High gradient magnetic separation versus expanded bed adsorption: a first principle comparison

被引:77
作者
Hubbuch, JJ [1 ]
Matthiesen, DB [1 ]
Hobley, TJ [1 ]
Thomas, ORT [1 ]
机构
[1] Tech Univ Denmark, Bioctr DTU, Ctr Proc Biotechnol, DK-2800 Lyngby, Denmark
关键词
affinity separation; batch adsorption; expanded bed adsorption; fluidised bed; high gradient magnetic separation; primary capture;
D O I
10.1023/A:1012034923621
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A robust new adsorptive separation technique specifically designed for direct product capture from crude bioprocess feedstreams is introduced and compared with the current bench mark technique, expanded bed adsorption. The method employs product adsorption onto sub-micron sized non-porous superparamagnetic supports followed by rapid separation of the `loaded' adsorbents from the feedstock using high gradient magnetic separation technology. For the recovery of Savinase(R) from a cell-free Bacillus clausii fermentation liquor using bacitracin-linked adsorbents, the integrated magnetic separation system exhibited substantially enhanced productivity over expanded bed adsorption when operated at processing velocities greater than 48 m h(-1). Use of the bacitracin-linked magnetic supports for a single cycle of batch adsorption and subsequent capture by high gradient magnetic separation at a processing rate of 12 m h(-1) resulted in a 2.2-fold higher productivity relative to expanded bed adsorption, while an increase in adsorbent collection rate to 72 m h(-1) raised the productivity to 10.7 times that of expanded bed adsorption. When the number of batch adsorption cycles was then increased to three, significant drops in both magnetic adsorbent consumption (3.6 fold) and filter volume required (1.3 fold) could be achieved at the expense of a reduction in productivity from 10.7 to 4.4 times that of expanded bed adsorption.
引用
收藏
页码:99 / 112
页数:14
相关论文
共 36 条
[1]   HIGH-PERFORMANCE LIQUID AFFINITY-CHROMATOGRAPHY WITH PHENYLBORONIC ACID, BENZAMIDINE, TRI-L-ALANINE, AND CONCANAVALIN-A IMMOBILIZED ON 3-ISOTHIOCYANATOPROPYLTRIETHOXYSILANE-ACTIVATED NONPOROUS MONODISPERSE SILICAS [J].
ANSPACH, FB ;
WIRTH, HJ ;
UNGER, KK ;
STANTON, P ;
DAVIES, JR ;
HEARN, MTW .
ANALYTICAL BIOCHEMISTRY, 1989, 179 (01) :171-181
[2]   Expanded-bed chromatography in primary protein purification [J].
Anspach, FB ;
Curbelo, D ;
Hartmann, R ;
Garke, G ;
Deckwer, WD .
JOURNAL OF CHROMATOGRAPHY A, 1999, 865 (1-2) :129-144
[3]   AMINO-ACID ANALYSIS - DETERMINATION OF CYSTEINE PLUS HALF-CYSTINE IN PROTEINS AFTER HYDROCHLORIC-ACID HYDROLYSIS WITH A DISULFIDE COMPOUND AS ADDITIVE [J].
BARKHOLT, V ;
JENSEN, AL .
ANALYTICAL BIOCHEMISTRY, 1989, 177 (02) :318-322
[4]  
Birrs R., 1981, PROGR FILTRATION SEP, V2, P171
[5]  
BRUMMELHUIS HGJ, 1980, METHODS PLASMA PROTE, P117
[6]  
Chang YK, 1996, BIOTECHNOL BIOENG, V49, P512, DOI 10.1002/(SICI)1097-0290(19960305)49:5<512::AID-BIT4>3.3.CO
[7]  
2-X
[8]   PURIFICATION OF PROTEINS BY ADSORPTION CHROMATOGRAPHY IN EXPANDED BEDS [J].
CHASE, HA .
TRENDS IN BIOTECHNOLOGY, 1994, 12 (08) :296-303
[9]   TECHNIQUES AND INSTRUMENTATION FOR PREPARATIVE IMMUNOSORBENT SEPARATIONS [J].
EVELEIGH, JW .
JOURNAL OF CHROMATOGRAPHY, 1978, 159 (01) :129-145
[10]   Interaction of mammalian cell culture broth with adsorbents in expanded bed adsorption of monoclonal antibodies [J].
Feuser, J ;
Halfar, M ;
Lütkemeyer, D ;
Ameskamp, N ;
Kula, MR ;
Thömmes, J .
PROCESS BIOCHEMISTRY, 1999, 34 (02) :159-165