Toward Advanced Ionic Liquids. Polar, Enzyme-friendly Solvents for Biocatalysis
Ionic liquids, also called molten salt, are mixtures of cations and anions that melt below 100℃. Typical ionic liquids are dialkylimidazolium cations with weakly coordinating anions such as (MeOSO₃) or (PF∧6). Advanced ionic liquids such as choline citrate have biodegradable, less expensive, and les...
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| Published in | Biotechnology and bioprocess engineering Vol. 15; no. 1; pp. 40 - 53 |
|---|---|
| Main Authors | , , |
| Format | Journal Article |
| Language | English |
| Published |
Heidelberg
The Korean Society for Biotechnology and Bioengineering
01.02.2010
Springer Nature B.V 한국생물공학회 |
| Subjects | |
| Online Access | Get full text |
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| Abstract | Ionic liquids, also called molten salt, are mixtures of cations and anions that melt below 100℃. Typical ionic liquids are dialkylimidazolium cations with weakly coordinating anions such as (MeOSO₃) or (PF∧6). Advanced ionic liquids such as choline citrate have biodegradable, less expensive, and less toxic anions and cations. Deep eutectic solvents are also included in the advanced ionic liquids. Deep eutectic solvents are mixtures of salts such as choline chloride and uncharged hydrogen bond donors such as urea, oxalic acid, or glycerol. For example, a mixture of choline chloride and urea in 1:2 molar ratio liquefies to form a deep eutectic solvent. Their properties are similar to those of ionic liquids. Water-miscible ionic liquids as cosolvents with water enhance the solubility of substrates or products. Although traditional water-miscible organic solvents also enhance solubility, they often inactivate enzymes, while ionic liquids do not. The enhanced solubility of substrates can increase the rate of reaction and often increases the regio- or enantioselectivity. Ionic liquids can also be solvents for non-aqueous reactions. In these cases, they are especially suited to dissolve polar substrates. Polar organic solvent alternatives inactivate enzymes, but ionic liquids do not even when they have similar polarities. Besides their solubility properties, ionic liquids and deep eutectic solvents may be greener than organic solvents because ionic liquids are nonvolatile, and can be made from nontoxic components. This review covers selected examples of enzyme catalyzed reaction in ionic liquids that demonstrate their advantages and unique properties, and point out opportunities for new applications. Most examples involve hydrolases, but oxidoreductases and even whole cell reactions have been reported in ionic liquids. |
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| AbstractList | Ionic liquids, also called molten salts, are mixtures of cations and anions that melt below 100°C. Typical ionic liquids are dialkylimidazolium cations with weakly coordinating anions such as (MeOSO
3
) or (PF
6
). Advanced ionic liquids such as choline citrate have biodegradable, less expensive, and less toxic anions and cations. Deep eutectic solvents are also included in the advanced ionic liquids. Deep eutectic solvents are mixtures of salts such as choline chloride and uncharged hydrogen bond donors such as urea, oxalic acid, or glycerol. For example, a mixture of choline chloride and urea in 1:2 molar ratio liquefies to form a deep eutectic solvent. Their properties are similar to those of ionic liquids. Water-miscible ionic liquids as cosolvents with water enhance the solubility of substrates or products. Although traditional water-miscible organic solvents also enhance solubility, they often inactivate enzymes, while ionic liquids do not. The enhanced solubility of substrates can increase the rate of reaction and often increases the regioor enantioselectivity. Ionic liquids can also be solvents for non-aqueous reactions. In these cases, they are especially suited to dissolve polar substrates. Polar organic solvent alternatives inactivate enzymes, but ionic liquids do not even when they have similar polarities. Besides their solubility properties, ionic liquids and deep eutectic solvents may be greener than organic solvents because ionic liquids are nonvolatile, and can be made from nontoxic components. This review covers selected examples of enzyme catalyzed reaction in ionic liquids that demonstrate their advantages and unique properties, and point out opportunities for new applications. Most examples involve hydrolases, but oxidoreductases and even whole cell reactions have been reported in ionic liquids. Ionic liquids, also called molten salts, are mixtures of cations and anions that melt below 100 °C. Typical ionic liquids are dialkylimidazolium cations with weakly coordinating anions such as [MeOSO3] or [PF6]. Advanced ionic liquids such as choline citrate have biodegradable, less expensive and less toxic anions and cations. Deep eutectic solvents are also included in the advanced ionic liquids. Deep eutectic solvents are mixtures of salts such as choline chloride and uncharged hydrogen bond donors such as urea, oxalic acid, or glycerol. For example, a mixture of choline chloride and urea in 1:2 molar ratio liquifies to form a deep eutectic solvent. Their properties are similar to those of ionic liquids. Water-miscible ionic liquids as cosolvents with water enhance the solubility of substrates or products. Although traditional water-miscible organic solvents also enhance solubility, they often inactivate enzymes, while ionic liquids do not. The enhanced solubility of substrates can increase the rate of reaction and often increases the regio- or enantioselectivity. Ionic liquids can also be solvents for non-aqueous reactions. In these cases, they are especially suited to dissolve polar substrates. Polar organic solvent alternatives inactivate enzymes, but ionic liquids do not even when they have similar polarities. Besides their solubility properties, ionic liquids and deep eutectic solvents may be greener than organic solvents because ionic liquids are non-volatile and can be made from non-toxic components. This review covers selected examples of enzyme catalyzed reaction ionic liquids that demonstrate their advantages and unique properties and point out opportunities for new applications. Most examples involve hydrolases, but oxidoreductases and even whole cell reactions have been reported in ionic liquids.Ionic liquids, also called molten salts, are mixtures of cations and anions that melt below 100 °C. Typical ionic liquids are dialkylimidazolium cations with weakly coordinating anions such as [MeOSO3] or [PF6]. Advanced ionic liquids such as choline citrate have biodegradable, less expensive and less toxic anions and cations. Deep eutectic solvents are also included in the advanced ionic liquids. Deep eutectic solvents are mixtures of salts such as choline chloride and uncharged hydrogen bond donors such as urea, oxalic acid, or glycerol. For example, a mixture of choline chloride and urea in 1:2 molar ratio liquifies to form a deep eutectic solvent. Their properties are similar to those of ionic liquids. Water-miscible ionic liquids as cosolvents with water enhance the solubility of substrates or products. Although traditional water-miscible organic solvents also enhance solubility, they often inactivate enzymes, while ionic liquids do not. The enhanced solubility of substrates can increase the rate of reaction and often increases the regio- or enantioselectivity. Ionic liquids can also be solvents for non-aqueous reactions. In these cases, they are especially suited to dissolve polar substrates. Polar organic solvent alternatives inactivate enzymes, but ionic liquids do not even when they have similar polarities. Besides their solubility properties, ionic liquids and deep eutectic solvents may be greener than organic solvents because ionic liquids are non-volatile and can be made from non-toxic components. This review covers selected examples of enzyme catalyzed reaction ionic liquids that demonstrate their advantages and unique properties and point out opportunities for new applications. Most examples involve hydrolases, but oxidoreductases and even whole cell reactions have been reported in ionic liquids. Ionic liquids, also called molten salts, are mixtures of cations and anions that melt below 100oC. Typical ionic liquids are dialkylimidazolium cations with weakly coordinating anions such as (MeOSO3) or (PF6). Advanced ionic liquids such as choline citrate have biodegradable, less expensive, and less toxic anions and cations. Deep eutectic solvents are also included in the advanced ionic liquids. Deep eutectic solvents are mixtures of salts such as choline chloride and uncharged hydrogen bond donors such as urea, oxalic acid, or glycerol. For example, a mixture of choline chloride and urea in 1:2 molar ratio liquefies to form a deep eutectic solvent. Their properties are similar to those of ionic liquids. Water-miscible ionic liquids as cosolvents with water enhance the solubility of substrates or products. Although traditional water-miscible organic solvents also enhance solubility, they often inactivate enzymes, while ionic liquids do not. The enhanced solubility of substrates can increase the rate of reaction and often increases the regioor enantioselectivity. Ionic liquids can also be solvents for non-aqueous reactions. In these cases, they are especially suited to dissolve polar substrates. Polar organic solvent alternatives inactivate enzymes, but ionic liquids do not even when they have similar polarities. Besides their solubility properties, ionic liquids and deep eutectic solvents may be greener than organic solvents because ionic liquids are nonvolatile, and can be made from nontoxic components. This review covers selected examples of enzyme catalyzed reaction in ionic liquids that demonstrate their advantages and unique properties, and point out opportunities for new applications. Most examples involve hydrolases, but oxidoreductases and even whole cell reactions have been reported in ionic liquids. KCI Citation Count: 158 Ionic liquids, also called molten salts, are mixtures of cations and anions that melt below 100°C. Typical ionic liquids are dialkylimidazolium cations with weakly coordinating anions such as (MeOSO^sub 3^) or (PF^sub 6^). Advanced ionic liquids such as choline citrate have biodegradable, less expensive, and less toxic anions and cations. Deep eutectic solvents are also included in the advanced ionic liquids. Deep eutectic solvents are mixtures of salts such as choline chloride and uncharged hydrogen bond donors such as urea, oxalic acid, or glycerol. For example, a mixture of choline chloride and urea in 1:2 molar ratio liquefies to form a deep eutectic solvent. Their properties are similar to those of ionic liquids. Water-miscible ionic liquids as cosolvents with water enhance the solubility of substrates or products. Although traditional water-miscible organic solvents also enhance solubility, they often inactivate enzymes, while ionic liquids do not. The enhanced solubility of substrates can increase the rate of reaction and often increases the regioor enantioselectivity. Ionic liquids can also be solvents for non-aqueous reactions. In these cases, they are especially suited to dissolve polar substrates. Polar organic solvent alternatives inactivate enzymes, but ionic liquids do not even when they have similar polarities. Besides their solubility properties, ionic liquids and deep eutectic solvents may be greener than organic solvents because ionic liquids are nonvolatile, and can be made from nontoxic components. This review covers selected examples of enzyme catalyzed reaction in ionic liquids that demonstrate their advantages and unique properties, and point out opportunities for new applications. Most examples involve hydrolases, but oxidoreductases and even whole cell reactions have been reported in ionic liquids.[PUBLICATION ABSTRACT] Ionic liquids, also called molten salt, are mixtures of cations and anions that melt below 100℃. Typical ionic liquids are dialkylimidazolium cations with weakly coordinating anions such as (MeOSO₃) or (PF∧6). Advanced ionic liquids such as choline citrate have biodegradable, less expensive, and less toxic anions and cations. Deep eutectic solvents are also included in the advanced ionic liquids. Deep eutectic solvents are mixtures of salts such as choline chloride and uncharged hydrogen bond donors such as urea, oxalic acid, or glycerol. For example, a mixture of choline chloride and urea in 1:2 molar ratio liquefies to form a deep eutectic solvent. Their properties are similar to those of ionic liquids. Water-miscible ionic liquids as cosolvents with water enhance the solubility of substrates or products. Although traditional water-miscible organic solvents also enhance solubility, they often inactivate enzymes, while ionic liquids do not. The enhanced solubility of substrates can increase the rate of reaction and often increases the regio- or enantioselectivity. Ionic liquids can also be solvents for non-aqueous reactions. In these cases, they are especially suited to dissolve polar substrates. Polar organic solvent alternatives inactivate enzymes, but ionic liquids do not even when they have similar polarities. Besides their solubility properties, ionic liquids and deep eutectic solvents may be greener than organic solvents because ionic liquids are nonvolatile, and can be made from nontoxic components. This review covers selected examples of enzyme catalyzed reaction in ionic liquids that demonstrate their advantages and unique properties, and point out opportunities for new applications. Most examples involve hydrolases, but oxidoreductases and even whole cell reactions have been reported in ionic liquids. Ionic liquids, also called molten salts, are mixtures of cations and anions that melt below 100 °C. Typical ionic liquids are dialkylimidazolium cations with weakly coordinating anions such as [MeOSO 3 ] or [PF 6 ]. Advanced ionic liquids such as choline citrate have biodegradable, less expensive and less toxic anions and cations. Deep eutectic solvents are also included in the advanced ionic liquids. Deep eutectic solvents are mixtures of salts such as choline chloride and uncharged hydrogen bond donors such as urea, oxalic acid, or glycerol. For example, a mixture of choline chloride and urea in 1:2 molar ratio liquifies to form a deep eutectic solvent. Their properties are similar to those of ionic liquids. Water-miscible ionic liquids as cosolvents with water enhance the solubility of substrates or products. Although traditional water-miscible organic solvents also enhance solubility, they often inactivate enzymes, while ionic liquids do not. The enhanced solubility of substrates can increase the rate of reaction and often increases the regio- or enantioselectivity. Ionic liquids can also be solvents for non-aqueous reactions. In these cases, they are especially suited to dissolve polar substrates. Polar organic solvent alternatives inactivate enzymes, but ionic liquids do not even when they have similar polarities. Besides their solubility properties, ionic liquids and deep eutectic solvents may be greener than organic solvents because ionic liquids are non-volatile and can be made from non-toxic components. This review covers selected examples of enzyme catalyzed reaction ionic liquids that demonstrate their advantages and unique properties and point out opportunities for new applications. Most examples involve hydrolases, but oxidoreductases and even whole cell reactions have been reported in ionic liquids. |
| Author | Kazlauskas, Romas, University of Minnesota, Minneapolis, MN, USA Gorke, Johnathan, University of Minnesota, Minneapolis, MN, USA Srienc, Friedrich, University of Minnesota, Minneapolis, MN, USA |
| AuthorAffiliation | b BioTechnology Institute, 240 Gortner Laboratory, University of Minnesota, 1479 Gortner Ave., Saint Paul, MN 55108, USA c Department of Chemical Engineering and Materials Science, University of Minnesota, 151 Amundson Hall, 421 Washington Ave. SE, Minneapolis, MN 55455, USA a Department of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota, 140 Gortner Laboratory, 1479 Gortner Ave., Saint Paul, MN 55108, USA |
| AuthorAffiliation_xml | – name: c Department of Chemical Engineering and Materials Science, University of Minnesota, 151 Amundson Hall, 421 Washington Ave. SE, Minneapolis, MN 55455, USA – name: a Department of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota, 140 Gortner Laboratory, 1479 Gortner Ave., Saint Paul, MN 55108, USA – name: b BioTechnology Institute, 240 Gortner Laboratory, University of Minnesota, 1479 Gortner Ave., Saint Paul, MN 55108, USA |
| Author_xml | – sequence: 1 fullname: Gorke, Johnathan, University of Minnesota, Minneapolis, MN, USA – sequence: 2 fullname: Srienc, Friedrich, University of Minnesota, Minneapolis, MN, USA – sequence: 3 fullname: Kazlauskas, Romas, University of Minnesota, Minneapolis, MN, USA |
| BackLink | https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART001422583$$DAccess content in National Research Foundation of Korea (NRF) |
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| Cites_doi | 10.1021/la803118q 10.1080/10242420500090219 10.1039/b608920h 10.1016/j.jbiotec.2007.04.001 10.1039/b714674d 10.1039/b505479f 10.1002/bit.260440120 10.1039/b716317g 10.1016/S0040-4039(02)02889-7 10.1023/A:1021305229969 10.1055/s-2007-967951 10.1039/b716602h 10.1016/S0958-1669(03)00100-9 10.1002/(SICI)1097-0290(20000720)69:2<227::AID-BIT12>3.0.CO;2-0 10.1002/adsc.200700303 10.1021/cr050946x 10.1016/S1381-1177(03)00147-4 10.1007/s10529-005-0023-y 10.2116/analsci.24.1231 10.1016/j.molcatb.2007.11.010 10.1039/b600930a 10.1039/b801489b 10.1039/b110008b 10.1007/s10529-006-0006-7 10.1016/j.tetlet.2004.10.015 10.1002/chir.20132 10.1016/j.eurpolymj.2005.12.021 10.1126/science.6729453 10.1039/b503010b 10.1039/b612106c 10.1016/j.procbio.2007.07.004 10.1080/10242420500292401 10.1021/ic00133a078 10.1002/(SICI)1099-0518(19990501)37:9<1265::AID-POLA6>3.0.CO;2-I 10.1023/A:1011697609756 10.1007/s10529-004-5087-6 10.1016/j.jbiotec.2006.01.023 10.1039/b514999a 10.1007/BF00127422 10.1002/chir.20078 10.1016/j.tetlet.2006.05.072 10.1016/j.tet.2003.11.063 10.1039/b009389k 10.1002/cbic.200800025 10.1039/b412848f 10.1016/j.tetasy.2007.10.010 10.1016/j.enzmictec.2005.02.014 10.1021/bp000094g 10.1021/ja048266j 10.1016/j.jbiotec.2005.12.004 10.1016/j.enzmictec.2005.11.002 10.1002/chem.200601043 10.1016/j.tetasy.2006.09.009 10.1039/b419172b 10.1016/j.enzmictec.2007.03.017 10.1021/jp0671998 10.1016/j.molcatb.2003.12.008 10.1039/b210714g 10.1002/cbic.200700128 10.1246/cl.2001.262 10.1039/b410467f 10.1002/bit.1177 10.1002/app.11511 10.1039/b600397d 10.1002/bit.21068 10.1002/anie.200460241 10.1295/polymj.34.94 10.1039/b716369j 10.1016/j.jbiotec.2006.10.001 10.1042/BA20040056 10.1016/j.jbiotec.2008.07.1133 10.1039/b513062j 10.1016/j.jbiotec.2008.08.008 10.1016/j.procbio.2008.05.001 10.1021/jo015761e 10.1021/ja028557x 10.1351/pac200072122275 10.1002/anie.200703305 10.1016/S1381-1177(02)00294-1 10.1016/S0958-1669(02)00353-1 10.1002/bit.21866 10.1002/bit.21534 10.1016/j.tetlet.2007.04.049 10.1021/bk-2003-0856.ch017 10.1021/ma061196b 10.1016/S0957-4166(03)00578-0 10.1039/b405712k 10.1021/ol015824f 10.1021/ol0511169 10.1016/j.procbio.2008.11.007 10.1039/b813529k 10.1021/ol006732d 10.1021/op0255231 10.1016/j.jbiotec.2007.11.001 10.1039/B813529K 10.1021/bk-2010-1038.ch014 10.1039/B513062J 10.1039/B600930A 10.1039/B600397D 10.1039/B612106C 10.1016/j.bbagen.2006.10.004 10.1039/B714674D |
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| References | Hongwei, Jinchuan, Bun (CR50) 2005; 17 Shipovskov, Gunaratne, Seddon, Stephens (CR86) 2008; 10 Uyama, Takamoto, Kobayashi (CR63) 2002; 34 Walden (CR1) 1914; 1800 Rumbau, Marcilla, Ochoteco, Pomposo, Mecerreyes (CR81) 2006; 39 Kragl, Eckstein, Kaftzik (CR9) 2002; 13 Nara, Harjani, Salunkhe, Mane, Wadgaonkar (CR64) 2003; 44 CR33 de Gonzalo, Lavandera, Durchschein, Wurm, Faber, Kroutil (CR90) 2007; 18 Zhao, Jackson, Song, Olubajo (CR31) 2006; 17 Yang, Pan (CR11) 2005; 37 Ganske, Bornscheuer (CR94) 2006; 28 Lou, Zong, Smith, Wu, Wang (CR27) 2006; 8 Wehofsky, Wespe, Cerovsky, Pech, Hoess, Rudolph, Bordusa (CR30) 2008; 9 Laszlo, Compton (CR70) 2001; 75 Sheldon, Madeira Lau, Sorgedrager, van Rantwijk, Seddon (CR7) 2002; 4 van Rantwijk, Sheldon (CR10) 2007; 107 Itoh, Akasaki, Kudo, Shirakami (CR15) 2001; 30 He, Zhou, Wang, Zu (CR95) 2009; 44 Marcilla, de Geus, Mecerreyes, Duxbury, Koning, Heise (CR66) 2006; 42 Lou, Zong, Smith (CR96) 2006; 8 Liu, Lou, Zong, Xu, Hong, Wu (CR26) 2005; 23 Lee, Nguyen, Koo, Ha (CR55) 2008; 43 Gamba, Lapis, Dupont (CR47) 2008; 350 Moniruzzaman, Kamiya, Goto (CR79) 2009; 25 Kaftzik, Neumann, Kula, Kragl, Rogers, Seddon (CR73) 2003 Madeira Lau, van Rantwijk, Seddon, Sheldon (CR13) 2000; 2 Nakashima, Maruyama, Kamiya, Goto (CR42) 2006; 4 Docherty, Kulpa (CR20) 2005; 7 Gorke, Okrasa, Louwagie, Kazlauskas, Srienc (CR67) 2007; 132 Sanfilippo, D’Antona, Nicolosi (CR83) 2004; 26 Chiappe, Neri, Pieraccini (CR84) 2006; 47 Pfruender, Amidjojo, Kragl, Weuster-Botz (CR98) 2004; 43 Xin, Zhao, Zhao, Zheng, Sheng, Xia, Li (CR51) 2005; 23 Lutz-Wahl, Trost, Wagner, Manns, Fischer (CR87) 2006; 124 Welton (CR8) 1999; 99 Malhotra, Zhao (CR53) 2005; 17 Shah, Gupta (CR71) 2007; 1770 Wasserscheid, Welton (CR3) 2008 Park, Kazlauskas (CR14) 2001; 66 Chiappe, Leandri, Hammock, Morisseau (CR38) 2007; 9 van Rantwijk, Secundo, Sheldon (CR40) 2006; 8 Dong, Cao, Li, Han, You, Shen (CR62) 1999; 37 Chin, Wheeler, Klibanov (CR39) 1994; 44 Roberts, Seago, Carey, Freer, Preston, Lye (CR24) 2004; 6 Itoh, Nishimura, Ouchi, Hayase (CR44) 2003; 26 Lozano, De Diego, Carrié, Vaultier, Iborra (CR43) 2001; 23 Abbott, Harris, Ryder (CR19) 2007; 111 Cull, Holbrey, Vargas-Mora, Seddon, Lye (CR12) 2000; 69 Persson, Bornscheuer (CR72) 2003; 22 Lee, Ha, Hiep, Chang, Koo (CR57) 2008; 133 CR68 Itoh, Matsushita, Abe, Han, Wada, Hayase, Kawatsura, Takai, Morimoto, Hirose (CR52) 2006; 12 Shi, Zong, Meng, Guo (CR88) 2005; 26 Zaks, Klibanov (CR22) 1984; 224 Chiappe, Leandri, Lucchesi, Pieraccini, Hammock, Morisseau (CR37) 2004; 27 Liu, Janssen, van Rantwijk, Sheldon (CR54) 2005; 7 Hinckley, Mozhaev, Budde, Khmelnitsky (CR76) 2002; 24 Park, Kazlauskas (CR5) 2003; 14 Kumar, Jain, Chauhan (CR78) 2007; 3 Okrasa, Guibé-Jampel, Therisod (CR80) 2003; 14 Lee, Dang, Ha, Chang, Koo (CR56) 2008; 99 Gorke, Srienc, Kazlauskas (CR28) 2008; 14 Pfruender, Jones, Weuster-Botz (CR99) 2006; 124 Wallert, Drauz, Grayson, Gröger, Dominguez de Maria, Bolm (CR29) 2005; 7 Lou, Zong, Wu (CR25) 2005; 41 Lang, Kamrat, Nidetzky (CR34) 2006; 95 Cornmell, Winder, Schuler, Goodacre, Stephens (CR97) 2008; 10 Wilkes, Levisky, Wilson, Hussey (CR2) 1982; 21 Zhao, Baker, Song, Olubajo, Crittlea, Peters (CR59) 2008; 10 Ha, Lan, Lee, Hwang, Koo (CR46) 2007; 41 Vafiadi, Topakas, Nahmias, Faulds, Christakopoulos (CR32) 2009; 139 Mischitz, Faber, Willetts (CR35) 1995; 17 Pinto, Saraiva, Lima (CR6) 2008; 24 Schofer, Kaftzik, Kragl, Wasserscheid (CR48) 2001; 5 Abbott, Boothby, Capper, Davies, Rasheed (CR18) 2004; 126 Karboune, Archelas, Baratti (CR36) 2006; 39 Kaar, Jesionowski, Berberich, Moulton, Russell (CR65) 2003; 125 Fujita, Nakamura, Igarashi, Samejima, Ohno (CR89) 2009; 11 Walker, Bruce (CR92) 2004; 60 Nakashima, Maruyama, Kamiya, Goto (CR41) 2005; 14 Tavares, Rodriguez, Macedo (CR85) 2008; 101 Erbeldinger, Mesiano, Russell (CR16) 2000; 16 Seddon, Stark, Torres (CR21) 2000; 72 Li, Lou, Smith, Zong, Wu, Wang (CR60) 2006; 8 Abbott, Capper, Davies, Rasheed, Tambyrajah (CR17) 2003; 1 Abe, Kude, Hayase, Kawatsura, Tsunashima, Itoh (CR45) 2008; 51 Walker, Bruce (CR93) 2004; 22 Okochi, Nakagawa, Kobayashi, Hayashi, Furusaki, Honda (CR91) 2007; 128 Dominquez de María (CR4) 2008; 47 Ganske, Bornscheuer (CR58) 2005; 7 Tee, Roccatano, Stolte, Arning, Jastorff, Schwaneberg (CR75) 2008; 10 Chefson, Auclair (CR74) 2007; 8 Alvarez, Manolache, Denes (CR82) 2003; 88 Xing, Li, Ming, Ran (CR69) 2007; 48 Kamal, Chouhan (CR49) 2004; 45 Machado, Saraiva (CR77) 2005; 27 Kim, Song, Choi, Kim (CR23) 2001; 3 Katsoura, Polydera, Katapodis, Kolisis, Stamatis (CR61) 2007; 42 S. J. Nara (3079_CR64) 2003; 44 Q. Liu (3079_CR54) 2005; 7 N. Wehofsky (3079_CR30) 2008; 9 C. Vafiadi (3079_CR32) 2009; 139 M. Lang (3079_CR34) 2006; 95 S. Lutz-Wahl (3079_CR87) 2006; 124 X. Shi (3079_CR88) 2005; 26 U. Kragl (3079_CR9) 2002; 13 A. P. Abbott (3079_CR18) 2004; 126 M. Okochi (3079_CR91) 2007; 128 J. He (3079_CR95) 2009; 44 A. Zaks (3079_CR22) 1984; 224 K. Kim (3079_CR23) 2001; 3 R. A. Sheldon (3079_CR7) 2002; 4 J. L. Kaar (3079_CR65) 2003; 125 R. J. Cornmell (3079_CR97) 2008; 10 K. Okrasa (3079_CR80) 2003; 14 S. G. Cull (3079_CR12) 2000; 69 N. Kaftzik (3079_CR73) 2003 W. Y. Lou (3079_CR27) 2006; 8 S. Shah (3079_CR71) 2007; 1770 P. Lozano (3079_CR43) 2001; 23 T. Welton (3079_CR8) 1999; 99 P. C. A. G. Pinto (3079_CR6) 2008; 24 K. Fujita (3079_CR89) 2009; 11 G. Gonzalo de (3079_CR90) 2007; 18 A. J. Walker (3079_CR93) 2004; 22 K. R. Seddon (3079_CR21) 2000; 72 M. Persson (3079_CR72) 2003; 22 C. Chiappe (3079_CR37) 2004; 27 P. Dominquez de María (3079_CR4) 2008; 47 C. Chiappe (3079_CR84) 2006; 47 H. Dong (3079_CR62) 1999; 37 3079_CR68 H. Uyama (3079_CR63) 2002; 34 S. H. Lee (3079_CR56) 2008; 99 F. Rantwijk van (3079_CR10) 2007; 107 Y. Abe (3079_CR45) 2008; 51 S. Karboune (3079_CR36) 2006; 39 W. Lou (3079_CR96) 2006; 8 J. Xin (3079_CR51) 2005; 23 H. Zhao (3079_CR31) 2006; 17 S. H. Ha (3079_CR46) 2007; 41 J. T. Chin (3079_CR39) 1994; 44 Y. Hongwei (3079_CR50) 2005; 17 M. F. Machado (3079_CR77) 2005; 27 A. Chefson (3079_CR74) 2007; 8 S. Shipovskov (3079_CR86) 2008; 10 C. Sanfilippo (3079_CR83) 2004; 26 M. Erbeldinger (3079_CR16) 2000; 16 A. P. Abbott (3079_CR17) 2003; 1 G. Hinckley (3079_CR76) 2002; 24 S. Park (3079_CR5) 2003; 14 T. Itoh (3079_CR44) 2003; 26 C. Chiappe (3079_CR38) 2007; 9 J. A. Laszlo (3079_CR70) 2001; 75 S. V. Malhotra (3079_CR53) 2005; 17 H. Pfruender (3079_CR98) 2004; 43 A. Kamal (3079_CR49) 2004; 45 P. Wasserscheid (3079_CR3) 2008 S. Alvarez (3079_CR82) 2003; 88 P. Walden (3079_CR1) 1914; 1800 W. Lou (3079_CR25) 2005; 41 F. Ganske (3079_CR58) 2005; 7 T. Itoh (3079_CR15) 2001; 30 3079_CR33 H. Pfruender (3079_CR99) 2006; 124 S. H. Lee (3079_CR55) 2008; 43 J. S. Wilkes (3079_CR2) 1982; 21 M. H. Katsoura (3079_CR61) 2007; 42 M. Moniruzzaman (3079_CR79) 2009; 25 J. T. Gorke (3079_CR28) 2008; 14 J. T. Gorke (3079_CR67) 2007; 132 S. H. Lee (3079_CR57) 2008; 133 K. Nakashima (3079_CR42) 2006; 4 M. Gamba (3079_CR47) 2008; 350 R. Marcilla (3079_CR66) 2006; 42 G. Xing (3079_CR69) 2007; 48 K. M. Docherty (3079_CR20) 2005; 7 Z. Yang (3079_CR11) 2005; 37 V. Rumbau (3079_CR81) 2006; 39 K. Nakashima (3079_CR41) 2005; 14 S. H. Schofer (3079_CR48) 2001; 5 F. Rantwijk van (3079_CR40) 2006; 8 X. Li (3079_CR60) 2006; 8 A. J. Walker (3079_CR92) 2004; 60 M. Mischitz (3079_CR35) 1995; 17 A. Kumar (3079_CR78) 2007; 3 S. Park (3079_CR14) 2001; 66 H. Zhao (3079_CR59) 2008; 10 S. Wallert (3079_CR29) 2005; 7 A. P. Abbott (3079_CR19) 2007; 111 A. P. M. Tavares (3079_CR85) 2008; 101 K. L. Tee (3079_CR75) 2008; 10 R. Madeira Lau (3079_CR13) 2000; 2 Y. Liu (3079_CR26) 2005; 23 F. Ganske (3079_CR94) 2006; 28 N. J. Roberts (3079_CR24) 2004; 6 T. Itoh (3079_CR52) 2006; 12 |
| References_xml | – volume: 25 start-page: 977 year: 2009 end-page: 982 ident: CR79 article-title: Biocatalysis in water-in-ionic liquid microemulsions: a case study with horseradish peroxidase publication-title: Langmuir doi: 10.1021/la803118q – volume: 23 start-page: 89 year: 2005 end-page: 95 ident: CR26 article-title: Increased enantioselectivity in the enzymatic hydrolysis of amino acid esters in the ionic liquid 1-butyl-3-methyl-imidazolium tetrafluoroborate publication-title: Biocatal. Bio transform. doi: 10.1080/10242420500090219 – volume: 4 start-page: 3462 year: 2006 end-page: 3467 ident: CR42 article-title: Homogeneous enzymatic reactions in ionic liquids with poly(ethylene glycol)-modified subtilisin publication-title: Org. Biomol. Chem. doi: 10.1039/b608920h – volume: 132 start-page: 306 year: 2007 end-page: 313 ident: CR67 article-title: Enzymatic synthesis of poly(hydroxylalkanoates) in ionic liquids publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2007.04.001 – ident: CR68 – volume: 10 start-page: 117 year: 2008 end-page: 123 ident: CR75 article-title: Ionic liquid effects on the activity of monooxygenase P450 BM-3 publication-title: Green Chem. doi: 10.1039/b714674d – volume: 14 start-page: 4297 year: 2005 end-page: 4299 ident: CR41 article-title: Comb-shaped poly(ethylene glycol)-modified subtilisin carlsberg is soluble and highly active in ionic liquids publication-title: Chem. Commun. doi: 10.1039/b505479f – volume: 99 start-page: 2071 year: 1999 end-page: 2083 ident: CR8 article-title: Room-temperature ionic liquids publication-title: Solvents for synthesis and catalysis. Chem. Rev. – volume: 44 start-page: 140 year: 1994 end-page: 145 ident: CR39 article-title: On protein solubility in organic solvents publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.260440120 – volume: 14 start-page: 1235 year: 2008 end-page: 1237 ident: CR28 article-title: Hydrolase-catalyzed biotransformations in deep eutectic solvents publication-title: Chem. Commun. doi: 10.1039/b716317g – volume: 44 start-page: 1371 year: 2003 end-page: 1373 ident: CR64 article-title: Lipase-catalysed polyester synthesis in 1-butyl-3-methylimidazolium hexafluorophosphate ionic liquid publication-title: Tetrahedron Lett. doi: 10.1016/S0040-4039(02)02889-7 – volume: 24 start-page: 2083 year: 2002 end-page: 2087 ident: CR76 article-title: Oxidative enzymes possess catalytic activity in systems with ionic liquids publication-title: Biotechnol. Lett. doi: 10.1023/A:1021305229969 – volume: 3 start-page: 411 year: 2007 end-page: 414 ident: CR78 article-title: Biomimetic oxidation of veratryl alcohol with H O catalyzed by iron(III) porphyrins and horseradish peroxidase in ionic liquid publication-title: Synlett doi: 10.1055/s-2007-967951 – volume: 10 start-page: 685 year: 2008 end-page: 691 ident: CR97 article-title: Using a biphasic ionic liquid/water reaction system to improve oxygenase-catalysed biotransformation with whole cells publication-title: Green Chem. doi: 10.1039/b716602h – volume: 26 start-page: 982 year: 2005 end-page: 986 ident: CR88 article-title: Catalytic characteristics of horse liver alcohol dehydrogenase in a medium containing ionic liquid [bmim]Cl publication-title: Chin. J. Catal. – volume: 14 start-page: 432 year: 2003 end-page: 437 ident: CR5 article-title: Biocatalysis in ionic liquids — advantages beyond green technology publication-title: Curr. Opin. Biotechnol. doi: 10.1016/S0958-1669(03)00100-9 – volume: 69 start-page: 227 year: 2000 end-page: 233 ident: CR12 article-title: Room-temperature ionic liquids as replacements for organic solvents in multiphase bioprocess operations publication-title: Biotechnol. Bioeng. doi: 10.1002/(SICI)1097-0290(20000720)69:2<227::AID-BIT12>3.0.CO;2-0 – volume: 350 start-page: 160 year: 2008 end-page: 165 ident: CR47 article-title: Supported ionic liquid enzymatic catalysis for the production of biodiesel publication-title: Adv. Synth. Catal. doi: 10.1002/adsc.200700303 – volume: 1770 start-page: 94 year: 2007 end-page: 98 ident: CR71 article-title: Obtaining high transesterification activity for subtilisin in ionic liquids publication-title: Biochim. Biophys. Acta. – volume: 107 start-page: 2757 year: 2007 end-page: 2785 ident: CR10 article-title: Biocatalysis in ionic liquids publication-title: Chem. Rev. doi: 10.1021/cr050946x – volume: 26 start-page: 41 year: 2003 end-page: 45 ident: CR44 article-title: 1-butyl-2,3-dimethylimidazolium tetrafluoroborate: the most desirable ionic liquid solvent for recycling use of enzyme in lipase-catalyzed transesterification using vinyl acetate as acyl donor publication-title: J. Mol. Catal. B: Enzym. doi: 10.1016/S1381-1177(03)00147-4 – volume: 27 start-page: 1233 year: 2005 end-page: 1239 ident: CR77 article-title: Thermal stability and activity regain of horseradish peroxidase in aqueous mixtures of imidazolium-based ionic liquids publication-title: Biotechnol. Lett. doi: 10.1007/s10529-005-0023-y – volume: 24 start-page: 1231 year: 2008 end-page: 1238 ident: CR6 article-title: Oxidoreductase behavior in ionic liquids: a review publication-title: Anal. Sci. doi: 10.2116/analsci.24.1231 – volume: 51 start-page: 81 year: 2008 end-page: 85 ident: CR45 article-title: Design of phosphonium ionic liquids for lipase-catalyzed transesterification publication-title: J. Mol. Catal. B: Enzym. doi: 10.1016/j.molcatb.2007.11.010 – volume: 8 start-page: 509 year: 2006 end-page: 512 ident: CR27 article-title: Impact of ionic liquids on papain: an investigation of structure-function relationships publication-title: Green Chem. doi: 10.1039/b600930a – volume: 10 start-page: 696 year: 2008 end-page: 705 ident: CR59 article-title: Designing enzyme-compatible ionic liquids that can dissolve carbohydrates publication-title: Green Chem. doi: 10.1039/b801489b – volume: 4 start-page: 147 year: 2002 end-page: 151 ident: CR7 article-title: Biocatalysis in ionic liquids publication-title: Green Chem. doi: 10.1039/b110008b – volume: 28 start-page: 465 year: 2006 end-page: 469 ident: CR94 article-title: Growth of Escherichia coli, Pichia pastoris, and Bacillus cereus in the presence of the ionic liquids [BMIM][BF ] and [BMIM][PF ] and organic solvents publication-title: Biotechnol. Lett. doi: 10.1007/s10529-006-0006-7 – volume: 45 start-page: 8801 year: 2004 end-page: 8805 ident: CR49 article-title: Chemoenzymatic synthesis of enantiomerically pure 1,2-diols employing immobilized lipase in the ionic liquid (bmim)PF publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2004.10.015 – volume: 17 start-page: S240 year: 2005 end-page: S242 ident: CR53 article-title: Enantioseparation of the esters of α- -acetylamino acids by lipase in ionic liquid publication-title: Chirality doi: 10.1002/chir.20132 – volume: 42 start-page: 1215 year: 2006 end-page: 1221 ident: CR66 article-title: Enzymatic polyester synthesis in ionic liquids publication-title: Eur. Polym. J. doi: 10.1016/j.eurpolymj.2005.12.021 – volume: 224 start-page: 1249 year: 1984 end-page: 1251 ident: CR22 article-title: Enzymatic catalysis in organic media at 100°C publication-title: Science doi: 10.1126/science.6729453 – volume: 7 start-page: 602 year: 2005 end-page: 605 ident: CR29 article-title: Ionic liquids as additives in the pig liver esterase (PLE) catalysed synthesis of chiral disubstituted malonates publication-title: Green Chem. doi: 10.1039/b503010b – volume: 9 start-page: 162 year: 2007 end-page: 168 ident: CR38 article-title: Effect of ionic liquids on epoxide hydrolase-catalyzed synthesis of chiral 1,2-diols publication-title: Green Chem. doi: 10.1039/b612106c – ident: CR33 – volume: 42 start-page: 1326 year: 2007 end-page: 1334 ident: CR61 article-title: Effect of different reaction parameters on the lipase-catalyzed selective acylation of polyhydroxylated natural compounds in ionic liquids publication-title: Proc. Biochem. doi: 10.1016/j.procbio.2007.07.004 – volume: 23 start-page: 353 year: 2005 end-page: 361 ident: CR51 article-title: Enzymatic resolution of ( )-naproxen in water-saturated ionic liquid publication-title: Biocata. Biotrans. doi: 10.1080/10242420500292401 – volume: 21 start-page: 1263 year: 1982 end-page: 1264 ident: CR2 article-title: Dialkylimidazolium chloroaluminate melts: a new class of room-temperature ionic liquids for electrochemistry, spectroscopy and synthesis publication-title: Inorg. Chem. doi: 10.1021/ic00133a078 – volume: 37 start-page: 1265 year: 1999 end-page: 1275 ident: CR62 article-title: Study on the enzymic polymerization mechanism of lactone and the strategy for improving the degree of polymerization publication-title: J. Polym. Sci. A: Polym. Chem. doi: 10.1002/(SICI)1099-0518(19990501)37:9<1265::AID-POLA6>3.0.CO;2-I – volume: 23 start-page: 1529 year: 2001 end-page: 1533 ident: CR43 article-title: Over-stabilization of lipase B by ionic liquids in ester synthesis publication-title: Biotechnol. Lett. doi: 10.1023/A:1011697609756 – volume: 26 start-page: 1815 year: 2004 end-page: 1819 ident: CR83 article-title: Chloroperoxidase from is active in the presence of an ionic liquid as co-solvent publication-title: Biotechnol. Lett. doi: 10.1007/s10529-004-5087-6 – volume: 124 start-page: 163 year: 2006 end-page: 171 ident: CR87 article-title: Performance of D-amino acid oxidase in presence of ionic liquids publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2006.01.023 – volume: 8 start-page: 147 year: 2006 end-page: 155 ident: CR96 article-title: Use of ionic liquids to improve whole-cell biocatalytic asymmetric reduction of acetyltrimethylsilane for efficient synthesis of enantiopure ( )-1-trimethylsilylethanol publication-title: Green Chem. doi: 10.1039/b514999a – volume: 17 start-page: 893 year: 1995 end-page: 898 ident: CR35 article-title: Isolation of a highly enantioselective epoxide hydrolase from NCIMB 11216 publication-title: Biotechnol. Lett. doi: 10.1007/BF00127422 – volume: 17 start-page: 16 year: 2005 end-page: 21 ident: CR50 article-title: Kinetic resolution of ibuprofen catalyzed by lipase in ionic liquids publication-title: Chirality doi: 10.1002/chir.20078 – volume: 47 start-page: 5089 year: 2006 end-page: 5093 ident: CR84 article-title: Application of hydrophilic ionic liquids as co-solvents in chloroperoxidase catalyzed oxidations publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2006.05.072 – volume: 60 start-page: 561 year: 2004 end-page: 568 ident: CR92 article-title: Combined biological and chemical catalysis in the preparation of oxycodone publication-title: Tetrahedron doi: 10.1016/j.tet.2003.11.063 – volume: 5 start-page: 425 year: 2001 end-page: 426 ident: CR48 article-title: Enzyme catalysis in ionic liquids: lipase catalysed kinetic resolution of 1-phenylethanol with improved enantioselectivity publication-title: Chem. Commun. doi: 10.1039/b009389k – volume: 9 start-page: 1493 year: 2008 end-page: 1499 ident: CR30 article-title: Ionic liquids and proteases: a clean alliance for semisynthesis publication-title: ChembioChem doi: 10.1002/cbic.200800025 – volume: 7 start-page: 39 year: 2005 end-page: 42 ident: CR54 article-title: Room-temperature ionic liquids that dissolve carbohydrates in high concentrations publication-title: Green Chem. doi: 10.1039/b412848f – volume: 18 start-page: 2541 year: 2007 end-page: 2546 ident: CR90 article-title: Asymmetric biocatalytic reduction of ketones using hydroxy-functionalised water-miscible ionic liquids as solvents publication-title: Tetrahedron Asymm. doi: 10.1016/j.tetasy.2007.10.010 – volume: 37 start-page: 19 year: 2005 end-page: 28 ident: CR11 article-title: Ionic liquids: Green solvents for nonaqueous biocatalysis publication-title: Enzym. Microb. Technol. doi: 10.1016/j.enzmictec.2005.02.014 – volume: 16 start-page: 1129 year: 2000 end-page: 1131 ident: CR16 article-title: Enzymatic catalysis of formation of Z-aspartame in ionic liquid — an alternative to enzymatic catalysis in organic solvents publication-title: Biotechnol. Prog. doi: 10.1021/bp000094g – volume: 126 start-page: 9142 year: 2004 end-page: 9147 ident: CR18 article-title: Deep eutectic solvents formed between choline chloride and carboxylic acids: versatile alternatives to ionic liquids publication-title: J. Am. Chem. Soc. doi: 10.1021/ja048266j – volume: 124 start-page: 182 year: 2006 end-page: 190 ident: CR99 article-title: Water immiscible ionic liquids as solvents for whole cell biocatalysis publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2005.12.004 – volume: 39 start-page: 318 year: 2006 end-page: 324 ident: CR36 article-title: Properties of epoxide hydrolase from for the hydrolytic kinetic resolution of epoxides in pure organic media publication-title: Enzym. Microb. Technol. doi: 10.1016/j.enzmictec.2005.11.002 – volume: 12 start-page: 9228 year: 2006 end-page: 9237 ident: CR52 article-title: Increased enantioselectivity and remarkable acceleration of lipase-catalyzed transesterification by using an imidazolium PEG-alkyl sulfate ionic liquid publication-title: Chem. Eur. J. doi: 10.1002/chem.200601043 – volume: 17 start-page: 2491 year: 2006 end-page: 2498 ident: CR31 article-title: Using ionic liquid (EMIM) (CH COO) as an enzyme-’friendly’ co-solvent for resolution of amino acids publication-title: Tetrahedron Asymmetr. doi: 10.1016/j.tetasy.2006.09.009 – volume: 7 start-page: 185 year: 2005 end-page: 189 ident: CR20 article-title: Toxicity and antimicrobial activity of imidazolium and pyridinium ionic liquids publication-title: Green Chem. doi: 10.1039/b419172b – volume: 41 start-page: 480 year: 2007 end-page: 483 ident: CR46 article-title: Lipase-catalyzed biodiesel production from soybean oil in ionic liquids publication-title: Enzym. Microb. Technol. doi: 10.1016/j.enzmictec.2007.03.017 – volume: 111 start-page: 4910 year: 2007 end-page: 4913 ident: CR19 article-title: Application of hole theory to define ionic liquids by their transport properties publication-title: J. Phys. Chem. B doi: 10.1021/jp0671998 – volume: 1800 start-page: 405 year: 1914 end-page: 422 ident: CR1 article-title: Molecular weights and electrical conductivity of several fused salts publication-title: Bull. Acad. Imper. Sci. (St. Petersburg) – volume: 27 start-page: 243 year: 2004 end-page: 248 ident: CR37 article-title: Biocatalysis in ionic liquids: the stereoconvergent hydrolysis of -β-methylstyrene oxide catalyzed by soluble epoxide hydrolase publication-title: J. Mol. Catal. B: Enzym. doi: 10.1016/j.molcatb.2003.12.008 – volume: 1 start-page: 70 year: 2003 end-page: 71 ident: CR17 article-title: Novel solvent properties of choline chloride/urea mixtures publication-title: Chem. Commun doi: 10.1039/b210714g – volume: 8 start-page: 1189 year: 2007 end-page: 1197 ident: CR74 article-title: CYP3A4 activity in the presence of organic cosolvents, ionic liquids, or water-immiscible organic solvents publication-title: ChemBioChem doi: 10.1002/cbic.200700128 – volume: 30 start-page: 262 year: 2001 end-page: 263 ident: CR15 article-title: Lipase-catalyzed enantioselective acylation in the ionic liquid solvent system: reaction of enzyme anchored to the solvent publication-title: Chem. Lett. doi: 10.1246/cl.2001.262 – volume: 22 start-page: 2570 year: 2004 end-page: 2571 ident: CR93 article-title: Cofactor-dependent enzyme catalysis in functionalized ionic solvents publication-title: Chem. Commun. doi: 10.1039/b410467f – volume: 75 start-page: 181 year: 2001 end-page: 186 ident: CR70 article-title: α-Chymotrypsin catalysis in imidazolium-based ionic liquids publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.1177 – volume: 88 start-page: 369 year: 2003 end-page: 379 ident: CR82 article-title: Synthesis of polyaniline using horseradish peroxidase immobilized on plasma-functionalized polyethylene surfaces as initiator publication-title: J. Appl. Polym. Sci. doi: 10.1002/app.11511 – volume: 8 start-page: 538 year: 2006 end-page: 544 ident: CR60 article-title: Efficient regioselective acylation of 1-β-D-arabinofuranosylcytosine catalyzed by lipase in ionic liquid containing systems publication-title: Green Chem. doi: 10.1039/b600397d – volume: 95 start-page: 1093 year: 2006 end-page: 1100 ident: CR34 article-title: Influence of ionic liquid cosolvent on transgalactosylation reactions catalyzed by thermostable β-glycosylhydrolase CelB from publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.21068 – volume: 43 start-page: 4529 year: 2004 end-page: 4531 ident: CR98 article-title: Efficient whole-cell biotransformation in a biphasic ionic liquid/water System publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.200460241 – volume: 34 start-page: 94 year: 2002 end-page: 96 ident: CR63 article-title: Enzymatic synthesis of polyesters in ionic liquids publication-title: Polym. J. doi: 10.1295/polymj.34.94 – volume: 10 start-page: 806 year: 2008 end-page: 810 ident: CR86 article-title: Catalytic activity of laccases in aqueous solutions of ionic liquids publication-title: Green Chem. doi: 10.1039/b716369j – volume: 128 start-page: 376 year: 2007 end-page: 382 ident: CR91 article-title: Enhanced activity of 3-α-hydroxysteroid dehydrogenase by addition of the cosolvent 1-butyl-3-methylimidazolium (L)-lactate in aqueous phase of biphasic systems for reductive production of steroids publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2006.10.001 – volume: 41 start-page: 151 year: 2005 end-page: 156 ident: CR25 article-title: Enzymic asymmetric hydrolysis of D,L- -hydroxyphenylglycine methyl ester in aqueous ionic liquid co-solvent mixtures publication-title: Biotechnol. Appl. Biochem. doi: 10.1042/BA20040056 – volume: 133 start-page: 486 year: 2008 end-page: 489 ident: CR57 article-title: Lipase-catalyzed synthesis of glucose fatty acid ester using ionic liquids mixtures publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2008.07.1133 – volume: 8 start-page: 282 year: 2006 end-page: 286 ident: CR40 article-title: Structure and activity of lipase B in ionic liquids publication-title: Green Chem. doi: 10.1039/b513062j – volume: 139 start-page: 124 year: 2009 end-page: 129 ident: CR32 article-title: Feruloyl esterase-catalysed synthesis of glycerol sinapate using ionic liquids mixtures publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2008.08.008 – year: 2008 ident: CR3 publication-title: Ionic liquids in synthesis – volume: 43 start-page: 1009 year: 2008 end-page: 1012 ident: CR55 article-title: Ultrasound-enhanced lipase activity in the synthesis of sugar ester using ionic liquids publication-title: Proc. Biochem. doi: 10.1016/j.procbio.2008.05.001 – volume: 66 start-page: 8395 year: 2001 end-page: 8401 ident: CR14 article-title: Improved preparation and use of room-temperature ionic liquids in lipasecatalyzed enantio- and regioselective acylations publication-title: J. Org. Chem. doi: 10.1021/jo015761e – volume: 125 start-page: 4125 year: 2003 end-page: 4131 ident: CR65 article-title: Impact of ionic liquid physical properties on lipase activity and stability publication-title: J. Am. Chem. Soc. doi: 10.1021/ja028557x – volume: 72 start-page: 2275 year: 2000 end-page: 2287 ident: CR21 article-title: Influence of chloride, water, and organic solvents on the physical properties of ionic liquids publication-title: Pure Appl. Chem. doi: 10.1351/pac200072122275 – volume: 47 start-page: 6960 year: 2008 end-page: 6968 ident: CR4 article-title: “Nonsolvent” applications of ionic liquids in biotransformations and organocatalysis publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.200703305 – volume: 22 start-page: 21 year: 2003 end-page: 27 ident: CR72 article-title: Increased stability of an esterase from in ionic liquids as compared to organic solvents publication-title: J. Mol. Catal. B: Enzym. doi: 10.1016/S1381-1177(02)00294-1 – volume: 13 start-page: 565 year: 2002 end-page: 571 ident: CR9 article-title: Enzyme catalysis in ionic liquids publication-title: Curr. Opin. Biotechnol. doi: 10.1016/S0958-1669(02)00353-1 – volume: 101 start-page: 201 year: 2008 end-page: 207 ident: CR85 article-title: Ionic liquids as alternative co-solvents for laccase: study of enzyme activity and stability publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.21866 – volume: 99 start-page: 1 year: 2008 end-page: 8 ident: CR56 article-title: Lipase-catalyzed synthesis of fatty acid sugar ester using extremely supersaturated sugar solution in ionic liquids publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.21534 – volume: 48 start-page: 4271 year: 2007 end-page: 4274 ident: CR69 article-title: Peptide bond formation catalyzed by α-chymotrypsin in ionic liquids publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2007.04.049 – start-page: 206 year: 2003 end-page: 211 ident: CR73 article-title: Enzymatic condensation reactions in ionic liquids publication-title: Ionic Liquids as Green Solvents doi: 10.1021/bk-2003-0856.ch017 – volume: 39 start-page: 8547 year: 2006 end-page: 8549 ident: CR81 article-title: Ionic liquid immobilized enzyme for biocatalytic synthesis of conducting polyaniline publication-title: Macromolecules doi: 10.1021/ma061196b – volume: 14 start-page: 2487 year: 2003 end-page: 2490 ident: CR80 article-title: Ionic liquids as a new reaction medium for oxidaseperoxidase-catalyzed sulfoxidation publication-title: Tetrahedron Asymm. doi: 10.1016/S0957-4166(03)00578-0 – volume: 6 start-page: 475 year: 2004 end-page: 482 ident: CR24 article-title: Lipase catalysed resolution of the lotrafiban intermediate 2,3,4,5-tetrahydro-4-methyl-3-oxo-1 -1,4-benzodiazepine-2-acetic acid methyl ester in ionic liquids: comparison to the industrial -butanol process publication-title: Green Chem. doi: 10.1039/b405712k – volume: 3 start-page: 1507 year: 2001 end-page: 1509 ident: CR23 article-title: Biocatalysis in ionic liquids: markedly enhanced enantioselectivity of lipase publication-title: Org. Lett. doi: 10.1021/ol015824f – volume: 7 start-page: 3097 year: 2005 end-page: 3098 ident: CR58 article-title: Lipasecatalyzed glucose fatty acid ester synthesis in ionic liquids publication-title: Org. Lett. doi: 10.1021/ol0511169 – volume: 44 start-page: 316 year: 2009 end-page: 321 ident: CR95 article-title: Microbial reduction of ethyl acetoacetate to ethyl ( )-3-hydroxybutyrate in an ionic liquid containing system publication-title: Proc. Biochem. doi: 10.1016/j.procbio.2008.11.007 – volume: 11 start-page: 351 year: 2009 end-page: 354 ident: CR89 article-title: Biocatalytic oxidation of cellobiose in a hydrated ionic liquid publication-title: Green Chem. doi: 10.1039/b813529k – volume: 2 start-page: 4189 year: 2000 end-page: 4191 ident: CR13 article-title: Lipase-catalyzed reactions in ionic liquids publication-title: Org. Lett. doi: 10.1021/ol006732d – ident: 3079_CR33 doi: 10.1021/op0255231 – volume: 3 start-page: 411 year: 2007 ident: 3079_CR78 publication-title: Synlett doi: 10.1055/s-2007-967951 – volume: 350 start-page: 160 year: 2008 ident: 3079_CR47 publication-title: Adv. Synth. Catal. doi: 10.1002/adsc.200700303 – volume: 75 start-page: 181 year: 2001 ident: 3079_CR70 publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.1177 – volume: 14 start-page: 2487 year: 2003 ident: 3079_CR80 publication-title: Tetrahedron Asymm. doi: 10.1016/S0957-4166(03)00578-0 – volume: 124 start-page: 182 year: 2006 ident: 3079_CR99 publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2005.12.004 – volume: 60 start-page: 561 year: 2004 ident: 3079_CR92 publication-title: Tetrahedron doi: 10.1016/j.tet.2003.11.063 – volume: 22 start-page: 21 year: 2003 ident: 3079_CR72 publication-title: J. Mol. Catal. B: Enzym. doi: 10.1016/S1381-1177(02)00294-1 – volume: 30 start-page: 262 year: 2001 ident: 3079_CR15 publication-title: Chem. Lett. doi: 10.1246/cl.2001.262 – volume: 47 start-page: 5089 year: 2006 ident: 3079_CR84 publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2006.05.072 – volume: 133 start-page: 486 year: 2008 ident: 3079_CR57 publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2007.11.001 – volume: 124 start-page: 163 year: 2006 ident: 3079_CR87 publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2006.01.023 – volume: 8 start-page: 1189 year: 2007 ident: 3079_CR74 publication-title: ChemBioChem doi: 10.1002/cbic.200700128 – volume: 14 start-page: 4297 year: 2005 ident: 3079_CR41 publication-title: Chem. Commun. doi: 10.1039/b505479f – volume: 126 start-page: 9142 year: 2004 ident: 3079_CR18 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja048266j – volume: 17 start-page: S240 year: 2005 ident: 3079_CR53 publication-title: Chirality doi: 10.1002/chir.20132 – volume: 42 start-page: 1326 year: 2007 ident: 3079_CR61 publication-title: Proc. Biochem. doi: 10.1016/j.procbio.2007.07.004 – volume: 4 start-page: 147 year: 2002 ident: 3079_CR7 publication-title: Green Chem. doi: 10.1039/b110008b – volume: 69 start-page: 227 year: 2000 ident: 3079_CR12 publication-title: Biotechnol. Bioeng. doi: 10.1002/(SICI)1097-0290(20000720)69:2<227::AID-BIT12>3.0.CO;2-0 – volume: 17 start-page: 2491 year: 2006 ident: 3079_CR31 publication-title: Tetrahedron Asymmetr. doi: 10.1016/j.tetasy.2006.09.009 – volume: 25 start-page: 977 year: 2009 ident: 3079_CR79 publication-title: Langmuir doi: 10.1021/la803118q – volume: 21 start-page: 1263 year: 1982 ident: 3079_CR2 publication-title: Inorg. Chem. doi: 10.1021/ic00133a078 – volume: 26 start-page: 1815 year: 2004 ident: 3079_CR83 publication-title: Biotechnol. Lett. doi: 10.1007/s10529-004-5087-6 – volume: 2 start-page: 4189 year: 2000 ident: 3079_CR13 publication-title: Org. Lett. doi: 10.1021/ol006732d – volume: 13 start-page: 565 year: 2002 ident: 3079_CR9 publication-title: Curr. Opin. Biotechnol. doi: 10.1016/S0958-1669(02)00353-1 – volume: 39 start-page: 8547 year: 2006 ident: 3079_CR81 publication-title: Macromolecules doi: 10.1021/ma061196b – volume: 224 start-page: 1249 year: 1984 ident: 3079_CR22 publication-title: Science doi: 10.1126/science.6729453 – volume: 17 start-page: 16 year: 2005 ident: 3079_CR50 publication-title: Chirality doi: 10.1002/chir.20078 – volume: 28 start-page: 465 year: 2006 ident: 3079_CR94 publication-title: Biotechnol. Lett. doi: 10.1007/s10529-006-0006-7 – volume: 7 start-page: 3097 year: 2005 ident: 3079_CR58 publication-title: Org. Lett. doi: 10.1021/ol0511169 – volume: 44 start-page: 316 year: 2009 ident: 3079_CR95 publication-title: Proc. Biochem. doi: 10.1016/j.procbio.2008.11.007 – volume: 24 start-page: 2083 year: 2002 ident: 3079_CR76 publication-title: Biotechnol. Lett. doi: 10.1023/A:1021305229969 – volume: 11 start-page: 351 year: 2009 ident: 3079_CR89 publication-title: Green Chem. doi: 10.1039/B813529K – volume: 7 start-page: 39 year: 2005 ident: 3079_CR54 publication-title: Green Chem. doi: 10.1039/b412848f – volume: 23 start-page: 1529 year: 2001 ident: 3079_CR43 publication-title: Biotechnol. Lett. doi: 10.1023/A:1011697609756 – volume: 42 start-page: 1215 year: 2006 ident: 3079_CR66 publication-title: Eur. Polym. J. doi: 10.1016/j.eurpolymj.2005.12.021 – volume: 99 start-page: 2071 year: 1999 ident: 3079_CR8 publication-title: Solvents for synthesis and catalysis. Chem. Rev. – volume: 44 start-page: 1371 year: 2003 ident: 3079_CR64 publication-title: Tetrahedron Lett. doi: 10.1016/S0040-4039(02)02889-7 – volume: 44 start-page: 140 year: 1994 ident: 3079_CR39 publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.260440120 – volume: 23 start-page: 353 year: 2005 ident: 3079_CR51 publication-title: Biocata. Biotrans. doi: 10.1080/10242420500292401 – volume: 72 start-page: 2275 year: 2000 ident: 3079_CR21 publication-title: Pure Appl. Chem. doi: 10.1351/pac200072122275 – volume: 3 start-page: 1507 year: 2001 ident: 3079_CR23 publication-title: Org. Lett. doi: 10.1021/ol015824f – volume: 39 start-page: 318 year: 2006 ident: 3079_CR36 publication-title: Enzym. Microb. Technol. doi: 10.1016/j.enzmictec.2005.11.002 – ident: 3079_CR68 doi: 10.1021/bk-2010-1038.ch014 – volume: 48 start-page: 4271 year: 2007 ident: 3079_CR69 publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2007.04.049 – volume: 101 start-page: 201 year: 2008 ident: 3079_CR85 publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.21866 – volume: 132 start-page: 306 year: 2007 ident: 3079_CR67 publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2007.04.001 – start-page: 206 volume-title: Ionic Liquids as Green Solvents year: 2003 ident: 3079_CR73 doi: 10.1021/bk-2003-0856.ch017 – volume: 9 start-page: 1493 year: 2008 ident: 3079_CR30 publication-title: ChembioChem doi: 10.1002/cbic.200800025 – volume: 8 start-page: 282 year: 2006 ident: 3079_CR40 publication-title: Green Chem. doi: 10.1039/B513062J – volume: 8 start-page: 509 year: 2006 ident: 3079_CR27 publication-title: Green Chem. doi: 10.1039/B600930A – volume: 27 start-page: 243 year: 2004 ident: 3079_CR37 publication-title: J. Mol. Catal. B: Enzym. doi: 10.1016/j.molcatb.2003.12.008 – volume: 17 start-page: 893 year: 1995 ident: 3079_CR35 publication-title: Biotechnol. Lett. doi: 10.1007/BF00127422 – volume: 37 start-page: 1265 year: 1999 ident: 3079_CR62 publication-title: J. Polym. Sci. A: Polym. Chem. doi: 10.1002/(SICI)1099-0518(19990501)37:9<1265::AID-POLA6>3.0.CO;2-I – volume: 128 start-page: 376 year: 2007 ident: 3079_CR91 publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2006.10.001 – volume: 88 start-page: 369 year: 2003 ident: 3079_CR82 publication-title: J. Appl. Polym. Sci. doi: 10.1002/app.11511 – volume: 6 start-page: 475 year: 2004 ident: 3079_CR24 publication-title: Green Chem. doi: 10.1039/b405712k – volume: 51 start-page: 81 year: 2008 ident: 3079_CR45 publication-title: J. Mol. Catal. B: Enzym. doi: 10.1016/j.molcatb.2007.11.010 – volume: 18 start-page: 2541 year: 2007 ident: 3079_CR90 publication-title: Tetrahedron Asymm. doi: 10.1016/j.tetasy.2007.10.010 – volume: 8 start-page: 538 year: 2006 ident: 3079_CR60 publication-title: Green Chem. doi: 10.1039/B600397D – volume: 16 start-page: 1129 year: 2000 ident: 3079_CR16 publication-title: Biotechnol. Prog. doi: 10.1021/bp000094g – volume: 12 start-page: 9228 year: 2006 ident: 3079_CR52 publication-title: Chem. Eur. J. doi: 10.1002/chem.200601043 – volume: 7 start-page: 185 year: 2005 ident: 3079_CR20 publication-title: Green Chem. doi: 10.1039/b419172b – volume: 22 start-page: 2570 year: 2004 ident: 3079_CR93 publication-title: Chem. Commun. doi: 10.1039/b410467f – volume: 8 start-page: 147 year: 2006 ident: 3079_CR96 publication-title: Green Chem. doi: 10.1039/b514999a – volume: 9 start-page: 162 year: 2007 ident: 3079_CR38 publication-title: Green Chem. doi: 10.1039/B612106C – volume: 4 start-page: 3462 year: 2006 ident: 3079_CR42 publication-title: Org. Biomol. Chem. doi: 10.1039/b608920h – volume: 37 start-page: 19 year: 2005 ident: 3079_CR11 publication-title: Enzym. Microb. Technol. doi: 10.1016/j.enzmictec.2005.02.014 – volume: 1770 start-page: 94 year: 2007 ident: 3079_CR71 publication-title: Biochim. Biophys. Acta. doi: 10.1016/j.bbagen.2006.10.004 – volume: 10 start-page: 117 year: 2008 ident: 3079_CR75 publication-title: Green Chem. doi: 10.1039/B714674D – volume: 95 start-page: 1093 year: 2006 ident: 3079_CR34 publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.21068 – volume: 43 start-page: 1009 year: 2008 ident: 3079_CR55 publication-title: Proc. Biochem. doi: 10.1016/j.procbio.2008.05.001 – volume: 1 start-page: 70 year: 2003 ident: 3079_CR17 publication-title: Chem. Commun doi: 10.1039/b210714g – volume: 24 start-page: 1231 year: 2008 ident: 3079_CR6 publication-title: Anal. Sci. doi: 10.2116/analsci.24.1231 – volume: 23 start-page: 89 year: 2005 ident: 3079_CR26 publication-title: Biocatal. Bio transform. doi: 10.1080/10242420500090219 – volume: 26 start-page: 982 year: 2005 ident: 3079_CR88 publication-title: Chin. J. Catal. – volume: 99 start-page: 1 year: 2008 ident: 3079_CR56 publication-title: Biotechnol. Bioeng. doi: 10.1002/bit.21534 – volume: 10 start-page: 685 year: 2008 ident: 3079_CR97 publication-title: Green Chem. doi: 10.1039/b716602h – volume: 43 start-page: 4529 year: 2004 ident: 3079_CR98 publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.200460241 – volume: 47 start-page: 6960 year: 2008 ident: 3079_CR4 publication-title: Angew. Chem. Int. Ed. doi: 10.1002/anie.200703305 – volume: 26 start-page: 41 year: 2003 ident: 3079_CR44 publication-title: J. Mol. Catal. B: Enzym. doi: 10.1016/S1381-1177(03)00147-4 – volume: 107 start-page: 2757 year: 2007 ident: 3079_CR10 publication-title: Chem. Rev. doi: 10.1021/cr050946x – volume: 10 start-page: 696 year: 2008 ident: 3079_CR59 publication-title: Green Chem. doi: 10.1039/b801489b – volume: 41 start-page: 480 year: 2007 ident: 3079_CR46 publication-title: Enzym. Microb. Technol. doi: 10.1016/j.enzmictec.2007.03.017 – volume: 41 start-page: 151 year: 2005 ident: 3079_CR25 publication-title: Biotechnol. Appl. Biochem. doi: 10.1042/BA20040056 – volume: 66 start-page: 8395 year: 2001 ident: 3079_CR14 publication-title: J. Org. Chem. doi: 10.1021/jo015761e – volume: 139 start-page: 124 year: 2009 ident: 3079_CR32 publication-title: J. Biotechnol. doi: 10.1016/j.jbiotec.2008.08.008 – volume: 5 start-page: 425 year: 2001 ident: 3079_CR48 publication-title: Chem. Commun. doi: 10.1039/b009389k – volume: 125 start-page: 4125 year: 2003 ident: 3079_CR65 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja028557x – volume: 10 start-page: 806 year: 2008 ident: 3079_CR86 publication-title: Green Chem. doi: 10.1039/b716369j – volume: 34 start-page: 94 year: 2002 ident: 3079_CR63 publication-title: Polym. J. doi: 10.1295/polymj.34.94 – volume: 45 start-page: 8801 year: 2004 ident: 3079_CR49 publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2004.10.015 – volume: 14 start-page: 432 year: 2003 ident: 3079_CR5 publication-title: Curr. Opin. Biotechnol. doi: 10.1016/S0958-1669(03)00100-9 – volume: 7 start-page: 602 year: 2005 ident: 3079_CR29 publication-title: Green Chem. doi: 10.1039/b503010b – volume-title: Ionic liquids in synthesis year: 2008 ident: 3079_CR3 – volume: 27 start-page: 1233 year: 2005 ident: 3079_CR77 publication-title: Biotechnol. Lett. doi: 10.1007/s10529-005-0023-y – volume: 1800 start-page: 405 year: 1914 ident: 3079_CR1 publication-title: Bull. Acad. Imper. Sci. (St. Petersburg) – volume: 14 start-page: 1235 year: 2008 ident: 3079_CR28 publication-title: Chem. Commun. doi: 10.1039/b716317g – volume: 111 start-page: 4910 year: 2007 ident: 3079_CR19 publication-title: J. Phys. Chem. B doi: 10.1021/jp0671998 |
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| Snippet | Ionic liquids, also called molten salt, are mixtures of cations and anions that melt below 100℃. Typical ionic liquids are dialkylimidazolium cations with... Ionic liquids, also called molten salts, are mixtures of cations and anions that melt below 100°C. Typical ionic liquids are dialkylimidazolium cations with... Ionic liquids, also called molten salts, are mixtures of cations and anions that melt below 100 °C. Typical ionic liquids are dialkylimidazolium cations with... Ionic liquids, also called molten salts, are mixtures of cations and anions that melt below 100oC. Typical ionic liquids are dialkylimidazolium cations with... |
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| SubjectTerms | Anions Biochemistry Biodegradation Biotechnology Catalysts Cations Chemical bonds Chemistry Chemistry and Materials Science deep eutectic solvents Enzymes Ethanol Glycerol HIDROLASAS Hydrogen bonds HYDROLASE HYDROLASES Industrial and Production Engineering ionic liquids Ions Liquids Organic solvents Oxalic acid OXIDOREDUCTASES OXIDORREDUCTASAS OXYDOREDUCTASE POLIMERIZACION POLYMERISATION POLYMERIZATION R&D Research & development Reviews Solubility Solvents Studies Urea Water 생물공학 |
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| Title | Toward Advanced Ionic Liquids. Polar, Enzyme-friendly Solvents for Biocatalysis |
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