2018
DOI: 10.1016/j.synbio.2018.10.008
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Nocardiopsistins A-C: New angucyclines with anti-MRSA activity isolated from a marine sponge-derived Nocardiopsis sp. HB-J378

Abstract: Marine natural products have become an increasingly important source of new drug leads during recent years. In an attempt to identify novel anti-microbial natural products by bioprospecting deep-sea Actinobacteria, three new angucyclines, nocardiopsistins A-C, were isolated from Nocardiopsis sp. strain HB-J378. Notably, the supplementation of the rare earth salt Lanthanum chloride (LaCl3) during fermentation of HB-J378 significantly increased the yield of these angucyclines. The structures of nocardiopsistins … Show more

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Cited by 35 publications
(25 citation statements)
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“…ROESY correlations between H-9 and H-12 positioned H-12/H-12' syn to H-9/H-9', whereas NOE correlations of methyl-16 with H-11 and H-13a signified that methyl-16/16' is in on the same face as H-11/11' (Figure 3). These The Δ 4,5 , Δ 6,7 , Δ 20,21 , Δ 22,23 double bonds were established as E and the Δ 8,9 , Δ 10,11 , Δ 20,21 , Δ 22,23 double bonds as Z configurated. The methyl substituted Δ 2,3 , Δ 16,17 , Δ 18,19 22 micromonosporin A (24 membered ring), 23 as well as lobosamide, mirilactam, micromonolactam, and sceliphrolactam (all with 26 membered rings).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…ROESY correlations between H-9 and H-12 positioned H-12/H-12' syn to H-9/H-9', whereas NOE correlations of methyl-16 with H-11 and H-13a signified that methyl-16/16' is in on the same face as H-11/11' (Figure 3). These The Δ 4,5 , Δ 6,7 , Δ 20,21 , Δ 22,23 double bonds were established as E and the Δ 8,9 , Δ 10,11 , Δ 20,21 , Δ 22,23 double bonds as Z configurated. The methyl substituted Δ 2,3 , Δ 16,17 , Δ 18,19 22 micromonosporin A (24 membered ring), 23 as well as lobosamide, mirilactam, micromonolactam, and sceliphrolactam (all with 26 membered rings).…”
Section: Resultsmentioning
confidence: 99%
“…19 Recently, three new angucyclines, nocardiopsistins A-C, with anti-Methicillin-Resistant Staphylococcus aureus (MRSA) activity were isolated from a marine sponge-derived Nocardiopsis sp. HB-J378, 20 and a new cytotoxic cyclic peptide was obtained from the marine sponge-associated Nocardiopsis sp. UR67.…”
mentioning
confidence: 99%
“…Three novel angucycline nocardiopsistins were isolated from marine sponge-derived Nocardiopsis sp. with anti-MRSA activity [ 100 ]. In a study of twenty strains of actinomycetes, from the mangrove ecosystem of the Andaman Islands, thirteen strains showed broad-spectrum activity against Gram-positive and Gram-negative bacteria.…”
Section: Medical Applicationsmentioning
confidence: 99%
“…HB‐J378 ( Table 1, Figure 1). Nocardiopsistin 2 showed the best anti‐Methicillin‐Resistant Staphylococcus Aureus (MRSA) activity with the same minimum inhibitory concentration (MIC=3.12 μg/mL), whereas both nocardiopsistins 1 and 3 merely possessed moderate potencies against MRSA with MIC value of 12.5 μg/mL [16] . The results indicated the carbonyl oxygen atom (=O) attached to the side‐ring of nocardiopsistin (C‐4) is essential for the anti‐MRSA activity.…”
Section: Marine‐based Polyketides With Diverse Bioactivitiesmentioning
confidence: 99%