Regulation of flavanone 3-hydroxylase gene involved in the flavonoid biosynthesis pathway in response to UV-B radiation and drought stress in the desert plant, Reaumuria soongorica

Copyright © 2013 Elsevier Masson SAS. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Plant physiology and biochemistry : PPB. - 1991. - 73(2013) vom: 14. Dez., Seite 161-7
1. Verfasser: Liu, Meiling (VerfasserIn)
Weitere Verfasser: Li, Xinrong, Liu, Yubing, Cao, Bo
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Plant physiology and biochemistry : PPB
Schlagworte:Journal Article Research Support, Non-U.S. Gov't 2-ODDs 2-oxoglutarate-dependent dioxygenases Drought F3H Flavonoid biosynthetic pathway HPLC MDA ORF mehr... RACE ROS Reaumuria soongorica RsF3H TBA TDR UV-B flavanone 3-hydroxylase high performance liquid chromatography malonaldehyde open reading frame qRT-PCR quantitative real-time RT-PCR rapid amplification of cDNA ends reactive oxygen species thiobarbituric acid time domain reflectometry Flavanones Flavonoids Plant Proteins Mixed Function Oxygenases EC 1.- flavanone 3-dioxygenase EC 1.14.11.9
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245 1 0 |a Regulation of flavanone 3-hydroxylase gene involved in the flavonoid biosynthesis pathway in response to UV-B radiation and drought stress in the desert plant, Reaumuria soongorica 
264 1 |c 2013 
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500 |a Date Completed 29.07.2014 
500 |a Date Revised 30.09.2020 
500 |a published: Print-Electronic 
500 |a Citation Status MEDLINE 
520 |a Copyright © 2013 Elsevier Masson SAS. All rights reserved. 
520 |a Flavonoid are known to have various functions in growth, development, reproduction, and also involved in diverse stress responses in plants. However, little is known about the roles of the key enzymes in the flavonoid biosynthetic pathway in response to environmental stress, such as UV-B radiation and drought. To understand this problem, we investigated the participation of flavanone 3-hydroxylase gene (F3H), a key enzyme in flavonoid biosynthetic pathway under UV-B radiation and drought stress in the desert plant Reaumuria soongorica. A novel cDNA sequence, named as RsF3H, was isolated from R. soongorica. The deduced amino acids showed high identities to other F3Hs. A phylogenetic analysis indicated that RsF3H appeared to be most homologous to F3H from Malus domestica (MdF3H). RsF3H protein structure contained all five conserved motifs for 2-oxoglutarate-dependent dioxygenases (2-ODDs) and an Arg-X-Ser motif, all of which were also found in other F3Hs. Quantitative real-time RT-PCR analysis showed that there was a rapid increase in gene expression of RsF3H under stress. Both UV-B radiation and drought stress induced an increase in RsF3H enzyme activity and the accumulation of the products in the flavonoid biosynthetic pathway (total flavonoid and anthocyanin). The antioxidant ability (inhibition of lipid oxidation) of total flavonoid was enhanced during this study. The results suggested that one explanation of the stress tolerance of R. soongorica may be a combination of an increase in RsF3H gene expression, RsF3H enzyme activity and the anti-oxidative ability of the metabolic end products in the flavonoid biosynthetic pathway in response to UV-B radiation and drought 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a 2-ODDs 
650 4 |a 2-oxoglutarate-dependent dioxygenases 
650 4 |a Drought 
650 4 |a F3H 
650 4 |a Flavonoid biosynthetic pathway 
650 4 |a HPLC 
650 4 |a MDA 
650 4 |a ORF 
650 4 |a RACE 
650 4 |a ROS 
650 4 |a Reaumuria soongorica 
650 4 |a RsF3H 
650 4 |a TBA 
650 4 |a TDR 
650 4 |a UV-B 
650 4 |a flavanone 3-hydroxylase 
650 4 |a high performance liquid chromatography 
650 4 |a malonaldehyde 
650 4 |a open reading frame 
650 4 |a qRT-PCR 
650 4 |a quantitative real-time RT-PCR 
650 4 |a rapid amplification of cDNA ends 
650 4 |a reactive oxygen species 
650 4 |a thiobarbituric acid 
650 4 |a time domain reflectometry 
650 7 |a Flavanones  |2 NLM 
650 7 |a Flavonoids  |2 NLM 
650 7 |a Plant Proteins  |2 NLM 
650 7 |a Mixed Function Oxygenases  |2 NLM 
650 7 |a EC 1.-  |2 NLM 
650 7 |a flavanone 3-dioxygenase  |2 NLM 
650 7 |a EC 1.14.11.9  |2 NLM 
700 1 |a Li, Xinrong  |e verfasserin  |4 aut 
700 1 |a Liu, Yubing  |e verfasserin  |4 aut 
700 1 |a Cao, Bo  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Plant physiology and biochemistry : PPB  |d 1991  |g 73(2013) vom: 14. Dez., Seite 161-7  |w (DE-627)NLM098178261  |x 1873-2690  |7 nnns 
773 1 8 |g volume:73  |g year:2013  |g day:14  |g month:12  |g pages:161-7 
856 4 0 |u http://dx.doi.org/10.1016/j.plaphy.2013.09.016  |3 Volltext 
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