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 |