制革工业土壤中苯修复细菌的分离、分子和代谢分析。

Polish journal of microbiology Pub Date : 2025-03-26 eCollection Date: 2025-03-01 DOI:10.33073/pjm-2025-003
Nadia Hussain, Farhan Mohiuddin, Fatima Muccee, Saboor Muarij Bunny, Amal H I Al Haddad
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引用次数: 0

摘要

苯是一种普遍存在的污染物和人类致癌物。由于成本高和苯降解不完全,传统的环境资源修复方法一直具有挑战性。本研究旨在从制革工业土壤中寻找具有苯降解潜力的高效细菌,以替代这些传统的苯去除方法。用苯(80 μl/ 1000 ml)加微量盐培养基(MSM)进行细菌分离。通过生长曲线分析、革兰氏染色、Remel RapID™NF PLUS系统(Thermo Scientific™、Thermo Fisher Scientific, Inc., USA)进行生化鉴定、抗生素敏感性分析、16S rRNA基因测序、苯去除效率评估、FTIR和GC-MS分析对分离株进行鉴定。本研究分离的5种细菌鉴定为aestuariparaccoccus PUB1、Bacillus tropicus PUB2、Bacillus albus PUB3、Bacillus subtilis PUB4和Bacillus cereus PUB6。除猪口假单胞菌PUB1外,其余均为革兰氏阳性。对苯的去除率最高(30 mg/l / 25 h)。对比细菌培养上清与对照的FTIR光谱,发现苯环键断裂引起的峰移。GC-MS分析鉴定了苯甲酸甲基化和苯甲醛途径的代谢中间体。这些细菌可以通过酶合成纳米颗粒或在生态友好的表达系统中克隆相关基因来降解苯。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolation, Molecular, and Metabolic Profiling of Benzene-Remediating Bacteria Inhabiting the Tannery Industry Soil.

Benzene is a pervasive contaminant and human carcinogen. Its remediation from environmental resources using conventional procedures has always been challenging due to high cost and incomplete benzene degradation. The present study was designed to explore highly efficient bacteria with benzene degrading potential from tannery industry soil, which might be used as an alternative to these conventional benzene removal remedies. Bacterial isolation was performed using benzene (80 μl/1,000 ml) supplemented with minimal salt media (MSM). Characterization of isolates was carried out by performing growth curve analysis, Gram staining, biochemical characterization via Remel RapID NF PLUS System (Thermo Scientific™, Thermo Fisher Scientific, Inc., USA), antibiotic sensitivity profiling, 16S rRNA gene sequencing, benzene removal efficiency estimation assay, FTIR, and GC-MS profiling. Five bacteria isolated in the present study were identified as Paracoccus aestuarii PUB1, Bacillus tropicus PUB2, Bacillus albus PUB3, Bacillus subtilis PUB4, and Bacillus cereus PUB6. All of these fast-growing bacteria were Gram-positive except P. aestuarii PUB1. Maximum benzene removal efficiency (30 mg/l per 25 h) was found in B. tropicus PUB2. Comparing the FTIR spectra of bacterial culture supernatant versus control revealed the peaks shifting corresponding to benzene ring bonds breaking. GC-MS analysis identified the metabolic intermediates from benzoate methylation and benzaldehyde pathways. These bacteria can be employed for benzene degradation via enzyme-based nanoparticle synthesis or cloning of relevant genes in eco-friendly expression systems.

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