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来自 spp. 的大环四醇类化合物对霜霉目游动孢子的游动孢子形成和运动性的抑制作用可能与线粒体中 ATP 酶活性增强有关。

Inhibitory Effects of Macrotetrolides from spp. On Zoosporogenesis and Motility of Peronosporomycete Zoospores Are Likely Linked with Enhanced ATPase Activity in Mitochondria.

作者信息

Islam Md Tofazzal, Laatsch Hartmut, von Tiedemann Andreas

机构信息

Division of Plant Pathology and Plant Protection, Department of Crop Sciences, Georg-August-Universität GöttingenGöttingen, Germany; Department of Biotechnology, Bangabandhu Sheikh Mujibur Rahman Agricultural UniversityGazipur, Bangladesh.

Institute of Organic and Biomolecular Chemistry, Georg-August-Universität Göttingen Göttingen, Germany.

出版信息

Front Microbiol. 2016 Nov 18;7:1824. doi: 10.3389/fmicb.2016.01824. eCollection 2016.

Abstract

The release of zoospores from sporangia and motility of the released zoospores are critical in the disease cycle of the Peronosporomycetes that cause devastating diseases in plants, fishes, animals and humans. Disruption of any of these asexual life stages eliminates the possibility of pathogenesis. In the course of screening novel bioactive secondary metabolites, we found that extracts of some strains of marine spp. rapidly impaired motility and caused subsequent lysis of zoospores of the grapevine downy mildew pathogen at 10 μg/ml. We tested a number of secondary metabolites previously isolated from these strains and found that macrotetrolide antibiotics such as nonactin, monactin, dinactin and trinactin, and nactic acids such as (+)-nonactic acid, (+)-homonactic acid, nonactic acid methyl ester, homonactic acid methyl ester, bonactin and feigrisolide C impaired motility and caused subsequent lysis of zoospores in a dose- and time-dependent manners with dinactin being the most active compound (MIC 0.3 μg/ml). A cation channel-forming compound, gramicidin, and a carrier of monovalent cations, nigericin also showed similar biological activities. Among all 12 compounds tested, gramicidin most potently arrested the motility of zoospores at concentrations starting from 0.1 μg/ml. All macrotetrolide antibiotics also displayed similar motility impairing activities against , and zoospores indicating non-specific biological effects of these compounds toward peronosporomyctes. Furthermore, macrotetrolide antibiotics and gramicidin also markedly suppressed the release of zoospores from sporangia of in a dose-dependent manner. As macrotetrolide antibiotics and gramicidin are known as enhancers of mitochondrial ATPase activity, inhibition of zoosporogenesis and motility of zoospores by these compounds are likely linked with hydrolysis of ATP through enhanced ATPase activity in mitochondria. This is the first report on motility inhibitory and lytic activities of macrotetrolide antibiotics and nactic acids against the zoospores of peronosporomycete phytopathogens.

摘要

游动孢子从孢子囊中释放以及释放出的游动孢子的运动能力,在卵菌纲的病害循环中至关重要,卵菌纲会在植物、鱼类、动物和人类中引发毁灭性疾病。这些无性生命阶段中的任何一个受到干扰,都会消除发病的可能性。在筛选新型生物活性次生代谢产物的过程中,我们发现一些海洋菌株的提取物在浓度为10μg/ml时,能迅速削弱葡萄霜霉病菌游动孢子的运动能力,并导致其随后裂解。我们测试了先前从这些菌株中分离出的多种次生代谢产物,发现大环四内酯抗生素如无活菌素、单活菌素、双活菌素和三活菌素,以及纳他霉素如(+)-无活酸、(+)-高纳他酸、无活酸甲酯、高纳他酸甲酯、博纳菌素和费格里索利德C,会以剂量和时间依赖的方式削弱游动孢子的运动能力并导致其随后裂解,其中双活菌素是最具活性的化合物(最低抑菌浓度为0.3μg/ml)。一种形成阳离子通道的化合物短杆菌肽,以及单价阳离子载体尼日利亚菌素也表现出类似的生物活性。在所有测试的12种化合物中,短杆菌肽在浓度从0.1μg/ml开始时就能最有效地阻止游动孢子的运动。所有大环四内酯抗生素对、和游动孢子也表现出类似的运动能力削弱活性,表明这些化合物对卵菌纲具有非特异性生物效应。此外,大环四内酯抗生素和短杆菌肽还以剂量依赖的方式显著抑制游动孢子从孢子囊的释放。由于大环四内酯抗生素和短杆菌肽是已知的线粒体ATP酶活性增强剂,这些化合物对游动孢子形成和运动能力的抑制可能与通过增强线粒体中的ATP酶活性来水解ATP有关。这是关于大环四内酯抗生素和纳他霉素对卵菌纲植物病原菌游动孢子的运动抑制和裂解活性的首次报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6829/5114239/f32bbe14008f/fmicb-07-01824-g0001.jpg

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