2013
DOI: 10.1016/j.molcatb.2013.01.019
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Enzymatic synthesis of 6- and 6′-O-linoleyl-α-d-maltose: From solvent-free to binary ionic liquid reaction media

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Cited by 35 publications
(12 citation statements)
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“…In contrast, biocatalytic synthesis occurs in mild reaction conditions, thereby reducing the formation of undesirable by-products and lowering energy consumption during processing [12]. In the literature, numerous approaches for lipase-catalyzed reactions have been conducted, including polar solvents [13][14][15], ionic liquids [16][17][18], microwave assistance [19], ultrasound irradiation [20], and supercritical carbon dioxide [21], to overcome the poor miscibility of acyl donors and acceptors reviewed in the publications [22,23].…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…In contrast, biocatalytic synthesis occurs in mild reaction conditions, thereby reducing the formation of undesirable by-products and lowering energy consumption during processing [12]. In the literature, numerous approaches for lipase-catalyzed reactions have been conducted, including polar solvents [13][14][15], ionic liquids [16][17][18], microwave assistance [19], ultrasound irradiation [20], and supercritical carbon dioxide [21], to overcome the poor miscibility of acyl donors and acceptors reviewed in the publications [22,23].…”
Section: Introductionmentioning
confidence: 99%
“…In contrast, biocatalytic synthesis occurs in mild reaction conditions, thereby reducing the formation of undesirable by-products and lowering energy consumption during processing [12]. In the literature, numerous approaches for lipase-catalyzed reactions have been conducted, including polar solvents [13][14][15], ionic liquids [16][17][18], microwave assistance [19], ultrasound irradiation [20], and supercritical carbon dioxide [21], to overcome the poor miscibility of acyl donors and acceptors reviewed in the publications [22,23].Recently, saccharide fatty acid esters have been enzymatically synthesized in solvent-free media in our laboratory, by making use of the desired product, monoester, to enhance the miscibility of acyl acceptor and donor, saccharide and fatty acid, respectively [24][25][26][27]. A closedloop bioreactor system operated under continuous recirculation was utilized in the preparation of sugar esters using a stoichiometrical feed of substrates on a 10-g scale consisting of a reservoir open to atmosphere at 65 °C on a hot plate, a peristaltic pump and a packed-bed bioreactor (PBBR) filled with immobilized Rhizomucor Abstract The effects of high-speed homogenization, high-intensity ultrasound, and their combination were evaluated for the reduction of the particle size of sucrose crystals to enhance solvent-free lipase-catalyzed synthesis of sucrose oleate at 65 °C.…”
mentioning
confidence: 99%
“…There have been recent reports on selective transformations of unprotected sugars and their derivatives using both biocatalytic 5,6,7,8 and chemical approaches 9,10,11 . De-oxygenation/dehydration of sugars is of particular interest and only a few approaches have been described.…”
Section: Introductionmentioning
confidence: 99%
“…Very recently, the lipase-catalyzed esterification [ 20 ], ester-hydrolysis [ 21 ], and transesterification [ 22 ] reactions in the IL media have been widely reported. Furthermore, many reports have demonstrated that the ILs with the anions PF 6 – and BF 4 – were suitable reaction media for the lipase-catalyzed transesterification [ 22 , 23 ] and esterification [ 24 , 25 ] reactions. However, the anions PF 6 – and BF 4 – are hydrolytically unstable, which results in a propensity to decompose and release corrosive HF [ 26 , 27 ].…”
Section: Introductionmentioning
confidence: 99%