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  • 1. Gelius, Eva
    et al.
    Persson, Carina
    Stockholm University, Faculty of Science, Department of Genetics, Microbiology and Toxicology.
    Karlsson, Jenny
    Stockholm University, Faculty of Science, Department of Genetics, Microbiology and Toxicology.
    Steiner, Håkan
    Stockholm University, Faculty of Science, Department of Genetics, Microbiology and Toxicology.
    A mammalian peptidoglycan recognition protein with N-acetylmuramoyl-L-alanine amidase activity2003In: Biochemical and Biophysical Research Communications - BBRC, ISSN 0006-291X, E-ISSN 1090-2104, Vol. 306, no 4, p. 988-994Article in journal (Refereed)
    Abstract [en]

    The family of peptidoglycan recognition proteins (PGRPs) is conserved from insects to mammals. Recently, Drosophila PGRP-SC1B was demonstrated to be an N-acetylmuramoyl- -alanine amidase (NAMLAA), an enzyme that cleaves the lactylamide bond between muramic acid and the peptide chain in peptidoglycan (PGN). We now show an M.mPGRP-L mRNA to be expressed in the liver. The recombinant M.mPGRP-L protein has NAMLAA activity and degrades PGN from both Escherichia coli and Staphylococcus aureus; however, the Gram-positive PGN was a better substrate after lysozyme treatment. The activity of M.mPGRP-L was further analysed using Bordetella pertussis tracheal toxin as a substrate. Cleavage products were separated on HPLC and identified using mass spectrometry. From these results we conclude that M.mPGRP-L has activity and other properties identifying it as the NAMLAA protein present in mammalian sera.

  • 2. Persson, Carina
    et al.
    Oldenvi, Sandra
    Steiner, Håkan
    Stockholm University, Faculty of Science, Department of Genetics, Microbiology and Toxicology.
    Peptidoglycan recognition protein LF, A negative regulator of Drosophila immunity.2007In: Insect Biochem Mol Biol, ISSN 0965-1748, Vol. 37, no 12, p. 1309-16Article in journal (Refereed)
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