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 inChemistry : a European journal Vol. 23; no. 67; pp. 16985 - 16989
Main Authors Olmedo, Andrés, Río, José C. del, Kiebist, Jan, Ullrich, René, Hofrichter, Martin, Scheibner, Katrin, Martínez, Angel T., Gutiérrez, Ana
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 01.12.2017
John Wiley and Sons Inc
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Online AccessGet full text
ISSN0947-6539
1521-3765
1521-3765
DOI10.1002/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.
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
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– 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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  surname: Olmedo
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Issue 67
Keywords oxidation
enzymes
chain shortening
carboxylic acids
hydrogen peroxide
Language English
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2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
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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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