Department of Civil and Environmental Engineering, McCormick School of Engineering and Applied Science, Northwestern University, Evanston, Illinois 60208, United States.
Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.
Environ Sci Technol. 2024 Oct 29;58(43):19338-19352. doi: 10.1021/acs.est.4c06645. Epub 2024 Oct 3.
bacteria are enriched on poly(ethylene terephthalate) (PET) microplastics in wastewaters and urban rivers, but the PET-degrading mechanisms remain unclear. Here, we investigated these mechanisms with KF-1, a wastewater isolate, by combining microscopy, spectroscopy, proteomics, protein modeling, and genetic engineering. Compared to minor dents on PET films, scanning electron microscopy revealed significant fragmentation of PET pellets, resulting in a 3.5-fold increase in the abundance of small nanoparticles (<100 nm) during 30-day cultivation. Infrared spectroscopy captured primarily hydrolytic cleavage in the fragmented pellet particles. Solution analysis further demonstrated double hydrolysis of a PET oligomer, bis(2-hydroxyethyl) terephthalate, to the bioavailable monomer terephthalate. Supplementation with acetate, a common wastewater co-substrate, promoted cell growth and PET fragmentation. Of the multiple hydrolases encoded in the genome, intracellular proteomics detected only one, which was found in both acetate-only and PET-only conditions. Homology modeling of this hydrolase structure illustrated substrate binding analogous to reported PET hydrolases, despite dissimilar sequences. Mutants lacking this hydrolase gene were incapable of PET oligomer hydrolysis and had a 21% decrease in PET fragmentation; re-insertion of the gene restored both functions. Thus, we have identified constitutive production of a key PET-degrading hydrolase in wastewater , which could be exploited for plastic bioconversion.
细菌在废水中和城市河流中的聚对苯二甲酸乙二醇酯 (PET) 微塑料上富集,但 PET 降解机制仍不清楚。在这里,我们通过将显微镜、光谱学、蛋白质组学、蛋白质建模和基因工程相结合,研究了废水分离株 KF-1 的这些机制。与 PET 薄膜上的小凹痕相比,扫描电子显微镜显示 PET 颗粒明显碎裂,导致在 30 天培养过程中小纳米颗粒(<100nm)的丰度增加了 3.5 倍。红外光谱主要捕获了碎裂颗粒中的水解裂解。溶液分析进一步证明了 PET 低聚物双(2-羟乙基)对苯二甲酸酯的双水解作用,生成可利用的单体对苯二甲酸。补充废水中常见的共基质乙酸盐可促进细胞生长和 PET 碎裂。在基因组中编码的多种水解酶中,细胞内蛋白质组学仅检测到一种,该酶在仅含乙酸盐和仅含 PET 的条件下均存在。该水解酶结构的同源建模说明了尽管序列不同,但与报道的 PET 水解酶类似的底物结合。缺乏该水解酶基因的突变体无法水解 PET 低聚物,PET 碎裂减少 21%;重新插入该基因恢复了这两种功能。因此,我们已经确定了在废水中持续产生关键的 PET 降解水解酶,这可能被用于塑料生物转化。