Biosynthesis, transport and combinatorial metabolic engineering of Tanacetum parthenium (feverfew) and Artemisia annua (sweet wormwood) sesquiterpene lactones

2018 ◽  
Author(s):  
Arman Beyraghdar Kashkooli
1999 ◽  
Vol 64 (7-8) ◽  
pp. 397-442 ◽  
Author(s):  
Slobodan Milosavljevic ◽  
Vanja Bulatovic ◽  
Milutin Stefanovic

1. Introduction 2. Results 3. Asteraceae 3.1. Genus Artemisia L. 3.1.1. Artemisia annua L. 3.1.2. Artemisia vulgaris L. 3.1.3. Artemisia absinthium L. (warmwood) 3.1.4. Artemisia scoparia W. et K. 3.1.5. Artemisia camprestris L. 3.2. Genus Ambrosia L. 3.2.1. Ambrosia artemisiifolia L. (the common rag weed) 3.3. Genus Tanacetum L. ( syn. Chrysanthemum L.) 3.3.1. Tanacetum parthenium L. (feverfew) 3.3.2. Tanacetum serotinum L. 3.3.3. Tanacetum vulgare L. (tansy) 3.3.4. Tanacetum macrophyllum Willd. 3.3.5. Tanacetum corymbosum L. 3.4. Genus Telekia Baumg. 3.4.1. Telekia speciosa (Schreb.) Baumg. 3.5. Genus Inula L. 3.5.1. Inula helenium L. 3.5.2. Inula spiraeifolia L. 3.6. Genus Eupatorium L. 3.6.1. Eupatorium cannabinum L. 3.7. Genus Achillea L. 3.7.1. Achillea abrotanoides Vis. 3.7.2. Achillea millefolium subsp. pannonica 3.7.3. Achillea crithmifolia W. et K. 3.7.4. Achillea clypeolata Sibth. et Sm. 3.7.5. Achillea serbica Nyman 3.7.6. Achillea depressa Janka 3.8. Genus Anthemis L. 3.8.1. Anthemis carpatica Willd. 3.8.2. Anthemis cretica L. subsp. cretica 3.9. Genus Centaurea L. 3.9.1. Centaurea derventana Vis. et Pan~. 3.9.2. Centaurea kosaninii Hayek 3.9.3. Centaurea solstitialis L. 4. Apiaceae 4.1. Genus Laserpitium L. 4.1.1. Laserpitium siler L. 4.1.2. Laserpitium marginatum L. 4.1.3. Laserpitium latifolium L. 4.1.4. Laserpitium alpinum W. K. 4.2. Genus Angelica L. 4.2.1. Angelica silvestris L. 4.3. Genus Peucedanum L. 4.3.1. Peucedanum austriacum (Jacq.) Koch


2021 ◽  
Vol 76 (3) ◽  
pp. 49-60
Author(s):  
Magdalena Sozoniuk

Asteraceae family is a rich source of many sesquiterpene lactones (STLs). These secondary metabolites exhibit multidirectional activity including anti-tumor, anti-inflammatory or antimicrobial, just to name a few. Promising approach of metabolic engineering offers a way of increasing the production of STLs by reconstruction  of  their  biosynthetic  pathway  in  a  heterologous system. Moreover, their production in host plants might be increased through overexpression of biosynthetic genes and/or transcription factors (TFs) positively regulating the pathway. Either of the strategies requires extensive knowledge on the genetic background of STLs biosynthesis pathway. This review summarizes molecular investigations concerning biosynthesis of these medicinally essential metabolites.


Author(s):  
Eric L. Yarnell ◽  
Kathy Abascal

1982 ◽  
Vol 21 (10) ◽  
pp. 2543-2549 ◽  
Author(s):  
Ferdinand Bohlmann ◽  
Christa Zdero

2010 ◽  
Vol 30 (5) ◽  
pp. 689-694 ◽  
Author(s):  
Benye Liu ◽  
Hong Wang ◽  
Zhigao Du ◽  
Guofeng Li ◽  
Hechun Ye

2012 ◽  
Vol 65 (9) ◽  
pp. 469-472 ◽  
Author(s):  
Guo-Zhen Zhao ◽  
Jie Li ◽  
Yu-Li Qin ◽  
Cui-Ping Miao ◽  
Da-Qiao Wei ◽  
...  

2020 ◽  
Vol 11 (04) ◽  
pp. 529-537
Author(s):  
John Nyoni ◽  
Tendai Madanzi ◽  
Joanah Midzi ◽  
Tavagwisa Muziri ◽  
Arnold Kapenzi

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