Expression profiling of proteins inL-threonine biosynthetic pathway ofEscherichia coli by using antibody microarray

PROTEOMICS ◽  
2006 ◽  
Vol 6 (22) ◽  
pp. 5929-5940 ◽  
Author(s):  
Min-Kyu Han ◽  
Mi-Young Hong ◽  
Dohoon Lee ◽  
Dong-Eun Lee ◽  
Geon Youp Noh ◽  
...  
2018 ◽  
Vol 125 (5) ◽  
pp. 1502-1517 ◽  
Author(s):  
M. Goswami ◽  
F. A. Khan ◽  
A. Ibrisevic ◽  
P.-E. Olsson ◽  
J. Jass

2015 ◽  
Vol 61 (2) ◽  
pp. 41-49
Author(s):  
Vladimír Repka ◽  
Roderik Fiala ◽  
Milada Čiamporová ◽  
Michal Martinka ◽  
Ján Pavlovkin

Abstract Here, we report the effectiveness of antibody microarray expression profiling (AbMEP) procedure to determine similarities and differences between two maize cultivars (Premia and Blitz) exposed to various concentration of cadmium (Cd), nickel (Ni), as well as simultaneous exposure to both metals (Cd + Ni) for 0, 12 and 24 h. After protein extraction from control (untreated) and heavy metals (HM)-treated root pairs and their fluorescent labelling, the protein extracts were used for the AbMEP procedure and western blot analysis. The results from the microarray were analysed using an internally normalised ratio. Using this highly parallel AbMEP-approach, the timing, dynamics and regulation of the expression of 101 specific genes in untreated and HM-treated roots of maize cultivars were determined. The microarray results revealed 23, 15 and 10 up-regulated/down-regulated proteins in Cd, Ni and Cd + Ni treated cv. Premia roots, respectively. In contrast, the microarray results revealed that 15, 11 and 7 proteins were up-regulated/down-regulated in Cd, Ni and Cd + Ni treated cv. Blitz roots, respectively. The data obtained from the AbMEP array experiment were validated by western blot analyses with more than 89% (the Pearson’s correlation coeficient Rr = 0.78) correlation between the two methods.


2015 ◽  
Vol 10 (12) ◽  
pp. 1934578X1501001
Author(s):  
Lijia Chen ◽  
Hui Tong ◽  
Mingxuan Wang ◽  
Jianhua Zhu ◽  
Jiachen Zi ◽  
...  

The biosynthetic pathway of terpene trilactones of Ginkgo biloba is unclear. In this present study, suspension cultured cells of G. biloba were used to explore the regulation of the mevalonic acid (MVA) and methylerythritol 4-phosphate (MEP) pathways in response to specific enzyme inhibitors (lovastatin and clomazone). The results showed that the biosynthesis of bilobalide was more highly correlated with the MVA pathway, and the biosynthesis of ginkgolides was more highly correlated with the MEP pathway. Meanwhile, according to the results, it could be speculated that bilobalide might be a product of ginkgolide metabolism.


2017 ◽  
Vol 19 (11) ◽  
pp. 4551-4563 ◽  
Author(s):  
Elio Rossi ◽  
Sara Motta ◽  
Alessandro Aliverti ◽  
Federica Cossu ◽  
Louise Gourlay ◽  
...  

2007 ◽  
Vol 7 (1) ◽  
pp. 163-169 ◽  
Author(s):  
X. Cynthia Song ◽  
Guanyuan Fu ◽  
Xufen Yang ◽  
Zhong Jiang ◽  
Yingjian Wang ◽  
...  

2017 ◽  
Vol 12 (7) ◽  
pp. 1934578X1701200
Author(s):  
Jianhua Zhu ◽  
Pu Wang ◽  
Minghua Qian ◽  
Chuxin Liang ◽  
Jiachen Zi ◽  
...  

Ginkgolides (GKs) and Bilobalide (BB) are rare terpene trilactones obtained from Ginkgo biloba, but their biosynthetic pathway is still unclear. In this paper, effects of levopimaradiene (LP) on increasing the production of terpene trilactones of G. biloba dedifferentiated cells (DDCs) and cambial meristematic cells (CMCs) were reported. The productions of ginkgolide A (GA) and ginkgolide B (GB) were 1.61 and 1.32 folds larger than that of the control groups when G. biloba DDCs was treated with LP, and the productions of ginkgolide C (GC) and BB reached 234 and 161 μg L−1 after treated with LP for 60 h. The production of GA, GB, GC and BB was 2.03, 1.43, 1.22 and 1.19 folds larger than that of the control groups in LP-treated CMCs groups. The results demonstrated that BB could be produced from the methylerythritol 4-phosphate (MEP) pathway. qRT-PCR experiments showed that LP was a significant precursor manipulated the biosynthesis of terpene trilactones via affecting the transcript levels of several related genes in the MEP pathway.


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