粘液样铜绿假单胞菌生物膜胞外聚合物网络的结构和流变行为

Biofilms Pub Date : 2005-10-01 DOI:10.1017/S1479050506002031
M. Wloka, H. Rehage, H. Flemming, J. Wingender
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引用次数: 43

摘要

对产生高分子量海藻酸盐的黏液型铜绿假单胞菌的生物膜进行了流变学研究,海藻酸盐是胞外聚合物质(EPS)的主要多糖成分。环境菌株SG81和临床菌株FRD1产生O -乙酰化的海藻酸盐,FRD1衍生的突变体FRD1153在海藻酸盐乙酰化方面存在缺陷。在假单胞菌分离琼脂上放置的膜过滤器上,36℃培养24 h,制备融合生物膜。用旋转圆盘流变仪分析了这些附着在膜过滤器上的纯培养生物膜的流变特性。所有黏液菌株的生物膜都表现出粘弹性,聚合物(海藻酸盐)交联主要是由缠结形式的物理相互作用引起的。在动态频率扫描测试中,我们观察到与时间相关的平台方案,描述了网络结构的动态。根据这些数据,我们可以得出铜绿假单胞菌SG81 24 h生物膜的弹性有效聚合物链浓度为5(±1)x 10 19链/l(极限为标准偏差)。松弛过程预测结点的平均寿命约为16(±10)s。与乙酰化缺陷菌株FRD1153相比,铜绿假单胞菌FRD1显示出更有弹性的聚合物网络,后者具有更粘性的生物膜结构。当生长培养基中添加10 mmol/l的钙时,生物膜的稳定性得到增强,这主要是基于二价钙离子与海藻酸盐羧酸基之间的库仑相互作用,缠结作用很小。与乙酰化缺陷菌株FRD1153相比,钙诱导的铜绿假单胞菌FRD1生物膜中聚合物网络稳定性的增加更大。这些结果表明,乙酰基作为海藻酸盐聚合物的低分子量取代基强烈影响黏液型铜绿假单胞菌生物膜的流变行为,并参与了在钙离子存在和不存在的情况下EPS基质聚合物网络的稳定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structure and rheological behaviour of the extracellular polymeric substance network of mucoid Pseudomonas aeruginosa biofilms
A rheological study was performed on biofilms of mucoid Pseudomonas aeruginosa strains producing high molecular weight alginate as the major polysaccharide component of the extracellular polymeric substances (EPS). Environmental strain SG81 and clinical strain FRD1 produced O -acetylated alginate, and mutant FRD1153 derived from strain FRD1 was defective in alginate acetylation. Confluent biofilms were prepared by cultivating the bacteria at 36 °C for 24 h on membrane filters placed on Pseudomonas isolation agar. The rheological properties of these pure culture biofilms attached to the membrane filters were analysed using a rotating disc rheometer. The biofilms of all mucoid strains showed viscoelastic properties, with polymer (alginate) cross-linking caused predominantly by physical interactions in the form of entanglements. In dynamic frequency-sweep tests, we observed time-dependent plateau regimens, describing the dynamics of network structures. From these data, we could derive the concentration of elastically effective polymer chains as 5 (±1) x 10 19 chains/l (limits are standard deviation) for 24 h old biofilms of P. aeruginosa SG81. Relaxation processes predicted an average lifetime of junction points of the order of 16 (±10) s. Pseudomona aeruginosa FRD1 revealed a more elastic polymer network when compared with the acetylation-defective strain FRD1153, which had a more viscous biofilm structure. With calcium (10 mmol/l) added to the growth medium, enhanced biofilm stability was observed, which was based mainly on Coulomb interactions between divalent calcium ions and the carboxylate groups of alginate, with entanglements making only minor contributions. The calcium-induced increase in polymer network stability was greater in biofilms of P. aeruginosa FRD1 than in the acetylation-defective strain FRD1153. These results indicate that acetyl groups as low molecular weight substituents of alginate polymers strongly influence the rheological behaviour of mucoid P. aeruginosa biofilms and are involved in the stabilization of polymer networks of the EPS matrix in both the absence and the presence of calcium ions.
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