2012
DOI: 10.1089/ind.2012.0008
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Selection of Enzyme Combination, Dose, and Temperature for Hydrolysis of Soybean White Flakes

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Cited by 7 publications
(3 citation statements)
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“…All sugar standards were purchase from Sigma-Aldrich (St. Louis, MO, USA) while all standards contained a purity of 99.9 %. The sugar standards were prepared using several concentrations and a calibration curve was constructed using concentration verus HPLC area previously established by Karunanithy, Karuppuchamy, Muthukumarappan, & Gibbons (2012).…”
Section: Residual Sugarsmentioning
confidence: 99%
“…All sugar standards were purchase from Sigma-Aldrich (St. Louis, MO, USA) while all standards contained a purity of 99.9 %. The sugar standards were prepared using several concentrations and a calibration curve was constructed using concentration verus HPLC area previously established by Karunanithy, Karuppuchamy, Muthukumarappan, & Gibbons (2012).…”
Section: Residual Sugarsmentioning
confidence: 99%
“…The soluble sugars in the supernatant was quantified by a high‐performance liquid chromatography (HPLC) system (Agilent Technologies, Santa Calara, CA, USA) equipped with a refractive index detector (Model G1362A) and a size‐exclusion chromatography column (SugarPak column I with pre‐column module; Waters Corporation, Milford, MA, USA) at a flow rate of 0.5 mL min −1 (50 ppm ethylenediaminetetraacetic acid in deionized water) and a column temperature of 85 °C. Sugar standards were prepared at various concentrations of (stachyose, raffinose, glucose, galactose, galactose‐mannose and arabinose) at 99.9% purity to build calibration curve of concentration versus HPLC peak area as previously reported by Karunanithy et al 32 . The sum of the soluble sugars was presented as total carbohydrates.…”
Section: Methodsmentioning
confidence: 99%
“…A HPLC system (Agilent Technologies, Santa Calara, CA, USA) equipped with a refractive index detector (Model G1362A), and a waters size‐exclusion chromatography column (SugarPak column I with pre‐column module, Waters Corporation, Milford, MA, USA) was used (mobile phase [50 ppm EDTA in deionized water], flow rate of 0.5 mL min −1 , column temperature of 85 °C). Sugar standards of stachyose, raffinose, glucose, galactose, galactose‐mannose, and arabinose were prepared at various concentration to set up calibration curve of concentration vs. HPLC area as previously described by (Karunanithy et al, 2012).…”
Section: Methodsmentioning
confidence: 99%