Literature DB >> 7622204

Evidence for glycosylation sites on the 45-kilodalton glycoprotein of Mycobacterium tuberculosis.

K M Dobos1, K Swiderek, K H Khoo, P J Brennan, J T Belisle.   

Abstract

The occurrence of glycosylated proteins in Mycobacterium tuberculosis has been widely reported. However, unequivocal proof for the presence of true glycosylated amino acids within these proteins has not been demonstrated, and such evidence is essential because of the predominance of soluble lipoglycans and glycolipids in all mycobacterial extracts. We have confirmed the presence of several putative glycoproteins in subcellular fractions of M. tuberculosis by reaction with the lectin concanavalin A. One such product, with a molecular mass of 45 kDa, was purified from the culture filtrate. Compositional analysis demonstrated that the protein was rich in proline and that mannose, galactose, glucose, and arabinose together represented about 4% of the total mass. The 45-kDa glycoprotein was subjected to proteolytic digestion with either the Asp-N or the Glu-C endopeptidase or subtilisin, peptides were resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and glycopeptides were identified by reaction with concanavalin A. Peptides were further separated, and when they were analyzed by liquid chromatography-electrospray mass spectrometry for neutral losses of hexoses (162 mass units), four peptides were identified, indicating that these were glycosylated with hexose residues. One peptide, with an average molecular mass of 1,516 atomic mass units (AMU), exhibited a loss of two hexose units. The N-terminal sequence of the 1,516-AMU glycopeptide was determined to be DPEPAPPVP, which was identical to the sequence of the amino terminus of the mature protein, DPEPAP PVPXTA. Furthermore, analysis of the glycopeptide by secondary ion mass spectrometry demonstrated that the complete sequence of the glycopeptide was DPEPAPPVPTTA. From this, it was determined that the 10th amino acid, threonine, was O-glycosidically linked to a disaccharide composed of two hexose residues, probably mannose. This report establishes that true, O-glycosylated proteins exist in mycobacteria.

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Year:  1995        PMID: 7622204      PMCID: PMC173386          DOI: 10.1128/iai.63.8.2846-2853.1995

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  53 in total

1.  The chemical composition of immunoaffinity-purified Mycobacterium tuberculosis antigen 5.

Authors:  T M Daniel
Journal:  Am Rev Respir Dis       Date:  1989-06

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Authors:  J E Shively; P Miller; M Ronk
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Review 3.  Biogenesis of lipoproteins in bacteria.

Authors:  H C Wu; M Tokunaga
Journal:  Curr Top Microbiol Immunol       Date:  1986       Impact factor: 4.291

4.  Specificity of Mycobacterium tuberculosis antigen 5 determined with mouse monoclonal antibodies.

Authors:  T M Daniel; N J Gonchoroff; J A Katzmann; G R Olds
Journal:  Infect Immun       Date:  1984-07       Impact factor: 3.441

5.  Microsequence analysis of peptides and proteins. V. Design and performance of a novel gas-liquid-solid phase instrument.

Authors:  D H Hawke; D C Harris; J E Shively
Journal:  Anal Biochem       Date:  1985-06       Impact factor: 3.365

6.  Purification and some properties of the endogenous, autolytic N-acetylmuramoylhydrolase of Streptococcus faecium, a bacterial glycoenzyme.

Authors:  T Kawamura; G D Shockman
Journal:  J Biol Chem       Date:  1983-08-10       Impact factor: 5.157

7.  Use of lectins for detection of electrophoretically separated glycoproteins transferred onto nitrocellulose sheets.

Authors:  W F Glass; R C Briggs; L S Hnilica
Journal:  Anal Biochem       Date:  1981-07-15       Impact factor: 3.365

8.  Lipoarabinomannan. Multiglycosylated form of the mycobacterial mannosylphosphatidylinositols.

Authors:  D Chatterjee; S W Hunter; M McNeil; P J Brennan
Journal:  J Biol Chem       Date:  1992-03-25       Impact factor: 5.157

9.  Synthetic lipopeptide analogs of bacterial lipoprotein are potent polyclonal activators for murine B lymphocytes.

Authors:  W G Bessler; M Cox; A Lex; B Suhr; K H Wiesmüller; G Jung
Journal:  J Immunol       Date:  1985-09       Impact factor: 5.422

10.  Characterization of Mycobacterium tuberculosis antigen 5 epitopes by using a panel of 19 monoclonal antibodies.

Authors:  G R Olds; A J Sanson; T M Daniel
Journal:  J Clin Microbiol       Date:  1987-03       Impact factor: 5.948

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  54 in total

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Authors:  M Schirm; S K Arora; A Verma; E Vinogradov; P Thibault; R Ramphal; S M Logan
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2.  MTSA-10, the product of the Rv3874 gene of Mycobacterium tuberculosis, elicits tuberculosis-specific, delayed-type hypersensitivity in guinea pigs.

Authors:  R Colangeli; J S Spencer; P Bifani; A Williams; K Lyashchenko; M A Keen; P J Hill; J Belisle; M L Gennaro
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3.  N-Terminal clustering of the O-glycosylation sites in the Mycobacterium tuberculosis lipoprotein SodC.

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4.  Influence of pilin glycosylation on Pseudomonas aeruginosa 1244 pilus function.

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5.  Purification of Mycobacterium bovis BCG Tokyo antigens by chromatofocusing, lectin-affinity chromatography, and hydrophobic interaction chromatography.

Authors:  E A Sugden; K Stilwell; D C Watson; E B Rohonczy; P Martineau
Journal:  Clin Diagn Lab Immunol       Date:  1996-09

Review 6.  Bacterial glycoproteins.

Authors:  P Messner
Journal:  Glycoconj J       Date:  1997-01       Impact factor: 2.916

7.  O-GLYCBASE version 2.0: a revised database of O-glycosylated proteins.

Authors:  J E Hansen; O Lund; K Rapacki; S Brunak
Journal:  Nucleic Acids Res       Date:  1997-01-01       Impact factor: 16.971

8.  Subcellular localization of the Iitracellular survival-enhancing Eis protein of Mycobacterium tuberculosis.

Authors:  J L Dahl; J Wei; J W Moulder; S Laal; R L Friedman
Journal:  Infect Immun       Date:  2001-07       Impact factor: 3.441

9.  Molecular cloning, expression, and immunogenicity of MTB12, a novel low-molecular-weight antigen secreted by Mycobacterium tuberculosis.

Authors:  J R Webb; T S Vedvick; M R Alderson; J A Guderian; S S Jen; P J Ovendale; S M Johnson; S G Reed; Y A Skeiky
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10.  Scale-up from shake flasks to bioreactor, based on power input and Streptomyces lividans morphology, for the production of recombinant APA (45/47 kDa protein) from Mycobacterium tuberculosis.

Authors:  Ramsés A Gamboa-Suasnavart; Luz D Marín-Palacio; José A Martínez-Sotelo; Clara Espitia; Luis Servín-González; Norma A Valdez-Cruz; Mauricio A Trujillo-Roldán
Journal:  World J Microbiol Biotechnol       Date:  2013-03-10       Impact factor: 3.312

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