J Gen Virol Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 71 (1990), 977-981; DOI 10.1099/0022-1317-71-4-977
© 1990 Society for General Microbiology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Spies, U.
Right arrow Articles by Müller, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Spies, U.
Right arrow Articles by Müller, H.
Agricola
Right arrow Articles by Spies, U.
Right arrow Articles by Müller, H.

Demonstration of enzyme activities required for cap structure formation in infectious bursal disease virus, a member of the birnavirus group

U. Spies and H. Müller

Institut für Virologie, Justus-Liebig-Universität Giessen, Frankfurter Strasse 107, D-6300 Giessen, F.R.G.

The putative viral transcriptase p90 in infectious bursal disease virus (IBDV) was shown to form an enzyme-guanylate intermediate which is indicative of guanylyltransferase activity. The p90-nucleotide bond is most likely to be a phosphodiester linkage, as it resisted treatment with HCl and NH2OH but was sensitive to NaOH. This is in contrast to phosphoamide bonds formed by reovirus cores. Methyltransferase activity was also demonstrated in IBDV, and is closely associated with transcription, suggesting that p90 may be a multifunctional enzyme.

Received 5 August 1989; accepted 3 January 1990.


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
J. Pan, V. N. Vakharia, and Y. J. Tao
The structure of a birnavirus polymerase reveals a distinct active site topology
PNAS, May 1, 2007; 104(18): 7385 - 7390.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
M. Liu and V. N. Vakharia
Nonstructural protein of infectious bursal disease virus inhibits apoptosis at the early stage of virus infection.
J. Virol., April 1, 2006; 80(7): 3369 - 3377.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
U. I. von Einem, A. E. Gorbalenya, H. Schirrmeier, S.-E. Behrens, T. Letzel, and E. Mundt
VP1 of infectious bursal disease virus is an RNA-dependent RNA polymerase
J. Gen. Virol., August 1, 2004; 85(8): 2221 - 2229.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
M. Brandt, K. Yao, M. Liu, R. A. Heckert, and V. N. Vakharia
Molecular Determinants of Virulence, Cell Tropism, and Pathogenic Phenotype of Infectious Bursal Disease Virus
J. Virol., December 15, 2001; 75(24): 11974 - 11982.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
H. J. Boot, A. A. H. M. ter Huurne, A. J. W. Hoekman, B. P. H. Peeters, and A. L. J. Gielkens
Rescue of Very Virulent and Mosaic Infectious Bursal Disease Virus from Cloned cDNA: VP2 Is Not the Sole Determinant of the Very Virulent Phenotype
J. Virol., August 1, 2000; 74(15): 6701 - 6711.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1990 by the Society for General Microbiology.