| 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 |