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Items: 17


Structural Perturbations of Rhodopseudomonas palustris Form II RuBisCO Mutant Enzymes That Affect CO2 Fixation.

Satagopan S, North JA, Arbing MA, Varaljay VA, Haines SN, Wildenthal JA, Byerly KM, Shin A, Tabita FR.

Biochemistry. 2019 Sep 17;58(37):3880-3892. doi: 10.1021/acs.biochem.9b00617. Epub 2019 Sep 3.


Isotope discrimination by form IC RubisCO from Ralstonia eutropha and Rhodobacter sphaeroides, metabolically versatile members of 'Proteobacteria' from aquatic and soil habitats.

Thomas PJ, Boller AJ, Satagopan S, Tabita FR, Cavanaugh CM, Scott KM.

Environ Microbiol. 2019 Jan;21(1):72-80. doi: 10.1111/1462-2920.14423. Epub 2018 Nov 21.


Synthetic CO2-fixation enzyme cascades immobilized on self-assembled nanostructures that enhance CO2/O2 selectivity of RubisCO.

Satagopan S, Sun Y, Parquette JR, Tabita FR.

Biotechnol Biofuels. 2017 Jul 6;10:175. doi: 10.1186/s13068-017-0861-6. eCollection 2017.


RubisCO of a nucleoside pathway known from Archaea is found in diverse uncultivated phyla in bacteria.

Wrighton KC, Castelle CJ, Varaljay VA, Satagopan S, Brown CT, Wilkins MJ, Thomas BC, Sharon I, Williams KH, Tabita FR, Banfield JF.

ISME J. 2016 Nov;10(11):2702-2714. doi: 10.1038/ismej.2016.53. Epub 2016 May 3.


RubisCO selection using the vigorously aerobic and metabolically versatile bacterium Ralstonia eutropha.

Satagopan S, Tabita FR.

FEBS J. 2016 Aug;283(15):2869-80. doi: 10.1111/febs.13774. Epub 2016 Jun 27.


Functional metagenomic selection of ribulose 1, 5-bisphosphate carboxylase/oxygenase from uncultivated bacteria.

Varaljay VA, Satagopan S, North JA, Witte B, Dourado MN, Anantharaman K, Arbing MA, Hoeft McCann S, Oremland RS, Banfield JF, Wrighton KC, Tabita FR.

Environ Microbiol. 2016 Apr;18(4):1187-99. doi: 10.1111/1462-2920.13138. Epub 2016 Jan 21.


Structure-function studies with the unique hexameric form II ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) from Rhodopseudomonas palustris.

Satagopan S, Chan S, Perry LJ, Tabita FR.

J Biol Chem. 2014 Aug 1;289(31):21433-50. doi: 10.1074/jbc.M114.578625. Epub 2014 Jun 18.


A Rubisco mutant that confers growth under a normally "inhibitory" oxygen concentration.

Satagopan S, Scott SS, Smith TG, Tabita FR.

Biochemistry. 2009 Sep 29;48(38):9076-83. doi: 10.1021/bi9006385.


Plant-like substitutions in the large-subunit carboxy terminus of Chlamydomonas Rubisco increase CO2/O2 specificity.

Satagopan S, Spreitzer RJ.

BMC Plant Biol. 2008 Jul 30;8:85. doi: 10.1186/1471-2229-8-85.


Phylogenetic and evolutionary relationships of RubisCO and the RubisCO-like proteins and the functional lessons provided by diverse molecular forms.

Tabita FR, Hanson TE, Satagopan S, Witte BH, Kreel NE.

Philos Trans R Soc Lond B Biol Sci. 2008 Aug 27;363(1504):2629-40. doi: 10.1098/rstb.2008.0023. Review.


Distinct form I, II, III, and IV Rubisco proteins from the three kingdoms of life provide clues about Rubisco evolution and structure/function relationships.

Tabita FR, Satagopan S, Hanson TE, Kreel NE, Scott SS.

J Exp Bot. 2008;59(7):1515-24. doi: 10.1093/jxb/erm361. Epub 2008 Feb 16. Review.


Structural and functional consequences of the replacement of proximal residues Cys(172) and Cys(192) in the large subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase from Chlamydomonas reinhardtii.

García-Murria MJ, Karkehabadi S, Marín-Navarro J, Satagopan S, Andersson I, Spreitzer RJ, Moreno J.

Biochem J. 2008 Apr 15;411(2):241-7.


Function, structure, and evolution of the RubisCO-like proteins and their RubisCO homologs.

Tabita FR, Hanson TE, Li H, Satagopan S, Singh J, Chan S.

Microbiol Mol Biol Rev. 2007 Dec;71(4):576-99. Review.


Phylogenetic engineering at an interface between large and small subunits imparts land-plant kinetic properties to algal Rubisco.

Spreitzer RJ, Peddi SR, Satagopan S.

Proc Natl Acad Sci U S A. 2005 Nov 22;102(47):17225-30. Epub 2005 Nov 10.

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