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Journal ArticleDOI

Molybdenum in nitrogenase

TLDR
The biochemical process described by nitrogen fixation is the reduction of N2 to NH3, which can then be used for the synthesis of amino acids, nucleic acids, and other essential nitrogenous compounds, which ranks with photosynthesis as a process of fundamental importance to all life on earth.
Abstract
Publisher Summary Nitrogen fixation ranks with photosynthesis as a process of fundamental importance to all life on earth. The biochemical process described by nitrogen fixation is the reduction of N2 to NH3, which can then be used for the synthesis of amino acids, nucleic acids, and other essential nitrogenous compounds. Intensive agricultural methods have led to increased use of and dependence on manufactured nitrogenous fertilizers with decreased emphasis on biological nitrogen fixation. However, with the depletion of fossil fuels, the cost of fertilizer production is rising, and this situation could easily lead to a worldwide food crisis. One aspect of nitrogen fixation that is receiving an increased amount of interest is the role of the element molybdenum. The enzyme nitrogenase that catalyzes the reduction of N2 to NH3 is one of a handful of enzymes that relies absolutely on Mo for catalytic activity. This fact has practical significance for agriculture since certain soils that could just barely support the growth of nitrogen-fixing legumes and could be greatly improved simply by addition of trace levels of Mo.

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Citations
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Journal ArticleDOI

Nitrogen fixation in freshwater, estuarine, and marine ecosystems. 2. Biogeochemical controls1

TL;DR: The tendency toward less nitrogen fixation by plankton in estuaries and coastal marine ecosystems than in lakes subject to similar loadings of nitrogen and phosphorus may be due to a lower availability in oxic seawater of one or more trace elements required for nitrogen fixation, such as molybdenum and iron.
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Biochemical disposal of excess H+ in growing plants?

TL;DR: This paper explores the possibility that a ‘biochemical’ disposal of these excess H+ could occur, thus allowing net NHJ assimilation to take place in the shoot of land plants and suggests that the H+-consuming processes, even in combination, probably cannot dispose of all of the H+.
Journal ArticleDOI

Biosynthesis of Nitrogenase Cofactors

TL;DR: This review provides a critical overview of discoveries on nitrogenase cofactor structure, function, and activity over the last four decades.
References
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Acetylene reduction by nitrogen-fixing preparations from Clostridium pasteurianum

TL;DR: It is suggested that the first step in N 2 reduction is a two-electron reduction leading to a non-dissociable intermediate at the oxidation level of diimide.
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Isolation of an iron-molybdenum cofactor from nitrogenase

TL;DR: The FeMoCo might be used as a model for synthesizing catalysts for chemical nitrogen fixation and knowledge of the structure of this cofactor should be useful for understanding the role of molybdenum at the active site of nitrogenase, role of ligands close to moly bdenum in electron and proton transfer, and the catalytic mechanism of nitrogen fixation.
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Regulation and characterization of protein products coded by the nif (nitrogen fixation) genes of Klebsiella pneumoniae.

TL;DR: Two hundred and thirty-five Nif- strains of Klebsiella pneumoniae were characterized by two-dimensional polyacrylamide gel electrophoresis, and nine nif-coded polypeptides were identified, and eight of these were assigned to specific nif genes.
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A Common Co-Factor for Nitrate Reductase and Xanthine Dehydrogenase which also Regulates the Synthesis of Nitrate Reductase

TL;DR: A Common Co-Factor for Nitrate Reductase and Xanthine Dehydrogenase which also Regulates the Synthesis of NitrateReductase.
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Nitrogenase and nitrogenase reductase associate and dissociate with each catalytic cycle.

TL;DR: The observations support the suggestion that it now is desirable to alter nomenclature to designate the MoFe protein as nitrogenase and the Fe protein as fertilizer, as shown by the occurrence of a lag phase approximately as long as the average turnover time of nitrogenase before hydrogen evolution occurs.
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