Enhanced degradation of phototreated recycled and unused low-density polyethylene films by Pleurotus ostreatus.

IF 4 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY World journal of microbiology & biotechnology Pub Date : 2024-08-24 DOI:10.1007/s11274-024-04116-6
Angel González-Márquez, Ariadna Denisse Andrade-Alvarado, Rosario González-Mota, Carmen Sánchez
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Abstract

Polyethylene, one of the most used petroleum-derived polymers, causes serious environmental pollution. The ability of Pleurotus ostreatus to degrade UV-treated and untreated recycled and unused (new) low-density polyethylene (LDPE) films was studied. We determined the fungal biomass production, enzyme production, and enzyme yield. Changes in the chemical structure and surface morphology of the LDPE after fungal growth were analyzed using FTIR spectroscopy and SEM. Functional group indices and contact angles were also evaluated. In general, the highest Lac (6013 U/L), LiP (2432 U/L), MnP (995 U/L) and UP (6671 U/L) activities were observed in irradiated recycled LDPE (IrRPE). The contact angle of all samples was negatively correlated with fermentation time; the smaller the contact angle, the longer the fermentation time, indicating effective biodegradation. The IrRPE samples exhibited the smallest contact angle (49°) at 4 weeks, and the samples were fragmented (into two pieces) at 5 weeks. This fungus could degrade unused (new) LDPE significantly within 6 weeks. The biodegradation of LDPE proceeded faster in recycled than in unused samples, which can be enhanced by exposing LDPE to UV radiation. Enzymatic production during fungal growth suggest that LDPE degradation is initiated by laccase (Lac) followed by lignin peroxidase (LiP), whereas manganese peroxidase (MnP) and unspecific peroxygenase (UP) are involved in the final degradation process. This is the first experimental study on the fungal growth and its main enzymes involved in LDPE biodegradation. This fungus has great promise as a safe, efficient, and environmentally friendly organism capable of degrading LDPE.

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褐藻对光照处理过的再生低密度聚乙烯薄膜和未使用过的低密度聚乙烯薄膜的降解作用增强。
聚乙烯是最常用的石油衍生聚合物之一,会造成严重的环境污染。我们研究了褐藻(Pleurotus ostreatus)降解紫外线处理过和未处理过的回收和未使用过的(新的)低密度聚乙烯(LDPE)薄膜的能力。我们测定了真菌的生物量产量、酶产量和产酶量。使用傅立叶变换红外光谱和扫描电镜分析了真菌生长后低密度聚乙烯化学结构和表面形态的变化。还对官能团指数和接触角进行了评估。一般来说,在辐照再生低密度聚乙烯(IrRPE)中观察到最高的 Lac(6013 U/L)、LiP(2432 U/L)、MnP(995 U/L)和 UP(6671 U/L)活性。所有样品的接触角与发酵时间呈负相关;接触角越小,发酵时间越长,表明生物降解效果越好。IrRPE 样品在 4 周时的接触角最小(49°),5 周时样品碎裂(分成两块)。这种真菌可在 6 周内显著降解未使用过的(新)低密度聚乙烯。低密度聚乙烯在回收样品中的生物降解速度比在未使用样品中快,将低密度聚乙烯置于紫外线辐射下可提高降解速度。真菌生长过程中产生的酶表明,低密度聚乙烯降解由漆酶(Lac)启动,然后是木质素过氧化物酶(LiP),而锰过氧化物酶(MnP)和非特异性过氧酶(UP)参与了最终降解过程。这是首次对真菌生长及其参与低密度聚乙烯生物降解的主要酶进行实验研究。这种真菌作为一种能够降解低密度聚乙烯的安全、高效和环境友好型生物,具有广阔的前景。
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来源期刊
World journal of microbiology & biotechnology
World journal of microbiology & biotechnology 工程技术-生物工程与应用微生物
CiteScore
6.30
自引率
2.40%
发文量
257
审稿时长
2.5 months
期刊介绍: World Journal of Microbiology and Biotechnology publishes research papers and review articles on all aspects of Microbiology and Microbial Biotechnology. Since its foundation, the Journal has provided a forum for research work directed toward finding microbiological and biotechnological solutions to global problems. As many of these problems, including crop productivity, public health and waste management, have major impacts in the developing world, the Journal especially reports on advances for and from developing regions. Some topics are not within the scope of the Journal. Please do not submit your manuscript if it falls into one of the following categories: · Virology · Simple isolation of microbes from local sources · Simple descriptions of an environment or reports on a procedure · Veterinary, agricultural and clinical topics in which the main focus is not on a microorganism · Data reporting on host response to microbes · Optimization of a procedure · Description of the biological effects of not fully identified compounds or undefined extracts of natural origin · Data on not fully purified enzymes or procedures in which they are applied All articles published in the Journal are independently refereed.
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