Eur J Clin Nutr. 1999 Nov;53(11):891-4.
learning notes
Saturday, 31 October 2015
Cowin 1999
Oboh 1998
J Chromatogr A. 1998 Oct 9;823(1-2):307-12.
Anti-nutritional constituents of six underutilized legumes grown in Nigeria.
Abstract
Martínez-Villaluenga 2005
J Food Prot. 2005 Jun;68(6):1246-52.
Raffinose family of oligosaccharides from lupin seeds as prebiotics: application in dairy products.
Abstract
Giannoccaro 2008
Comparison of two HPLC systems and an enzymatic method for quantification of soybean sugars.
Successful breeding programs need fast and reliable methods for analyzing sugar composition in new soybean (Glycine max (L.) Merrill) lines. The efficiency to quantify the major sugars, including glucose, fructose, sucrose, raffinose, and stachyose, in fivesoybean lines with two HPLC systems and an enzymatic procedure were compared. Soluble sugars in soybean were extracted with water at a solvent-to-sample ratio of 5:1 at 50°C for 15min, and analyzed by high-performance size exclusion chromatography with refractive index detection (HPSEC-RI), high-performance anion-exchange chromatography with pulsed-amperometric detection (HPAEC-PAD), and a raffinose-series oligosaccharides assay procedure. All three methods produced comparable and reproducible results. The HPAEC-PAD method was more sensitive, faster and capable of separating all five major sugars in soybean with improved peak resolution compared with the HPSEC-RI method, and is recommended for soybeanbreeding programs. The enzymatic procedure required no expensive instrumentation and less sample preparation, but could not quantify individual raffinose and stachyose.
Richmond 1981
Analysis of simple sugars and sorbitol in fruit by high-performance liquid chromatography
Michael L. Richmond; Sebastiao C. C. Brandao; J. Ian Gray; Pericles Markakis; Charles M. Stine
Journal of Agricultural and Food Chemistry. 1981;29(1):4-7.
Abstract
The application of a high-performance liquid chromatographic (LC) procedure for the determination of sugars and sorbitol in fresh fruits is described. This system combines the use of two bonded phase carbohydrate columns, joined in tandem; a ternary mobile phase (acetonitrile-water-ethanol) and a differential refractometer to accurately and precisely separate fructose, glucose, sorbitol, sucrose, and maltose. Total analysis time was 20 min for the five-sugar mixture. Twenty-four fruits were analyzed including eleven from the family Rosaceae, which often contain sorbitol. Sample recoveries ranged from 98% for fructose to 102% for maltose. © 1981 American Chemical Society.
Andersson 2009
J Agric Food Chem. 2009 Mar 11;57(5):2004-8. doi: 10.1021/jf801280f.
Content and molecular-weight distribution of dietary fiber components in whole-grain rye flour and bread.
Abstract
Sreenath 2008
Anal Bioanal Chem. 2008 May;391(2):609-15. doi: 10.1007/s00216-008-2016-x. Epub 2008 Mar 28.
Analysis of erythritol in foods by polyclonal antibody-based indirect competitive ELISA.
Sreenath K1, Venkatesh YP.Abstract
Sugar alcohols are widely used as food additives and drug excipients. Erythritol (INS 968) is an important four-carbon sugar alcohol in the food industry. Erythritol occurs naturally in certain fruits, vegetables, and fermented foods. Currently, HPLC and GC methods are in use for the quantification of erythritol in natural/processed foods. However, an immunoassay for erythritol has not been developed so far. We have utilized affinity-purified erythritol-specific antibodies generated earlier [9] to develop an indirect competitive ELISA. With erythritol–BSA conjugate (54 mol/mol; 100 ng/well) as the coating antigen, a calibration curve was prepared using known amounts of standard meso-erythritol (0.1–100,000 ng) in the immunoassay. Watermelon (Citrullus lanatus) and red wine were selected as the food sources containing meso-erythritol. The amount of meso-erythritol was calculated as 2.36 mg/100 g fresh weight of watermelon and 206.7 mg/L of red wine. The results obtained from the immunoassay are in close agreement with the reported values analyzed by HPLC and GC (22–24 mg/kg in watermelon and 130–300 mg/L in red wine). The recovery analyses showed that added amounts of meso-erythritol were recovered fairly accurately with recoveries of 86–105% (watermelon) and 85–93.3% (red wine). The method described here for erythritol is the first report of an immunoassay for a sugar alcohol.
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