NMR Spectroscopic Analysis of the First Two Steps of the Pentose-Phosphate Pathway Elucidates the Role of 6-Phosphogluconolactonase
The pentose-phosphate pathway provides reductive power and nucleotide precursors to the cell through oxidative and nonoxidative branches, respectively. 6-Phosphogluconolactonase is the second enzyme of the oxidative branch and catalyzes the hydrolysis of 6-phosphogluconolactones, the products of glu...
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Veröffentlicht in: | The Journal of biological chemistry 2001-09, Vol.276 (37), p.34840-34846 |
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creator | Miclet, Emeric Stoven, Véronique Michels, Paul A.M. Opperdoes, Fred R. Lallemand, Jean-Yves Duffieux, Francis |
description | The pentose-phosphate pathway provides reductive power and nucleotide precursors to the cell through oxidative and nonoxidative branches, respectively. 6-Phosphogluconolactonase is the second enzyme of the oxidative branch and catalyzes the hydrolysis of 6-phosphogluconolactones, the products of glucose 6-phosphate oxidation by glucose-6-phosphate dehydrogenase. The role of 6-phosphogluconolactonase was still questionable, because 6-phosphogluconolactones were believed to undergo rapid spontaneous hydrolysis. In this work, nuclear magnetic resonance spectroscopy was used to characterize the chemical scheme and kinetic features of the oxidative branch. We show that 6-phosphogluconolactones have in fact a nonnegligible lifetime and are highly electrophilic compounds. The δ form (1-5) of the lactone is the only product of glucose 6-phosphate oxidation. Subsequently, it leads to the γ form (1-4) by intramolecular rearrangement. However, only the δ form undergoes spontaneous hydrolysis, the γ form being a “dead end” of this branch. The δ form is the only substrate for 6-phosphogluconolactonase. Therefore, 6-phosphogluconolactonase activity accelerates hydrolysis of the δ form, thus preventing its conversion into the γ form. Furthermore, 6-phosphogluconolactonase guards against the accumulation of δ-6-phosphogluconolactone, which may be toxic through its reaction with endogenous cellular nucleophiles. Finally, the difference between activity of human,Trypanosoma brucei, and Plasmodium falciparum6-phosphogluconolactonases is reported and discussed. |
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The role of 6-phosphogluconolactonase was still questionable, because 6-phosphogluconolactones were believed to undergo rapid spontaneous hydrolysis. In this work, nuclear magnetic resonance spectroscopy was used to characterize the chemical scheme and kinetic features of the oxidative branch. We show that 6-phosphogluconolactones have in fact a nonnegligible lifetime and are highly electrophilic compounds. The δ form (1-5) of the lactone is the only product of glucose 6-phosphate oxidation. Subsequently, it leads to the γ form (1-4) by intramolecular rearrangement. However, only the δ form undergoes spontaneous hydrolysis, the γ form being a “dead end” of this branch. The δ form is the only substrate for 6-phosphogluconolactonase. Therefore, 6-phosphogluconolactonase activity accelerates hydrolysis of the δ form, thus preventing its conversion into the γ form. Furthermore, 6-phosphogluconolactonase guards against the accumulation of δ-6-phosphogluconolactone, which may be toxic through its reaction with endogenous cellular nucleophiles. Finally, the difference between activity of human,Trypanosoma brucei, and Plasmodium falciparum6-phosphogluconolactonases is reported and discussed.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M105174200</identifier><identifier>PMID: 11457850</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>6-Phosphogluconolactonase ; 6-phosphogluconolactones ; Carboxylic Ester Hydrolases - physiology ; Chemical Sciences ; glucose-6-phosphate ; Glucose-6-Phosphate - metabolism ; Humans ; Kinetics ; Magnetic Resonance Spectroscopy ; Organic chemistry ; Oxidation-Reduction ; Pentose Phosphate Pathway ; Plasmodium falciparum ; Substrate Specificity ; Trypanosoma brucei</subject><ispartof>The Journal of biological chemistry, 2001-09, Vol.276 (37), p.34840-34846</ispartof><rights>2001 © 2001 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c545t-50c3a53c3273a5f2c09c0a23da140e3f6688c25ed021f56213e03804c57d54a23</citedby><cites>FETCH-LOGICAL-c545t-50c3a53c3273a5f2c09c0a23da140e3f6688c25ed021f56213e03804c57d54a23</cites><orcidid>0000-0002-6250-1690 ; 0000-0003-0828-0759</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11457850$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://polytechnique.hal.science/hal-00954878$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Miclet, Emeric</creatorcontrib><creatorcontrib>Stoven, Véronique</creatorcontrib><creatorcontrib>Michels, Paul A.M.</creatorcontrib><creatorcontrib>Opperdoes, Fred R.</creatorcontrib><creatorcontrib>Lallemand, Jean-Yves</creatorcontrib><creatorcontrib>Duffieux, Francis</creatorcontrib><title>NMR Spectroscopic Analysis of the First Two Steps of the Pentose-Phosphate Pathway Elucidates the Role of 6-Phosphogluconolactonase</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>The pentose-phosphate pathway provides reductive power and nucleotide precursors to the cell through oxidative and nonoxidative branches, respectively. 6-Phosphogluconolactonase is the second enzyme of the oxidative branch and catalyzes the hydrolysis of 6-phosphogluconolactones, the products of glucose 6-phosphate oxidation by glucose-6-phosphate dehydrogenase. The role of 6-phosphogluconolactonase was still questionable, because 6-phosphogluconolactones were believed to undergo rapid spontaneous hydrolysis. In this work, nuclear magnetic resonance spectroscopy was used to characterize the chemical scheme and kinetic features of the oxidative branch. We show that 6-phosphogluconolactones have in fact a nonnegligible lifetime and are highly electrophilic compounds. The δ form (1-5) of the lactone is the only product of glucose 6-phosphate oxidation. Subsequently, it leads to the γ form (1-4) by intramolecular rearrangement. However, only the δ form undergoes spontaneous hydrolysis, the γ form being a “dead end” of this branch. The δ form is the only substrate for 6-phosphogluconolactonase. Therefore, 6-phosphogluconolactonase activity accelerates hydrolysis of the δ form, thus preventing its conversion into the γ form. Furthermore, 6-phosphogluconolactonase guards against the accumulation of δ-6-phosphogluconolactone, which may be toxic through its reaction with endogenous cellular nucleophiles. Finally, the difference between activity of human,Trypanosoma brucei, and Plasmodium falciparum6-phosphogluconolactonases is reported and discussed.</description><subject>6-Phosphogluconolactonase</subject><subject>6-phosphogluconolactones</subject><subject>Carboxylic Ester Hydrolases - physiology</subject><subject>Chemical Sciences</subject><subject>glucose-6-phosphate</subject><subject>Glucose-6-Phosphate - metabolism</subject><subject>Humans</subject><subject>Kinetics</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Organic chemistry</subject><subject>Oxidation-Reduction</subject><subject>Pentose Phosphate Pathway</subject><subject>Plasmodium falciparum</subject><subject>Substrate Specificity</subject><subject>Trypanosoma brucei</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUFv1DAQhS0EokvhyhHlgJA4ZBnHduIcV1VLkbZQtUXiZnknk8ZVNg6xt6s988fxsqv2hC8jPX9vNDOPsfcc5hwq-eVhhfMrDopXsgB4wWYctMiF4r9eshlAwfO6UPqEvQnhAdKTNX_NTjiXqtIKZuzP96ub7HYkjJMP6EeH2WKw_S64kPk2ix1lF24KMbvb-uw20vgkX9MQfaD8uvNh7GxMio3d1u6y836DrklK-Afe-J72pvKI-vv07wffW4x-sIHeslet7QO9O9ZT9vPi_O7sMl_--PrtbLHMUUkVcwUorBIoiirVtkCoEWwhGsslkGjLUmssFDVp61aVBRcEQoNEVTVKJvCUfT707Wxvxsmt7bQz3jpzuViavQZQK6kr_cgT--nAjpP_vaEQzdoFpL63A_lNMLzSda1KkcD5AcR0wDBR-9SZg9lHZFJE5jmiZPhw7LxZral5xo-ZJODjcUx3323dRGblPHa0NkVVGlEZIbXcY_qAUTrZo6PJBHQ0IDXJgtE03v1vhL_xYarA</recordid><startdate>20010914</startdate><enddate>20010914</enddate><creator>Miclet, Emeric</creator><creator>Stoven, Véronique</creator><creator>Michels, Paul A.M.</creator><creator>Opperdoes, Fred R.</creator><creator>Lallemand, Jean-Yves</creator><creator>Duffieux, Francis</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><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>M7N</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-6250-1690</orcidid><orcidid>https://orcid.org/0000-0003-0828-0759</orcidid></search><sort><creationdate>20010914</creationdate><title>NMR Spectroscopic Analysis of the First Two Steps of the Pentose-Phosphate Pathway Elucidates the Role of 6-Phosphogluconolactonase</title><author>Miclet, Emeric ; Stoven, Véronique ; Michels, Paul A.M. ; Opperdoes, Fred R. ; Lallemand, Jean-Yves ; Duffieux, Francis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c545t-50c3a53c3273a5f2c09c0a23da140e3f6688c25ed021f56213e03804c57d54a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>6-Phosphogluconolactonase</topic><topic>6-phosphogluconolactones</topic><topic>Carboxylic Ester Hydrolases - physiology</topic><topic>Chemical Sciences</topic><topic>glucose-6-phosphate</topic><topic>Glucose-6-Phosphate - metabolism</topic><topic>Humans</topic><topic>Kinetics</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Organic chemistry</topic><topic>Oxidation-Reduction</topic><topic>Pentose Phosphate Pathway</topic><topic>Plasmodium falciparum</topic><topic>Substrate Specificity</topic><topic>Trypanosoma brucei</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Miclet, Emeric</creatorcontrib><creatorcontrib>Stoven, Véronique</creatorcontrib><creatorcontrib>Michels, Paul A.M.</creatorcontrib><creatorcontrib>Opperdoes, Fred R.</creatorcontrib><creatorcontrib>Lallemand, Jean-Yves</creatorcontrib><creatorcontrib>Duffieux, Francis</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Miclet, Emeric</au><au>Stoven, Véronique</au><au>Michels, Paul A.M.</au><au>Opperdoes, Fred R.</au><au>Lallemand, Jean-Yves</au><au>Duffieux, Francis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NMR Spectroscopic Analysis of the First Two Steps of the Pentose-Phosphate Pathway Elucidates the Role of 6-Phosphogluconolactonase</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2001-09-14</date><risdate>2001</risdate><volume>276</volume><issue>37</issue><spage>34840</spage><epage>34846</epage><pages>34840-34846</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>The pentose-phosphate pathway provides reductive power and nucleotide precursors to the cell through oxidative and nonoxidative branches, respectively. 6-Phosphogluconolactonase is the second enzyme of the oxidative branch and catalyzes the hydrolysis of 6-phosphogluconolactones, the products of glucose 6-phosphate oxidation by glucose-6-phosphate dehydrogenase. The role of 6-phosphogluconolactonase was still questionable, because 6-phosphogluconolactones were believed to undergo rapid spontaneous hydrolysis. In this work, nuclear magnetic resonance spectroscopy was used to characterize the chemical scheme and kinetic features of the oxidative branch. We show that 6-phosphogluconolactones have in fact a nonnegligible lifetime and are highly electrophilic compounds. The δ form (1-5) of the lactone is the only product of glucose 6-phosphate oxidation. Subsequently, it leads to the γ form (1-4) by intramolecular rearrangement. However, only the δ form undergoes spontaneous hydrolysis, the γ form being a “dead end” of this branch. The δ form is the only substrate for 6-phosphogluconolactonase. Therefore, 6-phosphogluconolactonase activity accelerates hydrolysis of the δ form, thus preventing its conversion into the γ form. Furthermore, 6-phosphogluconolactonase guards against the accumulation of δ-6-phosphogluconolactone, which may be toxic through its reaction with endogenous cellular nucleophiles. Finally, the difference between activity of human,Trypanosoma brucei, and Plasmodium falciparum6-phosphogluconolactonases is reported and discussed.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11457850</pmid><doi>10.1074/jbc.M105174200</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-6250-1690</orcidid><orcidid>https://orcid.org/0000-0003-0828-0759</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 6-Phosphogluconolactonase 6-phosphogluconolactones Carboxylic Ester Hydrolases - physiology Chemical Sciences glucose-6-phosphate Glucose-6-Phosphate - metabolism Humans Kinetics Magnetic Resonance Spectroscopy Organic chemistry Oxidation-Reduction Pentose Phosphate Pathway Plasmodium falciparum Substrate Specificity Trypanosoma brucei |
title | NMR Spectroscopic Analysis of the First Two Steps of the Pentose-Phosphate Pathway Elucidates the Role of 6-Phosphogluconolactonase |
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