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Detection of Vibrio (Listonella) Anguillarum Porin Homologue Proteins and Their Source Bacteria from Coastal Seawater

机译:沿海海水中弧菌(李氏杆菌)猪同源蛋白及其源细菌的检测

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The molecular distribution of dissolved proteins in seawater from coastal marine environments in Uranouchi Bay, Kochi Prefecture, is first reported in this article. Occurrence of bacteria-derived dissolved proteins and their source bacteria were examined using a probe of the antibody (anti-Omp35La) against a porin outer membrane protein (Omp35La) of the fish pathogenic bacterium Vibrio (Listonella) anguillarum. The electrophoretograms of dissolved proteins from coastal seawater showed a large number of discrete and individual proteins overlapped each other over a wide range of molecular masses indicating active processes in coastal environments in transferring proteins from organisms to the inanimate dissolved protein pool. Among the dissolved proteins, 37 kDa- and 18 kDa-proteins reacted with the Omp35La. In order to isolate the source bacteria of such dissolved proteins, bacteria from seawater and diseased fish were screened by colony Western blotting with anti-Omp35La. The reactive strains were further examined in sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)/Western blotting to verify the presence of Omp35La homologues among the outer membrane proteins of such strains. Outer membrane proteins reacting with anti-Omp35La were detected in only 4 strains of the 129 strains that were positive in the colony Western blotting. The level of possible source bacteria of 37 kDa- and 18 kDa-dissolved proteins was suggested to be 5–6 orders of magnitude lower than the total bacterial count. The present study leads us to hypothesize that a minor portion of the bacterial assemblage is responsible for the dissolved proteins in the coastal waters.
机译:本文首次报道了高知县浦河内湾沿海海洋海水中溶解蛋白的分子分布。使用针对鱼类致病性细菌弧菌(Listonella)鳗的孔蛋白外膜蛋白(Omp35La)的抗体(anti-Omp35La)的探针来检查细菌来源的溶解蛋白及其来源细菌的发生。沿海海水中溶解的蛋白质的电泳图谱显示,大量离散的蛋白质和单个蛋白质在很宽的分子量范围内相互重叠,表明沿海环境中蛋白质从生物体转移到无生命的溶解蛋白质库中的活跃过程。在溶解的蛋白质中,有37 kDa和18 kDa的蛋白质与Omp35La反应。为了分离这种溶解的蛋白质的来源细菌,通过用抗Omp35La的菌落Western印迹来筛选海水和患病鱼类的细菌。在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)/蛋白质印迹中进一步检查反应菌株,以验证此类菌株的外膜蛋白中是否存在Omp35La同源物。在129株菌落Western blotting呈阳性的菌株中,仅4株检测到与抗Omp35La反应的外膜蛋白。建议将可能溶解37 kDa和18 kDa的蛋白质的来源细菌的水平比细菌总数减少5–6个数量级。本研究使我们假设细菌组合的一小部分负责沿海水域中的溶解蛋白。

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