首页> 外文期刊>Enzyme and Microbial Technology >Intracellular ferrireductase involved in Mn(IV)-educting enzyme enzyme system to supply Mn(II) for lignin biodegradation by white-rot fungus Phanerochaete sordida YK-624
【24h】

Intracellular ferrireductase involved in Mn(IV)-educting enzyme enzyme system to supply Mn(II) for lignin biodegradation by white-rot fungus Phanerochaete sordida YK-624

机译:胞内亚铁还原酶参与Mn(IV)还原酶系统,为白腐真菌Phanerochaete sordida YK-624降解木质素提供Mn(II)

获取原文
获取原文并翻译 | 示例
           

摘要

In the biobleaching of kraft pulp with white-rot Phanerochaete sordida YK-624, it was confirmed that manganese dioxide (Mn(IV)) in kraft pulp was reduced to Mn(II) by ESR analysis.By this reactions, the production of manganese peroxidase (MnP) by P.sordida YK-624 was triggered and then the kraft pulp was bleached with MnP. In the liquid culture, the reduction of manganese dioxide was observed by the washed mycelia of P.sordida YK-624 although smaller amount of Mn(II) was produced by the extracellular culture fluid.The reduction by the washed mycelia was dependent on Fe(II), a metal chlator ,and NAD(P)H. Moreover, the cell-free extract from P.Sordida YK-624 catalyzed the reduction of ferric chelate to ferrous chelate in the presence of NAD(P)H. It is likely , therefore , that ferrous chelate reduce manganese dioxide and that the produced ferric chelate is reduced by intracellular NAD(P)H-dependent, that ferrous chelate reduces manganese dioxide and that the produced ferric chelate is reduced by intracellular NAD(P)H-dependent reductase to regenerate ferrous chelate. An intracellular NADPH-dependent reducate , anmely NADPH-dependent ferrireductase (molecular weight 35 kDa, pI 5.1), was purified from P.sordida YK-624 .Moreover, there was a good correlation between the production of intracellular ferrireductase and that of extracellular MnP in a liquid culture containing manganese dioxide. These results suggest that the ferrireductase is involved in the production of MnP by the reduction of manganese dioxide to Mn(II)
机译:用白腐菌Phanerochaete sordida YK-624对牛皮纸浆进行生物漂白时,通过ESR分析证实牛皮纸浆中的二氧化锰(Mn(IV))被还原为Mn(II)。引发腐烂假单胞菌YK-624过氧化物酶(MnP),然后用MnP漂白牛皮纸浆。在液体培养中,尽管经细胞外培养液产生的Mn(II)量较少,但腐烂的毕赤酵母YK-624的菌丝体观察到二氧化锰的减少。洗涤的菌丝体的还原取决于Fe( II),金属螯合剂和NAD(P)H。此外,在NAD(P)H存在下,来自P.Sordida YK-624的无细胞提取物催化铁螯合物还原为亚铁螯合物。因此,螯合亚铁可能会还原二氧化锰,而细胞内NAD(P)H依赖性会降低生成的铁螯合物,螯合亚铁会还原二氧化锰,而细胞内NAD(P)可能会降低生成的铁螯合物H依赖性还原酶可再生螯合亚铁。从腐殖假单胞菌YK-624中纯化出一种细胞内NADPH依赖性还原酶,淀粉酶NADPH依赖性铁还原酶(分子量35 kDa,pI 5.1),此外,细胞内亚铁还原酶的产生与细胞外MnP的产生有良好的相关性。在含有二氧化锰的液体培养物中这些结果表明,亚铁还原酶通过将二氧化锰还原成Mn(II)参与MnP的生产。

著录项

相似文献

  • 外文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号