Search

Plant physiologists set about comprehending the genesis of the C4 photosynthetic pathway after its discovery by Hatch and Slack. They discovered that a sophisticated combination of morphological and biochemical adaptations allowed the plant to concentrate CO2 around RuBisCO to achieve maximum efficiency. We categorize the evolutionary events leading to C4 photosynthesis, beginning with anoxygenic photosynthesis and the evolution of RuBisCO to the cooling of Earth by the Great Oxygenation Event that led to the oxygenic photosynthesis. The evolutionary descent of the C4 plants is a phenomenon that occurred around 30 million years ago. Due to industrialization and population growth, improved photosynthetic efficiency and carbon fixation of C4 plants could contest the current global scenario of rising CO2 concentration. C3 crops engineered with C4 traits, implemented on a large scale, could impact the climate globally. Here we discuss the various strategies used to introduce C4 traits in the C3 plants and the potential techniques to be considered for successful hybridization. [ABSTRACT FROM AUTHOR]

Due to the progressive climate change on our planet, scientists are interested in solving this issue since it threatens not only certain regions or countries but also the world’s ecosystems and economies. Therefore, minimizing carbon dioxide (CO2) emissions and reducing atmospheric levels are global priorities. Thus, it is necessary at this moment to develop an appropriate approach to reduce or stabilize CO2 levels in the atmosphere. However, CO2 capture projects are long-term, low-profitable, and high-risk environmental projects. Consequently, it is necessary to find an appropriate and sustainable CO2 capture approach that is efficient in reducing atmospheric CO2 levels while having a safe impact on the environment. Although carbon (C) is the key basic component used to produce biological compounds by photosynthetic organisms in terrestrial plants, the C pathway is a key factor affecting the capture of CO2 by photosynthetic organisms. Among photosynthetic organisms, Paulownia, a multipurpose tree, is popular around the world for its timber and its potential role in CO2 sequestration. Paulownia spp. belongs to the Paulowniaceae family and comprises a group of trees. These trees are primarily found in southeastern Asia, particularly in China, and have been intentionally grown for more than two millennia due to their ornamental, cultural, and medicinal value. The number of Paulownia species varies depending on taxonomic classification, ranging from 6 to 17. Among them, Paulownia tomentosa, Paulownia elongata, Paulownia fortunei, and Paulownia catalpifolia are the most widely recognized and favored species. The present review provides a comprehensive technical-economic scenario for the capture of one million tons of CO2 by Paulownia trees (as a terrestrial plant model, grown on 2,400 ha−1). P. tomentosa can be utilized in agroforestry systems to mitigate greenhouse gas (GHG) emissions within urban cities and emphasize the carbon storage potential of agroforestry. In conclusion, Paulownia trees as an environmental mass project showed great encouragement to investors and governments to expand these types of projects to achieve global climate goals by 2050.

Anthropogenic emissions of carbon dioxide (CO2) contribute to global warming. Limiting temperature rise requires negative emission techniques to retract the emitted CO2 from the atmosphere. Through photosynthesis, ecosystems naturally sequester and store carbon. Enhancing these processes forms the basis of biological sequestration strategies. Ecosystems are a sink of atmospheric CO2 and significantly impact the global carbon cycle. The fixed carbon is converted into biomass, a portion of which enters the soil carbon pool and can be sequestered for millennia. The formation of stable soil organic carbon (SOC) depends on land use, management practices, and the use of amendments. Employing best management practices and carbon boosting approaches such as conservation agriculture, agroforestry, biochar, afforestation, and restoration of wetlands can improve SOC stocks and create a positive soil carbon budget, especially in degraded ecosystems. . Carbon fixation by plants and microbes is fundamental to biological sequestration. Regulating the properties and expression of the enzymes involved and introducing novel pathways for carbon capture can enhance carbon fixation efficiency and positively affect yield. This review discusses biological carbon sequestration strategies highlighting the recent findings in the effects and potential of soil carbon boosting approaches in carbon mitigation and the prospects of genetic engineering in enhancing carbon fixation.

As all plastids that have been investigated so far can be traced back to endosymbiotic uptake of cyanobacteria by heterotrophic host cells, they accordingly show a high similarity regarding photosynthesis, which includes both the photosystems and the biochemical reactions around the CO 2 fixation via the Calvin–Bassham cycle. Major differences between the different algal and plant groups may include the presence or absence of carbon concentrating mechanisms, pyrenoids, Rubisco activases, carbonic anhydrases as well as differences in the regulation of the Calvin–Bassham cycle. This review describes the diversity of primary carbon fixation steps in algae and plants and the respective regulatory mechanisms. [ABSTRACT FROM AUTHOR]

Agricultural yields have kept pace with the rising demands in the recent past as a result of the breeding and improved farming practices, but these practices alone will not be able to meet the demands of the future. The focus is now on the enhancement of the photosynthetic machinery. In photosynthesis, the rate limiting step is the one catalyzed by RuBisCO- Ribulose-1,5-bisphosphate carboxylase/oxygenase (4.1.1.39), which, because of its loose specificity and low turnover rate, is the primary target of most research programs directed towards improved photosynthesis. The other avenues of photosynthetic machinery that are under investigation to enhance it include-improved stomatal regulation and membrane permeability, RuBisCO with high specificity for CO and higher catalytic turnover; bypass of photorespiration and introduction of carbon concentrating mechanism (CCM) into the C plants. Carbon concentrating mechanisms cause accumulation of carbon dioxide in vicinity of RuBisCO producing a high CO/O ratio and hence an environment more suitable for carboxylation reactions than oxygenation reactions. This article includes the basic details of the major naturally occurring CCMs in various photosynthetic organisms to identify the knowledge gaps in each which could help study the prospects of its possible introduction into a non-native system as C plants which are devoid of any CCM. [ABSTRACT FROM AUTHOR]

The photosynthetic, unicellular green alga, Chlamydomonas reinhardtii, lives in environments that often contain low concentrations of CO and HCO, the utilizable forms of inorganic carbon (C). C. reinhardtii possesses a carbon concentrating mechanism (CCM) which can provide suitable amounts of C for growth and development. This CCM is induced when the CO concentration is at air levels or lower and is comprised of a set of proteins that allow the efficient uptake of C into the cell as well as its directed transport to the site where Rubisco fixes CO into biomolecules. While several components of the CCM have been identified in recent years, the picture is still far from complete. To further improve our knowledge of the CCM, we undertook a mutagenesis project where an antibiotic resistance cassette was randomly inserted into the C. reinhardtii genome resulting in the generation of 22,000 mutants. The mutant collection was screened using both a published PCR-based approach (Gonzalez-Ballester et al. ) and a phenotypic growth screen. The PCR-based screen did not rely on a colony having an altered growth phenotype and was used to identify colonies with disruptions in genes previously identified as being associated with the CCM-related gene. Eleven independent insertional mutations were identified in eight different genes showing the usefulness of this approach in generating mutations in CCM-related genes of interest as well as identifying new CCM components. Further improvements of this method are also discussed. [ABSTRACT FROM AUTHOR]

The articles in this special issue of Photosynthesis Research arose from the presentations given at the Eighth International Symposium on Inorganic Carbon Uptake by Aquatic Photosynthetic Organisms held from May 27 to June 1, 2013 in New Orleans, Louisiana USA. The meeting covered all the aspects of CO concentrating mechanisms (CCMs) present in photosynthetic bacteria, microalgae and macrophytes, and spanned disciplines from the molecular biology of CCMs to the importance of CCMs in aquatic ecosystems. The publications in this special issue represent our current understanding of CCMs and highlight recent advances in the field. The influences of CCMs on algal biofuel production as well as recent efforts to use the CCM to improve crop plants are also explored. [ABSTRACT FROM AUTHOR]

This review presents an overview of the two ways that cyanobacteria, algae, and plants have adapted to high O and low CO concentrations in the environment. First, the process of photorespiration enables photosynthetic organisms to recycle phosphoglycolate formed by the oxygenase reaction catalyzed by ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco). Second, there are a number of carbon concentrating mechanisms that increase the CO concentration around Rubisco which increases the carboxylase reaction enhancing CO fixation. This review also presents possibilities for the beneficial modification of these processes with the goal of improving future crop yields. [ABSTRACT FROM AUTHOR]

Cyanobacteria (as well as many chemoautotrophs) actively pump inorganic carbon (in the form of HCO) into the cytosol in order to enhance the overall efficiency of carbon fixation. The success of this approach is dependent upon the presence of carboxysomes-large, polyhedral, cytosolic bodies which sequester ribulose 1,5-bisphosphate carboxylase/oxygenase (RubisCO) and carbonic anhydrase. Carboxysomes seem to function by allowing ready passage of HCO into the body, but hindering the escape of evolved CO, promoting the accumulation of CO in the vicinity of RubisCO and, consequently, efficient carbon fixation. This selectivity is mediated by a thin shell of protein, which envelops the carboxysome's enzymatic core and uses narrow pores to control the passage of small molecules. In this review, we summarize recent advances in understanding the organization and functioning of these intriguing, and ecologically very important molecular machines. [ABSTRACT FROM AUTHOR]

Cyanobacteria show high metabolic plasticity by re-allocating macromolecular resources in response to variations in both environmental inorganic carbon (Ci) and light. We grew cultures of the picoplanktonic cyanobacterium Synechococcus elongatus Nägeli across a 50-fold range of growth irradiance at either a dissolved [Ci] <0.1 mM, sufficient to induce strongly the carbon-concentrating mechanism (CCM) or a dissolved [Ci] of ∼4 mM, sufficient to strongly induce the CCM to basal constitutive activity. There was no detectable growth cost of acclimation to low Ci across the entire range of irradiance and growth was nearly light saturated at 50 l mol photons·m−2·s−1. Cells acclimated to low Ci significantly re-allocated macromolecular resources to support their CCM, while maintaining near homeostatis of metabolic flux per unit photosynthetic complex. Changing growth irradiance also drove re-organization of the photosynthetic machinery to balance excitation flux and metabolic demands, but flux per complex varied widely across the range of tolerable growth irradiances. Across the range of growth irradiance, low Ci cells had significantly less phycocyanin than high Ci cells, which corresponded to a lower PSII absorbance capacity. Furthermore, low Ci cells maintained more PSI per cell−1 than high Ci cells under high growth irradiance. Low Ci cells could therefore maintain more of their PSII reaction centers open at high growth irradiance than could high Ci cells, which experienced a significant PSII closure. Thus, acclimation to growth under high available Ci actually constrained acclimation to high light by restricting electron transport downstream from PSII in S. elongatus. [ABSTRACT FROM AUTHOR]