TY - JOUR
T1 - Response of microbial membranes to butanol
T2 - Interdigitation: vs. Disorder
AU - Guo, Jingjing
AU - Ho, James C.S.
AU - Chin, Hokyun
AU - Mark, Alan E.
AU - Zhou, Cheng
AU - Kjelleberg, Staffan
AU - Liedberg, Bo
AU - Parikh, Atul N.
AU - Cho, Nam Joon
AU - Hinks, Jamie
AU - Mu, Yuguang
AU - Seviour, Thomas
N1 - Publisher Copyright:
© 2019 the Owner Societies.
PY - 2019
Y1 - 2019
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85067114154&partnerID=8YFLogxK
U2 - 10.1039/c9cp01469a
DO - 10.1039/c9cp01469a
M3 - Article
C2 - 31125035
AN - SCOPUS:85067114154
SN - 1463-9076
VL - 21
SP - 11903
EP - 11915
JO - Physical Chemistry Chemical Physics
JF - Physical Chemistry Chemical Physics
IS - 22
ER -