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Biotransformation of 5-hydroxymethylfurfural by Acinetobacter oleivorans S27 for the synthesis of furan derivatives

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dc.contributor.author Godan, T K
dc.contributor.author Rajesh, R O
dc.contributor.author Loreni, P C
dc.contributor.author Rai, A
dc.contributor.author Sahoo, D
dc.contributor.author Pandey, A
dc.contributor.author Binod, P
dc.date.accessioned 2019-07-19T14:30:38Z
dc.date.available 2019-07-19T14:30:38Z
dc.date.issued 2019-03-01
dc.identifier.citation Bioresource Technology; 282:88-93 en_US
dc.identifier.uri https://www.sciencedirect.com/science/article/pii/S0960852419303402?via%3Dihub
dc.identifier.uri http://10.10.100.66:8080/xmlui/handle/123456789/3424
dc.description.abstract Hydroxymethylfurfural (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.iso en en_US
dc.publisher Elsevier en_US
dc.subject Acinetobacter oleivorans S27 en_US
dc.subject 5-Hydroxymethyl furfural en_US
dc.subject 2,5-Furan dicarboxylic acid en_US
dc.subject 5-Hydroxymethyl 2-furancarboxylic acid en_US
dc.subject Response Surface Methodology en_US
dc.title Biotransformation of 5-hydroxymethylfurfural by Acinetobacter oleivorans S27 for the synthesis of furan derivatives en_US
dc.type Article en_US


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  • 2019
    Research articles authored by NIIST researchers published in 2019

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