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木质素过氧化物酶基因转录的氮调控

Nitrogen regulation of lignin peroxidase gene transcription.

作者信息

Li D, Alic M, Gold M H

机构信息

Department of Chemistry, Biochemistry, and Molecular Biology, Oregon Graduate Institute of Science and Technology, Portland 97291-1000.

出版信息

Appl Environ Microbiol. 1994 Sep;60(9):3447-9. doi: 10.1128/aem.60.9.3447-3449.1994.

Abstract

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).

摘要

用来自白腐担子菌黄孢原毛平革菌的木质素过氧化物酶(LiP)同工酶H8的多克隆抗体进行蛋白质免疫印迹(免疫印迹)分析表明,在5日龄和6日龄的氮限制(而非氮充足)培养物的细胞外培养基中可检测到LiP蛋白。RNA印迹分析表明,在氮限制(而非氮充足)培养条件下生长的5日龄和6日龄细胞中可检测到lip mRNA。这些结果表明,LiP的表达在基因转录水平上受营养氮的调控。由于黄孢原毛平革菌对木质素的降解在氮饥饿时会被解除抑制,因此在该生物体中木质素降解和LiP表达似乎是协同调控的。这些结果与最近一篇报道相矛盾,该报道得出结论认为LiP蛋白表达不受营养氮的调控(C.G.约翰斯顿和S.D.奥斯特,《生物化学与生物物理研究通讯》200:108 - 112,1994)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1cf/201829/804186e91645/aem00026-0422-a.jpg

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