Geobiological feedbacks, oxygen, and the evolution of nitrogenase

dc.contributor.authorMus, Florence
dc.contributor.authorColman, Daniel R.
dc.contributor.authorPeters, John W.
dc.contributor.authorBoyd, Eric S.
dc.date.accessioned2019-10-28T21:11:18Z
dc.date.available2019-10-28T21:11:18Z
dc.date.issued2019-02
dc.description.abstractBiological nitrogen fixation via the activity of nitrogenase is one of the most important biological innovations, allowing for an increase in global productivity that eventually permitted the emergence of higher forms of life. The complex metalloenzyme termed nitrogenase contains complex iron-sulfur cofactors. Three versions of nitrogenase exist that differ mainly by the presence or absence of a heterometal at the active site metal cluster (either Mo or V). Mo-dependent nitrogenase is the most common while V-dependent or heterometal independent (Fe-only) versions are often termed alternative nitrogenases since they have apparent lower activities for N2 reduction and are expressed in the absence of Mo. Phylogenetic data indicates that biological nitrogen fixation emerged in an anaerobic, thermophilic ancestor of hydrogenotrophic methanogens and later diversified via lateral gene transfer into anaerobic bacteria, and eventually aerobic bacteria including Cyanobacteria. Isotopic evidence suggests that nitrogenase activity existed at 3.2 Ga, prior to the advent of oxygenic photosynthesis and rise of oxygen in the atmosphere, implying the presence of favorable environmental conditions for oxygen-sensitive nitrogenase to evolve. Following the proliferation of oxygenic phototrophs, diazotrophic organisms had to develop strategies to protect nitrogenase from oxygen inactivation and generate the right balance of low potential reducing equivalents and cellular energy for growth and nitrogen fixation activity. Here we review the fundamental advances in our understanding of biological nitrogen fixation in the context of the emergence, evolution, and taxonomic distribution of nitrogenase, with an emphasis placed on key events associated with its emergence and diversification from anoxic to oxic environments.en_US
dc.identifier.citationMus, Florence, Daniel R. Colman, John W. Peters, and Eric S. Boyd. "Geobiological feedbacks, oxygen, and the evolution of nitrogenase." Free Radical Biology & Medicine (February 2019). DOI:10.1016/j.freeradbiomed.2019.01.050.en_US
dc.identifier.issn0891-5849
dc.identifier.urihttps://scholarworks.montana.edu/handle/1/15726
dc.rightsThis Item is protected by copyright and/or related rights. You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).en_US
dc.rights.urihttp://rightsstatements.org/vocab/InC/1.0/en_US
dc.titleGeobiological feedbacks, oxygen, and the evolution of nitrogenaseen_US
dc.typeArticleen_US
mus.citation.extentfirstpage250en_US
mus.citation.extentlastpage259en_US
mus.citation.journaltitleFree Radical Biology & Medicineen_US
mus.citation.volume140en_US
mus.contributor.orcidPeters, John W.|0000-0001-9117-9568en_US
mus.data.thumbpage35en_US
mus.identifier.doi10.1016/j.freeradbiomed.2019.01.050en_US
mus.relation.collegeCollege of Agricultureen_US
mus.relation.collegeCollege of Letters & Scienceen_US
mus.relation.departmentMicrobiology & Immunology.en_US
mus.relation.universityMontana State University - Bozemanen_US

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