Field assessment of sub-epidermal leaf anthocyanin, PSII photochemistry,and the xanthophyll-cycle as photoprotective mechanisms in two morphs of Agave striata

We tested the hypothesis that leaf epidermal pigments screen light of particular wavelengths from reaching the photosynthetic machinery, reducing dependence on the xanthophyll-cycle as an energy dissipation process. Under field conditions, photosynthesis and water relations were studied in two morphs of Agave striata that differ in leaf coloration (green vs. reddish-purple). Titratable acidity, chlorophyll fluorescence, and internal and surface leaf temperatures were measured under low irradiance by shading (30%) and full sunlight (100%) for six days. We also measured the reflectance ratio (R_RED: R_GREEN), an index of anthocyanin content and the change in photochemical reflectance index (ΔPRI), an index of xanthophyll-cycle de-epoxidation state (xanthophyll conversion). Our results showed that both morphs expressed typical CAM-activity with no significant differences under sun vs. shade. However, shading did reduce titratable acids in both morphs. Both morphs were well hydrated, with the relative water content (RWC) being greater than 93%. Leaf surface temperature was found to be significantly higher during the day in the green morph compared to the red morph under sun and shade. Dark level fluorescence (Fo), photochemical efficiency of PSII (Fv/Fm), and the quantum yield of PSII electron transport (Φ_PSII) were higher in the red morph under sun compared to the green morph. The value of qN (non-photochemical quenching) was significantly higher during the day for the green morph compared to the red morph and this higher qN value was associated with a greater xanthophyll conversion and surface leaf temperature. However, sunlight did not predispose either of the morphs to photoinhibition. It is clear that the sub-epidermal anthocyanins serve as a photoprotective mechanism in the red morph, screening light energy from reaching the photosynthetic machinery and reducing dependence on the xanthophyll-cycle. We concluded that under natural light conditions the leaves of two morphs tested utilized differential photoprotective mechanisms.     

Human immunodeficiency virus envelope-dependent cell-cell fusion: a quantitative fluorescence cytometric assay

BACKGROUND: In vitro fusion of transfected cells expressing the human immunodeficiency virus (HIV) envelope proteins gp120/gp41, with target cells expressing CD4, and a suitable chemokine coreceptor is used widely to investigate the mechanisms of molecular recognition and membrane fusion involved in the entry of the HIV genome into cells and in syncytia formation. METHODS: We developed an assay that uses two different fluorescent lipophilic probes to single label each reacting cell population and flow cytometry to quantify the extent of cellular fusion after coculture. RESULTS: Fused cells are detected as double-fluorescent particles in this assay, therefore permitting measurement of their proportion in the total cell population. The time course and extent of HIV-glycoprotein-related cellular fusion, the optimal cell ratio, the size and cell composition of the fusion products, and the inhibition of fusion caused by soluble CD4 and anti-CXCR4 antibody 12G5 were determined. The assay was applied to measure fusion between gp120/gp41 and CD4-expressing cells growing as monolayers (HeLa/CHO fusion), as well as to suspension lymphocyte cultures (Jurkat/Jurkat fusion). CONCLUSIONS: The method's simple technical and minimal cell-invasive procedures, as well as its non-ambiguous automatic numerical quantification should be useful for the study of factors influencing cell-cell fusion.     

Effects of a PAL inhibitor on phenolic accumulation and UV-B tolerance in Spirodela intermedia (Koch.)

Duckweed (Spirodela intermedia) was grown axenically on 1/2 strength Hutner's nutrient solution plus 1% sucrose, with the l-phenylalanine ammonia-lyase (PAL) inhibitor 2-aminoindan-2-phosphonic acid (AIP) at 0.0, 0.05, or 10 microM, at constant 25 degrees C and a light intensity of 300 micromol m(-2) s(-1) photosynthetically active radiation from CW fluorescent lamps. Growth with 10 microM AIP led to decreased frond area and fresh weight, but dry weight was unchanged. Microscopic examination of fronds revealed increased frond thickness and a lack of reticulate aerenchyma. Ultraviolet epifluorescence microscopy and UV-Vis spectroscopy of methanolic extracts confirmed the dose-dependent inhibition of secondary phenolic synthesis with the near total elimination of secondary phenolic accumulation at the 10 microM level. AIP-treated plants showed increased sensitivity to UV-B as shown by a reduced F(v)/F(m). The results provided direct evidence of the working hypothesis that phenols function to screen UV radiation from reaching photosynthetic tissues or damaging other sensitive tissues. A novel histochemical method employing zirconyl chloride to visualize phenols is discussed.     

A Central pattern generator to control a pyloric-based system

A central pattern generator (CPG) is built to control a mechanical device (plant) inspired by the pyloric chamber of the lobster. Conductance-based models are used to construct the neurons of the CPG. The plant has an associated function that measures the amount of food flowing through it per unit of time. We search for the best set of solutions that give a high positive flow of food in the maximization function. The plant is symmetric and the model neurons are identical to avoid any bias in the space of solutions. We find that the solution is not unique and that three neurons are sufficient to produce positive flow. We propose an effective principle for CPGs (effective on-off connectivity) and a few predictions to be corroborated in the pyloric system of the lobster.     

Self-organization in the olfactory system: one shot odor recognition in insects

We show in a model of spiking neurons that synaptic plasticity in the mushroom bodies in combination with the general fan-in, fan-out properties of the early processing layers of the olfactory system might be sufficient to account for its efficient recognition of odors. For a large variety of initial conditions the model system consistently finds a working solution without any fine-tuning, and is, therefore, inherently robust. We demonstrate that gain control through the known feedforward inhibition of lateral horn interneurons increases the capacity of the system but is not essential for its general function. We also predict an upper limit for the number of odor classes Drosophila can discriminate based on the number and connectivity of its olfactory neurons. Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.     

New information on the mechanism of forcible ascospore discharge from Ascobolus immersus

Many ascomycete fungi spurt their spores from asci pressurized by osmosis. This paper explores the details of this process in the coprophilous species Ascobolus immersus, through a combination of biomechanical and biochemical experiments, and mathematical modeling. A. immersus forms large asci that expel 8 spores as a single, mucilage-embedded projectile. Measurements of ascus turgor using a microprobe attached to a strain gauge showed a pressure of 0.3 MPa or 3 atm. Analysis of ascus sap using GC/MS identified glycerol as a major osmolyte, accounting for 0.1 MPa of the osmotic pressure within the ascus sap. A mathematical model indicated that a pressure of 0.2 MPa would be sufficient to propel the cluster of ascospores over the distance measured in previous studies. The difference between the measured and predicted pressures is ascribed to loss of pressure as the spores are forced through the tip of the open ascus.     

Validation of data collection for an American trypanosomiasis epidemiologic study in the State of Morelos, México]

The purpose of this paper is to show up the importance of the standardization concepts in American Trypanosomiasis epidemiological studies. The consistence in the measurement of some dwelling characteristics was evaluated. A validation of the Queretaro antigen for indirect hemagglutination reaction as a diagnostic test and the interobserver concordance for the serologic readings were also made. The observers were instructed in some sessions. The pretests were made in the laboratory with positive and negative sera, with sera from the studied population. Results show that the interobserver concordance after the instruction, for the dwelling variables ranged from 70% to 100%. Sensitivity of the Queretaro antigen was 100%, specificity 55%, the predictive value of a positive test 55%, and the predictive value of a negative test 93%. The interobserver concordance was 47%. The pretest and the pilot study are very important in getting the objectives of the principal study.