metabolism and highlights the regulatory effect of regulators with significantly perturbed activity during C8 challenge, as identified by network component analysis. Dashed lines indicate regulatory connections that were proposed in our previous analysis . Mechanisms for changes in transcription factor activity are discussed in the text.

    Journal: PLoS ONE

    Article Title: Transcriptomic Analysis of Carboxylic Acid Challenge in Escherichia coli : Beyond Membrane Damage

    doi: 10.1371/journal.pone.0089580

    Figure Lengend Snippet: MG1655 was challenged with sufficient octanoic acid to inhibit growth by 23% (10 mM) in MOPS minimal media at pH 7.0, 37°C, 150 rpm. This diagram shows central metabolism and highlights the regulatory effect of regulators with significantly perturbed activity during C8 challenge, as identified by network component analysis. Dashed lines indicate regulatory connections that were proposed in our previous analysis . Mechanisms for changes in transcription factor activity are discussed in the text.

    Article Snippet: MG1655 ATCC#700926 , F- lambda- ilvG- rfb-50 rph-1 , Wildtype.

    Techniques: Activity Assay

    E. coli MG1655 pJTD1 was grown to midlog in minimal media at pH(HCl). Values are the average of 4 biological replicates, with error bars indicating the standard deviation.

    Journal: PLoS ONE

    Article Title: Transcriptomic Analysis of Carboxylic Acid Challenge in Escherichia coli : Beyond Membrane Damage

    doi: 10.1371/journal.pone.0089580

    Figure Lengend Snippet: E. coli MG1655 pJTD1 was grown to midlog in minimal media at pH(HCl). Values are the average of 4 biological replicates, with error bars indicating the standard deviation.

    Article Snippet: MG1655 ATCC#700926 , F- lambda- ilvG- rfb-50 rph-1 , Wildtype.

    Techniques: Standard Deviation

    Measurements of the intracellular pH of E. coli MG1655 pJTD1 during C8 challenge while grown in the presence of supplemental arginine and glutamate. The cells were incubated for 3°C in MOPS media to allow utilization of the amino acid-dependent acid resistance systems. All concentrations are 10 mM.

    Journal: PLoS ONE

    Article Title: Transcriptomic Analysis of Carboxylic Acid Challenge in Escherichia coli : Beyond Membrane Damage

    doi: 10.1371/journal.pone.0089580

    Figure Lengend Snippet: Measurements of the intracellular pH of E. coli MG1655 pJTD1 during C8 challenge while grown in the presence of supplemental arginine and glutamate. The cells were incubated for 3°C in MOPS media to allow utilization of the amino acid-dependent acid resistance systems. All concentrations are 10 mM.

    Article Snippet: MG1655 ATCC#700926 , F- lambda- ilvG- rfb-50 rph-1 , Wildtype.

    Techniques: Incubation

    GABA measurements of MG1655 during log phase growth in MOPS with 2% dextrose at 37°C, 150 rpm. All concentrations are 10 mM. GABA: γ-amino butyric acid.

    Journal: PLoS ONE

    Article Title: Transcriptomic Analysis of Carboxylic Acid Challenge in Escherichia coli : Beyond Membrane Damage

    doi: 10.1371/journal.pone.0089580

    Figure Lengend Snippet: GABA measurements of MG1655 during log phase growth in MOPS with 2% dextrose at 37°C, 150 rpm. All concentrations are 10 mM. GABA: γ-amino butyric acid.

    Article Snippet: MG1655 ATCC#700926 , F- lambda- ilvG- rfb-50 rph-1 , Wildtype.

    Techniques:

    a: Membrane lipid profile of MG1655 and strains with altered cfa expression. Strains were incubated with 0–30 mM C8, pH = 7.0. Inset: specific growth rate in the log phase of E. coli with varying cfa expression. C16:0- palmitic acid, C16:1- palmitoleic acid, C17cyc- cyclopropane C17:0, C18:1- vaccenic acid, C18:0- stearic acid, C19cyc- cyclopropane C19:0. The complete lipid profiles are shown in of the Supporting Information. Membrane properties are calculated from a to obtain: b: saturated:unsaturated lipid ratio and c: average lipid length.

    Journal: PLoS ONE

    Article Title: Transcriptomic Analysis of Carboxylic Acid Challenge in Escherichia coli : Beyond Membrane Damage

    doi: 10.1371/journal.pone.0089580

    Figure Lengend Snippet: a: Membrane lipid profile of MG1655 and strains with altered cfa expression. Strains were incubated with 0–30 mM C8, pH = 7.0. Inset: specific growth rate in the log phase of E. coli with varying cfa expression. C16:0- palmitic acid, C16:1- palmitoleic acid, C17cyc- cyclopropane C17:0, C18:1- vaccenic acid, C18:0- stearic acid, C19cyc- cyclopropane C19:0. The complete lipid profiles are shown in of the Supporting Information. Membrane properties are calculated from a to obtain: b: saturated:unsaturated lipid ratio and c: average lipid length.

    Article Snippet: MG1655 ATCC#700926 , F- lambda- ilvG- rfb-50 rph-1 , Wildtype.

    Techniques: Expressing, Incubation

    Microbiological activities of gentamicin congeners against Gram-negative wild-type strains and an isogenic  E. coli  panel that harbored key aminoglycoside-modifying enzymes

    Journal: Antimicrobial Agents and Chemotherapy

    Article Title: Unraveling the Gentamicin Drug Product Complexity Reveals Variation in Microbiological Activities and Nephrotoxicity

    doi: 10.1128/AAC.00533-20

    Figure Lengend Snippet: Microbiological activities of gentamicin congeners against Gram-negative wild-type strains and an isogenic E. coli panel that harbored key aminoglycoside-modifying enzymes

    Article Snippet: However, gentamicin C1a had an MIC that was 4-fold more potent than that of the gentamicin mixture, which was significantly different. table ft1 table-wrap mode="anchored" t5 TABLE 1 caption a7 Panel Geometric mean MIC value (mg/liter) a Mix b C1a C2 C2a C1 Wild type E. coli ATCC 25922 0.5 0.5 0.5 0.5 0.5 P. aeruginosa ATCC 27853 0.5 0.25 0.25 0.25 1 A. baumannii M2 c 1 0.25 0.5 0.5 2 Isogenic e E. coli ATCC 700926 + empty vector d 0.25 0.125 0.125 0.125 0.125 E. coli ATCC 700926 + aac(6′)-Ib 1 4 0.5 32 0.25 E. coli ATCC 700926 + aac(3)-III 4 2 4 4 32 E. coli ATCC 700926 + aph(3′)-Ia 0.5 0.125 0.25 0.25 0.5 Open in a separate window a MIC values are the geometric mean of multiple independent measurements rounded to the nearest CLSI standard dilution increment. b “Mix” refers to batch of laboratory-grade gentamicin used to purify the gentamicin congeners. c Wild-type A. baumannii M2 has been previously characterized ( 34 ). d Parent E. coli strain containing the empty version of the pBBR1MCS-4 vector ( 35 ) used to carry the aminoglycoside-modifying enzyme genes in the isogenic panel. e Nine additional isogenic E. coli isolates with either aac(6′)-aph(2′′) , aph(3′)-II , aph(3′)-III , aph(3′)-IV , aph(3′)-V , aph(3′)-VII , aac(2′)-I , aac(3)-I , or aac(3)-X were also tested, and the MICs for each congener fell within ±1 log 2 dilution of the gentamicin “Mix” MIC.

    Techniques: Plasmid Preparation

    Microbiological activities of laboratory-grade gentamicin compared to artificial mixtures of gentamicin congeners that maximized gentamicin C1 and C2 (artificial mix 1) or minimized gentamicin C1 and C2 (artificial mix 2) within USP allowable ranges

    Journal: Antimicrobial Agents and Chemotherapy

    Article Title: Unraveling the Gentamicin Drug Product Complexity Reveals Variation in Microbiological Activities and Nephrotoxicity

    doi: 10.1128/AAC.00533-20

    Figure Lengend Snippet: Microbiological activities of laboratory-grade gentamicin compared to artificial mixtures of gentamicin congeners that maximized gentamicin C1 and C2 (artificial mix 1) or minimized gentamicin C1 and C2 (artificial mix 2) within USP allowable ranges

    Article Snippet: However, gentamicin C1a had an MIC that was 4-fold more potent than that of the gentamicin mixture, which was significantly different. table ft1 table-wrap mode="anchored" t5 TABLE 1 caption a7 Panel Geometric mean MIC value (mg/liter) a Mix b C1a C2 C2a C1 Wild type E. coli ATCC 25922 0.5 0.5 0.5 0.5 0.5 P. aeruginosa ATCC 27853 0.5 0.25 0.25 0.25 1 A. baumannii M2 c 1 0.25 0.5 0.5 2 Isogenic e E. coli ATCC 700926 + empty vector d 0.25 0.125 0.125 0.125 0.125 E. coli ATCC 700926 + aac(6′)-Ib 1 4 0.5 32 0.25 E. coli ATCC 700926 + aac(3)-III 4 2 4 4 32 E. coli ATCC 700926 + aph(3′)-Ia 0.5 0.125 0.25 0.25 0.5 Open in a separate window a MIC values are the geometric mean of multiple independent measurements rounded to the nearest CLSI standard dilution increment. b “Mix” refers to batch of laboratory-grade gentamicin used to purify the gentamicin congeners. c Wild-type A. baumannii M2 has been previously characterized ( 34 ). d Parent E. coli strain containing the empty version of the pBBR1MCS-4 vector ( 35 ) used to carry the aminoglycoside-modifying enzyme genes in the isogenic panel. e Nine additional isogenic E. coli isolates with either aac(6′)-aph(2′′) , aph(3′)-II , aph(3′)-III , aph(3′)-IV , aph(3′)-V , aph(3′)-VII , aac(2′)-I , aac(3)-I , or aac(3)-X were also tested, and the MICs for each congener fell within ±1 log 2 dilution of the gentamicin “Mix” MIC.

    Techniques: