Martínez-García Esteban, Fraile Sofía, Rodríguez Espeso David, Vecchietti Davide, Bertoni Giovanni, de Lorenzo Víctor
Systems Biology Program, Centro Nacional de Biotecnología (CNB-CSIC), Campus de Cantoblanco, 28049 Madrid, Spain.
Department of Biosciences, Università degli Studi di Milano, 20133 Milan, Italy.
ACS Synth Biol. 2020 Sep 18;9(9):2477-2492. doi: 10.1021/acssynbio.0c00272. Epub 2020 Aug 27.
Environmental bacteria are most often endowed with native surface-attachment programs that frequently conflict with efforts to engineer biofilms and synthetic communities with given tridimensional architectures. In this work, we report the editing of the genome of KT2440 for stripping the cells of most outer-facing structures of the bacterial envelope that mediate motion, binding to surfaces, and biofilm formation. To this end, 23 segments of the chromosome encoding a suite of such functions were deleted, resulting in the surface-naked strain EM371, the physical properties of which changed dramatically in respect to the wild type counterpart. As a consequence, surface-edited cells were unable to form biofilms on solid supports and, because of the swimming deficiency and other alterations, showed a much faster sedimentation in liquid media. Surface-naked bacteria were then used as carriers of interacting partners (e.g., Jun-Fos domains) ectopically expressed by means of an autotransporter display system on the now easily accessible cell envelope. Abstraction of individual bacteria as adhesin-coated spherocylinders enabled rigorous quantitative description of the multicell interplay brought about by thereby engineered physical interactions. The model was then applied to parametrize the data extracted from automated analysis of confocal microscopy images of the experimentally assembled bacterial flocks for analyzing their structure and distribution. The resulting data not only corroborated the value of EM371 over the parental strain as a platform for display artificial adhesins but also provided a strategy for rational engineering of catalytic communities.
环境细菌通常具有天然的表面附着程序,这些程序常常与构建具有特定三维结构的生物膜和合成群落的努力相冲突。在这项工作中,我们报告了对KT2440基因组的编辑,以去除细菌包膜中大多数介导运动、与表面结合和生物膜形成的最外层结构。为此,删除了编码一系列此类功能的23个染色体片段,产生了表面裸露的菌株EM371,其物理性质相对于野生型对应物发生了巨大变化。因此,表面编辑的细胞无法在固体支持物上形成生物膜,并且由于游动缺陷和其他改变,在液体培养基中沉降速度快得多。然后,表面裸露的细菌被用作相互作用伙伴(例如Jun-Fos结构域)的载体,这些伙伴通过自转运体展示系统在现在易于接近的细胞包膜上异位表达。将单个细菌抽象为粘附素包被的球圆柱体,能够对由此设计的物理相互作用所带来的多细胞相互作用进行严格的定量描述。然后应用该模型对从实验组装的细菌群的共聚焦显微镜图像自动分析中提取的数据进行参数化,以分析它们的结构和分布。所得数据不仅证实了EM371作为展示人工粘附素平台相对于亲本菌株的价值,还提供了一种合理设计催化群落的策略。