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卡特利链霉菌对含氟次生代谢产物的生物合成

Biosynthesis of fluorinated secondary metabolites by Streptomyces cattleya.

作者信息

Reid Karen A, Bowden Roy D, Dasaradhi Lakkaraju, Amin Muhammad R, Harper David B

机构信息

Microbial Biochemistry Section, Department of Food Science, The Queen's University of Belfast, Newforge Lane, Belfast BT9 5PX, UK.

Department of Chemistry, The University of Durham, Science Laboratories, South Road, Durham DH1 3LE, UK.

出版信息

Microbiology (Reading). 1995 Jun;141 ( Pt 6):1385-1393. doi: 10.1099/13500872-141-6-1385.

Abstract

The biosynthesis of organofluorine compounds by Streptomyces cattleya NRRL 8057 was examined using 19F NMR spectroscopy. The organism produced 1.2 mM fluoroacetate and 0.5 mM 4-fluorothreonine as secondary metabolites when cultured for 28 d on a chemically defined medium containing 2 mM fluoride. Cell suspensions from batch cultures harvested at the growth maximum of 4 d were not capable of fluoride uptake or fluorometabolite biosynthesis, but by 6 d had developed an efficient fluoride-uptake system and biosynthesized the two fluorometabolites in almost equal proportions. As the harvest age increased, the proportion of fluoroacetate to 4-fluorothreonine formed by cell suspensions rose progressively so that 16-d-old cells showed a ratio of 76:26 for the two compounds. Fluoride uptake and fluorometabolite production by cell suspensions were highly dependent on pH, with both processes showing a maximum rate at pH 6.0 but declining rapidly at higher pH values. This decrease was particularly marked in the case of fluoroacetate biosynthesis which was barely detectable at pH 7.5. Fluoroacetate and 4-fluorothreonine showed only low levels of interconversion by cell suspensions, suggesting that the carbon skeleton of neither was derived by metabolism of the other. The limited interconversion observed is explicable in terms of a small degree of biological defluorination occurring with each compound, followed by reincorporation of the resulting fluoride ion into the organic form by the active fluorinating system, a phenomenon also noted on incubation of cell suspensions with a number of other fluorinated biochemical intermediates.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用19F核磁共振光谱法研究了卡特利链霉菌NRRL 8057对有机氟化合物的生物合成。当在含有2 mM氟化物的化学限定培养基上培养28天时,该微生物产生了1.2 mM氟乙酸盐和0.5 mM 4-氟苏氨酸作为次级代谢产物。在4天生长高峰期收获的分批培养细胞悬液不能摄取氟化物或生物合成含氟代谢物,但到6天时已形成高效的氟化物摄取系统,并以几乎相等的比例生物合成了这两种含氟代谢物。随着收获时间的增加,细胞悬液形成的氟乙酸盐与4-氟苏氨酸的比例逐渐上升,因此16日龄的细胞中这两种化合物的比例为76:26。细胞悬液对氟化物的摄取和含氟代谢物的产生高度依赖于pH值,这两个过程在pH 6.0时显示出最大速率,但在较高pH值时迅速下降。这种下降在氟乙酸盐生物合成的情况下尤为明显,在pH 7.5时几乎检测不到。细胞悬液中氟乙酸盐和4-氟苏氨酸的相互转化水平很低,这表明两者的碳骨架都不是由另一种物质的代谢产生的。观察到的有限相互转化可以解释为每种化合物都发生了少量的生物脱氟,随后活性氟化系统将产生的氟离子重新掺入有机形式,在用许多其他氟化生化中间体孵育细胞悬液时也注意到了这种现象。(摘要截短至250字)

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