Peracetylated β-cyclodextrin as additive in enzymatic reactions: enhanced reaction rate and enantiomeric ratio in lipase-catalyzed transesterifications in organic solvents

2001 ◽  
Vol 12 (19) ◽  
pp. 2761-2766 ◽  
Author(s):  
Ashraf Ghanem ◽  
Volker Schurig
The Analyst ◽  
2015 ◽  
Vol 140 (6) ◽  
pp. 2023-2028 ◽  
Author(s):  
Tianchi Zhang ◽  
Chunli Shang ◽  
Ruixue Duan ◽  
Abdul Hakeem ◽  
Zhenyu Zhang ◽  
...  

Acceleration of the reaction rate by polar organic solvents during both simple and complicated DNA strand replacement reactions is reported.


Author(s):  
Edward MUNTEAN ◽  
Nicoleta MUNTEAN ◽  
Csaba PAIZS ◽  
Cecila ROMAN

Enzymatic hydrolysis of starch is one of the most important enzymatic technologies nowadays, leading to important amounts of sweeteners in food industry. It is accomplished at industrial scale using high starch concentrations; the present study deals with a less explored pathway, the one of low starch concentrations, originating from the residual starch in waste waters. The effective parameters of enzymatic starch hydrolysis were studied at laboratory scale, using a commercial enzymatic product (Dextrozyme® GA); experiments were carried out using low concentration starch systems, which were hydrolyzed monitoring the influence of pH, temperature, starch concentration and mixing rate on the reaction rate. Enzymatic reactions were monitored using high performance liquid chromatography, with a system enabling the quantification of glucose, fructose, saccharose and maltose. A complete factorial design at two levels was applied, the measured system’s response being the reaction rate. The obtained data demonstrated that the most important effect on saccharification is due to the pH, this being followed by starch concentration, temperature and mixing rate. Temperature, starch concentration and mixing rate are positively related with the reaction rate, while pH is inversely related with this. Analysis on the parameters’ interactions revealed that the most important interaction is the one between temperature and pH, followed by concentration-temperature and concentration-pH, while the combined interaction concentration-temperature-pH-mixing rate can be considered negligible


2001 ◽  
Vol 28 (4-5) ◽  
pp. 322-328 ◽  
Author(s):  
Georgia D.C. Machado ◽  
Lucia M.C. Paiva ◽  
Gerson F. Pinto ◽  
Enrique G. Oestreicher

1988 ◽  
Vol 45 (9) ◽  
pp. 705-712 ◽  
Author(s):  
Noritaka OHTANI ◽  
Masayoshi FURUYA ◽  
Kaoru HATAHJRA ◽  
Makoto YAMASAKI

2012 ◽  
Vol 90 (1) ◽  
pp. 1-16 ◽  
Author(s):  
Wing-Leung Wong ◽  
Kwok-Yin Wong

The recent development in the use of functionalized ionic liquids as both reaction media and promoters is reviewed. Ionic liquids designed with special functionality can enhance the reaction rate, selectivity, and productivity in various chemical reactions. In this context, some important chemical reactions involving C–C, C–O, C–N, and C–S bond formation in functionalized ionic liquids are discussed. These functionalized ionic liquids were found to provide distinct advantages over conventional organic solvents in these catalytic reactions.


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