Functional characterization and substrate promiscuity of sesquiterpene synthases from Tripterygium wilfordii

Author(s):  
Yuru Tong ◽  
Tianyuan Hu ◽  
Lichan Tu ◽  
Kang Chen ◽  
Tiezheng Liu ◽  
...  
2015 ◽  
Vol 56 (12) ◽  
pp. 2478-2493 ◽  
Author(s):  
Chuankui Song ◽  
Le Gu ◽  
Jingyi Liu ◽  
Shuai Zhao ◽  
Xiaotong Hong ◽  
...  

2021 ◽  
Vol 106 (1-2) ◽  
pp. 145-156
Author(s):  
Guopeng Miao ◽  
Juan Han ◽  
Yan-bo Huo ◽  
Cheng-run Wang ◽  
Shun-chang Wang

Plants ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 418
Author(s):  
Yanbo Huo ◽  
Bin Zhang ◽  
Ling Chen ◽  
Jing Zhang ◽  
Xing Zhang ◽  
...  

Miltiradiene synthase (MS) genes, TwTPS27a and TwTPS27b, are the key diterpene synthase genes in the biosynthesis of triptolide, which is an important medicinally active diterpenoid in Tripterygium wilfordii. However, the mechanism underlying the regulation of key genes TwTPS27a/b in triptolide biosynthesis remains unclear. In this study, the promoters of TwTPS27a (1496 bp) and TwTPS27b (1862 bp) were isolated and analyzed. Some hormone-/stress-responsive elements and transcription factor (TF) binding sites were predicted in both promoters, which might be responsible for the regulation mechanism of TwTPS27a/b. The β-glucuronidase (GUS) activity analysis in promoter deletion assays under normal and methyl jasmonate (MeJA) conditions showed that the sequence of −921 to −391 bp is the potential core region of the TwTPS27b promoter. And the TGACG-motif, a MeJA-responsive element found in this core region, might be responsible for MeJA-mediated stress induction of GUS activity. Moreover, the TGACG-motif is also known as the TGA TF-binding site. Yeast one-hybrid and GUS transactivation assays confirmed the interaction between the TwTPS27a/b promoters and the TwTGA1 TF (a MeJA-inducible TGA TF upregulating triptolide biosynthesis in T. wilfordii), indicating that TwTPS27a/b are two target genes regulated by TwTGA1. In conclusion, our results provide important information for elucidating the regulatory mechanism of MS genes, TwTPS27a and TwTPS27b, as two target genes of TwTGA1, in jasmonic acid (JA)-inducible triptolide biosynthesis.


2019 ◽  
Vol 39 (3) ◽  
pp. 409-418 ◽  
Author(s):  
Yuan Liu ◽  
Jiawei Zhou ◽  
Tianyuan Hu ◽  
Yun Lu ◽  
Linhui Gao ◽  
...  

Molecules ◽  
2018 ◽  
Vol 23 (2) ◽  
pp. 269 ◽  
Author(s):  
Bin Zhang ◽  
Yan Liu ◽  
Mengmeng Chen ◽  
Juntao Feng ◽  
Zhiqing Ma ◽  
...  

2017 ◽  
Vol 93 (1) ◽  
pp. 50-65 ◽  
Author(s):  
Ping Su ◽  
Hongyu Guan ◽  
Yujun Zhao ◽  
Yuru Tong ◽  
Meimei Xu ◽  
...  

Author(s):  
A. Engel ◽  
A. Holzenburg ◽  
K. Stauffer ◽  
J. Rosenbusch ◽  
U. Aebi

Reconstitution of solubilized and purified membrane proteins in the presence of phospholipids into vesicles allows their functions to be studied by simple bulk measurements (e.g. diffusion of differently sized solutes) or by conductance measurements after transformation into planar membranes. On the other hand, reconstitution into regular protein-lipid arrays, usually forming at a specific lipid-to-protein ratio, provides the basis for determining the 3-dimensional structure of membrane proteins employing the tools of electron crystallography.To refine reconstitution conditions for reproducibly inducing formation of large and highly ordered protein-lipid membranes that are suitable for both electron crystallography and patch clamping experiments aimed at their functional characterization, we built a flow-dialysis device that allows precise control of temperature and flow-rate (Fig. 1). The flow rate is generated by a peristaltic pump and can be adjusted from 1 to 500 ml/h. The dialysis buffer is brought to a preselected temperature during its travel through a meandering path before it enters the dialysis reservoir. A Z-80 based computer controls a Peltier element allowing the temperature profile to be programmed as function of time.


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