Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (6/6 displayed)

  • 2023Exploring Alkyl-O-Alkyl Ether Structures in Softwood Milled Wood Lignins9citations
  • 2020Fungal Treatment Modifies Kraft Lignin for Lignin- and Cellulose-Based Carbon Fiber Precursors25citations
  • 2020Applicability of Recombinant Laccases From the White-Rot Fungus Obba rivulosa for Mediator-Promoted Oxidation of Biorefinery Lignin at Low pH19citations
  • 2016Effect of Fatty Acid Esterification on the Thermal Properties of Softwood Kraft Lignin102citations
  • 2014Phenolic mediators enhance the manganese peroxidase catalyzed oxidation of recalcitrant lignin model compounds and synthetic lignin62citations
  • 2011Oxidation of lignans and lignin model compounds by laccase in aqueous solvent systems41citations

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Balakshin, Mikhail
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Zhu, Xuhai
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Rosenau, Thomas
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Potthast, Antje
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Maltari, Riku
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Hildén, Kristiina
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Kemell, Marianna Leena
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Mikkilä, Joona Aleksi
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Hummel, Michael
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Trogen, Mikaela
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Mäkelä, Miia R.
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Kontro, Jussi
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Dekere, Zane
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Kuuskeri, Jaana
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Koivu, Klaus A. Y.
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Nousiainen, Paula A.
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Nousiainen, Paula Annukka
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Kähkönen, Mika
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Nousiainen, Paula
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Argyropoulos, Dimitris S.
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Sadeghifar, Hasan
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Manner, Helmiina
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Hatakka, Annele
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Maijala, Pekka
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Viikari, Liisa
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Tamminen, Tarja
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Willför, Stefan
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Mattinen, Maija-Liisa
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Smeds, Annika
1 / 2 shared
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2020
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Co-Authors (by relevance)

  • Balakshin, Mikhail
  • Zhu, Xuhai
  • Rosenau, Thomas
  • Potthast, Antje
  • Maltari, Riku
  • Hildén, Kristiina
  • Kemell, Marianna Leena
  • Mikkilä, Joona Aleksi
  • Hummel, Michael
  • Trogen, Mikaela
  • Mäkelä, Miia R.
  • Kontro, Jussi
  • Dekere, Zane
  • Kuuskeri, Jaana
  • Koivu, Klaus A. Y.
  • Nousiainen, Paula A.
  • Nousiainen, Paula Annukka
  • Kähkönen, Mika
  • Nousiainen, Paula
  • Argyropoulos, Dimitris S.
  • Sadeghifar, Hasan
  • Manner, Helmiina
  • Hatakka, Annele
  • Maijala, Pekka
  • Viikari, Liisa
  • Tamminen, Tarja
  • Willför, Stefan
  • Mattinen, Maija-Liisa
  • Smeds, Annika
OrganizationsLocationPeople

article

Phenolic mediators enhance the manganese peroxidase catalyzed oxidation of recalcitrant lignin model compounds and synthetic lignin

  • Kontro, Jussi
  • Manner, Helmiina
  • Nousiainen, Paula
  • Hatakka, Annele
  • Sipilä, Jussi
Abstract

<p>Fungal oxidative enzymes, such as peroxidases and laccases, are the key catalysts in lignin biodegradation in vivo, and consequently provide an important source for industrial ligninolytic biocatalysts. Recently, it has been shown that some syringyl-type phenolics have potential as industrial co-oxidants or mediators, in laccase-catalyzed modification of lignocellulosic material. We have now studied the effect of such mediators with ligninolytic peroxidases on oxidation of the most recalcitrant lignin model compounds. We found that they are able to enhance the manganese peroxidase (MnP) catalyzed oxidation reactions of small non-phenolic compounds, veratryl alcohol and veratrylglycerol β-guaiacyl ether (adlerol), which are not usually oxidized by manganese peroxidases alone. In these experiments we compared two peroxidases from white-rot fungi, MnP from Phlebia sp. Nf b19 and versatile peroxidase (VP) from Bjerkandera adusta under two oxidation conditions: (i) the Mn(III) initiated mediated oxidation by syringyl compounds and (ii) the system involving MnP-dependent lipid peroxidation, both with production of (hydrogen) peroxides in situ to maintain the peroxidase catalytic cycle. It was found that both peroxidases produced α-carbonyl oxidation product of veratryl alcohol in clearly higher yields in reactions mediated by phenoxy radicals than in lipid-peroxyl radical system. The oxidation of adlerol, on the other hand, was more efficient in lipid-peroxidation-system. VP was more efficient than MnP in the oxidation of veratryl alcohol and showed its lignin peroxidase type activity in the reaction conditions indicated by some cleavage of Cα-Cβ-bond of adlerol. Finally, the mediator assisted oxidation conditions were applied in the oxidation of synthetic lignin (DHP) and the structural analysis of the oxidized polymers showed clear modifications in the polymer outcome, e.g. the oxidation resulted in reduced amount of aliphatic hydroxyls indicated by <sup>31</sup>P NMR.</p>

Topics
  • compound
  • polymer
  • experiment
  • Hydrogen
  • lignin
  • Nuclear Magnetic Resonance spectroscopy
  • Manganese
  • alcohol