通过照射尼古丁胺依赖酶以获得非自然反应性
Megan A Emmanuel1, Norman R Greenberg1, Daniel G Oblinsky1
1Department of Chemistry, Princeton University, Princeton, New Jersey 08544, USA.
Nature
|December 16, 2016
概括
研究人员开发了一种使用光和尼古丁胺辅助因子的酶催化新方法. 这种光诱导的酶变异使得新的化学转化成为可能,比如激素脱,以前传统的生物催化剂无法实现.
科学领域:
- 生物催化
- 酶工程
- 摄影化学
背景情况:
- 在不对称的催化过程中,酶提供了量身定制的选择性和效率.
- 现有的酶仅限于自然发生的反应,限制了催化多样性.
- 开发具有新型催化功能的酶是生物催化的一个关键挑战.
研究的目的:
- 开发一种方法来实现酶的催化性.
- 探索光激尼古丁胺辅助因子用于新的酶变化.
- 为了证明尼古丁胺依赖酶的新反应性.
主要方法:
- 在可见光照射下利用尼古丁胺辅助因子的光激发状态.
- 从碳缩酶转化为基基启动剂和性源.
- 已经证明了乳的反选择性基质脱.
主要成果:
- 实现了光诱导的酶杂交, 实现了新的催化功能.
- 减酶作为激素启动剂和原子源表现出新的反应性.
- 成功地进行了乳的高度反选择性激素脱,这是一个具有挑战性的反应.
结论:
- 这种方法代表了光诱导酶乱交的第一个例子.
- 生物辅助因子的激发状态可以释放现有酶的新反应性.
- 这种方法与传统的以光驱动的生物催化剂不同,以辅助因子再生为重点.
更多相关视频
06:56Near Infrared NIr Light Increases Expression of a Marker of Mitochondrial Function in the Mouse Vestibular Sensory Epithelium
Published on: March 14, 2015
10.5K
08:18Application of Laser Micro-irradiation for Examination of Single and Double Strand Break Repair in Mammalian Cells
Published on: September 5, 2017
10.3K
相关概念视频
Electron Transport Chain: Complex I and II
19.3K
The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
ROS generation is regulated and maintained at moderate levels necessary...
19.3K
Pharmacogenetics of Phase II Enzymes: N-acetyltransferase, Thiopurine S-methyltransferase, UDP-glucuronosyltransferase
52
Phase II biotransformation reactions are essential for detoxifying and eliminating xenobiotics, including many pharmaceutical compounds. These reactions typically involve conjugation, the covalent attachment of polar endogenous groups such as glucuronic acid, sulfate, methyl, or acetyl moieties to functional groups introduced during Phase I metabolism. The resulting conjugates are more water-soluble, enabling efficient renal or biliary excretion.The major classes of Phase II enzymes include...
52
