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
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