N-acetylputrescine as a characteristic constituent of cyanelle peptidoglycan in glaucocystophyte algae

Journal of Bacteriology

Volumn 178, Issue 23, 1996, Pages 6994-6997

  Pfanzagl, Beatrix ^a   Allmaier, Günter ^b   Schmid, Erich R ^b   De Pedro, Miguel A ^c   Löffelhardt, Wolfgang ^a  

^a UNIVERSITY OF VIENNA   (Austria)

^b Institute of Analytical Chemistry   (Austria)

^c UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

PEPTIDOGLYCAN; PUTRESCINE DERIVATIVE;

ALGA; ARTICLE; CELL ORGANELLE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MASS SPECTROMETRY; NONHUMAN; PRIORITY JOURNAL;

ALGAE; CYANOPHORA PARADOXA; CYANOPTYCHE GLOEOCYSTIS; GLAUCOCYSTIS NOSTOCHINEARUM; GLAUCOCYSTOPHYCEAE; GLOEOCYSTIS;

EID: 0029805179     PISSN: 00219193     EISSN: None     Source Type: Journal    
DOI: 10.1128/jb.178.23.6994-6997.1996     Document Type: Article

References (13)

1. Aitken, A., and R. Y. Stanier. 1979. Characterization of peptidoglycan from cyanelles of Cyanaphora paradoxa. J. Gen. Microbiol. 112:219-223.
2. Bhattachar, D., T. Helmchen, C. Bibeau, and M. Melkonian. 1995. Comparisons of nuclear-encoded small suhunit ribosomal RNAs reveal the evo lutionary position of the Glaucocystophyta. Mol. Biol. Evol. 12:415-420.
3. Bohnert, H. J., E. J. Crouse, J. Pouyet, H. Mucke, and W. Löffelhardt. 1982. The subcellular location of DNA components from Cyanophora paradoxa, a flagellate containing endosymbiotic cyanelles. Eur. J. Biochem. 126:381-388.
4. Demchick, P., and A. L. Koch. 1996. The permeability of the wall fabric of Escherichia coli and Bacillus subtilis. J. Bacteriol. 178:768-773.
5. Glauner, B. 1988. Separation and quantification of muropeptides with HPLC. Anal. Biochem. 172:451-464.
6. Hash, J. H., and M. V. Rothlauf. 1967. The N,O-diacetyl-muramidase of Chalaropsis species: purification and crystallisation. J. Biol. Chem. 242:5586-5590.
7. Helmchen, T. A., D. Bhattacharya, and M. Melkonian. 1995. Analyses of ribosomal RNA sequences from glaucocystophyte cyanelles provide new insights into evolutionary relationships of plastids. J. Mol. Evol. 41:203-210.
8. Herdman, M., and R. Y. Stanier. 1977. The cyanelle: chloroplast or endosymbiotic procaryote. FEMS Microbiol. Lett. 1:7-12.
9. +-oxidoreduetase from Cyanophora Pabadoxa into cyanelles and into pea chloroplasts. FEBS Lett. 381:153-155.
10. Kies, L. 1992. Glaucocrystophyccae and other protists harbouring procaryotic endocytobionts, p. 353-377. In W. Reisser (ed.), Algae and symbioses. Biopress Limited, Bristol, United Kingdom.
11. Mucke, H., W. Löffelhardt, and H. J. Bohnert. 1980. Partial characterization of the genome of the "endosymbiotic" cyanelles from Cyanophora paradosa. FEBS Lett. 111:347-352.
12. Pfanzagl, B., A. Zenker, E. Pittenauer, G. Allmaier, J. Martinez-Torrec-uadrada, E. R. Schmid, M. A. de Pedro, and W. Löffelhardt. 1996. Primary structure of cyanelle peptidoglycan of Cyanophora paradoxa: a prokaryotic cell wall as part of an organelle envelope. J. Bacteriol. 178:332-339.
13. 252-plasma desorption mass spectrometry and last atom bombardement/tandem mass spectrometry. Biol. Mass Spectrometry. 22:524-536.