优化固体复合菌剂对苯并[a]芘污染土壤的生物降解效果、微生物动力学变化及机制

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Bing Xiao, Jianli Jia, Xiaolong Gao, Mengyuan Zeng, Ben Zhang, Weiran Wang, Yichi Ma, Yuxin Han, Shuo Zhang
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引用次数: 0

摘要

固体复合细菌制剂(SCBA)为原位降解苯并[a]芘(BaP)提供了一种创新的生物修复策略,苯并[a]芘是一种顽固性化合物,对污染土壤的修复构成了重大挑战。本研究采用真空冷冻干燥技术制备了一种降解BaP的SCBA。采用响应面法优化保护剂配比,得到由14 %脱脂奶粉、8 %甘油、8 %蔗糖组成的复合配方。该制剂在SCBA中的冻干存活率为(89.65 %±2.04)%,有效活菌数为(1.50 ± 1.07)× 10 ¹ ¹CFU/g。BaP污染土壤修复60 d后,活化菌液联合共代谢底物(CMS) (JYC)组和SCBA联合CMS (JFC)组对BaP的降解率分别为57.23 %和45.33 %,较对照(CK)组分别提高了41.35 %和29.45 %。添加SCBA和CMS显著提高了微生物对BaP的修复效率,提高了土壤有机质、碱性氮含量以及双醋酸荧光素、过氧化氢酶和脱氢酶活性。此外,这种方法丰富了参与BaP降解的有益菌群,培养了一个更有效和稳定的微生物网络。微生物间信号的增强促进了更快的物质交换和更紧密的细菌间接触。CMS提供必需的营养物质,使微生物能够更快地适应环境,减少微生物修复。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimized solid composite bacterial agents for biodegradation of benzo[a]pyrene contaminated soils: Effects, microbial dynamic changes and mechanisms
Solid composite bacterial agents (SCBA) present an innovative bioremediation strategy for the in situ degradation of benzo[a]pyrene (BaP), a recalcitrant compound that poses significant challenges to remediation in contaminated soils. In this study, an SCBA for BaP degradation was prepared using vacuum freeze-drying technology. Response surface methodology was employed to optimize the protective agent ratio, resulting in a composite formulation comprising 14 % skimmed milk powder, 8 % glycerol, and 8 % sucrose. This formulation achieved a freeze-drying survival rate of (89.65 %±2.04)% and an effective viable bacterial count of (1.50 ± 1.07)× 10 ¹ ¹ CFU/g in the SCBA. After 60 days of BaP-contaminated soil remediation, the BaP degradation rates in the activated bacterial liquid combined with co-metabolized substrate (CMS) (JYC) and the SCBA combined with CMS (JFC) groups were 57.23 % and 45.33 %, respectively, reflecting increases of 41.35 % and 29.45 % compared to the control (CK) group. Incorporating SCBA and CMS significantly enhanced the microbial BaP remediation efficiency and improved soil organic matter, alkaline nitrogen content, as well as fluorescein diacetate, catalase, and dehydrogenase activity. Furthermore, this approach enriched the population of beneficial bacteria involved in BaP degradation, fostering a more efficient and stable microbial network. Enhanced signaling between microorganisms facilitated faster material exchange and closer inter-bacterial contact. The CMS provided essential nutrients, enabling microorganisms to adapt more rapidly to their environment and reducing microbial remediation.
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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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