Functional Diversification of Kaurene Synthase-Like Genes in Isodon rubescens . Issue 2 (5th April 2017)
- Record Type:
- Journal Article
- Title:
- Functional Diversification of Kaurene Synthase-Like Genes in Isodon rubescens . Issue 2 (5th April 2017)
- Main Title:
- Functional Diversification of Kaurene Synthase-Like Genes in Isodon rubescens
- Authors:
- Jin, Baolong
Cui, Guanghong
Guo, Juan
Tang, Jinfu
Duan, Lixin
Lin, Huixin
Shen, Ye
Chen, Tong
Zhang, Huabei
Huang, Luqi - Abstract:
- Abstract : Numerous kaurene synthase-like cyclases have been identified in Isodon rubescens, providing new perspectives into understanding the evolution of diterpenoid chemical diversity in Lamiaceae. Abstract: Ent -kaurene diterpenoids are the largest group of known Isodon diterpenoids. Among them, oridonin is accumulated in the leaves, and is the most frequently studied compound because of its antitumor and antibacterial activities. We have identified five copalyl diphosphate synthase (CPS) and six kaurene synthase-like (KSL) genes by transcriptome profiling of Isodon rubescens leaves. An in vitro assay assigns ten of them to five different diterpene biosynthesis pathways, except IrCPS3 that has a mutation in the catalytic motif. The Lamiaceae-specific clade genes (IrCPS1 and IrCPS2) synthesize the intermediate copalyl diphosphate (normal-CPP), while IrCPS4 and IrCPS5 synthesize the intermediate ent -copalyl diphosphate ( ent -CPP). IrKSL2, IrKSL4, and IrKSL5 react with ent -CPP to produce an ent -isopimaradiene-like compound, ent -atiserene and ent -kaurene, respectively. Correspondingly, the Lamiaceae-specific clade genes IrKSL1 or IrKSL3 combined with normal-CPP led to the formation of miltiradiene. The compound then underwent aromatization and oxidization with a cytochrome P450 forming two related compounds, abietatriene and ferruginol, which were detected in the root bark. IrKSL6 reacts with normal-CPP to produce isopimaradiene. IrKSL3 and IrKSL6 have the γβαAbstract : Numerous kaurene synthase-like cyclases have been identified in Isodon rubescens, providing new perspectives into understanding the evolution of diterpenoid chemical diversity in Lamiaceae. Abstract: Ent -kaurene diterpenoids are the largest group of known Isodon diterpenoids. Among them, oridonin is accumulated in the leaves, and is the most frequently studied compound because of its antitumor and antibacterial activities. We have identified five copalyl diphosphate synthase (CPS) and six kaurene synthase-like (KSL) genes by transcriptome profiling of Isodon rubescens leaves. An in vitro assay assigns ten of them to five different diterpene biosynthesis pathways, except IrCPS3 that has a mutation in the catalytic motif. The Lamiaceae-specific clade genes (IrCPS1 and IrCPS2) synthesize the intermediate copalyl diphosphate (normal-CPP), while IrCPS4 and IrCPS5 synthesize the intermediate ent -copalyl diphosphate ( ent -CPP). IrKSL2, IrKSL4, and IrKSL5 react with ent -CPP to produce an ent -isopimaradiene-like compound, ent -atiserene and ent -kaurene, respectively. Correspondingly, the Lamiaceae-specific clade genes IrKSL1 or IrKSL3 combined with normal-CPP led to the formation of miltiradiene. The compound then underwent aromatization and oxidization with a cytochrome P450 forming two related compounds, abietatriene and ferruginol, which were detected in the root bark. IrKSL6 reacts with normal-CPP to produce isopimaradiene. IrKSL3 and IrKSL6 have the γβα tridomain structure, as these proteins tend to possess the bidomain structure of IrKSL1, highlighting the evolutionary history of KSL gene domain loss and further elucidating chemical diversity evolution from a macroevolutionary stance in Lamiaceae. … (more)
- Is Part Of:
- Plant physiology. Volume 174:Issue 2(2017)
- Journal:
- Plant physiology
- Issue:
- Volume 174:Issue 2(2017)
- Issue Display:
- Volume 174, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 174
- Issue:
- 2
- Issue Sort Value:
- 2017-0174-0002-0000
- Page Start:
- 943
- Page End:
- 955
- Publication Date:
- 2017-04-05
- Subjects:
- Plant physiology -- Periodicals
Botany -- Periodicals
Periodicals
Electronic journals
571.2 - Journal URLs:
- https://academic.oup.com/plphys/issue ↗
http://www.plantphysiol.org/ ↗
http://www.jstor.org/journals/00320889.html ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=69 ↗
http://www-us.ebsco.com/online/direct.asp?JournalID=101725 ↗
http://www.oxfordjournals.org/ ↗ - DOI:
- 10.1104/pp.17.00202 ↗
- Languages:
- English
- ISSNs:
- 0032-0889
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 22687.xml