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林业科学 ›› 2014, Vol. 50 ›› Issue (2): 139-143.

• 研究简报 • 上一篇    下一篇

偏肿革裥菌Lg-mnp2基因在构巢曲霉中的表达

胡美美, 池玉杰   

  1. 东北林业大学林学院 哈尔滨 150040
  • 收稿日期:2013-01-01 修回日期:2013-08-11 出版日期:2014-02-25 发布日期:2014-03-11
  • 基金资助:

    国家自然科学基金项目(30671700)。

Expression of the Gene Lg-mnp2 Encoding for Manganese Peroxidase 2 (MnP2) from White-Rot Fungus Lenzites gibbosa in Aspergillus nidulans

Hu Meimei, Chi Yujie   

  1. School of Forestry, Northeast Forestry University Harbin 150040
  • Received:2013-01-01 Revised:2013-08-11 Online:2014-02-25 Published:2014-03-11
  • Contact: 池玉杰

关键词: 偏肿革裥菌, 锰过氧化物酶2基因, 构巢曲霉, 转化, 表达

Abstract:

The aim of this study was to enhance manganese peroxidase (MnP) gene express by Lenzites gibbosa MnP production for using Aspergillus nidulans. In this study, an auxotrophic strain, TN02A7, of A.nidulans was used as the host of L. gibbosa.The conidiophores of TN02A7 were used to produce the protoplasts by different cell wall lyases, including lywallzyme, cellulase and snailase which were mixed together by 1:1:1 for effectively break down the wall and produce protoplasts. PEG/CaCl2 were used to mediate transformation of L. gibbosa, containing a gene encoding for manganese peroxidase 2 (Lg-MnP2), into the TN02A7 protoplast. The newly obtained transformant strain, TN02A7-Lg-mnp2 , and TN02A7 were cultured in the same shaking medium containing lignin and the MnP activity was detected. The result showed that TN02A7-Lg-mnp2 could produce MnP activity up to 17 U ·L-1 in 96 h, while TN02A7 did not produce MnP activity at any time, indicating that the gene Lg-mnp2 had been successfully transformed into TN02A7-Lg-mnp2 and expressed in lignin environment. This study provided a new method to produce MnP.

Key words: Lenzites gibbosa, Lg-mnp2, Aspergillus nidulans, transformation, expression

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