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a vinelandii atcc 9046  (ATCC)


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    Structured Review

    ATCC a vinelandii atcc 9046
    Bacterial strains and plasmids used in this work
    A Vinelandii Atcc 9046, 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/a vinelandii atcc 9046/product/ATCC
    Average 90 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    a vinelandii atcc 9046 - by Bioz Stars, 2025-01
    90/100 stars

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    1) Product Images from "Azotobacter vinelandii Aldehyde Dehydrogenase Regulated by ? 54 : Role in Alcohol Catabolism and Encystment"

    Article Title: Azotobacter vinelandii Aldehyde Dehydrogenase Regulated by ? 54 : Role in Alcohol Catabolism and Encystment

    Journal:

    doi: 10.1128/JB.183.21.6169-6174.2001

    Bacterial strains and plasmids used in this work
    Figure Legend Snippet: Bacterial strains and plasmids used in this work

    Techniques Used: Plasmid Preparation, Subcloning, Mutagenesis

    Growth phenotypes of A. vinelandii ATCC 9046 (1), SG9A (2), SG9A::pSM9-Gm (3), and CN10 (4) at 30°C on Burk's medium supplemented with 10 mM NH4Cl as the nitrogen source and with 2.0% sucrose (A), 0.2% BHB (B), n-butanol (C), ethanol (D), or hexanol (E) as the sole carbon source.
    Figure Legend Snippet: Growth phenotypes of A. vinelandii ATCC 9046 (1), SG9A (2), SG9A::pSM9-Gm (3), and CN10 (4) at 30°C on Burk's medium supplemented with 10 mM NH4Cl as the nitrogen source and with 2.0% sucrose (A), 0.2% BHB (B), n-butanol (C), ethanol (D), or hexanol (E) as the sole carbon source.

    Techniques Used:

    Aldehyde dehydrogenase activity in A. vinelandii aldA mutant a
    Figure Legend Snippet: Aldehyde dehydrogenase activity in A. vinelandii aldA mutant a

    Techniques Used: Activity Assay, Mutagenesis

    Primer extension analysis of aldA transcription in strains ATCC 9046 and CN10. (A) DNA sequence of the 5′ end of aldA. The arrow indicates the start site of aldA transcription; the ς54 promoter is also indicated at the top. The ATG initiation codon is shown in boldface. The complementary sequence where the oligonucleotide used for primer extension was generated is underlined. (B) Primer extension of the aldA gene in strain ATCC 9046 (lane 1) and in strain CN10 (lane 2) incubated in Burk's medium plus ammonia with sucrose. The aldA sequence ladder (GATC) was produced with the oligonucleotide used for primer extension.
    Figure Legend Snippet: Primer extension analysis of aldA transcription in strains ATCC 9046 and CN10. (A) DNA sequence of the 5′ end of aldA. The arrow indicates the start site of aldA transcription; the ς54 promoter is also indicated at the top. The ATG initiation codon is shown in boldface. The complementary sequence where the oligonucleotide used for primer extension was generated is underlined. (B) Primer extension of the aldA gene in strain ATCC 9046 (lane 1) and in strain CN10 (lane 2) incubated in Burk's medium plus ammonia with sucrose. The aldA sequence ladder (GATC) was produced with the oligonucleotide used for primer extension.

    Techniques Used: Sequencing, Generated, Incubation, Produced

    Encystment in A. vinelandii aldA and rpoN mutants
    Figure Legend Snippet: Encystment in A. vinelandii aldA and rpoN mutants

    Techniques Used:



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    Bacterial strains and plasmids used in this work

    Journal:

    Article Title: Azotobacter vinelandii Aldehyde Dehydrogenase Regulated by ? 54 : Role in Alcohol Catabolism and Encystment

    doi: 10.1128/JB.183.21.6169-6174.2001

    Figure Lengend Snippet: Bacterial strains and plasmids used in this work

    Article Snippet: As expected, an increase in β-galactosidase activity was observed during incubation on n -butanol (Fig. ). fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG. 2 caption a7 Growth phenotypes of A. vinelandii ATCC 9046 (1), SG9A (2), SG9A::pSM9-Gm (3), and CN10 (4) at 30°C on Burk's medium supplemented with 10 mM NH 4 Cl as the nitrogen source and with 2.0% sucrose (A), 0.2% BHB (B), n -butanol (C), ethanol (D), or hexanol (E) as the sole carbon source. fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG. 3 caption a7 β-Galactosidase activity of strain SG9A, during incubation in solid Burk's medium with sucrose (open symbols) or n -butanol (closed symbols).

    Techniques: Plasmid Preparation, Subcloning, Mutagenesis

    Growth phenotypes of A. vinelandii ATCC 9046 (1), SG9A (2), SG9A::pSM9-Gm (3), and CN10 (4) at 30°C on Burk's medium supplemented with 10 mM NH4Cl as the nitrogen source and with 2.0% sucrose (A), 0.2% BHB (B), n-butanol (C), ethanol (D), or hexanol (E) as the sole carbon source.

    Journal:

    Article Title: Azotobacter vinelandii Aldehyde Dehydrogenase Regulated by ? 54 : Role in Alcohol Catabolism and Encystment

    doi: 10.1128/JB.183.21.6169-6174.2001

    Figure Lengend Snippet: Growth phenotypes of A. vinelandii ATCC 9046 (1), SG9A (2), SG9A::pSM9-Gm (3), and CN10 (4) at 30°C on Burk's medium supplemented with 10 mM NH4Cl as the nitrogen source and with 2.0% sucrose (A), 0.2% BHB (B), n-butanol (C), ethanol (D), or hexanol (E) as the sole carbon source.

    Article Snippet: As expected, an increase in β-galactosidase activity was observed during incubation on n -butanol (Fig. ). fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG. 2 caption a7 Growth phenotypes of A. vinelandii ATCC 9046 (1), SG9A (2), SG9A::pSM9-Gm (3), and CN10 (4) at 30°C on Burk's medium supplemented with 10 mM NH 4 Cl as the nitrogen source and with 2.0% sucrose (A), 0.2% BHB (B), n -butanol (C), ethanol (D), or hexanol (E) as the sole carbon source. fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG. 3 caption a7 β-Galactosidase activity of strain SG9A, during incubation in solid Burk's medium with sucrose (open symbols) or n -butanol (closed symbols).

    Techniques:

    Aldehyde dehydrogenase activity in A. vinelandii aldA mutant a

    Journal:

    Article Title: Azotobacter vinelandii Aldehyde Dehydrogenase Regulated by ? 54 : Role in Alcohol Catabolism and Encystment

    doi: 10.1128/JB.183.21.6169-6174.2001

    Figure Lengend Snippet: Aldehyde dehydrogenase activity in A. vinelandii aldA mutant a

    Article Snippet: As expected, an increase in β-galactosidase activity was observed during incubation on n -butanol (Fig. ). fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG. 2 caption a7 Growth phenotypes of A. vinelandii ATCC 9046 (1), SG9A (2), SG9A::pSM9-Gm (3), and CN10 (4) at 30°C on Burk's medium supplemented with 10 mM NH 4 Cl as the nitrogen source and with 2.0% sucrose (A), 0.2% BHB (B), n -butanol (C), ethanol (D), or hexanol (E) as the sole carbon source. fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG. 3 caption a7 β-Galactosidase activity of strain SG9A, during incubation in solid Burk's medium with sucrose (open symbols) or n -butanol (closed symbols).

    Techniques: Activity Assay, Mutagenesis

    Primer extension analysis of aldA transcription in strains ATCC 9046 and CN10. (A) DNA sequence of the 5′ end of aldA. The arrow indicates the start site of aldA transcription; the ς54 promoter is also indicated at the top. The ATG initiation codon is shown in boldface. The complementary sequence where the oligonucleotide used for primer extension was generated is underlined. (B) Primer extension of the aldA gene in strain ATCC 9046 (lane 1) and in strain CN10 (lane 2) incubated in Burk's medium plus ammonia with sucrose. The aldA sequence ladder (GATC) was produced with the oligonucleotide used for primer extension.

    Journal:

    Article Title: Azotobacter vinelandii Aldehyde Dehydrogenase Regulated by ? 54 : Role in Alcohol Catabolism and Encystment

    doi: 10.1128/JB.183.21.6169-6174.2001

    Figure Lengend Snippet: Primer extension analysis of aldA transcription in strains ATCC 9046 and CN10. (A) DNA sequence of the 5′ end of aldA. The arrow indicates the start site of aldA transcription; the ς54 promoter is also indicated at the top. The ATG initiation codon is shown in boldface. The complementary sequence where the oligonucleotide used for primer extension was generated is underlined. (B) Primer extension of the aldA gene in strain ATCC 9046 (lane 1) and in strain CN10 (lane 2) incubated in Burk's medium plus ammonia with sucrose. The aldA sequence ladder (GATC) was produced with the oligonucleotide used for primer extension.

    Article Snippet: As expected, an increase in β-galactosidase activity was observed during incubation on n -butanol (Fig. ). fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG. 2 caption a7 Growth phenotypes of A. vinelandii ATCC 9046 (1), SG9A (2), SG9A::pSM9-Gm (3), and CN10 (4) at 30°C on Burk's medium supplemented with 10 mM NH 4 Cl as the nitrogen source and with 2.0% sucrose (A), 0.2% BHB (B), n -butanol (C), ethanol (D), or hexanol (E) as the sole carbon source. fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG. 3 caption a7 β-Galactosidase activity of strain SG9A, during incubation in solid Burk's medium with sucrose (open symbols) or n -butanol (closed symbols).

    Techniques: Sequencing, Generated, Incubation, Produced

    Encystment in A. vinelandii aldA and rpoN mutants

    Journal:

    Article Title: Azotobacter vinelandii Aldehyde Dehydrogenase Regulated by ? 54 : Role in Alcohol Catabolism and Encystment

    doi: 10.1128/JB.183.21.6169-6174.2001

    Figure Lengend Snippet: Encystment in A. vinelandii aldA and rpoN mutants

    Article Snippet: As expected, an increase in β-galactosidase activity was observed during incubation on n -butanol (Fig. ). fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG. 2 caption a7 Growth phenotypes of A. vinelandii ATCC 9046 (1), SG9A (2), SG9A::pSM9-Gm (3), and CN10 (4) at 30°C on Burk's medium supplemented with 10 mM NH 4 Cl as the nitrogen source and with 2.0% sucrose (A), 0.2% BHB (B), n -butanol (C), ethanol (D), or hexanol (E) as the sole carbon source. fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window FIG. 3 caption a7 β-Galactosidase activity of strain SG9A, during incubation in solid Burk's medium with sucrose (open symbols) or n -butanol (closed symbols).

    Techniques: