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首页> 外文期刊>LWT-Food Science & Technology >Purification and characterization of dextransucrase from Weissella cibaria RBA12 and its application in in vitro synthesis of prebiotic oligosaccharides in mango and pineapple juices
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Purification and characterization of dextransucrase from Weissella cibaria RBA12 and its application in in vitro synthesis of prebiotic oligosaccharides in mango and pineapple juices

机译:从Weissella cibaria RBA12纯化和表征右旋胰蛋白酶及其在芒果和菠萝汁中益生元寡糖体外合成的应用

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Dextransucrase produced by Weissella cibaria RBA12 isolated from pummelo was purified by PEG-400 and PEG-1500 fractionation, followed by gel filtration. The enzyme purified by 0.25 mL/L PEG 400 gave specific activity 410 mu kat/g with 25-fold purification. Purified dextransucrase gave a single, homogeneous protein of molecular size similar to 180 kDa on analysis by SDS-PAGE. Purified dexransucrase was optimally active at 40 degrees C and pH 5.4. It gave maximum velocity (V-max) and Michaelis constant (K-m) of 488.3 mu kat/g and 19.2 mmol/L, respectively. The enzyme was thermally stable up to 30 degrees C and highest pH stability at pH 5.5 for 1 h Mg2+ and Ca2+ ions enhanced the enzyme activity by 40% and 25%, respectively. The in-situ production of isomalto-oligosaccharide was carried out by dextransucrase using mango and pineapple juices. The native sugars (sucrose, glucose and fructose) present in both juices were confirmed by HPLC. The glucose and fructose present in juices acted as acceptor molecules. In both juices, isomaltooligosaccharides from DP3 to DP5 along with isomaltose (DP2) and leucrose (DP2) were synthesized in situ by dextransucrase reaction utilizing the native sucrose. Sucrose content of the juices was eliminated resulting in its lower calorific value highlighting the potential of dextransucrase for production of functional foods. (C) 2017 Elsevier Ltd. All rights reserved.
机译:通过PEG-400和PEG-1500分馏纯化由Pummelo分离的Weissella Cibaria RBA12产生的葡聚糖蔗糖酶,然后纯化凝胶过滤。用0.25ml / l peg 400纯化的酶,得到特定的活性410μk/ g,纯化为25倍。纯化的右旋胰酶通过SDS-PAGE具有类似于180kDa的分子大小的单一,均相蛋白质。纯化的德红磺酰胺在40℃和pH 5.4的最佳活性活性活性。它分别为488.3μkat/ g和19.2mmol / l的最大速度(v-max)和michaelis常数(k-m)。将酶在pH 5.5下热稳定,最高30℃,最高的pH值为1 H mg2 +,Ca2 +离子分别使酶活性分别增强40%和25%。使用芒果和菠萝汁进行Isomalto-Oligosaccharide的原位生产。通过HPLC证实了两种果汁中存在的天然糖(蔗糖,葡萄糖和果糖)。果汁中存在的葡萄糖和果糖作用为受体分子。在两个果汁中,通过利用天然蔗糖的葡聚糖酶反应,通过葡聚糖菌反应原位合成来自DP3至DP5与异麦芽糖(DP2)和Leucrose(DP2)合成的异麦托隆核苷酸。消除了果汁的蔗糖含量,导致其较低的热值突出了右旋胰酶的潜力,用于生产功能性食品。 (c)2017 Elsevier Ltd.保留所有权利。

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