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木薯Linamarase基因的克隆、表达及酶学特性分析
引用本文:沈培峰,付莉莉,孙雪飘,张家明.木薯Linamarase基因的克隆、表达及酶学特性分析[J].中国农学通报,2012,28(12):164-168.
作者姓名:沈培峰  付莉莉  孙雪飘  张家明
作者单位:1. 海南大学农学院,海口570228;中国热带农业科学院热带生物技术研究所,海口571101;农业部热带作物生物学与遗传资源利用重点实验室,海口571101
2. 中国热带农业科学院热带生物技术研究所,海口,571101
3. 海南大学农学院,海口570228;中国热带农业科学院热带生物技术研究所,海口571101
基金项目:“973”项目“重要热带作物木薯新品种选育的基础研究”(2010CBl26600).
摘    要:亚麻仁苷酶(Linamarase)是存在于木薯、巴豆等作物中的降解生氰葡萄糖苷Linamarin(亚麻仁苷)的酶,在结构上与芥子酶有很大的相似性,对它的研究有利于揭示生氰葡萄糖苷酶和芥子酶之间的关系以及芥子酶的起源问题。通过真核表达的方法,克隆了木薯Linamarase基因,构建酵母表达载体,转化毕赤酵母GS115,经诱导表达和亲和纯化,获得纯化的Linamarase重组蛋白。SDS-PAGE分析表明,重组蛋白分子量集中在71 kD左右。该酶最适反应温度在37℃左右,最适pH约为5。以pNPG为底物时,Km为1.70 mmol/L,最大反应速率Vmax为8.36μmol/(min.mg)。

关 键 词:木薯  亚麻仁苷酶  生氰葡萄糖苷  重组蛋白  SDS-PAGE
收稿时间:2011/11/29 0:00:00
修稿时间:2011/12/31 0:00:00

Cloning, Expression of Linamarase in Cassava and Characterization of its Recombinant Protein Activity
Shen Peifeng , Fu Lili , Sun Xuepiao , Zhang Jiaming.Cloning, Expression of Linamarase in Cassava and Characterization of its Recombinant Protein Activity[J].Chinese Agricultural Science Bulletin,2012,28(12):164-168.
Authors:Shen Peifeng  Fu Lili  Sun Xuepiao  Zhang Jiaming
Institution:1 College of Agriculture, Hainan University, Haikou 570228; 2Institute of Tropical Bioscience and Biotechnology, Chinese Academy of Tropical Agricultural Science, Haikou 571101; 3Key Laboratory of Biology and Genetic Resources of Torpical Crops, Ministry of Agriculture, Haikou 571101)
Abstract:Abstract: Linamarase is a kind of enzyme, which can degrade Linamarin in cassava, croton and other crops. The structure of this enzyme is very similar with rnyrosinase. Our study on this enzyme was avail to announce the relationship between cyanogen glycosidase enzyme and myrosinase, at the same time also reveal the origin of myrosinase. Linamarase gene was cloned from cassava, the yeast expression vector was constructed and then transformed into piehia pastorios GSll5. Purified recombinant protein of Linamarase was obtained after induction and affinity purification. SDS-PAGE analysis showed that, the recombinant protein concentrated was in the 71 kD molecular weight around. The optimal temperature of this enzyme was about 37℃, and the optimal pH was about 5. The Km was 1.70 mmol/L, and Vmax was 8.36μmol/(min. mg), while pNPG was used as the substrate.
Keywords:cassava  Linamarase  cyanogenic glycoside  recombinant protein  SDS-PAGE
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