31 May 2021 to 4 June 2021
Europe/Berlin timezone

Self-assembly of Comamonas denitrificans: formation of a living bacterial gel

4 Jun 2021, 09:40
1h
Poster (+) Presentation (MS5) Biochemical processes and biofilms in porous media Poster +

Speaker

Sam Charlton (ETH Zurich)

Description

Bacterial autoaggregation is a phenomena widely exhibited by environmental and pathogenic bacterial species [1]. Autoaggregation is mediated through surface bound and secreted proteins and polysaccharides and can act as a precursor to surface bound biofilm formation. Aggregation is considered a survival strategy, commonly induced by unfavourable growth conditions and low metabolic activity [2]. Polymer bridging and depletion attraction have been demonstrated to trigger autoaggregation, typically forming structures of compact disconnected clusters [4, 5].

Comamonas denitrificans is a rod shaped filamentous bacterium found in abundance in wastewater environments which displays highly efficient denitrifying capabilities and exoelectrogenic activity in microbial fuel cells [6, 7, 8]. Our studies with this bacterium revealed autoaggregation which displays a distinct gelation phase transition at intermediate volume fractions (ϕ>0.008). In this work we apply multiscale techniques from the soft matter toolbox to investigate the aggregation kinetics of Comamonas denitrificans. For the first time we show that bacterial autoaggregation can lead to self-assembly of space spanning fractal networks akin to attractive colloidal gels. By altering dissolved oxygen conditions during cell culture, we are able to reliably tune cell aspect ratio distribution and gel porosity creating a controllable living colloidal system. Using optical microscopy, we study the aggregation dynamics of low and high aspect ratio distributions, in the presence and absence of bacterial growth and in density matched and mismatched conditions. We compare the bacterial gel dynamics against Brownian dynamics simulations to further access the impact of aspect ratio distribution on the bacterial gel connectivity and porosity, and consider the impact of uniform or polar bonding locations. This work is a first look into self-assembled bacterial ‘living gels’.

References

[1] T. Trunk, H. S. Khalil, and J. C. Leo, AIMS Microbiol., vol. 4, no. 1, pp. 140–164, 2018.
[2] J. Klebensberger, A. Birkenmaier, R. Geffers, S. Kjelleberg, and B. Philipp, Environ. Microbiol., vol. 11, no. 12, pp. 3073–3086, 2009.
[3] G. Dorken, G. P. Ferguson, C. E. French, and W. C. K. Poon, J. R. Soc. Interface, vol. 9, no. 77, pp. 3490–3502, 2012.
[4] N. Cohen, H. Zhou, A. G. Hay, and A. Radian, Colloids Surfaces B Biointerfaces, vol. 182, p. 110361, 2019.
[5] L. Laganenka, R. Colin, and V. Sourjik, Nat. Commun., vol. 7, no. 1, p. 12984, 2016.
[6] S. Andersson, G. Kuttuva Rajarao, C. J. Land, and G. Dalhammar, FEMS Microbiol. Lett., vol. 283, no. 1, pp. 83–90, 2008.
[7] D. Xing, S. Cheng, B. E. Logan, and J. M. Regan, Appl. Microbiol. Biotechnol., vol. 85, no. 5, pp. 1575–1587, 2010.
[8] L. Gumaelius, G. Magnusson, B. Pettersson, and G. Dalhammar, Int. J. Syst. Evol. Microbiol., vol. 51, no. 3, pp. 999–1006, 2001.

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Primary author

Sam Charlton (ETH Zurich)

Co-authors

Eleonora Secchi (ETH Zürich) Dr Gavin Melaugh (University of Edinburgh)

Presentation materials