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Enzymatic oxidation of cadmium and lead metals photodeposited on cadmium sulfide
Cadmium and lead metals deposited on CdS particles are shown to act as substrates — electron donors for enzymes, hydrogenase from Thiocapsa roseopersicina (HG), NAD-dependent hydrogenase from Alcaligenes eutrophus (NLH), and ferredoxin:NADP oxidoreductase (FNR) from Chlorella in the formation of hyd...
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Published in: | BIOELECTROCHEMISTRY 2001, Vol.53 (1), p.61-71 |
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creator | Nedoluzhko, Aleksey I Shumilin, Igor A Mazhorova, Lubov E Popov, Vladimir O Nikandrov, Vitaly V |
description | Cadmium and lead metals deposited on CdS particles are shown to act as substrates — electron donors for enzymes, hydrogenase from
Thiocapsa roseopersicina (HG), NAD-dependent hydrogenase from
Alcaligenes eutrophus (NLH), and ferredoxin:NADP oxidoreductase (FNR) from
Chlorella in the formation of hydrogen, NADH and NADPH, respectively. Adsorption of the enzyme on the surface of the metallized CdS particle is required for enzymatic oxidation of metal. The maximum rates for the formation of hydrogen and NADH catalyzed by hydrogenase and NAD-dependent hydrogenase with metals as electron donors are comparable with the rates obtained for these enzymes using soluble substrates. Kinetic analysis of the enzymatic oxidation of cadmium metal has revealed that the rate decreases mainly due to the formation of a solid product, which is supposed to be Cd(OH)
2. The deceleration of lead oxidation catalyzed by hydrogenase proceeds at the expense of the inhibitory effect of the formed Pb
2+. The enzymatic oxidation of electrochemically prepared cadmium metal is also shown. Based on these results, a new mechanism of action of the enzymes involved in anaerobic biocorrosion is proposed. By this mechanism, the enzyme accelerates the process of metal dissolution through a mediatorless catalysis of the reduction of the enzyme substrate. |
doi_str_mv | 10.1016/S0302-4598(00)00094-5 |
format | article |
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Thiocapsa roseopersicina (HG), NAD-dependent hydrogenase from
Alcaligenes eutrophus (NLH), and ferredoxin:NADP oxidoreductase (FNR) from
Chlorella in the formation of hydrogen, NADH and NADPH, respectively. Adsorption of the enzyme on the surface of the metallized CdS particle is required for enzymatic oxidation of metal. The maximum rates for the formation of hydrogen and NADH catalyzed by hydrogenase and NAD-dependent hydrogenase with metals as electron donors are comparable with the rates obtained for these enzymes using soluble substrates. Kinetic analysis of the enzymatic oxidation of cadmium metal has revealed that the rate decreases mainly due to the formation of a solid product, which is supposed to be Cd(OH)
2. The deceleration of lead oxidation catalyzed by hydrogenase proceeds at the expense of the inhibitory effect of the formed Pb
2+. The enzymatic oxidation of electrochemically prepared cadmium metal is also shown. Based on these results, a new mechanism of action of the enzymes involved in anaerobic biocorrosion is proposed. By this mechanism, the enzyme accelerates the process of metal dissolution through a mediatorless catalysis of the reduction of the enzyme substrate.</description><identifier>ISSN: 1567-5394</identifier><identifier>ISSN: 0302-4598</identifier><identifier>EISSN: 1878-562X</identifier><identifier>DOI: 10.1016/S0302-4598(00)00094-5</identifier><identifier>PMID: 11206926</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adsorption ; Algal Proteins - chemistry ; Algal Proteins - metabolism ; Bacterial Proteins - chemistry ; Bacterial Proteins - metabolism ; Biocorrosion ; Cadmium ; Cadmium - chemistry ; Cadmium Compounds - chemistry ; Catalysis ; CdS ; Charge transfer ; Deposition ; Electrochemical corrosion ; Electrochemistry - methods ; Electron transfer ; Enzymes, Immobilized - chemistry ; Enzymes, Immobilized - metabolism ; Ferredoxin-NADP Reductase - chemistry ; Ferredoxin-NADP Reductase - metabolism ; Hydrogenase ; Hydrogenase - chemistry ; Hydrogenase - metabolism ; Kinetics ; Lead ; Lead - chemistry ; Metal oxidation ; Models, Chemical ; NADH, NADPH Oxidoreductases - chemistry ; NADH, NADPH Oxidoreductases - metabolism ; Oxidation ; Oxidation-Reduction ; Oxidoreductases ; Oxidoreductases - chemistry ; Oxidoreductases - metabolism ; Photochemical reactions ; Photochemistry ; Semiconducting cadmium compounds ; Sulfides - chemistry</subject><ispartof>BIOELECTROCHEMISTRY, 2001, Vol.53 (1), p.61-71</ispartof><rights>2000 Elsevier Science S.A.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-f3d0329598a1fe09d4a219844af07fba881d5e17fd192afead7a41c080eb4b393</citedby><cites>FETCH-LOGICAL-c392t-f3d0329598a1fe09d4a219844af07fba881d5e17fd192afead7a41c080eb4b393</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11206926$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nedoluzhko, Aleksey I</creatorcontrib><creatorcontrib>Shumilin, Igor A</creatorcontrib><creatorcontrib>Mazhorova, Lubov E</creatorcontrib><creatorcontrib>Popov, Vladimir O</creatorcontrib><creatorcontrib>Nikandrov, Vitaly V</creatorcontrib><title>Enzymatic oxidation of cadmium and lead metals photodeposited on cadmium sulfide</title><title>BIOELECTROCHEMISTRY</title><addtitle>Bioelectrochemistry</addtitle><description>Cadmium and lead metals deposited on CdS particles are shown to act as substrates — electron donors for enzymes, hydrogenase from
Thiocapsa roseopersicina (HG), NAD-dependent hydrogenase from
Alcaligenes eutrophus (NLH), and ferredoxin:NADP oxidoreductase (FNR) from
Chlorella in the formation of hydrogen, NADH and NADPH, respectively. Adsorption of the enzyme on the surface of the metallized CdS particle is required for enzymatic oxidation of metal. The maximum rates for the formation of hydrogen and NADH catalyzed by hydrogenase and NAD-dependent hydrogenase with metals as electron donors are comparable with the rates obtained for these enzymes using soluble substrates. Kinetic analysis of the enzymatic oxidation of cadmium metal has revealed that the rate decreases mainly due to the formation of a solid product, which is supposed to be Cd(OH)
2. The deceleration of lead oxidation catalyzed by hydrogenase proceeds at the expense of the inhibitory effect of the formed Pb
2+. The enzymatic oxidation of electrochemically prepared cadmium metal is also shown. Based on these results, a new mechanism of action of the enzymes involved in anaerobic biocorrosion is proposed. By this mechanism, the enzyme accelerates the process of metal dissolution through a mediatorless catalysis of the reduction of the enzyme substrate.</description><subject>Adsorption</subject><subject>Algal Proteins - chemistry</subject><subject>Algal Proteins - metabolism</subject><subject>Bacterial Proteins - chemistry</subject><subject>Bacterial Proteins - metabolism</subject><subject>Biocorrosion</subject><subject>Cadmium</subject><subject>Cadmium - chemistry</subject><subject>Cadmium Compounds - chemistry</subject><subject>Catalysis</subject><subject>CdS</subject><subject>Charge transfer</subject><subject>Deposition</subject><subject>Electrochemical corrosion</subject><subject>Electrochemistry - methods</subject><subject>Electron transfer</subject><subject>Enzymes, Immobilized - chemistry</subject><subject>Enzymes, Immobilized - metabolism</subject><subject>Ferredoxin-NADP Reductase - chemistry</subject><subject>Ferredoxin-NADP Reductase - metabolism</subject><subject>Hydrogenase</subject><subject>Hydrogenase - chemistry</subject><subject>Hydrogenase - metabolism</subject><subject>Kinetics</subject><subject>Lead</subject><subject>Lead - chemistry</subject><subject>Metal oxidation</subject><subject>Models, Chemical</subject><subject>NADH, NADPH Oxidoreductases - chemistry</subject><subject>NADH, NADPH Oxidoreductases - metabolism</subject><subject>Oxidation</subject><subject>Oxidation-Reduction</subject><subject>Oxidoreductases</subject><subject>Oxidoreductases - chemistry</subject><subject>Oxidoreductases - metabolism</subject><subject>Photochemical reactions</subject><subject>Photochemistry</subject><subject>Semiconducting cadmium compounds</subject><subject>Sulfides - chemistry</subject><issn>1567-5394</issn><issn>0302-4598</issn><issn>1878-562X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqFkE1r3DAQhkVoaT7an5DgU0kOTmZkyZZOIYS0DQQaaAu9Ca00oiq2tbHskvTXV5vd0GNOM4dn5n15GDtGOEfA9uIbNMBrIbU6BTgDAC1quccOUHWqli3_-abssu1q2Wixzw5z_l0ghZ18x_YRObSatwfs_mb8-zTYOboqPUZfljRWKVTO-iEuQ2VHX_VkfTXQbPtcrX-lOXlapxxn8lWBX8i89CF6es_ehgLSh908Yj8-3Xy__lLfff18e311V7tG87kOjYeG61LfYiDQXliOWglhA3RhZZVCLwm74FFzG0qDzgp0oIBWYtXo5oh93P5dT-lhoTybIWZHfW9HSks2HUjVAHavghyFECg3oNyCbko5TxTMeoqDnZ4Mgtk4N8_Ozca5ATDPzo0sdye7gGU1kP9_tZNcgMstQMXHn0iTyS7S6MjHidxsfIqvRPwDidaReA</recordid><startdate>2001</startdate><enddate>2001</enddate><creator>Nedoluzhko, Aleksey I</creator><creator>Shumilin, Igor A</creator><creator>Mazhorova, Lubov E</creator><creator>Popov, Vladimir O</creator><creator>Nikandrov, Vitaly V</creator><general>Elsevier B.V</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></search><sort><creationdate>2001</creationdate><title>Enzymatic oxidation of cadmium and lead metals photodeposited on cadmium sulfide</title><author>Nedoluzhko, Aleksey I ; Shumilin, Igor A ; Mazhorova, Lubov E ; Popov, Vladimir O ; Nikandrov, Vitaly V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c392t-f3d0329598a1fe09d4a219844af07fba881d5e17fd192afead7a41c080eb4b393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adsorption</topic><topic>Algal Proteins - chemistry</topic><topic>Algal Proteins - metabolism</topic><topic>Bacterial Proteins - chemistry</topic><topic>Bacterial Proteins - metabolism</topic><topic>Biocorrosion</topic><topic>Cadmium</topic><topic>Cadmium - chemistry</topic><topic>Cadmium Compounds - chemistry</topic><topic>Catalysis</topic><topic>CdS</topic><topic>Charge transfer</topic><topic>Deposition</topic><topic>Electrochemical corrosion</topic><topic>Electrochemistry - methods</topic><topic>Electron transfer</topic><topic>Enzymes, Immobilized - chemistry</topic><topic>Enzymes, Immobilized - metabolism</topic><topic>Ferredoxin-NADP Reductase - chemistry</topic><topic>Ferredoxin-NADP Reductase - metabolism</topic><topic>Hydrogenase</topic><topic>Hydrogenase - chemistry</topic><topic>Hydrogenase - metabolism</topic><topic>Kinetics</topic><topic>Lead</topic><topic>Lead - chemistry</topic><topic>Metal oxidation</topic><topic>Models, Chemical</topic><topic>NADH, NADPH Oxidoreductases - chemistry</topic><topic>NADH, NADPH Oxidoreductases - metabolism</topic><topic>Oxidation</topic><topic>Oxidation-Reduction</topic><topic>Oxidoreductases</topic><topic>Oxidoreductases - chemistry</topic><topic>Oxidoreductases - metabolism</topic><topic>Photochemical reactions</topic><topic>Photochemistry</topic><topic>Semiconducting cadmium compounds</topic><topic>Sulfides - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nedoluzhko, Aleksey I</creatorcontrib><creatorcontrib>Shumilin, Igor A</creatorcontrib><creatorcontrib>Mazhorova, Lubov E</creatorcontrib><creatorcontrib>Popov, Vladimir O</creatorcontrib><creatorcontrib>Nikandrov, Vitaly V</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>BIOELECTROCHEMISTRY</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nedoluzhko, Aleksey I</au><au>Shumilin, Igor A</au><au>Mazhorova, Lubov E</au><au>Popov, Vladimir O</au><au>Nikandrov, Vitaly V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enzymatic oxidation of cadmium and lead metals photodeposited on cadmium sulfide</atitle><jtitle>BIOELECTROCHEMISTRY</jtitle><addtitle>Bioelectrochemistry</addtitle><date>2001</date><risdate>2001</risdate><volume>53</volume><issue>1</issue><spage>61</spage><epage>71</epage><pages>61-71</pages><issn>1567-5394</issn><issn>0302-4598</issn><eissn>1878-562X</eissn><abstract>Cadmium and lead metals deposited on CdS particles are shown to act as substrates — electron donors for enzymes, hydrogenase from
Thiocapsa roseopersicina (HG), NAD-dependent hydrogenase from
Alcaligenes eutrophus (NLH), and ferredoxin:NADP oxidoreductase (FNR) from
Chlorella in the formation of hydrogen, NADH and NADPH, respectively. Adsorption of the enzyme on the surface of the metallized CdS particle is required for enzymatic oxidation of metal. The maximum rates for the formation of hydrogen and NADH catalyzed by hydrogenase and NAD-dependent hydrogenase with metals as electron donors are comparable with the rates obtained for these enzymes using soluble substrates. Kinetic analysis of the enzymatic oxidation of cadmium metal has revealed that the rate decreases mainly due to the formation of a solid product, which is supposed to be Cd(OH)
2. The deceleration of lead oxidation catalyzed by hydrogenase proceeds at the expense of the inhibitory effect of the formed Pb
2+. The enzymatic oxidation of electrochemically prepared cadmium metal is also shown. Based on these results, a new mechanism of action of the enzymes involved in anaerobic biocorrosion is proposed. By this mechanism, the enzyme accelerates the process of metal dissolution through a mediatorless catalysis of the reduction of the enzyme substrate.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>11206926</pmid><doi>10.1016/S0302-4598(00)00094-5</doi><tpages>11</tpages></addata></record> |
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source | ScienceDirect Journals |
subjects | Adsorption Algal Proteins - chemistry Algal Proteins - metabolism Bacterial Proteins - chemistry Bacterial Proteins - metabolism Biocorrosion Cadmium Cadmium - chemistry Cadmium Compounds - chemistry Catalysis CdS Charge transfer Deposition Electrochemical corrosion Electrochemistry - methods Electron transfer Enzymes, Immobilized - chemistry Enzymes, Immobilized - metabolism Ferredoxin-NADP Reductase - chemistry Ferredoxin-NADP Reductase - metabolism Hydrogenase Hydrogenase - chemistry Hydrogenase - metabolism Kinetics Lead Lead - chemistry Metal oxidation Models, Chemical NADH, NADPH Oxidoreductases - chemistry NADH, NADPH Oxidoreductases - metabolism Oxidation Oxidation-Reduction Oxidoreductases Oxidoreductases - chemistry Oxidoreductases - metabolism Photochemical reactions Photochemistry Semiconducting cadmium compounds Sulfides - chemistry |
title | Enzymatic oxidation of cadmium and lead metals photodeposited on cadmium sulfide |
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