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Keywords: cyanobacteria
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Biochem J (2021) 478 (7): 1333–1346.
Published: 06 April 2021
... for all oxygen-evolving photosynthetic organisms. It has a highly conserved structure and composition [ 1–3 ]. PSI consists of 11–14 protein subunits coordinating 94–96 chlorophylls (Chls), ∼24 carotenoids (Cars) and other cofactors [ 4–6 ]. In cyanobacteria, PSI is usually found in a trimeric...
Includes: Supplementary data
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Biochem J (2020) 477 (7): 1309–1321.
Published: 17 April 2020
...Shoki Ito; Takashi Osanai Metabolite production from carbon dioxide using sugar catabolism in cyanobacteria has been in the spotlight recently. Synechocystis sp. PCC 6803 ( Synechocystis 6803) is the most studied cyanobacterium for metabolite production. Previous in vivo analyses revealed...
Includes: Supplementary data
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Biochem J (2020) 477 (5): 971–983.
Published: 06 March 2020
... Anabaena Cas7 CRISPR CRISPR type I-D cyanobacteria RNA-binding protein RNA was isolated using TRIzol TM LS reagent (Invitrogen) by following the manufacturer's protocol. RNA associated with Alr1562 obtained from different imidazole elution fractions (i.e. 50 mM, 100 mM or 250 mM imidazole...
Includes: Supplementary data
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Biochem J (2018) 475 (6): 1091–1105.
Published: 20 March 2018
... of G6PDH activity has also been reported in Anabaena 7120, and its related species Anabaena variabilis and Nostoc punctiforme ATCC 29133 [ 7 – 10 ]. G6PDH in these nitrogen-fixing cyanobacteria plays a crucial role in providing reducing power for nitrogenase. However, the molecular mechanism of redox...
Includes: Supplementary data
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Biochem J (2018) 475 (1): 151–168.
Published: 05 January 2018
... availability (Irr) [ 1 ]. Anabaena sp. PCC 7120 (hereinafter Anabaena sp.) contains three paralogues of the FUR family, namely FurA, FurB and FurC [ 2 ]. FurA is a global regulator in cyanobacteria and is mainly responsible for controlling iron homeostasis [ 3 ] and FurC has been proposed to act as a PerR...
Includes: Supplementary data
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Biochem J (2017) 474 (14): 2435–2447.
Published: 06 July 2017
...Manisha Banerjee; Dhiman Chakravarty; Anand Ballal Cysteine desulfurases, which supply sulfur for iron–sulfur cluster biogenesis, are broadly distributed in all phyla including cyanobacteria, the progenitors of plant chloroplasts. The SUF (sulfur utilization factor) system is responsible for Fe–S...
Includes: Supplementary data
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Biochem J (2016) 473 (24): 4559–4572.
Published: 09 December 2016
...Leah D. McGurn; Maryam Moazami-Goudarzi; Sean A. White; Tannu Suwal; Beant Brar; Jason Q. Tang; George S. Espie; Matthew S. Kimber CcaA is a β-carbonic anhydrase (CA) that is a component of the carboxysomes of a subset of β-cyanobacteria. This protein, which has a characteristic C-terminal...
Includes: Supplementary data
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Biochem J (2008) 410 (2): 347–357.
Published: 12 February 2008
... compilation © 2008 Biochemical Society 2008 bifunctional enzyme cyanobacteria linoleate diol synthase activity Nostoc sp. oxylipin prokaryotic lipoxygenase Eukaryotic algae have developed mechanisms involving lipid peroxidation by which they defend themselves against abiotic and biotic...
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Biochem J (2006) 398 (3): 361–369.
Published: 29 August 2006
... and Synechocystis apo-carotenoid oxygenases (NosACO and SynACO) cyanobacteria opsin retinal Retinal represents the chromophore of the widespread family of retinylidene proteins, commonly called rhodopsins. These light-responsive seven-helix transmembrane proteins are common in archaea, algae and animals...
Includes: Supplementary data
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Biochem J (2005) 390 (2): 513–520.
Published: 23 August 2005
...Pengpeng Zhang; Natalia Battchikova; Virpi Paakkarinen; Hirokazu Katoh; Masako Iwai; Masahiko Ikeuchi; Himadri B. Pakrasi; Teruo Ogawa; Eva-Mari Aro NDH (NADH-quinone oxidoreductase)-1 complexes in cyanobacteria have specific functions in respiration and cyclic electron flow as well as in active CO...
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Biochem J (2004) 383 (2): 277–283.
Published: 08 October 2004
...Dirk K. HINCHA; Martin HAGEMANN Many organisms accumulate compatible solutes under environmental stress conditions. Cyanobacteria accumulate compatible solutes in response to increased external salinity, with tolerance increasing from Suc (sucrose) or trehalose to 2- O -(α- D -glucopyranosyl...
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Biochem J (2003) 373 (3): 909–916.
Published: 01 August 2003
...Heike SIELAFF; Elke DITTMANN; Nicole TANDEAU de MARSAC; Christiane BOUCHIER; Hans von DÖHREN; Thomas BÖRNER; Torsten SCHWECKE Microcystins are hepatotoxic, non-ribosomal peptides produced by several genera of freshwater cyanobacteria. Among other enzymic activities, in particular those of peptide...
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