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弗氏链霉菌菌株提取物中S-腺苷-L-甲硫氨酸:大环菌素O-甲基转移酶的特性,这些菌株产生正常或高水平的泰乐菌素,以及在特定O-甲基化中受阻的突变体。

Properties of S-adenosyl-L-methionine:macrocin O-methyltransferase in extracts of Streptomyces fradiae strains which produce normal or elevated levels of tylosin and in mutants blocked in specific O-methylations.

作者信息

Seno E T, Baltz R H

出版信息

Antimicrob Agents Chemother. 1981 Sep;20(3):370-7. doi: 10.1128/AAC.20.3.370.

Abstract

An efficient assay for S-adenosyl-L-methionine:macrocin O-methyltransferase, the enzyme which carries out the terminal step in tylosin biosynthesis, is described. Macrocin O-methyltransferase requires Mg2+ and S-adenosyl-L-methionine for activity, has a temperature optimum of about 31 degrees C, and has a pH optimum of 7.5 to 8.2. Macrocin O-methyltransferase specifically converts macrocin to tylosin by O-methylation of the 3" ' position of macrocin. In vitro methylation studies with extracts from a tylosin-producing Streptomyces fradiae strain and from mutant strains blocked in 2" '- or 3" '-O-methylations indicated that: (i) the 2" '- and 3" '-O-methylations occur after 6-deoxy-D-allose is attached to the macrolide ring; (ii) the 2" '- and 3" '-O-methylations are carried out by separate enzymes; and (iii) the 2" '-O-methylation precedes the 3" '-O-methylation. Macrocin O-methyltransferase was inhibited by high levels of its substrate, macrocin, by its product, tylosin, and by other tylosin analogs which contained mycinose or demethyl analogs of mycinose. Macrocin O-methyltransferase was produced early in the tylosin fermentation cycle by S. fradiae and preceded the onset of rapid tylosin biosynthesis by about 24 h. The enzyme specific activity reached maximum at about 72 h and then slowly declined. A mutant strain of S. fradiae selected for increased tylosin production synthesized macrocin O-methyltransferase more rapidly and accumulated a higher enzyme specific activity than a wild-type strain.

摘要

本文描述了一种高效测定S-腺苷-L-甲硫氨酸:大环菌素O-甲基转移酶的方法,该酶催化泰乐菌素生物合成的最后一步反应。大环菌素O-甲基转移酶的活性需要Mg2+和S-腺苷-L-甲硫氨酸,最适温度约为31℃,最适pH为7.5至8.2。大环菌素O-甲基转移酶通过将大环菌素的3'' '位进行O-甲基化,特异性地将大环菌素转化为泰乐菌素。对一株产生泰乐菌素的弗氏链霉菌菌株以及在2'' '-或3'' '-O-甲基化过程中受阻的突变菌株提取物进行的体外甲基化研究表明:(i) 2'' '-和3'' '-O-甲基化在6-脱氧-D-阿洛糖连接到大环内酯环之后发生;(ii) 2'' '-和3'' '-O-甲基化由不同的酶催化;(iii) 2'' '-O-甲基化先于3'' '-O-甲基化。大环菌素O-甲基转移酶受到其底物大环菌素的高浓度、产物泰乐菌素以及其他含有霉糖或霉糖去甲基类似物的泰乐菌素类似物的抑制。弗氏链霉菌在泰乐菌素发酵周期早期产生大环菌素O-甲基转移酶,比快速的泰乐菌素生物合成开始提前约24小时。该酶的比活性在约72小时达到最大值,然后缓慢下降。一株为提高泰乐菌素产量而筛选的弗氏链霉菌突变菌株比野生型菌株更快地合成大环菌素O-甲基转移酶,并积累了更高的酶比活性。

相似文献

8
Terminal stages in the biosynthesis of tylosin.泰乐菌素生物合成的终末阶段。
Antimicrob Agents Chemother. 1977 Mar;11(3):455-61. doi: 10.1128/AAC.11.3.455.

引用本文的文献

本文引用的文献

9
Terminal stages in the biosynthesis of tylosin.泰乐菌素生物合成的终末阶段。
Antimicrob Agents Chemother. 1977 Mar;11(3):455-61. doi: 10.1128/AAC.11.3.455.

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