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  1. Artikel: Antibacterial Activity of Chromomycins from a Marine-Derived Streptomyces microflavus

    Cho, Eunji / Kwon, Oh-Seok / Chung, Beomkoo / Lee, Jayho / Sun, Jeongyoon / Shin, Jongheon / Oh, Ki-Bong

    Marine drugs. 2020 Oct. 21, v. 18, no. 10

    2020  

    Abstract: A marine-derived actinomycete (Streptomyces sp. MBTI36) exhibiting antibacterial activities was investigated in the present study. The strain was identified using genetic techniques. The 16S rDNA sequence of the isolate indicated that it was most closely ...

    Abstract A marine-derived actinomycete (Streptomyces sp. MBTI36) exhibiting antibacterial activities was investigated in the present study. The strain was identified using genetic techniques. The 16S rDNA sequence of the isolate indicated that it was most closely related to Streptomyces microflavus. Furthermore, a new chromomycin A₉ (1), along with chromomycin Ap (2), chromomycin A₂ (3), and chromomycin A₃ (4), were isolated from the ethyl acetate extract. Their structures were determined using extensive spectroscopic methods including 1D and 2D NMR, and HRMS, as well as comparisons with previously reported data. Compounds 1–4 showed potent antibacterial activities against Gram-positive bacteria including methicillin-resistant Staphylococcus aureus (MRSA). During a passage experiment, minimum inhibitory concentration (MIC) values for compounds 1–4 showed no more than a 4-fold increase from the starting MIC value, indicating that no resistance was detected over the 21 passages.
    Schlagwörter Gram-positive bacteria ; Streptomyces microflavus ; antibacterial properties ; drugs ; ethyl acetate ; genetic techniques and protocols ; methicillin-resistant Staphylococcus aureus ; minimum inhibitory concentration ; nucleotide sequences ; spectroscopy
    Sprache Englisch
    Erscheinungsverlauf 2020-1021
    Erscheinungsort Multidisciplinary Digital Publishing Institute
    Dokumenttyp Artikel
    Anmerkung NAL-light
    ZDB-ID 2175190-0
    ISSN 1660-3397
    ISSN 1660-3397
    DOI 10.3390/md18100522
    Datenquelle NAL Katalog (AGRICOLA)

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  2. Artikel ; Online: Antibacterial Activity of Chromomycins from a Marine-Derived

    Cho, Eunji / Kwon, Oh-Seok / Chung, Beomkoo / Lee, Jayho / Sun, Jeongyoon / Shin, Jongheon / Oh, Ki-Bong

    Marine drugs

    2020  Band 18, Heft 10

    Abstract: A marine-derived actinomycete ( ...

    Abstract A marine-derived actinomycete (
    Sprache Englisch
    Erscheinungsdatum 2020-10-21
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 2175190-0
    ISSN 1660-3397 ; 1660-3397
    ISSN (online) 1660-3397
    ISSN 1660-3397
    DOI 10.3390/md18100522
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Cytotoxic Scalarane Sesterterpenes from the Sponge

    Kwon, Oh-Seok / Kim, Donghwa / Kim, Chang-Kwon / Sun, Jeongyoon / Sim, Chung J / Oh, Dong-Chan / Lee, Sang Koo / Oh, Ki-Bong / Shin, Jongheon

    Marine drugs

    2020  Band 18, Heft 5

    Abstract: Twelve new sesterterpenes along with eight known sesterterpenes were isolated from the marine ... ...

    Abstract Twelve new sesterterpenes along with eight known sesterterpenes were isolated from the marine sponge
    Mesh-Begriff(e) Animals ; Antineoplastic Agents/chemistry ; Antineoplastic Agents/pharmacology ; Cell Cycle/drug effects ; Drug Screening Assays, Antitumor ; Hep G2 Cells/drug effects ; Humans ; Micronesia ; Oceans and Seas ; Porifera/chemistry ; Sesterterpenes/chemistry ; Sesterterpenes/pharmacology
    Chemische Substanzen Antineoplastic Agents ; Sesterterpenes
    Sprache Englisch
    Erscheinungsdatum 2020-05-13
    Erscheinungsland Switzerland
    Dokumenttyp Journal Article
    ZDB-ID 2175190-0
    ISSN 1660-3397 ; 1660-3397
    ISSN (online) 1660-3397
    ISSN 1660-3397
    DOI 10.3390/md18050253
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Structures and Biosynthetic Pathway of Pulvomycins B-D: 22-Membered Macrolides from an Estuarine

    Moon, Kyuho / Cui, Jinsheng / Kim, Eunji / Riandi, Evan Setiawan / Park, So Hyun / Byun, Woong Sub / Kal, Youngju / Park, Jun Young / Hwang, Sunghoon / Shin, Daniel / Sun, Jeongyoon / Oh, Ki-Bong / Cha, Sangwon / Shin, Jongheon / Lee, Sang Kook / Yoon, Yeo Joon / Oh, Dong-Chan

    Organic letters

    2020  Band 22, Heft 14, Seite(n) 5358–5362

    Abstract: Pulvomycins B-D ( ...

    Abstract Pulvomycins B-D (
    Mesh-Begriff(e) Antineoplastic Agents/chemistry ; Antineoplastic Agents/metabolism ; Antineoplastic Agents/pharmacology ; Cell Line, Tumor ; Humans ; Macrolides/chemistry ; Macrolides/metabolism ; Macrolides/pharmacology ; Streptomyces/metabolism
    Chemische Substanzen Antineoplastic Agents ; Macrolides
    Sprache Englisch
    Erscheinungsdatum 2020-07-06
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 1523-7052
    ISSN (online) 1523-7052
    DOI 10.1021/acs.orglett.0c01249
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel: Structures and Biosynthetic Pathway of Pulvomycins B–D: 22-Membered Macrolides from an Estuarine Streptomyces sp

    Moon, Kyuho / Cui, Jinsheng / Kim, Eunji / Riandi, Evan Setiawan / Park, So Hyun / Byun, Woong Sub / Kal, Youngju / Park, Jun Young / Hwang, Sunghoon / Shin, Daniel / Sun, Jeongyoon / Oh, Ki-Bong / Cha, Sangwon / Shin, Jongheon / Lee, Sang Kook / Yoon, Yeo Joon / Oh, Dong-Chan

    Organic letters. 2020 July 06, v. 22, no. 14

    2020  

    Abstract: Pulvomycins B–D (1–3) were discovered from an estuarine Streptomyces strain along with the known pulvomycin (4). The 22-membered macrocyclic lactone structures of 1–3 were determined based on the interpretation of NMR, UV, and MS data, the modified ... ...

    Abstract Pulvomycins B–D (1–3) were discovered from an estuarine Streptomyces strain along with the known pulvomycin (4). The 22-membered macrocyclic lactone structures of 1–3 were determined based on the interpretation of NMR, UV, and MS data, the modified Mosher’s method, and Kishi’s bidentate chiral solvent NMR spectroscopy. Genomic analysis of the bacterial strain revealed the biosynthetic gene cluster of pulvomycin and enabled us to propose the trans-acyltransferase polyketide biosynthetic pathway. Pulvomycin D displayed potent cytotoxic activity against various cancer cell lines.
    Schlagwörter Streptomyces ; biochemical pathways ; biosynthesis ; cytotoxicity ; estuaries ; genomics ; macrolides ; multigene family ; neoplasm cells ; nuclear magnetic resonance spectroscopy ; solvents
    Sprache Englisch
    Erscheinungsverlauf 2020-0706
    Umfang p. 5358-5362.
    Erscheinungsort American Chemical Society
    Dokumenttyp Artikel
    Anmerkung NAL-AP-2-clean
    ISSN 1523-7052
    DOI 10.1021/acs.orglett.0c01249
    Datenquelle NAL Katalog (AGRICOLA)

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