Cargando…

Identification of oxidosqualene cyclases associated with saponin biosynthesis from Astragalus membranaceus reveals a conserved motif important for catalytic function

INTRODUCTION: Triterpenoids and saponins have a broad range of pharmacological activities. Unlike most legumes which contain mainly oleanane-type scaffold, Astragalus membranaceus contains not only oleanane-type but also cycloartane-type saponins, for which the biosynthetic pathways are unknown. OBJ...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Kuan, Zhang, Meng, Xu, Lulu, Yi, Yang, Wang, Linlin, Wang, Haotian, Wang, Zilong, Xing, Jiangtao, Li, Pi, Zhang, Xiaohui, Shi, Xiaomeng, Ye, Min, Osbourn, Anne, Qiao, Xue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811366/
https://www.ncbi.nlm.nih.gov/pubmed/36585112
http://dx.doi.org/10.1016/j.jare.2022.03.014
_version_ 1784863518319706112
author Chen, Kuan
Zhang, Meng
Xu, Lulu
Yi, Yang
Wang, Linlin
Wang, Haotian
Wang, Zilong
Xing, Jiangtao
Li, Pi
Zhang, Xiaohui
Shi, Xiaomeng
Ye, Min
Osbourn, Anne
Qiao, Xue
author_facet Chen, Kuan
Zhang, Meng
Xu, Lulu
Yi, Yang
Wang, Linlin
Wang, Haotian
Wang, Zilong
Xing, Jiangtao
Li, Pi
Zhang, Xiaohui
Shi, Xiaomeng
Ye, Min
Osbourn, Anne
Qiao, Xue
author_sort Chen, Kuan
collection PubMed
description INTRODUCTION: Triterpenoids and saponins have a broad range of pharmacological activities. Unlike most legumes which contain mainly oleanane-type scaffold, Astragalus membranaceus contains not only oleanane-type but also cycloartane-type saponins, for which the biosynthetic pathways are unknown. OBJECTIVES: This work aims to study the function and catalytic mechanism of oxidosqualene cyclases (OSCs), one of the most important enzymes in triterpenoid biosynthesis, in A. membranaceus. METHODS: Two OSC genes, AmOSC2 and AmOSC3, were cloned from A. membranaceus. Their functions were studied by heterologous expression in tobacco and yeast, together with in vivo transient expression and virus-induced gene silencing. Site-directed mutagenesis and molecular docking were used to explain the catalytic mechanism for the conserved motif. RESULTS: AmOSC2 is a β-amyrin synthase which showed higher expression levels in underground parts. It is associated with the production of β-amyrin and soyasaponins (oleanane-type) in vivo. AmOSC3 is a cycloartenol synthase expressed in both aerial and underground parts. It is related to the synthesis of astragalosides (cycloartane-type) in the roots, and to the synthesis of cycloartenol as a plant sterol precursor. From AmOSC2/3, conserved triad motifs VFM/VFN were discovered for β-amyrin/cycloartenol synthases, respectively. The motif is a critical determinant of yield as proved by 10 variants from different OSCs, where the variant containing the conserved motif increased the yield by up to 12.8-fold. Molecular docking and mutagenesis revealed that Val, Phe and Met residues acted together to stabilize the substrate, and the cation-π interactions from Phe played the major role. CONCLUSION: The study provides insights into the biogenic origin of oleanane-type and cycloartane-type triterpenoids in Astragalus membranaceus. The conserved motif offers new opportunities for OSC engineering.
format Online
Article
Text
id pubmed-9811366
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-98113662023-01-05 Identification of oxidosqualene cyclases associated with saponin biosynthesis from Astragalus membranaceus reveals a conserved motif important for catalytic function Chen, Kuan Zhang, Meng Xu, Lulu Yi, Yang Wang, Linlin Wang, Haotian Wang, Zilong Xing, Jiangtao Li, Pi Zhang, Xiaohui Shi, Xiaomeng Ye, Min Osbourn, Anne Qiao, Xue J Adv Res Original Article INTRODUCTION: Triterpenoids and saponins have a broad range of pharmacological activities. Unlike most legumes which contain mainly oleanane-type scaffold, Astragalus membranaceus contains not only oleanane-type but also cycloartane-type saponins, for which the biosynthetic pathways are unknown. OBJECTIVES: This work aims to study the function and catalytic mechanism of oxidosqualene cyclases (OSCs), one of the most important enzymes in triterpenoid biosynthesis, in A. membranaceus. METHODS: Two OSC genes, AmOSC2 and AmOSC3, were cloned from A. membranaceus. Their functions were studied by heterologous expression in tobacco and yeast, together with in vivo transient expression and virus-induced gene silencing. Site-directed mutagenesis and molecular docking were used to explain the catalytic mechanism for the conserved motif. RESULTS: AmOSC2 is a β-amyrin synthase which showed higher expression levels in underground parts. It is associated with the production of β-amyrin and soyasaponins (oleanane-type) in vivo. AmOSC3 is a cycloartenol synthase expressed in both aerial and underground parts. It is related to the synthesis of astragalosides (cycloartane-type) in the roots, and to the synthesis of cycloartenol as a plant sterol precursor. From AmOSC2/3, conserved triad motifs VFM/VFN were discovered for β-amyrin/cycloartenol synthases, respectively. The motif is a critical determinant of yield as proved by 10 variants from different OSCs, where the variant containing the conserved motif increased the yield by up to 12.8-fold. Molecular docking and mutagenesis revealed that Val, Phe and Met residues acted together to stabilize the substrate, and the cation-π interactions from Phe played the major role. CONCLUSION: The study provides insights into the biogenic origin of oleanane-type and cycloartane-type triterpenoids in Astragalus membranaceus. The conserved motif offers new opportunities for OSC engineering. Elsevier 2022-03-26 /pmc/articles/PMC9811366/ /pubmed/36585112 http://dx.doi.org/10.1016/j.jare.2022.03.014 Text en © 2022 The Authors. Published by Elsevier B.V. on behalf of Cairo University. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Chen, Kuan
Zhang, Meng
Xu, Lulu
Yi, Yang
Wang, Linlin
Wang, Haotian
Wang, Zilong
Xing, Jiangtao
Li, Pi
Zhang, Xiaohui
Shi, Xiaomeng
Ye, Min
Osbourn, Anne
Qiao, Xue
Identification of oxidosqualene cyclases associated with saponin biosynthesis from Astragalus membranaceus reveals a conserved motif important for catalytic function
title Identification of oxidosqualene cyclases associated with saponin biosynthesis from Astragalus membranaceus reveals a conserved motif important for catalytic function
title_full Identification of oxidosqualene cyclases associated with saponin biosynthesis from Astragalus membranaceus reveals a conserved motif important for catalytic function
title_fullStr Identification of oxidosqualene cyclases associated with saponin biosynthesis from Astragalus membranaceus reveals a conserved motif important for catalytic function
title_full_unstemmed Identification of oxidosqualene cyclases associated with saponin biosynthesis from Astragalus membranaceus reveals a conserved motif important for catalytic function
title_short Identification of oxidosqualene cyclases associated with saponin biosynthesis from Astragalus membranaceus reveals a conserved motif important for catalytic function
title_sort identification of oxidosqualene cyclases associated with saponin biosynthesis from astragalus membranaceus reveals a conserved motif important for catalytic function
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811366/
https://www.ncbi.nlm.nih.gov/pubmed/36585112
http://dx.doi.org/10.1016/j.jare.2022.03.014
work_keys_str_mv AT chenkuan identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT zhangmeng identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT xululu identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT yiyang identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT wanglinlin identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT wanghaotian identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT wangzilong identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT xingjiangtao identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT lipi identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT zhangxiaohui identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT shixiaomeng identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT yemin identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT osbournanne identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction
AT qiaoxue identificationofoxidosqualenecyclasesassociatedwithsaponinbiosynthesisfromastragalusmembranaceusrevealsaconservedmotifimportantforcatalyticfunction