Studies of the CCM in cyanobacteria have led the field and have r

Studies of the CCM in cyanobacteria have led the field and have revealed a whole set of CCM components that fully account for the performance of the CCM in representative species of cyanobacteria. These studies have recently focused on the relationship between biochemical functions and the crystallographic structures of the carboxysome, a focal point for the CCM. Espie and Kimber (2011) and Kinney et al. (2011) reviewed the role of carboxysomes in CO2 fixation Galunisertib concentration in relationship to packaging topology of CsoS1/CcmK proteins and CsoS4/CcmL proteins; respectively, these proteins form shell facets and vertices of the icosahedral body of α- and β-carboxysomes.

This review also addressed key components of intracarboxysomal CO2 formation by carbonic anhydrases and the interior organization of the carboxysome by CcmM/CsoSCA. Kinney et al. (2011) further illustrated the dynamism of the

shell forming protein hexamers and pentamers and discussed that the possible small substrate molecules may pass through Selleck KU55933 the pores of these protein complex units with diameters and electrostatic charges of pore interiors. Long et al. (2011) reported the structural adjustment of the β-carboxysome in response to changes in CO2 concentration by demonstrating the tight correlation between the content of CcmM M58 and the carboxysomal CA, CcaA. Under limited CO2, CcmM M58 slightly increased over the other form M35 and concomitantly CcaA levels increased to flexibly optimize the CA content Racecadotril in the carboxysome. Also elucidated during the last decade is the participation of unique proteins components and their molecular mechanisms in the acquisition of dissolved inorganic carbon (DIC) by cyanobacteria. Price (2011) thoroughly summarized the current knowledge in his review describing

the three plasma membrane-localized HCO3 − transporters (CmpABCD, BicA, and SbtA) and the two CO2 converting systems of Ndh–Chp complexes that are CHIR98014 supplier located in the thylakoid membranes and possibly in the plasmalemma. Price’s (2011) review also illustrated the membrane topology of the 12 and 10 transmembrane helix domains of BicA and SbtA, respectively; this review will stimulate future study leading to an understanding of the fine regulatory mechanisms that control transporter activities in concert with environmental fluctuations. A highly efficient CCM system, “especially active in β-cyanobacteria,” possibly contributed to the evolutionary adaptations of α-cyanobacteria as these organisms shifted habitation from a marine/oligotrophic environment to a costal/freshwater environment (Rae et al. 2011). Rae et al. (2011) reported the interesting case of a “hybrid” CCM in the α-cyanobacterium, Synechococcus sp. WH5701. This organism possesses transcriptionally CO2-responsive β-type-Ci-transporters. Rae et al.

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