Capture of bacteriocins directly from non-clarified fermentation broth using macroporous monolithic cryogels with phenyl ligands

被引:22
作者
Deraz, Sahar
Plieva, Fatima M.
Galaev, Igor Yu.
Karlsson, Eva Nordberg
Mattiasson, Bo
机构
[1] Lund Univ, Ctr Chem & Chem Engn, Dept Biotechnol, SE-22100 Lund, Sweden
[2] Protista Biotechnol AB, SE-22370 Lund, Sweden
[3] Genet Engn & Biotechnol Res Inst, Mubarak City Sci, Alexandria, Egypt
关键词
bacteriocin; integrated product adsorption; macroporous monolith; cryogel in microtiter plate;
D O I
10.1016/j.enzmictec.2006.06.024
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
The bacteriocin, sakacin P was produced by the bacteriocin-producing strain Lactobacillus sakei CCUG 42687 at 20 degrees C without pH control. The bacteriocin was captured directly from the fermentation broth using macroporous octyl- and phenyl-monolith columns. The large size of the interconnected macropores (up to 100 mu m) in the macroporous monolith allowed for direct fermentation broth processing with no clarification needed. Screening for optimal bacteriocin binding demonstrated that at pH 6.2 about 80% of the bacteriocin activity could be recovered with a purification factor of 150-160 in the cell-free eluate. Capture of bacteriocins from the fermentation broth using macroporous monoliths in the 96-well plate format presents a promising approach for rapid analytical isolation of bacteriocins from numerous samples. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:786 / 793
页数:8
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