Suppr超能文献

来自光系统II中锰簇的S0态电子顺磁共振信号源于一个孤立的S = 1/2基态。

The S0 state EPR signal from the Mn cluster in photosystem II arises from an isolated S = 1/2 ground state.

作者信息

Ahrling K A, Peterson S, Styring S

机构信息

Department of Biochemistry, Center for Chemistry and Chemical Engineering, Lund University, Sweden.

出版信息

Biochemistry. 1998 Jun 2;37(22):8115-20. doi: 10.1021/bi980117o.

Abstract

During oxygen evolution, the Mn cluster in Photosystem II cycles through five oxidation states, S0-S4. S0 and S2 are paramagnetic, and can be monitored by electron paramagnetic resonance (EPR). Recently a new EPR signal from the S0 state was discovered [Ahrling et al. (1997) Biochemistry 36, 13148-13152, Messinger et al. (1997) J. Am. Chem. Soc. 119, 11349-11350]. Here, we present a well-resolved S0 spectrum, taken at high power and low temperature. The spectrum is wider and more resolved than previously thought, with structure over more than 2500 G, and appears to have at least 20 reproducible peaks on each side of g = 2. We also present the temperature dependence of the unsaturated S0 signal amplitude. A linear relationship was found between signal intensity and reciprocal temperature (1/T) in the region 5-25 K, clearly extrapolating to 0. This obeys the Curie law, indicating that the S0 state is a ground S = 1/2 state with no thermally accessible excited state. The data are consistent with a minimum energy gap of 30 cm-1 between the ground and first excited states.

摘要

在氧气释放过程中,光系统II中的锰簇会经历从S0到S4的五个氧化态循环。S0和S2是顺磁性的,可以通过电子顺磁共振(EPR)进行监测。最近发现了来自S0态的一个新的EPR信号[Ahrling等人(1997年)《生物化学》36卷,13148 - 13152页,Messinger等人(1997年)《美国化学会志》119卷,11349 - 11350页]。在此,我们展示了一个在高功率和低温下测得的分辨率良好的S0光谱。该光谱比之前认为的更宽且分辨率更高,结构跨越超过2500 G,并且在g = 2的两侧似乎各有至少20个可重复的峰。我们还展示了不饱和S0信号幅度的温度依赖性。在5 - 25 K区域内,发现信号强度与倒数温度(1/T)之间存在线性关系,明显外推至零。这符合居里定律,表明S0态是一个基态S = 1/2态,没有热可及的激发态。这些数据与基态和第一激发态之间至少30 cm-1的最小能隙一致。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验