Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/50473
標題: Identification acid characterization of the Escherichia coli-expressed RNA-dependent RNA polymerase of bamboo mosaic virus
作者: Li, Y.I.
蔡慶修
Cheng, Y.M.
Huang, Y.L.
Tsai, C.H.
Hsu, Y.H.
Meng, M.H.
徐堯煇
孟孟孝
關鍵字: protein secondary structure
hepatitis-c virus
nucleotide-sequence
enzymatic-activity
viral-rna
in-vitro
replication
region
initiation
potexvirus
期刊/報告no:: Journal of Virology, Volume 72, Issue 12, Page(s) 10093-10099.
摘要: Bamboo mosaic virus (BaMV), a member of the potexvirus group, infects primarily members of the Bambusoideae. The open reading frame 1 (ORF1) of BaMV encodes a 155-kDa polypeptide that was postulated to be involved in the replication and the formation of cap structure at the 5' end of the viral genome. To characterize the activities associated with the 155-kDa viral protein, it was expressed in Escherichia coli BL21(DE3) cells with thioredoxin, hexahistidine, and S Tag fused consecutively at its amino terminus, and the fusion protein was purified by metal affinity chromatography. Several RNA fragments, prepared by in vitro transcription, were tested as substrates for the RNA-dependent RNA polymerase (RdRp) activity. Among them, the expressed fusion enzyme was able to generate a P-32-labeled RNA product when 3'-end RNA fragments of the positive strand or negative strand of BaMV were included in the assay mixture. Dot hybridization assay revealed that the reaction products are complementary to their RNA substrates. Taken together, the evidence suggests that the 155-kDa protein encoded by ORF1 of BaMV has an RdRp activity and should be involved in the replication of BaMV, Mutational analyses demonstrate the importance of the GDD motif in the polymerase activity, and deletion studies suggest that the polymerase activity resides in the carboxyl terminus of the 155-kDa viral protein.
URI: http://hdl.handle.net/11455/50473
ISSN: 0022-538X
Appears in Collections:生物科技學研究所

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