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真核生物核糖体蛋白刺激大肠杆菌严谨因子合成鸟苷5'-二磷酸-3'-二磷酸(ppGpp)和鸟苷5'-三磷酸-3'-二磷酸(pppGpp)。

Eukaryotic ribosomal proteins stimulate Escherichia coli stringent factor to synthesize guanosine 5'-diphosphate, 3'-diphosphate (ppGpp) and guanosine 5'-triphosphate, 3'-diphosphate (ppGpp).

作者信息

Martini O, Richter D

出版信息

Mol Gen Genet. 1978 Nov 9;166(3):291-7. doi: 10.1007/BF00267621.

Abstract

When supplemented with Escherichia coli stringent factor, 80S ribosomes from various sources failed to support guanosine tetra- and pentaphosphate ((p)ppGpp) synthesis. In contrast, ribosomal proteins from 80S, 60S or 40S particles (mouse embryos, rabbit reticulocytes) crossreacted with the E. coli stringent factor. Significant stimulation of (p)ppGpp synthesis was achieved with a concentration as low as 5 micrograms of ribosomal proteins/ml. These observations may provide additional crtieria to detect homologies between eukaryotic and prokaryotic ribosomal proteins.

摘要

当补充大肠杆菌严谨因子时,来自各种来源的80S核糖体无法支持四磷酸鸟苷和五磷酸鸟苷((p)ppGpp)的合成。相比之下,80S、60S或40S颗粒(小鼠胚胎、兔网织红细胞)中的核糖体蛋白与大肠杆菌严谨因子发生交叉反应。每毫升低至5微克的核糖体蛋白就能显著刺激(p)ppGpp的合成。这些观察结果可能为检测真核生物和原核生物核糖体蛋白之间的同源性提供额外的标准。

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