Institute of Macromolecular Chemistry AS CR, vvi, Prague, Czech Republic.
J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Jul 15;879(22):2175-8. doi: 10.1016/j.jchromb.2011.05.043. Epub 2011 Jun 6.
Membrane ultrafiltration (UF) was used in sample preparation of the culture fluids of the human intestinal bacterium Clostridium paraputrificum strain J4 containing seven extracellular chitinolytic isoenzymes (38-90 kDa). The subsequent filtration of the bacteria-free supernatants was carried out through Millipore membranes with cut-off 100 and 30 kDa for separation of undigested components of the culture medium and bacterial metabolites with molecular weight higher and lower than that of the target enzymes. The chitinolytic enzymes, which were the minor components in the culture fluids, were concentrated at UF as well. The aim of the research consisted in evaluation of the effect of component composition of bacteria-free supernatants and the chemical nature of membrane active layer on partial fractionation of the chitinolytic enzymes, their recovery in retentates and purification degree. On the basis of the obtained experimental results, the sample preparation procedure of the culture fluids of C. paraputrificum J4 was established to be used further in chromatographic separations of the chitinolytic enzymes.
采用膜超滤(UF)技术对含有七种胞外几丁质水解同工酶(38-90 kDa)的人肠道细菌 Clostridium paraputrificum 菌株 J4 的培养液进行样品制备。然后,通过 Millipore 膜(截留分子量为 100 和 30 kDa)对无细菌的上清液进行过滤,以分离培养基中未消化的成分和分子量高于或低于目标酶的细菌代谢产物。在 UF 过程中,几丁质水解酶(培养液中的少量成分)也被浓缩。本研究的目的在于评估无细菌上清液的成分组成和膜活性层的化学性质对几丁质水解酶的部分分级分离、在截留物中的回收率和纯化程度的影响。基于获得的实验结果,建立了 C. paraputrificum J4 培养液的样品制备程序,以便进一步用于几丁质水解酶的色谱分离。