HARVEST OPERATIONS FOR RECOMBINANT PROTEINS

    公开(公告)号:US20230069966A1

    公开(公告)日:2023-03-09

    申请号:US17864255

    申请日:2022-07-13

    Abstract: The present invention contemplates a method of producing a recombinant protein comprising (a) fermenting a prokaryotic host cell wherein said prokaryotic host cell has been transformed with a nucleic acid encoding said recombinant protein, and (b) harvesting said recombinant protein under conditions where dO2 levels are greater than 0%, and (c) purifying said recombinant protein to a filtered bulk, wherein said filtered bulk does not contain detectable DHNA-recombinant protein adduct, as measured by an IEC assay at 310 nm. The present invention also contemplates a method of producing a recombinant protein comprising (a) fermenting a menE gene-deleted prokaryotic host cell wherein said prokaryotic host cell has been transformed with a nucleic acid encoding said recombinant protein, (b) harvesting said recombinant protein; and (c) purifying said recombinant protein to a filtered bulk, wherein said filtered bulk does not contain detectable DHNA-recombinant protein adduct, as measured by an IEC assay at 310 nm, and wherein the recombinant protein yield is increased by about 20% or greater.

    HARVEST OPERATIONS FOR RECOMBINANT PROTEINS

    公开(公告)号:US20210171997A1

    公开(公告)日:2021-06-10

    申请号:US17067059

    申请日:2020-10-09

    Abstract: The present invention contemplates a method of producing a recombinant protein comprising (a) fermenting a prokaryotic host cell wherein said prokaryotic host cell has been transformed with a nucleic acid encoding said recombinant protein, and (b) harvesting said recombinant protein under conditions where dO2 levels are greater than 0%, and (c) purifying said recombinant protein to a filtered bulk, wherein said filtered bulk does not contain detectable DHNA-recombinant protein adduct, as measured by an IEC assay at 310 nm. The present invention also contemplates a method of producing a recombinant protein comprising (a) fermenting a menE gene-deleted prokaryotic host cell wherein said prokaryotic host cell has been transformed with a nucleic acid encoding said recombinant protein, (b) harvesting said recombinant protein; and (c) purifying said recombinant protein to a filtered bulk, wherein said filtered bulk does not contain detectable DHNA-recombinant protein adduct, as measured by an IEC assay at 310 nm, and wherein the recombinant protein yield is increased by about 20% or greater.

    HARVEST OPERATIONS FOR RECOMBINANT PROTEINS
    15.
    发明申请
    HARVEST OPERATIONS FOR RECOMBINANT PROTEINS 审中-公开
    重组蛋白的收获操作

    公开(公告)号:US20160130624A1

    公开(公告)日:2016-05-12

    申请号:US14734848

    申请日:2015-06-09

    CPC classification number: C12P21/00 C07K16/00

    Abstract: The present invention contemplates a method of producing a recombinant protein comprising (a) fermenting a prokaryotic host cell wherein said prokaryotic host cell has been transformed with a nucleic acid encoding said recombinant protein, and (b) harvesting said recombinant protein under conditions where dO2 levels are greater than 0%, and (c) purifying said recombinant protein to a filtered bulk, wherein said filtered bulk does not contain detectable DHNA-recombinant protein adduct, as measured by an IEC assay at 310 nm. The present invention also contemplates a method of producing a recombinant protein comprising (a) fermenting a menE gene-deleted prokaryotic host cell wherein said prokaryotic host cell has been transformed with a nucleic acid encoding said recombinant protein, (b) harvesting said recombinant protein; and (c) purifying said recombinant protein to a filtered bulk, wherein said filtered bulk does not contain detectable DHNA-recombinant protein adduct, as measured by an IEC assay at 310 nm, and wherein the recombinant protein yield is increased by about 20% or greater.

    Abstract translation: 本发明涉及生产重组蛋白的方法,其包括(a)发酵原核宿主细胞,其中所述原核宿主细胞已经用编码所述重组蛋白的核酸转化,和(b)在dO2水平的条件下收获所述重组蛋白 大于0%,和(c)将所述重组蛋白纯化至过滤的体积,其中所述过滤的体积不含可检测的DHNA重组蛋白加合物,如通过IEC测定在310nm测量的。 本发明还涉及一种生产重组蛋白的方法,其包括(a)发酵menE基因缺失的原核宿主细胞,其中所述原核宿主细胞已用编码所述重组蛋白的核酸转化,(b)收获所述重组蛋白; 和(c)将所述重组蛋白纯化至过滤体积,其中所述过滤的体积不含可检测的DHNA重组蛋白质加合物,如通过IEC测定在310nm测量的,并且其中重组蛋白质产量增加约20%或 更大

    HARVEST OPERATIONS FOR RECOMBINANT PROTEINS
    17.
    发明公开

    公开(公告)号:US20240158825A1

    公开(公告)日:2024-05-16

    申请号:US18419368

    申请日:2024-01-22

    CPC classification number: C12P21/00 C07K16/00

    Abstract: The present invention contemplates a method of producing a recombinant protein comprising (a) fermenting a prokaryotic host cell wherein said prokaryotic host cell has been transformed with a nucleic acid encoding said recombinant protein, and (b) harvesting said recombinant protein under conditions where dO2 levels are greater than 0%, and (c) purifying said recombinant protein to a filtered bulk, wherein said filtered bulk does not contain detectable DHNA-recombinant protein adduct, as measured by an IEC assay at 310 nm. The present invention also contemplates a method of producing a recombinant protein comprising (a) fermenting a menE gene-deleted prokaryotic host cell wherein said prokaryotic host cell has been transformed with a nucleic acid encoding said recombinant protein, (b) harvesting said recombinant protein; and (c) purifying said recombinant protein to a filtered bulk, wherein said filtered bulk does not contain detectable DHNA-recombinant protein adduct, as measured by an IEC assay at 310 nm, and wherein the recombinant protein yield is increased by about 20% or greater.

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