Bioseparations and Downstream Processing
Application of a 22L scale membrane bioreactor and cross-flow ultrafiltration to obtain purified chondroitin
Article first published online: 22 JUN 2012
DOI: 10.1002/btpr.1566
Copyright © 2012 American Institute of Chemical Engineers (AIChE)
Additional Information
How to Cite
Schiraldi, C., Alfano, A., Cimini, D., Rosa, M. D., Panariello, A., Restaino, O. F. and Rosa, M. D. (2012), Application of a 22L scale membrane bioreactor and cross-flow ultrafiltration to obtain purified chondroitin. Biotechnol Progress, 28: 1012–1018. doi: 10.1002/btpr.1566
Publication History
- Issue published online: 7 AUG 2012
- Article first published online: 22 JUN 2012
- Accepted manuscript online: 23 MAY 2012 01:30AM EST
- Manuscript Revised: 7 MAY 2012
- Manuscript Received: 10 FEB 2012
Funded by
- Ministero dell'Istruzione dell'Università e della Ricerca (MIUR). Grant Number: L.297 project “Produzione biotecnologica di condroitina.”
- Abstract
- Article
- References
- Cited By
Keywords:
- ultrafiltration;
- purification;
- membrane reactor;
- chondroitin;
- capsular polysaccharide
Abstract
Recently, the possibility of producing fructosylated chondroitin from the capsular polysaccharide of Escherichia coli O5:K4:H4, in fed-batch and microfiltration experiments was assessed on a 2 L bioreactor. In this work, a first scale-up step was set on a 22 L membrane reactor with modified baffles to insert ad hoc designed microfiltration modules permanently inside the bioreactor vessel. Moreover, the downstream polysaccharide purification process, recently established on the A¨KTA cross-flow instrument, was translated to a UNIFLUX-10, a tangential flow filtration system suitable for prepilot scale. In particular, the microfiltered permeates obtained throughout the fermentation, and the supernatant recovered from the centrifuged broth at the end of the process, were treated as two separate samples in the following ultrafiltration procedure, and the differences in the two streams and how these affected the ultrafiltration/diafiltration process performance were analysed. The total amount of K4 capsular polysaccharide was about 85% in the broth and 15% in the microfiltered permeates. However, the downstream treatment was more efficient when applied to the latter. The major contaminant, the lipopolysaccharide, could easily be separated by a mild hydrolysis that also results in the elimination of the unwanted fructosyl residue, which is linked to the C-3 of glucuronic acid residues. The tangential ultrafiltration/diafiltration protocols developed in a previous work were effectively scaled-up, and therefore in this research proof of principle was established for the biotechnological production of chondroitin from the wild-type strain E. coli O5:K4:H4. The complete downstream procedure yielded about 80% chondroitin with 90% purity. © 2012 American Institute of Chemical Engineers Biotechnol. Prog., 28: 1012–1018, 2012

1520-6033/asset/BTPR_left.gif?v=1&s=a5be2ff5a0fe6ccdaad74a6d128c142e5f71a8da)
1520-6033/asset/BTPR_right.gif?v=1&s=992d113a3e61fc9d3571812359165df86cf830e4)
