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bacteriophage vii  (ATCC)


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    Structured Review

    ATCC bacteriophage vii
    Genomic maps of the regions surrounding the 5-HMUDK gene of <t>bacteriophages</t> listed in . GenBank accession numbers as well as the name and host of the bacteriophages are indicated. Notably, 5-HMUDK coassociates with dUMP hydroxymethyltransferase (dU hmt), a member of the thymidylate synthase superfamily.
    Bacteriophage Vii, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/bacteriophage vii/product/ATCC
    Average 93 stars, based on 5 article reviews
    bacteriophage vii - by Bioz Stars, 2026-02
    93/100 stars

    Images

    1) Product Images from "Identification and biosynthesis of thymidine hypermodifications in the genomic DNA of widespread bacterial viruses"

    Article Title: Identification and biosynthesis of thymidine hypermodifications in the genomic DNA of widespread bacterial viruses

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    doi: 10.1073/pnas.1714812115

    Genomic maps of the regions surrounding the 5-HMUDK gene of bacteriophages listed in . GenBank accession numbers as well as the name and host of the bacteriophages are indicated. Notably, 5-HMUDK coassociates with dUMP hydroxymethyltransferase (dU hmt), a member of the thymidylate synthase superfamily.
    Figure Legend Snippet: Genomic maps of the regions surrounding the 5-HMUDK gene of bacteriophages listed in . GenBank accession numbers as well as the name and host of the bacteriophages are indicated. Notably, 5-HMUDK coassociates with dUMP hydroxymethyltransferase (dU hmt), a member of the thymidylate synthase superfamily.

    Techniques Used:

    Restriction digests of modified and unmodified bacteriophage genomic DNAs. Genomic DNA extracted from the indicated bacteriophages was incubated with restriction enzymes AccI, EcoRI, HinfI, and NdeI. The predicted number of cut sites in each bacteriophage sequence is shown in parentheses next to the given enzyme; λ contains canonical DNA bases only. Phage SP8 DNA contains 5-hmdU, replacing thymidine. Phages SP10 and ΦW-14 contain hypermodified thymidines.
    Figure Legend Snippet: Restriction digests of modified and unmodified bacteriophage genomic DNAs. Genomic DNA extracted from the indicated bacteriophages was incubated with restriction enzymes AccI, EcoRI, HinfI, and NdeI. The predicted number of cut sites in each bacteriophage sequence is shown in parentheses next to the given enzyme; λ contains canonical DNA bases only. Phage SP8 DNA contains 5-hmdU, replacing thymidine. Phages SP10 and ΦW-14 contain hypermodified thymidines.

    Techniques Used: Modification, Incubation, Sequencing

    HPLC traces and MS analysis of bacteriophage M6 and ViI nucleosides. The trace in Top was obtained from bacteriophage λ to show the retention of canonical nucleosides. M6 and ViI show a fifth major peak corresponding to the hypermodified base. The protonated molecular ion detected for each hypermodified base is indicated as well as a hypothetical combination of atoms to account for the observed masses. dA, 2′-deoxyadenosine; dG, 2′-deoxyguanosine; dC, 2′-deoxycytidine; dT, thymidine.
    Figure Legend Snippet: HPLC traces and MS analysis of bacteriophage M6 and ViI nucleosides. The trace in Top was obtained from bacteriophage λ to show the retention of canonical nucleosides. M6 and ViI show a fifth major peak corresponding to the hypermodified base. The protonated molecular ion detected for each hypermodified base is indicated as well as a hypothetical combination of atoms to account for the observed masses. dA, 2′-deoxyadenosine; dG, 2′-deoxyguanosine; dC, 2′-deoxycytidine; dT, thymidine.

    Techniques Used:

    Proposed structures of phage M6 ( A ) and ViI ( B ) modifications. 5- N edU and 5- N e O mdU are shown to be the actual modifications in this work.
    Figure Legend Snippet: Proposed structures of phage M6 ( A ) and ViI ( B ) modifications. 5- N edU and 5- N e O mdU are shown to be the actual modifications in this work.

    Techniques Used:



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    bacteriophage vii  (ATCC)
    93
    ATCC bacteriophage vii
    Genomic maps of the regions surrounding the 5-HMUDK gene of <t>bacteriophages</t> listed in . GenBank accession numbers as well as the name and host of the bacteriophages are indicated. Notably, 5-HMUDK coassociates with dUMP hydroxymethyltransferase (dU hmt), a member of the thymidylate synthase superfamily.
    Bacteriophage Vii, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/bacteriophage vii/product/ATCC
    Average 93 stars, based on 1 article reviews
    bacteriophage vii - by Bioz Stars, 2026-02
    93/100 stars
    		  Buy from Supplier

    Image Search Results


    Genomic maps of the regions surrounding the 5-HMUDK gene of bacteriophages listed in . GenBank accession numbers as well as the name and host of the bacteriophages are indicated. Notably, 5-HMUDK coassociates with dUMP hydroxymethyltransferase (dU hmt), a member of the thymidylate synthase superfamily.

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Identification and biosynthesis of thymidine hypermodifications in the genomic DNA of widespread bacterial viruses

    doi: 10.1073/pnas.1714812115

    Figure Lengend Snippet: Genomic maps of the regions surrounding the 5-HMUDK gene of bacteriophages listed in . GenBank accession numbers as well as the name and host of the bacteriophages are indicated. Notably, 5-HMUDK coassociates with dUMP hydroxymethyltransferase (dU hmt), a member of the thymidylate synthase superfamily.

    Article Snippet: The following strains were purchased from the American Type Culture Collection (ATCC): bacteriophage ViI (ATCC 27870-B1), the ViI host Salmonella enterica ssp. enterica serovar Typhi (ATCC 27870), bacteriophage M6 (ATCC BAA-31-B1), and the M6 host Pseudomonas aeruginosa (ATCC BAA-31).

    Techniques:

    Restriction digests of modified and unmodified bacteriophage genomic DNAs. Genomic DNA extracted from the indicated bacteriophages was incubated with restriction enzymes AccI, EcoRI, HinfI, and NdeI. The predicted number of cut sites in each bacteriophage sequence is shown in parentheses next to the given enzyme; λ contains canonical DNA bases only. Phage SP8 DNA contains 5-hmdU, replacing thymidine. Phages SP10 and ΦW-14 contain hypermodified thymidines.

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Identification and biosynthesis of thymidine hypermodifications in the genomic DNA of widespread bacterial viruses

    doi: 10.1073/pnas.1714812115

    Figure Lengend Snippet: Restriction digests of modified and unmodified bacteriophage genomic DNAs. Genomic DNA extracted from the indicated bacteriophages was incubated with restriction enzymes AccI, EcoRI, HinfI, and NdeI. The predicted number of cut sites in each bacteriophage sequence is shown in parentheses next to the given enzyme; λ contains canonical DNA bases only. Phage SP8 DNA contains 5-hmdU, replacing thymidine. Phages SP10 and ΦW-14 contain hypermodified thymidines.

    Article Snippet: The following strains were purchased from the American Type Culture Collection (ATCC): bacteriophage ViI (ATCC 27870-B1), the ViI host Salmonella enterica ssp. enterica serovar Typhi (ATCC 27870), bacteriophage M6 (ATCC BAA-31-B1), and the M6 host Pseudomonas aeruginosa (ATCC BAA-31).

    Techniques: Modification, Incubation, Sequencing

    HPLC traces and MS analysis of bacteriophage M6 and ViI nucleosides. The trace in Top was obtained from bacteriophage λ to show the retention of canonical nucleosides. M6 and ViI show a fifth major peak corresponding to the hypermodified base. The protonated molecular ion detected for each hypermodified base is indicated as well as a hypothetical combination of atoms to account for the observed masses. dA, 2′-deoxyadenosine; dG, 2′-deoxyguanosine; dC, 2′-deoxycytidine; dT, thymidine.

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Identification and biosynthesis of thymidine hypermodifications in the genomic DNA of widespread bacterial viruses

    doi: 10.1073/pnas.1714812115

    Figure Lengend Snippet: HPLC traces and MS analysis of bacteriophage M6 and ViI nucleosides. The trace in Top was obtained from bacteriophage λ to show the retention of canonical nucleosides. M6 and ViI show a fifth major peak corresponding to the hypermodified base. The protonated molecular ion detected for each hypermodified base is indicated as well as a hypothetical combination of atoms to account for the observed masses. dA, 2′-deoxyadenosine; dG, 2′-deoxyguanosine; dC, 2′-deoxycytidine; dT, thymidine.

    Article Snippet: The following strains were purchased from the American Type Culture Collection (ATCC): bacteriophage ViI (ATCC 27870-B1), the ViI host Salmonella enterica ssp. enterica serovar Typhi (ATCC 27870), bacteriophage M6 (ATCC BAA-31-B1), and the M6 host Pseudomonas aeruginosa (ATCC BAA-31).

    Techniques:

    Proposed structures of phage M6 ( A ) and ViI ( B ) modifications. 5- N edU and 5- N e O mdU are shown to be the actual modifications in this work.

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Identification and biosynthesis of thymidine hypermodifications in the genomic DNA of widespread bacterial viruses

    doi: 10.1073/pnas.1714812115

    Figure Lengend Snippet: Proposed structures of phage M6 ( A ) and ViI ( B ) modifications. 5- N edU and 5- N e O mdU are shown to be the actual modifications in this work.

    Article Snippet: The following strains were purchased from the American Type Culture Collection (ATCC): bacteriophage ViI (ATCC 27870-B1), the ViI host Salmonella enterica ssp. enterica serovar Typhi (ATCC 27870), bacteriophage M6 (ATCC BAA-31-B1), and the M6 host Pseudomonas aeruginosa (ATCC BAA-31).

    Techniques: