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6-Hydroxy-5-nitrobenzo[d]oxazol-2(3H)-one-A degradable derivative of natural 6-Hydroxybenzoxazolin-2(3H)-one produced by Pantoea ananatis.
Schulz, Margot; Sicker, Dieter; Schackow, Oliver; Hennig, Lothar; Hofmann, Diana; Disko, Ulrich; Ventura, Marina; Basyuk, Kateryna.
Afiliação
  • Schulz M; IMBIO Institute of Molecular Physiology and Biotechnology of Plants, University of Bonn, Bonn, Germany.
  • Sicker D; Institut für Organische Chemie, Universität Leipzig, Leipzig, Germany.
  • Schackow O; Institut für Organische Chemie, Universität Leipzig, Leipzig, Germany.
  • Hennig L; Institut für Organische Chemie, Universität Leipzig, Leipzig, Germany.
  • Hofmann D; IBG-3: Agrosphäre, Forschungszentrum Jülich GmbH, Jülich, Germany.
  • Disko U; IBG-3: Agrosphäre, Forschungszentrum Jülich GmbH, Jülich, Germany.
  • Ventura M; IMBIO Institute of Molecular Physiology and Biotechnology of Plants, University of Bonn, Bonn, Germany.
  • Basyuk K; IMBIO Institute of Molecular Physiology and Biotechnology of Plants, University of Bonn, Bonn, Germany.
Commun Integr Biol ; 10(3): e1302633, 2017.
Article em En | MEDLINE | ID: mdl-28702124
ABSTRACT
Pantoea ananatis is a bacterium associated with other microorganisms on Abutilon theophrasti Medik. roots. It converts 6-hydroxybenzoxazolin-2(3H)-one (BOA-6-OH), a hydroxylated derivative of the allelochemical benzoxazolin-2(3H)-one, into 6-hydroxy-5-nitrobenzo[d]oxazol-2(3H)-one. The compound was identified by NMR and mass spectrometric methods. In vitro synthesis succeeded with Pantoea protein, with isolated proteins from the Abutilon root surface or with horseradish peroxidase in the presence of nitrite and H2O2. Nitro-BOA-6-OH is completely degraded further by Pantoea ananatis and Abutilon root surface proteins. Under laboratory conditions, 6-hydroxy-5-nitrobenzo[d]oxazol-2(3H)-one inhibits Lepidium sativum seedling growth whereas Abutilon theophrasti is much less affected. Although biodegradable, an agricultural use of 6-hydroxy-5-nitrobenzo[d]oxazol-2(3H)-one is undesirable because of the high toxicity of nitro aromatic compounds to mammals.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article