Novel enzymes involved in the biotransformation of oxytetracycline by Arthrobacter nicotianae OTC-16

文献类型： 外文期刊

第一作者： Wang, Beibei

作者： Wang, Beibei;Xu, Weijie;Wang, Keke;Zhang, Xin;Lin, Hui;Ahmad, Zulfiqar

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关键词： oxytetracycline; transcriptomics; proteomics; degradation mechanisms; biodegradation enzymes

期刊名称：MICROBIOLOGY SPECTRUM （ 影响因子：3.8； 五年影响因子：4.1 ）

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年卷期： 2025 年 13 卷 9 期

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收录情况： SCI

摘要： Current research on the microbial degradation of antibiotic residues primarily focuses on isolating degrading bacteria and characterizing their metabolites. The enzymatic mechanisms underlying these biotransformation processes remain poorly understood. Here, we investigated the molecular mechanisms involved in the biodegradation of oxytetracycline (OTC) by Arthrobacter nicotianae OTC-16 using integrated transcriptomic and proteomic sequencing analyses. OTC exposure significantly altered gene expression, identifying 1,158 and 863 differentially expressed genes on days 2 and 4, respectively. Proteomics revealed 352 and 818 differentially expressed proteins, predominantly involved in compound binding and redox processes. Integrated analysis identified AlkB (DNA oxidative demethylase), uaZ (urate oxidase), and prpD (2-methylcitrate dehydratase) as key enzymes mediating OTC biodegradation through decarboxylation, carbon-carbon bond reduction, and dehydration reactions, confirmed by RT-qPCR. Protein-protein interactions subsequently highlighted supportive proteins, including glutathione S-transferase, ABC transporter ATP-binding protein, prpB, prpE, MarR regulators, and glyoxalase. Notably, prpD and uaZ were successfully expressed in Escherichia coli, and their OTC degradation-promoting activities were validated through in vitro assays. This study is the first to report the roles of prpD and uaZ in antibiotic residue degradation, providing novel insights into the enzymatic mechanisms and laying a foundation for future genetic engineering and practical applications.IMPORTANCEOxytetracycline (OTC), a widely used antibiotic in agriculture and animal husbandry, frequently accumulates in the environment, posing significant ecological and human health risks by promoting antibiotic resistance. Understanding the microbial enzymatic pathways for OTC biodegradation is crucial for developing effective bioremediation strategies. This study provides a comprehensive molecular analysis of the OTC degradation process by Arthrobacter nicotianae OTC-16, identifying three key enzymes (AlkB, uaZ, and prpD) involved in OTC removal. Successfully expressing prpD and uaZ in Escherichia coli and validating their biodegradation activity in vivo further underscores their potential for biotechnological applications. These findings significantly enhance the knowledge of microbial antibiotic degradation mechanisms, offering practical molecular targets for environmental detoxification strategies.

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