PMID- 37051271 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20230415 IS - 2296-4185 (Print) IS - 2296-4185 (Electronic) IS - 2296-4185 (Linking) VI - 11 DP - 2023 TI - Immobilizing lead and copper in aqueous solution using microbial- and enzyme-induced carbonate precipitation. PG - 1146858 LID - 10.3389/fbioe.2023.1146858 [doi] LID - 1146858 AB - Inappropriate irrigation could trigger migration of heavy metals into surrounding environments, causing their accumulation and a serious threat to human central nervous system. Traditional site remediation technologies are criticized because they are time-consuming and featured with high risk of secondary pollution. In the past few years, the microbial-induced carbonate precipitation (MICP) is considered as an alternative to traditional technologies due to its easy maneuverability. The enzyme-induced carbonate precipitate (EICP) has attracted attention because bacterial cultivation is not required prior to catalyzing urea hydrolysis. This study compared the performance of lead (Pb) and copper (Cu) remediation using MICP and EICP respectively. The effect of the degree of urea hydrolysis, mass and species of carbonate precipitation, and chemical and thermodynamic properties of carbonates on the remediation efficiency was investigated. Results indicated that ammonium ion (NH(4) (+)) concentration reduced with the increase in lead ion (Pb(2+)) or copper ion (Cu(2+)) concentration, and for a given Pb(2+) or Cu(2+) concentration, it was much higher under MICP than EICP. Further, the remediation efficiency against Cu(2+) is approximately zero, which is way below that against Pb(2+) (approximately 100%). The Cu(2+) toxicity denatured and even inactivated the urease, reducing the degree of urea hydrolysis and the remediation efficiency. Moreover, the reduction in the remediation efficiency against Pb(2+) and Cu(2+) appeared to be due to the precipitations of cotunnite and atacamite respectively. Their chemical and thermodynamic properties were not as good as calcite, cerussite, phosgenite, and malachite. The findings shed light on the underlying mechanism affecting the remediation efficiency against Pb(2+) and Cu(2+). CI - Copyright (c) 2023 Wang, Cheng, Xue, Rahman, Xie and Hu. FAU - Wang, Lin AU - Wang L AD - School of Civil Engineering, Xi'an University of Architecture and Technology, Xi'an, China. AD - Shaanxi Key Laboratory of Geotechnical and Underground Space Engineering (XAUAT), Xi'an, China. FAU - Cheng, Wen-Chieh AU - Cheng WC AD - School of Civil Engineering, Xi'an University of Architecture and Technology, Xi'an, China. AD - Shaanxi Key Laboratory of Geotechnical and Underground Space Engineering (XAUAT), Xi'an, China. FAU - Xue, Zhong-Fei AU - Xue ZF AD - School of Civil Engineering, Xi'an University of Architecture and Technology, Xi'an, China. AD - Shaanxi Key Laboratory of Geotechnical and Underground Space Engineering (XAUAT), Xi'an, China. FAU - Rahman, Md Mizanur AU - Rahman MM AD - UniSA STEM, SIRM, University of south Australia, Adelaide, SA, Australia. FAU - Xie, Yi-Xin AU - Xie YX AD - School of Civil Engineering, Xi'an University of Architecture and Technology, Xi'an, China. AD - Shaanxi Key Laboratory of Geotechnical and Underground Space Engineering (XAUAT), Xi'an, China. FAU - Hu, Wenle AU - Hu W AD - School of Civil Engineering, Xi'an University of Architecture and Technology, Xi'an, China. AD - Shaanxi Key Laboratory of Geotechnical and Underground Space Engineering (XAUAT), Xi'an, China. LA - eng PT - Journal Article DEP - 20230327 PL - Switzerland TA - Front Bioeng Biotechnol JT - Frontiers in bioengineering and biotechnology JID - 101632513 PMC - PMC10083330 OTO - NOTNLM OT - EICP OT - MICP OT - heavy metal OT - remediation efficiency OT - thermodynamic properties COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2023/04/14 06:00 MHDA- 2023/04/14 06:01 PMCR- 2023/01/01 CRDT- 2023/04/13 01:59 PHST- 2023/01/18 00:00 [received] PHST- 2023/03/16 00:00 [accepted] PHST- 2023/04/14 06:01 [medline] PHST- 2023/04/13 01:59 [entrez] PHST- 2023/04/14 06:00 [pubmed] PHST- 2023/01/01 00:00 [pmc-release] AID - 1146858 [pii] AID - 10.3389/fbioe.2023.1146858 [doi] PST - epublish SO - Front Bioeng Biotechnol. 2023 Mar 27;11:1146858. doi: 10.3389/fbioe.2023.1146858. eCollection 2023.