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首页> 外文期刊>Applied and Environmental Microbiology >Oligopolyphenylenevinylene-Conjugated Oligoelectrolyte Membrane Insertion Molecules Selectively Disrupt Cell Envelopes of Gram-Positive Bacteria
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Oligopolyphenylenevinylene-Conjugated Oligoelectrolyte Membrane Insertion Molecules Selectively Disrupt Cell Envelopes of Gram-Positive Bacteria

机译:Oligopolyphenylenevinylene共轭的Oligo电解质膜插入分子选择性地破坏革兰氏阳性细菌的细胞包膜。

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摘要

The modification of microbial membranes to achieve biotechnological strain improvement with exogenous small molecules, such as oligopolyphenylenevinylene-conjugated oligoelectrolyte (OPV-COE) membrane insertion molecules (MIMs), is an emerging biotechnological field. Little is known about the interactions of OPV-COEs with their target, the bacterial envelope. We studied the toxicity of three previously reported OPV-COEs with a selection of Gram-negative and Gram-positive organisms and demonstrated that Gram-positive bacteria are more sensitive to OPV-COEs than Gram-negative bacteria. Transmission electron microscopy demonstrated that these MIMs disrupt microbial membranes and that this occurred to a much greater degree in Gram-positive organisms. We used a number of mutants to probe the nature of MIM interactions with the microbial envelope but were unable to align the membrane perturbation effects of these compounds to previously reported membrane disruption mechanisms of, for example, cationic antimicrobial peptides. Instead, the data support the notion that OPV-COEs disrupt microbial membranes through a suspected interaction with diphosphatidylglycerol (DPG), a major component of Gram-positive membranes. The integrity of model membranes containing elevated amounts of DPG was disrupted to a greater extent by MIMs than those prepared from Escherichia coli total lipid extracts alone.
机译:微生物膜的修饰以利用外源性小分子,例如寡聚苯撑乙烯撑共轭的低聚电解质(OPV-COE)膜插入分子(MIMs)来实现生物技术菌株的改良,是一个新兴的生物技术领域。关于OPV-COE与靶标,细菌包膜的相互作用知之甚少。我们用选择的革兰氏阴性和革兰氏阳性生物研究了三种先前报道的OPV-COE的毒性,并证明革兰氏阳性细菌比革兰氏阴性细菌对OPV-COE更敏感。透射电子显微镜表明,这些MIM破坏了微生物膜,并且这种现象在革兰氏阳性生物体中的发生率更高。我们使用了许多突变体来探测MIM与微生物包膜的相互作用性质,但无法将这些化合物的膜扰动效应与先前报道的例如阳离子抗微生物肽的膜破坏机制进行比对。取而代之的是,数据支持了OPV-COE通过怀疑与革兰氏阳性膜的主要成分二磷脂酰甘油(DPG)相互作用而破坏微生物膜的观点。与仅由大肠杆菌总脂质提取物制备的膜相比,MIM更大程度地破坏了含DPG量升高的模型膜的完整性。

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