Kinetics of the reaction of phosphoenol pyruvic acid with tetranitrosyl iron complex with penicylamine ligands – nitrogen monoxide donor

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Аннотация

The kinetic patterns of the reaction of phosphoenolpyruvic acid (PEP) with the NO donor – nitrosyl iron complex with penicillamine ligands (PEN) were studied using mass spectrometric analysis. It has been established that the PEP molecule in an aqueous solution interacts with PEN. The kinetic curves demonstrate the complex multi-stage nature of the reaction. A kinetic model of the process is proposed that quantitatively describes the experimental data.

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Авторлар туралы

B. Psikha

Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences

Email: easar@icp.ac.ru
Ресей, Chernogolovka

E. Saratovskikh

Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences

Хат алмасуға жауапты Автор.
Email: easar@icp.ac.ru
Ресей, Chernogolovka

N. Sanina

Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences; Lomonosov Moscow State University , Faculty of Fundamental Physical and Chemical Engineering; Moscow State Regional University

Email: easar@icp.ac.ru

Moscow State Regional University, Scientific and Educational Center “Medical Chemistry”

Ресей, Chernogolovka; Moscow; Mytishchi

Әдебиет тізімі

  1. R. Stark, R.G. Kibbey. Biochim. Biophys. Acta 1840, 1313 (2014). https://doi.org/10.1016/j.bbagen.2013.10.033
  2. P. Pérez-Martinez, A. Garcia-Rios, J. Delgado-Lista et al. Clinical Nutrition 32, 630 (2013). https://doi.org/10.1016/j.clnu.2012.10.003
  3. P. Dizengremel, M.N. Vaultier, D. Le Thiec et al. New Phytologist 195, 512 (2012). https://doi.org/10.1111/j.1469-8137.2012.04211.x
  4. L.N. Shishkina, M.V. Kozlov, T.V. Konstantinova, A.N. Smirnova, V.O. Shvydkiy. Russ. J. Phys. Chem. B. 17, 141 (2023). https://doi.org/10.1134/S1990793123010104
  5. S.V. Molodochkina, D.V. Loshadkin, E.M. Pliss. Russ. J. Phys. Chem. B. 18, 136 (2024). https://doi.org/10.1134/S1990793124010160
  6. N.I. Kol′tsov. Russ. J. Phys. Chem. B. 16, 18 (2022). https://doi.org/10.1134/S1990793122010080
  7. A. Marín-Hernández, J.C. Gallardo-Pérez, S. Rodríguez-Enríquez et al. Biochim. Biophys. Acta 1807, 755 (2011). https://doi.org/10.1016/j.bbabio.2010.11.006
  8. H.R. Christofk, M.G. Vander Heiden, N. Wu, J.M. Asara, L.C. Cantley. Nature. 452, 181 (2008). https://doi.org/10.1038/nature06667
  9. M.G. Khrenova, I.V. Polyakov, A. V. Nemukhin. Russ. J. Phys. Chem. B. 16, 455 (2022). https://doi.org/10.1134/S1990793122030174
  10. O.V. Pokidova, A. Yu. Kormukhina, A. I. Kotelnikov, et al. Inorg. Chim. Acta 524, 120453 (2021). https://doi.org/10.1016/j.ica.2021.120453
  11. S.M. Aldoshin, N.A. Sanina. Fundamental sciences – medicine. (MAKS Press, Moscow, 2015).
  12. T.A. Ivanova, E.N. Golubeva. Russ. J. Phys. Chem. B. 16, 426 (2022). https://doi.org/10.1134/S1990793122030162
  13. L. Syrtsova, N. Sanina, K. Lyssenka et al. Bioinorg. Chem. Appl. 2014. 641407 (2014). https://doi.org/10.1155/2014/641407
  14. A.Yu. Kormukhina, A.B. Kusyapkulova, N.S. Emel´yanova, O. V. Pokidova, N.A. Sanina. Russ. J. Phys. Chem. B. 18, 244 (2024). https://doi.org/10.1134/S1990793124010305
  15. N.A. Sanina, L.I. Serebryakova, V.S. Shulzhenko et al. The use of a binuclear sulfur-nitrosyl complex of iron cationic type as a vasodilator drug: Patent RF 2460531 (2012). Inventions. Utility models. Official Bull. Federal Service for Intellect. Property 25. (2012).
  16. A.A. Zanina, E.A. Saratovskikh, V.M. Martynenko et al. Russ. Chem. Bull. 66, 927 (2017). https://doi.org/10.1007/s11172-017-1832-6
  17. Chemist’s Handbook. Chemistry and chemical technology. http://chem21.info/info/1765362
  18. MassBank Record: KOX00489 MERGED SPECTRUM. http://www.massbank.jp/jsp/Dispatcher.jsp?type=disp&id=KOX00489&site=0
  19. T.Lis. Acta Crystallographica C52, 2720 (1996). https://doi.org/10.1107/S0108270196007445
  20. V.R. Williams, H.R. Williams. Basic physical chemistry for the life. (W.H. Freedman &Co Lmt., San Francisco, 1973).
  21. B.L. Psikha, E. A. Saratovskikh, I.V. Sulimenkov et al. Inorg. Chim. Acta. 531, 120709 (2022). https://doi.org/10.1016/j.ica.2021.120709
  22. B.L. Psikha, E.A. Saratovskikh, N.A. Sanina. Russ. Chem. Bull. 61, 1810 (2012).

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Әрекет
1. JATS XML
2. Fig. 1. Structural formula of phosphoenolpyruvic acid (PEP).

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3. Fig. 2. Structural formula of tris(hydroxymethyl)-aminomethane hydrochloride (Tris-HCl).

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4. Fig. 3. Structure of the dication of the tetranitrosyl iron complex with penicillamine ligands – NO donor (PEN).

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5. Fig. 4. Mass spectrum of a solution of FEP in water. Ionization type – ESI, eluent – ​​acetonitrile-water; spectra were assigned based on the distribution of negatively charged ions.

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6. Fig. 5. Change in intensity over time of the MS peak of FEP (m/z = 167 [M–H]) during the reaction with the PEN complex. The initial concentration ratio of FEN: PEN in M: 1 – 1 : 1; 2 – 1 : 2; 3 – 1 : 3.

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7. Fig. 6. Kinetic curves of FEP consumption during interaction with PEN. Initial concentrations of B, mol l–1: 1 – [FEP] = 9.5 10–4, [C] = 9.7 10–4; 2 – [FEP] = 9.3 10–4, [C] = 20.4 10–4; 3 – [FEP] = 8.8 10–4, [C] = 30.2 10–4. Dots are experimental values, solid lines are calculated curves.

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