scholarly journals Enhancement of Peroxidase Stability Against Oxidative Self-Inactivation by Co-immobilization with a Redox-Active Protein in Mesoporous Silicon and Silica Microparticles

2016 ◽  
Vol 11 (1) ◽  
Author(s):  
P. Sahare ◽  
M. Ayala ◽  
R. Vazquez-Duhalt ◽  
U. Pal ◽  
A. Loni ◽  
...  
2015 ◽  
Vol 17 (6) ◽  
pp. 4025-4028 ◽  
Author(s):  
Charuksha Walgama ◽  
Nicolas Means ◽  
Nicholas F. Materer ◽  
Sadagopan Krishnan

Edge-to-edge interaction between carbon nanotubes and edge plane electrodes is suggested to favor enhanced π–π stacking of a pyrenyl compound and subsequent high density redox active protein immobilization.


2013 ◽  
Vol 41 (1) ◽  
pp. 171-181 ◽  
Author(s):  
Masato Yashiro ◽  
Hirokazu Tsukahara ◽  
Akihiro Matsukawa ◽  
Mutsuko Yamada ◽  
Yosuke Fujii ◽  
...  

2012 ◽  
Vol 116 (30) ◽  
pp. 16080-16088 ◽  
Author(s):  
Simone Ciampi ◽  
Bin Guan ◽  
Nadim Darwish ◽  
Peter J. Reece ◽  
J. Justin Gooding

2003 ◽  
Vol 168 (9) ◽  
pp. 1075-1083 ◽  
Author(s):  
Tomoaki Hoshino ◽  
Hajime Nakamura ◽  
Masaki Okamoto ◽  
Seiya Kato ◽  
Shinichi Araya ◽  
...  

2013 ◽  
Vol 125 (2) ◽  
pp. 109-112
Author(s):  
Masato Yashiro ◽  
Hirokazu Tsukahara ◽  
Akihiro Matsukawa ◽  
Mutsuko Yamada ◽  
Yosuke Fujii ◽  
...  

Author(s):  
Ruifeng Shi ◽  
Wenya Hou ◽  
Zhao-Qi Wang ◽  
Xingzhi Xu

Iron–sulfur (Fe/S) clusters (ISCs) are redox-active protein cofactors that their synthesis, transfer, and insertion into target proteins require many components. Mitochondrial ISC assembly is the foundation of all cellular ISCs in eukaryotic cells. The mitochondrial ISC cooperates with the cytosolic Fe/S protein assembly (CIA) systems to accomplish the cytosolic and nuclear Fe/S clusters maturation. ISCs are needed for diverse cellular functions, including nitrogen fixation, oxidative phosphorylation, mitochondrial respiratory pathways, and ribosome assembly. Recent research advances have confirmed the existence of different ISCs in enzymes that regulate DNA metabolism, including helicases, nucleases, primases, DNA polymerases, and glycosylases. Here we outline the synthesis of mitochondrial, cytosolic and nuclear ISCs and highlight their functions in DNA metabolism.


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