首页> 外文期刊>FEMS Microbiology Letters >Improvement of ligninolytic properties in the hyper lignin-degrading fungus Phanerochaete sordida YK-624 using a novel gene promoter
【24h】

Improvement of ligninolytic properties in the hyper lignin-degrading fungus Phanerochaete sordida YK-624 using a novel gene promoter

机译:使用新型基因启动子改善木质素过度降解真菌Phanerochaete sordida YK-624的木质素分解特性

获取原文
获取原文并翻译 | 示例
           

摘要

We identified a highly expressed protein (BUNA2) by two-dimensional gel electrophoresis from the hyper lignin-degrading fungus Phanerochaete sordida YK-624 under wood-rotting conditions. Partial amino acid sequences of BUNA2 were determined by LC-MS/MS analysis, and BUNA2 gene (bee2) and promoter region were PCR-cloned and sequenced. The bee2 promoter was used to drive the expression of the manganese peroxidase gene (mnp4) in P. sordida YK-624. Eighteen mnp4-expressing clones were obtained, with most showing higher ligninolytic activity and selectivity than wild-type YK-624. Examination of the ligninolytic properties of the most effective lignin-degrading transformant, BM-65, cultured on wood meal revealed that this strain exhibited higher lignin degradation and MnP activities than those of wild type. Transcriptional analysis confirmed the increased expression of recombinant mnp4 in the transformant. These results indicate that use of the bee2 promoter to drive the expression of ligninolytic enzymes may be an effective approach for improving the lignin-degrading properties of white-rot fungi.
机译:我们通过二维凝胶电泳从木质素降解条件下的高木质素降解真菌Phanerochaete sordida YK-624鉴定了高表达蛋白(BUNA2)。通过LC-MS / MS分析确定BUNA2的部分氨基酸序列,并对BUNA2基因(bee2)和启动子区域进行PCR克隆和测序。使用bee2启动子来驱动锰过氧化物酶基因(mnp4)在P. sordida YK-624中表达。获得了18个表达mnp4的克隆,其中大多数显示出比野生型YK-624更高的木质素分解活性和选择性。在木粉上培养的最有效的降解木质素的转化体BM-65的木质素分解特性研究表明,该菌株比野生型具有更高的木质素降解和MnP活性。转录分析证实了重组mnp4在转化体中的表达增加。这些结果表明,使用bee2启动子驱动木质素分解酶的表达可能是改善白腐真菌木质素降解特性的有效方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 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