University of Duisburg-Essen, Faculty of Chemistry, Biofilm Centre, Department of Aquatic Microbiology, Geibelstrasse 41, D-47057 Duisburg, Germany.
Heinrich-Heine-University of Duesseldorf, Institute for Molecular Enzyme Technology, Research Centre Juelich, Stetternicher Forst, D-52425 Juelich, Germany.
Microbiology (Reading). 2010 Jul;156(Pt 7):2239-2252. doi: 10.1099/mic.0.037036-0. Epub 2010 Apr 1.
Pseudomonas aeruginosa secretes a variety of hydrolases, many of which contribute to virulence or are thought to play a role in the nutrition of the bacterium. As most studies concerning extracellular enzymes have been performed on planktonic cultures of non-mucoid P. aeruginosa strains, knowledge of the potential role of these enzymes in biofilm formation in mucoid (alginate-producing) P. aeruginosa remains limited. Here we show that mucoid P. aeruginosa produces extracellular hydrolases during biofilm growth. Overexpression of the extracellular lipases LipA and LipC, the esterase EstA and the proteolytic elastase LasB from plasmids revealed that some of these hydrolases affected the composition and physicochemical properties of the extracellular polymeric substances (EPS). While no influence of LipA was observed, the overexpression of estA and lasB led to increased concentrations of extracellular rhamnolipids with enhanced levels of mono-rhamnolipids, elevated amounts of total carbohydrates and decreased alginate concentrations, resulting in increased EPS hydrophobicity and viscosity. Moreover, we observed an influence of the enzymes on cellular motility. Overexpression of estA resulted in a loss of twitching motility, although it enhanced the ability to swim and swarm. The lasB-overexpression strain showed an overall enhanced motility compared with the parent strain. Moreover, the EstA- and LasB-overproduction strains completely lost the ability to form 3D biofilms, whereas the overproduction of LipC increased cell aggregation and the heterogeneity of the biofilms formed. Overall, these findings indicate that directly or indirectly, the secreted enzymes EstA, LasB and LipC can influence the formation and architecture of mucoid P. aeruginosa biofilms as a result of changes in EPS composition and properties, as well as the motility of the cells.
铜绿假单胞菌分泌多种水解酶,其中许多与毒力有关,或被认为在细菌营养中发挥作用。由于大多数关于细胞外酶的研究都是在非黏液型铜绿假单胞菌浮游培养物上进行的,因此,对于这些酶在黏液型(产生藻酸盐)铜绿假单胞菌生物膜形成中的潜在作用的了解仍然有限。在这里,我们表明黏液型铜绿假单胞菌在生物膜生长过程中产生细胞外水解酶。通过质粒过表达细胞外脂肪酶 LipA 和 LipC、酯酶 EstA 和蛋白水解弹性蛋白酶 LasB 表明,这些水解酶中的一些会影响细胞外聚合物物质 (EPS) 的组成和理化性质。虽然观察到 LipA 没有影响,但 estA 和 lasB 的过表达导致细胞外鼠李糖脂浓度增加,单鼠李糖脂水平升高,总碳水化合物含量增加,藻酸盐浓度降低,导致 EPS 疏水性和粘度增加。此外,我们观察到这些酶对细胞运动性的影响。estA 的过表达导致扭转型运动丧失,尽管它增强了游泳和群集的能力。与亲本菌株相比,lasB 过表达菌株的整体运动性增强。此外,EstA 和 LasB 过表达菌株完全丧失了形成 3D 生物膜的能力,而 LipC 的过表达增加了细胞聚集和形成生物膜的异质性。总体而言,这些发现表明,分泌的酶 EstA、LasB 和 LipC 可以通过改变 EPS 组成和特性以及细胞的运动性,直接或间接地影响黏液型铜绿假单胞菌生物膜的形成和结构。