Upper ocean oxygenation, evolution of RuBisCO and the Phanerozoic succession of phytoplankton

Evidence is compiled to demonstrate a redox scale within Earth's photosynthesisers that correlates the specificity of their RuBisCO with organismal metabolic tolerance to anoxia, and ecological selection by dissolved O2/CO2 and nutrients. The Form 1B RuBisCO found in the chlorophyte green algae...

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Veröffentlicht in:Free radical biology & medicine 2019-08, Vol.140, p.295-304
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description Evidence is compiled to demonstrate a redox scale within Earth's photosynthesisers that correlates the specificity of their RuBisCO with organismal metabolic tolerance to anoxia, and ecological selection by dissolved O2/CO2 and nutrients. The Form 1B RuBisCO found in the chlorophyte green algae, has a poor selectivity between the two dissolved substrates, O2 and CO2, at the active site. This enzyme appears adapted to lower O2/CO2 ratios, or more “anoxic” conditions and therefore requires additional energetic or nutrient investment in a carbon concentrating mechanism (CCM) to boost the intracellular CO2/O2 ratio and maintain competitive carboxylation rates under increasingly high O2/CO2 conditions in the environment. By contrast the coccolithophores and diatoms evolved containing the more selective Rhodophyte Form 1D RuBisCO, better adapted to a higher O2/CO2 ratio, or more oxic conditions. This Form 1D RuBisCO requires lesser energetic or nutrient investment in a CCM to attain high carboxylation rates under environmentally high O2/CO2 ratios. Such a physiological relationship may underpin the succession of phytoplankton in the Phanerozoic oceans: the coccolithophores and diatoms took over the oceanic realm from the incumbent cyanobacteria and green algae when the upper ocean became persistently oxygenated, alkaline and more oligotrophic. The facultatively anaerobic green algae, able to tolerate the anoxic conditions of the water column and a periodically inundated soil, were better poised to adapt to the fluctuating anoxia associated with periods of submergence and emergence and transition onto the land. The induction of a CCM may exert a natural limit to the improvement of RuBisCO efficiency over Earth history. Rubisco specificity appears to adapt on the timescale of ∼100 Myrs. So persistent elevation of CO2/O2 ratios in the intracellular environment around the enzyme, may induce a relaxation in RuBisCO selectivity for CO2 relative to O2. The most efficient RuBisCO for net carboxylation is likely to be found in CCM-lacking algae that have been exposed to hyperoxic conditions for at least 100 Myrs, such as intertidal brown seaweeds. [Display omitted] •Dissolved O2/CO2 selects for a redox scale of phytoplankton Rubisco substrate selectivity and anaerobic metabolic ability.•Increasing O2/CO2 induced a positive feedback selecting for red-algal derived plastids at the start of the Mesozoic.•The relative affinity of RuBisCO for O2 and CO2 tunes to compensate fo
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The Form 1B RuBisCO found in the chlorophyte green algae, has a poor selectivity between the two dissolved substrates, O2 and CO2, at the active site. This enzyme appears adapted to lower O2/CO2 ratios, or more “anoxic” conditions and therefore requires additional energetic or nutrient investment in a carbon concentrating mechanism (CCM) to boost the intracellular CO2/O2 ratio and maintain competitive carboxylation rates under increasingly high O2/CO2 conditions in the environment. By contrast the coccolithophores and diatoms evolved containing the more selective Rhodophyte Form 1D RuBisCO, better adapted to a higher O2/CO2 ratio, or more oxic conditions. This Form 1D RuBisCO requires lesser energetic or nutrient investment in a CCM to attain high carboxylation rates under environmentally high O2/CO2 ratios. Such a physiological relationship may underpin the succession of phytoplankton in the Phanerozoic oceans: the coccolithophores and diatoms took over the oceanic realm from the incumbent cyanobacteria and green algae when the upper ocean became persistently oxygenated, alkaline and more oligotrophic. The facultatively anaerobic green algae, able to tolerate the anoxic conditions of the water column and a periodically inundated soil, were better poised to adapt to the fluctuating anoxia associated with periods of submergence and emergence and transition onto the land. The induction of a CCM may exert a natural limit to the improvement of RuBisCO efficiency over Earth history. Rubisco specificity appears to adapt on the timescale of ∼100 Myrs. So persistent elevation of CO2/O2 ratios in the intracellular environment around the enzyme, may induce a relaxation in RuBisCO selectivity for CO2 relative to O2. The most efficient RuBisCO for net carboxylation is likely to be found in CCM-lacking algae that have been exposed to hyperoxic conditions for at least 100 Myrs, such as intertidal brown seaweeds. 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The Form 1B RuBisCO found in the chlorophyte green algae, has a poor selectivity between the two dissolved substrates, O2 and CO2, at the active site. This enzyme appears adapted to lower O2/CO2 ratios, or more “anoxic” conditions and therefore requires additional energetic or nutrient investment in a carbon concentrating mechanism (CCM) to boost the intracellular CO2/O2 ratio and maintain competitive carboxylation rates under increasingly high O2/CO2 conditions in the environment. By contrast the coccolithophores and diatoms evolved containing the more selective Rhodophyte Form 1D RuBisCO, better adapted to a higher O2/CO2 ratio, or more oxic conditions. This Form 1D RuBisCO requires lesser energetic or nutrient investment in a CCM to attain high carboxylation rates under environmentally high O2/CO2 ratios. Such a physiological relationship may underpin the succession of phytoplankton in the Phanerozoic oceans: the coccolithophores and diatoms took over the oceanic realm from the incumbent cyanobacteria and green algae when the upper ocean became persistently oxygenated, alkaline and more oligotrophic. The facultatively anaerobic green algae, able to tolerate the anoxic conditions of the water column and a periodically inundated soil, were better poised to adapt to the fluctuating anoxia associated with periods of submergence and emergence and transition onto the land. The induction of a CCM may exert a natural limit to the improvement of RuBisCO efficiency over Earth history. Rubisco specificity appears to adapt on the timescale of ∼100 Myrs. So persistent elevation of CO2/O2 ratios in the intracellular environment around the enzyme, may induce a relaxation in RuBisCO selectivity for CO2 relative to O2. The most efficient RuBisCO for net carboxylation is likely to be found in CCM-lacking algae that have been exposed to hyperoxic conditions for at least 100 Myrs, such as intertidal brown seaweeds. [Display omitted] •Dissolved O2/CO2 selects for a redox scale of phytoplankton Rubisco substrate selectivity and anaerobic metabolic ability.•Increasing O2/CO2 induced a positive feedback selecting for red-algal derived plastids at the start of the Mesozoic.•The relative affinity of RuBisCO for O2 and CO2 tunes to compensate for environmental O2/CO2 on timescales of 100–1000 yrs.•Induction of a CCM relaxes enzyme specificity over ∼ 100 Myrs providing a limit to improvement of RuBisCO selectivity.•Persistently high O2/CO2 ratios in restricted intertidal zones selects the most efficient RuBisCO in species lacking a CCM.</description><subject>Carbon Dioxide - metabolism</subject><subject>Cyanobacteria - genetics</subject><subject>Cyanobacteria - metabolism</subject><subject>Diatoms - genetics</subject><subject>Diatoms - metabolism</subject><subject>Oceans and Seas</subject><subject>Oxygen - metabolism</subject><subject>Photosynthesis - genetics</subject><subject>Phytoplankton - genetics</subject><subject>Phytoplankton - metabolism</subject><subject>Ribulose-Bisphosphate Carboxylase - genetics</subject><subject>Ribulose-Bisphosphate Carboxylase - metabolism</subject><issn>0891-5849</issn><issn>1873-4596</issn><issn>1873-4596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkVFrFDEQx4Mo9qx-BVnwxQd3TXY32QRB0KPVQqFF7KOE7Oykl3MvWZPdw-und4-7FvvWpwTym_9M5kfIO0YLRpn4uC5sRIyma13YYFeUlKmC8oJS8YwsmGyqvOZKPCcLKhXLuazVCXmV0ppSWvNKviQnFaMNr1WzIL9uhgFjFgCNz8Lf3S16M7rgP2S4Df20v2bBZj-mry4trzLju2xcYXa9Mh5juAsOsjQBYEpHcljtxjD0xv8eg39NXljTJ3xzPE_JzfnZz-X3_PLq28Xyy2UOtWJjDgqEMdTYEoURdVlW0HRWtC0DZkoFIKuSt7yxFnmrsGQSLArABnlTUwrVKfl8yB2mdl4JoB-j6fUQ3cbEnQ7G6ccv3q30bdhqIbloGJ8D3h8DYvgzYRr1xiXAfv4HhinpeSSmqOSSzuinAwoxpBTRPrRhVO8F6bV-JEjvBWnK9Sxorn77_6QPtfdGZuDsAOC8r63DqBM49ICdiwij7oJ7UqN_t3etdw</recordid><startdate>20190820</startdate><enddate>20190820</enddate><creator>Rickaby, Rosalind E.M.</creator><creator>Eason Hubbard, M.R.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190820</creationdate><title>Upper ocean oxygenation, evolution of RuBisCO and the Phanerozoic succession of phytoplankton</title><author>Rickaby, Rosalind E.M. ; Eason Hubbard, M.R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c491t-c9c6aa0af2e6a64223c7df6bb1c1a29cc8325b57ffe5b9e218cfe6ce7e57400c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Carbon Dioxide - metabolism</topic><topic>Cyanobacteria - genetics</topic><topic>Cyanobacteria - metabolism</topic><topic>Diatoms - genetics</topic><topic>Diatoms - metabolism</topic><topic>Oceans and Seas</topic><topic>Oxygen - metabolism</topic><topic>Photosynthesis - genetics</topic><topic>Phytoplankton - genetics</topic><topic>Phytoplankton - metabolism</topic><topic>Ribulose-Bisphosphate Carboxylase - genetics</topic><topic>Ribulose-Bisphosphate Carboxylase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rickaby, Rosalind E.M.</creatorcontrib><creatorcontrib>Eason Hubbard, M.R.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Free radical biology &amp; medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rickaby, Rosalind E.M.</au><au>Eason Hubbard, M.R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Upper ocean oxygenation, evolution of RuBisCO and the Phanerozoic succession of phytoplankton</atitle><jtitle>Free radical biology &amp; medicine</jtitle><addtitle>Free Radic Biol Med</addtitle><date>2019-08-20</date><risdate>2019</risdate><volume>140</volume><spage>295</spage><epage>304</epage><pages>295-304</pages><issn>0891-5849</issn><issn>1873-4596</issn><eissn>1873-4596</eissn><abstract>Evidence is compiled to demonstrate a redox scale within Earth's photosynthesisers that correlates the specificity of their RuBisCO with organismal metabolic tolerance to anoxia, and ecological selection by dissolved O2/CO2 and nutrients. The Form 1B RuBisCO found in the chlorophyte green algae, has a poor selectivity between the two dissolved substrates, O2 and CO2, at the active site. This enzyme appears adapted to lower O2/CO2 ratios, or more “anoxic” conditions and therefore requires additional energetic or nutrient investment in a carbon concentrating mechanism (CCM) to boost the intracellular CO2/O2 ratio and maintain competitive carboxylation rates under increasingly high O2/CO2 conditions in the environment. By contrast the coccolithophores and diatoms evolved containing the more selective Rhodophyte Form 1D RuBisCO, better adapted to a higher O2/CO2 ratio, or more oxic conditions. This Form 1D RuBisCO requires lesser energetic or nutrient investment in a CCM to attain high carboxylation rates under environmentally high O2/CO2 ratios. Such a physiological relationship may underpin the succession of phytoplankton in the Phanerozoic oceans: the coccolithophores and diatoms took over the oceanic realm from the incumbent cyanobacteria and green algae when the upper ocean became persistently oxygenated, alkaline and more oligotrophic. The facultatively anaerobic green algae, able to tolerate the anoxic conditions of the water column and a periodically inundated soil, were better poised to adapt to the fluctuating anoxia associated with periods of submergence and emergence and transition onto the land. The induction of a CCM may exert a natural limit to the improvement of RuBisCO efficiency over Earth history. Rubisco specificity appears to adapt on the timescale of ∼100 Myrs. So persistent elevation of CO2/O2 ratios in the intracellular environment around the enzyme, may induce a relaxation in RuBisCO selectivity for CO2 relative to O2. The most efficient RuBisCO for net carboxylation is likely to be found in CCM-lacking algae that have been exposed to hyperoxic conditions for at least 100 Myrs, such as intertidal brown seaweeds. [Display omitted] •Dissolved O2/CO2 selects for a redox scale of phytoplankton Rubisco substrate selectivity and anaerobic metabolic ability.•Increasing O2/CO2 induced a positive feedback selecting for red-algal derived plastids at the start of the Mesozoic.•The relative affinity of RuBisCO for O2 and CO2 tunes to compensate for environmental O2/CO2 on timescales of 100–1000 yrs.•Induction of a CCM relaxes enzyme specificity over ∼ 100 Myrs providing a limit to improvement of RuBisCO selectivity.•Persistently high O2/CO2 ratios in restricted intertidal zones selects the most efficient RuBisCO in species lacking a CCM.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>31075497</pmid><doi>10.1016/j.freeradbiomed.2019.05.006</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Carbon Dioxide - metabolism
Cyanobacteria - genetics
Cyanobacteria - metabolism
Diatoms - genetics
Diatoms - metabolism
Oceans and Seas
Oxygen - metabolism
Photosynthesis - genetics
Phytoplankton - genetics
Phytoplankton - metabolism
Ribulose-Bisphosphate Carboxylase - genetics
Ribulose-Bisphosphate Carboxylase - metabolism
title Upper ocean oxygenation, evolution of RuBisCO and the Phanerozoic succession of phytoplankton
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