Dextranase: Hyper production of dextran degrading enzyme from newly isolated strain of Bacillus licheniformis

► New Bacillus strain for dextranase production was isolated. ► High production of dextranase was reported first time from Bacillus licheniformis. ► New medium was developed for the production of dextranase. ► Novel dextranase was produced capable of degrading low molecular weight dextran. Dextranas...

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Veröffentlicht in:Carbohydrate polymers 2013-02, Vol.92 (2), p.2149-2153
Hauptverfasser: Zohra, Rashida Rahmat, Aman, Afsheen, Zohra, Raheela Rahmat, Ansari, Asma, Ghani, Maria, Qader, Shah Ali Ul
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Sprache:eng
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Zusammenfassung:► New Bacillus strain for dextranase production was isolated. ► High production of dextranase was reported first time from Bacillus licheniformis. ► New medium was developed for the production of dextranase. ► Novel dextranase was produced capable of degrading low molecular weight dextran. Dextranase, 6-alpha-d-glucan 6-glucanohydrolase catalyzes the degradation of dextran (polymer of d-glucose) in to low molecular weight fractions. Dextranolytic bacterial strains were isolated from various natural sources and plate assay methods were developed for screening of highest extracellular dextranase producing isolate. Bacillus licheniformis, identified on the basis of taxonomic characterization was subjected to UV radiation and highest enzyme producing mutant obtained led to 7 times more dextranase production than wild. Optimization of major physico-chemical parameters affecting enzyme production; including medium composition, pH, cultivation time and temperature revealed that maximum enzyme production was obtained in a self designed medium (pH 6.0) containing 1% Dextran 5000Da, after 24h culture incubation at 37°C. Dextranase reported in this study is of great commercial importance as it is strictly inducible in nature and B. licheniformis being non-pathogenic removes the safety concerns associated with production of dextran fractions for clinical and pharmaceutical usage.
ISSN:0144-8617
1879-1344
DOI:10.1016/j.carbpol.2012.11.044