The release of iron from horse spleen ferritin by reduced flavins
Ferritin-Fe(III) was rapidly and quantitatively reduced and liberated as Fe(II) by FMNH(2), FADH(2) and reduced riboflavin. Dithionite also released Fe(II) from ferritin but at less than 1% of the rate with FMNH(2). Cysteine, glutathione and ascorbate gave a similar slower rate and yielded less than...
Gespeichert in:
Veröffentlicht in: | Biochemical journal 1974-11, Vol.143 (2), p.311-315 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 315 |
---|---|
container_issue | 2 |
container_start_page | 311 |
container_title | Biochemical journal |
container_volume | 143 |
creator | Sirivech, S Frieden, E Osaki, S |
description | Ferritin-Fe(III) was rapidly and quantitatively reduced and liberated as Fe(II) by FMNH(2), FADH(2) and reduced riboflavin. Dithionite also released Fe(II) from ferritin but at less than 1% of the rate with FMNH(2). Cysteine, glutathione and ascorbate gave a similar slower rate and yielded less than 20% of the total iron from ferritin within a few hours. The reduction of ferritin-Fe(III) by the three riboflavin compounds gave complex second-order kinetics with overlapping fast and slow reactions. The fast reaction appeared to be non-specific and may be due to a reduction of Fe(III) of a lower degree of polymerization, equilibrated with ferritin iron. The amount of this Fe(3+) ion initially reduced was small, less than 0.3% of the total iron. Addition of FMN to the ferritin-dithionite system enhanced the reduction; this is due to the reduction of FMN by dithionite to form FMNH(2) which then reduces ferritin-Fe(III). A comparison of the thermodynamic parameters of FMNH(2)-ferritin and dithionite-ferritin complex formation showed that FMNH(2) required a lower activation energy and a negative entropy change, whereas dithionite required 50% more activation energy and showed a positive entropy change in ferritin reduction. The effectiveness of FMNH(2) in ferritin-Fe(III) reduction may be due to a specific binding of the riboflavin moiety to the protein portion of the ferritin molecule. |
doi_str_mv | 10.1042/bj1430311 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1168386</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>82707242</sourcerecordid><originalsourceid>FETCH-LOGICAL-c436t-988377b1eb8be85daa90c3d5b45ce1c1aeb00792c86022630066a33cf3ed85e3</originalsourceid><addsrcrecordid>eNpVkEtLAzEUhYMotVYX_gBhVoKL0ZvHZNKNUIovKLjpPiSZOzZlOqnJTKH_3pGWoqsL536ccziE3FJ4pCDYk11TwYFTekbGVJSQq5KpczIGJkUugdFLcpXSGoAKEDAiIyEkK4pyTGbLFWYRGzQJs1BnPoY2q2PYZKsQByltG8RBwRh959vM7ge66h1WWd2YnW_TNbmoTZPw5ngnZPn6spy_54vPt4_5bJE7wWWXT5XiZWkpWmVRFZUxU3C8KqwoHFJHDVqAcsqcGvoyyQGkNJy7mmOlCuQT8nyw3fZ2g5XDtoum0dvoNybudTBe__-0fqW_wk5TKhVXcjC4PxrE8N1j6vTGJ4dNY1oMfdKKlVAywQbw4QC6GFKKWJ9CKOjfufVp7oG9-9vqRB735T8rlXsV</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>82707242</pqid></control><display><type>article</type><title>The release of iron from horse spleen ferritin by reduced flavins</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Sirivech, S ; Frieden, E ; Osaki, S</creator><creatorcontrib>Sirivech, S ; Frieden, E ; Osaki, S</creatorcontrib><description>Ferritin-Fe(III) was rapidly and quantitatively reduced and liberated as Fe(II) by FMNH(2), FADH(2) and reduced riboflavin. Dithionite also released Fe(II) from ferritin but at less than 1% of the rate with FMNH(2). Cysteine, glutathione and ascorbate gave a similar slower rate and yielded less than 20% of the total iron from ferritin within a few hours. The reduction of ferritin-Fe(III) by the three riboflavin compounds gave complex second-order kinetics with overlapping fast and slow reactions. The fast reaction appeared to be non-specific and may be due to a reduction of Fe(III) of a lower degree of polymerization, equilibrated with ferritin iron. The amount of this Fe(3+) ion initially reduced was small, less than 0.3% of the total iron. Addition of FMN to the ferritin-dithionite system enhanced the reduction; this is due to the reduction of FMN by dithionite to form FMNH(2) which then reduces ferritin-Fe(III). A comparison of the thermodynamic parameters of FMNH(2)-ferritin and dithionite-ferritin complex formation showed that FMNH(2) required a lower activation energy and a negative entropy change, whereas dithionite required 50% more activation energy and showed a positive entropy change in ferritin reduction. The effectiveness of FMNH(2) in ferritin-Fe(III) reduction may be due to a specific binding of the riboflavin moiety to the protein portion of the ferritin molecule.</description><identifier>ISSN: 0264-6021</identifier><identifier>EISSN: 1470-8728</identifier><identifier>DOI: 10.1042/bj1430311</identifier><identifier>PMID: 4462557</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; Ascorbic Acid ; Cysteine ; Dithionite ; Ferritins ; Flavins ; Glutathione ; Horses ; In Vitro Techniques ; Iron ; Kinetics ; Oxidation-Reduction ; Protein Binding ; Proteins ; Riboflavin ; Spleen ; Thermodynamics</subject><ispartof>Biochemical journal, 1974-11, Vol.143 (2), p.311-315</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-988377b1eb8be85daa90c3d5b45ce1c1aeb00792c86022630066a33cf3ed85e3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1168386/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1168386/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,724,777,781,882,27906,27907,53773,53775</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/4462557$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sirivech, S</creatorcontrib><creatorcontrib>Frieden, E</creatorcontrib><creatorcontrib>Osaki, S</creatorcontrib><title>The release of iron from horse spleen ferritin by reduced flavins</title><title>Biochemical journal</title><addtitle>Biochem J</addtitle><description>Ferritin-Fe(III) was rapidly and quantitatively reduced and liberated as Fe(II) by FMNH(2), FADH(2) and reduced riboflavin. Dithionite also released Fe(II) from ferritin but at less than 1% of the rate with FMNH(2). Cysteine, glutathione and ascorbate gave a similar slower rate and yielded less than 20% of the total iron from ferritin within a few hours. The reduction of ferritin-Fe(III) by the three riboflavin compounds gave complex second-order kinetics with overlapping fast and slow reactions. The fast reaction appeared to be non-specific and may be due to a reduction of Fe(III) of a lower degree of polymerization, equilibrated with ferritin iron. The amount of this Fe(3+) ion initially reduced was small, less than 0.3% of the total iron. Addition of FMN to the ferritin-dithionite system enhanced the reduction; this is due to the reduction of FMN by dithionite to form FMNH(2) which then reduces ferritin-Fe(III). A comparison of the thermodynamic parameters of FMNH(2)-ferritin and dithionite-ferritin complex formation showed that FMNH(2) required a lower activation energy and a negative entropy change, whereas dithionite required 50% more activation energy and showed a positive entropy change in ferritin reduction. The effectiveness of FMNH(2) in ferritin-Fe(III) reduction may be due to a specific binding of the riboflavin moiety to the protein portion of the ferritin molecule.</description><subject>Animals</subject><subject>Ascorbic Acid</subject><subject>Cysteine</subject><subject>Dithionite</subject><subject>Ferritins</subject><subject>Flavins</subject><subject>Glutathione</subject><subject>Horses</subject><subject>In Vitro Techniques</subject><subject>Iron</subject><subject>Kinetics</subject><subject>Oxidation-Reduction</subject><subject>Protein Binding</subject><subject>Proteins</subject><subject>Riboflavin</subject><subject>Spleen</subject><subject>Thermodynamics</subject><issn>0264-6021</issn><issn>1470-8728</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1974</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkEtLAzEUhYMotVYX_gBhVoKL0ZvHZNKNUIovKLjpPiSZOzZlOqnJTKH_3pGWoqsL536ccziE3FJ4pCDYk11TwYFTekbGVJSQq5KpczIGJkUugdFLcpXSGoAKEDAiIyEkK4pyTGbLFWYRGzQJs1BnPoY2q2PYZKsQByltG8RBwRh959vM7ge66h1WWd2YnW_TNbmoTZPw5ngnZPn6spy_54vPt4_5bJE7wWWXT5XiZWkpWmVRFZUxU3C8KqwoHFJHDVqAcsqcGvoyyQGkNJy7mmOlCuQT8nyw3fZ2g5XDtoum0dvoNybudTBe__-0fqW_wk5TKhVXcjC4PxrE8N1j6vTGJ4dNY1oMfdKKlVAywQbw4QC6GFKKWJ9CKOjfufVp7oG9-9vqRB735T8rlXsV</recordid><startdate>19741101</startdate><enddate>19741101</enddate><creator>Sirivech, S</creator><creator>Frieden, E</creator><creator>Osaki, S</creator><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><scope>5PM</scope></search><sort><creationdate>19741101</creationdate><title>The release of iron from horse spleen ferritin by reduced flavins</title><author>Sirivech, S ; Frieden, E ; Osaki, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-988377b1eb8be85daa90c3d5b45ce1c1aeb00792c86022630066a33cf3ed85e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1974</creationdate><topic>Animals</topic><topic>Ascorbic Acid</topic><topic>Cysteine</topic><topic>Dithionite</topic><topic>Ferritins</topic><topic>Flavins</topic><topic>Glutathione</topic><topic>Horses</topic><topic>In Vitro Techniques</topic><topic>Iron</topic><topic>Kinetics</topic><topic>Oxidation-Reduction</topic><topic>Protein Binding</topic><topic>Proteins</topic><topic>Riboflavin</topic><topic>Spleen</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sirivech, S</creatorcontrib><creatorcontrib>Frieden, E</creatorcontrib><creatorcontrib>Osaki, S</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochemical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sirivech, S</au><au>Frieden, E</au><au>Osaki, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The release of iron from horse spleen ferritin by reduced flavins</atitle><jtitle>Biochemical journal</jtitle><addtitle>Biochem J</addtitle><date>1974-11-01</date><risdate>1974</risdate><volume>143</volume><issue>2</issue><spage>311</spage><epage>315</epage><pages>311-315</pages><issn>0264-6021</issn><eissn>1470-8728</eissn><abstract>Ferritin-Fe(III) was rapidly and quantitatively reduced and liberated as Fe(II) by FMNH(2), FADH(2) and reduced riboflavin. Dithionite also released Fe(II) from ferritin but at less than 1% of the rate with FMNH(2). Cysteine, glutathione and ascorbate gave a similar slower rate and yielded less than 20% of the total iron from ferritin within a few hours. The reduction of ferritin-Fe(III) by the three riboflavin compounds gave complex second-order kinetics with overlapping fast and slow reactions. The fast reaction appeared to be non-specific and may be due to a reduction of Fe(III) of a lower degree of polymerization, equilibrated with ferritin iron. The amount of this Fe(3+) ion initially reduced was small, less than 0.3% of the total iron. Addition of FMN to the ferritin-dithionite system enhanced the reduction; this is due to the reduction of FMN by dithionite to form FMNH(2) which then reduces ferritin-Fe(III). A comparison of the thermodynamic parameters of FMNH(2)-ferritin and dithionite-ferritin complex formation showed that FMNH(2) required a lower activation energy and a negative entropy change, whereas dithionite required 50% more activation energy and showed a positive entropy change in ferritin reduction. The effectiveness of FMNH(2) in ferritin-Fe(III) reduction may be due to a specific binding of the riboflavin moiety to the protein portion of the ferritin molecule.</abstract><cop>England</cop><pmid>4462557</pmid><doi>10.1042/bj1430311</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0264-6021 |
ispartof | Biochemical journal, 1974-11, Vol.143 (2), p.311-315 |
issn | 0264-6021 1470-8728 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_1168386 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection |
subjects | Animals Ascorbic Acid Cysteine Dithionite Ferritins Flavins Glutathione Horses In Vitro Techniques Iron Kinetics Oxidation-Reduction Protein Binding Proteins Riboflavin Spleen Thermodynamics |
title | The release of iron from horse spleen ferritin by reduced flavins |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T09%3A06%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20release%20of%20iron%20from%20horse%20spleen%20ferritin%20by%20reduced%20flavins&rft.jtitle=Biochemical%20journal&rft.au=Sirivech,%20S&rft.date=1974-11-01&rft.volume=143&rft.issue=2&rft.spage=311&rft.epage=315&rft.pages=311-315&rft.issn=0264-6021&rft.eissn=1470-8728&rft_id=info:doi/10.1042/bj1430311&rft_dat=%3Cproquest_pubme%3E82707242%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=82707242&rft_id=info:pmid/4462557&rfr_iscdi=true |