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Improvement of Thermostability and Activity of Firefly Luciferase Through [TMG][Ac] Ionic Liquid Mediator
Authors:Mehdi Ebrahimi  Saman Hosseinkhani  Akbar Heydari  Ramazan Ali Khavari-Nejad  Jafar Akbari
Affiliation:1. Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran
2. Department of Biochemistry, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran
3. Department of Chemistry, Faculty of Science, Tarbiat Modares University, Tehran, Iran
Abstract:Firefly luciferase catalyzes production of light from luciferin in the presence of Mg2+?CATP and oxygen. This enzyme has wide range of applications in biotechnology and development of biosensors. The low thermal stability of wild-type firefly luciferase is a limiting factor in most applications. Improvements in activity and stability of few enzymes in the presence of ionic liquids were shown in many reports. In this study, kinetic and thermal stability of firefly luciferase from Photinus pyralis in the presence of three tetramethylguanidine-based ionic liquids was investigated. The enzyme has shown improved activity in the presence of [1, 1, 3, 3-tetramethylguanidine][acetate], but in the presence of [TMG][trichloroacetate] and [TMG][triflouroacetate] activity, it decreased or unchanged significantly. Among these ionic liquids, only [TMG][Ac] has increased the thermal stability of luciferase. Incubation of [TMG][Ac] with firefly luciferase brought about with decrease of K m for ATP.
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