Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3424
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dc.contributor.authorGodan, T K-
dc.contributor.authorRajesh, R O-
dc.contributor.authorLoreni, P C-
dc.contributor.authorRai, A-
dc.contributor.authorSahoo, D-
dc.contributor.authorPandey, A-
dc.contributor.authorBinod, P-
dc.date.accessioned2019-07-19T14:30:38Z-
dc.date.available2019-07-19T14:30:38Z-
dc.date.issued2019-03-01-
dc.identifier.citationBioresource Technology; 282:88-93en_US
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0960852419303402?via%3Dihub-
dc.identifier.urihttp://10.10.100.66:8080/xmlui/handle/123456789/3424-
dc.description.abstractHydroxymethylfurfural (HMF) is an industrially important chemical which is a starting material in the production of plenty of platform chemicals. In this study, a complete biotransformation of HMF was achieved using a novel isolate, Acinetobacter oleivorans S27. This strain could tolerate up to 3000 mg/L of HMF concentration and convert to other furan derivatives. The conversion products includes high-value chemicals like 5-hydroxymethyl-2-furancarboxylic acid (HMFCA), a known interleukin inhibitor and 2,5-furan dicarboxylic acid (FDCA), an alternate of terephthalic acid in polyester industries. The biotransformation efficiency was found to be 100%, as there is complete conversion of HMF to other chemicals. Most importantly, it is an environmental friendly process for the production of furan derivatives.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectAcinetobacter oleivorans S27en_US
dc.subject5-Hydroxymethyl furfuralen_US
dc.subject2,5-Furan dicarboxylic aciden_US
dc.subject5-Hydroxymethyl 2-furancarboxylic aciden_US
dc.subjectResponse Surface Methodologyen_US
dc.titleBiotransformation of 5-hydroxymethylfurfural by Acinetobacter oleivorans S27 for the synthesis of furan derivativesen_US
dc.typeArticleen_US
Appears in Collections:2019

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