Generic placeholder image

Protein & Peptide Letters

Editor-in-Chief

ISSN (Print): 0929-8665
ISSN (Online): 1875-5305

Research Article

Some Minor Characteristics of Spectrophotometric Determination of Antioxidant System and Phenolic Metabolism Enzyme Activity in Wood Plant Tissues of Pinus sylvestris L.

Author(s): Maria A. Ershova*, Kseniya M. Nikerova, Natalia A. Galibina, Irina N. Sofronova and Marina N. Borodina

Volume 29, Issue 8, 2022

Published on: 10 August, 2022

Page: [711 - 720] Pages: 10

DOI: 10.2174/0929866529666220414104747

Price: $65

Abstract

Introduction: A comprehensive study of enzymes of the antioxidant system (AOS) and phenolic metabolism is an actual subject of biochemical research; changes in the activity of these enzymes can be used as a diagnostic sign. At the same time, practically little attention has been paid to describing the regularities of these enzymatic reactions. The article presents the chemical kinetics study of reactions catalyzed by superoxide dismutase, catalase, peroxidase, polyphenol oxidase, and phenylalanine ammonia-lyase in Scots pine trunk tissues (Pinus sylvestris L.). The dependence of the enzyme reaction rate on the enzyme concentration and the substrate concentration is presented, and the pH-optimum for each reaction is established.

Background: Determination of AOS enzyme activity and PAL activity in woody plants has many difficulties. The chemical composition of pine trunk tissues affects determining AOS enzyme activity and PAL activity. Spectrophotometric determination of AOS enzyme activity and PAL activity gives perfect results when considering all additional controls by taking into account minor characteristics.

Objective: This study aimed at determining the AOS enzyme activity in 40-year-old Scots pine (Pinus sylvestris L.) plants growing in the Karelian (Russia) forest seed plantation.

Methods: Plant tissues were ground in liquid nitrogen to a uniform mass and homogenized at 4 °C in the buffer containing 50 mM HEPES (pH 7.5), 1 mM EDTA, 1 mM EGTA, 3 mM DTT, 5 mM MgCl2, and 0.5 mM PMSF. After 15-min of extraction, the homogenate was centrifuged at 12000 g for 10 min (MPW-351R centrifuge, Poland). The supernatant was purified on 20 cm3 columns with Sephadex G-250. Aliquots with the highest protein amount were collected. In tissues, the protein concentration was 10-50 μg/ml. Proteins in the extracts were quantified by a Bradford assay. The enzyme activity was determined spectrophotometrically on a SpectroStar Nano plate spectrophotometer (BMG Labtech, Germany).

Results: Our study made it possible to modify the methods for determining the activity of superoxide dismutase, catalase, peroxidase, polyphenol oxidase, and phenylalanine ammonia-lyase in Scots pine trunk tissues. The enzymatic reaction rate dependence on the enzyme concentration and the substrate concentration was determined, and pH-optimum was also noted. This methodological article also provides formulas for calculating the activities of the enzymes.

Conclusion: We found that determining AOS enzyme activity and PAL activity in woody plants is challenging. The chemical composition of the xylem and phloem of pine affects determining AOS enzyme activity and PAL activity. Spectrophotometric determination of AOS enzyme activity and PAL activity gives perfect results when considering all additional controls by taking into account minor characteristics.

Keywords: Pinus sylvestris L., xylem, phloem, superoxide dismutase, catalase, peroxidase, polyphenol oxidase, phenylalanine ammonia-lyase.

[1]
Nikerova, K.M.; Galibina, N.A.; Moshchenskaya, Y.U.L.; Borodina, M.N.; Sofronova, I.N. Determination of Superoxide Dismutase and Polyphenol Oxidase Activity in Betula pendula var. carelica (Betulaceae) Wood with Different Degree of Xylogenesis Disturbance. Rastit. Resur., 2019, 55(2), 213-230.
[http://dx.doi.org/10.1134/S0033994619020134]
[2]
Abdalla, M. Beneficial effects of diatomite on the growth, the biochemical contents and polymorphic DNA in Lupinus albus plants grown under water stress. Agric. Biol. J. N. Am., 2011, 2(2), 207-220.
[http://dx.doi.org/10.5251/abjna.2011.2.2.207.220]
[3]
Nikerova, K.M. Aktivnost’ fermentovantioksidantnoysistemyprii zmeneniistsenarievksilogeneza u Betulapendula Rothi PinussylvestrisL; Dis. Kand. Biol. Nauk: Petrozavodsk, 2020, 201, .
[4]
Antonova, G.F.; Stasova, V.V. [Seasonal development of phloem in Scots pine stems]. Ontogenez, 2006, 37(5), 368-383.
[PMID: 17066978]
[5]
Dixon, R.A.; Paiva, N.L. Stress-induced phenylpropanoid metabolism. Plant Cell, 1995, 7(7), 1085-1097.
[http://dx.doi.org/10.2307/3870059] [PMID: 12242399]
[6]
Cakmak, I.; Römheld, V. Boron deficiency-induced impairments of cellular functions in plants. Plant Soil, 1997, 193(2), 71-83.
[http://dx.doi.org/10.1023/A:1004259808322]
[7]
Nikerova, K.M.; Galibina, N.A.; Moshchenskaya, Y.L.; Tarelkina, T.V.; Borodina, M.N.; Sofronova, I.N.; Semenova, L.I.; Ivanova, D.S.; Novitskaya, L.L. Upregulation of antioxidant enzymes is a biochemical indicator of abnormal xylogenesis in Karelian birch. Trees (Berl.), 2022, 36, 517-529.
[http://dx.doi.org/10.1007/s00468-021-02225-5]
[8]
Mittler, R.; Zilinskas, B.A. Purification and characterization of pea cytosolic ascorbate peroxidase. Plant Physiol., 1991, 97(3), 962-968.
[http://dx.doi.org/10.1104/pp.97.3.962] [PMID: 16668537]
[9]
Serdyukov, Y.A.; Novitskii, Y.I. Impact of weak permanent magnetic field on antioxidant enzyme activities in radish seedlings. Russ. J. Plant Physiol., 2013, 60(1), 69-76.
[http://dx.doi.org/10.1134/S1021443713010068]
[10]
Zagoskina, N.V.; Nazarenko, L.V. Active oxygen species and antioxidant system of plants. Nat. Sci., 2016, (22), 9-23.
[11]
Vatankhah, E.; Niknam, V.; Ebrahimzadeh, H. Activity of antioxidant enzyme during in vitro organogenesis in Crocus sativus. Biol. Plant., 2010, 54(3), 509-514.
[http://dx.doi.org/10.1007/s10535-010-0089-9]
[12]
Dziri, S.; Hosni, K. Effects of cement dust on volatile oil constituents and antioxidative metabolism of Aleppo pine (Pinus halepensis) needles. Acta Physiol. Plant., 2012, 34(5), 1669-1678.
[http://dx.doi.org/10.1007/s11738-012-0962-6]
[13]
Lange, B.M.; Trost, M.; Heller, W.; Langebartels, C.; Sandermann, H. Jr Elicitor-induced formation of free and cell-wall-bound stilbenes in cell-suspension cultures of Scots pine (Pinus sylvestris L.). Planta, 1994, 194(1), 143-148.
[http://dx.doi.org/10.1007/BF00201045]
[14]
MacAllister, S. L. Regeneration of Scots pine (Pinus sylvestris L.) under drought. 2016.
[15]
Pan, Y.; Zhao, T.; Krokene, P.; Yu, Z.; Qiao, M.; Lu, J.; Chen, P.; Ye, H. Bark beetle-associated blue-stain fungi increase antioxidant enzyme activities and monoterpene concentrations in Pinus yunnanensis. Front. Plant Sci., 2018, 9, 1731.
[http://dx.doi.org/10.3389/fpls.2018.01731] [PMID: 30559751]
[16]
Schützendübel, A.; Schwanz, P.; Teichmann, T.; Gross, K.; Langenfeld-Heyser, R.; Godbold, D.L.; Polle, A. Cadmium-induced changes in antioxidative systems, hydrogen peroxide content, and differentiation in Scots pine roots. Plant Physiol., 2001, 127(3), 887-898.
[http://dx.doi.org/10.1104/pp.010318] [PMID: 11706171]
[17]
Tang, W.; Newton, R.J. Increase of polyphenol oxidase and decrease of polyamines correlate with tissue browning in Virginia pine (Pinus virginiana Mill.). Plant Sci., 2004, 167(3), 621-628.
[http://dx.doi.org/10.1016/j.plantsci.2004.05.024]
[18]
Zhang, L.L.; Zhu, X.M.; Kuang, Y.W. Responses of Pinus massoniana seedlings to lead stress. Biol. Plant., 2017, 61(4), 785-790.
[http://dx.doi.org/10.1007/s10535-017-0710-2]
[19]
Mayer, A.M. Polyphenol oxidases in plants and fungi: Going places? A review. Phytochemistry, 2006, 67(21), 2318-2331.
[http://dx.doi.org/10.1016/j.phytochem.2006.08.006] [PMID: 16973188]
[20]
Gao, D.; Gao, Q.; Xu, H.Y.; Ma, F.; Zhao, C.M.; Liu, J.Q. Physiological responses to gradual drought stress in the diploid hybrid Pinus densata and its two parental species. Trees (Berl.), 2009, 23(4), 717-728.
[http://dx.doi.org/10.1007/s00468-009-0314-3]
[21]
Wang, F.; Liang, D.; Pei, X.; Zhang, Q.; Zhang, P.; Zhang, J.; Lu, Z.; Yang, Y.; Liu, G.; Zhao, X. Study on the physiological indices of Pinus sibirica and Pinus koraiensis seedlings under cold stress. J. For. Res., 2019, 30(4), 1255-1265.
[http://dx.doi.org/10.1007/s11676-018-0833-0]
[22]
Gould, N.; Reglinski, T.; Northcott, G.L.; Spiers, M.; Taylor, J.T. Physiological and biochemical responses in Pinus radiata seedlings associated with methyl jasmonate-induced resistance to Diplodia pinea. Physiol. Mol. Plant Pathol., 2009, 74(2), 121-128.
[http://dx.doi.org/10.1016/j.pmpp.2009.10.002]
[23]
Laukkanen, H.; Rautiainen, L.; Taulavuori, E.; Hohtola, A. Changes in cellular structures and enzymatic activities during browning of Scots pine callus derived from mature buds. Tree Physiol., 2000, 20(7), 467-475.
[http://dx.doi.org/10.1093/treephys/20.7.467] [PMID: 12651442]
[24]
Andersone, U.; Ievinsh, G. Changes of morphogenic competence in mature Pinus sylvestris L. buds in vitro. Ann. Bot. (Lond.), 2002, 90(2), 293-298.
[http://dx.doi.org/10.1093/aob/mcf176] [PMID: 12197528]
[25]
Andersone, U.; Ievinsh, G. Medium pH affects regeneration capacity and oxidative enzyme activity of Pinus sylvestris in tissue culture. Acta Uni. Latv., 2008, 745, 25-35.
[26]
Guo, H.; Sun, Y.; Li, Y.; Liu, X.; Zhang, W.; Ge, F. Elevated CO 2 decreases the response of the ethylene signaling pathway inM edicago truncatula and increases the abundance of the pea aphid. New Phytol., 2014, 201(1), 279-291.
[http://dx.doi.org/10.1111/nph.12484] [PMID: 24015892]
[27]
Shein, I.V.; Shibistova, O.B.; Zrazhevskaya, G.K.; Astrakhantseva, N.G.; Polyakova, G.G. The content of phenolic compounds and the activity of key enzymes of their synthesis in Scots pine hypocotyls infected with Fusarium. Russ. J. Plant Physiol., 2003, 50(4), 516-521.
[http://dx.doi.org/10.1023/A:1024776924788]

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy