dc.creator | Liu, Qing | |
dc.creator | Manzano, David | |
dc.creator | Tanić, Nikola | |
dc.creator | Pešić, Milica | |
dc.creator | Banković, Jasna Z. | |
dc.creator | Pateraki, Irini | |
dc.creator | Ricard, Lea | |
dc.creator | Ferrer, Albert | |
dc.creator | de Vos, Ric | |
dc.creator | van de Krol, Sander | |
dc.creator | Bouwmeester, Harro | |
dc.date.accessioned | 2016-05-23T11:00:34Z | |
dc.date.issued | 2014 | |
dc.identifier.issn | 1096-7184 | |
dc.identifier.uri | https://radar.ibiss.bg.ac.rs/handle/123456789/2218 | |
dc.description.abstract | Parthenolide, the main bioactive compound of the medicinal plant
feverfew (Tanacetum parthenium), is a promising anti-cancer drug.
However, the biosynthetic pathway of parthenolide has not been
elucidated yet. Here we report on the isolation and characterization of
all the genes from feverfew that are required for the biosynthesis of
parthenolide, using a combination of 454 sequencing of a feverfew
glandular trichome cDNA library, co-expression analysis and
metabolomics. When parthenolide biosynthesis was reconstituted by
transient co-expression of all pathway genes in Nicotiana benthamiana,
up to 1.4 mu g g(-1) parthenolide was produced, mostly present as
cysteine and glutathione conjugates. These relatively polar conjugates
were highly active against colon cancer cells, with only slightly lower
activity than free parthenolide. In addition to these biosynthetic
genes, another gene encoding a costunolide and parthenolide 3
beta-hydroxylase was identified opening up further options to improve
the water solubility of parthenolide and therefore its potential as a
drug. (C) 2014 International Metabolic Engineering Society. Published by
Elsevier Inc. All rights reserved. | en |
dc.description.sponsorship | European Commission (EU) {[}227448]; Netherlands Metabolomics Centre as
part of the Netherlands Genomics Initiative/Netherlands Organization for
Scientific Research; Centre for BioSystems Genomics as part of the
Netherlands Genomics Initiative/Netherlands Organization for Scientific
Research | en |
dc.language | English | |
dc.rights | restrictedAccess | |
dc.source | Metabolic Engineering | |
dc.subject | Parthenolide | |
dc.subject | Biosynthetic pathway reconstitution | |
dc.subject | Feverfew | |
dc.subject | Metabolic
engineering | |
dc.title | Elucidation and in planta reconstitution of the parthenolide
biosynthetic pathway | en |
dc.type | article | |
dc.rights.license | ARR | |
dcterms.abstract | Таниц, Никола; Песиц, Милица; Патераки, Ирини; Боуwмеестер, Харро; Банковић, Јасна З.; Феррер, Aлберт; де Вос, Риц; Манзано, Давид; Лиу, Qинг; Рицард, Леа; ван де Крол, Сандер; | |
dc.citation.volume | 23 | |
dc.identifier.doi | 10.1016/j.ymben.2014.03.005 | |
dc.identifier.scopus | 2-s2.0-84898867034 | |
dc.identifier.wos | 000335385500015 | |
dc.citation.spage | 145 | |
dc.citation.epage | 153 | |
dc.type.version | publishedVersion | en |