Transport of beta-casein-derived peptides by the oligopeptide transport system is a crucial step in the proteolytic pathway of Lactococcus lactis.

TitleTransport of beta-casein-derived peptides by the oligopeptide transport system is a crucial step in the proteolytic pathway of Lactococcus lactis.
Publication TypeJournal Article
Year of Publication1995
AuthorsKunji, ERS, Hagting, A, De Vries, CJ, Juillard, V, Haandrikman, AJ, Poolman, B, Konings, WN
JournalJ Biol Chem
Volume270
Issue4
Pagination1569-74
Date Published1995 Jan 27
ISSN0021-9258
KeywordsAmino Acids, Animals, Bacterial Proteins, Biological Transport, Carrier Proteins, Caseins, Cattle, Genotype, Kinetics, Lactococcus lactis, Lipoproteins, Milk, Oligopeptides, Peptide Fragments, Serine Endopeptidases, Subtilisins
Abstract

In the proteolytic pathway of Lactococcus lactis, milk proteins (caseins) are hydrolyzed extracellularly to oligopeptides by the proteinase (PrtP). The fate of these peptides, i.e. extracellular hydrolysis followed by amino acid uptake or transport followed by intracellular hydrolysis, has been addressed. Mutants have been constructed that lack a functional di-tripeptide transport system (DtpT) and/or oligopeptide transport system (Opp) but do express the P1-type proteinase (specific for hydrolysis of beta- and to a lesser extent kappa-casein). The wild type strain and the DtpT- mutant accumulate all beta-casein-derived amino acids in the presence of beta-casein as protein substrate and glucose as a source of metabolic energy. The amino acids are not accumulated significantly inside the cells by the Opp- and DtpT- Opp- mutants. When cells are incubated with a mixture of amino acids mimicking the composition of beta-casein, the amino acids are taken up to the same extent in all four strains. Analysis of the extracellular peptide fraction, formed by the action of PrtP on beta-casein, indicates that distinct peptides disappear only when the cells express an active Opp system. These and other experiments indicate that (i) oligopeptide transport is essential for the accumulation of all beta-casein-derived amino acids, (ii) the activity of the Opp system is sufficiently high to support high growth rates on beta-casein provided leucine and histidine are present as free amino acids, and (iii) extracellular peptidase activity is not present in L. lactis.

DOI10.1074/jbc.270.4.1569
Alternate JournalJ. Biol. Chem.
Citation Key10.1074/jbc.270.4.1569
PubMed ID7829486