使用辅助4Fe-5S集群插入硫的生物合成酶的发现
Jake C Lachowicz1, David Lennox-Hvenekilde2,3, Nils Myling-Petersen3
1Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York 10461, United States.
Journal of the American Chemical Society
|January 12, 2024
概括
一种对维生素B7产生至关重要的新型生物合成酶 (BioB) 使用了4Fe-5S集群而不是以前已知的2Fe-2S集群. 这一发现揭示了厌氧生物与有氧生物生物合成的不同策略.
科学领域:
- 生物化学
- 酵素学
- 生物有机化学
背景情况:
- 生物合成酶 (BioB) 催化生物生物合成,将一个硫原子插入到生物中.
- 硫原子的来源被争论,但现在被认为来自于I型生物B中的牺牲性2Fe-2S集群.
- 包括BioB在内的激进SAM酶在各种生物途径中至关重要.
研究的目的:
- 研究生物素合成酶 (BioB) 的多样性.
- 在无氧生物中发现的一种新型BioB的特征.
- 阐明不同BioB铁硫集群类型的机制和进化影响.
主要方法:
- 对生物B序列的生物信息分析.
- 在体外生化特征酶活性.
- 进行X射线结晶学以确定酶结构.
主要成果:
- 在使用4Fe-5S集群的有义务无氧生物中发现了一种新型II BioB.
- 4Fe-5S集群包含一种被提议作为生物形成的硫供体的结合硫化物.
- 晶体结构显示了II型生物B中辅助铁硫集群的协调.
- I型BioB (大肠杆菌) 使用2Fe-2S集群,与II型相反.
结论:
- 在无氧生物中,一种新的BioB类 (II型) 具有4Fe-5S集群.
- 这一发现突出了无氧和有氧环境中生物合成的不同生化策略.
- 这项研究促进了对酶的铁硫功能和演变的理解.
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