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Measurement of Ascorbic Acid and Glutathione Content in Cyanobacterium Synechocystis sp. PCC 6803.

Bio-protocol (2021-03-05)
Anabella Aguilera, Charlotte Steelheart, Matías Alegre, Federico Berdun, Graciela Salerno, Carlos Bartoli, Gabriela Pagnussat, María Victoria Martin
RESUMEN

Ascorbic acid (AsA) and gluthathione (GSH) are two key components of the antioxidant machinery of eukaryotic and prokaryotic cells. The cyanobacterium Synechocystis sp. PCC 6803 presents both compounds in different concentrations (AsA, 20-100 μM and GSH, 2-5 mM). Therefore, it is important to have precise and sensitive methods to determine the redox status in the cell and to detect variations in this antioxidants. In this protocol, we describe an improved method to estimate the content of both antioxidants (in their reduced and oxidized forms) from the same sample obtained from liquid cultures of Synechocystis sp. PCC 6803.

MATERIALES
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Sigma-Aldrich
Metanol, suitable for HPLC, ≥99.9%
Sigma-Aldrich
DL-Ditiotreitol, ≥98% (HPLC), ≥99.0% (titration)
Sigma-Aldrich
L-Glutatión reducido, ≥98.0%
Sigma-Aldrich
Ácido 5,5′-ditiobis(2-nitrobenzoico), ≥98%, BioReagent, suitable for determination of sulfhydryl groups
Sigma-Aldrich
Ácido L-ascórbico, BioXtra, ≥99.0%, crystalline
Sigma-Aldrich
L-Glutationa oxidada, ≥98% (HPLC)
Sigma-Aldrich
Glutatión reductasa from baker′s yeast (S. cerevisiae), ammonium sulfate suspension, 100-300 units/mg protein (biuret)
Sigma-Aldrich
ββ-Nicotinamida adenina dinucleótico 2′-fosfato reducido tetrasodium salt hydrate, ≥93% (HPLC)
Glass beads, acid-washed, 150-212 μm (70-100 U.S. sieve)