Version 1
: Received: 7 December 2019 / Approved: 8 December 2019 / Online: 8 December 2019 (17:24:19 CET)
How to cite:
Bhamare, H.; Sayyed, R.; Marraiki, N.; Elgorban, A.; Syed, A.; Enshasy, H. Extracellular Laccase Produced by Tree Bark Scrape Isolate : A Potential Source for Bioremediation of Non-Textile Dyes. Preprints2019, 2019120104
Bhamare, H.; Sayyed, R.; Marraiki, N.; Elgorban, A.; Syed, A.; Enshasy, H. Extracellular Laccase Produced by Tree Bark Scrape Isolate : A Potential Source for Bioremediation of Non-Textile Dyes. Preprints 2019, 2019120104
Bhamare, H.; Sayyed, R.; Marraiki, N.; Elgorban, A.; Syed, A.; Enshasy, H. Extracellular Laccase Produced by Tree Bark Scrape Isolate : A Potential Source for Bioremediation of Non-Textile Dyes. Preprints2019, 2019120104
APA Style
Bhamare, H., Sayyed, R., Marraiki, N., Elgorban, A., Syed, A., & Enshasy, H. (2019). Extracellular Laccase Produced by Tree Bark Scrape Isolate : A Potential Source for Bioremediation of Non-Textile Dyes. Preprints. https://doi.org/
Chicago/Turabian Style
Bhamare, H., Asad Syed and Hesham Enshasy. 2019 "Extracellular Laccase Produced by Tree Bark Scrape Isolate : A Potential Source for Bioremediation of Non-Textile Dyes" Preprints. https://doi.org/
Abstract
Although laccase has been recognized as a wonder molecule, and green enzyme, the use of low yielding fungal strains, poor production, purification, and low enzyme kinetics have hampered its larger-scale applications. Hence the present research was aimed to select high yielding fungal strains and to optimize the production, purification, and kinetics of laccase of Aspergillus sp. HB_RZ4. Aspergillus sp. HB_RZ4 produced a copious amount of laccase on under meso-acidophillic shaking conditions in a medium containing glucose and yeast extract. A 25 µM of CuSO4 enhanced the enzyme yield. The enzyme was best purified on Sephadex G-100 column. Purified enzyme resembled with the laccase of A. flavus. Kinetics of purified enzyme revealed the high substrate specificity and good velocity of reaction with ABTS as substrate. The enzyme was stable over a wide range of pH and temperature. The peptide structure of the purified enzyme resembled with the laccase of A. kawachii IFO 4308. The fungus decolorized various dyes independent of the requirement of a laccase mediator system (LMS). Aspergillus sp. HB_RZ4 came out as a potent natural producer of laccase, it decolorized the dyes even in absence of LMS and thus can be used for bioremediation.
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
