CO2 concentrating mechanisms in cyanobacteria: molecular components, their diversity and evolution.
By M. Badger, G. Price. Journal of Experimental Botany, 2003
823 citations recorded by the source corpus.
Subfields: Ecology, Molecular Biology, Renewable Energy, Sustainability and the Environment
View Paper: https://www.semanticscholar.org/paper/2cc287c9acf0950ee5c2c763465c61787b315c5b
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Ecology
- D. Hutchins
- Feixue Fu
- Mark E. Warner
- Yuanyuan Feng
- M. Mulholland
- Yaohong Zhang
- J. Raven
- John Beardall
In Molecular Biology
In Renewable Energy, Sustainability and the Environment
- J. Raven
- John Beardall
- M. Mulholland
- B. M. Long
- Fiona J. Woodger
- Mohd Firdaus Abdul Wahab
- A. Idi
- Arun Kumar
Citations in the corpus
- Carbon Acquisition Mechanisms of Algae: Carbon Dioxide Diffusion and Carbon Dioxide Concentrating Mechanisms (2003, background): “These mechanisms have been investigated in [3 cyanobacteria (Badger, Hanson and Price, 2002; Badger and Price, 2003 ) such as the Synechocyistis and some strains ofSynechcoccus for which complete gene sequences are available.”
- Response of photosynthesis to ocean acidification (2015, background): “Energy sources for DIC transport can include ATP, NADPH, or reduced ferredoxin, or alternatively, transport can be coupled to an electrochemical Na+ gradient (Badger and Price, 2003).”
- Picophytoplankton : Bottom-up and top-down controls on ecology and evolution (2005, neutral): “The problem is exacerbated for cyanobacteria by the low CO2 affinity, and low CO2/O2 selectivity, of both the Form IA and Form IB ribulose bisphosphate carboxylaseoxygenases or Rubiscos (Horken & Tabita 1999, Badger & Price 2003, Giordano et al. 2005).”
- Elevated CO2 enhances nitrogen fixation and growth in the marine cyanobacterium Trichodesmium (2007, background): “The function and efficiency of the CCM have been studied extensively (see reviews by Kaplan & Reinhold, 1999; Badger et al., 2002; Badger & Price, 2003) focusing prominently on the potential of some species to concentrate Ci intracellularly up to 1000-fold more than ambient concentrations.”
- EFFECTS OF INCREASED TEMPERATURE AND CO2 ON PHOTOSYNTHESIS, GROWTH, AND ELEMENTAL RATIOS IN MARINE SYNECHOCOCCUS AND PROCHLOROCOCCUS (CYANOBACTERIA) 1 (2007, background): “Many eukaryotic and prokaryotic algal groups possess a wide variety of phylogenetically diverse carbon-concentrating systems that transport and ⁄ or interconvert CO2 and HCO3 ) (Raven 1997, Kaplan and Reinhold 1999, Beardall and Giordano 2002, Badger and Price 2003).”
- Cyanobacteria: A Precious Bio-resource in Agriculture, Ecosystem, and Environmental Sustainability (2016, positive): “…from the power plants contains high concentrations of CO 2 and has high temperatures (about 120 C), the cyanobacterial bio-fixation of CO 2 may warrants the use of thermophilic cyanobacterial species that are tolerant to both high CO 2 and temperature (Badger and Price, 2003; Ono and Cuello, 2007).”
- GEOMICROBIOLOGY IN CAVE ENVIRONMENTS: PAST, CURRENT AND FUTURE PERSPECTIVES (2007, background): “In cyanobacterial species, fixation of CO2 increases the concentration of bicarbonate ions, which may be excreted into the extracellular medium, causing CaCO3 precipitation if calcium ions are present (Badger and Price 2003; Hammes and Verstraete 2002).”
- Advances in understanding the cyanobacterial CO2-concentrating-mechanism (CCM): functional components, Ci transporters, diversity, genetic regulation and prospects for engineering into plants. (2008, methodology): “Energy sources for Ci uptake may include ATP (BCT1 HCO 3 transporter), NADPH or reduced ferredoxin (CO2 uptake) or coupling to an electrochemical Na+ gradient (SbtA or BicA HCO 3 transport) (Badger et al., 2002; Badger and Price, 2003).”
- Recent advances in CO2 uptake and fixation mechanism of cyanobacteria and microalgae (2016, background): “During the past two decades, many CCM components have been recognized and characterized at the molecular and cellular levels (Omata et al., 2001, 1999; Rocap et al., 2002; Badger and Price, 2003; Price et al., 2004; Seckbach et al., 2013).”
- Ecological Genomics of Marine Picocyanobacteria (2009, background): “have the longest RuBisCo gene region, since they possess three genes involved in low-affinity carbon transport (homologs to Synechocystis ndhD4 [cluster 8090] and ndhF4 [cluster 1422] genes [11, 12]) and carbon hydration (chpX [cluster 1423]) that are missing in all Prochlorococcus strains (56).”
- Contrasting effects of ocean acidification on the microbial food web under different trophic conditions (2016, background): “Cyanobacteria are known to use CCMs to actively transport inorganic C species and maintain their growth even at low external dissolved inorganic carbon concentrations (Badger and Price, 2003).”