Accumulation of ionic liquids in Escherichia coli cells

被引:67
作者
Cornmell, Robert J. [1 ]
Winder, Catherine L. [2 ]
Tiddy, Gordon J. T. [1 ]
Goodacre, Royston [2 ]
Stephens, Gill [1 ]
机构
[1] Univ Manchester, Manchester Interdisciplinary Bioctr, Sch Chem Engn & Analyt Sci, Manchester M1 7DN, Lancs, England
[2] Univ Manchester, Manchester Interdisciplinary Bioctr, Sch Chem, Manchester M1 7DN, Lancs, England
关键词
D O I
10.1039/b807214k
中图分类号
O6 [化学];
学科分类号
0703 [化学];
摘要
Ionic liquids accumulate within Escherichia coli cells and can be detected by Fourier transform infrared (FT-IR) spectroscopy. Harvested cells were incubated with the biocompatible, water-immiscible ionic liquids, trihexyltetradecylphosphonium bis(trifluoromethylsulfonyl) imide ([P-6,P-6,P-6,P-14][NTf2]) and methyltrioctylammonium bis(trifluoromethylsulfonyl) imide ([N-1,N-8,N-8,N-8][NTf2]), and with the toxic chlorides, [P-6,P-6,P-6,P-14][Cl] and [N-1,N-8,N-8,N-8][Cl]. The cells were harvested, washed and dried, and their FT-IR spectra were recorded. The ionic liquid spectra could be detected against the background spectra of the cells, demonstrating that they were accumulating within the cells. The toxic ionic liquids accumulated more rapidly than the biocompatible ionic liquids. Principal components analysis followed by discriminant function analysis showed that, compared to control cells, the toxic ionic liquids produced much bigger changes in the FT-IR fingerprint of the cellular chemicals than the biocompatible ionic liquids. Subcellular fractionation, followed by FT-IR analysis, demonstrated that [P-6,P-6,P-6,P-14][NTf2] accumulated specifically in the membrane fraction of the cells and not the cytoplasm.
引用
收藏
页码:836 / 841
页数:6
相关论文
共 36 条
[1]
[Anonymous], 1966, Multivariate Analysis
[2]
The complete genome sequence of Escherichia coli K-12 [J].
Blattner, FR ;
Plunkett, G ;
Bloch, CA ;
Perna, NT ;
Burland, V ;
Riley, M ;
ColladoVides, J ;
Glasner, JD ;
Rode, CK ;
Mayhew, GF ;
Gregor, J ;
Davis, NW ;
Kirkpatrick, HA ;
Goeden, MA ;
Rose, DJ ;
Mau, B ;
Shao, Y .
SCIENCE, 1997, 277 (5331) :1453-+
[3]
Biocatalysis in non-conventional media-ionic liquids, supercritical fluids and the gas [J].
Cantone, Sara ;
Hanefeld, Ulf ;
Basso, Alessandra .
GREEN CHEMISTRY, 2007, 9 (09) :954-971
[4]
Using a biphasic ionic liquid/water reaction system to improve oxygenase-catalysed biotransformation with whole cells [J].
Cornmell, Robert J. ;
Winder, Catherine L. ;
Schuler, Stephanie ;
Goodacre, Royston ;
Stephens, Gill .
GREEN CHEMISTRY, 2008, 10 (06) :685-691
[5]
Deetlefs M, 2006, CHIM OGGI, V24, P16
[6]
Measuring the metabolome: current analytical technologies [J].
Dunn, WB ;
Bailey, NJC ;
Johnson, HE .
ANALYST, 2005, 130 (05) :606-625
[7]
Metabolic fingerprinting in disease diagnosis: biomedical applications of infrared and Raman spectroscopy [J].
Ellis, David I. ;
Goodacre, Royston .
ANALYST, 2006, 131 (08) :875-885
[8]
Detection of the dipicolinic acid biomarker in Bacillus spores using Curie-point pyrolysis mass spectrometry and fourier transform infrared spectroscopy [J].
Goodacre, R ;
Shann, B ;
Gilbert, RJ ;
Timmins, ÉM ;
McGovern, AC ;
Alsberg, BK ;
Kell, DB ;
Logan, NA .
ANALYTICAL CHEMISTRY, 2000, 72 (01) :119-127
[10]
Metabolomics by numbers: acquiring and understanding global metabolite data [J].
Goodacre, R ;
Vaidyanathan, S ;
Dunn, WB ;
Harrigan, GG ;
Kell, DB .
TRENDS IN BIOTECHNOLOGY, 2004, 22 (05) :245-252