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Dimeric chlorite dismutase from the nitrogen‐fixing cyanobacterium C yanothece sp. PCC7425

It is demonstrated that cyanobacteria (both azotrophic and non‐azotrophic) contain heme b oxidoreductases that can convert chlorite to chloride and molecular oxygen (incorrectly denominated chlorite ‘dismutase’, Cld). Beside the water‐splitting manganese complex of photosystem II, this metalloenzyme...

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Detalles Bibliográficos
Autores principales: Schaffner, Irene, Hofbauer, Stefan, Krutzler, Michael, Pirker, Katharina F., Bellei, Marzia, Stadlmayr, Gerhard, Mlynek, Georg, Djinovic‐Carugo, Kristina, Battistuzzi, Gianantonio, Furtmüller, Paul G., Daims, Holger, Obinger, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973843/
https://www.ncbi.nlm.nih.gov/pubmed/25732258
http://dx.doi.org/10.1111/mmi.12989
Descripción
Sumario:It is demonstrated that cyanobacteria (both azotrophic and non‐azotrophic) contain heme b oxidoreductases that can convert chlorite to chloride and molecular oxygen (incorrectly denominated chlorite ‘dismutase’, Cld). Beside the water‐splitting manganese complex of photosystem II, this metalloenzyme is the second known enzyme that catalyses the formation of a covalent oxygen–oxygen bond. All cyanobacterial Clds have a truncated N‐terminus and are dimeric (i.e. clade 2) proteins. As model protein, Cld from C yanothece sp. PCC7425 (CCld) was recombinantly produced in E scherichia coli and shown to efficiently degrade chlorite with an activity optimum at pH 5.0 [k (cat) 1144 ± 23.8 s(−1), K(M) 162 ± 10.0 μM, catalytic efficiency (7.1 ± 0.6) × 10(6) M(−1) s(−1)]. The resting ferric high‐spin axially symmetric heme enzyme has a standard reduction potential of the Fe(III)/Fe(II) couple of −126 ± 1.9 mV at pH 7.0. Cyanide mediates the formation of a low‐spin complex with k (on) = (1.6 ± 0.1) × 10(5) M(−1) s(−1) and k (off) = 1.4 ± 2.9 s(−1) (K(D) ∼ 8.6 μM). Both, thermal and chemical unfolding follows a non‐two‐state unfolding pathway with the first transition being related to the release of the prosthetic group. The obtained data are discussed with respect to known structure–function relationships of Clds. We ask for the physiological substrate and putative function of these O(2)‐producing proteins in (nitrogen‐fixing) cyanobacteria.