首页> 美国卫生研究院文献>Beilstein Journal of Organic Chemistry >Two new 2-alkylquinolones inhibitory to the fish skin ulcer pathogen Tenacibaculum maritimum produced by a rhizobacterium of the genus Burkholderia sp.
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Two new 2-alkylquinolones inhibitory to the fish skin ulcer pathogen Tenacibaculum maritimum produced by a rhizobacterium of the genus Burkholderia sp.

机译:由Burkholderia sp。的一种根瘤菌产生的两种新的2-烷基喹诺酮类药物对鱼皮肤溃疡病原体Tenacibaculum maritimum具有抑制作用。

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摘要

Exploration of rhizobacteria of the genus Burkholderia as an under-tapped resource of bioactive molecules resulted in the isolation of two new antimicrobial 2-alkyl-4-quinolones. (E)-2-(Hept-2-en-1-yl)quinolin-4(1H)-one (>1) and (E)-2-(non-2-en-1-yl)quinolin-4(1H)-one (>3) were isolated from the culture broth of strain MBAF1239 together with four known alkylquinolones (>2 and >4–>6), pyrrolnitrin (>7), and BN-227 (>8). The structures of >1 and >3 were unambiguously characterized using NMR spectroscopy and mass spectrometry. Compounds >1–>8 inhibited the growth of the marine bacterium Tenacibaculum maritimum, an etiological agent of skin ulcers in marine fish, offering new opportunities to develop antibacterial drugs for fish farming.
机译:探索伯克霍尔德氏菌属的根瘤菌作为生物活性分子的开发资源不足,导致分离出两种新的抗菌剂2-烷基-4-喹诺酮。 (E)-2-(庚-2-烯-1-基)喹啉-4(1H)-1(> 1 )和(E)-2-(non-2-en-1从菌株MBAF1239的培养液中分离出-yl)quinolin-4(1H)-one(> 3 )和四个已知的烷基喹诺酮类(> 2 和> 4 < / strong> – > 6 ),吡咯硝酸(> 7 )和BN-227(> 8 )。使用NMR光谱法和质谱法明确地表征了> 1 和> 3 的结构。化合物> 1 – > 8 抑制海洋细菌Tenacibaculum maritimum(海洋鱼类皮肤溃疡的病原体)的生长,为开发用于鱼类养殖的抗菌药物提供了新的机会。

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