Literature DB >> 10733873

Kinetics and mechanism of the decomposition of S-nitrosoglutathione by l-ascorbic acid and copper ions in aqueous solution to produce nitric oxide.

J N Smith1, T P Dasgupta.   

Abstract

S-Nitrosothiols serve as a good source of nitric oxide ((*)NO) mainly due to the ease of cleavage of the S-N bond which consequently produces (*)NO. The reductive decomposition of S-nitrosoglutathione (GSNO) by l-ascorbic acid (vitamin C) yields (*)NO which was monitored both electrochemically (using NO-probe) and spectrophotometrically. The rate of reaction and (*)NO release was found to be pH dependent in a manner which drastically increases with pH demonstrating that the l-ascorbic acid dianion (A(2-)) is by far the most reactive species of l-ascorbic acid (H(2)A). The derived rate expression (measuring the disappearance of the absorption at ca. 336 nm due to GSNO) was established as rate = -d[GSNO](t)/dt = ((k(a)[H(+)](2) + k(b)[H(+)]K(1) + k(c)K(1)K(2))/([H(+)](2) + K(1)[H(+)] + K(1)K(2)))[GSNO](t)[H(2)A](t). k(a), k(b), and k(c) are second-order rate constants via the H(2)A, HA(-), and A(2-) pathways, respectively, while K(1) and K(2) represent the first and second equilibrium dissociation constants of l-ascorbic acid. There is little or no reaction at low pH (below 5.5), where H(2)A is a predominant species, and as a result the rate constant (k(a)) via this route was found to be negligible. At 25 degrees C, k(b) = 5.23 +/- 1.47 x 10(-3) dm(3) mol(-1) s(-1) and k(c) = 1.22 +/- 0.04 x 10(3) dm(3) mol(-1) s(-1), activation parameters DeltaH(double dagger)(b) = 54.4 +/- 4.3 kJ mol(-1), DeltaS(double dagger)(b) = -106 +/- 16 J K(-1) mol(-1), DeltaH(double dagger)(c) = 80.5 +/- 7.5 kJ mol(-1), DeltaS(double dagger)(c) = 84 +/- 7 kJ mol(-1). The experimental rate and activation parameters suggest that this redox process follows an outer-sphere electron transfer mechanism. GSNO is relatively stable in the dark, aqueous medium and even in the presence of trace quantities of Cu(2+). Induced catalytic decomposition of GSNO only becomes significant above ca. 10 microM Cu(2+), but after this it shows linear dependency. To nullify any catalysis by Cu(2+) or any other transition metal ions, EDTA was added to all experimental reactions except those where catalysis by Cu(2+) was studied. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10733873     DOI: 10.1006/niox.2000.0272

Source DB:  PubMed          Journal:  Nitric Oxide        ISSN: 1089-8603            Impact factor:   4.427


  17 in total

Review 1.  Proteomic methods for analysis of S-nitrosation.

Authors:  Nicholas J Kettenhofen; Katarzyna A Broniowska; Agnes Keszler; Yanhong Zhang; Neil Hogg
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2007-02-25       Impact factor: 3.205

2.  Conjugated polymer-based fluorescence turn-on sensor for nitric oxide.

Authors:  Rhett C Smith; Andrew G Tennyson; Mi Hee Lim; Stephen J Lippard
Journal:  Org Lett       Date:  2005-08-04       Impact factor: 6.005

3.  Do nitric oxide donors mimic endogenous NO-related response in plants?

Authors:  J Floryszak-Wieczorek; G Milczarek; M Arasimowicz; A Ciszewski
Journal:  Planta       Date:  2006-06-14       Impact factor: 4.116

4.  Zinc induces distinct changes in the metabolism of reactive oxygen and nitrogen species (ROS and RNS) in the roots of two Brassica species with different sensitivity to zinc stress.

Authors:  Gábor Feigl; Nóra Lehotai; Árpád Molnár; Attila Ördög; Marta Rodríguez-Ruiz; José M Palma; Francisco J Corpas; László Erdei; Zsuzsanna Kolbert
Journal:  Ann Bot       Date:  2014-12-22       Impact factor: 4.357

Review 5.  Function of S-nitrosoglutathione reductase (GSNOR) in plant development and under biotic/abiotic stress.

Authors:  Marina Leterrier; Mounira Chaki; Morad Airaki; Raquel Valderrama; José M Palma; Juan B Barroso; Francisco J Corpas
Journal:  Plant Signal Behav       Date:  2011-06-01

6.  Estradiol-17beta stimulates specific receptor and endogenous nitric oxide-dependent dynamic endothelial protein S-nitrosylation: analysis of endothelial nitrosyl-proteome.

Authors:  Hong-Hai Zhang; Lin Feng; Itamar Livnat; Jeong-Kyu Hoh; Jae-Yoon Shim; Wu-Xiang Liao; Dong-Bao Chen
Journal:  Endocrinology       Date:  2010-06-02       Impact factor: 4.736

7.  Role of quinones in the ascorbate reduction rates of S-nitrosoglutathione.

Authors:  Pedro Sanchez-Cruz; Carmelo Garcia; Antonio E Alegria
Journal:  Free Radic Biol Med       Date:  2010-08-05       Impact factor: 7.376

8.  Signaling through reactive oxygen and nitrogen species is differentially modulated in sunflower seedling root and cotyledon in response to various nitric oxide donors and scavengers<sup/>.

Authors:  Neha Singh; Satish C Bhatla
Journal:  Plant Signal Behav       Date:  2017-09-01

9.  Nitric oxide-based protein modification: formation and site-specificity of protein S-nitrosylation.

Authors:  Izabella Kovacs; Christian Lindermayr
Journal:  Front Plant Sci       Date:  2013-05-14       Impact factor: 5.753

10.  Copper dependence of the biotin switch assay: modified assay for measuring cellular and blood nitrosated proteins.

Authors:  Xunde Wang; Nicholas J Kettenhofen; Sruti Shiva; Neil Hogg; Mark T Gladwin
Journal:  Free Radic Biol Med       Date:  2008-01-04       Impact factor: 7.376

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