Laboratory of Natural Products Chemistry, Graduate School of Science and Technology, Faculty of Agriculture Shizuoka, Shizuoka University, Suruga-ku, Shizuoka, Japan.
J Sep Sci. 2011 Oct;34(19):2759-64. doi: 10.1002/jssc.201100508. Epub 2011 Aug 24.
Centrifugal precipitation chromatography and a high-speed counter-current chromatography system equipped with a spiral tubing support rotor (spHSCCC) were successfully applied for the identification and isolation of carotenoid cleavage-like enzymes from Enteromorpha compressa (L.) Nees. This is the first study separating active enzymes from a complex natural matrix by spHSCCC. The target enzymes were identified after fractionation of the proteins in an acetone Tris-buffer gradient by centrifugal precipitation chromatography. Also, an aqueous two-phase solvent system consisting of PEG 1000 and mono- and dibasic potassium phosphate was used for the isolation of the enzymes by spHSCCC. The purified fractions contained two proteins of 65 and 72 kDa, respectively. The enzymes could cleave β-carotene and β-apo-8'-carotenal to produce β-ionone.
离心沉淀色谱和高速逆流色谱系统配备螺旋管支撑转子(spHSCCC)成功应用于从肠浒苔(L.)Nees 中鉴定和分离类胡萝卜素裂解酶。这是首次通过 spHSCCC 从复杂的天然基质中分离活性酶。通过离心沉淀色谱在丙酮 Tris-缓冲梯度中对蛋白质进行分级后,分离出目标酶。此外,还使用由聚乙二醇 1000 和单、二碱基磷酸钾组成的双水相溶剂系统通过 spHSCCC 分离酶。纯化的馏分分别含有两种 65 和 72 kDa 的蛋白质。这些酶可以切割 β-胡萝卜素和 β-apo-8'-胡萝卜醛,产生 β-紫罗兰酮。