Moving adsorption belt system for continuous bioproduct recovery utilizing composite fibrous adsorbents

被引:1
|
作者
Guo, Yijia [1 ]
Kangwa, Martin [1 ]
Ali, Wael [2 ,3 ]
Mayer-Gall, Thomas [2 ,3 ]
Gutmann, Jochen S. [2 ,3 ]
Zenneck, Claus [4 ]
Winter, Martina [5 ]
Jungbauer, Alois [5 ]
Lahore, Hector Marcelo Fernandez [1 ,6 ]
机构
[1] Jacobs Univ Bremen gGmbH, Sch Sci, Bremen, Germany
[2] Deutsch Textilforschungszentrum Nord West gGmbH, Krefeld, Germany
[3] Univ Duisburg Essen, Ctr Nanointegrat CENIDE, Dept Phys Chem, Essen, Germany
[4] MDX Biotech Int GmbH, Norten Hardenberg, Germany
[5] Univ Nat Resources & Life Sci, Inst Bioproc Sci & Engn, Dept Biotechnol, Vienna, Austria
[6] Luxembourg Inst Sci & Technol, Dept Environm Res & Innovat, Unit Biotechnol, Esch Sur Alzette, Luxembourg
关键词
nylon; 6; strong cation-exchanger; moving belt system; continuous bioproduct recovery; Humira monoclonal antibody; CONTINUOUS PURIFICATION; NANOFIBER ADSORBENTS; HIGH-CAPACITY; EXCHANGE; FIBER; CHROMATOGRAPHY;
D O I
10.3389/fbioe.2023.1135447
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A continuous protein recovery and purification system based on the true moving bed concept is presented. A novel adsorbent material, in the form of an elastic and robust woven fabric, served as a moving belt following the general designs observed in known belt conveyors. The composite fibrous material that forms the said woven fabric showed high protein binding capacity, reaching a static binding capacity equal to 107.3 mg/g, as determined via isotherm experiments. Moreover, testing the same cation exchange fibrous material in a packed bed format resulted in excellent dynamic binding capacity values (54.5 mg/g) even when operating at high flow rates (480 cm/h). In a subsequent step, a benchtop prototype was designed, constructed, and tested. Results indicated that the moving belt system could recover a model protein (hen egg white lysozyme) with a productivity up to 0.5 mg/cm(2)/h. Likewise, a monoclonal antibody was directly recovered from unclarified CHO_K1 cell line culture with high purity, as judged by SDS-PAGE, high purification factor (5.8), and in a single step, confirming the suitability and selectivity of the purification procedure.
引用
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页数:10
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