Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5145036 | Bioelectrochemistry | 2017 | 23 Pages |
Abstract
A new plant peroxidase was isolated from the leaves of guinea grass (Panicum maximum) and partially purified using a biphasic polymer system (poly(ethylene glycol) - ammonium sulfate) followed by size-exclusion chromatography and ultracentrifugation until obtaining a homogeneous extract containing a high peroxidase activity. The novel peroxidase was characterized as having a specific activity of 408 U/mg and a molecular weight of 30 kDa. The pH for its optimum activity was 8.0 and exhibited a high thermostability at 66 °C with a kinact of 8.0 Ã 10â 3 minâ 1. The best substrates for peroxidase from guinea grass are o-dianisidine and 2,2â²-azino-bis-(3-ethylbenzthiazoline-6-sulfonic acid). POD from guinea grass was directly immobilized on the surface of a graphene screen printed electrode and cyclic voltammograms in the presence of potassium ferrocyanide ([Fe(CN)6]3 â / 4 â) as a redox species demonstrated an increase in the electron transfer process. The graphene- modified electrode exhibits excellent electrocatalytic activity to the reduction of H2O2, with a linear response in the 100 μM to 3.5 mM concentration range and a detection limit of 150 μM. The new peroxidase from guinea grass allowed the modification of a graphene electrode providing a potential sensor detection system for determination of H2O2 in real samples with some biomedical or environmental importance.
Related Topics
Physical Sciences and Engineering
Chemistry
Electrochemistry
Authors
Diana A. Centeno, Xuxan H. Solano, John J. Castillo,