Titlebook: Catalysts for Nitrogen Fixation; Nitrogenases, Releva Barry E. Smith,Raymond L. Richards,William E. Newt Book 2004 Springer Science+Busines

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Mamadou Thiongane,Wyean Chan,Pierre L’Ecuyerenabled us to produce enough nitrogen fertiliser to feed the current world population, to provide enough explosive to fight as many minor wars as seems desirable to desperate enough people, and to be able to do this for the foreseeable future.

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Springer Tracts in Modern PhysicsSystems for the steady-state assay of the molybdenum-, vanadium-, and iron-only nitrogenases share a number of common requirements.

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Nitrogen Fixation: An Historical Perspective,nd nitrate (NO. .) the most common. These and other related usable forms of nitrogen are most often the limiting factor for the growth of organisms; a situation that is clearly highlighted in production agriculture. The element nitrogen is not, however, in short supply on this planet, which is bless

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The Structures of The Nitrogenase Proteins and Stabilized Complexes,matic nitrogen reduction. Nitrogenase structure/function has been a rich area of research for several decades (reviewed in Kim and Rees, 1994; Peters ., 1995; Howard and Rees, 1996; Rees and Howard, 1999; 2000; Rees 2002; Lawson and Smith, 2002) and the advent of detailed structures of the nitrogena

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Strategies for the Functional Analysis of the , MoFe Protein and its Active Site FeMo-Cofactor,ction (Burgess and Lowe, 1996). As described elsewhere in this volume, reducing equivalents are delivered during catalysis from the Fe protein to the MoFe protein in a reaction coupled to MgATP hydrolysis. Although the nucleotide-binding sites are located on the Fe protein, it does not catalyze MgAT

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Chemical Models, Theoretical Calculations, and the Reactivity of Isolated Iron-Molybdenum Cofactor, the M-centre or the iron-molybdenum cofactor (FeMo-cofactor or FeMoco) (see Figure 1). This fascinating cluster has the stoichiometry [MoFe.S.X-homocitrate], where X is a light atom, most probably nitrogen, at the centre of the inorganic part of the cofactor. Over several decades, coordination chem

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