Yin Chao-Fan, Pan Piaopiao, Li Tao, Song Xin, Xu Ying, Zhou Ning-Yi
State Key Laboratory of Microbial Metabolism, Joint International Research Laboratory of Metabolic & Developmental Sciences, and School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, 200240, China.
State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing, 211135, China.
Microbiome. 2025 Mar 7;13(1):68. doi: 10.1186/s40168-025-02065-2.
Acetaminophen, a widely used analgesic and antipyretic drug, has become a significant aquatic micro-pollutant due to its extensive global production and increased consumption, particularly during the COVID-19 pandemic. Its high-water solubility leads to its pervasive presence in wastewater treatment plants (WWTPs), posing substantial risks to the environment and human health. Biological treatment is one of the promising approaches to remove such pollutants. Although previous studies have isolated acetaminophen-degrading pure cultures and proposed catabolic pathways, the interactions between microbiotas and acetaminophen, the distribution feature of acetaminophen degradation genes, and the gene-driven fate of acetaminophen in the real-world environment remain largely unexplored.
Among the water samples from 20 WWTPs across China, acetaminophen was detected from 19 samples at concentrations ranging from 0.06 to 29.20 nM. However, p-aminophenol, a more toxic metabolite, was detected in all samples at significantly higher concentrations (23.93 to 108.68 nM), indicating the presence of a catabolic bottleneck in WWTPs. Metagenomic analysis from both the above 20 samples and global datasets revealed a consistently higher abundance of initial acetaminophen amidases compared to downstream enzymes, potentially having explained the reason for the bottleneck. Meanwhile, a close correlation between initial amidases and Actinomycetota revealed by genome-based taxonomy suggests a species-dependent degradation pattern. Additionally, a distinct amidase ApaA was characterized by newly isolated Rhodococcus sp. NyZ502 (Actinomycetota), represents a predominant category of amidase in WWTPs. Significant phylogenetic and structural diversity observed among putative amidases suggest versatile acetaminophen hydrolysis potential in WWTPs.
This study enhances our understanding of acetaminophen's environmental fate and highlights the possible occurrence of ecological risks driven by imbalanced genes in the process of acetaminophen degradation in global WWTPs. Video Abstract.
对乙酰氨基酚是一种广泛使用的解热镇痛药,由于其全球产量的大幅增长以及消费量的增加,尤其是在新冠疫情期间,它已成为一种重要的水生微污染物。其高水溶性导致它在污水处理厂中普遍存在,对环境和人类健康构成重大风险。生物处理是去除此类污染物的一种有前景的方法。尽管先前的研究已经分离出降解对乙酰氨基酚的纯培养物并提出了分解代谢途径,但微生物群与对乙酰氨基酚之间的相互作用、对乙酰氨基酚降解基因的分布特征以及在现实环境中基因驱动的对乙酰氨基酚归宿仍 largely 未被探索。
在中国 20 个污水处理厂的水样中,19 个样本检测到了对乙酰氨基酚,浓度范围为 0.06 至 29.20 nM。然而,在所有样本中均检测到了毒性更强的代谢产物对氨基苯酚,其浓度显著更高(23.93 至 108.68 nM),这表明污水处理厂中存在分解代谢瓶颈。对上述 20 个样本以及全球数据集的宏基因组分析表明,与下游酶相比,初始对乙酰氨基酚酰胺酶的丰度始终更高,这可能解释了瓶颈产生的原因。同时,基于基因组的分类学显示初始酰胺酶与放线菌门之间存在密切相关性,这表明存在物种依赖性降解模式。此外,新分离的红球菌属 NyZ502(放线菌门)鉴定出了一种独特的酰胺酶 ApaA,它是污水处理厂中酰胺酶的主要类别。在假定的酰胺酶中观察到的显著系统发育和结构多样性表明污水处理厂中存在多种对乙酰氨基酚水解潜力。
本研究增进了我们对乙酰氨基酚环境归宿的理解,并强调了全球污水处理厂中对乙酰氨基酚降解过程中基因失衡可能引发的生态风险。视频摘要。