首页> 外文OA文献 >Metabolic regulation in Streptomyces parvulus during actinomycin D synthesis, studied with 13C- and 15N-labeled precursors by 13C and 15N nuclear magnetic resonance spectroscopy and by gas chromatography-mass spectrometry.
【2h】

Metabolic regulation in Streptomyces parvulus during actinomycin D synthesis, studied with 13C- and 15N-labeled precursors by 13C and 15N nuclear magnetic resonance spectroscopy and by gas chromatography-mass spectrometry.

机译:用13C和15N标记的前体通过13C和15N核磁共振波谱和气相色谱-质谱法研究了放线菌素D合成过程中小链霉菌的代谢调控。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Recent studies have suggested that the onset of synthesis of actinomycin D in Streptomyces parvulus is due to a release from L-glutamate catabolic repression. In the present investigation we showed that S. parvulus has the capacity to maintain high levels of intracellular glutamate during the synthesis of actinomycin D. The results seem contradictory, since actinomycin D synthesis cannot start before a release from L-glutamate catabolic repression, but a relatively high intracellular pool of glutamate is needed for the synthesis of actinomycin D. Utilizing different labeled precursors, D-[U-13C]fructose and 13C- and 15N-labeled L-glutamate, and nuclear magnetic resonance techniques, we showed that carbon atoms of an intracellular glutamate pool of S. parvulus were not derived biosynthetically from the culture medium glutamate source but rather from D-fructose catabolism. A new intracellular pyrimidine derivative whose nitrogen and carbon skeletons were derived from exogenous L-glutamate was obtained as the main glutamate metabolite. Another new pyrimidine derivative that had a significantly reduced intracellular mobility and that was derived from D-fructose catabolism was identified in the cell extracts of S. parvulus during actinomycin D synthesis. These pyrimidine derivatives may serve as a nitrogen store for actinomycin D synthesis. In the present study, the N-trimethyl group of a choline derivative was observed by 13C nuclear magnetic resonance spectroscopy in growing S. parvulus cells. The choline group, as well as the N-methyl groups of sarcosine, N-methyl-valine, and the methyl groups of an actinomycin D chromophore, arose from D-fructose catabolism. The 13C enrichments found in the peptide moieties of actinomycin D were in accordance with a mechanism of actinomycin D synthesis from L-glutamate and D-fructose.
机译:最近的研究表明,小链霉菌中放线菌素D的合成是由于L-谷氨酸分解代谢抑制释放。在本研究中,我们表明细小链霉菌具有在合成放线菌素D期间维持高水平细胞内谷氨酸的能力。结果似乎是矛盾的,因为放线菌素D的合成不能在L-谷氨酸分解代谢抑制释放之前开始,而是合成放线菌素D需要较高的细胞内谷氨酸池。利用不同的标记前体,D- [U-13C]果糖以及13C和15N标记的L-谷氨酸,以及核磁共振技术,我们证明了碳原子小分子链球菌的细胞内谷氨酸池的一部分不是从合成的谷氨酸来源生物合成而来的,而是从D-果糖分解代谢产生的。获得了一种新的胞内嘧啶衍生物,其氮和碳骨架均来自外源性L-谷氨酸,作为主要的谷氨酸代谢物。在放线菌素D合成过程中,在细小链球菌的细胞提取物中鉴定出了另一种新的嘧啶衍生物,该衍生物具有显着降低的细胞内迁移率,并且衍生自D-果糖分解代谢。这些嘧啶衍生物可以用作放线菌素D合成的氮存储。在本研究中,通过13 C核磁共振波谱法在生长的小生链霉菌细胞中观察到了胆碱衍生物的N-三甲基。 D-果糖分解代谢产生了胆碱基团以及肌氨酸,N-甲基缬氨酸的N-甲基和放线菌素D生色团的甲基。在放线菌素D的肽部分中发现的13 C富集与从L-谷氨酸和D-果糖合成放线菌素D的机理一致。

著录项

  • 作者

    Inbar, L; Lapidot, A;

  • 作者单位
  • 年度 1988
  • 总页数
  • 原文格式 PDF
  • 正文语种 en
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号