2009
DOI: 10.3354/ab01315
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Contributions of anoxygenic and oxygenic phototrophy and chemolithotrophy to carbon and oxygen fluxes in aquatic environments

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Cited by 50 publications
(68 citation statements)
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“…The anammox process is inhibited by oxygen, yet organisms quickly resume their activity once anaerobic conditions are restored (Strous et al 1999). Genomic and enzymatic studies of anammox bacteria provided initial evidence for usage of the WL-pathway for carbon fixation (Schouten et al 2004, Strous et al 2006, making this pathway potentially of wider significance in the pelagic realm, with a potential contribution of up to 3.5 Tg C y −1 (Raven 2009). Interestingly, CO dehydrogenase, the key enzyme of the WL-pathway, is very oxygen sensitive and, so far, the WL-pathway is only known to operate in anaerobic organisms growing under highly reducing conditions (Berg et al 2010a), unlike conditions prevailing in OMZs.…”
Section: Wwwannualreviewsorg • Beyond the Calvin Cyclementioning
confidence: 98%
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“…The anammox process is inhibited by oxygen, yet organisms quickly resume their activity once anaerobic conditions are restored (Strous et al 1999). Genomic and enzymatic studies of anammox bacteria provided initial evidence for usage of the WL-pathway for carbon fixation (Schouten et al 2004, Strous et al 2006, making this pathway potentially of wider significance in the pelagic realm, with a potential contribution of up to 3.5 Tg C y −1 (Raven 2009). Interestingly, CO dehydrogenase, the key enzyme of the WL-pathway, is very oxygen sensitive and, so far, the WL-pathway is only known to operate in anaerobic organisms growing under highly reducing conditions (Berg et al 2010a), unlike conditions prevailing in OMZs.…”
Section: Wwwannualreviewsorg • Beyond the Calvin Cyclementioning
confidence: 98%
“…Although other so-called alternative carbon fixation pathways have been known to exist for a long time, recognition of their relative contribution to local organic matter production and an appreciation of the ecological role of the organisms using these pathways have occurred only this past decade (Raven 2009). Presently, five CO 2 fixation pathways are known in addition to the CBB cycle: the reductive tricarboxylic acid (rTCA) cycle; the reductive acetyl-CoA, or Wood-Ljungdahl (WL) pathway; and the 3-hydroxypropionate (3-HP) bicycle; as well as the 3-hydroxypropionate/4-hydroxybutyrate (3-HP/4-HB) and dicarboxylate/4-hydroxybutyrate (DC/4-HB) cycles (Ljungdahl 1986, Buchanan & Arnon 1990, Berg et al 2007, Huber et al 2008, Zarzycki et al 2009).…”
Section: Introductionmentioning
confidence: 99%
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“…3), Calvin cycle, reverse TCA cycle, reductive acetyl CoA pathway, and dicarboxylatehydroxybutyrate cycle. This prediction becomes relevant in light of the described importance of the Calvin cycle in primary productivity estimations, [44][45][46][47][48][49][50] but the other CO 2¯x ation pathways remain understudied. [51][52][53][54] The EFM analysis is constrained by stoichiometry and does not violate the conservation of mass law, therefore it becomes useful to estimate the potential role of relevant metabolic pathways, including the alternative CO 2¯x ation pathways, coupling metagenomic datasets, and ecophysiological rates to limit the solution°ux space of the EFMs and make predictions for the rates of CO 2¯x ation pathways involved.…”
Section: Efm Analysis Of Metabolic Networkmentioning
confidence: 97%
“…The CBB cycle is also used by chemolithoautotrophic bacteria to fix carbon in the dark ocean (Badger and Bek, 2007;Walsh et al, 2009). Thus, the CBB cycle, being one of the six carbon fixation pathways described to date (Berg, 2011;Hügler and Sievert, 2011), is the main carbon fixation mechanism utilized by extant autotrophic organisms (Raven, 2009;Berg, 2011).…”
Section: Introductionmentioning
confidence: 99%