在Pyrroloiminoquinone生物合成过程中的意想不到的转化
Josseline Ramos Figueroa1, Lingyang Zhu1, Wilfred A van der Donk1
1Department of Chemistry and Howard Hughes Medical Institute, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, United States.
Journal of the American Chemical Society
|May 8, 2024
概括
比以前想象的更复杂的生物合成. 这项研究显示,氨基基组通过tRNA依赖的途径从甘氨酸,氨酸和白氨酸中结合起来,挑战了之前提出的途径.
科学领域:
- 自然产品生物合成
- 酵素学
- 分子进化
背景情况:
- 罗胺基是一种生物活性天然产物,由酸衍生.
- 它们的生物合成途径在很大程度上是未知的.
- 之前的研究发现PEptide Aminoacyl- tRNA Ligase (PEARL) 通过托连接启动阿莫萨米德合成.
研究的目的:
- 阐明罗胺基的复杂生物合成途径.
- 识别这些化合物中包含的氨基基群的来源.
- 调查该路径中的关键酶的进化起源.
主要方法:
- 来自两个基因集群的四种额外酶的分析.
- 研究tRNA依赖性氨基基组的结合.
- 一个FAD依赖的甘氨酸氧化酶 (Amm14) 和一个缩酶的生物化学特征.
主要成果:
- 之前提出的ammosamides的生物合成途径被发现是不正确的.
- 类胺基中的氨基群来源于甘氨酸,氨酸和白氨酸,通过tRNA依赖机制结合在一起.
- Amm14和一个缩酶对于分别从甘氨酸,氨酸和氨酸中加入气至关重要.
结论:
- 自然界对胺基的途径比预期的要复杂得多.
- 它们的生物合成涉及多种氨基酸来源和tRNA依赖机制.
- 珍珠和相关酶可能是从ATP-GRASP蛋白家族进化而来的.
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