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@ARTICLE{Krmer:256486,
author = {Krämer, Christina E. M. and Singh, Abhijeet and Helfrich,
Stefan and Grünberger, Alexander and Wiechert, Wolfgang and
Nöh, Katharina and Kohlheyer, Dietrich},
title = {{N}on-{I}nvasive {M}icrobial {M}etabolic {A}ctivity
{S}ensing at {S}ingle {C}ell {L}evel by {P}erfusion of
{C}alcein {A}cetoxymethyl {E}ster},
journal = {PLoS one},
volume = {10},
number = {10},
issn = {1932-6203},
address = {Lawrence, Kan.},
publisher = {PLoS},
reportid = {FZJ-2015-06382},
pages = {e0141768},
year = {2015},
abstract = {Phase contrast microscopy cannot give sufficient
information on bacterial metabolic activity, or if a cell is
dead, it has the fate to die or it is in a viable but
non-growing state. Thus, a reliable sensing of the metabolic
activity helps to distinguish different categories of
viability. We present a non-invasive instantaneous sensing
method using a fluorogenic substrate for online monitoring
of esterase activity and calcein efflux changes in growing
wild type bacteria. The fluorescent conversion product of
calcein acetoxymethyl ester (CAM) and its efflux indicates
the metabolic activity of cells grown under different
conditions at real-time. The dynamic conversion of CAM and
the active efflux of fluorescent calcein were analyzed by
combining microfluidic single cell cultivation technology
and fluorescence time lapse microscopy. Thus, an
instantaneous and non-invasive sensing method for apparent
esterase activity was created without the requirement of
genetic modification or harmful procedures. The metabolic
activity sensing method consisting of esterase activity and
calcein secretion was demonstrated in two applications.
Firstly, growing colonies of our model organism
Corynebacterium glutamicum were confronted with intermittent
nutrient starvation by interrupting the supply of iron and
carbon, respectively. Secondly, bacteria were exposed for
one hour to fatal concentrations of antibiotics. Bacteria
could be distinguished in growing and non-growing cells with
metabolic activity as well as non-growing and
non-fluorescent cells with no detectable esterase activity.
Microfluidic single cell cultivation combined with high
temporal resolution time-lapse microscopy facilitated
monitoring metabolic activity of stressed cells and
analyzing their descendants in the subsequent recovery
phase. Results clearly show that the combination of CAM with
a sampling free microfluidic approach is a powerful tool to
gain insights in the metabolic activity of growing and
non-growing bacteria.},
cin = {IBG-1},
ddc = {500},
cid = {I:(DE-Juel1)IBG-1-20101118},
pnm = {581 - Biotechnology (POF3-581)},
pid = {G:(DE-HGF)POF3-581},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000363920300081},
doi = {10.1371/journal.pone.0141768},
url = {https://juser.fz-juelich.de/record/256486},
}