A new cytosine glycoside from Streptomyces griseochromogenes produced by the use in vivo of enzyme inhibitors.

A new cytosine glycoside from Streptomyces griseochromogenes produced by the use in vivo of enzyme inhibitors.
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一种来自灰产色链霉菌的新型胞嘧啶糖苷,通过体内使用酶抑制剂产生。

DOI:
10.1021/np970468o
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发表时间:
1998
期刊:
Journal of natural products.
影响因子:
--
通讯作者:
Zabriskie,TM
Zabriskie,TM
中科院分区:
--
文献类型:
--
作者:
Zhang,Q;Gould,SJ;Zabriskie,TM

文献摘要

相似文献

采用体内酶抑制法研究了抗真菌抗生素杀稻瘟菌素S(1)生物合成途径中新的胞嘧啶糖苷和中间体的鉴定。研究发现,添加精氨酸类似物精氨酸或精氨酸琥珀酸合成酶抑制剂2-甲基天冬氨酸的灰产色链霉菌(Streptomycesgriseochromogenes)发酵可产生一种新的代谢产物(7)。
The identification of new cytosine glycosides and intermediates in the biosynthetic pathway of the antifungal antibiotic blasticidin S (1) was investigated using in vivo enzyme inhibition. Fermentations ofStreptomyces griseochromogenes, the organism that produces1, supplemented with the arginine analogue argininic acid or the argininosuccinate synthase inhibitor 2-methylaspartic acid were found to produce a new metabolite (7).