Catalytic properties of yellow laccase from Pleurotus ostreatus D1

2004 ◽  
Vol 30 (1) ◽  
pp. 19-24 ◽  
Author(s):  
N.N Pozdnyakova ◽  
J Rodakiewicz-Nowak ◽  
O.V Turkovskaya
2006 ◽  
Vol 42 (1) ◽  
pp. 56-61 ◽  
Author(s):  
N. N. Pozdnyakova ◽  
O. V. Turkovskaya ◽  
E. N. Yudina ◽  
Ya. Rodakiewicz-Nowak

2009 ◽  
Vol 26 (2) ◽  
pp. 205-211 ◽  
Author(s):  
Natalia N. Pozdnyakova ◽  
Svetlana V. Nikiforova ◽  
Oleg E. Makarov ◽  
Marina P. Chernyshova ◽  
Kirill E. Pankin ◽  
...  

2009 ◽  
Vol 58 (6) ◽  
pp. 554-558 ◽  
Author(s):  
Svetlana V. Nikiforova ◽  
Natalia N. Pozdnyakova ◽  
Olga V. Turkovskaya

Microbiology ◽  
2010 ◽  
Vol 79 (4) ◽  
pp. 456-460 ◽  
Author(s):  
S. V. Nikiforova ◽  
N. N. Pozdnyakova ◽  
O. E. Makarov ◽  
M. P. Chernyshova ◽  
O. V. Turkovskaya

2010 ◽  
Vol 5 (1) ◽  
pp. 83-94 ◽  
Author(s):  
Natalia Pozdnyakova ◽  
Svetlana Nikiforova ◽  
Olga Turkovskaya

AbstractPolycyclic aromatic hydrocarbons (PAHs), their derivatives, and their degradation products were assayed for the ability to enhance activities of ligninolytic enzymes (laccase and versatile peroxidase) of the fungus Pleurotus ostreatus D1. The activities of both laccase and versatile peroxidase were induced by the PAHs, their derivatives, and their degradation products. Laccase was produced mostly in the first 7–10 days, whereas the production of versatile peroxidase began after 5–7 days of cultivation. Non-denaturing PAGE showed the presence of additional forms of laccase and versatile peroxidase in the presence of the xenobiotics in the cultivation medium. The difference in the production time for these enzymes may reflect that laccases are involved in the first stages of PAHs degradation and that versatile peroxidase can be necessary for oxidation of some degradation products. This is the first report on versatile peroxidase induction by PAHs and their derivatives.


Author(s):  
L.D. Schmidt ◽  
K. R. Krause ◽  
J. M. Schwartz ◽  
X. Chu

The evolution of microstructures of 10- to 100-Å diameter particles of Rh and Pt on SiO2 and Al2O3 following treatment in reducing, oxidizing, and reacting conditions have been characterized by TEM. We are able to transfer particles repeatedly between microscope and a reactor furnace so that the structural evolution of single particles can be examined following treatments in gases at atmospheric pressure. We are especially interested in the role of Ce additives on noble metals such as Pt and Rh. These systems are crucial in the automotive catalytic converter, and rare earths can significantly modify catalytic properties in many reactions. In particular, we are concerned with the oxidation state of Ce and its role in formation of mixed oxides with metals or with the support. For this we employ EELS in TEM, a technique uniquely suited to detect chemical shifts with ∼30Å resolution.


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