Novozymes A/S, Biologiens Vej 2, 2800, Kgs. Lyngby, Denmark.
Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet B220, 2800, Kgs. Lyngby, Denmark.
Microb Cell Fact. 2021 May 1;20(1):93. doi: 10.1186/s12934-021-01582-7.
Poly(ethylene terephthalate) (PET) is the world's most abundant polyester plastic, and its ongoing accumulation in nature is causing a global environmental problem. Currently, the main recycling processes utilize thermomechanical or chemical means, resulting in the deterioration of the mechanical properties of PET. Consequently, polluting de novo synthesis remains preferred, creating the need for more efficient and bio-sustainable ways to hydrolyze the polymer. Recently, a PETase enzyme from the bacterium Ideonella sakaiensis was shown to facilitate PET biodegradation, albeit at slow rate. Engineering of more efficient PETases is required for industrial relevance, but progress is currently hampered by the dependency on intracellular expression in Escherichia coli. To create a more efficient screening platform in E. coli, we explore different surface display anchors for fast and easy assaying of PETase activity. We show that PETases can be functionally displayed on the bacterial cell surface, enabling screening of enzyme activity on PET microparticles - both while anchored to the cell and following solubilization of the enzymes.
聚对苯二甲酸乙二醇酯(PET)是世界上最丰富的聚酯塑料,其在自然界中的不断积累正在造成全球性的环境问题。目前,主要的回收工艺利用热机械或化学手段,导致 PET 的机械性能恶化。因此,新的污染合成仍然是首选,这就需要更有效和生物可持续的方法来水解聚合物。最近,一种来自 Ideonella sakaiensis 细菌的 PETase 酶被证明可以促进 PET 的生物降解,尽管速度很慢。为了实现工业相关性,需要对更有效的 PETases 进行工程改造,但目前的进展受到在大肠杆菌中依赖细胞内表达的阻碍。为了在大肠杆菌中创建一个更有效的筛选平台,我们探索了不同的表面展示锚,以便快速、轻松地测定 PETase 活性。我们表明,PETases 可以在细菌细胞表面上进行功能展示,从而可以在 PET 微球上筛选酶活性,既可以在酶固定在细胞上时进行,也可以在酶溶解后进行。