Young Eric J, Burton Rodney, Mahalik Jyoti P, Sumpter Bobby G, Fuentes-Cabrera Miguel, Kerfeld Cheryl A, Ducat Daniel C
Biochemistry and Molecular Biology, Michigan State University, East LansingMI, United States.
MSU-DOE Plant Research Laboratory, East LansingMI, United States.
Front Microbiol. 2017 Jul 31;8:1441. doi: 10.3389/fmicb.2017.01441. eCollection 2017.
As synthetic biology advances the intricacy of engineered biological systems, the importance of spatial organization within the cellular environment must not be marginalized. Increasingly, biological engineers are investigating means to control spatial organization within the cell, mimicking strategies used by natural pathways to increase flux and reduce cross-talk. A modular platform for constructing a diverse set of defined, programmable architectures would greatly assist in improving yields from introduced metabolic pathways and increasing insulation of other heterologous systems. Here, we review recent research on the shell proteins of bacterial microcompartments and discuss their potential application as "building blocks" for a range of customized intracellular scaffolds. We summarize the state of knowledge on the self-assembly of BMC shell proteins and discuss future avenues of research that will be important to realize the potential of BMC shell proteins as predictively assembling and programmable biological materials for bioengineering.
随着合成生物学推动工程生物系统的复杂性不断提高,细胞环境中空间组织的重要性绝不能被忽视。越来越多的生物工程师正在研究控制细胞内空间组织的方法,模仿自然途径所采用的策略来提高通量并减少串扰。构建各种定义明确、可编程架构的模块化平台将极大地有助于提高引入的代谢途径的产量,并增强其他异源系统的隔离性。在此,我们综述了关于细菌微区室外壳蛋白的最新研究,并讨论了它们作为一系列定制细胞内支架“构建模块”的潜在应用。我们总结了BMC外壳蛋白自组装的知识现状,并讨论了未来重要的研究途径,这些途径对于实现BMC外壳蛋白作为用于生物工程的可预测组装和可编程生物材料的潜力至关重要。