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生物膜中二氧化碳产生速率所指示的代谢分化。

Metabolic differentiation in biofilms as indicated by carbon dioxide production rates.

机构信息

Department of Chemical Engineering and Applied Chemistry, University of Toronto, 200 College Street, Toronto, Ontario, Canada M5S3E51.

出版信息

Appl Environ Microbiol. 2010 Feb;76(4):1189-97. doi: 10.1128/AEM.01719-09. Epub 2009 Dec 18.

Abstract

The measurement of carbon dioxide production rates as an indication of metabolic activity was applied to study biofilm development and response of Pseudomonas sp. biofilms to an environmental disturbance in the form of a moving air-liquid interface (i.e., shear). A differential response in biofilm cohesiveness was observed after bubble perturbation, and the biofilm layers were operationally defined as either shear-susceptible or non-shear-susceptible. Confocal laser scanning microscopy and image analysis showed a significant reduction in biofilm thickness and biomass after the removal of the shear-susceptible biofilm layer, as well as notable changes in the roughness coefficient and surface-to-biovolume ratio. These changes were accompanied by a 72% reduction of whole-biofilm CO2 production; however, the non-shear-susceptible region of the biofilm responded rapidly after the removal of the overlying cells and extracellular polymeric substances (EPS) along with the associated changes in nutrient and O2 flux, with CO2 production rates returning to preperturbation levels within 24 h. The adaptable nature and the ability of bacteria to respond to environmental conditions were further demonstrated by the outer shear-susceptible region of the biofilm; the average CO2 production rate of cells from this region increased within 0.25 h from 9.45 +/- 5.40 fmol of CO2 x cell(-1) x h(-1) to 22.6 +/- 7.58 fmol of CO2 x cell(-1) x h(-1) when cells were removed from the biofilm and maintained in suspension without an additional nutrient supply. These results also demonstrate the need for sufficient monitoring of biofilm recovery at the solid substratum if mechanical methods are used for biofouling control.

摘要

采用二氧化碳生成速率的测量作为代谢活性的指示,研究了生物膜的发展以及假单胞菌生物膜对环境干扰(即剪切力)的响应。在气泡扰动后,观察到生物膜的内聚性出现差异响应,并且将生物膜层操作定义为剪切敏感或非剪切敏感。共聚焦激光扫描显微镜和图像分析显示,在去除剪切敏感的生物膜层后,生物膜厚度和生物量显著减少,粗糙度系数和表面积与生物体积比也发生了显著变化。这些变化伴随着整个生物膜 CO2 生成量减少了 72%;然而,在去除上层细胞和细胞外聚合物(EPS)以及相关的营养物质和 O2 通量变化后,非剪切敏感区域的生物膜迅速做出响应,CO2 生成速率在 24 小时内恢复到扰动前的水平。通过生物膜外层的剪切敏感区域进一步证明了细菌适应环境条件的能力和响应能力;当从生物膜中去除细胞并在没有额外营养供应的情况下保持悬浮状态时,该区域细胞的平均 CO2 生成速率在 0.25 小时内从 9.45 +/- 5.40 fmol 的 CO2 x 细胞(-1) x h(-1)增加到 22.6 +/- 7.58 fmol 的 CO2 x 细胞(-1) x h(-1)。这些结果还表明,如果使用机械方法进行生物污垢控制,则需要对固体基底上的生物膜恢复进行充分监测。

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