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作为大肠杆菌中近紫外诱导合成四磷酸鸟苷靶点的硫醇化嘧啶转运核糖核酸

tRNA thiolated pyrimidines as targets for near-ultraviolet-induced synthesis of guanosine tetraphosphate in Escherichia coli.

作者信息

Thomas G, Thiam K, Favre A

出版信息

Eur J Biochem. 1981 Oct;119(2):381-7. doi: 10.1111/j.1432-1033.1981.tb05619.x.

Abstract

Illumination with near-ultraviolet light triggers synthesis of ppGpp (guanosine 3'-diphosphate 5'-diphosphate) not only in growing Escherichia coli cells containing the putative chromophore 4-thiouridine in their tRNAs [Ramabhadran, T. V and Jagger, J. (1976) Proc. Natl Acad. Sci. USA, 73, 59--69], but also in nuv- cells which lack 4-thiouridine. The burst of ppGpp in nuv- cells is, however, induced exclusively by light of wavelengths shorter than 350 nm. Its maximum level is half that obtained in the parental strain. This ppGpp synthesis is also under the control of the relA gene, indicating that it is due to the accumulation of uncharged tRNAs. A candidate likely to trigger this effect is a 5-methylaminomethyl-2-thiouracil residues present in the first position of the anticodon loop of tRNAGlu, tRNALys and one tRNAGln isoacceptor. In conditions in vitro, this base is highly photoreactive at wavelengths shorter than 350 nm. Furthermore, near-ultraviolet-photomodified tRNAGlu and tRNALys become poor substrates of their acylation enzyme.

摘要

近紫外光照射不仅会在其tRNA中含有假定发色团4-硫尿苷的生长中的大肠杆菌细胞中触发ppGpp(鸟苷3'-二磷酸5'-二磷酸)的合成[Ramabhadran, T. V和Jagger, J. (1976) Proc. Natl Acad. Sci. USA, 73, 59 - 69],而且在缺乏4-硫尿苷的nuv-细胞中也会触发。然而,nuv-细胞中ppGpp的爆发仅由波长小于350 nm的光诱导。其最大水平是亲代菌株中所获得水平的一半。这种ppGpp合成也受relA基因的控制,表明这是由于无电荷tRNA的积累所致。一个可能触发这种效应的候选物是存在于tRNAGlu、tRNALys和一种tRNAGln同功受体反密码子环第一位的5-甲基氨基甲基-2-硫尿嘧啶残基。在体外条件下,该碱基在波长小于350 nm时具有高度光反应性。此外,近紫外光光修饰的tRNAGlu和tRNALys成为其酰化酶的不良底物。

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