Effects of permanent magnetic fields on in vitro growth of Cymbidium and Spathiphyllum shoots

Magnetic fields affect biological systems. However, this is the first study on the effects of permanent magnetic fields (MFs) on the micropropagation of two ornamental plants, Spathiphyllum cv. i.e ‘Merry’ and Cymbidium Music Hour ‘Maria’. Cymbidium and Spathiphyllum shoots cultured in the ‘Miracle Pack’? culture system were exposed to MFs of different intensities, polarities, and duration of exposure. The results show that by increasing intensity from 5 × 10⁻⁶ Tesla (T) as the geo-magnetic field to 0.1, 0.15, and 0.2 T negatively influenced height and fresh mass of roots of Cymbidium plants (except for 0.1 T–S and 0.2 T–N treatments), but had no significant effect on other plantlet parameters. Long-term exposure (1, 2, or 3 mo) of Cymbidium shoots to 0.15 T–MFs negatively influenced plant height, positively affected the number of leaves (with the exception of 0.15 T–S—1 mo), and had no clear effect on other parameters compared to the control. MFs (0.1, 0.15, and 0.2 T), regardless of their polarity, increased chlorophyll content (SPAD value) and the number of leaves, but slightly decreased the dry mass of Spathiphyllum shoots. Different exposure duration to 0.15 T (i.e., 2, 4, or 8 wk) had no significant influence on Spathiphyllum plantlet development other than increasing the SPAD value. These two ornamentals could serve as model systems to study plant development, space production, yield maximization, and the development of new morphotypes essential for the floricultural market.     

Discovery of Dihydrochalcone as Potential Lead for Alzheimer’s Disease: In Silico and In Vitro Study

By the virtual screening method we have screened out Dihydrochalcone as a top-lead for the Alzheimer’s disease using the database of about 32364 natural compounds. The binding affinity of this ligand to amyloid beta (A) fibril has been thoroughly studied by computer simulation and experiment. Using the Thioflavin T (ThT) assay we have obtained the inhibition constant IC50 M. This result is in good agreement with the estimation of the binding free energy obtained by the molecular mechanic-Poisson Boltzmann surface area method and all-atom simulation with the force field CHARMM 27 and water model TIP3P. Cell viability assays indicated that Dihydrochalcone could effectively reduce the cytotoxicity induced by A. Thus, both in silico and in vitro studies show that Dihydrochalcone is a potential drug for the Alzheimers disease.     

Allelopathic actions of the alkaloid 12-epi-hapalindole E isonitrile and calothrixin A from cyanobacteria of the genera Fischerella and Calothrix

The alkaloids 12-epi-hapalindole E isonitrile,isolated from the cyanobacterium Fischerellasp., and the indolophenanthridine calothrixin A, fromCalothrix sp., were characterized in terms oftheir ability to kill several organisms and celltypes, and their biochemical modes of action. Bothcompounds inhibited RNA synthesis, and consequentlyprotein synthesis, in Bacillus subtilis. Calothrixin A also inhibited DNA replication, thehapalindole having little effect on this process. Measurements of in vitro RNA synthesis confirmedthe in vivo results and suggested that bothcompounds inhibit RNA polymerase directly; the degreeof inhibition was independent of the DNAconcentration, but strongly dependent on thepolymerase concentration.     

Infection and transmission studies with the N-3 strain of Plasmodium fieldi in the Macaca mulatta monkey

Seven different anophelines--Anopheles freeborni, An. dirus, An. maculatus, An. atroparvus, An. stephensi, An. albimanus, and An. quadrimaculatus--were shown to be susceptible to infection with the N-3 strain of Plasmodium fieldi. Transmission was obtained via the bites of An. dirus, An. stephensi, and An. maculatus mosquitoes to Macaca mulatta monkeys. Sporozoites dissected from An. freeborni were also shown to be infectious. Anopheles dirus and An. stephensi were the most suitable mosquitoes for transmission studies. Prepatent periods in M. mulatta monkeys following sporozoite inoculation ranged from 9 to 18 days with a mean of 12.3 days. Maximum parasitemias in intact animals following sporozoite inoculation ranged from 5,460 to 32,800 per mm3. Mean maximum parasitemia in splenectomized monkeys inoculated with parasitized blood was 146,000 per mm3.     

Photobleaching recovery and anisotropy decay of green fluorescent protein GFP-S65T in solution and cells: cytoplasmic viscosity probed by green fluorescent protein translational and rotational diffusion.

The green fluorescent protein (GFP) was used as a noninvasive probe to quantify the rheological properties of cell cytoplasm. GFP mutant S65T was purified from recombinant bacteria for solution studies, and expressed in CHO cell cytoplasm. GFP-S65T was brightly fluorescent in solution (lambda ex 492 nm, lambda em 509 nm) with a lifetime of 2.9 ns and a rotational correlation time (tc) of 20 ns. Recovery of GFP fluorescence after photobleaching was complete with a half-time (t1/2) in aqueous saline of 30 +/- 2 ms (5-micron diameter spot), giving a diffusion coefficient of 8.7 x 10(-7) cm2/s. The t1/2 was proportional to solution viscosity and was dependent on spot diameter. In contrast to fluorescein. GFP photobleaching efficiency was not affected by solution O2 content, triplet state quenchers, singlet oxygen scavengers, and general radical quenchers. In solutions of higher viscosity, an additional, rapid GFP recovery process was detected and ascribed to reversible photobleaching. The t1/2 for reversible photobleaching was 1.5-5.5 ms (relative viscosity 5-250), was independent of spot diameter, and was unaffected by O2 or quenchers. In cell cytoplasm, time-resolved microfluorimetry indicated a GFP lifetime of 2.6 ns and a tc of 36 +/- 3 ns, giving a relative viscosity (cytoplasm versus water) of 1.5. Photobleaching recovery of GFP in cytoplasm was 82 +/- 2% complete with a t1/2 of 83 +/- 6 ms, giving a relative viscosity of 3.2. GFP translational diffusion increased 4.7-fold as cells swelled from a relative volume of 0.5 to 2. Taken together with measurements of GFP translation and rotation in aqueous dextran solutions, the data in cytoplasm support the view that the primary barrier to GFP diffusion is collisional interactions between GFP and macromolecular solutes.     

Spectroscopy, electrochemistry, and nucleophilicity of nickel and cobalt complexes of 2′-pyridine carboxaldehyde 2′-pyridyl hydrazone (papyH)

Nickel and cobalt complexes of pyridine-2-carboxaldehyde-2′-pyridylhydrazone (papyH) and N-methyl(pyridine-2-carboxaldehyde-2′-pyridyl-hydrazone) (papyMe) have been fully characterized through electrochemistry, titration, and alkylation with methyl iodide and compared with existing data on zinc and iron complexes. Both rate constants for alkylation and ligand pKa depend on the coordinated metal and can be understood based on the influence of d electrons on the ligand molecular orbitals.     

An expert system applied to the physiological analysis of early stage of beer fermentation

A fuzzy expert system was applied to the knowledge analysis of yeast physiology in the early stage of beer fermentation, when the wort was aerated. We used ergosterol and glycogen concentration in the wort as a suitable marker of physiological state of the cell population. The amount of both compounds influences the rate of fermentation, cell growth and the final taste of beer. The concentrations of ergosterol and glycogen including the number of cells can not be measured immediately during the relatively short aeration period, and incomplete experimental data are therefore found in laboratory logbooks. We therefore suggested that the fuzzy relation between the directly measurable dissolved oxygen concentration and the rate of ergosterol or glycogen formation should be identified and a fuzzy expert system should be used to analyze the behavior of the yeast.