Cationic state distribution over the chlorophyll d-containing PD1/PD2 pair in photosystem II

Most of the chlorophyll (Chl) cofactors in photosystem II (PSII) from Acaryochloris marina are Chld, although a few Chla molecules are also present. To evaluate the possibility that Chla may participate in the P_D1/P_D2 Chl pair in PSII from A. marina, the P_D1^?+/P_D2^?+ charge ratio was investigated using the PSII crystal structure analyzed at 1.9-Å resolution, while considering all possibilities for the Chld-containing P_D1/P_D2 pair, i.e., Chld/Chld, Chla/Chld, and Chld/Chla pairs. Chld/Chld and Chla/Chld pairs resulted in a large P_D1^?+ population relative to P_D2^?+, as identified in Chla/Chla homodimer pairs in PSII from other species, e.g., Thermosynechococcus elongatus PSII. However, the Chld/Chla pair possessed a P_D1^?+/P_D2^?+ ratio of approximately 50/50, which is in contrast to previous spectroscopic studies on A. marina PSII. The present results strongly exclude the possibility that the Chld/Chla pair serves as P_D1/P_D2 in A. marina PSII. This article is part of a Special Issue entitled: Photosynthesis Research for Sustainability: from Natural to Artificial.     

A comparative study of microalgae isolated from flooded rice paddies: light-limited growth,C fixation,growth efficiency and relative N and P requirement

Seven unialgal isolates from rice paddies,Ankistrodesmus convolutus, Chlorella sp.,Scenedesmus quadricauda, Frustulia vulgaris, Anabaena sp.,Microcystis aeruginosa andPhormidium mucicola, were investigated for their light-limited growth and photosynthetic characteristics, growth efficiency, and relative requirement for N and P as well as their storage potentials. The maximum growth rate (μ_max) ranged from 1.27 to 2.72 d^?1 among species. The slope of light-limited growth (α_g) showed only small interspecies differences (0.126–0.204 d^?1 W^?1 m²) except inS. quadricauda (0.092 d^?1 W^?1 m²). Similarly, the ratio of μ_max to α_g, I_k(g), varied within a narrow range (8.7–13.9 W m^?2) with the exception ofS. quadricauda (19.5 W m^?2). The slope of the photosynthetic curve based on chlorophylla (chla), α_p(a), was significantly higher in cyanobacteria (0.118–0.189 mg C mg chla ^?1h^?1W^?1m²) than in other species (0.070–0.094 mg C mg chla ^?1h^?1W^?1m²). The maximum photosynthetic rate based on chla (P_max(a)) was similar (2.95–3.83 mg C mg chla ^?1 h^?1) with the exception of a high value (6.17 mg C mg chla ^?1 h^?1) inM. aeruginosa. A significant correlation (P<0.001) existed between α_p(a) and P_max(a). The C-specific maximum photosynthetic rate (P_max(c)) was inversely correlated to the C/chla ratio. Growth efficiency (μ_eff), the efficiency to retain photosynthetically-fixed C for growth, showed an interspecies variation ranging from 73–93% and was correlated to the μ_max:P_max(c) ratio. Cyanobacteria exhibited higher efficiency than others. The ratio of P_max:α_p, I_k(p), was higher than I_k(g) by 2.0 to 3.8 times. The optimum N:P ratio, determined as the ratio of minimum cell quotas of N to P (q_oN:q_oP), showed a wide interspecies variability. It was highest inP. mucicola (54) and lowest inF. vulgaris (10). The maximum storage capacity for excess P and N also varied among species; the maximum capacity for P ranged from 2 to 14 times of its immediate need and the capacity for N varied from 1.2 to 4 times.     

Role of pheophytin a in the primary charge separation of photosystem I from Acaryochloris marina: Femtosecond optical studies of excitation energy and electron transfer reactions

Photosystem I (PSI) of the cyanobacterium Acaryochloris marina is capable of performing an efficient photoelectrochemical conversion of far-red light due to its unique suite of cofactors. Chlorophyll d (Chl-d) has been long known as the major antenna pigment in the PSI from A. marina, while the exact cofactor composition of the reaction centre (RC) was established only recently by cryo-electron microscopy. The RC consists of four Chl-d molecules, and, surprisingly, two molecules of pheophytin a (Pheo-a), which provide a unique opportunity to resolve, spectrally and kinetically, the primary electron transfer reactions. Femtosecond transient absorption spectroscopy was here employed to observe absorption changes in the 400–860 nm spectral window occurring in the 0.1–500 ps timescale upon unselective antenna excitation and selective excitation of the Chl-d special pair P₇₄₀ in the RC. A numerical decomposition of the absorption changes, including principal component analysis, allowed the identification of P₇₄₀⁽⁺⁾Chl_d2⁽⁻⁾ as the primary charge separated state and P₇₄₀⁽⁺⁾Pheo_a3⁽⁻⁾ as the successive, secondary, radical pair. A remarkable feature of the electron transfer reaction between Chl_d2 and Pheo_a3 is the fast, kinetically unresolved, equilibrium with an estimated ratio of 1:3. The energy level of the stabilised ion-radical state P₇₄₀⁽⁺⁾Pheo_a3⁽⁻⁾ was determined to be ~60 meV below that of the RC excited state. In this regard, the energetics and the structural implications of the presence of Pheo-a in the electron transfer chain of PSI from A. marina are discussed, also in comparison with those of the most diffused Chl-a binding RC.     

A theoretical explanation for some effects of calcium on the facilitation of neurotransmitter release

A quantal model developed earlier by the authors is recast in terms of common macroscopic variables and applied to the well-documented T, P, N/L, AE neuron network of a leech ganglion. The electrical potential of a neuron (φ) and the ion potentials (φ_a) for Na⁺, K⁺, Cl^? and Ca²⁺ are featured, though it proves possible to reduce the resulting set of coupled non-linear diffusion equations to a single pair whose admissible solutions are defined by a simple algebraic dispersion relation. Less than 30 s is required to solve the system for a functional interval of 2·25 s on a CYBER 175 computer using a modified Runge-Kutta algorithm, the program for which is given. Irreversible effects are included but reversibility is stressed, since the neurons are seen to exchange energy with their environment only in the immediate neighborhood of firing peaks. Plasma oscillations, resulting from a disruption of the Debye layer, offer a sound physical mechanism whereby transient currents and ion exchanges of the observed magnitudes may be generated.The total energy H and information rate Γ_I transferred across the neural membrane are also calculated in terms of φ and φ_a. It is shown that while φ is determined primarily by the K⁺ potential, Γ_I depends mainly on the Ca²⁺ potential together with its time derivatives, and H depends on both the K⁺ and Ca²⁺ potentials. This also makes it possible, not only to compare φ (t) solutions for each of the neurons in the incrementally-loaded network to experimental measurements of φ(t) made for similar stimulus levels, but also to trace the correlated flows of energy and information through the system. Nearly all of the distinctive features of the experimental curves are reproduced, despite the presence of such complexities as wide variations in pulse frequencies and amplitudes, sudden suppression of firing in one neuron when another begins to fire, refractory phases of different durations, and facilitation building to plateau values only slightly less than peak amplitudes for the sensory neurons.While both the energy and information curves possess sharp maxima which coincide with the firing pulses of the potential curves, those for Γ_I (t) are bimodal with rounded maxima that must represent transmissions associated with ion motions instead of polarization effects. In the case of the L and AE neurons, these curves exhibit a series of discrete energy/information packets that could easily produce the proportional increases in muscle tension actually observed.     

Design and synthesis of spirotryprostatin-inspired diketopiperazine systems from prolyl spirooxoindolethiazolidine derivatives

Based on the spirotryprostatin-A structure, we designed, synthesized, and evaluated different series of compounds belonging to the diketopiperazine structural class as potential cell cycle modulators and cytotoxic agents. Starting from the spirooxoindolthiazolidine scaffold, amide coupling with Pro derivatives and intramolecular cyclization reactions are suitable synthetic methods to generate chemically diverse diketopiperazine system, such as hexahydropyrrolo[1,2-a][1,3]thiazolo[3,2-d]pyrazine-5,10-dione (structure I), hexahydropyrrolo[1,2-a] [1,3]thiazolo[3,4-d]pyrazine-5,10-dione (structure II) and spiroindol-2-one[3,3′]hexahydro-5,10H-pyrrolo[1,2-a][1,3]thiazolo[3,4-d]pyrazine-5,10-dione (structure III). Some of these compounds, especially those who belong to the series I and II, showed interesting cytotoxic activity.     

18O Labeling of Chlorophyll d in Acaryochloris marina Reveals That Chlorophyll a and Molecular Oxygen Are Precursors

The cyanobacterium Acaryochloris marina was cultured in the presence of either H₂¹⁸O or ¹⁸O₂, and the newly synthesized chlorophylls (Chl a and Chl d) were isolated using high performance liquid chromatography and analyzed by mass spectroscopy. In the presence of H₂¹⁸O, newly synthesized Chl a and d, both incorporated up to four isotopic ¹⁸O atoms. Time course H₂¹⁸O labeling experiments showed incorporation of isotopic ¹⁸O atoms originating from H₂¹⁸O into Chl a, with over 90% of Chl a ¹⁸O-labeled at 48 h. The incorporation of isotopic ¹⁸O atoms into Chl d upon incubation in H₂¹⁸O was slower compared with Chl a with ∼50% ¹⁸O-labeled Chl d at 115 h. The rapid turnover of newly synthesized Chl a suggested that Chl a is the direct biosynthetic precursor of Chl d. In the presence of ¹⁸O₂ gas, one isotopic ¹⁸O atom was incorporated into Chl a with approximately the same kinetic incorporation rate observed in the H₂¹⁸O labeling experiment, reaching over 90% labeling intensity at 48 h. The incorporation of two isotopic ¹⁸O atoms derived from molecular oxygen (¹⁸O₂) was observed in the extracted Chl d, and the percentage of double isotopic ¹⁸O-labeled Chl d increased in parallel with the decrease of non-isotopic-labeled Chl d. This clearly indicated that the oxygen atom in the C3¹-formyl group of Chl d is derived from dioxygen via an oxygenase-type reaction mechanism.     

A new series of iodocarbonyl ruthenium (II) complexes with unsymmetrical phosphine-phosphine sulfide ligands of the type Ph2P(CH2)nP(S)Ph2, n = 1-4: Isolation and structural investigation

Hexa-coordinated chelate complex cis-[Ru(CO)₂I₂(P∩S)] (1a) {P∩S = η²-(P,S)-coordinated} and penta-coordinated non-chelate complexes cis-[Ru(CO)₂I₂(P∼S)] (1b-d) {P∼S = η¹-(P)-coordinated} are produced by the reaction of polymeric [Ru(CO)₂I₂]_n with equimolar quantity of the ligands Ph₂P(CH₂)_nP(S)Ph₂ {n = 1(a), 2(b), 3(c), 4(d)} in dichloromethane at room temperature. The bidentate nature of the ligand a in the complex 1a leads to the formation of five-membered chelate ring which confers extra stability to the complex. On the other hand, 1:2 (Ru:L) molar ratio reaction affords the hexa-coordinated non-chelate complexes cis,cis,trans-[Ru(CO)₂I₂(P∼S)₂] (2a-d) irrespective of the ligands. All the complexes show two equally intense terminal ν(CO) bands in the range 2028-2103 cm⁻¹. The ν(PS) band of complex 1a occurs 23 cm⁻¹ lower region compared to the corresponding free ligand suggesting chelation via metal-sulfur bond formation. X-ray crystallography reveals that the Ru(II) atom occupies the center of a slightly distorted octahedral geometry. The complexes have also been characterized by elemental analysis, ¹H, ¹³C and ³¹P NMR spectroscopy.     

Armonización de bases de datos para el estudio de la fragilidad en personas mayores: Estudio INTAFRADE

ObjectivesThe main objective of the present work is to evaluate the feasibility of harmonising the available information from different independent databases, in order to build an integrated database to study frailty.Material and methodsThis work is based on the European project, Integral Approach to the Transition between Frailty and Dependence on older adults: Patterns of occurrence, identification tools and model of care (INTAFRADE), developed by 4 groups, 3 in Spain and one in France. Each partner provided their databases related to the study of frailty. As a previous step to the creation of an integrated database the characteristics and variables included in each study were mapped, specifying whether their harmonisation was possible or not.ResultsA total of 30 different variables that corresponded to 8 dimensions were identified: Sociodemographic and social characteristics, health status, lifestyle habits, anthropometric measures, other physical measurements, use of health services, and adverse health results. Of them all, 28 (93%) variables were harmonisable, although only 20% were present in all databases, with 47% in 3 of them. In relation to the frailty instruments, all of them were lacking at least 50% of the items. The harmonisation process will allow us to jointly analyse information available on 2,361 people.ConclusionsThe European INTAFRADE study will allow a deeper understanding of the frailty process in older people by harmonising information from heterogeneous databases.     

Crystal structure of [Sm(OPMePh2)4I2]I. A cationic octahedral complex of samarium(III)

The crystal structure of [Sm(OPMePh₂)₄I₂]I, 1, was determined by X-ray diffraction and refined anisotropically to a final R value of 0.067 from 3040 reflections with I>3.0σ(I). The space group was P2/a and Z=2. The unit cell dimensions were: a= 17.777(6), b=13.559(2), c=11.656(4) Å, α=γ= 90.0 and β=97.25(3)°. The cation geometry was octahedral with the Sm(III) bonded to two mutually trans I⁻ ions and four OPMePh₂ groups. A third non-bonded I⁻ was present elsewhere in the cell. The SmI and SmO distances were 3.077(1) and 2.27(1) Å respectively. Two of the SmOP angles were 172.1(6)° and the other two were 162.0(6)°.     

CXCR4-A Prognostic and Clinicopathological Biomarker for Pancreatic Ductal Adenocarcinoma: A Meta-Analysis

Adenocarcinomas of the pancreatic duct (PDAC) are characteristically aggressive tumors that are extremely challenging to treat as curative surgical resection, the definitive treatment, is seldom possible. Regretably, most patients are diagnosed with metastatic disease at the time of initial presentation. In addition, current chemotherapeutic concepts that are used for advanced disease stages show frustrating results. Thus, there is an urgent need to identify novel therapeutic molecular targets that are associated with PDAC disease. Recently, the chemokine receptor CXCR4 has been demonstrated to be highly expressed in metastatic PDAC. However, the results of the published data on CXCR4 and its association with clinicopathological variables and prognosis in PDAC seem to be heterogeneous. Consequently, to clarify the relevance of CXCR4 as a biomarker in PDAC we performed a comprehensive literature search by using PubMed and Web of Science databases to identify articles that focused on the expression of CXCR4 in PDAC by using immunohistochemistry. Subsequently, data from nine relevant studies, encompassing 1183 patients were extracted, qualitatively assessed, and entered into a meta-analysis. By using a random effects model, the pooled hazard ratio of the seven studies that reported on patients overall survival revealed a correlation between expression of CXCR4 and poor prognosis (HR 1.49; 95% CI: 1.04-2.14; P = 0.03; I² = 74%). Although heterogeneity became evident, subgroup analyses confirmed the prognostic value of CXCR4 in PDAC, especially in high-quality studies that performed multivariate analysis. In addition, meta-analysis revealed a strong association of CXCR4 expression with the UICC stage (OR: 3.40; 95% CI: 1.67-6.92; P = 0.0007; I² = 0%) and metastatic disease (N-status: OR: 2.55; 95% CI: 1.56-4.15; P = 0.0002; I² = 26%; recurrence to the liver: OR: 2.80; 95% CI: 1.48-5.29; P = 0.001; I² = 0%). Taken together, our meta-analysis suggests that CXCR4 represents a useful prognostic biomarker in PDAC and might therefore be evaluated as a potential therapeutic target in the treatment of metastatic cancer disease of the pancreas.     

Both chlorophylls a and d are essential for the photochemistry in photosystem II of the cyanobacteria, Acaryochloris marina

We have measured the flash-induced absorbance difference spectrum attributed to the formation of the secondary radical pair, P⁺Q⁻, between 270 nm and 1000 nm at 77 K in photosystem II of the chlorophyll d containing cyanobacterium, Acaryochloris marina. Despite the high level of chlorophyll d present, the flash-induced absorption difference spectrum of an approximately 2 ms decay component shows a number of features which are typical of the difference spectrum seen in oxygenic photosynthetic organisms containing no chlorophyll d. The spectral shape in the near-UV indicates that a plastoquinone is the secondary acceptor molecule (Q_A). The strong C-550 change at 543 nm confirms previous reports that pheophytin a is the primary electron acceptor. The bleach at 435 nm and increase in absorption at 820 nm indicates that the positive charge is stabilized on a chlorophyll a molecule. In addition a strong electrochromic band shift, centred at 723 nm, has been observed. It is assigned to a shift of the Qy band of the neighbouring accessory chlorophyll d, Chl_D1. It seems highly likely that it accepts excitation energy from the chlorophyll d containing antenna. We therefore propose that primary charge separation is initiated from this chlorophyll d molecule and functions as the primary electron donor. Despite its lower excited state energy (0.1 V less), as compared to chlorophyll a, this chlorophyll d molecule is capable of driving the plastoquinone oxidoreductase activity of photosystem II. However, chlorophyll a is used to stabilize the positive charge and ultimately to drive water oxidation.     

Changes in specific photosynthetic rate of oceanic phytoplankton from the northeast Pacific Ocean

The study is based on data (n=244) from light-saturation experiments utilizing artificial incubation under fluorescent light. Values of maximum photosynthetic rate,P _max, and the light intensity at which it takes place,I _max, are estimated by non-linear regression using stepwise Gauss-Newton iterations. Estimated values ofP _max ranged from 0.85 to 5.48 mg C (mg Chla·h)^?1;I _max varied from 2.35 to 5.52 cal (cm²·h)^?1. The effects of time (months) and depth (illumination levels) and their interaction are evaluated by analysis of covariance using a linear model. A significant time-depth interaction is noted: The maximum specific primary productivity occurred in the surface layers during March, at the 50% light level during April, and at 1% level during May. Estimates ofP _max from simulated in situ primary productivity experiments for the same period are lower than those from light-saturation experiments. A comparison of data from light-saturation and simulated in situ experiments indicated that effects of duration of experiments and the quality of available light may affect primary productivity data considerably.     

New structure–activity relationship studies in a series of N,N-bis(cyclohexanol)amine aryl esters as potent reversers of P-glycoprotein-mediated multidrug resistance (MDR)

As a continuation of previous research on a new series of potent and efficacious P-gp-dependent multidrug resistant (MDR) reversers with a N,N-bis(cyclohexanol)amine scaffold, we have designed and synthesized several analogs by modulation of the two aromatic moieties linked through ester functions to the N,N-bis(cyclohexanol)amine, aiming to optimize activity and to extend structure–activity relationships (SAR) within the series. This scaffold, when esterified with two different aromatic carboxylic acids, gives origin to four geometric isomers (cis/trans, trans/trans, cis/cis and trans/cis).The new compounds were tested on doxorubicin-resistant erythroleukemia K562 cells (K562/DOX) in the pirarubicin uptake assay. Most of them resulted in being potent modulators of the extrusion pump P-gp, showing potency values ([I]_0.5) in the submicromolar and nanomolar range. Of these, compounds 2b, 2c, 3d, 5a–d and 6d, showed excellent efficacy with a α_max close to 1. Selected compounds (2d, 3a, 3b, 5a–d) were further studied to evaluate their doxorubicin cytotoxicity potentiation (RF) on doxorubicin-resistant erythroleukemia K562 cells and were found able to enhance significantly doxorubicin cytotoxicity on K562/DOX cells.The results of both pirarubicin uptake and the cytotoxicity assay, indicate that the new compounds of the series are potent P-gp-mediated MDR reversers. They present a structure with a mix of flexible and rigid moieties, a property that seems critical to allow the molecules to choose the most productive of the several binding modes possible in the transporter recognition site.In particular, compounds 5c and 5d, similar to the already reported analogous isomers 1c and 1d,²⁹ are potent and efficacious modulators of P-gp-dependent MDR and may be promising leads for the development of MDR-reversal drugs.     

Seasonal variation in light-shade adaptation of natural populations of the symbiotic sea anemone Aiptasiapulchella (Carlgren, 1943) in Hawaii

The productivity and biomass parameters of the symbiotic anemone Aiptasia pulchella (Carlgren, 1943) from a shaded mangrove lagoon (maximum summer irradiance of 100 μE m⁻² · s⁻¹) and a sunlit reef flat (maximum summer irradiance of 1400 μE · m⁻² · s⁻¹) were examined in Hawaii. Light-shade adaptation was evident in the summer populations (1981) but not observed during the fall (1982). In the summer, zooxanthellae from the lagoon A. pulchella (shade anemones) contained 2.97 pg Chl a cell ⁻¹ and those from the reef flat (sun anemones) contained 1.70 pg Chl a · cell⁻¹; but Chl a : c₂ ratios were 2.5 in zooxanthellae from both shade and sun anemones. During the fall, there were no significant differences in Chl a and c₂ of zooxanthellae (2.25 pg Chl a · cell⁻¹) in shade and sun anemones, but Chl a : c₂ ratios averaged 3.9. During both seasons, shade anemones were larger and contained higher densities of zooxanthellae than sun anemones. In addition to differences between shade and sun habitats, there was localized photoadaptation of zooxanthellae within individual anemones due to microhabitat variations in ambient irradiance. Growth rates of zooxanthellae in A. pulchella differed in shade and sun anemones. Specific growth rates for zooxanthellae in situ were the same for shade populations in both summer and fall (0.016 day⁻¹). However, zooxanthellae in sun anemones grew four times faster in the fall (0.033 day⁻¹) than during the summer (0.008 day⁻¹). These results suggest that growth of zooxanthellae in these anemones was independent of ambient irradiance. Photosynthesis-irradiance (P-I) responses of shade and sun anemones during the summer showed that shade anemones had greater photosynthetic efficiencies (α) but lower photosynthetic capacities (P_max) than sun anemones. Dark-respiration rates of sun anemones were twice those obtained with shade anemones. In the fall, these populations of anemones did not exhibit P-I responses characteristic of light-shade adaptation. Both α and P_max of shade and sun anemones were higher in the fall, indicating that zooxanthellae in A. pulchella adapted to seasonal reduction in irradiance.     

The covariance of relatives derived from a random mating population.

Attention is drawn to errors common in the derivation of forms for the genotypic covariance of noninbred relatives from a Hardy-Weinberg population of diploids. A synthesis of Fisher's least-squares method of partitioning the genotypic variance and Malécot's probability method of expressing kinship, yields a general form. For one locus, the form is $\text{(P}{}_{\mathrm{ss}}\text{+ P}{}_{\mathrm{sd}}\text{+ P}{}_{\mathrm{ds}}\text{+ P}{}_{\mathrm{dd}}\text{)}\text{1}\text{2}\text{σ}{}_{\mathrm{a}}{}^2\text{+ (P}{}_{\mathrm{ss}}\text{P}{}_{\mathrm{dd}}\text{+ P}{}_{\mathrm{sd}}\text{P}{}_{\mathrm{ds}}\text{) σa}{}_{\mathrm{d}}{}^2$, where σ_a² is the additive genetic variance, α_d² is the variance of dominance deviations, p_ij is the probability that parental gamete i is identical by descent to parental gamete j, i = s, d indexes the parents of one relative, and j = s, d indexes those of the other. The form provides a framework for obtaining the covariance of relatives from an equilibrium population with linkage.     

Membrane d-lactate oxidase in Zymomonas mobilis: evidence for a branched respiratory chain

Respiratory chain composition of the ethanol-producing bacterium Zymomonas mobilis was studied. Its membrane d-lactate oxidase was characterised. With NADH, but not d-lactate as substrate, a cytochrome o-like component was seen in CO difference spectra. Chlorpromazine specifically inhibited reduction of cytochrome d, while myxothiazol eliminated the cytochrome o-like features in CO difference spectra. It is suggested that electrons from NADH are distributed between branches terminated by the cytochrome o-like component, cytochrome a, and cytochrome d. With d-lactate, electrons are transported to cytochrome a, or an unidentified CN⁻-sensitive oxidase, and cytochrome d.     

Potential of a dust grain in a nitrogen plasma with a condensed disperse phase at room and cryogenic temperatures

The first numerical study is presented of the self-consistent potential of a dust grain in a nitrogen plasma with a condensed disperse phase at room and cryogenic temperatures and at high gas pressures for which the electron and ion transport in the plasma can be described in the hydrodynamic approximation. It is shown that the potential of the dust grain is described with good accuracy by the Debye potential, in which case, however, the screening radius turns out to be larger than the electron Debye radius. The difference between the radii is especially large in a plasma with high ionization rates (about 10¹⁶–10¹⁸ cm^?3 s^?1) at room temperature. It is found that, in a certain range of the parameters of a nitrogen dusty plasma, the parameter describing the interaction between the grains exceeds the critical value above which one would expect the formation of plasma-dust structures such as Coulomb crystals. For a plasma at cryogenic temperature (T=77 K), this range is significantly wider.     

Formation and decay of radical-pair state P+I− in Chloroflexus aurantiacus reaction centers

We have examined the room temperature kinetics of the absorption changes associated with the formation of state P⁺I⁻ (P⁺BPh⁻) and its subsequent decay to state P⁺Q⁻_A in reaction centers from Chloroflexus aurantiacus. Our data, acquired using 30-ps excitation flashes, strongly suggest that formation of P⁺I⁻ (P⁺BPh⁻) takes longer in Chloroflexus than in reaction centers from Rhodopseudomonas sphaeroides. The reduction of the photoactive bacteriopheophytin (BPh) could take as long as 13 ps. Absorption changes different from those due to P⁺I⁻ are observed early in the excitation flash, but the detailed identity of the transient remains unclear. We also find that the kinetics observed subsequent to P⁺I⁻ formation differ with detection wavelength. The time constant measured in the anion band (I⁻) at 655 nm is 324 ± 20 ps and probably reflects the rate of electron transfer from I⁻ (BPh⁻) to Q_A. However, the kinetics measured in the BPh ground-state absorption bands are slightly longer: 365 ± 19 and 367 ± 21 ps at 538 and 760 nm, respectively. At 810 nm, a wavelength normally associated with the monomeric bacteriochlorophyll (BChl) in the Chloroflexus reaction center, a slightly faster (281 ± 19 ps) time constant is observed. This detection-wavelength dependence of the kinetics is similar to that observed recently in Rps. sphaeroides reaction centers. Comparison of these results suggests that the kinetics observed in the ground-state absorption bands of the BPhs and BChls in Chloroflexus may contain contributions from readjustments of the pigments and/or protein in response to the charge separation process.     

Inner Ear Morphology Is Perturbed in Two Novel Mouse Models of Recessive Deafness

Human MYO7A mutations can cause a variety of conditions involving the inner ear. These include dominant and recessive non-syndromic hearing loss and syndromic conditions such as Usher syndrome. Mouse models of deafness allow us to investigate functional pathways involved in normal and abnormal hearing processes. We present two novel mouse models with mutations in the Myo7a gene with distinct phenotypes. The mutation in Myo7a^I487N/I487N ewaso is located within the head motor domain of Myo7a. Mice exhibit a profound hearing loss and manifest behaviour associated with a vestibular defect. A mutation located in the linker region between the coiled-coil and the first MyTH4 domains of the protein is responsible in Myo7a^F947I/F947I dumbo. These mice show a less severe hearing loss than in Myo7a^I487N/I487N ewaso; their hearing loss threshold is elevated at 4 weeks old, and progressively worsens with age. These mice show no obvious signs of vestibular dysfunction, although scanning electron microscopy reveals a mild phenotype in vestibular stereocilia bundles. The Myo7a^F947I/F947I dumbo strain is therefore the first reported Myo7a mouse model without an overt vestibular phenotype; a possible model for human DFNB2 deafness. Understanding the molecular basis of these newly identified mutations will provide knowledge into the complex genetic pathways involved in the maintenance of hearing, and will provide insight into recessively inherited sensorineural hearing loss in humans.