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    • 1. 发明授权
    • KDO aldolase and condensation reactions employed therewith
    • KDO醛缩酶和与其一起使用的缩合反应
    • US06423834B1
    • 2002-07-23
    • US09247164
    • 1999-02-09
    • Chi-Huey WongTakeshi SugaiGwo-Jenn Shen
    • Chi-Huey WongTakeshi SugaiGwo-Jenn Shen
    • C07H1500
    • C12P19/02C07H7/027C12N9/88C12P7/58C12P9/00Y10S435/822
    • Aureobacterium barkerei strain KDO-37-2 (ATCC 49977) and KDO aldolase (EC 4.1.2.23) isolated therefrom are disclosed. The KDO aldolase is further disclosed to have a broad substrate specificity with respect to its reverse reaction, i.e. the condensation of aldoses with pyruvate to form a wide range of 2-keto-3-deoxy-onic acids, including 2-keto-3-deoxy-nonulosonic acid, 2-keto-3-deoxy-octulosonic acid, 2-keto-3-deoxy-heptulosonic acid, and 2-keto-3-deoxy-hexulosonic acid. In particular, 3-deoxy-D-manno-2-octulosonic acid (D-KDO), a vital component of lipopolysaccharides found in the bacterial outer membrane may be synthesized from D-arabinose and pyruvate in 67% yield. Additionally, protected forms of the KDO aldolase products, e.g. hexaacetyl 2-keto-3-deoxy-nonulosonic acid and pentaacetyl 2-keto-3-deoxy-octulosonic acid, may be decarboxylated to form the corresponding 2-deoxy-aldoses, e.g. 2-deoxy-octulose and 2-deoxy-heptulose respectively.
    • 公开了从其分离的巴氏杆菌菌株KDO-37-2(ATCC 49977)和KDO醛缩酶(EC 4.1.2.23)。 进一步公开KDO醛缩酶相对于其逆反应具有广泛的底物特异性,即醛糖与丙酮酸的缩合形成宽范围的2-酮-3-脱氧ic酸,包括2-酮-3- 脱氧 - 非酮酸,2-酮-3-脱氧 - 八环酮酸,2-酮-3-脱氧 - 庚酮酸和2-酮-3-脱氧 - 己酸。 特别地,在D-细菌外膜中发现的脂多糖的重要组分3-脱氧-D-壬烯-2-辛酮酸(D-KDO)可由D-阿拉伯糖和丙酮酸合成,产率67%。 另外,保护形式的KDO醛缩酶产物,例如, 六乙酰基2-酮-3-脱氧 - 非酮酸和五乙酰基2-酮-3-脱氧 - 八环酸可以脱羧以形成相应的2-脱氧醛糖,例如, 2-脱氧 - 八酮糖和2-脱氧 - 七氟醚。
    • 2. 发明授权
    • Biologically pure culture of aureobacterium barkeri KDO-37-2
    • 生物纯培养的巴氏杆菌KDO-37-2
    • US5869316A
    • 1999-02-09
    • US767182
    • 1996-12-16
    • Chi-Huey WongTakeshi SugaiGwo-Jenn Shen
    • Chi-Huey WongTakeshi SugaiGwo-Jenn Shen
    • C07H7/027C12N9/88C12P7/58C12P9/00C12P19/02C12N1/20
    • C12P19/02C07H7/027C12N9/88C12P7/58C12P9/00Y10S435/822
    • Aureobacterium barkeri strain KDO-37-2 (ATCC 49977) and KDO aldolase (EC 4.1.2.23) isolated therefrom are disclosed. The KDO aldolase is further disclosed to have a broad substrate specificity with respect to its reverse reaction, i.e. the condensation of aldoses with pyruvate to form a wide range of 2-keto-3-deoxy-onic acids, including 2-keto-3-deoxy-nonulosonic acid, 2-keto-3-deoxy-octulosonic acid, 2-keto-3-deoxy-heptulosonic acid, and 2-keto-3-deoxy-hexulosonic acid. In particular, 3-deoxy-D-manno-2-octulosonic acid (D-KDO), a vital component of lipopolysaccharides found in the bacterial outer membrane may be synthesized from D-arabinose and pyruvate in 67% yield. Additionally, protected forms of the KDO aldolase products, e.g. hexaacetyl 2-keto-3-deoxy-nonulosonic acid and pentaacetyl 2-keto-3-deoxy-octulosonic acid, may be decarboxylated to form the corresponding 2-deoxy-aldoses, e.g. 2-deoxy-octulose and 2-deoxy-heptulose respectively.
    • 公开了分离自巴斯德氏菌杆菌菌株KDO-37-2(ATCC 49977)和KDO醛缩酶(EC 4.1.2.23)。 进一步公开KDO醛缩酶相对于其逆反应具有广泛的底物特异性,即醛糖与丙酮酸的缩合形成宽范围的2-酮-3-脱氧ic酸,包括2-酮-3- 脱氧 - 非酮酸,2-酮-3-脱氧 - 八环酮酸,2-酮-3-脱氧 - 庚酮酸和2-酮-3-脱氧 - 己酸。 特别地,在D-细菌外膜中发现的脂多糖的重要组分3-脱氧-D-壬烯-2-辛酮酸(D-KDO)可由D-阿拉伯糖和丙酮酸合成,产率67%。 另外,保护形式的KDO醛缩酶产物,例如, 六乙酰基2-酮-3-脱氧 - 非酮酸和五乙酰基2-酮-3-脱氧 - 八环酸可以脱羧以形成相应的2-脱氧醛糖,例如, 2-脱氧 - 八酮糖和2-脱氧 - 七氟醚。
    • 3. 发明授权
    • KDO Aldolase and condensation reactions employed therewith
    • KDO醛缩酶和与其一起使用的缩合反应
    • US5358859A
    • 1994-10-25
    • US993140
    • 1992-12-18
    • Chi-Huey WongTakeshi SugaiGwo-Jenn Shen
    • Chi-Huey WongTakeshi SugaiGwo-Jenn Shen
    • C07H7/027C12N9/88C12P7/58C12P9/00C12P19/02
    • C12P19/02C07H7/027C12N9/88C12P7/58C12P9/00Y10S435/822
    • Aureobacterium barkerei strain KDO-37-2 (ATCC 49977) KDO aldolase (EC 4.1.2.23) isolated therefrom are disclosed. The DKDO aldolase is further disclosed to have a broad substrate specificity with respect to its reverse reaction, i.e. the condensation of aldoses with pyruvate to form a wide range of 2-keto-3-deoxy-onic acids, including 2-keto-3-deoxy-nonulosonic acid, 2-keto-3-deoxy-octulosonic acid, 2-keto-3-deoxy-heptulosonic acid, and 2-keto-3-deoxy-hexulosonic acid. In particular, 3-deoxy-D-manno-2-octulosonic acid (D-KDO), a vital component of lipopolysaccharides found in the bacterial outer membrane may be synthesized from D-arabinose and pyruvate in 67% yield. Additionally, protected forms of the KDO aldolase products, e.g. hexaacetyl 2-keto-3-deoxy-nonulosonic acid and pentaacetyl 2-keto-3-deoxy-octulosonic acid, may be decarboxylated to form the corresponding 2-deoxy-aldoses, e.g. 2-deoxy-octulose and 2-deoxy-heptulose respectively.
    • 公开了从其分离的巴氏杆菌菌株KDO-37-2(ATCC 49977)KDO醛缩酶(EC 4.1.2.23)。 进一步公开了DKDO醛缩酶对于其逆反应具有广泛的底物特异性,即醛糖与丙酮酸的缩合形成宽范围的2-酮-3-脱氧酸,包括2-酮-3- 脱氧 - 非酮酸,2-酮-3-脱氧 - 八环酮酸,2-酮-3-脱氧 - 庚酮酸和2-酮-3-脱氧 - 己酸。 特别地,在D-细菌外膜中发现的脂多糖的重要组分3-脱氧-D-壬烯-2-辛酮酸(D-KDO)可由D-阿拉伯糖和丙酮酸合成,产率67%。 另外,保护形式的KDO醛缩酶产物,例如, 六乙酰基2-酮-3-脱氧 - 非酮酸和五乙酰基2-酮-3-脱氧 - 八环酸可以脱羧以形成相应的2-脱氧醛糖,例如, 2-脱氧 - 八酮糖和2-脱氧 - 七氟醚。
    • 5. 发明授权
    • Method and composition for synthesizing sialylated glycosyl compounds
    • 合成唾液酸化糖基化合物的方法和组成
    • US5278299A
    • 1994-01-11
    • US670701
    • 1991-03-18
    • Chi-Huey WongYoshitaka IchikawaGwo-Jenn Shen
    • Chi-Huey WongYoshitaka IchikawaGwo-Jenn Shen
    • C12N1/21C12N9/12C12P19/04C12P19/18C12P19/26C07H1/00C12N9/24
    • C12N9/1241C12P19/04C12P19/18C12P19/26
    • The present invention provides a method for synthesizing a sialylated glycosyl compound comprising reacting in the presence of each other a sialic acid, a glycosyl compound, a CMP-sialic acid regenerating system, a pyrophosphate scavenger and catalytic amounts of a CMP-sialic acid synthetase and a sialyl transferase having substrate specificity for the glycosyl compound. The present invention also provides a composition for sialylating glycosyl compounds comprising a sialic acid, CMP-sialic acid regenerating system, a pyrophosphate scavenger and a catalytic amount of CMP-sialic acid synthetase. The composition can further comprise an aqueous solvent having a suitable buffer and enzyme cofactors as well as a catalytic amount of a sialyl transferase having substrate specificity for the glycosyl compound. A phagemid-transformed E. coli. that overproduces CMP-sialic acid synthetase is also disclosed.
    • 本发明提供了合成唾液酸化糖基化合物的方法,包括在唾液酸,糖基化合物,CMP-唾液酸再生系统,焦磷酸盐清除剂和催化量的CMP-唾液酸合成酶的存在下彼此反应,以及 具有对糖基化合物具有底物特异性的唾液酸转移酶。 本发明还提供了用于唾液酸化糖基化合物的组合物,其包含唾液酸,CMP-唾液酸再生系统,焦磷酸盐清除剂和催化量的CMP-唾液酸合成酶。 组合物还可以包含具有合适的缓冲液和酶辅因子的水性溶剂以及催化量的对糖基化合物具有底物特异性的唾液酸转移酶。 噬菌粒转化的大肠杆菌。 也公开了过度生产CMP-唾液酸合成酶。