Weinberger Simone, Beyer Reinhard, Schüller Christoph, Strauss Joseph, Pellis Alessandro, Ribitsch Doris, Guebitz Georg M
Department of Agrobiotechnology, Institute of Environmental Biotechnology, University of Natural Resources and Life Sciences, Vienna, Austria.
Austrian Center of Industrial Biotechnology (ACIB), Tulln an der Donau, Austria.
Front Microbiol. 2020 Apr 24;11:554. doi: 10.3389/fmicb.2020.00554. eCollection 2020.
There is a strong need for novel and more efficient polyester hydrolyzing enzymes in order to enable the development of more environmentally friendly plastics recycling processes allowing the closure of the carbon cycle. In this work, a high throughput system on microplate scale was used to screen a high number of fungi for their ability to produce polyester-hydrolyzing enzymes. For induction of responsible enzymes, the fungi were cultivated in presence of aliphatic and aromatic polyesters [poly(1,4-butylene adipate terephthalate) (PBAT), poly(lactic acid) (PLA) and poly(1,4-butylene succinate) (PBS)], and the esterase activity in the culture supernatants was compared to the culture supernatants of fungi grown without polymers. The results indicate that the esterase activity of the culture supernatants was induced in about 10% of the tested fungi when grown with polyesters in the medium, as indicated by increased activity (to >50 mU/mL) toward the small model substrate -nitrophenylbutyrate (pNPB). Incubation of these 50 active culture supernatants with different polyesters (PBAT, PLA, PBS) led to hydrolysis of at least one of the polymers according to liquid chromatography-based quantification of the hydrolysis products terephthalic acid, lactic acid and succinic acid, respectively. Interestingly, the specificities for the investigated polyesters varied among the supernatants of the different fungi.
为了开发更环保的塑料回收工艺以实现碳循环的闭合,对新型且更高效的聚酯水解酶有强烈需求。在这项工作中,使用了一种微孔板规模的高通量系统来筛选大量真菌产生聚酯水解酶的能力。为了诱导相关酶的产生,将真菌在脂肪族和芳香族聚酯[聚(1,4 - 丁二醇己二酸对苯二甲酸酯)(PBAT)、聚乳酸(PLA)和聚(1,4 - 丁二醇琥珀酸酯)(PBS)]存在的情况下进行培养,并将培养上清液中的酯酶活性与在无聚合物条件下生长的真菌的培养上清液进行比较。结果表明,当在培养基中与聚酯一起生长时,约10%的受试真菌培养上清液中的酯酶活性被诱导,这表现为对小模型底物对硝基苯丁酸酯(pNPB)的活性增加(至>50 mU/mL)。根据基于液相色谱对水解产物对苯二甲酸、乳酸和琥珀酸的定量分析,将这50种活性培养上清液与不同聚酯(PBAT、PLA、PBS)一起孵育导致至少一种聚合物发生水解。有趣的是,不同真菌的上清液对所研究聚酯的特异性各不相同。