氧化抑制糖基酶及其活性酶
Juan Carlos Cáceres1, Nathan G Michellys2, Brandon L Greene1,2
1Interdisciplinary Program in Quantitative Biosciences, University of California Santa Barbara, Santa Barbara, California 93106, United States.
Journal of the American Chemical Society
|March 25, 2025
概括
氧化 (NO) 抑制无氧代谢中的关键酶,如酸甲酸酶 (PFL),破坏细菌的生长. 这种NO介导的糖基酶抑制可能在肠道免疫中起作用.
科学领域:
- 微生物学
- 生物化学
- 免疫学
背景情况:
- 天生的免疫细胞产生氧化 (NO) 来对抗病原体.
- 已知NO对有氧代谢酶的抗菌作用.
- 它在无氧代谢中的目标仍然不太清楚.
研究的目的:
- 研究无氧代谢中NO的分子点.
- 为了确定NO对大肠杆菌的糖基酶酸甲酸酶 (PFL) 的作用.
主要方法:
- 电子磁共振 (EPR) 光谱.
- 位点定向的突变发生.
- 全细胞EPR和代谢流量分析.
- 研究的PFL及其激活酶 (PFL-AE).
主要成果:
- 通过破坏其糖基,NO 无法逆转地抑制PFL.
- NO使PFL-AE失活,将铁硫转化为二铁复合物.
- 在大肠杆菌中抑制PFL和PFL-AE,减少生长和转移新陈代谢.
- 对III类核酸减少酶 (RNR) 和其激活酶 (RNR- AE) 进行了类似的抑制.
结论:
- NO广泛抑制糖基酶化学,包括PFL和RNR途径.
- 这种抑制有助于NO的细菌静止作用.
- 通过向肠道中的无氧代谢酶,NO可能具有免疫功能.
相关概念视频
Nitric Oxide Signaling Pathway
4.9K
Nitric oxide (NO), an inorganic gas, acts as a potent second messenger in most animal and plant tissues. NO diffuses out of the cells that produce it and enters the neighboring cells to generate a downstream response. NO synthase (NOS) catalyzes NO production by the deamination of the amino acid arginine. There are three isoforms of NOS. Endothelial cells have endothelial NOS (eNOS), nerve and muscle cells have neuronal NOS (nNOS), and macrophages produce inducible NOS (iNOS) upon exposure...
4.9K
Antihypertensive Drugs: Vasodilators
449
Vasodilators, primarily affecting the smooth muscles within arterial and venous walls, are commonly used for hypertension treatment. Medications such as minoxidil and hydralazine primarily target arteries and arterioles, while sodium nitroprusside acts on arterioles and venules. Minoxidil, functioning as a prodrug, is metabolized by hepatic sulfotransferase into its active form, minoxidil sulfate, after oral administration. This metabolite binds to the sulfonylurea receptor (SUR) component of...
449
Antianginal Drugs: Nitrates and β-Blockers
479
In cardiovascular health, antianginal drugs combat angina pectoris — a condition marked by chest pain owing to diminished blood flow to the heart.
Organic nitrates, such as nitroglycerin, play a pivotal role. Once metabolized, they liberate nitric oxide, a molecular marvel. Nitric oxide triggers guanylyl cyclase and augments cGMP production. This biochemical cascade orchestrates the relaxation of vascular smooth muscles, ushering in vasodilation and enhancing coronary blood flow....
Organic nitrates, such as nitroglycerin, play a pivotal role. Once metabolized, they liberate nitric oxide, a molecular marvel. Nitric oxide triggers guanylyl cyclase and augments cGMP production. This biochemical cascade orchestrates the relaxation of vascular smooth muscles, ushering in vasodilation and enhancing coronary blood flow....
479
Radical Autoxidation
2.1K
The oxidation of an organic compound in the presence of air or oxygen is called autoxidation. For example, cumene reacts with oxygen to form hydroperoxide. Autoxidation involves initiation, propagation, and termination steps. Many organic compounds are susceptible to autoxidation—especially ethers in the presence of oxygen, which form hydroperoxides. Even though this reaction is slow, old ether bottles contain small amounts of peroxide, which leads to laboratory explosions during ether...
2.1K
meta-Directing Deactivators: –NO2, –CN, –CHO, –⁠CO2R, –COR, –CO2H
5.3K
All meta-directing substituents are deactivating groups. These substituents withdraw electrons from the aromatic ring, making the ring less reactive toward electrophilic substitution. For example, the nitration of nitrobenzene is 100,000 times slower than that of benzene because of the deactivating effect of the nitro group. The first step in an electrophilic aromatic substitution is the addition of an electrophile to form a resonance-stabilized carbocation. The energy diagrams for...
5.3K
GPCRs Regulate Adenylyl Cylase Activity
5.1K
Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
5.1K


