Abstract
The foremost requirement of quantification of cellulases expressed in genetically modified sugarcane is an efficient sample clean-up. This work investigates the feasibility of isotachophoresis for this purpose. An electrolyte system comprising a leading electrolyte of 10 mM formic acid at pH 9.0 and a terminating electrolyte of 10 mM β-alanine was devised and used to perform isotachophoresis of cellulases. The use of a simple front cutting method removed a majority of interfering species in the juice, thereby resulting in the formation of a distinct zone of desired proteins. In comparison to techniques such as ultrafiltration and liming, the analysis time and loss of desired proteins was lower when the sample was prepared by using isotachophoresis. Hence, isotachophoresis was an ideal choice for purification of the proteins in question from the remaining components in the juice. © 2010 Elsevier B.V.
Original language | English |
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Pages (from-to) | 8026-8031 |
Number of pages | 5 |
Journal | Journal of Chromatography A |
Volume | 1217 |
Issue number | 51 |
DOIs | |
Publication status | Published - 17 Dec 2010 |
Keywords
- Bio-ethanol
- Bovine serum albumin (BSA)
- Cellulases
- Isotachophoresis
- Sample preparation
- Sugarcane