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红霉素合成中甲基丙二酰辅酶A的来源:来自红色链霉菌的甲基丙二酰辅酶A变位酶。

Source of methylmalonyl-coenzyme A for erythromycin synthesis: methylmalonyl-coenzyme A mutase from Streptomyces erythreus.

作者信息

Hunaiti A A, Kolattukudy P E

出版信息

Antimicrob Agents Chemother. 1984 Feb;25(2):173-8. doi: 10.1128/AAC.25.2.173.

Abstract

Streptomyces erythreus produces erythromycin, presumably from methylmalonyl-coenzyme A (CoA), which could be generated by the isomerization of succinyl-CoA. In S. erythreus cultures, [1,4-14C,2,3-3H]succinate was incorporated into erythromycin with a doubling of the 3H/14C ratio. This result is consistent with the hypothesis that succinyl-CoA is isomerized to methylmalonyl-CoA before incorporation into the macrocyclic lactone of erythromycin. The presence of methylmalonyl-CoA mutase, which catalyzes this isomerization, was demonstrated in cell-free extracts prepared from this organism. Consistent with the suggested role for this enzyme, methylmalonyl-CoA mutase activity increased over 12-fold at the time of the most rapid antibiotic production, and the activity level drastically declined when the antibiotic production ceased. The mutase was partially purified from this organism with DEAE-cellulose, ammonium sulfate precipitation, and affinity chromatography on a B12-coenzyme Sepharose column. The enzyme was stimulated 2.5-fold by the addition of B12-coenzyme. The enzyme showed a typical Michaelis-Menten type substrate saturation patterns, with KmS of 0.31 mM and 0.09 microM for methylmalonyl-CoA and B12-coenzyme, respectively, and a V of 0.5 mumol/min per mg. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of the purified enzyme showed a major band with a molecular weight of 63,000. The properties of this enzyme appear to be fairly similar to those of the mutase previously obtained from other sources.

摘要

红色链霉菌产生红霉素,推测其来源于甲基丙二酰辅酶A(CoA),而甲基丙二酰辅酶A可由琥珀酰辅酶A异构化生成。在红色链霉菌培养物中,[1,4-14C,2,3-3H]琥珀酸盐被掺入红霉素中,3H/14C比值翻倍。这一结果与琥珀酰辅酶A在掺入红霉素大环内酯之前异构化为甲基丙二酰辅酶A的假说一致。在从该生物体制备的无细胞提取物中证实了催化这种异构化的甲基丙二酰辅酶A变位酶的存在。与该酶的推测作用一致,甲基丙二酰辅酶A变位酶活性在抗生素产生最快时增加了12倍以上,而当抗生素产生停止时,活性水平急剧下降。通过DEAE-纤维素、硫酸铵沉淀以及在钴胺素-辅酶琼脂糖柱上进行亲和层析,从该生物体中部分纯化了该变位酶。添加钴胺素-辅酶可使该酶活性提高2.5倍。该酶呈现典型的米氏型底物饱和模式,甲基丙二酰辅酶A和钴胺素-辅酶的KmS分别为0.31 mM和0.09 microM,V为每毫克0.5微摩尔/分钟。纯化酶的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳显示一条主要条带,分子量为63,000。该酶的性质似乎与先前从其他来源获得的变位酶相当相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a38f/185468/c0647befdf3a/aac00191-0032-a.jpg

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