Catechol oxidase activity associated with sporogenesis inHaplosporidium malacobdellae, a balanosporidan endoparasite of the hoplonemerteanAmphiporus lactifloreus

1981 ◽  
Vol 65 (2) ◽  
pp. 153-162 ◽  
Author(s):  
I. M. Varndell
2012 ◽  
Vol 36 (9) ◽  
pp. 1828 ◽  
Author(s):  
Ronan Marion ◽  
Nidal M. Saleh ◽  
Nicolas Le Poul ◽  
Didier Floner ◽  
Olivier Lavastre ◽  
...  

2018 ◽  
Vol 47 (43) ◽  
pp. 15555-15564
Author(s):  
Adriana M. Magherusan ◽  
Daniel N. Nelis ◽  
Brendan Twamley ◽  
Aidan R. McDonald

Dicopper complexes proved to be more reactive catechol oxidase mimics when compared to dimanganese complexes supported by identical ligand frameworks.


2002 ◽  
Vol 41 (15) ◽  
pp. 3983-3989 ◽  
Author(s):  
Stéphane Torelli ◽  
Catherine Belle ◽  
Sylvain Hamman ◽  
Jean-Louis Pierre ◽  
Eric Saint-Aman

1970 ◽  
Vol 119 (1) ◽  
pp. 89-94 ◽  
Author(s):  
P. F. T. Vaughan ◽  
V. S. Butt

1. Under defined conditions, the hydroxylation of p-coumaric acid catalysed by a phenolase from leaves of spinach beet (Beta vulgaris L.) was observed to develop its maximum rate only after a lag period. 2. By decreasing the reaction rate with lower enzyme concentrations or by increasing it with higher concentrations of reductants, the length of the lag period was inversely related to the maximum rate subsequently developed. 3. Low concentrations of caffeic acid or other o-dihydric phenols abolished this lag period. With caffeic acid, the rate of hydroxylation was independent of the reductant employed. 4. Hydroxylation was inhibited by diethyldithiocarbamate, but with low inhibitor concentrations hydroxylation recovered after a lag period. This lag could again be abolished by the addition of high concentrations of caffeic acid or other o-dihydric phenols. 5. Catechol oxidase activity showed no lag period, and did not recover from diethyldithiocarbamate inhibition. 6. The purified enzyme contained 0.17–0.33% copper; preparations with the highest specific activity were found to have the highest copper content. 7. The results are interpreted to suggest that the oxidation of o-dihydric phenols converts the enzymic copper into a species catalytically active in hydroxylation. This may represent the primary function for the catechol oxidase activity of the phenolase complex. The electron donors are concerned mainly, but not entirely, in the reduction of o-quinones produced in this reaction.


2016 ◽  
Vol 45 (34) ◽  
pp. 13576-13589 ◽  
Author(s):  
Tufan Singha Mahapatra ◽  
Dipmalya Basak ◽  
Santanu Chand ◽  
Jeff Lengyel ◽  
Michael Shatruk ◽  
...  

The synthetic procedures, magnetic properties and catecholase-like activity of a V-shaped [CoII3L4] and planar disc-like [CoII7L6] complexes have been discussed.


2003 ◽  
Vol 42 (1-2) ◽  
pp. 25-26
Author(s):  
Hayrullah Yilmaz ◽  
Halis Şakiroǧlu ◽  
Ö.Ïrfan Küfrevioǧlu

2017 ◽  
Vol 41 (11) ◽  
pp. 4689-4701 ◽  
Author(s):  
Leena Mandal ◽  
Shuvankar Mandal ◽  
Sasankasekhar Mohanta

One phenoxo–hydroxo bridged tetranuclear cluster and one phenoxo-µ1,1-azido-µ1,3-azido bridged one-dimensional coordination polymer of copper(ii) derived from a Schiff base ligand are described.


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