Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8330188 | International Journal of Biological Macromolecules | 2016 | 35 Pages |
Abstract
A novel pullulanase gene, PulSS4, was identified from the gut microflora of Hermetia illucens by a function-based metagenome screening. The PulSS4 gene had an open reading frame of 4455 base pairs, and encoded a mature protein of 1484 amino acids, with a signal peptide sequence of 44 amino acids. The deduced amino acid sequence of PulSS4 gene showed 51% identity with that of the amylopullulanase of Amphibacillus xylanus, exhibiting no significant sequence homology to already known pullulanases. A conserved domain analysis revealed it to be a pullulanase type II with respective active sites at the N-terminal pullulanase and C-terminal amylase domain. PulSS4 was active in the temperature range of 10-50 °C, with an optimum activity at 40 °C. It was active in the pH range of 6.5-10.5, with optimum pH at 9.0, and retained more than 80% of its original activity in a broad pH range of 5-11 for 24 h at 30 °C. Also, PulSS4 was highly stable against many different chemical reagents, including 10% polar organic solvents and 1% non-ionic detergents. Overall, PulSS4 is expected to have the strong potential for application in biotechnological industries that require high activity at moderate temperature and alkaline conditions.
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Authors
Young-Seok Lee, So-Hyeon Seo, Sang-Hong Yoon, Su-Yeon Kim, Bum-Soo Hahn, Joon-Soo Sim, Bon-Sung Koo, Chang-Muk Lee,