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噻孢霉素产生菌,卡特利链霉菌对氟苏氨酸和氟乙酸的生物合成。

Biosynthesis of fluorothreonine and fluoroacetic acid by the thienamycin producer, Streptomyces cattleya.

作者信息

Sanada M, Miyano T, Iwadare S, Williamson J M, Arison B H, Smith J L, Douglas A W, Liesch J M, Inamine E

出版信息

J Antibiot (Tokyo). 1986 Feb;39(2):259-65. doi: 10.7164/antibiotics.39.259.

Abstract

An antimetabolite, THX, was isolated from fermentation broths of the thienamycin producer, Streptomyces cattleya, when the organism was grown in the presence of a fluorine-containing substrate. THX was subsequently identified as one of the four possible stereoisomers of 4-fluorothreonine. Inorganic fluoride or any one of a number of organofluorine compounds can be used as precursors of 4-fluorothreonine. In addition, 19F NMR has provided evidence that the organism synthesizes fluoroacetate under the same fermentation conditions. The in vitro antibacterial spectrum of 4-fluorothreonine is also presented.

摘要

一种抗代谢物THX是从硫霉素产生菌——卡特利链霉菌的发酵液中分离得到的,当时该微生物是在含氟底物存在的情况下生长的。THX随后被鉴定为4-氟苏氨酸四种可能的立体异构体之一。无机氟化物或多种有机氟化合物中的任何一种都可以用作4-氟苏氨酸的前体。此外,19F核磁共振提供了证据,表明该微生物在相同的发酵条件下合成氟乙酸。文中还介绍了4-氟苏氨酸的体外抗菌谱。

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