Leaching loss of NO3-N and dissolved P from manure and fertilizer during turfgrass establishment

Cycling of manure nutrients through turfgrass sod could affect groundwater quality. The fate of nutrients in transplanted fertilizer- or manure-grown sod of Tifway bermudagrass (Cynodon dactylon L. Pers. X C. transvaalensis Burtt-Davey) was compared with that in composted dairy manure (CDM) applied to a sprigged treatment. Leaching loss of NO₃-N and dissolved P (DP) in filtrate (<0.45 μm) of leachate was compared among sodded and sprigged treatments during periods 0–50, 60–110, and 330–380 d after planting in lysimeters. In addition, recovery of N and P in turfgrass clippings and a sand medium was quantified. Maintenance applications of CDM or fertilizer P were top-dressed starting 60 d after planting. Leachate was collected and sampled over three simulated rain events during each of the three sampling periods. From 0 d to 50 d after planting, leaching loss of NO₃-N from sprigged Tifway totaled 2.0 g m⁻² and was 10 times greater than loss from CDM-grown or fertilizer-grown sod. In contrast, DP loss in leachate was ≤0.02 g m⁻² and similar among treatments. Surface applications of CDM and fertilizer P and N increased concentration and mass of total Kjeldahl N (TKN) and soil-test P (STP) in surface or subsurface layers of the sand medium. Yet, NO₃-N mass in leachate collected over three simulated rain events ranged from 0.0 to only 1.0% of applied N from 60–110 d and 330–380 d after planting. Leaching loss of NO₃-N did not differ between the sodded and sprigged treatments after two topdressings of CDM. Similarly, the DP mass recovered in leachate was small (≤0.013 g m⁻¹) and did not differ among treatments during the latter two sampling periods. The mass loss of DP in leachate was typically less than the DP mass applied through irrigation or simulated rain. Importing CDM in sod reduces NO₃-N leaching loss compared to sprigged turfgrass amended with CDM, but NO₃-N and DP leaching losses are similar during maintenance of CDM-grown and fertilizer-grown sod from 60–110 d to 330–380 d after transplanting. Responsible Editor: Bernard Nicolardot.     

Seasonal dynamics of soil micronutrients in compost-amended bermudagrass turf

Compost application to turfgrasses can increase plant-available nutrient concentrations in soil and improve growth, but may alter micronutrient dynamics and increase leaching and runoff losses. The objectives of this study were to investigate the influence of compost on the seasonal dynamics of plant-available Mn, Fe, Cu, and Zn in soil after a single application to bermudagrass [Cynodon dactylon (L.) Pers.] turf. Extractable Mn increased from 270 to 670 mg kg(-1) and Cu from 0.36 to 9.89 mg kg(-1) from 0 to 29 months. In contrast, extractable Fe and Zn decreased by 52% and 57% during the same time period. Seasonal trends in extractable Mn and Cu were closely related to dissolved organic C (DOC), and appeared influenced by bermudagrass growth and dormancy patterns and subsequent impacts on DOC. Losses of Mn and Cu from the soil surface occurred after high levels of precipitation during winter dormancy but not during the growing season, while Fe and Zn exhibited an opposite pattern. Thus, seasonal variation of soil micronutrients was likely related to seasonal patterns of bermudagrass growth and dormancy and their effects on DOC, and precipitation events which probably leached DOC and complexed nutrients from surface soil. Composts only influenced the magnitude of changes in micronutrient concentrations, as similar seasonal trends occurred for both compost-amended and unamended soils.     

Identification of MarvelD3 as a tight junction-associated transmembrane protein of the occludin family

Background

Protein translocation across the membrane of the Endoplasmic Reticulum (ER) is the first step in the biogenesis of secretory and membrane proteins. Proteins enter the ER by the Sec61 translocon, a proteinaceous channel composed of three subunits, α, β and γ. While it is known that Sec61α forms the actual channel, the function of the other two subunits remains to be characterized.

Results

In the present study we have investigated the function of Sec61β in Drosophila melanogaster. We describe its role in the plasma membrane traffic of Gurken, the ligand for the Epidermal Growth Factor (EGF) receptor in the oocyte. Germline clones of the mutant allele of Sec61β show normal translocation of Gurken into the ER and transport to the Golgi complex, but further traffic to the plasma membrane is impeded. The defect in plasma membrane traffic due to absence of Sec61β is specific for Gurken and is not due to a general trafficking defect.

Conclusion

Based on our study we conclude that Sec61β, which is part of the ER protein translocation channel affects a post-ER step during Gurken trafficking to the plasma membrane. We propose an additional role of Sec61β beyond protein translocation into the ER.     

Sequence of a cDNA for mouse thymidylate synthase reveals striking similarity with the prokaryotic enzyme

We report the nucleotide sequence of a cloned cDNA, pMTS-3, that contains a 1-kb insert corresponding to mouse thymidylate synthase (E.C. 2.1.1.45). The open reading frame of 921 nucleotides from the first AUG to the termination codon specifies a protein with a molecular mass of 34,962 daltons. The predicted amino acid sequence is 90% identical with that of the human enzyme. The mouse sequence also has an extremely high degree of similarity (as much as 55% identity) with prokaryotic thymidylate synthase sequences, indicating that thymidylate synthase is among the most highly conserved proteins studied to date. The similarity is especially pronounced (as much as 80% identity) in the 44-amino-acid region encompassing the binding site for deoxyuridylic acid. The cDNA sequence also suggests that mouse thymidylate synthase mRNA lacks a 3' untranslated region, since the termination codon, UAA, is followed immediately by a poly(A) segment.      

Role of the reticulum in the stability and shape of the isolated human erythrocyte membrane

In order to examine the widely held hypothesis that the reticulum of proteins which covers the cytoplamsic surface of the human erythrocyte membrane controls cell stability and shape, we have assessed some of its properties. The reticulum, freed of the bilayer by extraction with Triton X-100, was found to be mechanically stable at physiological ionic strength but physically unstable at low ionic strength. The reticulum broke down after a characteristic lag period which decreased 500-fold between 0 degrees and 37 degrees C. The release of polypeptide band 4.1 from the reticulum preceded that of spectrin and actin, suggesting that band 4.1 might stabilize the ensemble but is not essential to its integrity. The time-course of breakdown was similar for ghosts, the reticulum inside of ghosts, and the isolated reticulum. However, at very low ionic strength, the reticulum was less stable within the ghost than when free; at higher ionic strength, the reverse was true. Over a wide range of conditions the membrane broke down to vesicles just as the reticulum disintegrated, presumably because the bilayer was mechanically stabilized by this network. The volume of both ghosts and naked reticula varied inversely and reversibly with ionic strength. The volume of the naked reticulum varied far more widely than the ghost, suggesting that its deformation was normally limited by the less extensible bilayer. The contour of the isolated reticulum was discoid and often dimpled or indented, as visualized in the fluorescence microscope after labeling of the ghosts with fluoroscein isothiocyanate. Reticula derived from ghosts which had lost the ability to crenate in isotonic saline were shriveled, even though the bilayer was smooth and expanded. Conversly, ghosts crenated by dinitrophenol yielded smooth, expanded reticula. We conclude that the reticulum is a durable, flexible, and elastic network which assumes and stabilizes the contour of the membrane but is not responsible for its crenation.     

Molecular evolution of a multigene family in group A streptococci

The emm genes are members of a gene family in group A streptococci (GAS) that encode for antiphagocytic cell-surface proteins and/or immunoglobulin-binding proteins. Previously sequenced genes in this family have been named "emm," "fcrA," "enn," "arp," "protH," and "mrp"; herein they will be referred to as the "emm gene family." The genes in the emm family are located in a cluster occupying 3-6 kb between the genes mry and scpA on the chromosome of Streptococcus pyogenes. Most GAS strains contain one to three tandemly arranged copies of emm-family genes in the cluster, but the alleles within the cluster vary among different strains. Phylogenetic analysis of the conserved sequences at the 3' end of these genes differentiates all known members of this family into four evolutionarily distinct emm subfamilies. As a starting point to analyze how the different subfamilies are related evolutionarily, the structure of the emm chromosomal region was mapped in a number of diverse GAS strains by using subfamily-specific primers in the polymerase chain reaction. Nine distinct chromosomal patterns of the genes in the emm gene cluster were found. These nine chromosomal patterns support a model for the evolution of the emm gene family in which gene duplication followed by sequence divergence resulted in the generation of four major-gene subfamilies in this locus.      

Diversity of lactic acid bacteria of the bioethanol process

Background  

Bacteria may compete with yeast for nutrients during bioethanol production process, potentially causing economic losses. This is the first study aiming at the quantification and identification of Lactic Acid Bacteria (LAB) present in the bioethanol industrial processes in different distilleries of Brazil.     

Feasibility of using cryopreserved lymphoblastoid cells to diagnose some lysosomal storage diseases

Objectives: The Epstein–Barr virus (EBV) is utilized as a tool in the study of cellular biology because of its capacity to transform B‐lymphocytes. For this reason, EBV is used in conservation of human B‐lymphocytes for long periods for subsequent evaluation of lysosomal hydrolase activity. Lymphoblastoid cell lines have several advantages for use over other cell types, such as prompt availability and possibility to develop, characterize and standardize cell banks, to test effects of promising pharmaceutical reagents. The study below presents biochemical data that demonstrate validity of lymphoblastoid cell lines for diagnosis of GM1‐gangliosidosis, Gaucher, Fabry and Pompe diseases and mucopolysaccharidosis type I. Materials and methods: Cultures were prepared from peripheral blood, collected from 25 normal subjects and 13 affected individuals. Enzyme activities and immunohistochemistry (IHC) were measured. Activities of enzymes β‐galactosidase, β‐glucosidase, α‐iduronidase, α‐galactosidase and α‐glucosidase were measured before and after cryopreservation for 180 days. Enzymatic activity was measured when transformation was confirmed by IHC. Results: We observed some significant alterations in enzymatic activity of non‐cultured cells when compared to others that had been cultured for 12 days and kept frozen for 180 days. Conclusions: However, these alterations did not invalidate use of the technology of transformation of lymphoblastoid cell lines with EBV, to diagnose the diseases mentioned above, in view of the fact that the cultured cells, before and after freezing, demonstrated similar enzymatic activities.