Phosphorylation-mediated regulation of the Bacillus anthracis phosphoglycerate mutase by the Ser/Thr protein kinase PrkC.

Bacillus anthracis Ser/Thr protein kinase PrkC is necessary for phenotypic memory and spore germination, and the loss of PrkC-dependent phosphorylation events affect the spore development. During sporulation, Bacillus sp. can store 3-Phosphoglycerate (3-PGA) that will be required at the onset of germination when ATP will be necessary. The Phosphoglycerate mutase (Pgm) catalyzes the isomerization of 2-PGA and 3-PGA and is important for spore germination as a key metabolic enzyme that maintains 3-PGA pool at later events. Therefore, regulation of Pgm is important for an efficient spore germination process and metabolic switching. While the increased expression of Pgm in B. anthracis decreases spore germination efficiency, it remains unexplored if PrkC could directly influence Pgm activity. Here, we report the phosphorylation and regulation of Pgm by PrkC and its impact on Pgm stability and catalytic activity. Mass spectrometry revealed Pgm phosphorylation on seven threonine residues. In silico mutational analysis highlighted the role of Thr459 residue towards metal and substrate binding. Altogether, we demonstrated that PrkC-mediated Pgm phosphorylation negatively regulates its activity that is essential to maintain Pgm in its apo-like isoform before germination. This study advances the role of Pgm regulation that represents an important switch for B. anthracis resumption of metabolism and spore germination.

Exploring the superhydrophilicity of nanosecond laser textured silicon: a Raman analysis.

We present Raman analysis of nanosecond laser textured silicon. The samples have also been characterized by field emission scanning electron microscopy (FESEM) and x ray diffraction. Contact angles (CAs) are measured to trace the hydrophilic nature. Characterization of the textured samples in argon and air shows that cleavage cracks are developed during texturing. CA measurements reveal the superhydrophilic nature of textured samples obtained in the presence of ambient oxygen and argon. In vacuum, however, the hydrophilicity is decreased. Micro-Raman analysis indicates the formation of nano-sized cleavage cracks that impart stable superhydrophilic properties to textured silicon is supported from FESEM images also. On the other hand, in vacuum textured silicon, evidence of such cracks is not noticed, which is also supported by Raman analysis. Further, the hydrophilicity is decreased. A definitive trend appears to exist between Raman signatures and hydrophilicity. We believe that the study will further the understanding of the mechanistic aspect in designing textured silicon with a high degree of self-cleaning capability.

Förster Resonance Energy Transfer between Fluorescent Organic Semiconductors: Poly(9,9-dioctylfluorene-alt-benzothiadiazole) and 6,13-Bis(triisopropylsilylethynyl)pentacene.

In the present study, an investigation of the electronic excitation energy transfer between two p-type fluorescent semiconductors, F8BT [poly(9,9-dioctylfluorene-alcohol-benzothiadiazole] and TIPS-P [6,13-bis(triisopropylsilylethynyl)pentacene], has been carried out in a chloroform solution using steady-state and time-domain fluorescence techniques. The spectral overlap integral between donor (F8BT) emission and acceptor (TIPS-P) absorption is 2.04 × 1015 nm4/(M cm), and the corresponding critical transfer distance is 53.12 Å. In donor decay dynamics, at the lower acceptor concentrations, the observed results deviate from the Förster theory due to the combined effect of diffusion and energy migration. However, it does not exhibit energy migration and distribution for higher acceptor concentrations, and the system follows the Förster model of resonance excitation energy transfer (FRET). The higher value of the donor-acceptor interaction strength than self-interaction (donor-donor interaction) appears to be responsible for this behavior. Further, in acceptor decay, the appearance of the rise time and its decrease with the acceptor concentration confirms FRET from F8BT to TIPS-P.

Observation of ion acceleration in nanosecond laser generated plasma on a nickel thin film under rear ablation geometry.

In this article we report acceleration observed for the ions produced in a 50-nm-thick nickel film coated on a quartz substrate, under nanosecond laser ablation, in the rear ablation geometry. A detailed study with varying background pressure and laser energy is done. Spectroscopic study including spectroscopic time of flight (STOF) measurements of ionic and other neutral transitions from the plasma has been undertaken. The STOF spectra recorded for ionic transition clearly show an enhancement in the velocity of the slow component as the background pressure increases. In addition, a large asymmetric spectral broadening in the 712.22-nm neutral line is observed, which increases with background pressure. While these observations have similarity to some of the reported studies on the acceleration of ionic species through double-layer formation, the electric fields calculated from the measured acceleration appear to be anomalously higher, and a double-layer concept seems to be inadequate. Moreover, the large asymmetry observed in the neutral line profile is indicative of microelectric fields present inside the laser produced plasma plume, which may play a role in the continuous acceleration of the ions. Interestingly, this asymmetry in spectral broadening exhibits temporal and spatial dependence, which indicates that significant electric field is present in the plasma plume even for longer duration and larger distance from the target. These spectroscopic observations of acceleration have also been complemented by triple Langmuir probe measurements. To the best of our information, such observations regarding large ion acceleration for the rather low laser intensities as used in this experiment have not been reported in literature so far.

Therapeutic potential of pharmacological agents targeting TRP channels in CNS disorders.

Central nervous system (CNS) disorders like Alzheimer's disease (AD), Parkinson disease (PD), stroke, epilepsy, depression, and bipolar disorder have a high impact on both medical and social problems due to the surge in their prevalence. All of these neuronal disorders share some common etiologies including disruption of Ca2+ homeostasis and accumulation of misfolded proteins. These misfolded proteins further disrupt the intracellular Ca2+ homeostasis by disrupting the activity of several ion channels including transient receptor potential (TRP) channels. TRP channel families include non-selective Ca2+ permeable channels, which act as cellular sensors activated by various physio-chemical stimuli, exogenous, and endogenous ligands responsible for maintaining the intracellular Ca2+ homeostasis. TRP channels are abundantly expressed in the neuronal cells and disturbance in their activity leads to various neuronal diseases. Under the pathological conditions when the activity of TRP channels is perturbed, there is a disruption of the neuronal homeostasis through increased inflammatory response, generation of reactive oxygen species, and mitochondrial dysfunction. Therefore, there is a potential of pharmacological interventions targeting TRP channels in CNS disorders. This review focuses on the role of TRP channels in neurological diseases; also, we have highlighted the current insights into the pharmacological modulators targeting TRP channels.

Comment on the article "Investigation of Fluorescence Resonance Energy Transfer between Fluorescein and Rhodamine 6G".

In this comment we, report the missing of relevant literature regarding Forster energy transfer (FRET) between fluorescein and rhodamine 6G in a recent paper (Spectrochim. Acta A, 149 (2015) 143-149). In this paper, the authors claim that "a new FRET pair" has been identified, which is absolutely incorrect. In fact, studies on FRET in this dye pair under different conditions have been done earlier. Further, the estimated critical transfer distance may have uncertainty because of donor quantum yield which is not clarified in the paper.

Slow excited state phototautomerization in 3-hydroxyisoquinoline.

In the present work we report the spectral and photophysical properties of 3-hydroxyisoquinoline in various protic/aprotic solvents. Our steady state and time resolved fluorescence data indicates that in the monomer form of 3HIQ phototautomerization can take place in the excited state through excited state intramolecular proton, while as per earlier suggestions phototautomerization in 3HIQ occurs in dimer or complex (in the presence of acetic acid) form. Moreover, we find rather slow tautomerization (occurring on the nanosecond scale). It is found that proton transfer occurs both in the ground as well as excited states and is controlled by the polarity of the solvent.

Steady state and time-resolved fluorescence study of isoquinoline: reinvestigation of excited state proton transfer.

In the present work we report some hitherto unnoticed features in the steady state and time-resolved measurements of isoquinoline in water and trifluoroethanol (TFE). Absorption spectra reveal that in water, neutrals as well cationic species are present. Emission spectrum shows structured features at shorter wavelengths accompanied with a broad band around 375 nm, which correspond to neutrals and cations respectively. However, time-resolved data indicate that protonation does not take place in the excited state in water. On the contrary, in stronger hydrogen bonding solvent TFE, distribution of decay components is observed and at longer wavelengths a small rise time is present. This is ascribed to neutral and cation-like species present in the ground as well as in the excited state. The difference in the results is explained in terms of different excited state potential energy surfaces for water and TFE; particularly, the presence of a rather small barrier for protonation in case of TFE.

Fluorescence characteristics of 5-amino salicylic acid: An iodide recognition study.

In this paper we report the effect of iodide on the fluorescence of 5-amino salicylic acid (5-ASA). In the absence of iodide, prominent blue green (BG) emission band at ∼465nm (broad) is observed in aprotic solvents whereas violet (V) emission at ∼408nm, blue green (BG) at ∼480nm and green (G) at ∼500nm are observed in case of protic solvents. On the addition of iodide ion (I(-)), the intensity of BG fluorescence is enhanced in case of aprotic solvents. On the other hand the G band is enhanced in protic solvents and decrease in the intensity of the V band is observed. The effect of hydrogen bonding as well as the interplay of neutral and ionic species is invoked to explain the observed results. The study projects the application of this system in iodide recognition in protic/aprotic environments.

In vitro biomechanical properties of linear, circular, and hybrid external skeletal fixation devices for use in large ruminants.

OBJECTIVE: To report the biomechanical properties of 3 external skeletal fixation (ESF) devices for use in large ruminants. STUDY DESIGN: In vitro biomechanical testing of ESF constructs. SAMPLE POPULATION: Adult buffalo (weighing, 250-350 kg) tibiae (n=27). METHODS: ESF constructs (bilateral linear fixator [BLF], 4-ring circular external fixator [CEF], and hybrid fixator [HF]) were made using mild (low carbon) steel implants plated with nickel and cadaveric buffalo tibiae. After ESF application, a 1 cm mid-diaphyseal gap was created. Constructs were loaded to failure, on a materials testing machine, in axial compression (n=5/ESF type) and craniocaudal bending (n=3/ESF type). In addition, 3 CEF constructs were tested in intact tibiae under craniocaudal bending. RESULT: In compression, HF was the strongest and most rigid construct; yield load was significantly higher for HF than for BLF or CEF. Under bending, both CEF and HF had similar strength and modulus of elasticity. Strength for BLF was higher than CEF and HF, whereas the reverse was true for modulus of elasticity. CONCLUSIONS: ESF made from mild steel for use in large ruminants could withstand

Evaluation of two dynamic axial fixators for large ruminants.

OBJECTIVES: To evaluate healing of a radial osteotomy repaired by application of dynamic axial fixation devices (DAF) in large ruminants. STUDY DESIGN: In vivo study of bone healing after application of 2 DAF types. Model I had 2 sidebars, each with a central cylindrical cuff (internally threaded) with 2 detachable connecting rods telescoping within the cuff. Model II had 2 side bars with 2 moveable clamps with multiple holes. SAMPLE POPULATION: Bull calves (n=8; aged, 1.5-2.0 years; weighing, 175-250 kg). METHODS: A mid-diaphyseal radial osteotomy was repaired by use of a model I (n=4) or model II (n=4) DAF. Calves were monitored for weight bearing, stability of fixation, and radiographically for fracture reduction, alignment and healing at intervals for 6 months. Fixators were removed when there was radiographic evidence of healing. RESULTS: Both the fixators were well tolerated with free movement of adjacent joints. Fragment fixation was maintained until healing in all but 1 model I calf where failure occurred within 7 days. Model II DAF provided more rigid fixation as indicated by early full weight bearing and fracture healing with less callus formation. Functional recovery of repaired limbs occurred within 60 days in surviving calves. CONCLUSIONS: Both bilateral DAFs were easy to apply; however, the model II DAF provided better fixation. CLINICAL RELEVANCE: The model II DAF made of low carbon steel was economical and may be useful for treating long bone fractures in large ruminants.