TY - JOUR
T1 - Listeria monocytogenes cell wall constituents exert a charge effect on electroporation threshold
AU - Golberg, Alex
AU - Rae, Chris S.
AU - Rubinsky, Boris
N1 - Funding Information:
We thank Prof. Daniel Portnoy from UC Berkeley for providing assistance concerning the microbiological aspects of this project. The work was partly supported by NIH grants PO1 A1063302 and PO1 A127655 to DP. AG and BR acknowledge AngioDynamics Inc. for the gift supporting the electroporation research.
PY - 2012/3
Y1 - 2012/3
N2 - Genetically engineered cells with mutations of relevance to electroporation, cell membrane permeabilization by electric pulses, can become a promising new tool for fundamental research on this important biotechnology. Listeria monocytogenes mutants lacking DltA or MprF and assayed for sensitivity to the cathelicidin like anti-microbial cationic peptide (mCRAMP), were developed to study the effect of cell wall charge on electroporation. Working in the irreversible electroporation regime (IRE), we found that application of a sequence of 50 pulses, each 50 μs duration, 12.5 kV/cm field, delivered at 2 Hz led to 2.67 ± 0.29 log reduction in wild-type L. monocytogenes, log 2.60 ± 0.19 in the MprF-minus mutant, and log 1.33 ± 0.13 in the DltA-minus mutant. The experimental observation that the DltA-minus mutant was highly susceptible to cationic mCRAMP and resistant to IRE suggests that the charge on the bacterial cell wall affects electroporation and shows that this approach may be promising for fundamental studies on electroporation.
AB - Genetically engineered cells with mutations of relevance to electroporation, cell membrane permeabilization by electric pulses, can become a promising new tool for fundamental research on this important biotechnology. Listeria monocytogenes mutants lacking DltA or MprF and assayed for sensitivity to the cathelicidin like anti-microbial cationic peptide (mCRAMP), were developed to study the effect of cell wall charge on electroporation. Working in the irreversible electroporation regime (IRE), we found that application of a sequence of 50 pulses, each 50 μs duration, 12.5 kV/cm field, delivered at 2 Hz led to 2.67 ± 0.29 log reduction in wild-type L. monocytogenes, log 2.60 ± 0.19 in the MprF-minus mutant, and log 1.33 ± 0.13 in the DltA-minus mutant. The experimental observation that the DltA-minus mutant was highly susceptible to cationic mCRAMP and resistant to IRE suggests that the charge on the bacterial cell wall affects electroporation and shows that this approach may be promising for fundamental studies on electroporation.
KW - Electroporation threshold
KW - Irreversible electroporation
KW - Lipoteichoic acid
KW - Listeria monocytogenes
KW - Membrane charge
UR - http://www.scopus.com/inward/record.url?scp=84855719944&partnerID=8YFLogxK
U2 - 10.1016/j.bbamem.2011.11.003
DO - 10.1016/j.bbamem.2011.11.003
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AN - SCOPUS:84855719944
SN - 0005-2736
VL - 1818
SP - 689
EP - 694
JO - Biochimica et Biophysica Acta - Biomembranes
JF - Biochimica et Biophysica Acta - Biomembranes
IS - 3
ER -