Fatty Acid Chain Shortening by a Fungal Peroxygenase
A recently discovered peroxygenase from the fungus Marasmius rotula (MroUPO) is able to catalyze the progressive one‐carbon shortening of medium and long‐chain mono‐ and dicarboxylic acids by itself alone, in the presence of H2O2. The mechanism, analyzed using H218O2, starts with an α‐oxidation cata...
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Published in | Chemistry : a European journal Vol. 23; no. 67; pp. 16985 - 16989 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Wiley Subscription Services, Inc
01.12.2017
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0947-6539 1521-3765 1521-3765 |
DOI | 10.1002/chem.201704773 |
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Abstract | A recently discovered peroxygenase from the fungus Marasmius rotula (MroUPO) is able to catalyze the progressive one‐carbon shortening of medium and long‐chain mono‐ and dicarboxylic acids by itself alone, in the presence of H2O2. The mechanism, analyzed using H218O2, starts with an α‐oxidation catalyzed by MroUPO generating an α‐hydroxy acid, which is further oxidized by the enzyme to a reactive α‐keto intermediate whose decarboxylation yields the one‐carbon shorter fatty acid. Compared with the previously characterized peroxygenase of Agrocybe aegerita, a wider heme access channel, enabling fatty acid positioning with the carboxylic end near the heme cofactor (as seen in one of the crystal structures available) could be at the origin of the unique ability of MroUPO shortening carboxylic acid chains.
Magic from a mushroom: A peroxygenase from the fungus Marasmius rotula catalyzes the stepwise chain shortening of carboxylic acids by one carbon atom, in the presence of H2O2 as the sole co‐substrate. |
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AbstractList | A recently discovered peroxygenase from the fungus Marasmius rotula (MroUPO) is able to catalyze the progressive one‐carbon shortening of medium and long‐chain mono‐ and dicarboxylic acids by itself alone, in the presence of H2O2. The mechanism, analyzed using H218O2, starts with an α‐oxidation catalyzed by MroUPO generating an α‐hydroxy acid, which is further oxidized by the enzyme to a reactive α‐keto intermediate whose decarboxylation yields the one‐carbon shorter fatty acid. Compared with the previously characterized peroxygenase of Agrocybe aegerita, a wider heme access channel, enabling fatty acid positioning with the carboxylic end near the heme cofactor (as seen in one of the crystal structures available) could be at the origin of the unique ability of MroUPO shortening carboxylic acid chains.
Magic from a mushroom: A peroxygenase from the fungus Marasmius rotula catalyzes the stepwise chain shortening of carboxylic acids by one carbon atom, in the presence of H2O2 as the sole co‐substrate. A recently discovered peroxygenase from the fungus Marasmius rotula (MroUPO) is able to catalyze the progressive one-carbon shortening of medium and long-chain mono- and dicarboxylic acids by itself alone, in the presence of H O . The mechanism, analyzed using H O , starts with an α-oxidation catalyzed by MroUPO generating an α-hydroxy acid, which is further oxidized by the enzyme to a reactive α-keto intermediate whose decarboxylation yields the one-carbon shorter fatty acid. Compared with the previously characterized peroxygenase of Agrocybe aegerita, a wider heme access channel, enabling fatty acid positioning with the carboxylic end near the heme cofactor (as seen in one of the crystal structures available) could be at the origin of the unique ability of MroUPO shortening carboxylic acid chains. A recently discovered peroxygenase from the fungus Marasmius rotula (MroUPO) is able to catalyze the progressive one-carbon shortening of medium and long-chain mono- and dicarboxylic acids by itself alone, in the presence of H2 O2 . The mechanism, analyzed using H218 O2 , starts with an α-oxidation catalyzed by MroUPO generating an α-hydroxy acid, which is further oxidized by the enzyme to a reactive α-keto intermediate whose decarboxylation yields the one-carbon shorter fatty acid. Compared with the previously characterized peroxygenase of Agrocybe aegerita, a wider heme access channel, enabling fatty acid positioning with the carboxylic end near the heme cofactor (as seen in one of the crystal structures available) could be at the origin of the unique ability of MroUPO shortening carboxylic acid chains.A recently discovered peroxygenase from the fungus Marasmius rotula (MroUPO) is able to catalyze the progressive one-carbon shortening of medium and long-chain mono- and dicarboxylic acids by itself alone, in the presence of H2 O2 . The mechanism, analyzed using H218 O2 , starts with an α-oxidation catalyzed by MroUPO generating an α-hydroxy acid, which is further oxidized by the enzyme to a reactive α-keto intermediate whose decarboxylation yields the one-carbon shorter fatty acid. Compared with the previously characterized peroxygenase of Agrocybe aegerita, a wider heme access channel, enabling fatty acid positioning with the carboxylic end near the heme cofactor (as seen in one of the crystal structures available) could be at the origin of the unique ability of MroUPO shortening carboxylic acid chains. A recently discovered peroxygenase from the fungus Marasmius rotula (MroUPO) is able to catalyze the progressive one-carbon shortening of medium and long-chain mono- and dicarboxylic acids by itself alone, in the presence of H2O2. The mechanism, analyzed using H218O2, starts with an [alpha]-oxidation catalyzed by MroUPO generating an [alpha]-hydroxy acid, which is further oxidized by the enzyme to a reactive [alpha]-keto intermediate whose decarboxylation yields the one-carbon shorter fatty acid. Compared with the previously characterized peroxygenase of Agrocybe aegerita, a wider heme access channel, enabling fatty acid positioning with the carboxylic end near the heme cofactor (as seen in one of the crystal structures available) could be at the origin of the unique ability of MroUPO shortening carboxylic acid chains. A recently discovered peroxygenase from the fungus Marasmius rotula ( Mro UPO) is able to catalyze the progressive one‐carbon shortening of medium and long‐chain mono‐ and dicarboxylic acids by itself alone, in the presence of H 2 O 2 . The mechanism, analyzed using H 2 18 O 2 , starts with an α‐oxidation catalyzed by Mro UPO generating an α‐hydroxy acid, which is further oxidized by the enzyme to a reactive α‐keto intermediate whose decarboxylation yields the one‐carbon shorter fatty acid. Compared with the previously characterized peroxygenase of Agrocybe aegerita , a wider heme access channel, enabling fatty acid positioning with the carboxylic end near the heme cofactor (as seen in one of the crystal structures available) could be at the origin of the unique ability of Mro UPO shortening carboxylic acid chains. |
Author | Hofrichter, Martin Río, José C. del Martínez, Angel T. Scheibner, Katrin Olmedo, Andrés Ullrich, René Gutiérrez, Ana Kiebist, Jan |
AuthorAffiliation | 4 Centro de Investigaciones Biológicas, CSIC Ramiro de Maeztu 9 28040 Madrid Spain 1 Instituto de Recursos Naturales y Agrobiología de Sevilla, CSIC Reina Mercedes 10 41012 Seville Spain 2 JenaBios GmbH Löbstedter Str. 80 07749 Jena Germany 3 TU Dresden Markt 23 02763 Zittau Germany |
AuthorAffiliation_xml | – name: 4 Centro de Investigaciones Biológicas, CSIC Ramiro de Maeztu 9 28040 Madrid Spain – name: 3 TU Dresden Markt 23 02763 Zittau Germany – name: 1 Instituto de Recursos Naturales y Agrobiología de Sevilla, CSIC Reina Mercedes 10 41012 Seville Spain – name: 2 JenaBios GmbH Löbstedter Str. 80 07749 Jena Germany |
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Keywords | oxidation enzymes chain shortening carboxylic acids hydrogen peroxide |
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Snippet | A recently discovered peroxygenase from the fungus Marasmius rotula (MroUPO) is able to catalyze the progressive one‐carbon shortening of medium and long‐chain... A recently discovered peroxygenase from the fungus Marasmius rotula ( Mro UPO) is able to catalyze the progressive one‐carbon shortening of medium and... A recently discovered peroxygenase from the fungus Marasmius rotula (MroUPO) is able to catalyze the progressive one-carbon shortening of medium and long-chain... |
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SubjectTerms | Agrocybe - enzymology Carboxylic acids Catalysis chain shortening Chains Chemistry Communication Communications Crystal structure Decarboxylation Dicarboxylic acids enzymes Fatty acids Fatty Acids - chemistry Fungal Proteins - chemistry Heme Heme - chemistry Hydrogen - chemistry Hydrogen peroxide Kinetics Mixed Function Oxygenases - chemistry Molecular Structure Oxidation Oxidation-Reduction Oxygen - chemistry Thermodynamics |
Title | Fatty Acid Chain Shortening by a Fungal Peroxygenase |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fchem.201704773 https://www.ncbi.nlm.nih.gov/pubmed/29083064 https://www.proquest.com/docview/1970572273 https://www.proquest.com/docview/1957767020 https://pubmed.ncbi.nlm.nih.gov/PMC5725704 |
Volume | 23 |
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