Direct electron transfer to a metagenome-derived laccase fused to affinity tags near the electroactive copper site

2013 ◽  
Vol 15 (47) ◽  
pp. 20585 ◽  
Author(s):  
Seiya Tsujimura ◽  
Masafumi Asahi ◽  
Maiko Goda-Tsutsumi ◽  
Osamu Shirai ◽  
Kenji Kano ◽  
...  
2007 ◽  
Vol 601 (1-2) ◽  
pp. 119-124 ◽  
Author(s):  
Yuji Kamitaka ◽  
Seiya Tsujimura ◽  
Kunishige Kataoka ◽  
Takeshi Sakurai ◽  
Tokuji Ikeda ◽  
...  

2005 ◽  
Vol 385 (3) ◽  
pp. 745-754 ◽  
Author(s):  
Sergey SHLEEV ◽  
Andreas CHRISTENSON ◽  
Vladimir SEREZHENKOV ◽  
Dosymzhan BURBAEV ◽  
Alexander YAROPOLOV ◽  
...  

Mediatorless, electrochemically driven, redox transformations of T1 (type 1) and T2 copper sites in Trametes hirsuta laccase were studied by cyclic voltammetry and spectroelectrochemical redox titrations using bare gold electrode. DET (direct electron transfer) between the electrode and the enzyme was observed under anaerobic conditions. From analysis of experimental data it is concluded that the T2 copper site is in DET contact with gold. It was found that electron transfer between the gold surface and the T1 copper site progresses through the T2 copper site. From EPR measurements and electrochemical data it is proposed that the redox potential of the T2 site for high-potential ‘blue’ laccase is equal to about 400 mV versus NHE (normal hydrogen electrode) at pH 6.5. The hypothesis that the redox potentials of the T2 copper sites in low- and high-potential laccases/oxidases from totally different sources might be very similar, i.e. approx. 400 mV, is discussed.


Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4525
Author(s):  
Franziska Schachinger ◽  
Hucheng Chang ◽  
Stefan Scheiblbrandner ◽  
Roland Ludwig

The accurate determination of analyte concentrations with selective, fast, and robust methods is the key for process control, product analysis, environmental compliance, and medical applications. Enzyme-based biosensors meet these requirements to a high degree and can be operated with simple, cost efficient, and easy to use devices. This review focuses on enzymes capable of direct electron transfer (DET) to electrodes and also the electrode materials which can enable or enhance the DET type bioelectrocatalysis. It presents amperometric biosensors for the quantification of important medical, technical, and environmental analytes and it carves out the requirements for enzymes and electrode materials in DET-based third generation biosensors. This review critically surveys enzymes and biosensors for which DET has been reported. Single- or multi-cofactor enzymes featuring copper centers, hemes, FAD, FMN, or PQQ as prosthetic groups as well as fusion enzymes are presented. Nanomaterials, nanostructured electrodes, chemical surface modifications, and protein immobilization strategies are reviewed for their ability to support direct electrochemistry of enzymes. The combination of both biosensor elements—enzymes and electrodes—is evaluated by comparison of substrate specificity, current density, sensitivity, and the range of detection.


2021 ◽  
pp. 107818
Author(s):  
Miriam Izzo ◽  
Silvio Osella ◽  
Margot Jacquet ◽  
Małgorzata Kiliszek ◽  
Ersan Harputlu ◽  
...  

1982 ◽  
Vol 141 ◽  
pp. 23-32 ◽  
Author(s):  
Robert M. Ianniello ◽  
Thomas J. Lindsay ◽  
Alexander M. Yacynych

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