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Cyanobacterial Ultrastructure in Light of Genomic Sequence Data

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Journal Photosynth Res
Publisher Springer
Date 2016 Jun 27
PMID 27344651
Citations 17
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Abstract

Cyanobacteria are physiologically and morphologically diverse photosynthetic microbes that play major roles in the carbon and nitrogen cycles of the biosphere. Recently, they have gained attention as potential platforms for the production of biofuels and other renewable chemicals. Many cyanobacteria were characterized morphologically prior to the advent of genome sequencing. Here, we catalog cyanobacterial ultrastructure within the context of genomic sequence information, including high-magnification transmission electron micrographs that represent the diversity in cyanobacterial morphology. We place the image data in the context of tabulated protein domains-which are the structural, functional, and evolutionary units of proteins-from the 126 cyanobacterial genomes comprising the CyanoGEBA dataset. In particular, we identify the correspondence between ultrastructure and the occurrence of genes encoding protein domains related to the formation of cyanobacterial inclusions. This compilation of images and genome-level domain occurrence will prove useful for a variety of analyses of cyanobacterial sequence data and provides a guidebook to morphological features.

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References
1.
Schirrmeister B, Gugger M, Donoghue P . Cyanobacteria and the Great Oxidation Event: evidence from genes and fossils. Palaeontology. 2016; 58(5):769-785. PMC: 4755140. DOI: 10.1111/pala.12178. View

2.
Tsang T, Roberson R, Vermaas W . Polyhydroxybutyrate particles in Synechocystis sp. PCC 6803: facts and fiction. Photosynth Res. 2013; 118(1-2):37-49. DOI: 10.1007/s11120-013-9923-1. View

3.
Lang N . The fine structure of blue-green algae. Annu Rev Microbiol. 1968; 22:15-46. DOI: 10.1146/annurev.mi.22.100168.000311. View

4.
Vogel C, Bashton M, Kerrison N, Chothia C, Teichmann S . Structure, function and evolution of multidomain proteins. Curr Opin Struct Biol. 2004; 14(2):208-16. DOI: 10.1016/j.sbi.2004.03.011. View

5.
Schirrmeister B, Antonelli A, Bagheri H . The origin of multicellularity in cyanobacteria. BMC Evol Biol. 2011; 11:45. PMC: 3271361. DOI: 10.1186/1471-2148-11-45. View