Issue 22, 2019

Response of microbial membranes to butanol: interdigitation vs. disorder

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.

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

Supplementary files

Article information

Article type
Paper
Submitted
15 Mar 2019
Accepted
07 May 2019
First published
08 May 2019

Phys. Chem. Chem. Phys., 2019,21, 11903-11915

Response of microbial membranes to butanol: interdigitation vs. disorder

J. Guo, J. C. S. Ho, H. Chin, A. E. Mark, C. Zhou, S. Kjelleberg, B. Liedberg, A. N. Parikh, N. Cho, J. Hinks, Y. Mu and T. Seviour, Phys. Chem. Chem. Phys., 2019, 21, 11903 DOI: 10.1039/C9CP01469A

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