<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hou YN</submitter><funding>Guizhou Science and Technology Department</funding><pagination>88</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7214591</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(1)</volume><pubmed_abstract>Biotransformation has the advantages of low cost and environmental protection and is a preferred method for production of compounds. At present, most 2,5-dihydroxymethylfuran (DHMF) is synthesized by chemical methods. In this study, 12.008 μg/mL DHMF was produced from 9.045 μg/mL 5-hydroxymethylfurfural (5-HMF) with a yield of 1.33 g/g using the crude enzymes from fungus Ganoderma sessile. To elucidate the toxic potential for both compounds, cytotoxicity tests and acute toxicity were evaluated respectively. 5-HMF induced weak cytotoxicity in HCT-8, A549 and SGC-7901 cells and DHMF exerted no cytotoxicity on HCT-8 while induced inhibition proliferation of A549 and SGC-7901 cells. The acute toxicity study showed no mortality happened in any group even at the single dose of 2000 mg/kg body we</pubmed_abstract><journal>AMB Express</journal><pubmed_title>Biotransformation of 5-hydroxymethylfurfural into 2,5-dihydroxymethylfuran by Ganoderma sessile and toxicological assessment of both compounds.</pubmed_title><pmcid>PMC7214591</pmcid><funding_grant_id>[2016] 2592</funding_grant_id><pubmed_authors>Feng K</pubmed_authors><pubmed_authors>Wang YR</pubmed_authors><pubmed_authors>Hou YN</pubmed_authors><pubmed_authors>Zheng CH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Biotransformation of 5-hydroxymethylfurfural into 2,5-dihydroxymethylfuran by Ganoderma sessile and toxicological assessment of both compounds.</name><description>Biotransformation has the advantages of low cost and environmental protection and is a preferred method for production of compounds. At present, most 2,5-dihydroxymethylfuran (DHMF) is synthesized by chemical methods. In this study, 12.008 μg/mL DHMF was produced from 9.045 μg/mL 5-hydroxymethylfurfural (5-HMF) with a yield of 1.33 g/g using the crude enzymes from fungus Ganoderma sessile. To elucidate the toxic potential for both compounds, cytotoxicity tests and acute toxicity were evaluated respectively. 5-HMF induced weak cytotoxicity in HCT-8, A549 and SGC-7901 cells and DHMF exerted no cytotoxicity on HCT-8 while induced inhibition proliferation of A549 and SGC-7901 cells. The acute toxicity study showed no mortality happened in any group even at the single dose of 2000 mg/kg body we</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 May</publication><modification>2025-04-22T00:53:36.876Z</modification><creation>2020-05-22T20:10:55Z</creation></dates><accession>S-EPMC7214591</accession><cross_references><pubmed>32394214</pubmed><doi>10.1186/s13568-020-01023-5</doi></cross_references></HashMap>