1998
DOI: 10.7164/antibiotics.51.145
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New Quinolone Compounds from Pseudonocardia sp. with Selective and Potent Anti-Helicobacter pylori Activity: Taxonomy of Producing Strain, Fermentation, Isolation, Structural Elucidation and Biological Activities.

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Cited by 67 publications
(60 citation statements)
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“…5, Supplementary Table S8). Such an interaction can be theorized to happen due to an antimicrobial activity that Pseudonocardina is known to have 43 . These interpretations show that SparCC computed taxonomic correlations can therefore provide reasonably relevant targets for hypothesis building and evaluation of co-operative and competitive interactions in the environment.…”
Section: Resultsmentioning
confidence: 99%
“…5, Supplementary Table S8). Such an interaction can be theorized to happen due to an antimicrobial activity that Pseudonocardina is known to have 43 . These interpretations show that SparCC computed taxonomic correlations can therefore provide reasonably relevant targets for hypothesis building and evaluation of co-operative and competitive interactions in the environment.…”
Section: Resultsmentioning
confidence: 99%
“…Therefore, it seems likely that quinolone antibiotics were present in nature before the widespread use of man-made quinolones. In fact, many quinolone compounds have been reported as natural products of animals, plants and bacteria [27] and some of them are reported to have antimicrobial activities [28]. Therefore, it is not surprising that certain bacteria producing nybomycins arose in the soil to compete with a substantial number of quinolone-resistant bacteria carrying quinolone-insensitive DNA gyrase [26].…”
Section: Discussionmentioning
confidence: 98%
“…Owing to their structural similarity to vitamin K, they act as potent inhibitors of electron transport in the respiratory chain. [2] The structurally related isoprenylated quinoline antibiotics are potent growth inhibitors of Helicobacter pylori, [8] while two members of the 4-hydroxy-2-alkylquinoline family (HAQs), 3,4-dihydroxy-2-heptylquinoline (PQS) [9] and 4-hydroxy-2-heptylquinoline, function as signaling molecules in cell-cell communication in Pseudomonas aeruginosa. [10] HAQ biosynthesis has been shown to result from the "head-to-head" condensation of anthranilic acid (1) and bketo fatty acids.…”
mentioning
confidence: 99%