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丝裂霉素C诱导细菌和原生质体中recA蛋白的合成

Induction by mitomycin C of recA protein synthesis in bacteria and spheroplasts.

作者信息

Giacomoni P U

出版信息

J Biol Chem. 1982 Dec 25;257(24):14932-6.

PMID:6816801
Abstract

The effect of mitomycin C on the synthesis of recA protein in Escherichia coli has been analyzed in a variety of conditions, using an immunoradiometric assay (Paoletti, C., Salles, B., and Giacomoni, P. U. (1982) Biochimie 64, 239-246). In exponentially growing cultures of E. coli AB 1157, the addition of mitomycin C (5 micrograms/ml) promotes a 15-fold increase of the content of recA protein with respect to the basal level. Kinetic analysis of this induction shows that the maximum is reached 60 to 90 min after the addition of the drug and then the level decreases. In an uvrA mutant treated with mitomycin C the level of recA protein reaches a maximum within an hour and afterwards it does not decrease. Treatment of exponentially growing cells with EDTA and lysozyme induces a 3-fold increase of recA protein content, in comparison to the basal level. When such spheroplasts are added with mitomycin or nalidixic acid, a striking increase of the recA protein content in the spheroplast suspension is observed, which tends to level off an hour and a half after the addition of the drugs. The maximum level of recA protein content is five times the level measured after lysozyme treatment, i.e. 15 times the basal level in exponentially growing cells.

摘要

运用免疫放射分析方法(Paoletti, C., Salles, B., and Giacomoni, P. U. (1982) Biochimie 64, 239 - 246),在多种条件下分析了丝裂霉素C对大肠杆菌中recA蛋白合成的影响。在大肠杆菌AB 1157的指数生长培养物中,添加丝裂霉素C(5微克/毫升)可使recA蛋白含量相对于基础水平增加15倍。对这种诱导作用的动力学分析表明,在添加药物后60至90分钟达到最大值,然后水平下降。在用丝裂霉素C处理的uvrA突变体中,recA蛋白水平在一小时内达到最大值,之后不再下降。用EDTA和溶菌酶处理指数生长的细胞,与基础水平相比,recA蛋白含量增加3倍。当向这种原生质体添加丝裂霉素或萘啶酸时,在原生质体悬浮液中观察到recA蛋白含量显著增加,在添加药物后一个半小时趋于稳定。recA蛋白含量的最高水平是溶菌酶处理后测量水平的5倍,即指数生长细胞中基础水平的15倍。

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