scholarly journals Proteomics of Carbon Fixation Energy Sources in Halothiobacillus neapolitanus

Author(s):  
Jonathan Hunter ◽  
Maria Marasco ◽  
Ilerioluwa Sowande ◽  
Newton Hilliard
Author(s):  
David W. Deamer

The two quotes in the epigraph, in juxtaposition, always make me smile, and I tried to keep them in mind while writing this chapter. The first eight chapters of this book have the effect of eliminating the impossible by investigating the facts to which Twain is referring. Perhaps he would consider them trifling, but I doubt that Twain ever performed an experiment to test an idea. Every working scientist knows that science is not just a set of facts but is also a set of questions. The best way to begin answering a question is to pose a hypothesis and that hypothesis begins as a conjecture. Only when we have a hypothesis, can we design experiments to test it, and if we are lucky, the results of those experiments lead us a little closer to the truth. This chapter summarizes facts that lead to an alternative scenario for life’s origin in freshwater hydrothermal conditions rather than a marine origin in saltwater hydrothermal vents. As stated in the introduction to this book, when assumptions are part of the story they will be made explicit so that the logic that arises from them will be clear. What follows in this overview is a list of ten prerequisites we assume are necessary for cellular life to begin, followed by eight assumptions underlying the scenario to be presented here. Prerequisite conditions for life to begin: Dilute solutions of potential reactants are available, together with a process by which they can be sufficiently concentrated to react. Energy sources available in the environment can drive reactions such as carbon fixation, primitive metabolism, and polymerization. Products of reactions accumulate within the site rather than dispersing into the bulk phase environment. Amphiphiles assemble into membranous compartments over the range of temperatures, salt concentrations, and pH values related to each site. Biologically relevant polymers are synthesized with chain lengths sufficient to act as catalysts or incorporate genetic information. A plausible physical mechanism can produce encapsulated polymers as protocells then subject them to combinatorial selection. Organic solutes in aqueous solutions become biochemical solutes within protocells and then substrates supporting a primitive metabolism.


2012 ◽  
Vol 450-451 ◽  
pp. 1082-1085
Author(s):  
Qiao Ling Luo ◽  
Qing Ming Zhan

This paper discusses the theory and practice of low-carbon communities. The paper suggests that the following points should be considered when constructing a low-carbon community: (1) mixed-functions; (2) public transport; (3) carbon fixation through forestry; (4) green building design; (5) water recycling; (6) energy-saving building design and the use of renewable energy sources.


2021 ◽  
Author(s):  
Sean K. Bay ◽  
David W. Waite ◽  
Xiyang Dong ◽  
Osnat Gillor ◽  
Steven L. Chown ◽  
...  

AbstractDesert soils harbour diverse communities of aerobic bacteria despite lacking substantial organic carbon inputs from vegetation. A major question is therefore how these communities maintain their biodiversity and biomass in these resource-limiting ecosystems. Here, we investigated desert topsoils and biological soil crusts collected along an aridity gradient traversing four climatic regions (sub-humid, semi-arid, arid, and hyper-arid). Metagenomic analysis indicated these communities vary in their capacity to use sunlight, organic compounds, and inorganic compounds as energy sources. Thermoleophilia, Actinobacteria, and Acidimicrobiia were the most abundant and prevalent bacterial classes across the aridity gradient in both topsoils and biocrusts. Contrary to the classical view that these taxa are obligate organoheterotrophs, genome-resolved analysis suggested they are metabolically flexible, with the capacity to also use atmospheric H2 to support aerobic respiration and often carbon fixation. In contrast, Cyanobacteria were patchily distributed and only abundant in certain biocrusts. Activity measurements profiled how aerobic H2 oxidation, chemosynthetic CO2 fixation, and photosynthesis varied with aridity. Cell-specific rates of atmospheric H2 consumption increased 143-fold along the aridity gradient, correlating with increased abundance of high-affinity hydrogenases. Photosynthetic and chemosynthetic primary production co-occurred throughout the gradient, with photosynthesis dominant in biocrusts and chemosynthesis dominant in arid and hyper-arid soils. Altogether, these findings suggest that the major bacterial lineages inhabiting hot deserts use different strategies for energy and carbon acquisition depending on resource availability. Moreover, they highlight the previously overlooked roles of Actinobacteriota as abundant primary producers and trace gases as critical energy sources supporting productivity and resilience of desert ecosystems.


2017 ◽  
Vol 326 ◽  
pp. 249-256 ◽  
Author(s):  
Ya-nan Wang ◽  
Yiu Fai Tsang ◽  
Lei Wang ◽  
Xiaohua Fu ◽  
Huan Li ◽  
...  

2016 ◽  
Vol 198 (9) ◽  
pp. 1423-1428 ◽  
Author(s):  
Lisa G. Kuhns ◽  
Stéphane L. Benoit ◽  
Krishnareddy Bayyareddy ◽  
Darryl Johnson ◽  
Ron Orlando ◽  
...  

ABSTRACTA molecular hydrogen (H2)-stimulated, chemolithoautotrophic growth mode for the gastric pathogenHelicobacter pyloriis reported. In a culture medium containing peptides and amino acids, H2-supplied cells consistently achieved 40 to 60% greater growth yield in 16 h and accumulated 3-fold more carbon from [14C]bicarbonate (on a per cell basis) in a 10-h period than cells without H2. Global proteomic comparisons of cells supplied with different atmospheric conditions revealed that addition of H2led to increased amounts of hydrogenase and the biotin carboxylase subunit of acetyl coenzyme A (acetyl-CoA) carboxylase (ACC), as well as other proteins involved in various cellular functions, including amino acid metabolism, heme synthesis, or protein degradation. In agreement with this result, H2-supplied cells contained 3-fold more ACC activity than cells without H2. Other possible carbon dioxide (CO2) fixation enzymes were not up-expressed under the H2-containing atmosphere. As the gastric mucus is limited in carbon and energy sources and the bacterium lacks mucinase, this new growth mode may contribute to the persistence of the pathogenin vivo. This is the first time that chemolithoautotrophic growth is described for a pathogen.IMPORTANCEMany pathogens must survive within host areas that are poorly supplied with carbon and energy sources, and the gastric pathogenHelicobacter pyloriresides almost exclusively in the nutritionally stringent mucus barrier of its host. Although this bacterium is already known to be highly adaptable to gastric niches, a new aspect of its metabolic flexibility, whereby molecular hydrogen use (energy) is coupled to carbon dioxide fixation (carbon acquisition) via a described carbon fixation enzyme, is shown here. This growth mode, which supplements heterotrophy, is termed chemolithoautotrophy and has not been previously reported for a pathogen.


2004 ◽  
Vol 186 (3) ◽  
pp. 623-630 ◽  
Author(s):  
Anthony K.-C. So ◽  
George S. Espie ◽  
Eric B. Williams ◽  
Jessup M. Shively ◽  
Sabine Heinhorst ◽  
...  

ABSTRACT A significant portion of the total carbon fixed in the biosphere is attributed to the autotrophic metabolism of prokaryotes. In cyanobacteria and many chemolithoautotrophic bacteria, CO2 fixation is catalyzed by ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO), most if not all of which is packaged in protein microcompartments called carboxysomes. These structures play an integral role in a cellular CO2-concentrating mechanism and are essential components for autotrophic growth. Here we report that the carboxysomal shell protein, CsoS3, from Halothiobacillus neapolitanus is a novel carbonic anhydrase (ε-class CA) that has an evolutionary lineage distinct from those previously recognized in animals, plants, and other prokaryotes. Functional CAs encoded by csoS3 homologues were also identified in the cyanobacteria Prochlorococcus sp. and Synechococcus sp., which dominate the oligotrophic oceans and are major contributors to primary productivity. The location of the carboxysomal CA in the shell suggests that it could supply the active sites of RuBisCO in the carboxysome with the high concentrations of CO2 necessary for optimal RuBisCO activity and efficient carbon fixation in these prokaryotes, which are important contributors to the global carbon cycle.


2021 ◽  
Author(s):  
Yaqi Sun ◽  
Victoria M. Harman ◽  
James R. Johnson ◽  
Taiyu Chen ◽  
Gregory F. Dykes ◽  
...  

AbstractCarboxysomes are anabolic bacterial microcompartments that play an essential role in carbon fixation in cyanobacteria and some chemoautotrophs. This self-assembling organelle encapsulates the key CO2-fixing enzymes, Rubisco, and carbonic anhydrase using a polyhedral protein shell that is constructed by hundreds of shell protein paralogs. The α-carboxysome from the chemoautotroph Halothiobacillus neapolitanus serves as a model system in fundamental studies and synthetic engineering of carboxysomes. Here we adopt a QconCAT-based quantitative mass spectrometry to determine the absolute stoichiometric composition of native α-carboxysomes from H. neapolitanus. We further performed an in-depth comparison of the protein stoichiometry of native and recombinant α-carboxysomes heterologously generated in Escherichia coli to evaluate the structural variability and remodeling of α-carboxysomes. Our results provide insight into the molecular principles that mediate carboxysome assembly, which may aid in rational design and reprogramming of carboxysomes in new contexts for biotechnological applications.


Author(s):  
Gunnel Karlsson ◽  
Jan-Olov Bovin ◽  
Michael Bosma

RuBisCO (D-ribulose-l,5-biphosphate carboxylase/oxygenase) is the most aboundant enzyme in the plant cell and it catalyses the key carboxylation reaction of photosynthetic carbon fixation, but also the competing oxygenase reaction of photorespiation. In vitro crystallized RuBisCO has been studied earlier but this investigation concerns in vivo existance of RuBisCO crystals in anthers and leaves ofsugarbeets. For the identification of in vivo protein crystals it is important to be able to determinethe unit cell of cytochemically identified crystals in the same image. In order to obtain the best combination of optimal contrast and resolution we have studied different staining and electron accelerating voltages. It is known that embedding and sectioning can cause deformation and obscure the unit cell parameters.


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