Enhanced removal of PHE-Cd2+ co-contamination by the mixed bacterial cultures of Pseudomonas putida and Arthrobacter sp.: Performance and mechanism

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Biochemical Engineering Journal Pub Date : 2024-07-18 DOI:10.1016/j.bej.2024.109433
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Abstract

The strain species resource is essential for microbial remediation of PHE (phenanthrene)-Cd2+ co-contamination. In this study, the mixed bacterial culture (M) was established to intensively remediate PHE-Cd2+ co-contamination using PAHs-degrading bacteria Pseudomonas putida and Arthrobacter sp. with different Cd2+ tolerance. The PHE degradation efficiency of the mixed bacterial cultures (M) was 65 %-81 % under different Cd2+ concentration of 10–50 mg/L, respectively, which was 1.40–2.98 times that of the individual strains. In addition, strain metabolic enzyme activity, intracellular structure and extracellular polymeric substances (EPS) were carried out under Cd2+ stress. Results showed that the catechol 1,2-dioxygenase enzyme (C120) and the electron transport system activity (ETSA) were less adversely affected by Cd2+ in mixed bacterial cultures. Transmission electron microscopy images showed that the cells surface of the mixed bacterial cultures (M) could be adsorbed more Cd2+ compared to the single strain. The analysis of cell functional groups suggested that C-O-C and C-O groups in EPS mediated the removal of Cd2+ in the mixed bacterial culture. Moreover, the Cd2+ removal proportion by EPS adsorption of the mixed bacterial cultures accounted for 92 %, 67 %, 57 %, and 52 % under Cd2+ stress of 0.5, 10, 25, and 50 mg/L, respectively, which were superior to that of individual strains. This study confirmed the potential application and technical reference of the specific mixed bacterial cultures in the enhanced bioremediation of PHE-Cd2+ co-contamination.

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利用假单胞菌(Pseudomonas putida)和节杆菌(Arthrobacter sp:性能与机理
菌种资源对 PHE(菲)-Cd2+ 共污染的微生物修复至关重要。本研究利用不同耐Cd2+能力的多环芳烃降解菌假单胞菌(Pseudomonas putida)和节杆菌(Arthrobacter sp.在 10-50 mg/L 的不同 Cd2+浓度下,混合细菌培养物(M)的 PHE 降解效率分别为 65 %-81 %,是单个菌株的 1.40-2.98 倍。此外,还对 Cd2+ 胁迫下菌株的代谢酶活性、胞内结构和胞外聚合物质(EPS)进行了研究。结果表明,在混合细菌培养物中,儿茶酚 1,2-二氧化酶(C120)和电子传递系统活性(ETSA)受 Cd2+ 的不利影响较小。透射电子显微镜图像显示,与单一菌株相比,混合细菌培养物(M)的细胞表面能吸附更多的 Cd2+。细胞功能基团分析表明,EPS 中的 C-O-C 和 C-O 基团介导了混合细菌培养物对 Cd2+ 的去除。此外,在 0.5、10、25 和 50 mg/L 的 Cd2+ 胁迫下,混合细菌培养物通过 EPS 吸附去除 Cd2+ 的比例分别为 92%、67%、57% 和 52%,均优于单个菌株。该研究证实了特定混合细菌培养物在增强 PHE-Cd2+ 共污染生物修复中的潜在应用和技术参考价值。
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来源期刊
Biochemical Engineering Journal
Biochemical Engineering Journal 工程技术-工程:化工
CiteScore
7.10
自引率
5.10%
发文量
380
审稿时长
34 days
期刊介绍: The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology. The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields: Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics Biosensors and Biodevices including biofabrication and novel fuel cell development Bioseparations including scale-up and protein refolding/renaturation Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells Bioreactor Systems including characterization, optimization and scale-up Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis Protein Engineering including enzyme engineering and directed evolution.
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