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Osmolyte effect on enzymatic stability and reaction equilibrium of formate dehydrogenase
Osmolytes are well-known biocatalyst stabilisers as they promote the folded state of proteins, and a stabilised biocatalyst might also improve reaction kinetics. In this work, the influence of four osmolytes (betaine, glycerol, trehalose, and trimethylamine N -oxide) on the activity and stability of...
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Published in: | Physical chemistry chemical physics : PCCP 2022-11, Vol.24 (45), p.2793-27939 |
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creator | Gajardo-Parra, Nicolás F Akrofi-Mantey, Harold Ascani, Moreno Cea-Klapp, Esteban Garrido, José Matias Sadowski, Gabriele Held, Christoph |
description | Osmolytes are well-known biocatalyst stabilisers as they promote the folded state of proteins, and a stabilised biocatalyst might also improve reaction kinetics. In this work, the influence of four osmolytes (betaine, glycerol, trehalose, and trimethylamine
N
-oxide) on the activity and stability of
Candida bondinii
formate dehydrogenase
cb
FDH was studied experimentally and theoretically. Scanning differential fluorimetric studies were performed to assess the thermal stability of
cb
FDH, while UV detection was used to reveal changes in
cb
FDH activity and reaction equilibrium at osmolyte concentrations between 0.25 and 1 mol kg
−1
. The thermodynamic model ePC-SAFT advanced allowed predicting the effects of osmolyte on the reaction equilibrium by accounting for interactions involving osmolyte, products, substrates, and water. The results show that osmolytes at low concentrations were beneficial for both, thermal stability and
cb
FDH activity, while keeping the equilibrium yield at high level. Molecular dynamics simulations were used to describe the solvation around the
cb
FDH surface and the volume exclusion effect, proofing the beneficial effect of the osmolytes on
cb
FDH activity, especially at low concentrations of trimethylamine
N
-oxide and betaine. Different mechanisms of stabilisation (dependent on the osmolyte) show the importance of studying solvent-protein dynamics towards the design of optimised biocatalytic processes.
The effect of osmolytes was studied on FDH properties: termal stability, initial enzyme activity, long-term stability and reaction equilibrium by experimental methods (UV-VIS and fluorimetrics) supported by theory (PC-SAFT and MD simulations). |
doi_str_mv | 10.1039/d2cp04011e |
format | article |
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N
-oxide) on the activity and stability of
Candida bondinii
formate dehydrogenase
cb
FDH was studied experimentally and theoretically. Scanning differential fluorimetric studies were performed to assess the thermal stability of
cb
FDH, while UV detection was used to reveal changes in
cb
FDH activity and reaction equilibrium at osmolyte concentrations between 0.25 and 1 mol kg
−1
. The thermodynamic model ePC-SAFT advanced allowed predicting the effects of osmolyte on the reaction equilibrium by accounting for interactions involving osmolyte, products, substrates, and water. The results show that osmolytes at low concentrations were beneficial for both, thermal stability and
cb
FDH activity, while keeping the equilibrium yield at high level. Molecular dynamics simulations were used to describe the solvation around the
cb
FDH surface and the volume exclusion effect, proofing the beneficial effect of the osmolytes on
cb
FDH activity, especially at low concentrations of trimethylamine
N
-oxide and betaine. Different mechanisms of stabilisation (dependent on the osmolyte) show the importance of studying solvent-protein dynamics towards the design of optimised biocatalytic processes.
The effect of osmolytes was studied on FDH properties: termal stability, initial enzyme activity, long-term stability and reaction equilibrium by experimental methods (UV-VIS and fluorimetrics) supported by theory (PC-SAFT and MD simulations).</description><identifier>ISSN: 1463-9076</identifier><identifier>EISSN: 1463-9084</identifier><identifier>DOI: 10.1039/d2cp04011e</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Biocatalysts ; Dehydrogenases ; Design optimization ; Equilibrium ; Formate dehydrogenase ; Low concentrations ; Molecular dynamics ; Proteins ; Reaction kinetics ; Solvation ; Stability analysis ; Substrates ; Thermal stability ; Thermodynamic models ; Trehalose ; Trimethylamine</subject><ispartof>Physical chemistry chemical physics : PCCP, 2022-11, Vol.24 (45), p.2793-27939</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c280t-5a807158d0879038f054fbba554e38652c89b44fadab206f38f9e7d60dde803c3</citedby><cites>FETCH-LOGICAL-c280t-5a807158d0879038f054fbba554e38652c89b44fadab206f38f9e7d60dde803c3</cites><orcidid>0000-0002-3571-4973 ; 0000-0001-9989-7206 ; 0000-0003-1389-8836 ; 0000-0002-2238-1807 ; 0000-0002-3189-3628 ; 0000-0002-5038-9152 ; 0000-0003-1074-177X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Gajardo-Parra, Nicolás F</creatorcontrib><creatorcontrib>Akrofi-Mantey, Harold</creatorcontrib><creatorcontrib>Ascani, Moreno</creatorcontrib><creatorcontrib>Cea-Klapp, Esteban</creatorcontrib><creatorcontrib>Garrido, José Matias</creatorcontrib><creatorcontrib>Sadowski, Gabriele</creatorcontrib><creatorcontrib>Held, Christoph</creatorcontrib><title>Osmolyte effect on enzymatic stability and reaction equilibrium of formate dehydrogenase</title><title>Physical chemistry chemical physics : PCCP</title><description>Osmolytes are well-known biocatalyst stabilisers as they promote the folded state of proteins, and a stabilised biocatalyst might also improve reaction kinetics. In this work, the influence of four osmolytes (betaine, glycerol, trehalose, and trimethylamine
N
-oxide) on the activity and stability of
Candida bondinii
formate dehydrogenase
cb
FDH was studied experimentally and theoretically. Scanning differential fluorimetric studies were performed to assess the thermal stability of
cb
FDH, while UV detection was used to reveal changes in
cb
FDH activity and reaction equilibrium at osmolyte concentrations between 0.25 and 1 mol kg
−1
. The thermodynamic model ePC-SAFT advanced allowed predicting the effects of osmolyte on the reaction equilibrium by accounting for interactions involving osmolyte, products, substrates, and water. The results show that osmolytes at low concentrations were beneficial for both, thermal stability and
cb
FDH activity, while keeping the equilibrium yield at high level. Molecular dynamics simulations were used to describe the solvation around the
cb
FDH surface and the volume exclusion effect, proofing the beneficial effect of the osmolytes on
cb
FDH activity, especially at low concentrations of trimethylamine
N
-oxide and betaine. Different mechanisms of stabilisation (dependent on the osmolyte) show the importance of studying solvent-protein dynamics towards the design of optimised biocatalytic processes.
The effect of osmolytes was studied on FDH properties: termal stability, initial enzyme activity, long-term stability and reaction equilibrium by experimental methods (UV-VIS and fluorimetrics) supported by theory (PC-SAFT and MD simulations).</description><subject>Biocatalysts</subject><subject>Dehydrogenases</subject><subject>Design optimization</subject><subject>Equilibrium</subject><subject>Formate dehydrogenase</subject><subject>Low concentrations</subject><subject>Molecular dynamics</subject><subject>Proteins</subject><subject>Reaction kinetics</subject><subject>Solvation</subject><subject>Stability analysis</subject><subject>Substrates</subject><subject>Thermal stability</subject><subject>Thermodynamic models</subject><subject>Trehalose</subject><subject>Trimethylamine</subject><issn>1463-9076</issn><issn>1463-9084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpd0U1LxDAQBuAgCq6rF-9CwIsI1UnTtOlR1vUDFtaDgreSJhPt0ja7SXuov96uKyt4mmF4eBlmCDlncMOA57cm1mtIgDE8IBOWpDzKQSaH-z5Lj8lJCCsAYILxCXlfhsbVQ4cUrUXdUddSbL-GRnWVpqFTZVVX3UBVa6hHpbtqCzb9OC191TfUWWqdHzlSg5-D8e4DWxXwlBxZVQc8-61T8vYwf509RYvl4_PsbhHpWEIXCSUhY0IakFkOXFoQiS1LJUSCXKYi1jIvk8Qqo8oYUjuKHDOTgjEogWs-JVe73LV3mx5DVzRV0FjXqkXXhyLOeMrHUJGM9PIfXbnet-N2W5VDzMRop-R6p7R3IXi0xdpXjfJDwaDYHrm4j2cvP0eej_hih33Qe_f3BP4N_cp5Jw</recordid><startdate>20221123</startdate><enddate>20221123</enddate><creator>Gajardo-Parra, Nicolás F</creator><creator>Akrofi-Mantey, Harold</creator><creator>Ascani, Moreno</creator><creator>Cea-Klapp, Esteban</creator><creator>Garrido, José Matias</creator><creator>Sadowski, Gabriele</creator><creator>Held, Christoph</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-3571-4973</orcidid><orcidid>https://orcid.org/0000-0001-9989-7206</orcidid><orcidid>https://orcid.org/0000-0003-1389-8836</orcidid><orcidid>https://orcid.org/0000-0002-2238-1807</orcidid><orcidid>https://orcid.org/0000-0002-3189-3628</orcidid><orcidid>https://orcid.org/0000-0002-5038-9152</orcidid><orcidid>https://orcid.org/0000-0003-1074-177X</orcidid></search><sort><creationdate>20221123</creationdate><title>Osmolyte effect on enzymatic stability and reaction equilibrium of formate dehydrogenase</title><author>Gajardo-Parra, Nicolás F ; Akrofi-Mantey, Harold ; Ascani, Moreno ; Cea-Klapp, Esteban ; Garrido, José Matias ; Sadowski, Gabriele ; Held, Christoph</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c280t-5a807158d0879038f054fbba554e38652c89b44fadab206f38f9e7d60dde803c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biocatalysts</topic><topic>Dehydrogenases</topic><topic>Design optimization</topic><topic>Equilibrium</topic><topic>Formate dehydrogenase</topic><topic>Low concentrations</topic><topic>Molecular dynamics</topic><topic>Proteins</topic><topic>Reaction kinetics</topic><topic>Solvation</topic><topic>Stability analysis</topic><topic>Substrates</topic><topic>Thermal stability</topic><topic>Thermodynamic models</topic><topic>Trehalose</topic><topic>Trimethylamine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gajardo-Parra, Nicolás F</creatorcontrib><creatorcontrib>Akrofi-Mantey, Harold</creatorcontrib><creatorcontrib>Ascani, Moreno</creatorcontrib><creatorcontrib>Cea-Klapp, Esteban</creatorcontrib><creatorcontrib>Garrido, José Matias</creatorcontrib><creatorcontrib>Sadowski, Gabriele</creatorcontrib><creatorcontrib>Held, Christoph</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Physical chemistry chemical physics : PCCP</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gajardo-Parra, Nicolás F</au><au>Akrofi-Mantey, Harold</au><au>Ascani, Moreno</au><au>Cea-Klapp, Esteban</au><au>Garrido, José Matias</au><au>Sadowski, Gabriele</au><au>Held, Christoph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Osmolyte effect on enzymatic stability and reaction equilibrium of formate dehydrogenase</atitle><jtitle>Physical chemistry chemical physics : PCCP</jtitle><date>2022-11-23</date><risdate>2022</risdate><volume>24</volume><issue>45</issue><spage>2793</spage><epage>27939</epage><pages>2793-27939</pages><issn>1463-9076</issn><eissn>1463-9084</eissn><abstract>Osmolytes are well-known biocatalyst stabilisers as they promote the folded state of proteins, and a stabilised biocatalyst might also improve reaction kinetics. In this work, the influence of four osmolytes (betaine, glycerol, trehalose, and trimethylamine
N
-oxide) on the activity and stability of
Candida bondinii
formate dehydrogenase
cb
FDH was studied experimentally and theoretically. Scanning differential fluorimetric studies were performed to assess the thermal stability of
cb
FDH, while UV detection was used to reveal changes in
cb
FDH activity and reaction equilibrium at osmolyte concentrations between 0.25 and 1 mol kg
−1
. The thermodynamic model ePC-SAFT advanced allowed predicting the effects of osmolyte on the reaction equilibrium by accounting for interactions involving osmolyte, products, substrates, and water. The results show that osmolytes at low concentrations were beneficial for both, thermal stability and
cb
FDH activity, while keeping the equilibrium yield at high level. Molecular dynamics simulations were used to describe the solvation around the
cb
FDH surface and the volume exclusion effect, proofing the beneficial effect of the osmolytes on
cb
FDH activity, especially at low concentrations of trimethylamine
N
-oxide and betaine. Different mechanisms of stabilisation (dependent on the osmolyte) show the importance of studying solvent-protein dynamics towards the design of optimised biocatalytic processes.
The effect of osmolytes was studied on FDH properties: termal stability, initial enzyme activity, long-term stability and reaction equilibrium by experimental methods (UV-VIS and fluorimetrics) supported by theory (PC-SAFT and MD simulations).</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2cp04011e</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-3571-4973</orcidid><orcidid>https://orcid.org/0000-0001-9989-7206</orcidid><orcidid>https://orcid.org/0000-0003-1389-8836</orcidid><orcidid>https://orcid.org/0000-0002-2238-1807</orcidid><orcidid>https://orcid.org/0000-0002-3189-3628</orcidid><orcidid>https://orcid.org/0000-0002-5038-9152</orcidid><orcidid>https://orcid.org/0000-0003-1074-177X</orcidid><oa>free_for_read</oa></addata></record> |
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source | Royal Society of Chemistry Journals |
subjects | Biocatalysts Dehydrogenases Design optimization Equilibrium Formate dehydrogenase Low concentrations Molecular dynamics Proteins Reaction kinetics Solvation Stability analysis Substrates Thermal stability Thermodynamic models Trehalose Trimethylamine |
title | Osmolyte effect on enzymatic stability and reaction equilibrium of formate dehydrogenase |
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