Talib Y Y, Karve M S, Bhide S V, Kale N R
Department of Chemistry, University of Poona, India.
Prep Biochem. 1988;18(2):199-203. doi: 10.1080/00327488808062521.
The defatted starch was dispersed in NaOH (1 M) and neutralized with HCl (1 M). The amylose 1-butanol complex is adsorbed on defatted cellulose powder in the solvent system containing acetate buffer (pH 4.8,0.1 M) + urea (2 M) + 1-butanol (8.5%, v/v). The complex adsorbed on cellulose powder is separated by centrifugation (2418 g). The sediment is washed with the solvent system-I to obtain the intermediate fraction. The adsorbed amylose is eluted with urea (2 M) in acetate buffer (pH 4.8, 0.1 M). The amylose, intermediate fraction and amylopectin were precipitated with ethanol, washed free of urea and air dried. They were characterized by determining their blue value and beta -amylolysis limit.
将脱脂淀粉分散于1M的氢氧化钠中,并用1M的盐酸中和。直链淀粉-正丁醇复合物在含有醋酸盐缓冲液(pH 4.8,0.1M)+尿素(2M)+正丁醇(8.5%,v/v)的溶剂体系中吸附于脱脂纤维素粉末上。吸附在纤维素粉末上的复合物通过离心(2418g)分离。沉淀物用溶剂体系-I洗涤以获得中间级分。吸附的直链淀粉用醋酸盐缓冲液(pH 4.8,0.1M)中的2M尿素洗脱。直链淀粉、中间级分和支链淀粉用乙醇沉淀,洗涤除去尿素并风干。通过测定它们的蓝色值和β-淀粉酶解极限对其进行表征。