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    • 1. 发明授权
    • Isolated DNA encoding recombinant glucose isomerase
    • 分离的DNA编码重组葡萄糖异构酶
    • US08067561B2
    • 2011-11-29
    • US12723918
    • 2010-03-15
    • Jun WangCaike JinRongzhao FuDong Shen
    • Jun WangCaike JinRongzhao FuDong Shen
    • C12N9/00C12N9/92C12N1/20C12N15/00C07H21/04
    • C12N9/92C12P19/24
    • This invention provides a series of recombinant Thermoanaerobacterium saccharolyticum glucose isomerases with improved catalytic activity and thermostability obtained by using recombinant techniques. These recombinant glucose isomerases comprise amino acid variation including phenylalanine (Phe) at position 139, alanine (Ala) at position 182, serine (Ser) at position 187, and glutamine (Gin) at position 299, and carry at least one additional mutated amino acid at position 87, position 217, position 260 or position 276, and possess a higher catalytic activity than that of the wild-type when using D-glucose as substrate. These recombinant glucose isomerases can be used for direct production of high fructose corn syrup containing 55% [wt] or higher concentration of fructose.
    • 本发明提供了一系列通过使用重组技术获得的具有改进的催化活性和热稳定性的重组热酵母杆菌葡萄糖异构酶。 这些重组葡萄糖异构酶包括氨基酸变异,包括139位的苯丙氨酸(Phe),182位的丙氨酸(Ala),187位的丝氨酸(Ser)和299位的谷氨酰胺(Gin),并携带至少一种其它的突变氨基 在第87位,217位,260位或276位具有较高的酸性,当使用D-葡萄糖作为底物时,其具有比野生型更高的催化活性。 这些重组葡萄糖异构酶可用于直接生产含有55%(重量)或更高浓度果糖的高果糖玉米糖浆。
    • 2. 发明授权
    • Glucose isomerase mutants, DNA thereof and use thereof
    • 葡萄糖异构酶突变体,其DNA及其用途
    • US07704719B2
    • 2010-04-27
    • US12093859
    • 2006-10-30
    • Jun WangCaike JinRongzhao FuDong Shen
    • Jun WangCaike JinRongzhao FuDong Shen
    • C12N9/00C12N9/92C12N1/20C12N15/00C07H21/04
    • C12N9/92C12P19/24
    • This invention provides a series of recombinant Thermoanaerobacterium saccharolyticum glucose isomerases with improved catalytic activity and thermostability obtained by using recombinant techniques. These recombinant glucose isomerases comprise amino acid variation including phenylalanine (Phe) at position 139, alanine (Ala) at position 182, serine (Ser) at position 187, and glutamine (Gln) at position 299, and carry at least one additional mutated amino acid at position 87, position 217, position 260 or position 276, and possess a higher catalytic activity than that of the wild-type when using D-glucose as substrate. These recombinant glucose isomerases can be used for direct production of high fructose corn syrup containing 55.% [wt] or higher concentration of fructose.
    • 本发明提供了一系列通过使用重组技术获得的具有改进的催化活性和热稳定性的重组热酵母杆菌葡萄糖异构酶。 这些重组葡萄糖异构酶包括氨基酸变异,包括139位的苯丙氨酸(Phe),182位的丙氨酸(Ala),187位的丝氨酸(Ser)和299位的谷氨酰胺(Gln),并携带至少一种另外的突变氨基 在第87位,217位,260位或276位具有较高的酸性,当使用D-葡萄糖作为底物时,其具有比野生型更高的催化活性。 这些重组葡萄糖异构酶可用于直接生产含有55%(wt)或更高浓度果糖的高果糖玉米糖浆。
    • 4. 发明申请
    • Glucose Isomerase Mutants, Dna Thereof and Use Thereof
    • 葡萄糖异构酶突变体及其用途
    • US20080305529A1
    • 2008-12-11
    • US12093859
    • 2006-10-30
    • Jun WangCaike JinRongzhao FuDong Shen
    • Jun WangCaike JinRongzhao FuDong Shen
    • C12P19/24C12N9/92C07H21/04
    • C12N9/92C12P19/24
    • This invention provides a series of recombinant Thermoanaerobacterium saccharolyticum glucose isomerases with improved catalytic activity and thermostability obtained by using recombinant techniques. These recombinant glucose isomerases comprise amino acid variation including phenylalanine Phe) at position 139, alanine (Ala) at position 182, serine (Ser) at position 187, and glutamine (Gln) at position 299, and carry at least one additional mutated amino acid at position 87, position 217, position 260 or position 276, and possess a higher catalytic activity than that of the wild-type when using D-glucose as substrate. These recombinant glucose isomerases can be used for direct production of high fructose corn syrup containing 55.% [wt] or higher concentration of fructose.
    • 本发明提供了一系列通过使用重组技术获得的具有改进的催化活性和热稳定性的重组热酵母杆菌葡萄糖异构酶。 这些重组葡萄糖异构酶包含位置139的氨基酸变异,包括苯丙氨酸Phe),182位丙氨酸(Ala),第187位的丝氨酸(Ser)和299位的谷氨酰胺(Gln),并携带至少一种另外的突变的氨基酸 在位置87,位置217,位置260或位置276,并且当使用D-葡萄糖作为底物时,具有比野生型更高的催化活性。 这些重组葡萄糖异构酶可用于直接生产含有55%(wt)或更高浓度果糖的高果糖玉米糖浆。
    • 5. 发明授权
    • Methods of using isolated glucose isomerase
    • 使用分离的葡萄糖异构酶的方法
    • US07923222B2
    • 2011-04-12
    • US12723833
    • 2010-03-15
    • Jun WangCaike JinRongzhao FuDong Shen
    • Jun WangCaike JinRongzhao FuDong Shen
    • C12P19/24C12N9/00C12N9/92C12N1/20C12N15/00C07H21/04
    • C12N9/92C12P19/24
    • This invention provides a series of recombinant Thermoanaerobacterium saccharolyticum glucose isomerases with improved catalytic activity and thermostability obtained by using recombinant techniques. These recombinant glucose isomerases comprise amino acid variation including phenylalanine (Phe) at position 139, alanine (Ala) at position 182, serine (Ser) at position 187, and glutamine (Gin) at position 299, and carry at least one additional mutated amino acid at position 87, position 217, position 260 or position 276, and possess a higher catalytic activity than that of the wild-type when using D-glucose as substrate. These recombinant glucose isomerases can be used for direct production of high fructose corn syrup containing 55% [wt] or higher concentration of fructose.
    • 本发明提供了一系列通过使用重组技术获得的具有改进的催化活性和热稳定性的重组热酵母杆菌葡萄糖异构酶。 这些重组葡萄糖异构酶包括氨基酸变异,包括139位的苯丙氨酸(Phe),182位的丙氨酸(Ala),187位的丝氨酸(Ser)和299位的谷氨酰胺(Gin),并携带至少一种其它的突变氨基 在第87位,217位,260位或276位具有较高的酸性,当使用D-葡萄糖作为底物时,其具有比野生型更高的催化活性。 这些重组葡萄糖异构酶可用于直接生产含有55%(重量)或更高浓度果糖的高果糖玉米糖浆。
    • 6. 发明申请
    • DNA comprising a DNA SEQ. of isolated glucose isomerase
    • DNA包含DNA SEQ。 的葡萄糖异构酶
    • US20100228016A1
    • 2010-09-09
    • US12723918
    • 2010-03-15
    • Jun WangCaike JinRongzhao FuDong Shen
    • Jun WangCaike JinRongzhao FuDong Shen
    • C07H21/04
    • C12N9/92C12P19/24
    • This invention provides a series of recombinant Thermoanaerobacterium saccharolyticum glucose isomerases with improved catalytic activity and thermostability obtained by using recombinant techniques. These recombinant glucose isomerases comprise amino acid variation including phenylalanine (Phe) at position 139, alanine (Ala) at position 182, serine (Ser) at position 187, and glutamine (Gln) at position 299, and carry at least one additional mutated amino acid at position 87, position 217, position 260 or position 276, and possess a higher catalytic activity than that of the wild-type when using D-glucose as substrate. These recombinant glucose isomerases can be used for direct production of high fructose corn syrup containing 55% [wt] or higher concentration of fructose.
    • 本发明提供了一系列通过使用重组技术获得的具有改进的催化活性和热稳定性的重组热酵母杆菌葡萄糖异构酶。 这些重组葡萄糖异构酶包括氨基酸变异,包括139位的苯丙氨酸(Phe),182位的丙氨酸(Ala),187位的丝氨酸(Ser)和299位的谷氨酰胺(Gln),并携带至少一种另外的突变氨基 在第87位,217位,260位或276位具有较高的酸性,当使用D-葡萄糖作为底物时,其具有比野生型更高的催化活性。 这些重组葡萄糖异构酶可用于直接生产含有55%(重量)或更高浓度果糖的高果糖玉米糖浆。
    • 7. 发明申请
    • Methods of using isolated glucose isomerase
    • 使用分离的葡萄糖异构酶的方法
    • US20100227365A1
    • 2010-09-09
    • US12723833
    • 2010-03-15
    • Jun WangCaike JinRongzhao FuDong Shen
    • Jun WangCaike JinRongzhao FuDong Shen
    • C12P19/24
    • C12N9/92C12P19/24
    • This invention provides a series of recombinant Thermoanaerobacterium saccharolyticum glucose isomerases with improved catalytic activity and thermostability obtained by using recombinant techniques. These recombinant glucose isomerases comprise amino acid variation including phenylalanine (Phe) at position 139, alanine (Ala) at position 182, serine (Ser) at position 187, and glutamine (Gin) at position 299, and carry at least one additional mutated amino acid at position 87, position 217, position 260 or position 276, and possess a higher catalytic activity than that of the wild-type when using D-glucose as substrate. These recombinant glucose isomerases can be used for direct production of high fructose corn syrup containing 55% [wt] or higher concentration of fructose.
    • 本发明提供了一系列通过使用重组技术获得的具有改进的催化活性和热稳定性的重组热酵母杆菌葡萄糖异构酶。 这些重组葡萄糖异构酶包括氨基酸变异,包括139位的苯丙氨酸(Phe),182位的丙氨酸(Ala),187位的丝氨酸(Ser)和299位的谷氨酰胺(Gin),并携带至少一种其它的突变氨基 在第87位,217位,260位或276位具有较高的酸性,当使用D-葡萄糖作为底物时,其具有比野生型更高的催化活性。 这些重组葡萄糖异构酶可用于直接生产含有55%(重量)或更高浓度果糖的高果糖玉米糖浆。