Center of Biophysics and Quantitative Biology, University of Illinois Urbana-Champaign, Urbana, Illinois 61801, United States.
Department of Bioengineering, University of Illinois Urbana-Champaign, Urbana, Illinois 61801, United States.
ACS Synth Biol. 2022 Nov 18;11(11):3714-3723. doi: 10.1021/acssynbio.2c00322. Epub 2022 Nov 6.
One important direction of synthetic biology is to establish desired spatial structures from microbial populations. Underlying this structural development process are different driving factors, among which bacterial motility and chemotaxis serve as a major force. Here, we present an individual-based, biophysical computational framework for mechanistic and multiscale simulation of the spatiotemporal dynamics of motile and chemotactic microbial populations. The framework integrates cellular movement with spatial population growth, mechanical and chemical cellular interactions, and intracellular molecular kinetics. It is validated by a statistical comparison of single-cell chemotaxis simulations with reported experiments. The framework successfully captures colony range expansion of growing isogenic populations and also reveals chemotaxis-modulated, spatial patterns of a two-species amensal community. Partial differential equation-based models subsequently validate these simulation findings. This study provides a versatile computational tool to uncover the fundamentals of microbial spatial ecology as well as to facilitate the design of synthetic consortia for desired spatial patterns.
合成生物学的一个重要方向是从微生物群体中建立所需的空间结构。在这个结构发展过程的背后是不同的驱动因素,其中细菌的运动和趋化性起着主要作用。在这里,我们提出了一个基于个体的、生物物理的计算框架,用于对运动和趋化微生物群体的时空动力学进行机制和多尺度模拟。该框架将细胞运动与空间种群增长、机械和化学细胞相互作用以及细胞内分子动力学结合起来。通过对单细胞趋化性模拟与报道实验的统计比较进行验证。该框架成功地捕获了生长同基因群体的菌落范围扩展,还揭示了趋化调节的两种共生群落的空间模式。基于偏微分方程的模型随后验证了这些模拟结果。这项研究提供了一个通用的计算工具,用于揭示微生物空间生态学的基本原理,并有助于设计用于所需空间模式的合成联合体。