在白素生物合成过程中涉及作为硫供体的激素S-adenosyl-l-methionine FeS集群
Richiro Ushimaru1,2,3,4,5, Ziyang Zheng1,5, Jin Xiong6,5
1Department of Chemistry, The University of Texas at Austin, Austin, TX, USA.
激进的S-adenosyl-l-methionine (SAM) 酶被证明可以催化一种新的硫-氧交换反应. 这一发现揭示了抗菌化合物阿尔波米的硫黄核心来源,并突出了SAM激素催化的多样性功能.
科学领域:
- 生物化学
- 有机化学
- 酵素学
背景情况:
- 自然产品中的碳-硫键形成通常使用易斯酸/化学.
- 极端的S-adenosyl-l-methionine (SAM) 酶很少参与其中,并且通常利用辅助铁-硫集群催化硫插入C-H键.
研究的目的:
- 调查白素生物合成中的 thiofuranose 的机制.
- 在已知的硫插入反应之外探索激素SAM酶的催化能力.
主要方法:
- 从阿尔波米辛生物合成基因集群中对AbmM的酶表征.
- 在AbmM催化反应中分析硫源.
主要成果:
- 激素SAM酶AbmM催化硫替代氧的反应.
- AbmM将黄环转化为硫黄部分,这对菌素的抗菌活性至关重要.
- 激素SAM的催化集群似乎是硫的捐赠者.
结论:
- 这项研究阐明了阿尔波米中的硫黄核的起源.
- 它展示了一种由SAM激素酶催化的新型硫与氧交换反应.
- 这一发现扩大了生物合成中SAM激素催化已知的功能范围.
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