Vanadium elicitation of Trifolium pratense L. cell culture and possible pathways of produced isoflavones transport across the plasma membrane
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
SVV 260 416
Ministry of Education, Youth and Sports of the Czech Republic
PubMed
30770962
DOI
10.1007/s00299-019-02397-y
PII: 10.1007/s00299-019-02397-y
Knihovny.cz E-zdroje
- Klíčová slova
- Abiotic elicitation, Plasma-membrane transport, Red clover, Secondary metabolites,
- MeSH
- biologický transport účinky léků MeSH
- buněčná membrána účinky léků metabolismus MeSH
- isoflavony metabolismus MeSH
- Trifolium účinky léků metabolismus MeSH
- vanad farmakologie MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- isoflavony MeSH
- vanad MeSH
Vanadium compounds increased the content and release of distinct isoflavones in a Trifolium pratense suspension culture. Regarding transport-mechanism inhibitors, the process was mostly facilitated by ABC proteins and vesicular transport. The transport of isoflavones and other secondary metabolites is an important part of metabolism within plants and cultures in vitro regarding their role in defence against various abiotic and biotic stressors. This research focuses on the way how to increase production and exudation of isoflavones by application of chemical elicitor and the basic identification of their transport mechanisms across cell membranes. The release of five isoflavones (genistin, genistein, biochanin A, daidzein, and formononetin) into a nutrient medium was determined in a Trifolium pratense var. DO-8 suspension culture after two vanadium compound treatments and cultivation for 24 and 48 h. The NH4VO3 solution caused a higher concentration of isoflavones in the medium after 24 h. This increased content of secondary metabolites was subsequently suppressed by distinct transport-mechanism inhibitors. The transport of isoflavones in T. pratense was mostly affected by ABC inhibitors from the multidrug-resistance-associated protein subfamily, but the genistein concentration in the medium was lower after treatment with multidrug-resistance protein subfamily inhibitors. Brefeldin A, which blocks vesicular transport, also decreased the concentration of some isoflavones in the nutrient medium.
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Arch Biochem Biophys. 2000 Jan 1;373(1):102-9 PubMed
Plant J. 2000 Feb;21(3):289-304 PubMed
Br J Pharmacol. 2001 Feb;132(3):778-84 PubMed
Plant Physiol. 2002 Feb;128(2):726-33 PubMed
Curr Opin Plant Biol. 2002 Jun;5(3):218-23 PubMed
FEBS Lett. 2003 Nov 6;554(1-2):23-9 PubMed
Chem Rev. 2004 Feb;104(2):849-902 PubMed
Epilepsy Res. 2004 Feb;58(2-3):85-91 PubMed
FEBS Lett. 2004 May 21;566(1-3):1-5 PubMed
Biotechnol Adv. 2005 Jun;23(4):283-333 PubMed
Endocr J. 2006 Feb;53(1):7-20 PubMed
J Hazard Mater. 2006 Sep 21;137(2):649-53 PubMed
Plant Physiol. 1984 Jul;75(3):586-91 PubMed
Annu Rev Plant Biol. 2007;58:347-75 PubMed
FEBS Lett. 2007 May 25;581(12):2204-14 PubMed
Plant Physiol. 2007 Aug;144(4):2000-8 PubMed
Plant Cell. 2007 Jun;19(6):2023-38 PubMed
Plant Physiol. 2007 Oct;145(2):478-90 PubMed
Phytochemistry. 2007 Nov-Dec;68(22-24):2881-6 PubMed
Adv Biochem Eng Biotechnol. 2008;111:187-228 PubMed
Plant Physiol. 2009 Feb;149(2):708-18 PubMed
Phytother Res. 2009 Mar;23(3):439-46 PubMed
Plant Cell. 2009 Aug;21(8):2323-40 PubMed
Trends Plant Sci. 2010 Feb;15(2):72-80 PubMed
Proc Natl Acad Sci U S A. 2010 Feb 2;107(5):2355-60 PubMed
Plant Physiol Biochem. 2010 Dec;48(12):909-30 PubMed
Fitoterapia. 2011 Jun;82(4):513-23 PubMed
Acta Biochim Pol. 2011;58(2):217-23 PubMed
Acta Biochim Pol. 2011;58(2):211-6 PubMed
FEBS Lett. 1990 Dec 10;276(1-2):189-91 PubMed
ScientificWorldJournal. 2012;2012:746412 PubMed
Acta Biochim Pol. 2012;59(2):195-200 PubMed
Plant Sci. 2012 Nov;196:67-76 PubMed
J Exp Bot. 2013 Feb;64(4):1005-15 PubMed
Plant Physiol Biochem. 2013 Nov;72:21-34 PubMed
Planta. 1989 Feb;177(2):160-8 PubMed
J Plant Physiol. 2014 Jan 15;171(2):63-8 PubMed
Nat Prod Res. 2014;28(24):2253-63 PubMed
Molecules. 2014 Oct 10;19(10):16240-65 PubMed
Molecules. 2014 Nov 05;19(11):18033-56 PubMed
Prog Lipid Res. 2015 Apr;58:1-13 PubMed
PLoS One. 2015 Mar 17;10(3):e0118578 PubMed
Trends Plant Sci. 2015 Sep;20(9):576-85 PubMed
Plant Cell Rep. 2017 Feb;36(2):235-242 PubMed
Environ Toxicol Pharmacol. 2018 Sep;62:20-29 PubMed
Molecules. 2018 Jul 03;23(7):null PubMed
Exp Cell Res. 1968 Apr;50(1):151-8 PubMed
Circ Res. 1983 Aug;53(2):186-91 PubMed
J Biol Chem. 1984 Apr 25;259(8):4971-8 PubMed
Toxicology. 1996 Jan 8;106(1-3):27-38 PubMed
J Biol Chem. 1996 Feb 9;271(6):3163-71 PubMed
J Bioenerg Biomembr. 1996 Jun;28(3):279-84 PubMed
Endocrinology. 1998 Oct;139(10):4252-63 PubMed