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首页> 外文期刊>biofouling >Comparison of microcolony formation betweenVibriosp. strain S141 and a flagellum#x2010;negative mutant developing on agar and glass substrata
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Comparison of microcolony formation betweenVibriosp. strain S141 and a flagellum#x2010;negative mutant developing on agar and glass substrata

机译:弧菌之间微菌落形成的比较。菌株 S141 和鞭毛阴性突变体在琼脂和玻璃基质上发育

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A flagellum#x2010;negative mutant, M8.2, of the marine bacteriumVibriosp. S141 was produced by transposon mutagenesis. Time#x2010;lapse video imaging of surface colonisation behaviour and microcolony formation of S141 compared to M8.2 cells was carried out to investigate the role of the flagellum ofVibriosp. S141 in microcolony formation on agar and glass substrata. On an agar surface, S141 cells formed a tetrad pattern after the first two cell divisions, during initial surface colonisation. Developed microcolonies consisted of tight circular arrangements of cells with infrequent branching of cells from the main body. In contrast, M8.2 cells did not form tetrad patterns and micro#x2010;colonies generally showed enhanced branching and did not develop circular arrangements of cells. On a glass surface under flow conditions, S141 cells displayed several types of movement behaviours at the surface which may have assisted microcolony formation. M8.2 cells appeared unable to develop micro#x2010;colonies, but rather displayed a behaviour which enabled them to spread out across the substratum. Laser scanning confocal microscopy revealed S141 mature biofilms consisted of characteristic towers of bacterial growth with scattered troughs. The flagellum#x2010;negative M8.2 biofilm did not form such architecture, displaying a homogeneous distribution of cells throughout the biofilm and across the entire substratum. Although not required for attachment to the glass substratum, the flagellum was required for alignment as well as specific movement behaviours by S141 cells.
机译:海洋细菌弧菌的鞭毛阴性突变体M8.2。S141由转座子诱变产生。与M8.2细胞相比,对S141的表面定植行为和微菌落形成进行了延时视频成像,以研究弧菌鞭毛的作用。S141在琼脂和玻璃基质上形成微菌落。在琼脂表面,S141细胞在前两次细胞分裂后,在初始表面定植期间形成四分体模式。发达的微菌落由紧密的圆形细胞排列组成,细胞很少从主体分支。相比之下,M8.2细胞没有形成四分体模式,微菌落通常表现出增强的分支,并且没有形成细胞的环状排列。在流动条件下的玻璃表面上,S141细胞在表面表现出几种类型的运动行为,这些行为可能有助于微菌落的形成。M8.2细胞似乎无法形成微集落,而是表现出一种行为,使它们能够在整个基质中扩散。激光扫描共聚焦显微镜显示,S141成熟的生物膜由细菌生长的特征塔和分散的低谷组成。鞭毛阴性的M8.2生物膜没有形成这样的结构,显示出整个生物膜和整个基质中细胞的均匀分布。虽然鞭毛不是附着在玻璃基质上所必需的,但 S141 细胞的排列和特定运动行为是必需的。

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