TY - JOUR ID - 14788 TI - Biochemical and computational study of an alginate lyase produced by Pseudomonas aeruginosa strain S21 JO - Iranian Journal of Basic Medical Sciences JA - IJBMS LA - en SN - 2008-3866 AU - Piroozmand, Firoozeh AU - Ghadam, Parinaz AU - Zarrabi, Mahboobe AU - Abdi Ali, Ahya AD - Department of Biotechnology, Faculty of Biological Sciences, Alzahra University, Tehran, Iran AD - Department of Microbiology, Faculty of Biological sciences, Alzahra University, Tehran, Iran Y1 - 2020 PY - 2020 VL - 23 IS - 4 SP - 454 EP - 460 KW - Alginate KW - Alginate lyase KW - Computational biology KW - Enzyme assay KW - Pseudomonas aeruginosa KW - Strain S21 DO - 10.22038/ijbms.2020.37277.8874 N2 - Objective(s): Alginates play a key role in mucoid Pseudomonas aeruginosa colonization, biofilm formation, and driving out of cationic antibiotics. P. aeruginosa alginate lyase (AlgL) is a periplasmic enzyme that is necessary for alginate synthesis and secretion. It also has a role in depolymerization of alginates. Using AlgLs in cystic fibrosis patients along with antibiotics enhances bacterial killing and host healing. In this study, we investigated the different biochemical properties of a newly isolated AlgL from P. aeruginosa S21 to complete the databank of AlgLsMaterials and Methods: The enzyme was extracted from the periplasmic space of the bacteria by the heat shock method. Using the TBA method, the enzyme activity and biochemical properties were assessed. The mutability of P. aeruginosa S21 AlgL to increase its thermal stability was investigated. The most favorable mutations were studied computationally. The molecular dynamics simulation (MDS) package GROMACS was used for determining the effect of S34R mutation on enzyme’s thermal stability.Results: Data showed that this enzyme has the best activity at 37 °C and pH 7.5 and it can degrade mannuronate blocks, guluronate blocks, and sodium alginate. After 7 hr at 80 °C, 45% of the enzyme activity was retained. This enzyme needed 15 min to completely degrade accessible sodium alginate.  Tris buffer, pH 8.5 and Britton-Robinson buffer, pH 7.0 were the preferable buffers for the enzyme activity. MDS of native and mutated enzymes showed desirable results.Conclusion: P. aeruginosa S21 AlgL can be used in medical and industrial applications to degrade alginates. UR - https://ijbms.mums.ac.ir/article_14788.html L1 - https://ijbms.mums.ac.ir/article_14788_098ee43aa148f3558057f72d42b539c8.pdf ER -