紫外和γ辐照大肠杆菌体内腺苷酸环化酶活性。

A Chatterjee, A K Bhattacharya
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引用次数: 2

摘要

以大肠杆菌B/r全细胞将[14C]腺嘌呤掺入环AMP片段作为体内腺苷酸环化酶活性的衡量指标。60Co γ射线或杀菌灯紫外线照射可显著抑制细胞的这种活性,提示抑制环AMP的合成。低剂量(50-100 Gy) γ射线照射后的细胞孵育,体内腺苷酸环化酶活性显著增加,而高剂量(150 Gy及以上)照射后的细胞体内腺苷酸环化酶活性无显著变化。用紫外光(54 J m-2)照射后的细胞进行暗孵育,酶活性恢复到未照射细胞的水平。因此,紫外线和γ照射诱导的l -阿拉伯糖异构酶的分解代谢抑制似乎是由于照射细胞中环AMP合成的减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vivo adenylate cyclase activity in ultraviolet- and gamma-irradiated Escherichia coli.

The incorporation of [14C]adenine into the cyclic AMP fraction by whole cells of Escherichia coli B/r was taken as a measure of the in vivo adenylate cyclase activity. This activity was significantly inhibited by irradiation of the cells either with 60Co gamma-rays or with UV light from a germicidal lamp, suggesting inhibition of cyclic AMP synthesis. The incubation of cells after irradiation with lower doses (50-100 Gy) of gamma-rays produced a significant increase of in vivo adenylate cyclase activity, whereas there was no significant change after higher doses (150 Gy and above). Dark incubation of cells after irradiation with UV light (54 J m-2) led to recovery of enzyme activity to the level measured in unirradiated cells. Thus it appears that the catabolite repression of L-arabinose isomerase induced by UV light, as well as gamma-irradiation, is due to reduced cyclic AMP synthesis in irradiated cells.

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