| Home > Publications database > Ionic Liquides as Performance Additives for Electroenzymatic Syntheses > print |
| 001 | 5895 | ||
| 005 | 20180208233523.0 | ||
| 024 | 7 | _ | |2 pmid |a pmid:19777513 |
| 024 | 7 | _ | |2 DOI |a 10.1002/chem.200901046 |
| 024 | 7 | _ | |2 WOS |a WOS:000271992100033 |
| 037 | _ | _ | |a PreJuSER-5895 |
| 041 | _ | _ | |a eng |
| 082 | _ | _ | |a 540 |
| 084 | _ | _ | |2 WoS |a Chemistry, Multidisciplinary |
| 100 | 1 | _ | |0 P:(DE-Juel1)VDB39656 |a Kohlmann, C. |b 0 |u FZJ |
| 245 | _ | _ | |a Ionic Liquides as Performance Additives for Electroenzymatic Syntheses |
| 260 | _ | _ | |a Weinheim |b Wiley-VCH |c 2009 |
| 300 | _ | _ | |a 11692 - 11700 |
| 336 | 7 | _ | |0 PUB:(DE-HGF)16 |2 PUB:(DE-HGF) |a Journal Article |
| 336 | 7 | _ | |2 DataCite |a Output Types/Journal article |
| 336 | 7 | _ | |0 0 |2 EndNote |a Journal Article |
| 336 | 7 | _ | |2 BibTeX |a ARTICLE |
| 336 | 7 | _ | |2 ORCID |a JOURNAL_ARTICLE |
| 336 | 7 | _ | |2 DRIVER |a article |
| 440 | _ | 0 | |0 1226 |a Chemistry-a European Journal |v 15 |x 0947-6539 |y 43 |
| 500 | _ | _ | |a The authors thank Lilia Harter, Stephanie Corsten and Zubeyda Dogan for excellent work in the lab and the GK 1166 "BioNoCo" for fruitful discussion and funding. L.G. thanks the cluster of excellence "Tailor-Made Fuels from Biomass" (TMFB) for support. |
| 520 | _ | _ | |a Electroenzymatic syntheses combine oxidoreductase-catalysed reactions with electrochemical reactant supply. The use of ionic liquids as performance additives can contribute to overcoming existing limitations of these syntheses. Here, we report on the influence of different water-miscible ionic liquids on critical parameters such as conductivity, biocatalyst activity and stability or substrate solubility for three typical electroenzymatic syntheses. In these investigations promising ionic liquids were identified and have been used as additives for batch electrolyses on preparative scale for the three electroenzymatic systems. It was possible to improve the space-time-yield for the electrochemical regeneration of NADPH by a factor of three. For an amino acid oxidase catalysed resolution of a methionine racemate with ferrocene-mediated electrochemical regeneration of the enzyme-bound cofactor FAD a 50% increase in space time yield and 140% increase in catalyst utilisation (TTN) were achieved. Furthermore, for the chloroperoxidase-catalysed synthesis of (R)-phenylmethylsulfoxide with electrochemical generation of the required cosubstrate H2O2 the space time yield and the catalyst utilisation were improved by a factor of up to 4.2 depending on the ionic liquids used. |
| 536 | _ | _ | |0 G:(DE-Juel1)FUEK410 |2 G:(DE-HGF) |a Biotechnologie |c PBT |x 0 |
| 588 | _ | _ | |a Dataset connected to Web of Science, Pubmed |
| 650 | _ | 2 | |2 MeSH |a Amino Acid Oxidoreductases: metabolism |
| 650 | _ | 2 | |2 MeSH |a Biocatalysis |
| 650 | _ | 2 | |2 MeSH |a Chloride Peroxidase: metabolism |
| 650 | _ | 2 | |2 MeSH |a Electrochemical Techniques |
| 650 | _ | 2 | |2 MeSH |a Flavin-Adenine Dinucleotide: metabolism |
| 650 | _ | 2 | |2 MeSH |a Hydrogen Peroxide: metabolism |
| 650 | _ | 2 | |2 MeSH |a Ionic Liquids: chemistry |
| 650 | _ | 2 | |2 MeSH |a NADP: metabolism |
| 650 | _ | 2 | |2 MeSH |a Solubility |
| 650 | _ | 7 | |0 0 |2 NLM Chemicals |a Ionic Liquids |
| 650 | _ | 7 | |0 146-14-5 |2 NLM Chemicals |a Flavin-Adenine Dinucleotide |
| 650 | _ | 7 | |0 53-59-8 |2 NLM Chemicals |a NADP |
| 650 | _ | 7 | |0 7722-84-1 |2 NLM Chemicals |a Hydrogen Peroxide |
| 650 | _ | 7 | |0 EC 1.11.1.10 |2 NLM Chemicals |a Chloride Peroxidase |
| 650 | _ | 7 | |0 EC 1.4.- |2 NLM Chemicals |a Amino Acid Oxidoreductases |
| 650 | _ | 7 | |2 WoSType |a J |
| 653 | 2 | 0 | |2 Author |a biocatalysis |
| 653 | 2 | 0 | |2 Author |a biotechnology |
| 653 | 2 | 0 | |2 Author |a electroenzymatic synthesis |
| 653 | 2 | 0 | |2 Author |a ionic liquids |
| 653 | 2 | 0 | |2 Author |a sustainable chemistry |
| 700 | 1 | _ | |0 P:(DE-HGF)0 |a Greiner, L. |b 1 |
| 700 | 1 | _ | |0 P:(DE-HGF)0 |a Leitner, W. |b 2 |
| 700 | 1 | _ | |0 P:(DE-Juel1)129071 |a Wandrey, C. |b 3 |u FZJ |
| 700 | 1 | _ | |0 P:(DE-Juel1)VDB978 |a Lütz, S. |b 4 |u FZJ |
| 773 | _ | _ | |0 PERI:(DE-600)1478547-x |a 10.1002/chem.200901046 |g Vol. 15, p. 11692 - 11700 |p 11692 - 11700 |q 15<11692 - 11700 |t Chemistry |v 15 |x 0947-6539 |y 2009 |
| 856 | 7 | _ | |u http://dx.doi.org/10.1002/chem.200901046 |
| 909 | C | O | |o oai:juser.fz-juelich.de:5895 |p VDB |
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| 914 | 1 | _ | |y 2009 |
| 915 | _ | _ | |0 StatID:(DE-HGF)0010 |a JCR/ISI refereed |
| 915 | _ | _ | |0 StatID:(DE-HGF)0030 |2 StatID |a Peer review |
| 920 | 1 | _ | |0 I:(DE-Juel1)VDB56 |g IBT |k IBT-2 |l Biotechnologie 2 |x 0 |z ab 31.10.10 weitergeführt IBG-1 |
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| 980 | _ | _ | |a UNRESTRICTED |
| 981 | _ | _ | |a I:(DE-Juel1)IBG-1-20101118 |
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