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Di-(2-ethylhexyl) phthalate-degrading functional microorganisms were identified in black soil based on high throughput analysis

基因组 放线菌门 邻苯二甲酸盐 微生物 蛋白质细菌 微生物种群生物学 土壤水分 微生物降解 降级(电信) 环境化学 生物 土壤微生物学 污染物 微生物群 丰度(生态学) 生物强化 微生物代谢 环境科学 土工试验 生态学 污染 鞘脂单胞菌属 土壤污染物 土壤污染 功能多样性 相对物种丰度 土壤分类 微塑料 土壤有机质
作者
Wenli Zhang,Heqi Guo,Weihui Xu,Wenjing Chen,Yunlong Hu,Zhigang Wang
出处
期刊:Current research in microbial sciences [Elsevier BV]
卷期号:9: 100479-100479
标识
DOI:10.1016/j.crmicr.2025.100479
摘要

• Through high-throughput sequencing and analysis of multiple soil genomes, functional microorganisms involved in DEHP degradation were elucidated. • The combination of soil extract and inorganic salt medium was used to screen DEHP-degrading bacterial communities with good degradability, which was consistent with the bioinformatics data. Di-(2-ethylhexyl) phthalate (DEHP) has become an increasingly serious pollutant in soils. Microbial degradation represents a highly promising approach for its remediation. In this study, four black soils were used to simulate the natural degradation of DEHP over a 75-day microenvironmental experiment. High-throughput analysis was conducted to investigate the distribution and abundance of functional genes in soil microorganisms, aiming to explore functional microbial information. The degradation efficiency of DEHP in black soils was 76.37%, 74.16%, 92.21%, and 75.35%. The α-diversity of microbial community was positively correlated with the degradation rate. Actinobacteria and Proteobacteria exhibited sensitivity to DEHP contamination. Xanthomonaceae, Sphingomonadaceae, Hypomicrobiaceae, and Comamonadaceae contributed to the upstream metabolism of DEHP. The abundances of Rhodococcus, Sphingomonas, Nocardioides , and Arthrobacter were positively correlated with the abundance of functional genes enriched in the black soil for benzoate degradation. Concurrently, 10 DEHP-degrading bacterial communities were identified, and the taxonomic and functional profiles of certain members within these communities were consistent with the metagenomic data. Bacterial communities JQ104, JQ52, and JQ129 degraded more than 98% of DEHP (400 mg/L) in 48 h, demonstrating remarkable degradation efficiency. This study demonstrated the dynamic impact of the indigenous microbiome on DEHP contamination and verified the degradation capabilities of key functional microorganisms.

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