MOE Lab for Bioinformatics, Center for Synthetic and Systems Biology, School of Life Sciences, Tsinghua-Peking Center for Life Sciences, Tsinghua University, Beijing 100084, China.
MOE Lab for Bioinformatics, Center for Synthetic and Systems Biology, School of Life Sciences, Tsinghua-Peking Center for Life Sciences, Tsinghua University, Beijing 100084, China; Center for Nano and Micro Mechanics, Tsinghua University, Beijing 100084, China; MOE Key Lab for Industrial Biocatalysis, Tsinghua University, Beijing 100084, China; Manchester Institute of Biotechnology, University of Manchester, 131 Princess Street, Manchester M1 7DN, UK.
Metab Eng. 2018 Jan;45:32-42. doi: 10.1016/j.ymben.2017.11.010. Epub 2017 Nov 24.
The rigidity of bacterial cell walls synthesized by a complicated pathway limit the cell shapes as coccus, bar or ellipse or even fibers. A less rigid bacterium could be beneficial for intracellular accumulation of poly-3-hydroxybutyrate (PHB) as granular inclusion bodies. To understand how cell rigidity affects PHB accumulation, E. coli cell wall synthesis pathway was reinforced and weakened, respectively. Cell rigidity was achieved by thickening the cell walls via insertion of a constitutive gltA (encoding citrate synthase) promoter in front of a series of cell wall synthesis genes on the chromosome of several E. coli derivatives, resulting in 1.32-1.60 folds increase of Young's modulus in mechanical strength for longer E. coli cells over-expressing fission ring FtsZ protein inhibiting gene sulA. Cell rigidity was weakened by down regulating expressions of ten genes in the cell wall synthesis pathway using CRISPRi, leading to elastic cells with more spaces for PHB accumulation. The regulation on cell wall synthesis changes the cell rigidity: E. coli with thickened cell walls accumulated only 25% PHB while cell wall weakened E. coli produced 93% PHB. Manipulation on cell wall synthesis mechanism adds another possibility to morphology engineering of microorganisms.
细菌细胞壁的刚性由复杂途径合成,限制了细胞形状为球菌、棒状或椭圆形,甚至是纤维状。刚性较低的细菌可能有利于多聚 3-羟基丁酸酯 (PHB) 作为颗粒状包涵体的细胞内积累。为了了解细胞刚性如何影响 PHB 的积累,分别增强和削弱了大肠杆菌细胞壁的合成途径。通过在大肠杆菌衍生菌的染色体上一系列细胞壁合成基因的前面插入组成型 gltA(编码柠檬酸合酶)启动子,使细胞壁变厚,从而实现细胞刚性,导致过度表达分裂环 FtsZ 蛋白抑制基因 sulA 的大肠杆菌细胞的杨氏模量在机械强度上增加 1.32-1.60 倍。通过使用 CRISPRi 下调细胞壁合成途径中的十个基因的表达,削弱了细胞刚性,导致具有更多 PHB 积累空间的弹性细胞。细胞壁合成的调节改变了细胞的刚性:细胞壁变厚的大肠杆菌仅积累了 25%的 PHB,而细胞壁削弱的大肠杆菌产生了 93%的 PHB。对细胞壁合成机制的操纵为微生物的形态工程增加了另一种可能性。