Monitoring single cell bioenergetic status and cell lysis in dense and differentiating Bacillus subtilis cultures
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Bacillus subtilis is a major model organism for studying population heterogeneity in clonal bacterial cultures due to its high genetic tractability and ability to differentiate into subpopulations with distinct biological functions. It is also a key industrial production host, responsible for synthesizing a range of commercially valuable enzymes and metabolites. However, cell differentiation processes can pose a challenge for the optimal biotechnological utilization of B. subtilis , particularly when emerging subpopulations do not contribute to product biosynthesis. Here, we present robust assays that facilitate the analysis of two previously difficult-to-study population properties of B. subtilis : (i) the energization levels of individual cells within dense cultures and (ii) the extent of cell lysis that can occur under such conditions. Our findings reveal an unappreciated level of heterogeneity in cell energization within dense B. subtilis cultures, and a surprisingly high degree of cell lysis in seemingly healthy, actively growing populations. These insights add to our understanding of the biological complexities and single-cell heterogeneities present in superficially simple bacterial clonal cultures, establish analytical tools to study the associated processes, and provide a foundation for further optimizing B. subtilis as an industrial production host.
IMPORTANCE
Bacillus subtilis and its close relatives are important industrial microorganisms, responsible for the production of a range of commercially valuable enzymes, antibiotics and metabolites. In recent years, considerable research efforts have been aimed at increasing the productivity of these organisms. However, their ability to undergo physiological and morphological differentiation processes at high cell densities ultimately limits their productivity. Our research reveals how the resulting heterogeneity impacts the population-level energy status of individual cells in the culture and the surprisingly high extent of population-level cell lysis. It also provides tools for determining these important productivity criteria as well as guiding the development of the production host.
