ArticlePhotosynthesis research2006
Evidence for a plasmalemma-based CO2 concentrating mechanism in Laminaria saccharina.
Article in Photosynthesis research, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 32 citations in OpenAlex.
- The role of irradiance and C-use strategies in tropical macroalgae photosynthetic response to ocean acidification.Scientific reports · 2018Article
- Acquisition and metabolism of carbon in the Ochrophyta other than diatoms.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017Review
- Increased pCOPlanta · 2017Article
- Photosynthetic use of inorganic carbon in deep-water kelps from the Strait of Gibraltar.Photosynthesis research · 2016Article
- An Ocean Acidification Acclimatised Green Tide Alga Is Robust to Changes of Seawater Carbon Chemistry but Vulnerable to Light Stress.PloS one · 2016Article
- Effects of ocean acidification on the photosynthetic performance, carbonic anhydrase activity and growth of the giant kelp Macrocystis pyrifera.Photosynthesis research · 2015Article
- Article
- Ecophysiology of photosynthesis in macroalgae.Photosynthesis research · 2012Review
- Photosynthetic carbon acquisition in Sargassum henslowianum (Fucales, Phaeophyta), with special reference to the comparison between the vegetative and reproductive tissues.Photosynthesis research · 2011Article
- Photosynthetic utilization of bicarbonate in Zostera marina is reduced by inhibitors of mitochondrial ATPase and electron transport.Plant physiology · 2008Article
Corrections and comments
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Authors and funding
5 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A kinetic analysis of the photosynthesis inhibition by buffers allowed quantification of some components of the carbon concentrating mechanism (CCM) of the brown macroalga Laminaria saccharina. The CCM was based on the presence of acid regions outside the plasma membrane that increased the CO(2) concentration available for photosynthesis by 10-20 times above that of the bulk medium at alkaline pH. Furthermore, the results suggested that the CCM is located mainly on the cell membrane and not in the chloroplast, as suggested for most macroalgae. The degree of dissipation of the acid regions by a buffer was related to the buffer anion concentration (B(-)), estimated from the titration of the buffer from bulk medium pH to a pH endpoint value close to the first pK (a) of the carbonic acid system. A kinetic model describing the relationship between inhibition of photosynthesis by a buffer and B(-) was developed suggesting that buffers act as competitive inhibitors with IC(50) (the concentration of the buffer anion which reduces the reaction velocity by half) of 5.0 mol m(-3). This model can be used to estimate the inhibitory effect of any buffer on the photosynthesis of L. saccharina. Nevertheless, some buffers tested showed a lower effect than that predicted from the hyperbolic model suggesting that their strength as inhibitors depended on: (1) the pK (a) in relation to the first pK (a) of the carbonic acid system and (2) its molecular weight (i.e. its mobility).
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