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How is the activity of shikimate dehydrogenase from the root of Petroselinum crispum (parsley) regulated and which side reactions are catalyzed?

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dc.title How is the activity of shikimate dehydrogenase from the root of Petroselinum crispum (parsley) regulated and which side reactions are catalyzed? en
dc.contributor.author Hýsková, Veronika
dc.contributor.author Bělonožníková, Kateřina
dc.contributor.author Šmeringaiová, Ingrida
dc.contributor.author Kavan, Daniel
dc.contributor.author Ingr, Marek
dc.contributor.author Ryšlavá, Helena
dc.relation.ispartof Phytochemistry
dc.identifier.issn 0031-9422 Scopus Sources, Sherpa/RoMEO, JCR
dc.date.issued 2021
utb.relation.volume 190
dc.type article
dc.language.iso en
dc.publisher Elsevier Ltd
dc.identifier.doi 10.1016/j.phytochem.2021.112881
dc.relation.uri https://www.sciencedirect.com/science/article/pii/S0031942221002302
dc.subject apiaceae en
dc.subject chlorogenic acid en
dc.subject dehydroshikimate en
dc.subject gallic acid en
dc.subject hydroxycinnamic acids en
dc.subject petroselinum crispum en
dc.subject simple phenols en
dc.subject tannic acid en
dc.description.abstract Inhibitors of the shikimate pathway are widely used as herbicides, antibiotics, and anti-infectious drugs. However, the regulation of the shikimic pathway is complex, and little is known about the feedback regulation of the shikimate dehydrogenase (SDH, EC 1.1.1.25) in plants. Thus, the aim of this study was to elucidate the kinetic mechanism of SDH purified from the root of Petroselinum crispum (parsley), to determine all possible reaction products and to identify phenylpropanoid compounds that affect its activity. Our results showed that the bisubstrate reaction catalyzed by P. crispum SDH follows a sequential ordered mechanism, except for three dead-end complexes. The main and lateral reactions of SDH were monitored by mass spectrometry, thereby detecting protocatechuic acid as a byproduct. Gallic acid was formed non-enzymatically, whereas quinate was not detected. Several polyphenolic compounds inhibited SDH activity, especially tannic, caffeic and chlorogenic acids, with IC50 0.014 mM, 0.15 mM, and 0.19 mM, respectively. The number of hydroxyl groups influenced their inhibition effect on SDH, and p-coumaric, t-ferulic, sinapic, syringic and salicylic acids were less effective SDH inhibitors. Nevertheless, one branch of the phenylpropanoid pathway may affect SDH activity through feedback regulation. © 2021 Elsevier Ltd en
utb.faculty Faculty of Technology
dc.identifier.uri http://hdl.handle.net/10563/1010491
utb.identifier.obdid 43883055
utb.identifier.scopus 2-s2.0-85111940569
utb.identifier.wok 000687318400012
utb.identifier.pubmed 34365296
utb.identifier.coden PYTCA
utb.source j-scopus
dc.date.accessioned 2021-08-17T13:56:41Z
dc.date.available 2021-08-17T13:56:41Z
dc.description.sponsorship Charles University [SVV260572/2020]
dc.description.sponsorship Univerzita Karlova v Praze, UK: SVV260572/2020
utb.ou Department of Physics and Materials Engineering
utb.contributor.internalauthor Ingr, Marek
utb.fulltext.affiliation Veronika Hýsková a,* , Kateřina Bělonožníková a, Ingrida Šmeringaiová a, Daniel Kavan a,Marek Ingr a,b, Helena Ryšlavá a a Department of Biochemistry, Faculty of Science, Charles University, Hlavova 2030, Prague 2, 128 40, Czech Republic b Tomas Bata University in Zlín, Faculty of Technology, Department of Physics and Materials Engineering, Nam. T.G. Masaryka 5555, 760 01, Zlín, Czech Republic
utb.fulltext.dates Received 25 March 2021; Received in revised form 18 May 2021; Accepted 6 July 2021
utb.fulltext.sponsorship This work was supported (in part) by Charles University (SVV260572/2020). The authors thank Dr. Carlos V. Melo for English editing the manuscript.
utb.wos.affiliation [Hyskova, Veronika; Belonoznikova, Katerina; Smeringaiova, Ingrida; Kavan, Daniel; Ingr, Marek; Ryslava, Helena] Charles Univ Prague, Fac Sci, Dept Biochem, Hlavova 2030, Prague 12840 2, Czech Republic; [Ingr, Marek] Tomas Bata Univ Zlin, Fac Technol, Dept Phys & Mat Engn, Nam TG Masaryka 5555, Zlin 76001, Czech Republic
utb.scopus.affiliation Department of Biochemistry, Faculty of Science, Charles University, Hlavova 2030, Prague 2128 40, Czech Republic; Tomas Bata University in Zlín, Faculty of Technology, Department of Physics and Materials Engineering, Nám. T.G. Masaryka 5555, Zlín, 760 01, Czech Republic
utb.fulltext.projects SVV260572/2020
utb.fulltext.faculty Faculty of Technology
utb.fulltext.ou Department of Physics and Materials Engineering
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