Characterization of urease active calcite-producing strain YX-3 combined with the whole genome
Urease found in a wide range of microorganisms plays a vital role in ureolytic induced calcite precipitation (UICP). However, the genomic information on urease-producing strains is limited, and there is a need for further in-depth studies on aspects such as the regulation of urease activity by nicke...
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description | Urease found in a wide range of microorganisms plays a vital role in ureolytic induced calcite precipitation (UICP). However, the genomic information on urease-producing strains is limited, and there is a need for further in-depth studies on aspects such as the regulation of urease activity by nickel ligand residues. The present study delved into the elucidation of urease activity in a newly isolated strain YX-3 coupled with nickel-ligand residues by employing the genetic architecture of biomineralization-controlled growth, molecular docking, molecular dynamics simulation (MDS), and site-directed mutagenesis. Genome-wide sequencing showed the presence of urease gene clusters, comprising structural genes ureA, ureB, and ureC, alongside auxiliary genes ureD, ureE, ureF, and ureG. RT-qPCR analysis showed that the addition of NiCl2 resulted in a significant up-regulation of ureC expression. His267, His294, and Gly325 in the domain of UreC were further proved to coordinate with nickel ions and urea simultaneously through homology modeling and molecular docking, and molecular dynamics simulations (MDS) showed the urease-urea docking complexes exhibited degressive binding stability by four metrics including root mean square deviations (RMSD) when those residues were mutated into alanine respectively. Western blotting exhibited that mutations of H267A, H294A, and G325A led to a reduction in the relative expression of urease, wherein urease activity was about 62%, 45%, and 20% times that of the wild type (WT), respectively. The overexpression results further confirmed the importance of these residues for urease activity and CaCO3 precipitation. These results would help to deepen the understanding of urease-producing strains at a molecular level and expand the theoretical basis for modulating urease activity.
[Display omitted]
•Sphingobacterium thalpophilum YX-3 exhibits the ability to precipitate calcium carbonate.•The whole genome sequencing data of Sphingobacterium thalpophilum YX-3 was elucidated.•Mutations at His267, His294, and Gly325 result in decreased urease binding to urea.•Alterations in critical residues involved in nickel and urea coordination diminish UreC expression and urease activity. |
doi_str_mv | 10.1016/j.envres.2024.119855 |
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[Display omitted]
•Sphingobacterium thalpophilum YX-3 exhibits the ability to precipitate calcium carbonate.•The whole genome sequencing data of Sphingobacterium thalpophilum YX-3 was elucidated.•Mutations at His267, His294, and Gly325 result in decreased urease binding to urea.•Alterations in critical residues involved in nickel and urea coordination diminish UreC expression and urease activity.</description><identifier>ISSN: 0013-9351</identifier><identifier>ISSN: 1096-0953</identifier><identifier>EISSN: 1096-0953</identifier><identifier>DOI: 10.1016/j.envres.2024.119855</identifier><identifier>PMID: 39208972</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Calcium Carbonate - chemistry ; Calcium Carbonate - metabolism ; Genome analysis ; Genome, Bacterial ; MDS ; Molecular Docking Simulation ; Molecular Dynamics Simulation ; Nickel - metabolism ; Nickel ion ; Site-directed mutagenesis ; Sphingobacterium thalpophilum ; Sporosarcina - enzymology ; Sporosarcina - genetics ; Urease - chemistry ; Urease - genetics ; Urease - metabolism ; Western blotting</subject><ispartof>Environmental research, 2024-12, Vol.262 (Pt 1), p.119855, Article 119855</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c241t-3a23690a1ee66f222ec0cc1148981294f2f2f74e9c3fb3f13f7c6832131fa74b3</cites><orcidid>0000-0002-2590-4351</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0013935124017602$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39208972$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Shuqi</creatorcontrib><creatorcontrib>Liu, Shichuang</creatorcontrib><creatorcontrib>Chen, Mengyao</creatorcontrib><creatorcontrib>Lu, Juncheng</creatorcontrib><creatorcontrib>Ma, Yanling</creatorcontrib><title>Characterization of urease active calcite-producing strain YX-3 combined with the whole genome</title><title>Environmental research</title><addtitle>Environ Res</addtitle><description>Urease found in a wide range of microorganisms plays a vital role in ureolytic induced calcite precipitation (UICP). However, the genomic information on urease-producing strains is limited, and there is a need for further in-depth studies on aspects such as the regulation of urease activity by nickel ligand residues. The present study delved into the elucidation of urease activity in a newly isolated strain YX-3 coupled with nickel-ligand residues by employing the genetic architecture of biomineralization-controlled growth, molecular docking, molecular dynamics simulation (MDS), and site-directed mutagenesis. Genome-wide sequencing showed the presence of urease gene clusters, comprising structural genes ureA, ureB, and ureC, alongside auxiliary genes ureD, ureE, ureF, and ureG. RT-qPCR analysis showed that the addition of NiCl2 resulted in a significant up-regulation of ureC expression. His267, His294, and Gly325 in the domain of UreC were further proved to coordinate with nickel ions and urea simultaneously through homology modeling and molecular docking, and molecular dynamics simulations (MDS) showed the urease-urea docking complexes exhibited degressive binding stability by four metrics including root mean square deviations (RMSD) when those residues were mutated into alanine respectively. Western blotting exhibited that mutations of H267A, H294A, and G325A led to a reduction in the relative expression of urease, wherein urease activity was about 62%, 45%, and 20% times that of the wild type (WT), respectively. The overexpression results further confirmed the importance of these residues for urease activity and CaCO3 precipitation. These results would help to deepen the understanding of urease-producing strains at a molecular level and expand the theoretical basis for modulating urease activity.
[Display omitted]
•Sphingobacterium thalpophilum YX-3 exhibits the ability to precipitate calcium carbonate.•The whole genome sequencing data of Sphingobacterium thalpophilum YX-3 was elucidated.•Mutations at His267, His294, and Gly325 result in decreased urease binding to urea.•Alterations in critical residues involved in nickel and urea coordination diminish UreC expression and urease activity.</description><subject>Calcium Carbonate - chemistry</subject><subject>Calcium Carbonate - metabolism</subject><subject>Genome analysis</subject><subject>Genome, Bacterial</subject><subject>MDS</subject><subject>Molecular Docking Simulation</subject><subject>Molecular Dynamics Simulation</subject><subject>Nickel - metabolism</subject><subject>Nickel ion</subject><subject>Site-directed mutagenesis</subject><subject>Sphingobacterium thalpophilum</subject><subject>Sporosarcina - enzymology</subject><subject>Sporosarcina - genetics</subject><subject>Urease - chemistry</subject><subject>Urease - genetics</subject><subject>Urease - metabolism</subject><subject>Western blotting</subject><issn>0013-9351</issn><issn>1096-0953</issn><issn>1096-0953</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1rGzEQhkVpaBy3_6AUHXtZRyPtly6FYPIFhlxSSC4RsnYUy-yuHElrk_76rNk0xzCHYYb3nY-HkJ_AFsCgPN8usN8HjAvOeL4AkHVRfCEzYLLMmCzEVzJjDEQmRQGn5CzG7VhCIdg3ciokZ7Ws-Iw8LTc6aJMwuH86Od9Tb-kQUEekY9vtkRrdGpcw2wXfDMb1zzSmoF1PHx8yQY3v1q7Hhh5c2tC0QXrY-BbpM_a-w-_kxOo24o_3PCd_ry7vlzfZ6u76dnmxygzPIWVCc1FKpgGxLC3nHA0zBiCvZQ1c5paPUeUojbBrYUHYypS14CDA6ipfizn5Pc0dj3wZMCbVuWiwbXWPfohKMCkrKcvRMSf5JDXBxxjQql1wnQ6vCpg6klVbNZFVR7JqIjvafr1vGNYdNh-m_yhHwZ9JgOOfe4dBReOwN9i4gCapxrvPN7wBwt2MAA</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Zhang, Shuqi</creator><creator>Liu, Shichuang</creator><creator>Chen, Mengyao</creator><creator>Lu, Juncheng</creator><creator>Ma, Yanling</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2590-4351</orcidid></search><sort><creationdate>20241201</creationdate><title>Characterization of urease active calcite-producing strain YX-3 combined with the whole genome</title><author>Zhang, Shuqi ; Liu, Shichuang ; Chen, Mengyao ; Lu, Juncheng ; Ma, Yanling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c241t-3a23690a1ee66f222ec0cc1148981294f2f2f74e9c3fb3f13f7c6832131fa74b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Calcium Carbonate - chemistry</topic><topic>Calcium Carbonate - metabolism</topic><topic>Genome analysis</topic><topic>Genome, Bacterial</topic><topic>MDS</topic><topic>Molecular Docking Simulation</topic><topic>Molecular Dynamics Simulation</topic><topic>Nickel - metabolism</topic><topic>Nickel ion</topic><topic>Site-directed mutagenesis</topic><topic>Sphingobacterium thalpophilum</topic><topic>Sporosarcina - enzymology</topic><topic>Sporosarcina - genetics</topic><topic>Urease - chemistry</topic><topic>Urease - genetics</topic><topic>Urease - metabolism</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Shuqi</creatorcontrib><creatorcontrib>Liu, Shichuang</creatorcontrib><creatorcontrib>Chen, Mengyao</creatorcontrib><creatorcontrib>Lu, Juncheng</creatorcontrib><creatorcontrib>Ma, Yanling</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Shuqi</au><au>Liu, Shichuang</au><au>Chen, Mengyao</au><au>Lu, Juncheng</au><au>Ma, Yanling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of urease active calcite-producing strain YX-3 combined with the whole genome</atitle><jtitle>Environmental research</jtitle><addtitle>Environ Res</addtitle><date>2024-12-01</date><risdate>2024</risdate><volume>262</volume><issue>Pt 1</issue><spage>119855</spage><pages>119855-</pages><artnum>119855</artnum><issn>0013-9351</issn><issn>1096-0953</issn><eissn>1096-0953</eissn><abstract>Urease found in a wide range of microorganisms plays a vital role in ureolytic induced calcite precipitation (UICP). However, the genomic information on urease-producing strains is limited, and there is a need for further in-depth studies on aspects such as the regulation of urease activity by nickel ligand residues. The present study delved into the elucidation of urease activity in a newly isolated strain YX-3 coupled with nickel-ligand residues by employing the genetic architecture of biomineralization-controlled growth, molecular docking, molecular dynamics simulation (MDS), and site-directed mutagenesis. Genome-wide sequencing showed the presence of urease gene clusters, comprising structural genes ureA, ureB, and ureC, alongside auxiliary genes ureD, ureE, ureF, and ureG. RT-qPCR analysis showed that the addition of NiCl2 resulted in a significant up-regulation of ureC expression. His267, His294, and Gly325 in the domain of UreC were further proved to coordinate with nickel ions and urea simultaneously through homology modeling and molecular docking, and molecular dynamics simulations (MDS) showed the urease-urea docking complexes exhibited degressive binding stability by four metrics including root mean square deviations (RMSD) when those residues were mutated into alanine respectively. Western blotting exhibited that mutations of H267A, H294A, and G325A led to a reduction in the relative expression of urease, wherein urease activity was about 62%, 45%, and 20% times that of the wild type (WT), respectively. The overexpression results further confirmed the importance of these residues for urease activity and CaCO3 precipitation. These results would help to deepen the understanding of urease-producing strains at a molecular level and expand the theoretical basis for modulating urease activity.
[Display omitted]
•Sphingobacterium thalpophilum YX-3 exhibits the ability to precipitate calcium carbonate.•The whole genome sequencing data of Sphingobacterium thalpophilum YX-3 was elucidated.•Mutations at His267, His294, and Gly325 result in decreased urease binding to urea.•Alterations in critical residues involved in nickel and urea coordination diminish UreC expression and urease activity.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>39208972</pmid><doi>10.1016/j.envres.2024.119855</doi><orcidid>https://orcid.org/0000-0002-2590-4351</orcidid></addata></record> |
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subjects | Calcium Carbonate - chemistry Calcium Carbonate - metabolism Genome analysis Genome, Bacterial MDS Molecular Docking Simulation Molecular Dynamics Simulation Nickel - metabolism Nickel ion Site-directed mutagenesis Sphingobacterium thalpophilum Sporosarcina - enzymology Sporosarcina - genetics Urease - chemistry Urease - genetics Urease - metabolism Western blotting |
title | Characterization of urease active calcite-producing strain YX-3 combined with the whole genome |
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