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The interstitial atom of the nitrogenase FeMo-cofactor: ENDOR and ESEEM evidence that it is not a nitrogen.

Authors :
Yang TC
Maeser NK
Laryukhin M
Lee HI
Dean DR
Seefeldt LC
Hoffman BM
Source :
Journal of the American Chemical Society [J Am Chem Soc] 2005 Sep 21; Vol. 127 (37), pp. 12804-5.
Publication Year :
2005

Abstract

X-ray crystallographic study of the nitrogenase MoFe protein revealed electron density from an atom (denoted X) inside the active-site metal cluster, the [MoFe7S9:homocitrate] FeMo-cofactor. The electron density associated with X is consistent with a single N, O, or C atom. We now have tested whether X is an N or not by comparing the Q-band ENDOR and ESEEM signals from resting-state (S = 3/2) MoFe protein and NMF-extracted FeMo-co from bacteria grown with either 14N or 15N as the exclusive N source. All of the 14N or 15N signals associated with the protein are lost upon extraction of the FeMo-co. We interpret this as strong evidence that X is not an N.

Details

Language :
English
ISSN :
0002-7863
Volume :
127
Issue :
37
Database :
MEDLINE
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
16159266
Full Text :
https://doi.org/10.1021/ja0552489