enzyme recycle
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2010 ◽  
Vol 97 (1) ◽  
pp. 24-30 ◽  
Author(s):  
Carlos A. Prieto ◽  
Emilia M. Guadix ◽  
Antonio Guadix

Author(s):  
Yanpin Lu ◽  
Bin Yang ◽  
David Gregg ◽  
John N. Saddler ◽  
Shawn D. Mansfield

2002 ◽  
Vol 98-100 (1-9) ◽  
pp. 641-654 ◽  
Author(s):  
Yanpin Lu ◽  
Bin Yang ◽  
David Gregg ◽  
John N. Saddler ◽  
Shawn D. Mansfield

1989 ◽  
Vol 56 (3) ◽  
pp. 323-333 ◽  
Author(s):  
Servaas Visser ◽  
Henk J. Noorman ◽  
Charles J. Slangen ◽  
Harry S. Rollema

SummaryThe degradation of bovine β-casein by plasmin was used as a model system to investigate the applicability of an enzyme recycle reactor for the continuous production and isolation of peptide fractions. A simple, ultrafiltration-type membrane reactor was used incorporating a commercially available hollow-fiber module normally employed for dialysis purposes (artificial kidney). The results were compared with those obtained in a batch reactor process, using HPLC to monitor the course of proteolysis.Peptide fragments were isolated and were characterized using amino-acid analysis and N-terminal end-group determination. Sixteen peptide fragments were identified, which together accounted for virtually all the potential cleavage sites in β-casein. In the system studied the N-terminal half of β-casein appeared to be more sensitive to plasmic hydrolysis than the rest of the molecule.


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