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[红霉素超级生产菌红链霉菌1571中自身抗生素两种保护系统的协同作用]

[Cooperative functioning of 2 systems of protection against its own antibiotic in Str. erythreus 1571, a superproducer of erythromycin].

作者信息

Griaznova N S, Beliavskaia I V, Subbotina N A, Listvinova S N, Orlova N V

出版信息

Antibiotiki. 1982 Feb;27(2):105-17.

PMID:7065644
Abstract

Protein synthesis in the mycelium of various ages and the protoplasts of Str. erythreus 1571 was slightly sensitive even to high concentrations of erythromycin and lincomycin. Oxytetracycline and neomycin in low concentrations induced marked inhibition of the protein synthesis. 14C-Erythromycin was binding with the mycelium of the organism producing it in much lower amounts than with the mycelium of Str. roseolus, a lincomycin-producing culture. No products of erythromycin biotransformation by the cell-free preparations of Str. erythreus containing cofactors for enzymatic phosphorylation and demethylation were detected with the methods of microbiological titration and radiochromatography. Enzymatic N-demethylation of lincomycin was observed in the cell-free preparations of Str. erythreus. Erythromycin and lincomycin had practically no effect on polylysine synthesis in the cell-free system of Str. erythreus with poly-A and inhibited the synthesis of this polypeptide in the cell-free systems of E. coli MRE 600 and B. subtilis ATCC 6633. These antibiotics had either no effect on the fragment (puromycin) reaction with the ribosomes of Str. erythreus. In case of the ribosomes of E. coli MRE 600 the fragment reaction was sensitive to lincomycin but not to erythromycin. The ribosomes isolated from Str. erythreus and their 50S subunits bound 14C-erythromycin in much lower amounts than those isolated from E. coli and their 50S subunits. The data are indicative of the presence of 2 systems protecting the culture from erythromycin in Str. erythreus 1571, i.e. at the level of ribosomes and at the level of the cytoplasmic membrane.

摘要

不同菌龄的红霉菌丝体以及红霉菌1571原生质体中的蛋白质合成,即便对高浓度的红霉素和林可霉素也只是稍有敏感性。低浓度的土霉素和新霉素会显著抑制蛋白质合成。14C-红霉素与产生它的菌株的菌丝体结合的量,比与产生林可霉素的玫瑰色链霉菌的菌丝体结合的量要低得多。采用微生物滴定法和放射色谱法,未检测到含有用于酶促磷酸化和去甲基化辅因子的红霉菌无细胞制剂对红霉素的生物转化产物。在红霉菌的无细胞制剂中观察到林可霉素的酶促N-去甲基化。红霉素和林可霉素对红霉菌无细胞体系中以多聚腺苷酸为模板的多聚赖氨酸合成几乎没有影响,且抑制了大肠杆菌MRE 600和枯草芽孢杆菌ATCC 6633无细胞体系中该多肽的合成。这些抗生素对红霉菌核糖体上的片段(嘌呤霉素)反应均无影响。对于大肠杆菌MRE 600的核糖体,片段反应对林可霉素敏感,但对红霉素不敏感。从红霉菌中分离出的核糖体及其50S亚基与14C-红霉素的结合量,比从大肠杆菌中分离出的核糖体及其50S亚基低得多。这些数据表明,红霉菌1571中存在两种保护培养物免受红霉素影响的系统,即在核糖体水平和细胞质膜水平。

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