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Full-Text Articles in Plant Sciences
Risk-Based Oversight Of Experiments In The Environment, Henry I. Miller, Robert H. Burris, Anne K. Vidaver, Nelson A. Wivel
Risk-Based Oversight Of Experiments In The Environment, Henry I. Miller, Robert H. Burris, Anne K. Vidaver, Nelson A. Wivel
Department of Plant Pathology: Faculty Publications
The new biology has come of age. Basic research in fields ranging from immunology to plant biology has been transformed so as to be almost unrecognizable to those whose biology education ended before 1970. The spillover into commercial development likewise has been remarkable. Hardly a week passes without news of some new advance in an area such as therapeutics, vaccines, or plants and animals for food, feed, or fiber. These uses of biotechnology in "contained" laboratories, pilot plants, greenhouses, and production facilities have engendered little controversy. The National Institutes of Health Guidelines for Research Involving Recombinant DNA have exempted from …
Towards An Improved Taxonomy Of Xanthomonas, L. Vauterin, J. Swings, K. Kersters, M. Gillis, T. W. Mew, M. N. Schroth, N. J. Palleroni, D. C. Hildebrand, D. E. Stead, E. L. Civerolo, A. C. Hayward, H. Maraîte, R. E. Stall, A. K. Vidaver, J. F. Bradbury
Towards An Improved Taxonomy Of Xanthomonas, L. Vauterin, J. Swings, K. Kersters, M. Gillis, T. W. Mew, M. N. Schroth, N. J. Palleroni, D. C. Hildebrand, D. E. Stead, E. L. Civerolo, A. C. Hayward, H. Maraîte, R. E. Stall, A. K. Vidaver, J. F. Bradbury
Department of Plant Pathology: Faculty Publications
Improvement of the taxonomy of the genus Xanthomonas and especially of Xanthomonas campestris, which is subdivided into more than 125 pathovars, is discussed. Recent contributions to the taxonomy of Xanthomonas are reviewed, and on the basis of these data and unpublished data from several laboratories, the usefulness of different phenotypic, chemotaxonomic, and genotypic techniques is discussed. The heterogeneity of several X. campestris pathovars has been demonstrated by sodium dodecyl sulfate electrophoresis of whole-cell proteins and fatty acid fingerprinting. The host selectivity of the pathovars is not correlated with their relationships as revealed by DNA-DNA hybridization experiments. In order to …
Capping Of Tobacco Mosaic Virus Rna: Analysis Of Viral-Coded Guanylyltransferase-Like Activity, David Dunigan, Milton Zaitlin
Capping Of Tobacco Mosaic Virus Rna: Analysis Of Viral-Coded Guanylyltransferase-Like Activity, David Dunigan, Milton Zaitlin
Department of Plant Pathology: Faculty Publications
The 5’ end of tobacco mosaic virus (TMV) genomic RNA is capped with 7- methylguanosine. A virus-coded polypeptide with guanylyltransferase activity has been investigated. This enzyme is responsible for forming the 5’→5’ linkage of guanosine 5’-monophosphate to the 5’- diphosphate of an acceptor RNA, thereby forming the cap. A critical step in the mechanism for cap formation in the eukaryotic nucleus is for guanylyltransferase to bind covalently to guanosine 5’- monophosphate with the hydrolysis of pyrophosphate when guanosine 5’- triphosphate is the substrate. The TMV 126-kilodalton protein, which is most probably a component of the TMV replicase, was found to …
Degradation Of Wheat Streak Mosaic Virus Capsid Protein During Leaf Senescence, Myron K. Brakke, Rose N. Skopp, L. C. Lane
Degradation Of Wheat Streak Mosaic Virus Capsid Protein During Leaf Senescence, Myron K. Brakke, Rose N. Skopp, L. C. Lane
Department of Plant Pathology: Faculty Publications
Wheat streak mosaic virus capsid protein degraded in vivo by proteolysis as leaves senesced. The capsid protein of virus purified from young systemically infected leaves had an apparent size or 45 kDa in 12% sodium dodecyl sulfate-polyacrylamide gels with minor amounts of 43, 42, 33, and 3E kDa proteins. The proportion of smaller proteins increased with the age of the leaf. In some virus preparations only 3 1 kDa capsid protein was detected. In vitro proteolysis of virions with 45 kDa protein produced virions with 31 kDa protein. Virions with 31 kDa capsid protein sedimented slightly more slowly than those …
Identification Of Single Meloidogyne Juveniles By Polymerase Chain Reaction Amplification Of Mitochondrial Dna, T. S. Harris, L. J. Sandall, Thomas O. Powers
Identification Of Single Meloidogyne Juveniles By Polymerase Chain Reaction Amplification Of Mitochondrial Dna, T. S. Harris, L. J. Sandall, Thomas O. Powers
Department of Plant Pathology: Faculty Publications
Polymerase chain reaction (PCR) was used to amplify a specific 1.8-kb sequence of mitochondrial DNA from single juveniles and eggs from 17 populations of Meloidogyne incognita, M. hapla, M. javanica, and M. arenaria. Approximately 2 μg amplified product were produced per reaction. Restriction digestion of the amplified product with HinfI permitted discrimination of clonal lineages of the four species. Meloidogyne javanica, however, could not be separated from M. hapla by the enzymes used in these experiments. Various amplification conditions and nematode lysis procedures were examined in order to optimize the speed and quality of …