Suppr超能文献

栅藻和菠菜铁氧化还原蛋白中的穆斯堡尔效应。植物型铁硫蛋白中的电子转移机制。

Mössbauer effect in Scenedesmus and spinach ferredoxins. The mechanism of electron transfer in plant-type iron-sulphur proteins.

作者信息

Rao K K, Cammack R, Hall D O, Johnson C E

出版信息

Biochem J. 1971 Apr;122(3):257-65. doi: 10.1042/bj1220257.

Abstract
  1. The Mössbauer spectra of Scenedesmus ferredoxin enriched in (57)Fe were measured and found to be identical with those of two other plant-type ferredoxins (from spinach and Euglena) that had been previously measured. Better resolved Mössbauer spectra of spinach ferredoxin are also reported from protein enriched in (57)Fe. All these iron-sulphur proteins are known to contain two iron atoms in a molecule that takes up one electron on reduction. 2. The Mössbauer spectra at 195 degrees K have electric hyperfine structure only and show that on reduction the electron goes to one of the iron atoms, the other appearing to remain unchanged. 3. In the oxidized state, both iron atoms are in a similar chemical state, which appears from the chemical shift and quadrupole splitting to be high-spin Fe(3+), but they are in slightly different environments. In the reduced state the iron atoms are different and the molecule appears to contain one high-spin Fe(2+) and one high-spin Fe(3+) atom. 4. At lower temperatures (77 and 4.2 degrees K) the spectra of both iron atoms in the reduced proteins show magnetic hyperfine structure which suggests that the iron in the oxidized state also has unpaired electrons. This provides experimental evidence for earlier suggestions that in the oxidized state there is antiferromagnetic exchange coupling, which would result in a low value for the magnetic susceptibility. 5. In a small magnetic field the spectrum of the reduced ferredoxin shows a Zeeman splitting with hyperfine field (H(n)) of 180kG at the nuclei. On application of a strong magnetic field H the spectrum splits into two spectra with effective fields H(n)+/-H, thus confirming the presence of the two antiferromagnetically coupled iron atoms. 6. These results are in agreement with the model proposed by Gibson, Hall, Thornley & Whatley (1966); in the oxidized state there are two Fe(3+) atoms (high spin) antiferromagnetically coupled and on reduction of the ferredoxin by one electron one of the ferric atoms becomes Fe(2+) (high spin).
摘要
  1. 对富含(57)Fe的斜生栅藻铁氧化还原蛋白的穆斯堡尔谱进行了测量,发现其与之前测量的另外两种植物型铁氧化还原蛋白(来自菠菜和眼虫)的谱相同。还报道了从富含(57)Fe的蛋白质中得到的菠菜铁氧化还原蛋白分辨率更高的穆斯堡尔谱。所有这些铁硫蛋白已知在一个分子中含有两个铁原子,在还原时接受一个电子。2. 195K时的穆斯堡尔谱仅具有电超精细结构,表明在还原时电子进入其中一个铁原子,另一个似乎保持不变。3. 在氧化态下,两个铁原子处于相似的化学状态,从化学位移和四极分裂来看似乎是高自旋Fe(3+),但它们处于略有不同的环境中。在还原态下,铁原子不同,分子似乎含有一个高自旋Fe(2+)和一个高自旋Fe(3+)原子。4. 在较低温度(77和4.2K)下,还原蛋白中两个铁原子的谱都显示出磁超精细结构,这表明氧化态的铁也有未成对电子。这为早期的推测提供了实验证据,即在氧化态下存在反铁磁交换耦合,这将导致磁化率值较低。5. 在小磁场中,还原铁氧化还原蛋白的谱显示出塞曼分裂,核处的超精细场(H(n))为

相似文献

5
Mossbauer spectroscopy of the iron-sulfur proteins.铁硫蛋白的穆斯堡尔光谱学
Proc Natl Acad Sci U S A. 1969 Aug;63(4):1234-8. doi: 10.1073/pnas.63.4.1234.

引用本文的文献

本文引用的文献

9
The amino acid sequence of taro ferredoxin.芋头铁氧还蛋白的氨基酸序列。
Biochem Biophys Res Commun. 1970 Feb 6;38(3):500-6. doi: 10.1016/0006-291x(70)90742-4.
10
Mossbauer spectroscopy of the iron-sulfur proteins.铁硫蛋白的穆斯堡尔光谱学
Proc Natl Acad Sci U S A. 1969 Aug;63(4):1234-8. doi: 10.1073/pnas.63.4.1234.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验