TY - JOUR
T1 - Lysozyme fractionation from egg white at pilot scale by means of tangential flow membrane adsorbers
T2 - Investigation of the flow conditions
AU - Brand, Janina
AU - Voigt, Katharina
AU - Zochowski, Bianca
AU - Kulozik, Ulrich
N1 - Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/3/18
Y1 - 2016/3/18
N2 - The application of membrane adsorbers instead of classical packed bed columns for protein fractionation is still a growing field. In the case of egg white protein fractionation, the application of classical chromatography is additionally limited due to its high viscosity that impairs filtration. By using tangential flow membrane adsorbers as stationary phase this limiting factor can be left out, as they can be loaded with particle containing substrates. The flow conditions existing in tangential flow membrane adsorbers are not fully understood yet. Thus, the aim of the present study was to gain a deeper understanding of the transport mechanisms in tangential flow membrane adsorbers. It was found that loading in recirculation mode instead of single pass mode increased the binding capacity (0.39 vs. 0.52 mg cm-2). Further, it was shown that either higher flow rates (0.39 mg cm-2 vs. 0.57 mg cm-2 at 1 CV min-1 or 20 CV min-1, respectively) or higher amounts of the target protein in the feed (0.24 mg cm-2 vs. 0.85 mg cm-2 for 2.5 or 39.0 g lysozyme, respectively) led to more protein binding. These results show that, in contrast to radial flow or flat sheet membrane adsorbers, the transport in tangential flow membrane adsorbers is not purely based on convection, but on a mix of convection and diffusion. Additionally, investigations concerning the influence of fouling formation were performed that can lead to transport limitations. It was found that this impact is neglectable. It can be concluded that the usage of tangential flow membrane adsorbers is very recommendable for egg white protein fractionations, although the transport is partly diffusion-limited.
AB - The application of membrane adsorbers instead of classical packed bed columns for protein fractionation is still a growing field. In the case of egg white protein fractionation, the application of classical chromatography is additionally limited due to its high viscosity that impairs filtration. By using tangential flow membrane adsorbers as stationary phase this limiting factor can be left out, as they can be loaded with particle containing substrates. The flow conditions existing in tangential flow membrane adsorbers are not fully understood yet. Thus, the aim of the present study was to gain a deeper understanding of the transport mechanisms in tangential flow membrane adsorbers. It was found that loading in recirculation mode instead of single pass mode increased the binding capacity (0.39 vs. 0.52 mg cm-2). Further, it was shown that either higher flow rates (0.39 mg cm-2 vs. 0.57 mg cm-2 at 1 CV min-1 or 20 CV min-1, respectively) or higher amounts of the target protein in the feed (0.24 mg cm-2 vs. 0.85 mg cm-2 for 2.5 or 39.0 g lysozyme, respectively) led to more protein binding. These results show that, in contrast to radial flow or flat sheet membrane adsorbers, the transport in tangential flow membrane adsorbers is not purely based on convection, but on a mix of convection and diffusion. Additionally, investigations concerning the influence of fouling formation were performed that can lead to transport limitations. It was found that this impact is neglectable. It can be concluded that the usage of tangential flow membrane adsorbers is very recommendable for egg white protein fractionations, although the transport is partly diffusion-limited.
KW - Egg white
KW - Ion exchange chromatography
KW - Lysozyme
KW - Particle containing substrate
KW - Tangential flow membrane adsorber
UR - http://www.scopus.com/inward/record.url?scp=85027946423&partnerID=8YFLogxK
U2 - 10.1016/j.chroma.2016.02.023
DO - 10.1016/j.chroma.2016.02.023
M3 - Article
C2 - 26898148
AN - SCOPUS:85027946423
SN - 0021-9673
VL - 1438
SP - 143
EP - 149
JO - Journal of Chromatography A
JF - Journal of Chromatography A
ER -