<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(1)</volume><submitter>Ding Y</submitter><pubmed_abstract>The immobilization technology provides a potential pathway for enzyme recycling. Here, we evaluated the potential of using dextranase immobilized onto hydroxyapatite nanoparticles as a promising inorganic material. The optimal immobilization temperature, reaction time, and pH were determined to be 25 °C, 120 min, and pH 5, respectively. Dextranase could be loaded at 359.7 U/g. The immobilized dextranase was characterized by field emission gun-scanning electron microscope (FEG-SEM), X-ray diffraction (XRD), and Fourier-transformed infrared spectroscopy (FT-IR). The hydrolysis capacity of the immobilized enzyme was maintained at 71% at the 30th time of use. According to the constant temperature acceleration experiment, it was estimated that the immobilized dextranase could be stored for 99 d</pubmed_abstract><journal>Materials (Basel, Switzerland)</journal><pagination>E130</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7796272</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Immobilization of Dextranase on Nano-Hydroxyapatite as a Recyclable Catalyst.</pubmed_title><pmcid>PMC7796272</pmcid><pubmed_authors>Dong D</pubmed_authors><pubmed_authors>Lyu M</pubmed_authors><pubmed_authors>Ding Y</pubmed_authors><pubmed_authors>Wang C</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Zu H</pubmed_authors><pubmed_authors>Wang X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immobilization of Dextranase on Nano-Hydroxyapatite as a Recyclable Catalyst.</name><description>The immobilization technology provides a potential pathway for enzyme recycling. Here, we evaluated the potential of using dextranase immobilized onto hydroxyapatite nanoparticles as a promising inorganic material. The optimal immobilization temperature, reaction time, and pH were determined to be 25 °C, 120 min, and pH 5, respectively. Dextranase could be loaded at 359.7 U/g. The immobilized dextranase was characterized by field emission gun-scanning electron microscope (FEG-SEM), X-ray diffraction (XRD), and Fourier-transformed infrared spectroscopy (FT-IR). The hydrolysis capacity of the immobilized enzyme was maintained at 71% at the 30th time of use. According to the constant temperature acceleration experiment, it was estimated that the immobilized dextranase could be stored for 99 d</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2025-04-25T20:47:13.228Z</modification><creation>2025-04-06T08:28:07.09Z</creation></dates><accession>S-EPMC7796272</accession><cross_references><pubmed>33396810</pubmed><doi>10.3390/ma14010130</doi></cross_references></HashMap>