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铜绿假单胞菌生物膜与有毒可溶性金发生反应并使其沉淀。

Pseudomonas aeruginosa biofilms react with and precipitate toxic soluble gold.

作者信息

Karthikeyan S, Beveridge T J

机构信息

Department of Microbiology, College of Biological Science, University of Guelph, Guelph, Ontario, Canada N1G 2W1.

出版信息

Environ Microbiol. 2002 Nov;4(11):667-75. doi: 10.1046/j.1462-2920.2002.00353.x.

Abstract

The interaction between biofilms of Pseudomonas aeruginosa PAO1 and 0.01-5 mM gold chloride was investigated using flow-cells. Scanning confocal laser microscopy (SCLM) of these biofilms revealed the formation of two distinct structural features: (i) confluent areas of uniform thickness and (ii) cell clusters which often emerged as 30-40 micro m, tall narrow pillars (or pedestals) of cells and exopolymeric substance (EPS). When 5-day-old, quasi-steady state biofilms (as indicated by the stability of film thickness and overall structure) were exposed to relatively high AuCl3 (i.e. 0.5-5 mM) for 30 min at 20 degrees C, reduction of the auric ion resulted in the formation of both extracellular and intracellular metallic gold colloids, as revealed by transmission electron microscopy (TEM). Most mineralization occurred on cell surfaces with lesser amounts within cells and little throughout the EPS. Little to no mineralization of gold was seen at 0.01-0.1 mM concentrations. As initial AuCl3 concentrations approached 0.5 mM or greater, more gold particles were seen and cell viability, as determined by a BacLight live/dead viability probe, approached zero. At an intermediate concentration of 0.1 mM, the live:dead ratio increased to 4:1. However, when planktonic cells were exposed to this same 0.1 mM concentration, it resulted in a 4-log reduction in viable counts as determined by plating. The higher resistance of biofilm cells to 0.1 mM gold can be attributed to its binding to the EPS and cell surfaces of the biofilm which ensured a (presumably) low effective cytoplasmic concentration of gold (i.e. no gold crystals were seen in cells by TEM). In addition, SCLM revealed the formation of larger extracellular gold crystals at the substratum (coverslip) level of the biofilms, with a higher proportion of crystals detected beneath pillars (cell cluster structures), suggesting the possibility of unique cell types, more reduced microenvironments at the base of each cluster, or a combination of both. These results suggest that the biomineralization of gold is impacted by biofilm structure.

摘要

使用流动小室研究了铜绿假单胞菌PAO1生物膜与0.01 - 5 mM氯化金之间的相互作用。对这些生物膜进行扫描共聚焦激光显微镜(SCLM)观察,发现形成了两种不同的结构特征:(i)厚度均匀的融合区域;(ii)细胞簇,其通常呈现为30 - 40微米高的狭窄细胞柱(或基座)以及胞外聚合物(EPS)。当5天大的准稳态生物膜(通过膜厚度和整体结构的稳定性表明)在20℃下暴露于相对较高浓度的AuCl3(即0.5 - 5 mM)30分钟时,金离子的还原导致细胞外和细胞内金属金胶体的形成,这通过透射电子显微镜(TEM)得以揭示。大多数矿化发生在细胞表面,细胞内较少,EPS中更少。在0.01 - 0.1 mM浓度下几乎看不到或看不到金的矿化。随着初始AuCl3浓度接近0.5 mM或更高,观察到更多的金颗粒,并且通过BacLight活/死活力探针测定的细胞活力接近零。在0.1 mM的中间浓度下,活细胞与死细胞的比例增加到4:1。然而,当浮游细胞暴露于相同的0.1 mM浓度时,通过平板计数法测定,活细胞数量减少了4个对数级。生物膜细胞对0.1 mM金具有更高抗性可归因于其与生物膜的EPS和细胞表面结合,这确保了(推测)细胞内金的有效细胞质浓度较低(即通过TEM在细胞中未看到金晶体)。此外,SCLM显示在生物膜的基质(盖玻片)水平形成了更大的细胞外金晶体,在柱体(细胞簇结构)下方检测到的晶体比例更高,这表明可能存在独特的细胞类型、每个簇底部的微环境更还原或两者兼而有之。这些结果表明金的生物矿化受到生物膜结构的影响。

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