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诺尔斯链霉菌JA 3890b合成链丝菌素的链霉胍部分。

Biosynthesis of streptolidine moiety of streptothricins by Streptomyces noursei JA 3890b.

作者信息

Gräfe U, Reinhardt G, Bocker H, Thrum H

出版信息

J Antibiot (Tokyo). 1977 Jan;30(1):106-10. doi: 10.7164/antibiotics.30.106.

Abstract

The incorporation of uniformly 14C-labeled compounds into the streptothricin-type antibiotic nourseothricin was studied with a strain of Streptomyces noursei JA 3890b. 6.5% of radioactivity from U-14C-L-arginine was incorporated into the antibiotic, while glutamic acid, aspartic acid, alanine, proline, glycine and leucine displayed much lower incorporations. Furhtermore, 95% of the activity incorporated from arginine was located in the streptolidine moiety supporting the suggestion that this subunit of streptothricin antibiotics is formed via the dehydroarginine pathway.

摘要

使用诺尔斯链霉菌JA 3890b菌株研究了均匀14C标记的化合物掺入链丝菌素型抗生素诺尔丝菌素的情况。来自U-14C-L-精氨酸的6.5%放射性掺入了抗生素中,而谷氨酸、天冬氨酸、丙氨酸、脯氨酸、甘氨酸和亮氨酸的掺入率则低得多。此外,从精氨酸掺入的活性中有95%位于链霉胍部分,支持了链丝菌素类抗生素的这个亚基是通过脱氢精氨酸途径形成的这一观点。

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