...
首页> 外文期刊>Biocontrol Science >Phenol-Oxidizing Enzyme Expression in Lentinula edodes by the Addition of Sawdust Extract, Aromatic Compounds, or Copper in Liquid Culture Media
【24h】

Phenol-Oxidizing Enzyme Expression in Lentinula edodes by the Addition of Sawdust Extract, Aromatic Compounds, or Copper in Liquid Culture Media

机译:通过添加木屑提取物,芳香族化合物或铜在液体培养基中的香菇中的苯酚氧化酶表达。

获取原文
           

摘要

This study examined how the addition of a sawdust extract from Castanopsis cuspidata , several aromatic compounds, and copper affected the expression of a phenol-oxidizing enzyme in the white-rot basidiomycete, Lentinula edodes . Compared to liquid media that had not been supplemented with sawdust extract (MYPG), MYPG containing low (MYPG-S_(100)) or high (MYPG-S_(500)) concentrations of sawdust extract had a marked effect on the promotion of mycelial growth. No manganese peroxidase (MnP) production was observed in either MYPG or MYPG-S_(100) media until 35 days after inoculation. However, MnP production was enhanced by culture in MYPG-S_(500), with a marked increase observed suddenly at 14 days after inoculation. Northern blot analysis revealed that the transcription of the lemnp2 gene coding extracellular MnP was initially observed at detectable levels at day 10 after the initial inoculation of MYPG-S_(500), increasing gradually thereafter until days 22-25. However, laccase (Lcc) production was not observed in any of the media until 35 days after inoculation. Addition of 10 mM aromatic compounds - 1,2-benzenediol, 2-methoxyphenol, hydroquinone, and 4-anisidine - into the MYPG-S_(500) medium completely inhibited MnP production and did not enhance any Lcc production. While the addition of 1 or 2 mM Cu~(2+) (CuSO_(4)?5H_(2)O) to MYPG-S_(500) medium completely inhibited MnP production, this Cu~(2+ )addition caused a marked increase in Lcc production at 17 and 6 days after the addition, respectively.
机译:这项研究检查了添加来自 Castanopsis cuspidata的锯末提取物,几种芳香族化合物和铜如何影响白腐烂担子菌 Lentinula edodes中酚氧化酶的表达。与未添加木屑提取物(MYPG)的液体培养基相比,低浓度(MYPG-S_(100))或高浓度(MYPG-S_(500))的MYPG对菌丝体的促进作用明显。增长。接种后35天,在MYPG或MYPG-S_(100)培养基中均未观察到锰过氧化物酶(MnP)的产生。但是,通过在MYPG-S_(500)中进行培养可以提高MnP的产量,在接种后第14天突然观察到明显的增加。 Northern印迹分析显示,最初接种MYPG-S_(500)后第10天,最初以可检测的水平观察到编码细胞外MnP的Ilemmp2基因的转录,此后逐渐增加直至22-25天。然而,直到接种后35天,在任何培养基中都未观察到漆酶(Lcc)的产生。向MYPG-S_(500)介质中添加10 mM芳香族化合物-1,2-苯二醇,2-甲氧基苯酚,对苯二酚和4-茴香胺-完全抑制了MnP的产生,并且没有提高任何Lcc的产生。向MYPG-S_(500)介质中添加1或2 mM Cu〜(2+)(CuSO_(4)?5H_(2)O)完全抑制了MnP的产生,但Cu〜(2+)的添加引起了明显的抑制作用。添加后第17天和第6天Lcc产量分别增加。

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