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微生物膜对丁醇的响应:交错与无序。

Response of microbial membranes to butanol: interdigitation vs. disorder.

机构信息

Singapore Centre for Environmental Sciences Engineering (SCELSE), Nanyang Technological University, 60 Nanyang Drive, 637551, Singapore.

出版信息

Phys Chem Chem Phys. 2019 Jun 5;21(22):11903-11915. doi: 10.1039/c9cp01469a.

DOI:10.1039/c9cp01469a
PMID:31125035
Abstract

Biobutanol production by fermentation is potentially a sustainable alternative to butanol production from fossil fuels. However, the toxicity of butanol to fermentative bacteria, resulting largely from cell membrane fluidization, limits production titers and is a major factor limiting the uptake of the technology. Here, studies were undertaken, in vitro and in silico, on the butanol effects on a representative bacterial (i.e. Escherichia coli) inner cell membrane. A critical butanol : lipid ratio for stability of 2 : 1 was observed, computationally, consistent with complete interdigitation. However, at this ratio the bilayer was ∼20% thicker than for full interdigitation. Furthermore, butanol intercalation induced acyl chain bending and increased disorder, measured as a 27% lateral diffusivity increase experimentally in a supported lipid bilayer. There was also a monophasic Tm reduction in butanol-treated large unilamellar vesicles. Both behaviours are inconsistent with an interdigitated gel. Butanol thus causes only partial interdigitation at physiological temperatures, due to butanol accumulating at the phospholipid headgroups. Acyl tail disordering (i.e. splaying and bending) fills the subsequent voids. Finally, butanol short-circuits the bilayer and creates a coupled system where interdigitated and splayed phospholipids coexist. These findings will inform the design of strategies targeting bilayer stability for increasing biobutanol production titers.

摘要

生物丁醇发酵生产是一种潜在的可持续替代化石燃料丁醇生产的方法。然而,丁醇对发酵细菌的毒性,主要来自细胞膜的流变性,限制了生产滴度,是限制该技术采用的主要因素。在此,通过体外和计算机模拟研究了丁醇对代表性细菌(即大肠杆菌)内膜的影响。计算结果表明,在 2:1 的关键丁醇:脂质比例下,稳定性达到临界值,与完全交错一致。然而,在这个比例下,双层比完全交错厚约 20%。此外,丁醇插入诱导酰基链弯曲和增加无序性,在支撑脂质双层中实验测量的侧向扩散性增加了 27%。在丁醇处理的大单室脂质体中,还观察到单峰 Tm 降低。这两种行为都与交错凝胶不一致。因此,由于丁醇在磷脂头部堆积,丁醇在生理温度下仅导致部分交错。酰基尾部无序(即张开和弯曲)填充了随后的空隙。最后,丁醇使双层短路,并创建了一个交错和张开的磷脂共存的偶联系统。这些发现将为提高生物丁醇生产滴度的靶向双层稳定性的策略设计提供信息。

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