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Journal of Virology, December 1998, p. 10207-10212, Vol. 72, No. 12
NERC Institute of Virology and Environmental
Microbiology,
Received 17 March 1998/Accepted 10 September 1998
Confocal immunofluorescence microscopy was used to demonstrate that
the Autographa californica nucleopolyhedrovirus
(AcMNPV) chitinase was localized within the endoplasmic
reticulum (ER) of virus-infected insect cells. This was consistent with
removal of the signal peptide from the chitinase and an ER localization motif (KDEL) at the carboxyl end of the protein. Chitinase release from
cells, a prerequisite for liquefaction of virus-infected insect larvae,
appears to be aided by synthesis of the p10 protein. Deletion of
p10 from the AcMNPV genome delayed the
appearance of chitinase activity in the medium of virus-infected cells
by 24 h and also delayed liquefaction of virus-infected
Trichoplusia ni larvae by the same period.
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Localization of a Baculovirus-Induced
Chitinase in the Insect Cell Endoplasmic Reticulum
*
Corresponding author. Mailing address: NERC Institute
of Virology and Environmental Microbiology, Mansfield Rd., Oxford OX1 3SR, United Kingdom. Phone: 44 1865 281663. Fax: 44 1865 281696. E-mail: rpossee{at}worf.molbiol.ox.ac.uk.
Journal of Virology, December 1998, p. 10207-10212, Vol. 72, No. 12
0022-538X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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