Taxeidis George, Nikolaivits Efstratios, Siaperas Romanos, Gkountela Christina, Vouyiouka Stamatina, Pantelic Brana, Nikodinovic-Runic Jasmina, Topakas Evangelos
Industrial Biotechnology & Biocatalysis Group, Biotechnology Laboratory, School of Chemical Engineering, National Technical University of Athens, Athens, Greece.
Laboratory of Polymer Technology, School of Chemical Engineering, National Technical University of Athens, Athens, Greece.
Environ Pollut. 2023 May 15;325:121460. doi: 10.1016/j.envpol.2023.121460. Epub 2023 Mar 20.
The uncontrollable disposal of plastic waste has raised the concern of the scientific community, which tries to face this environmental burden by discovering and applying new techniques. Regarding the biotechnology field, several important microorganisms possessing the necessary enzymatic arsenal to utilize recalcitrant synthetic polymers as an energy source have been discovered. In the present study, we screened various fungi for their ability to degrade intact polymers, such as ether-based polyurethane (PU) and low-density polyethylene (LDPE). For this, ImpranIil® DLN-SD and a mixture of long-chain alkanes were used as sole carbon sources, indicating not only the most promising strains in agar plate screening but also inducing the secretion of depolymerizing enzymatic activities, useful for polymer degradation. The agar plate screening revealed three fungal strains belonging to Fusarium and Aspergillus genera, whose secretome was further studied for its ability to degrade the aforementioned non-treated polymers. Specifically for ether-based PU, the secretome of a Fusarium species reduced the sample mass and the average molecular weight of the polymer by 24.5 and 20.4%, respectively, while the secretome of an Aspergillus species caused changes in the molecular structure of LDPE, as evidenced by FTIR. The proteomics analysis revealed that the enzymatic activities induced in presence of Impranil® DLN-SD can be associated with urethane bond cleavage, a fact which was also supported by the observed degradation of the ether-based PU. Although, the mechanism of LDPE degradation was not completely elucidated, the presence of oxidative enzymes could be the main factor contributing to polymer modification.
塑料垃圾的无节制处理引发了科学界的关注,科学界试图通过发现和应用新技术来应对这一环境负担。在生物技术领域,已经发现了几种重要的微生物,它们拥有必要的酶库,能够将难降解的合成聚合物作为能源加以利用。在本研究中,我们筛选了各种真菌,以评估它们降解完整聚合物的能力,如醚基聚氨酯(PU)和低密度聚乙烯(LDPE)。为此,使用了ImpranIil® DLN-SD和长链烷烃混合物作为唯一碳源,这不仅表明了在琼脂平板筛选中最有前景的菌株,还诱导了可用于聚合物降解的解聚酶活性的分泌。琼脂平板筛选揭示了三种属于镰刀菌属和曲霉属的真菌菌株,对其分泌组降解上述未处理聚合物的能力进行了进一步研究。具体而言,对于醚基PU,一种镰刀菌属物种的分泌组使聚合物的样品质量和平均分子量分别降低了24.5%和20.4%,而一种曲霉属物种的分泌组导致了LDPE分子结构的变化,傅里叶变换红外光谱(FTIR)证明了这一点。蛋白质组学分析表明,在ImpranIil® DLN-SD存在下诱导的酶活性可能与氨基甲酸酯键的断裂有关,醚基PU的降解也证实了这一事实。尽管LDPE降解的机制尚未完全阐明,但氧化酶的存在可能是导致聚合物改性的主要因素。