A Single Oxidosqualene Cyclase Produces the Seco-Triterpenoid α-Onocerin . Issue 2 (4th December 2017)
- Record Type:
- Journal Article
- Title:
- A Single Oxidosqualene Cyclase Produces the Seco-Triterpenoid α-Onocerin . Issue 2 (4th December 2017)
- Main Title:
- A Single Oxidosqualene Cyclase Produces the Seco-Triterpenoid α-Onocerin
- Authors:
- Almeida, Aldo
Dong, Lemeng
Khakimov, Bekzod
Bassard, Jean-Etienne
Moses, Tessa
Lota, Frederic
Goossens, Alain
Appendino, Giovanni
Bak, Søren - Abstract:
- Abstract : In Ononis spinosa, a single oxidosqualene cyclase interacts with squalene epoxidases to produce α-onocerin from squalene dioxide, demonstrating that α-onocerin pathways evolved convergently in plants. Abstract: 8, 14- seco -Triterpenoids are characterized by their unusual open C-ring. Their distribution in nature is rare and scattered in taxonomically unrelated plants. The 8, 14- seco -triterpenoid α-onocerin is only known from the evolutionarily distant clubmoss genus Lycopodium and the leguminous genus Ononis, which makes the biosynthesis of this seco -triterpenoid intriguing from an evolutionary standpoint. In our experiments with Ononis spinosa, α-onocerin was detected only in the roots. Through transcriptome analysis of the roots, an oxidosqualene cyclase, OsONS1, was identified that produces α-onocerin from squalene-2, 3;22, 23-dioxide when transiently expressed in Nicotiana bethamiana . In contrast, in Lycopodium clavatum, two sequential cyclases, LcLCC and LcLCD, are required to produce α-onocerin in the N. benthamiana transient expression system. Expression of OsONS1 in the lanosterol synthase knockout yeast strain GIL77, which accumulates squalene-2, 3;22, 23-dioxide, verified the α-onocerin production. A phylogenetic analysis predicts that OsONS1 branches off from specific lupeol synthases and does not group with the known L. clavatum α-onocerin cyclases. Both the biochemical and phylogenetic analyses of OsONS1 suggest convergent evolution of theAbstract : In Ononis spinosa, a single oxidosqualene cyclase interacts with squalene epoxidases to produce α-onocerin from squalene dioxide, demonstrating that α-onocerin pathways evolved convergently in plants. Abstract: 8, 14- seco -Triterpenoids are characterized by their unusual open C-ring. Their distribution in nature is rare and scattered in taxonomically unrelated plants. The 8, 14- seco -triterpenoid α-onocerin is only known from the evolutionarily distant clubmoss genus Lycopodium and the leguminous genus Ononis, which makes the biosynthesis of this seco -triterpenoid intriguing from an evolutionary standpoint. In our experiments with Ononis spinosa, α-onocerin was detected only in the roots. Through transcriptome analysis of the roots, an oxidosqualene cyclase, OsONS1, was identified that produces α-onocerin from squalene-2, 3;22, 23-dioxide when transiently expressed in Nicotiana bethamiana . In contrast, in Lycopodium clavatum, two sequential cyclases, LcLCC and LcLCD, are required to produce α-onocerin in the N. benthamiana transient expression system. Expression of OsONS1 in the lanosterol synthase knockout yeast strain GIL77, which accumulates squalene-2, 3;22, 23-dioxide, verified the α-onocerin production. A phylogenetic analysis predicts that OsONS1 branches off from specific lupeol synthases and does not group with the known L. clavatum α-onocerin cyclases. Both the biochemical and phylogenetic analyses of OsONS1 suggest convergent evolution of the α-onocerin pathways. When OsONS1 was coexpressed in N. benthamiana leaves with either of the two O. spinosa squalene epoxidases, OsSQE1 or OsSQE2, α-onocerin production was boosted, most likely because the epoxidases produce higher amounts of squalene-2, 3;22, 23-dioxide. Fluorescence lifetime imaging microscopy analysis demonstrated specific protein-protein interactions between OsONS1 and both O. spinosa squalene epoxidases. Coexpression of OsONS1 with the two OsSQE s suggests that OsSQE2 is the preferred partner of OsONS1 in planta. Our results provide an example of the convergent evolution of plant specialized metabolism. … (more)
- Is Part Of:
- Plant physiology. Volume 176:Issue 2(2018)
- Journal:
- Plant physiology
- Issue:
- Volume 176:Issue 2(2018)
- Issue Display:
- Volume 176, Issue 2 (2018)
- Year:
- 2018
- Volume:
- 176
- Issue:
- 2
- Issue Sort Value:
- 2018-0176-0002-0000
- Page Start:
- 1469
- Page End:
- 1484
- Publication Date:
- 2017-12-04
- 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.17.01369 ↗
- 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:
- 16650.xml