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Considering this complex morphology, it was postulated that certain subsection V-specific (cytoskeletal) proteins could be responsible for this phenotype. However, no specific gene was identified whose distribution was specifically correlated with the cell morphology among different cyanobacterial subsections.
Polyhedral bodies were discovered by transmission electron microscopy in the cyanobacterium Phormidium uncinatum in 1956. [11] These were later observed in other cyanobacteria [12] and in some chemotrophic bacteria that fix carbon dioxide—many of them are sulfur oxidizers or nitrogen fixers (for example, Halothiobacillus, Acidithiobacillus, Nitrobacter and Nitrococcus; all belonging to ...
The function of the cyanobiont depends on its host species. Abundant marine cyanobacteria in the genus Synechococcus form symbionts with dinoflagellates in the genera Ornithocercus, Histionesis and Citharistes, where it is hypothesized to benefit its host through the provision of fixed nitrogen in oligotrophic, subtropical waters. [24]
SynechoNET is a specialized cyanobacterial protein-protein interaction database. It shows feasible cyanobacterial domain-domain interactions, as well as their protein level interactions using the model cyanobacterium, Synechocystis sp. PCC 6803. Additionally, SynechoNET provides transmembrane topology and domain information, as well as ...
Cyanobacteria are variable in morphology, ranging from unicellular and filamentous to colonial forms. Filamentous forms exhibit functional cell differentiation such as heterocysts (for nitrogen fixation), akinetes (resting stage cells), and hormogonia (reproductive, motile filaments).
Cyanobacteria are a phylum of bacteria that obtain their energy through the process of photosynthesis. [1] [2] Although cyanobacteria metabolize photoautotrophically like eukaryotic plants, they have prokaryotic cell structure. Cyanophages can be found in both freshwater and marine environments. [3]
Synechococcus is one of the most important components of the prokaryotic autotrophic picoplankton in the temperate to tropical oceans. The genus was first described in 1979, [5] [6] and was originally defined to include "small unicellular cyanobacteria with ovoid to cylindrical cells that reproduce by binary traverse fission in a single plane and lack sheaths". [7]
Spiral bacteria are another major bacterial cell morphology. [2] [30] [31] [32] Spiral bacteria can be sub-classified as spirilla, spirochetes, or vibrios based on the number of twists per cell, cell thickness, cell flexibility, and motility. [33] Bacteria are known to evolve specific traits to survive in their ideal environment. [34]