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Nitrogen regulation of lignin peroxidase gene transcription.

机译:木质素过氧化物酶基因转录的氮调节。

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Western blot (immunoblot) analysis with a polyclonal antibody to lignin peroxidase (LiP) isozyme H8 from the white rot basidiomycete Phanerochaete chrysosporium demonstrates that LiP protein is detectable in the extracellular media of 5- and 6-day-old nitrogen-limited, but not nitrogen-sufficient, cultures. Northern (RNA) blot analysis demonstrates that lip mRNA is detectable from 5- and 6-day old cells grown in nitrogen-limited, but not nitrogen-sufficient, cultures. These results indicate that LiP expression is regulated at the level of gene transcription by nutrient nitrogen. Since lignin degradation by P. chrysosporium is derepressed by nitrogen starvation, it appears that lignin degradation and LiP expression are coordinately regulated in this organism. These results contradict a recent report which concluded that LiP protein expression is not regulated by nutrient nitrogen (C. G. Johnston and S. D. Aust, Biochem. Biophys. Res. Commun. 200:108-112, 1994).
机译:使用针对来自白色腐烂担子菌Phanerochaete chrysosporium的木质素过氧化物酶(LiP)同工酶H8的多克隆抗体进行的蛋白质印迹(免疫印迹)分析表明,LiP蛋白可在5天和6天大氮限制的细胞外培养基中检测到,但不是氮充足,培养。 Northern(RNA)印迹分析表明,从在氮有限但不富氮的培养物中生长的5天和6天龄细胞中可检测到嘴唇mRNA。这些结果表明,LiP的表达受营养氮调控在基因转录水平上。由于氮饥饿会抑制金黄色葡萄球菌对木质素的降解,因此似乎在该生物中协调地调节了木质素的降解和LiP的表达。这些结果与最近的报告相矛盾,该报告得出结论,LiP蛋白的表达不受营养氮的调节(C.G.Johnston和S.D.Aust,Biochem.Biophys.Res.Commun.200:108-112,1994)。

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