Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3367
Title: Biotransformation of 5-hydroxymethylfurfural by Acinetobacter oleivorans S27 for the synthesis of furan derivatives
Authors: Godan, T K
Rajesh, R O
Loreni, P C
Rai, A K
Sahoo, D
Pandey, A
Binod, P
Keywords: Acinetobacter oleivorans S27
5-Hydroxymethyl furfura
2,5-Furan dicarboxylic acid
5-Hydroxymethyl 2-furancarboxylic acid
Response Surface Methodology
Issue Date: Jul-2019
Publisher: Elsevier
Citation: Bioresource Technology; 282:88-93
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 5hydroxymethyl-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.
URI: https://www.sciencedirect.com/science/article/pii/S0960852419303402?via%3Dihub
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Appears in Collections:2019

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