Cloning and characterization of an elicitor-responsive gene encoding 3-hydroxy-3-methylglutaryl coenzyme A reductase involved in 20-hydroxyecdysone production in cell cultures of Cyanotis arachnoidea

Copyright © 2014 Elsevier Masson SAS. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Plant physiology and biochemistry : PPB. - 1991. - 84(2014) vom: 18. Nov., Seite 1-9
1. Verfasser: Wang, Qiu Jun (VerfasserIn)
Weitere Verfasser: Zheng, Li Ping, Zhao, Pei Fei, Zhao, Yi Lu, Wang, Jian Wen
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2014
Zugriff auf das übergeordnete Werk:Plant physiology and biochemistry : PPB
Schlagworte:Journal Article Research Support, Non-U.S. Gov't 20-Hydroxyecdysterone 3-Hydroxy-3-methylglutaryl coenzyme A reductase Cyanotis arachnoidea Elicitation Gene expression Acetates Acyl Coenzyme A Carboxylic Acids mehr... Cyclopentanes Naphthalenes Oxylipins 3-hydroxy-3-methylglutaryl-coenzyme A 1553-55-5 1-naphthoic acid 2NIV4O66BH Ecdysterone 5289-74-7 methyl jasmonate 900N171A0F
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245 1 0 |a Cloning and characterization of an elicitor-responsive gene encoding 3-hydroxy-3-methylglutaryl coenzyme A reductase involved in 20-hydroxyecdysone production in cell cultures of Cyanotis arachnoidea 
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500 |a Date Revised 18.03.2022 
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520 |a Copyright © 2014 Elsevier Masson SAS. All rights reserved. 
520 |a Cyanotis arachnoidea contains a rich source of bioactive phytoecdysteroids (i.e. analogues of insect steroid hormones). 3-Hydroxy-3-methylglutaryl coenzyme A reductase (HMGR) supplies mevalonate for the synthesis of many secondary metabolites including 20-hydroxyecdysone (20E), one of metabolism-enhancing phytoecdysteroids. In this study, in order to develop a sustainable source of 20E, cell suspension cultures were established from shoot cultures of C. arachnoidea, and a full length cDNA encoding HMGR (designated as CaHMGR) was cloned and characterized. The cDNA contained 2037 nucleotides with a complete open reading frame (ORF) of 1800 nucleotides, which was predicted to encode a peptide of 599 amino acids. Expression analysis by real-time PCR revealed that CaHMGR mRNA was abundant in C. arachnoidea stems, roots and leaves. When cultivated in Murashige & Skoog medium supplemented with 0.2 mg L(-1) 1-naphthlcetic acid (NAA) and 3.0 mg L(-1) 6-benzyladenine (6-BA), C. arachnoidea cells in suspension culture grew rapidly, yielding 20E (124.14 μg L(-1)) after 12 days. The content of 20E in cell cultures elicited by 0.2 mM methyl jasmonate (MeJA), 100 mg L(-1) yeast elicitor (YE) or 25 μM AgNO3 was increased 8-, 2-, and 6-fold over the control, respectively. Quantitative real-time PCR analysis showed that CaHMGR was expressed at a higher level under the treatment of MeJA or Ag(+) elicitor. Our results suggested that 20E accumulation may be the result of the expression up-regulation of CaHMGR involved in the biosynthesis under the treatment of various elicitors 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 4 |a 20-Hydroxyecdysterone 
650 4 |a 3-Hydroxy-3-methylglutaryl coenzyme A reductase 
650 4 |a Cyanotis arachnoidea 
650 4 |a Elicitation 
650 4 |a Gene expression 
650 7 |a Acetates  |2 NLM 
650 7 |a Acyl Coenzyme A  |2 NLM 
650 7 |a Carboxylic Acids  |2 NLM 
650 7 |a Cyclopentanes  |2 NLM 
650 7 |a Naphthalenes  |2 NLM 
650 7 |a Oxylipins  |2 NLM 
650 7 |a 3-hydroxy-3-methylglutaryl-coenzyme A  |2 NLM 
650 7 |a 1553-55-5  |2 NLM 
650 7 |a 1-naphthoic acid  |2 NLM 
650 7 |a 2NIV4O66BH  |2 NLM 
650 7 |a Ecdysterone  |2 NLM 
650 7 |a 5289-74-7  |2 NLM 
650 7 |a methyl jasmonate  |2 NLM 
650 7 |a 900N171A0F  |2 NLM 
700 1 |a Zheng, Li Ping  |e verfasserin  |4 aut 
700 1 |a Zhao, Pei Fei  |e verfasserin  |4 aut 
700 1 |a Zhao, Yi Lu  |e verfasserin  |4 aut 
700 1 |a Wang, Jian Wen  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Plant physiology and biochemistry : PPB  |d 1991  |g 84(2014) vom: 18. Nov., Seite 1-9  |w (DE-627)NLM098178261  |x 1873-2690  |7 nnns 
773 1 8 |g volume:84  |g year:2014  |g day:18  |g month:11  |g pages:1-9 
856 4 0 |u http://dx.doi.org/10.1016/j.plaphy.2014.08.021  |3 Volltext 
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