Phosphopeptides from Grana Padano cheese: nature, origin and changes during ripening

1997 ◽  
Vol 64 (4) ◽  
pp. 601-615 ◽  
Author(s):  
PASQUALE FERRANTI ◽  
FRANCESCA BARONE ◽  
LINA CHIANESE ◽  
FRANCESCO ADDEO ◽  
ANDREA SCALONI ◽  
...  

Casein phosphopeptides (CPP) which develop in Grana Padano cheese at different ages were isolated by precipitation with Ba2+ and analysed by HPLC. Profiles were complex throughout the period between 4 and 38 months. CPP in a cheese sample 14 months old were identified by a combination of fast atom bombardment–mass spectrometry and Edman degradation. They were found to consist of a mixture of components derived from three parent peptides, β-CNf(7–28)4P, αs1-CNf(61–79)4P and αs1-CNf(7–21)4P. In total, 45 phosphopeptides were identified: 24 from β-CN, 16 from αs1-CN and 5 from αs2-CN. The presence of aminopeptidase activity during cheese ripening was deduced from the presence of a number of CPP of different lengths with the loss of one or more residues from the N-terminus. The longest had C-terminal lysine and seemed to be progressively hydrolysed by carboxypeptidases A and B to shorter peptides. CPP in cheese appeared to be shortened plasmin-mediated products. Moreover, those most resistant to further hydrolysis contained at least three closely located phosphoserine residues. The anticariogenic activity of CPP is also discussed.

2000 ◽  
Vol 83 (12) ◽  
pp. 2733-2739 ◽  
Author(s):  
A. Gaiaschi ◽  
B. Beretta ◽  
C. Poiesi ◽  
A. Conti ◽  
M.G. Giuffrida ◽  
...  

2010 ◽  
Vol 20 (5) ◽  
pp. 352-359 ◽  
Author(s):  
Fabio Masotti ◽  
Johannes A. Hogenboom ◽  
Veronica Rosi ◽  
Ivano De Noni ◽  
Luisa Pellegrino

2001 ◽  
Vol 84 (1) ◽  
pp. 60-65 ◽  
Author(s):  
A. Gaiaschi ◽  
B. Beretta ◽  
C. Poiesi ◽  
A. Conti ◽  
M.G. Giuffrida ◽  
...  

1983 ◽  
Vol 50 (4) ◽  
pp. 469-480 ◽  
Author(s):  
Paul A. Grieve ◽  
Barry J. Kitchen ◽  
John R. Dulley ◽  
John Bartley

SUMMARYAn extract ofKluyveromyces lactis416 and a β-galactosidase preparation (Maxilact 40000) contaminated with proteinase, showed similar pH profiles of caseinolytic activity. Similar modes of casein hydrolysis (κ-, > αs-, ≥ β-) were observed at pH 5·0 (the pH of Cheddar cheese), without detection of bitterness. The contaminated Maxilact preparation contained similar proteinase types to those detected in an autolysate ofK. lactis. Both the autolysate and the Maxilact preparation contained acid endopeptidase (proteinase A), serine endopeptidase (proteinase B) and serine exopeptidase (carboxypeptidase Y) activities. Some aminopeptidase activity was also detected in both preparations. There were some differences in apparent molecular weight and charge properties between proteinase A and B and carboxypeptidase Y from the 2 proteinase sources.


2003 ◽  
Vol 77 (1) ◽  
pp. 43-48 ◽  
Author(s):  
E.P. Masler

AbstractThe cytosolic fraction of homogenates from the free-living soil nematodeCaenorhabditis elegansis capable of metabolizing the insect neuropeptide adipokinetic hormone, a decapeptide blocked at the N-terminus by a pGlu residue. Analysis of digests by RP-HPLC and LC-MS revealed that an initial endoproteolytic cleavage step produced a heptapeptide with an unblocked N-terminus that can serve as a substrate for aminopeptidases. The aminopeptidase activity is depressed in the presence of the inhibitor amastatin; the initial product of the endoproteolytic step accumulates during incubation, and expected aminopeptidase product peptides are reduced in amount, as assessed by chromatographic peak size. The absence of some expected peptide fragments in the reaction mixtures suggests that multiple proteases contribute to short peptide half-lives. Comparison of the adipokinetic hormone digestion inC. elegansto that reported previously for insects reveals the same general pattern of peptide fragment production.


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