TY - JOUR
T1 - Swimming bacteria power microspin cycles
AU - Hamby, Alex E.
AU - Vig, Dhruv K.
AU - Safonova, Sasha
AU - Wolgemuth, Charles W.
N1 - Funding Information:
We thank R. Bourret for providing E. coli (RBB1050) and S. Parkinson, M. McEvoy, and M. Harman for useful discussions. This research was supported by NIH grant R01 GM072004 and NSF grant CMMI 1361987 (to C.W.W.), NIH training grant GM0884905 (to D.K.V.), and NIH training grant GM008659 (to A.E.H.).
Publisher Copyright:
Copyright © 2018 The Authors,
PY - 2018/12/19
Y1 - 2018/12/19
N2 - Dense suspensions of swimming bacteria are living fluids, an archetype of active matter. For example, Bacillus subtilis confined within a disc-shaped region forms a persistent stable vortex that counterrotates at the periphery. Here, we examined Escherichia coli under similar confinement and found that these bacteria, instead, form microspin cycles: a single vortex that periodically reverses direction on time scales of seconds. Using experimental perturbations of the confinement geometry, medium viscosity, bacterial length, density, and chemotaxis pathway, we show that morphological alterations of the bacteria transition a stable vortex into a periodically reversing one. We develop a mathematical model based on single-cell biophysics that quantitatively recreates the dynamics of these vortices and predicts that density gradients power the reversals. Our results define how microbial physics drives the active behavior of dense bacterial suspensions and may allow one to engineer novel micromixers for biomedical and other microfluidic applications.
AB - Dense suspensions of swimming bacteria are living fluids, an archetype of active matter. For example, Bacillus subtilis confined within a disc-shaped region forms a persistent stable vortex that counterrotates at the periphery. Here, we examined Escherichia coli under similar confinement and found that these bacteria, instead, form microspin cycles: a single vortex that periodically reverses direction on time scales of seconds. Using experimental perturbations of the confinement geometry, medium viscosity, bacterial length, density, and chemotaxis pathway, we show that morphological alterations of the bacteria transition a stable vortex into a periodically reversing one. We develop a mathematical model based on single-cell biophysics that quantitatively recreates the dynamics of these vortices and predicts that density gradients power the reversals. Our results define how microbial physics drives the active behavior of dense bacterial suspensions and may allow one to engineer novel micromixers for biomedical and other microfluidic applications.
UR - http://www.scopus.com/inward/record.url?scp=85058970314&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85058970314&partnerID=8YFLogxK
U2 - 10.1126/sciadv.aau0125
DO - 10.1126/sciadv.aau0125
M3 - Article
C2 - 30585288
AN - SCOPUS:85058970314
SN - 2375-2548
VL - 4
JO - Science advances
JF - Science advances
IS - 12
M1 - eaau0125
ER -