Article ID Journal Published Year Pages File Type
4997263 Bioresource Technology 2017 24 Pages PDF
Abstract
A recombinant Pichia pastoris harbouring the cyanate hydratase gene (rTl-Cyn) from the thermophilic fungus Thermomyces lanuginosus SSBP yielded a high titre of extracellular cyanate hydratase (100 ± 13 U mL−1) which was ∼10-fold higher than the native fungal strain. The purified rTl-Cyn had a molecular mass of ∼20 kDa on SDS-PAGE, with Km, Vmax, kcat and kcat/Km values of 0.34 mM, 2857.14 µmoles mg−1 min−1, 2.14 × 104 s−1 and 6.3 × 107 M−1 s−1, respectively. Its properties of thermostability, pH stability, and heavy metals insensitivity, make it a suitable candidate for bioremediation in extreme environments. The rTl-Cyn was able to degrade toxic cyanate completely with the liberation of ammonia, which was confirmed by FTIR analysis. This is the first report of any known cyanate hydratase that has been expressed in P. pastoris, characterized and effectively evaluated for cyanate detoxification.
Related Topics
Physical Sciences and Engineering Chemical Engineering Process Chemistry and Technology
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