利用宏基因组学研究不同粒径零价铁对污泥中温和嗜热厌氧消化的影响

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jianglin Chen , Wenqian Li , Lina Pang , Efthalia Chatzisymeon , Yuanyuan Lu , Ping Yang
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引用次数: 0

摘要

本研究研究了在中温(MAD)和亲热(TAD)温度下,三种粒径下污泥厌氧消化(AD)对零价铁(ZVI)添加的机理。结果表明,纳米级zvi、微米级zvi和废铁均能提高两种AD工艺的累计甲烷产量。此外,纳米zvi在MAD中的累积甲烷产率最高(83.92 mL/g VS),这可能刺激了MAD的水解和酸化过程。此外,宏基因组研究结果表明,纳米zvi的优势产甲烷途径和功能微生物(如Candidatus_Microthrix和Methanothrix属)的丰富,以及与水化和甲基甲烷生成途径相关的酶的丰富,可能是MAD具有最佳性能的潜在原因。该研究为在固体废物厌氧消化中部署ZVI以有效管理和处理废物并增加生物甲烷产量的机制提供了知识基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Using metagenomics to reveal the effects of zero-valent iron with different sizes on the mesophilic and thermophilic anaerobic digestion of sludge
This work investigated the mechanisms of anaerobic digestion (AD) of sludge to the addition of zero-valent iron (ZVI) at three particle sizes under mesophilic (MAD) and thermophilic (TAD) temperatures. Results showed that nano-ZVI, micron-ZVI, and iron scrap all enhanced the cumulative methane production in two AD processes. Besides, the highest cumulative methane yield (83.92 mL/g VS) was achieved in MAD with nano-ZVI, which possibly stimulated the hydrolysis and acidification processes in MAD. Moreover, metagenomic results revealed that the more abundant predominant methanogenic pathways and functional microbes like genera Candidatus_Microthrix and Methanothrix, and the enriched enzymes associated with hydrotrophic and methyl methanogenesis pathways, might be the underlying reasons for the best performance of MAD with nano-ZVI. This study provides knowledge underpinning the mechanisms for the deployment of ZVI in solid waste anaerobic digestion to effectively manage and treat waste and increase biomethane production.
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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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