首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Hydrogen Peroxide Production as a Limiting Factor in Xenobiotic Compound Oxidation by Nitrogen-Sufficient Cultures of Bjerkandera sp. Strain BOS55 Overproducing Peroxidases
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Hydrogen Peroxide Production as a Limiting Factor in Xenobiotic Compound Oxidation by Nitrogen-Sufficient Cultures of Bjerkandera sp. Strain BOS55 Overproducing Peroxidases

机译:Bjerkandera sp。的氮充足培养物将过氧化氢的产生作为异源复合物氧化的限制因素。菌株BOS55过度生产过氧化物酶

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摘要

The overproduction of ligninolytic peroxidase by the N-deregulated white rot fungus Bjerkandera sp. strain BOS55 under nitrogen-sufficient conditions had no noteworthy effect on the oxidation of anthracene or the decolorization of the polymeric aromatic dye Poly R-478 in 6-day-old cultures. Only when the endogenous production of H(inf2)O(inf2) was increased by the addition of extra oxygen and glucose could a 2.5-fold increase in the anthracene oxidation rate and a 6-fold increase in the Poly R-478 decolorization rate be observed in high-N cultures with 10- to 35-fold higher peroxidase activities than N-limited cultures. Further increase of the H(inf2)O(inf2) generation rate in high-N cultures with glucose oxidase led to an additional 3.5-fold increase in the anthracene oxidation rate (350 mg liter(sup-1) day(sup-1)) and a 10-fold increase in the Poly R-478 decolorization rate. These results indicate that xenobiotic compound oxidation by white rot fungi cannot be improved by overproducing peroxidases without increasing the endogenous production of H(inf2)O(inf2). The absence of Mn, which decreased the manganese peroxidase titers and increased the lignin peroxidase titers, was associated with up to 95% improvements in the anthracene oxidation rate. The simultaneous presence of Mn and veratryl alcohol was observed to have a synergistic negative effect on the oxidation of anthracene and the decolorization of Poly R-478.
机译:N端白腐真菌Bjerkandera sp。产生的木质素过氧化物酶过量生产。氮充足的条件下,BOS55菌株对蒽的氧化或6天龄培养物中聚合芳香族染料Poly R-478的脱色没有显着影响。仅当通过添加额外的氧气和葡萄糖增加H(inf2)O(inf2)的内生产量时,蒽氧化速率才会增加2.5倍,而Poly R-478脱色速度则会增加6倍。在高氮培养物中观察到过氧化物酶活性比氮有限的培养物高10到35倍。葡萄糖氧化酶在高氮培养物中H(inf2)O(inf2)生成速率的进一步增加导致蒽氧化速率进一步增加3.5倍(350 mg升(sup-1)天(sup-1) ),而Poly R-478的脱色率提高了10倍。这些结果表明,在不增加H(inf2)O(inf2)内源性生产的情况下,过氧化物酶的过量生产不能改善白腐真菌的异生化合物氧化。锰的缺乏会降低锰过氧化物酶的效价并增加木质素过氧化物酶的效价,这与蒽氧化率提高高达95%有关。观察到同时存在锰和藜芦醇对蒽的氧化和聚R-478的脱色具有协同的负面影响。

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