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Allen, J. F.

Publications and source records attributed to Allen, J. F..

2 recordsLinked to original sources

Nitrogenase inhibition limited oxygenation of the Proterozoic atmosphere

Cyanobacteria produced the atmospheric O2 that began accumulating 2.4 billion years ago1, leading to Earths Great Oxidation Event (GOE)2. For nearly 2 billion years following the GOE, O2 production was restricted and atmospheric oxygen remained low2-5. Oxygen rose again sharply with the advent of land plants roughly 450 million years ago, which increased atmospheric O2 through carbon burial4-5. Why did the O2 content of the atmosphere remain constant and low for more than a billion years despite the existence of O2-producing cyanobacteria? While geological limitations have been explored2-7, the limiting factor may have been biological, and enzymatic. Here we propose that O2 was kept low by oxygen inhibition of nitrogenase activity. Nitrogenase is the sole N2-fixing enzyme on Earth, and is inactive in air containing 2% or more O2 by volume8. No O2-resistant nitrogenase enzyme is known9-12. We further propose that nitrogenase inhibition by O2 kept atmospheric O2 low until upright terrestrial plants physically separated O2 production in aerial photosynthetic tissues from N2 fixation in soil, liberating nitrogenase from inhibition by atmospheric O2.

evolutionary biology↗

Oligomeric States In Sodium Ion-Dependent Regulation Of Cyanobacterial Histidine Kinase-2

Two-component signal transduction systems (TCSs) consist of sensor histidine kinases and response regulators. TCSs mediate adaptation to environmental changes in bacteria, plants, fungi, and protists. Histidine kinase 2 (Hik2) is a sensor histidine kinase found in all known cyanobacteria and as chloroplast sensor kinase in eukaryotic algae and plants. Sodium ions have been shown to inhibit the autophosphorylation activity of Hik2 that precedes phosphoryl transfer to response regulators, but the mechanism of inhibition has not been determined. We report on the mechanism of Hik2 activation and inactivation probed by chemical crosslinking and size exclusion chromatography together with direct visualisation of the kinase using negative-stain transmission electron microscopy of single particles. We show that the functional form of Hik2 is a higher order oligomer such as a hexamer or octamer. Increased NaCl concentration converts the active hexamer into an inactive tetramer. Furthermore, the action of NaCl appears to be confined to the Hik2 kinase domain.\n\nIMPORTANCEBacteria sense change and respond to it by means of two-component regulatory systems. The sensor component is a protein that becomes covalently modified by a phosphate group on a histidine side chain. The response regulator accepts the phosphate group onto an aspartate, with structural and functional consequences, often for gene transcription. Histidine kinase 2 is a sensor of sodium ion concentration and redox potential, regulating transcription of genes for light-harvesting and reaction center proteins of photosynthesis in cyanobacteria and chloroplasts of algae and plants. Using radiolabeling, chemical crosslinking, chromatography and electron microscopy, we find that sodium ion concentration governs the oligomeric state of Histidine Kinase 2 and its phosphorylation by ATP.

biochemistry↗