Characterization of ureolysis and microbially induced calcium carbonate precipitation under different incubation and reaction conditions

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Hyun-Woo Joo , Matthew H. Fyfe , Irene Verdú , Seyed Ali Rahmaninezhad , Christopher M. Sales , Wil V. Srubar III , Mija H. Hubler
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引用次数: 0

Abstract

Understanding the factors influencing ureolysis and calcium carbonate precipitation is essential for optimizing microbially induced calcium carbonate precipitation (MICP) processes, yet comparative insights into different bacterial species under varying conditions remain inconclusive. This study investigates the ureolysis and MICP characteristics of Sporosarcina pasteurii and Lysinibacillus sphaericus under varying incubation and reaction conditions. Batch experiments were conducted to assess the effects of incubation duration and pH, bacterial cell density, and reagent (i.e., urea and calcium ion) concentrations on ureolysis and CaCO3 precipitation. The findings indicate that both bacteria exhibit higher urease activity after 24 h of incubation compared to 48 h, regardless of incubation pH. S. pasteurii exhibits maximum specific urease activity when incubated at an alkaline pH (pH 9.0), whereas L. sphaericus peaks after incubation at a neutral pH (pH 7.2). Moreover, the ureolysis performance of S. pasteurii shows greater sensitivity to incubation conditions, while L. sphaericus maintains consistently. At low cell density (OD600 ∼0.1), specific urease activity and early-stage mineralization efficiency are improved, whereas high density (OD600 ∼1.0) enhances overall CaCO3 precipitation and prolonged vaterite presence. High reagent concentrations (1.0 and 1.5 M) further enhance urease activity and precipitation rates and lead to vaterite dominance (> 93 %), while low concentration (0.3 M) favors calcite formation over time. These findings provide insights into evaluating and optimizing MICP performance under varying incubation and reaction conditions.
不同孵育和反应条件下尿素溶解和微生物诱导碳酸钙沉淀的表征
了解影响尿解和碳酸钙沉淀的因素对于优化微生物诱导碳酸钙沉淀(MICP)过程至关重要,但在不同条件下对不同细菌种类的比较研究尚无定论。本研究研究了不同孵育和反应条件下巴氏孢弧菌和球形赖氨酸芽孢杆菌的解尿和MICP特性。进行了批量实验,以评估孵育时间、pH、细菌细胞密度和试剂(即尿素和钙离子)浓度对尿解和CaCO3沉淀的影响。结果表明,两种细菌在孵育24 h后比48 h表现出更高的脲酶活性,无论孵育pH值如何。巴氏杆菌在碱性pH (pH 9.0)下孵育时表现出最大的特异性脲酶活性,而球形乳杆菌在中性pH (pH 7.2)下孵育后达到峰值。此外,巴氏杆菌的溶尿性能对孵育条件的敏感性更高,而球形乳杆菌则保持一致。在低细胞密度(OD600 ~ 0.1)下,特定脲酶活性和早期矿化效率得到改善,而高密度(OD600 ~ 1.0)增强了CaCO3的总体沉淀和延长了水蛭体的存在。高浓度试剂(1.0和1.5 M)进一步提高脲酶活性和沉淀率,并导致水蛭优势(>;93 %),而低浓度(0.3 M)有利于方解石随时间的形成。这些发现为在不同的孵育和反应条件下评估和优化MICP性能提供了见解。
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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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