Schulz Margot, Sicker Dieter, Schackow Oliver, Hennig Lothar, Hofmann Diana, Disko Ulrich, Ventura Marina, Basyuk Kateryna
IMBIO Institute of Molecular Physiology and Biotechnology of Plants, University of Bonn, Bonn, Germany.
Institut für Organische Chemie, Universität Leipzig, Leipzig, Germany.
Commun Integr Biol. 2017 Mar 13;10(3):e1302633. doi: 10.1080/19420889.2017.1302633. eCollection 2017.
is a bacterium associated with other microorganisms on Medik. roots. It converts 6-hydroxybenzoxazolin-2(3)-one (BOA-6-OH), a hydroxylated derivative of the allelochemical benzoxazolin-2(3)-one, into 6-hydroxy-5-nitrobenzo[]oxazol-2(3)-one. The compound was identified by NMR and mass spectrometric methods. synthesis succeeded with protein, with isolated proteins from the root surface or with horseradish peroxidase in the presence of nitrite and HO. Nitro-BOA-6-OH is completely degraded further by and root surface proteins. Under laboratory conditions, 6-hydroxy-5-nitrobenzo[]oxazol-2(3)-one inhibits seedling growth whereas is much less affected. Although biodegradable, an agricultural use of 6-hydroxy-5-nitrobenzo[]oxazol-2(3)-one is undesirable because of the high toxicity of nitro aromatic compounds to mammals.
是一种与Medik.根上的其他微生物相关的细菌。它将化感物质苯并恶唑啉-2(3)-酮的羟基化衍生物6-羟基苯并恶唑啉-2(3)-酮(BOA-6-OH)转化为6-羟基-5-硝基苯并[]恶唑啉-2(3)-酮。该化合物通过核磁共振和质谱方法鉴定。在有蛋白质、从根表面分离的蛋白质或在亚硝酸盐和HO存在下用辣根过氧化物酶时合成成功。硝基-BOA-6-OH会被和根表面蛋白质进一步完全降解。在实验室条件下,6-羟基-5-硝基苯并[]恶唑啉-2(3)-酮抑制幼苗生长,而受到的影响小得多。尽管6-羟基-5-硝基苯并[]恶唑啉-2(3)-酮可生物降解,但由于硝基芳香化合物对哺乳动物具有高毒性,其农业用途并不理想。