The complex and dynamic compositions of biofilms, along
with their
sophisticated structural assembly mechanisms, endow them with exceptional
capabilities to thrive in diverse conditions that are typically unfavorable
for individual cells. Characterizing biofilms in their native state
is significantly challenging due to their intrinsic complexities and
the limited availability of noninvasive techniques. Here, we utilized
solid-state nuclear magnetic resonance (NMR) spectroscopy to analyze Bacillus subtilis biofilms in-depth. Our data uncover
a dynamically distinct organization within the biofilm: a dominant,
hydrophilic, and mobile framework interspersed with minor, rigid cores
of limited water accessibility. In these heterogeneous rigid cores,
the major components are largely self-assembled. TasA fibers, the
most robust elements, further provide a degree of mechanical support
for the cell aggregates and some lipid vesicles. Notably, rigid cell
aggregates can persist even without the major extracellular polymeric
substance (EPS) polymers, although this leads to slight variations
in their rigidity and water accessibility. Exopolysaccharides are
exclusively present in the mobile domain, playing a pivotal role in
its water retention property. Specifically, all water molecules are
tightly bound within the biofilm matrix. These findings reveal a dual-layered
defensive strategy within the biofilm: a diffusion barrier through
limited water mobility in the mobile phase and a physical barrier
posed by limited water accessibility in the rigid phase. Complementing
these discoveries, our comprehensive, in situ compositional
analysis is not only essential for delineating the sophisticated biofilm
architecture but also reveals the presence of alternative genetic
mechanisms for synthesizing exopolysaccharides beyond the known pathway