Deoxyribonucleic
acid (DNA) evolved as a tool for storing and transmitting
genetic information within cells, but outside the cell, DNA can also
serve as “construction material” present in microbial
biofilms or various body fluids, such as cystic fibrosis, sputum,
and pus. In the present work, we investigate the mechanics of biofilms
formed from Pseudomonas aeruginosa Xen
5, Staphylococcus aureus Xen 30, and Candida albicans 1408 using oscillatory shear rheometry
at different levels of compression and recreate these mechanics in
systems of entangled DNA and cells. The results show that the compression-stiffening
and shear-softening effects observed in biofilms can be reproduced
in DNA networks with the addition of an appropriate number of microbial
cells. Additionally, we observe that these effects are cell-type dependent.
We also identify other mechanisms that may significantly impact the
viscoelastic behavior of biofilms, such as the compression-stiffening
effect of DNA cross-linking by bivalent cations (Mg2+,
Ca2+, and Cu2+) and the stiffness-increasing
interactions of P. aeruginosa Xen 5
biofilm with Pf1 bacteriophage produced by P. aeruginosa. This work extends the knowledge of biofilm mechanobiology and demonstrates
the possibility of modifying biopolymers toward obtaining the desired
biophysical properties.