Effect of Time of Application on the Action of Foliar Sprays of Oxamyl on Meloidogyne hapla in Tomato

Foliar sprays containing 3,000 or 4,000 ppm oxamyl applied before inoculation with Meloidogyne hapla completely protected tomato plants from intection for up to 36 days but sprays containing 1,000 or 2,000 ppm provided only partial protection. Postinoculation sprays were less effective than preinoculation sprays but they decreased the numbers of females and their rate of development and increased the numbers of males. Similar amounts of oxamyl applied to the soil as a drench or as granules controlled M. hapla more effectively than foliar sprays but the longer treatment was delayed after infection the fewer the larvae that were killed and the more that became male.     

Selective neutrality of glucose-6-phosphate dehydrogenase allozymes in Escherichia coli

Six naturally occurring alleles representing four electromorphs of the enzyme glucose-6-phosphate dehydrogenase were transferred by P1- mediated transduction from natural isolates of Escherichia coli into the genetic background of E. coli K12 and were studied in pairwise competition in chemostats limited for glucose in order to estimate differences in growth rate associated with the alleles. Although the level of resolution of such experiments is a growth rate differential of approximately 0.002 h-1, no significant differences among the strains were found. Studies of apparent Km and Vmax in crude enzyme extracts of the strains also failed to reveal any significant differences among the electromorphs. These results support the view that the alleles are selectively neutral or nearly neutral under these conditions.      

Purification and properties of cyclopentanone oxygenase of Pseudomonas NCIB 9872.

1. Cyclopentanone oxygenase from Pseudomonas NCIB 9872 has been purified some 40-fold. It gives a single peak in the ultracentrifuge and a single major protein band on polyacrylamide gels contaminated with about 5% of a slower migrating impurity. Flavin dissociates from the protein during electrophoresis. 2. The enzyme has a molecular weight of about 200000 and is a homopolymeric assemblage of either three of four subunits of molecular weight 54000-58000. 3. The prosthetic group is FAD and values of about 2.5 are typically obtained for the number of moles bound to each mole of holoenzyme. Some FAD probably dissociates during purification and it seems likely that each subunit binds one FAD in the undamaged protein.     

Ingestion,Retention, and Transmission of two Strains of Raspberry Ring-spot Virus by Longidorus macrosoma

The transmission of two strains of raspberry ringspot virus (RRV) by small numbers of nematodes was compared. A strain of RRV from Scotland (RRV-S), originally found in the field associated with Longidorus elongatus, was transmitted frequently by L. elongatus but only once by L. macrosoma. A strain from England (RRV-E) associated with L. macrosoma in the field was transmitted infrequently by each species of nematode. The reasons why L. macrosoma infected only a small proportion of bait plants with virus were investigated, and it was found that most of the nematodes tested had fed on the source plants and many had ingested virus. Most nematodes exposed to RRV-E or RRV-S had fed on the roots of the bait plants and, when thin sections were examined by electron microscope, had retained particles (thought to be those of the virus) in the region of the anterior odontostyle, Thus, most nematodes seem to have had ample opportunity to transmit virus, and the low frequency of transmission may have been due to a failure of the virus particles to be released from the site of retention or to a lack of infectivity of the virus when L. macrosoma was the vector and Petunia hybrida was the host.     

Utility of nematode community analysis as an integrated measure of the functional state of soils: perspectives and challenges

Soil nematode communities have the potential to provide unique insights into many aspects of soil processes. Since most nematodes are active in soil throughout the year, they can potentially provide a holistic measure of the biotic and functional status of soils. In contrast to other soil microbial groups, representative samples of soil nematode communities are relatively easy to obtain. However, most current nematode ecological information has been survey-based or purely observational in nature, with a persistent focus on detailed taxonomic analysis of nematode communities. The development of a Maturity Index, MI, represents a significant advance in classifying communities and it continues to be refined and developed. But, to develop a wide capacity to use soil nematode information for diagnostic and predictive purposes, particularly for agricultural soils, we need a new, more robust approach, which does not require extensive taxonomic skill and includes more functional criteria. One of the key attributes of nematodes is the relationship between structural form (principally oesophagal feeding apparatus) and function (i.e. trophic group). Nematode form is readily determinable by direct observation of extracted nematodes and high-level taxonomic skills are not needed to assign the major community components to their different trophic and ecological groups. Consequently, the trophic structure of nematode communities is relatively easy to determine and can provide an integrated measure of the status of the other groups on which they feed. Similarly, population numbers and proportions of juveniles and adults can be readily determined, permitting calculation of relative biomass and dynamics of population growth. The size distribution of individuals within the community is likely also to be an indicator of the structural status of soils from a biotic standpoint. However, fundamental gaps remain in our understanding which limit our ability to relate differences in nematode communities to functional differences. There needs to be a greater emphasis on the development and experimental testing of hypotheses, a greater integration of nematology into soil-process related studies, and the development of a specific, soil-nematode related theoretical framework for understanding epidemiological and soil colonisation processes. This revised version was published online in June 2006 with corrections to the Cover Date.     

Tissue type-specific expression of intermediate filament proteins in a cultured epithelial cell line from bovine mammary gland

Different clonal cell lines have been isolated from cultures of mammary gland epithelium of lactating cow’s udder and have been grown in culture media containing high concentrations of hydrocortisone, insulin, and prolactin. These cell (BMGE+H), which grow in monolayers of typical epithelial appearance, are not tightly packed, but leave intercellular spaces spanned by desmosomal bridges. The cells contain extended arrays of cytokeratin fibrils, arranged in bundles attached to desmosomes. Gel electophoresis show that they synthesize cytokeratins similar, if not identical, to those found in bovine epidermis and udder, including two large (mol wt 58,500 and 59,000) and basic (pH range: 7-8) and two small (mol wt 45,500 and 50,000) and acidic (pH 5.32 and 5.36) components that also occur in phosphorylated forms. Two further cytokeratins of mol wts 44,000 (approximately pH 5.7) and 53,000 (pH 6.3) are detected as minor cytokeratins in some cell clones. BMGE+H cells do not produce vimentin filaments as determined by immunofluorescence microscopy and gel electrophoresis. By contrast, BMGE-H cells, which have emerged from the same original culture but have been grown without hormones added, are not only morphologically different, but also contain vimentin filaments and a different set of cytokeratins, the most striking difference being the absence of the two acidic cytokeratins of mol wt 50,000 and 45,500. Cells of the BMGE+H line are characterized by an unusual epithelial morphology and represent the first example of a nonmalignant permanent cell line in vitro that produces cytokeratin but not vimentin filaments. The results show that (a) tissue-specific patterns of intermediate filament expression can be maintained in permanent epithelial cell lines in culture, at least under certain growth conditions; (b) loss of expression of relatively large, basic cytokeratins is not an inevitable consequence of growth of epithelial cells in vitro. Our results further show that, during culturing, different cell clones with different cytoskeletal composition can emerge from the same cell population and suggest that the presence of certain hormones may have an influence on the expression of intermediate filament proteins.     

Multiple forms of cyclohexanone oxygenase from Nocardia globerula CL1.

The cyclohexanone 1,2-monooxygenase of Nocardia globerula CL1 exists as two electrophoretically distinct forms. These are present in crude cell extracts and are not artifacts of enzyme purification or electrophoresis. They have been separated in mg amounts by preparative polyacrylamide gel electrophoresis and shown to have essentially identical kinetic, spectral and physical characteristics. They do differ in pH-activity profile and temperature stability. Whether or not they are conformational isoenzymes or arise by gene duplication and divergent evolution has not been established. Cyclohexanone oxygenase constitutes 8% of the soluble protein of induced cells. This high level would correlate well with the presence of duplicate genes. It is proposed that the presence of a large amount of cyclohexanone oxygenase may confer an ecological advantage on the organism.