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Enzymatic production of difructose dianhydride IV from sucrose and relevant enzymes and genes coding for them

机译:由蔗糖及相关酶和编码它们的基因酶法生产果糖二酐IV

摘要

Disclosed is the production of difructose dianhydride IV from sugar. A sugar solution is subjected to reaction at room temperature or lower in an acidic buffer of pH 3.0-7.0 in the presence of a levansucrase derived from Z. mobilis to produce levan. The levansucrase is prepared by culturing E. coli BL21 (DE3)/pEL12 (KCTC 8661), harvesting and homogenizing the cells, and isolating levansucrase from the cell homogenate. Levan is purified from the reaction solution and subjected to reaction at 25-50° C. for 3-10 hours in an acidic buffer of pH 3.0-7.0 in the presence of a levan fructotransferase to produce difructose dianhydride IV. The levan fructotransferase is obtained from E. coli JUD81 (KCTC 0877BP). Also, disclosed are a gene coding for the levan fructotransferase and an expression vector pUDAF81 carrying the gene.
机译:公开了由糖生产二果糖二酐IV。在衍生自I Z的葡糖蔗糖酶的存在下,使糖溶液在pH 3.0-7.0的酸性缓冲液中于室温或更低温度下反应。动员产生levan。糖蔗糖酶通过培养 E制备。大肠杆菌 BL21(DE3)/ pEL12(KCTC 8661),收获并匀浆细胞,并从细胞匀浆中分离出蔗糖酶。从反应溶液中纯化Levan,并在levan果糖转移酶的存在下在pH 3.0-7.0的酸性缓冲液中在25-50℃下使其反应3-10小时,以产生二果糖二酐IV。左旋果糖转移酶获自。大肠杆菌 JUD81(KCTC 0877BP)。还公开了编码左旋果糖转移酶的基因和携带该基因的表达载体pUDAF81。

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