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1 Department of Plant Pathology
and2 Biochemistry, University of Illinois at Urbana-Champaign, Illinois 61801, U.S.A.
The 5' terminus of barley yellow dwarf virus RNA did not become labelled with 32P after dephosphorylation was attempted with calf intestinal alkaline phosphatase and subsequent treatment with [
-32P]ATP and T4 polynucleotide kinase. Treatment of BYDV RNA with 125I-Bolton-Hunter reagent yielded 125I-labelled BYDV RNA, as shown by acid precipitation analysis. Treatment with RNase yielded a protein of approximate Mr 17 000 that was destroyed by treatment with Pronase and was serologically distinct from BYDV coat protein. BYDV therefore appears to have a genome-linked protein.
Keywords: BYDV, genome-linked protein
Present address: Department of Plant Pathology, College of Agriculture, University of Kentucky, Lexington, Kentucky 40546-0091, U.S.A.
Received 6 February 1989;
accepted 20 April 1989.
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