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生物甲基化对丝裂霉素A生物合成的影响

INFLUENCE OF BIOLOGICAL METHYLATION ON THE BIOSYNTHESIS OF MITOMYCIN A.

作者信息

KIRSCH E J, KORSHALLA J D

出版信息

J Bacteriol. 1964 Feb;87(2):247-55. doi: 10.1128/jb.87.2.247-255.1964.

Abstract

Kirsch, E. J. (Lederle Laboratories, Pearl River, N.Y.), and J. D. Korshalla. Influence of biological methylation on the biosynthesis of mitomycin A. J. Bacteriol. 87:247-255. 1964.-Methionine-methyl-C(14) was shown to contribute radioactive carbon to the mitomycin antibiotic complex synthesized by Streptomyces verticillatus in a simple synthetic medium containing glucose and inorganic salts. The position of radioactivity in mitomycin A was determined by selective hydrolysis of the 7 and 9a methoxyl functions. Essentially all of the radioactivity incorporated was distributed evenly between these two substituent groups. Mitomycin A, synthesized by washed resting cells of S. verticillatus at the expense of internal metabolites, also incorporated methyl label. When the methionine antagonist, d,l-ethionine, was added to resting cells at a concentration causing 65% inhibition of antibiotic synthesis, incorporation of radioactive methyl groups was reduced to the same extent. Synthetic medium supplemented with d,l-ethionine supported about 90% maximal growth of the culture, but antibiotic biosynthesis was markedly inhibited. The addition of the inhibitor during the period of rapid antibiotic synthesis resulted in cessation of further increases in antibiotic titer. l-Methionine was shown to be capable of reversing ethionine inhibition; the extent of reversal was dependent on the concentration, as well as on the time of addition of amino acid. The data suggest the critical nature of a methyl transfer system in the biogenesis of biologically active mitomycins.

摘要

基尔希,E. J.(莱德利实验室,纽约州珍珠河),以及J. D. 科尔沙拉。生物甲基化对丝裂霉素A生物合成的影响。《细菌学杂志》87:247 - 255。1964年。- 已表明在含有葡萄糖和无机盐的简单合成培养基中,甲硫氨酸 - 甲基 - C¹⁴ 为轮枝链霉菌合成的丝裂霉素抗生素复合物贡献放射性碳。通过对7位和9a位甲氧基官能团进行选择性水解来确定丝裂霉素A中放射性的位置。基本上所有掺入的放射性均匀分布在这两个取代基之间。由轮枝链霉菌的洗涤后静止细胞以内部代谢物为代价合成的丝裂霉素A也掺入了甲基标记。当将甲硫氨酸拮抗剂d,l - 乙硫氨酸以导致抗生素合成65%抑制的浓度添加到静止细胞中时,放射性甲基的掺入也降低到相同程度。添加了d,l - 乙硫氨酸的合成培养基支持培养物约90%的最大生长,但抗生素生物合成受到明显抑制。在抗生素快速合成期间添加抑制剂导致抗生素效价不再进一步升高。已表明l - 甲硫氨酸能够逆转乙硫氨酸的抑制作用;逆转程度取决于氨基酸的浓度以及添加时间。数据表明甲基转移系统在具有生物活性的丝裂霉素生物合成中的关键性质。

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