喹啉- dna碱基加合物QGI的仿生制备及结构测定。QGI是一种在4-硝基喹啉- 1-氧化物处理的细胞中形成的碱基加合物。

Gan Pub Date : 1984-11-01
M Tada, K H Kohda, Y Kawazoe
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引用次数: 0

摘要

其中一种喹啉- dna碱基加合物QGI是在4-硝基喹啉- 1-氧化物处理的细胞中形成的,在ATP、l -丝氨酸和丝氨酸tRNA合成酶的存在下,很容易在体外由GMP或dGMP和4-羟基氨基喹啉- 1-氧化物制备而成。合成的seryl-AMP可以取代酶激活体系形成QGI。对所制备的加合物进行化学和光谱分析表明,QGI可形成N4-(guanan -8-yl)-4-氨基喹啉1-氧化物,其结构与脱氧鸟苷-喹啉加合物中修饰的碱基结构相同,dGIII (Loucheux-Lefebvre等人的命名)是用4HAQO的单乙酰和双乙酰衍生物对脱氧鸟苷进行化学修饰得到的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biomimetic preparation and structure determination of QGI, one of the quinoline-DNA base adducts formed in cells treated with 4-nitroquinoline 1-oxide.

One of the quinoline-DNA base adducts, QGI, formed in cells treated with 4-nitroquinoline 1-oxide, was readily prepared in vitro from GMP or dGMP and 4-hydroxy-aminoquinoline 1-oxide in the presence of ATP, L-serine, and seryl tRNA synthetase. Synthetic seryl-AMP could be substituted for the enzymatic activation system for QGI formation. Chemical and spectral analyses of the adduct thus prepared revealed that QGI can be formulated as N4-(guan-8-yl)-4-aminoquinoline 1-oxide, the structure of which is identical with the modified base structure involved in the deoxyguanosine-quinoline adduct, dGIII (nomenclature of Loucheux-Lefebvre et al.) obtained by the chemical modification of deoxyguanosine with monoacetyl and diacetyl derivatives of 4HAQO.

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Gan
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