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    • 6. 发明授权
    • Process for producing 2-O-alpha-D-glucopyranosyl-L-ascorbic acid
    • 制备2-O-α-D-吡喃葡萄糖基-L-抗坏血酸的方法
    • US08759030B2
    • 2014-06-24
    • US10523920
    • 2003-07-07
    • Kazuhisa MukaiKeiji TsusakiMichio KubotaShigeharu FukudaToshio Miyake
    • Kazuhisa MukaiKeiji TsusakiMichio KubotaShigeharu FukudaToshio Miyake
    • C12P19/44
    • C12P19/60
    • The object of the present invention is to provide a method and a process for producing 2-O-α-glucopyranosyl-L-ascorbic acid where 5-O-α-glucopyranosyl-L-ascorbic acid and 6-O-α-glucopyranosyl-L-ascorbic acid are not formed or formed in such a small amount that the formation of these can nor be detected. The present invention solves the above object by providing a process for producing 2-O-α-glucopyranosyl-L-ascorbic acid comprising the steps of allowing α-isomaltosyl glucosaccharide-forming enzyme together with or without cyclomaltodextrin glucanotransferase (EC 2.4.1.19) to act on a solution comprising L-ascorbic acid and, an α-glucosyl saccharide to form 2-O-α-glucopyranosyl-L-ascorbic acid and collecting the formed 2-O-α-glucopyranosyl-L-ascorbic acid.
    • 本发明的目的是提供一种生产2-O-α-吡喃葡萄糖基-L-抗坏血酸的方法和方法,其中5-O-α-吡喃葡萄糖基-L-抗坏血酸和6-O-α-吡喃葡萄糖基 - L-抗坏血酸不是以这样的少量形成或形成,也可以不形成。 本发明通过提供一种生产2-O-α-吡喃葡萄糖基-L-抗坏血酸的方法来解决上述目的,其包括以下步骤:将α-异麦芽糖基葡萄糖形成酶与或不与环糊精葡聚糖转移酶(EC 2.4.1.19)一起 作用于包含L-抗坏血酸和α-葡萄糖基糖的溶液中以形成2-O-α-吡喃葡萄糖基-L-抗坏血酸并收集形成的2-O-α-吡喃葡萄糖基-L-抗坏血酸。
    • 7. 发明申请
    • Process for producing 2-0-alpha-d-glucopyranosyl-l-ascorbic acid
    • 制备2-0-α-d-吡喃葡萄糖基-1-抗坏血酸的方法
    • US20060216792A1
    • 2006-09-28
    • US10523920
    • 2003-07-07
    • Kazuhisa MukaiKeiji TsusakiMichio KubotaShigeharu FukudaToshio Miyake
    • Kazuhisa MukaiKeiji TsusakiMichio KubotaShigeharu FukudaToshio Miyake
    • C12P19/44
    • C12P19/60
    • The object of the present invention is to provide a method and a process for producing 2-O-α-glucopyranosyl-L-ascorbic acid where 5-O-α-glucopyranosyl-L-ascorbic acid and 6-O-α-glucopyranosyl-L-ascorbic acid are not formed or formed in such a small amount that the formation of these can nor be detected. The present invention solves the above object by providing a process for producing 2-O-α-glucopyranosyl-L-ascorbic acid comprising the steps of allowing α-isomaltosyl glucosaccharide-forming enzyme together with or without cyclomaltodextrin glucanotransferase (EC 2.4.1.19) to act on a solution comprising L-ascorbic acid and, an α-glucosyl saccharide to form 2-O-α-glucopyranosyl-L-ascorbic acid and collecting the formed 2-O-α-glucopyranosyl-L-ascorbic acid.
    • 本发明的目的是提供一种生产2-O-α-glucopyranosyl-L-抗坏血酸的方法和方法,其中5-O-α-吡喃葡萄糖基-L-抗坏血酸和6-O-α-吡喃葡萄糖基-L- L-抗坏血酸不是以这样的少量形成或形成,也可以不形成。 本发明通过提供一种生产2-O-α-吡喃葡萄糖基-L-抗坏血酸的方法来解决上述目的,其包括以下步骤:将α-异麦芽糖基糖糖形成酶与或不与环糊精葡聚糖转移酶(EC 2.4.1.19)一起使用 作用于包含L-抗坏血酸和α-葡糖基糖的溶液以形成2-O-α-吡喃葡萄糖基-L-抗坏血酸并收集形成的2-O-α-吡喃葡萄糖基-L-抗坏血酸。
    • 9. 发明申请
    • PROCESS FOR PRODUCING ISOMALTOSE AND USES THEREOF
    • 生产异构体的方法及其用途
    • US20080241904A1
    • 2008-10-02
    • US11777044
    • 2007-07-12
    • Michio KubotaTomoyuki NishimotoTakanobu HigashiyamaHikaru WatanabeShigeharu FukudaToshio Miyake
    • Michio KubotaTomoyuki NishimotoTakanobu HigashiyamaHikaru WatanabeShigeharu FukudaToshio Miyake
    • C12N9/10
    • C12P19/12
    • A novel process for producing isomaltose and uses thereof and comprising the steps of contacting saccharides, which have a glucose polymerization degree of at least two and α-1,4 glucosidic linkage as a linkage at the non-reducing end, with an α-isomaltosylglucosaccharide-forming enzyme, in the presence or the absence of α-isomaltosyl-transferring enzyme to form a-isomaltosylglucosaccharides, which have a glucose polymerization degree of at least three, α-1,6 glucosidic linkage as a linkage at the non-reducing end, and α-1,4 glucosidic linkage as a linkage other than the non-reducing end, and/or to form cyclo{→6)-α-D-glucopyranosyl-(1→3)-α-D-glucopyranosyl-(1→6)-α-D-glucopyranosyl-(1″3)-α-D-glucopyranosyl-(1→}; contacting the saccharides so formed with isomaltose-releasing enzyme to release isomaltose; and collecting the released isomaltose; and uses thereof.
    • 一种制备异麦芽糖的新方法及其用途,包括以下步骤:将具有至少两个葡萄糖聚合度的至少两个和非1,4-还原末端的α-1,4糖苷键的糖与α-异麦芽糖基葡萄糖 在α-异麦芽糖基转移酶的存在或不存在下形成α-异麦芽糖基糖,其具有在非还原末端具有至少三个α-1,6糖苷键作为键的葡萄糖聚合度 和α-1,4糖苷键作为非还原末端之外的键,和/或形成环{ - > 6)-al-D-glucopyranosyl-(1-> 3)-al-D-glucopyranosyl - (1-> 6)-al-D-glucopyranosyl-(1''3)-alpha-D-吡喃葡萄糖基 - (1->};使所形成的糖与异麦芽糖释放酶接触以释放异麦芽糖; 释放的异麦芽糖;及其用途。
    • 10. 发明申请
    • Method for transferring a glucosyl residue
    • 转移葡糖基残基的方法
    • US20070154996A1
    • 2007-07-05
    • US10587711
    • 2005-01-27
    • Tomoyuki NishimotoMichio KubotaShigeharu FukudaToshio Miyake
    • Tomoyuki NishimotoMichio KubotaShigeharu FukudaToshio Miyake
    • C12P19/04
    • C12P19/18C12P19/44
    • An object of the present invention is to provide novel methods for forming glucosyl-transferred polyalcohols, glucosyl-transferred glucuronic acid, and glucosyl-transferred derivatives of glucose whose C-6 hydroxyl group bound to a saccharide by using an enzymatic reaction. The present invention solves the above object by providing a method for transferring a glucosyl residue to polyalcohols, glucuronic acid and/or derivatives of glucose whose C-6 hydroxyl group bound to a saccharide, comprising a step of: allowing a trehalose phosphorylase to act on a saccharide containing glucose as a component sugar and one or more polyalcohols selected from the group consisting of inositol, ribitol, erythritol, and glycerol; glucuronic acid and/or a salt thereof; and/or one or more derivatives of glucose whose C-6 hydroxyl group bound to a saccharide selected from the group consisting of isomaltose, gentiobiose, melibiose, isomaltotriose, and isopanose.
    • 本发明的目的是提供通过酶促反应形成C-6羟基与糖结合的葡萄糖转移的多元醇,葡糖基转移的葡萄糖醛酸和葡萄糖转移的葡萄糖转移衍生物的新方法。 本发明通过提供一种将葡糖基残基转移到多糖,葡糖醛酸和/或其C-6羟基与糖结合的葡萄糖的衍生物的方法,包括以下步骤:使海藻糖磷酸化酶作用于 含有葡萄糖作为组分糖和一种或多种选自肌醇,核糖醇,赤藓糖醇和甘油的多元醇的糖; 葡萄糖醛酸和/或其盐; 和/或一种或多种C-6羟基结合于选自异麦芽糖,龙胆糖,蜜二糖,异麦芽三糖和异丙糖的糖的葡萄糖衍生物。