Correlation between the chemical shift values and precise interglycosidic measurements in the cyclic glucan of Burkholderia solanacearum

Journal of the American Chemical Society

Volumn 118, Issue 30, 1996, Pages 7227-7228

  Lippens, G ^a   Wieruszeski, J M ^a   Talaga, P ^b   Bohin, J P ^b   Desvaux, H ^c,d  

^a INSTITUT PASTEUR DE LILLE   (France)

^b CNRS   (France)

^c FLORIDA STATE UNIVERSITY   (United States)

^d CEA SACLAY   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCAN;

ARTICLE; DRUG STRUCTURE; NUCLEAR MAGNETIC RESONANCE;

EID: 0029785337     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja954344e     Document Type: Article

References (17)

1. Breedveld, M. W.; Miller, K. J. Microbiol. Rev. 1994, 58, 145.
2. (a) Lippens, G.; Talaga, P.; Wieruszeski, J.-M.; Bohin, J. P. In Spectroscopy of Biological Molecules; Merlin, J. C., Turrell, S., Huvenne, J.-P., Eds.; Kluwer Academic Publishers: Dordrecht, The Netherlands, 1995.
3. (b) Talaga, P.; Stahl, B.; Wieruszeski, J.-M.; Hillenkamp, F.; Tsuyumu, S.; Lippens, G.; Bohin, J. P. J. Bacteriol. 1996, 178, 2263-2271.
4. York, W. S. Carbohydr. Res. 1995, 278, 205-225.
5. Jarvis, M. C. Carbohydr. Res. 1994, 259, 311.
6. The glycosidic torsional angles are defined as Φ = H1-C1-O-C2′ and Ψ = C1-O-C2′-H2′.
7. (a) Sabesan, S.; Duus, J. O.; Fukunaga, T.; Bock, K.; Ludvigsen, S. J. Am. Chem. Soc. 1992, 113, 3236.
8. (b) Widmalm, G.; Byrd, R. A.; Egan, W. Carbohydr. Res. 1992, 229, 195.
9. (c) Peters, T.; Weimar, T. J. Biomol. NMR 1994, 4, 97.
10. Desvaux, H.; Berthault, P.; Birlirakis, N.; Goldman, M. J. Magn. Reson. A 1994, 108, 219.
11. Desvaux, H.; Berthault, P.; Birlirakis, N. Chem. Phys. Lett. 1995, 233, 545.
12. Macura, S.; Farmer, B. T., II; Brown, L. R. J. Magn. Reson. 1986, 70, 493.
13. 2 seems to be due to a slight amount of spin diffusion for this pair.
14. Berthault, P.; Birlirakis, N.; Rubinstenn, G.; Sinay, P.; Desvaux, H. J. Biomol. NMR, in press.
15. Estimating a maximal error of 10% in the cross and diagonal peak volumes, intrinsic upper limits on the error bars are ±0.05 Å for the distances and ±0.04 ns for the correlation times. Of course, these values do not take into account the bias associated with the assumed model of motions. However, it has been demonstrated for an equivalent molecule (ref 11) that the effect of this bias on found distances is smaller than that obtained using an internal distance reference. The distance ranges observed for group 1 and group 2 are therefore significantly different.
16. (a) Dowd, M. K.; French, A. D.; Reilly, P. J. Carbohydr. Res. 1992, 233, 15.
17. (b) André, I.; Mazeau, K.; Taravel, F. R.; Tvaroska, I. New J. Chem. 1995, 19, 331.