Human Artificial Chromosome with a Conditional Centromere for Gene Delivery and Gene Expression

Human artificial chromosomes (HACs), which carry a fully functional centromere and are maintained as a single-copy episome, are not associated with random mutagenesis and offer greater control over expression of ectopic genes on the HAC. Recently, we generated a HAC with a conditional centromere, which includes the tetracycline operator (tet-O) sequence embedded in the alphoid DNA array. This conditional centromere can be inactivated, loss of the alphoid^tet-O (tet-O HAC) by expression of tet-repressor fusion proteins. In this report, we describe adaptation of the tet-O HAC vector for gene delivery and gene expression in human cells. A loxP cassette was inserted into the tet-O HAC by homologous recombination in chicken DT40 cells following a microcell-mediated chromosome transfer (MMCT). The tet-O HAC with the loxP cassette was then transferred into Chinese hamster ovary cells, and EGFP transgene was efficiently and accurately incorporated into the tet-O HAC vector. The EGFP transgene was stably expressed in human cells after transfer via MMCT. Because the transgenes inserted on the tet-O HAC can be eliminated from cells by HAC loss due to centromere inactivation, this HAC vector system provides important novel features and has potential applications for gene expression studies and gene therapy.     

Protein expression during Flammulina velutipes fruiting body formation

Formation of the Flammulina velutipes fruiting body can be induced by lowering the ambient temperature (first treatment) in complete darkness. Fruiting bodies formed under these conditions elongate without pileus formation (pinhead fruiting body), suggesting that they cannot mature in complete darkness. However, after light treatment of the pinhead fruiting body (second treatment), a pileus develops immediately, and the stipe also thickens and becomes increasingly pigmented. The apical region swells as a result of cell division starting 2 days after light treatment, the pileus–stipe junction fracture and hymenium primordia form on day 4, and gills appear at day 6. Pf1 and Pf3 are specifically expressed after exposure to low temperature without light. The cell wall-associated protein [pileus-specific hydrophobin-like protein (PSH)] is specifically induced in the pileus, but not in the stipe, following the second light treatment to the pinhead fruiting body. These results suggest that Pf1 and Pf3 would be involved in fruiting body induction and that PSH would be involved in pileus formation. These phenomena will aid further histological and molecular biological investigations into the mechanisms behind fruiting body development in F. velutipes.     

Distribution of the oriental weatherloach, Misgurnus anguillicaudatus, in paddy fields and its implications for conservation in Sado Island, Japan

The distribution of the oriental weatherloach, Misgurnus anguillicaudatus, together with related environmental factors were surveyed at 185 paddy field locations on Sado Island in Japan. This was associated with the reintroduction of the Japanese crested ibis, Nipponia nippon, which prefers to feed on the loach. Loach were found to be present at 90 locations (49%). Analysis with GIS, GLM and AIC revealed that positive factors for the loach distribution included the presence of an earth ditch, the connections at outlets and the proportion of paddy field area within an 800 m radius. Conversely, pumping-up water irrigation and flow irrigation affected loach distribution negatively. In an interview survey that was conducted concurrently, older farmers in the area recalled that the loach had once been distributed over almost the entire island (89/96, 93%) about half a century ago. The farmers also suggested that the impact of agricultural chemicals was one of the main reasons for loach reduction or local extinction. A map of the current potential loach distribution was made using the best fit model from GIS variables. The loach was expected to be distributed in the Kuninaka region with high probability (60–100%) and in patches in the Osado and Kosado regions with low–medium probability (10–50%). As a feasible scenario for the conservation of the loach, another predictive map of the loach distributions was made using a model fit based on the GIS variables and outlet connection, in which the all of the outlets were presumed to be connected to the ditches without gaps. In this case, the loach were expected to be distributed almost throughout the paddy fields with medium–high probability (40–100%). In another scenario that presumed the complete land consolidation of all the paddy fields, the probability of loach occurrence was low (0–30%) throughout the island with the exception of the island’s center in the Kuninaka region.     

Short- and medium-chain fatty acids enhance the cell surface expression and transport capacity of the bile salt export pump (BSEP/ABCB11)

The reduced expression of the bile salt export pump (BSEP/ABCB11) at the canalicular membrane is associated with cholestasis-induced hepatotoxicity due to the accumulation of bile acids in hepatocytes. We previously reported that 4-phenylbutyrate (4PBA), an approved drug for urea cycle disorders, is a promising agent for intrahepatic cholestasis because it increases both the cell surface expression and the transport capacity of BSEP. In the present study, we searched for effective compounds other than 4PBA by focusing on short- and medium-chain fatty acids, which have similar characteristics to 4PBA such as their low-molecular-weight and a carboxyl group. In transcellular transport studies using Madin–Darby canine kidney (MDCK) II cells, all short- and medium-chain fatty acids tested except for formate, acetate, and hexanoic acid showed more potent effects on wild type (WT) BSEP-mediated [³H]taurocholate transport than did 4PBA. The increase in WT BSEP transport with butyrate and octanoic acid treatment correlated with an increase in its expression at the cell surface. Two PFIC2-type variants, E297G and D482G BSEP, were similarly affected with both compounds treatment. The prolonged half-life of cell surface-resident WT BSEP was responsible for this increased octanoic acid-stimulated transport, but not for that of butyrate. In conclusion, short- and medium-chain fatty acids have potent effects on the increase in WT and PFIC2-type BSEP-mediated transport in MDCK II cells. Although both short- and medium-chain fatty acids enhance the transport capacity of WT and PFIC2-type BSEP by inducing those expressions at the cell surface, the underlying mechanism seems to differ between fatty acids.     

Analysis of stream water temperature changes during rainfall events in forested watersheds

Despite continued interest in stream water temperature (Tw) analysis, there are few studies of Tw response to rainfall events at forested watersheds. We examined 61 sets of data on Tw for 21 rainfall events at 16 watersheds with various slope gradients (from 0.08 to 0.56) in four regions of Japan from June 2004 to December 2005. The investigation focused on the changes of specific discharge (ΔQs) and ΔTw at medium-sized watersheds (0.5–100 ha). The results clearly demonstrated different flow patterns expressed by Qs vs. Tw hysteretic loops. Those were clockwise in Period I (April–September) and counterclockwise in Period II (October–March), except for lower slope gradient at Aichi, where counterclockwise loops were observed in both periods. These differences in hysteretic loops could be explained by the differences in Tw and in response times to rainfall between surface/subsurface and groundwater flows. The response times were probably determined by the slope gradient and the vertical level of groundwater. We also found that the changes in air temperature (ΔTa) influenced ΔTw to a lesser degree than Qs. The average rainfall intensities in Period I and Period II (9.3 ± 1.7 and 5.4 ± 0.2 mm/h, respectively) affected the average values of ΔQs and ΔTw (6.62 ± 4.08 mm/h and 1.7 ± 0.4°C; 0.85 ± 0.68 mm/h and 0.9 ± 0.3°C, respectively). This indicates that slope gradient and Qs influenced ΔTw by changing the relative proportions of flow paths. In addition, the water table changes influenced the percentage of groundwater flow to the stream.     

Catalytic Biomineralization of Fluorescent Calcite by the Thermophilic Bacterium Geobacillus thermoglucosidasius

The thermophilic Geobacillus bacterium catalyzed the formation of 100-μm hexagonal crystals at 60°C in a hydrogel containing sodium acetate, calcium chloride, and magnesium sulfate. Under fluorescence microscopy, crystals fluoresced upon excitation at 365 ± 5, 480 ± 20, or 545 ± 15 nm. X-ray diffraction indicated that the crystals were magnesium-calcite in calcite-type calcium carbonate.Biomineralization is defined as the synthesis of inorganic crystalline or amorphous mineral-like materials by living organisms. Most of the crystals formed through biomineralization consist of inorganic minerals, but they may also contain trace amounts of organic compounds, which are thought to regulate the biomineralization process. A Japanese researcher first coined the term biomineralization in the 1940s, and interest in this field of research soon began to grow (28, 29). Biomineralization is a universal process, occurring in both prokaryotes and eukaryotes, including mammals. Biomineralization research is also a diverse and multidisciplinary field, encompassing microscopic analyses of biominerals and tissues (21, 23), mineralogy (25), organic chemistry (30), paleontology (3), and cellular biochemistry (19).Bacteria are capable of forming inorganic crystals either intracellularly (12, 14) or extracellularly (9). Calcite (calcium carbonate) precipitation is a well-known example of extracellular bacterial biomineralization. Certain species of marine bacteria have been shown to precipitate minerals in water supplemented with artificial marine salt media and differing ratios of Mg²⁺ to Ca²⁺ concentrations (20). Several groups have investigated the geobiochemical significance of the presence of calcium carbonate in seafloor sediments in terms of calcite formation by marine bacteria (17). Boquet et al. (4) reported calcite formation by 210 species of soil bacteria cultured on solid growth medium containing calcium acetate, yeast extract, and glucose. Sánchez-Román et al. (22) found that 19 species of moderately halophilic bacteria, grown in nutrient liquid media, catalyzed the precipitation of calcite, magnesium calcite, and struvite in variable proportions depending on the ratio of Mg²⁺ to Ca²⁺ in the media.Researchers and engineers in materials science have only recently begun to focus on biomineralization (2). There is currently great interest in the development of mimic materials based on biomineralization. In our own research, we found that a moderately thermophilic bacterium isolated from thermophilically composted organic waste catalyzes the formation of inorganic crystals extracellularly under oligotrophic conditions. In this paper, we describe the physiological properties of this isolated thermophilic bacterium, the conditions under which it catalyzes the formation of crystals, the elemental composition and photoluminescent properties of the crystals, and the technological implications of our findings.Composted organic waste (0.4 g) was suspended in 20 ml of sterilized water and streaked onto soybean-casein digest (SCD) agar (Nissui Pharmaceutical Co., Ltd., Tokyo, Japan), and the agar plate was incubated at 60°C for 48 h. A single visible colony was picked and recultured by streaking on a fresh SCD agar plate incubated at 60°C. Another single colony was isolated from this plate and cultured in the same manner to obtain a pure culture of the thermophilic bacterium. Gram staining was carried out according to conventional methodology. Morphology and photoluminescence properties were observed using a fluorescence microscope (Axioskop 2 plus; Zeiss, Oberkochen, Germany). Growth under anaerobic conditions was evaluated by culturing the bacterium in an anaerobic chamber.The organism we isolated from composted organic waste was a Gram-positive, rod-shaped (0.5 μm wide and 2 to 5 μm long), facultative aerobic bacterium. Oval-shaped endospores were readily discerned microscopically by their intracellular terminal sites. The bacterium was categorized as moderately thermophilic, as it grew maximally in SCD broth (pH 7.0) at 60°C but did not grow above 70°C or below 45°C (5, 32). The inability of the bacterium to grow at 37°C indicated that the organism was an obligate thermophile (16). The maximal pH for growth in SCD broth culture at 60°C was 6.0 to 7.0, but a pH of 5.0 strongly inhibited growth. There was no growth under acidic conditions (pH 3.0 to 4.0).Total DNA was extracted from 1.5 ml of cultured thermophilic bacteria (approximately 0.04 g of cells) using a DNA extraction kit (InstaGene Matrix; Bio-Rad, CA) according to the manufacturer''s instructions. Sense and antisense primers were designed (5′-GAGTTTGATCCTGGCTCAG-3′ and 5′-GGCTACCTTGTTACGA-3′, respectively) and used in PCR with total DNA serving as the template. The reaction mixture contained 5 μg of total DNA, 400 pmol of each oligonucleotide primer, and 0.1 U of Taq DNA polymerase in a volume of 50 μl. Thirty thermal cycles of 94°C for 1 min, 50°C for 1 min, and 72°C for 1 min were carried out. PCR products were purified by agarose gel electrophoresis, and the resulting DNA fragment (approximately 1,500 bp) was ligated into a pCRII vector (Invitrogen, CA). The PCR-amplified fragment was sequenced using the dideoxy-chain termination method.The small subunit rRNA gene of the isolated bacterium was amplified from bulk genomic DNA by PCR, and it constituted 1,483 bp of the 1,500 bp that were originally amplified by PCR. Searches for similar sequences were carried out using the BLAST program. According to the GenBank/DDBJ/EMBL database, the sequence of this gene showed 100% homology with Geobacillus thermoglucosidasius ACTT43742 ({"type":"entrez-nucleotide","attrs":{"text":"AB021197","term_id":"7209544","term_text":"AB021197"}}AB021197 in GenBank). The isolated bacterium was thus identified as Geobacillus thermoglucosidasius and designated strain NY05.For crystal formation on a gel surface, bacteria were first inoculated onto an SCD agar plate and incubated at 60°C for 18 h. A total of 1 mg (wet weight) of bacterial cells were inoculated with a loop onto a crystal-promoting hydrogel (25 mM sodium acetate, 7.0 mM calcium chloride, 2.0 mM magnesium sulfate, and 1.5% [wt/vol] agar) and incubated at 60°C for 24 h (hydrogel method).When cells were cultured using the hydrogel method, crystals of about 20 μm in size appeared in and around bacterial colonies during the course of a 3- to 4-h incubation. As shown in Fig. ​Fig.11 B, 100- to 200-μm hexagon-like crystals appeared when incubation was extended to 24 h. The importance of metabolic activity for crystal formation was evidenced by the absence of crystallization in control experiments, i.e., those performed without bacteria, or with cultures that had been autoclaved. These results demonstrate that bacteria are not simply heterogeneous nuclei for crystallization but actively mediate the process.Open in a separate windowFIG. 1.(A and B) Polarized (A) and light (B) microscopic observation of crystals formed using the hydrogel method. (C to E) Fluorescence microscopic image of crystals excited at 480 ± 20 nm, (C) 365 ± 5 nm (D), and 545 ± 15 nm (E).To isolate crystals formed using the hydrogel method, the part of gel on which crystals formed was excised using a sterilized spatula and solubilized in buffer QX1 (Qiagen, CA) in a test tube at room temperature. Crystals were recovered at the bottom of the test tube and washed repeatedly with sterilized distilled water and ethanol and then dried at 60°C. Crystals were observed using an Eclipse-ME600 polarized microscope (Nikon, Tokyo, Japan) and an Axioskop 2 plus fluorescence microscope. For fluorescence microscopy, the following filter blocks were used: exciter, 360 to 370 nm, 460 to 500 nm, and 530 to 560 nm; dichroic mirror, 380 nm, 505 nm, and 570 nm; emitter, >399, 510 to 560 nm, and 573 to 684 nm.The exceptionally strong polarizing property of crystals when examined under polarized microscopy confirmed that the material was composed of crystallized inorganic mineral (Fig. ​(Fig.1A).1A). The remarkable fluorescent property of the crystals was demonstrated by fluorescence microscopy. As shown in Fig. 1C to E, the crystals fluoresced green, blue, and red when excited at 480 ± 20 nm, 365 ± 5 nm, and 545 ± 15 nm, respectively.Geobacillus catalyzed the formation of crystals on gel media containing 25 mM sodium acetate, 7.0 mM calcium chloride, and 2.0 mM magnesium sulfate. Gels lacking magnesium sulfate did not prevent bacteria from catalyzing crystal formation, but the removal of sodium acetate or calcium chloride from media did preclude crystal formation. Thus, calcium and carboxyl carbon were both essential for crystal formation, while magnesium sulfate was inessential. Crystals formed when incubation temperatures were in the range of 60 to 70°C, but when the temperature was kept in the range of 40 to 50°C, fewer crystals formed. Crystallization was precluded by incubation above 80°C and below 30°C. The optimal temperature for crystal formation was therefore chosen to be 60°C. Crystal formation was observed only under aerobic conditions, suggesting that atmospheric oxygen and/or biological oxidative molecules are essential for the catalytic processes leading to crystal formation. The effect of sodium acetate concentration on crystal formation was also investigated using the hydrogel method. The concentrations of calcium chloride and magnesium sulfate were maintained at 7.0 mM and 2.0 mM, respectively, while the concentration of sodium acetate was varied. Sodium acetate in the range of 12.5 mM to 50 mM induced satisfactory crystal formation. However, at a concentration of 75 mM, sodium acetate decreased the efficiency of crystal formation, and no crystals were formed on gels with 100 mM sodium acetate. The effect of different sources of carbon on the ability of Geobacillus to catalyze crystal formation was investigated using the hydrogel method. The presence of sodium formate or acetate at 25 mM induced calcite formation, but 25 mM sodium propionate, sodium citrate, methyl alcohol, and ethyl alcohol did not promote crystal formation. These results indicated that Geobacillus-catalyzed crystal formation requires a carbon source derived from C₁ and C₂ carboxylates. The optimal concentration of calcium ion for crystal formation was also determined using the hydrogel method, in which the concentrations of sodium acetate and magnesium sulfate were 25 mM and 2.0 mM, respectively. More than 200 crystals per milligram (wet weight) of cells were obtained using 40 mM calcium chloride.The effect of heavy metal ions on crystal formation was investigated by doping the hydrogel with heavy metal ions (CuCl₂, NiCl₂, CdCl₂) at concentrations ranging from 0.01 to 0.5 mM. In general, results obtained for hydrogel doped with Cu²⁺ showed that a high concentration (0.5 mM) of heavy metal ions completely inhibited crystal formation. Doping hydrogel with 0.1 mM Cd²⁺ strongly inhibited crystal formation. On the other hand, low concentrations (0.01 mM) of metal ions did not impede crystal formation. The presence of Ni²⁺ at a concentration of 0.01 mM enhanced crystal formation.Crystals were examined for fluorescence properties using an SPEX Fluorolog LF3-22-Tau3 fluorescence spectrophotometer (Horiba, Tokyo, Japan). Crystals were studied at room temperature, and matrix scanning was employed for the measurement of fluorescence spectra. Wavelength scans were performed at 250 to 400 nm at step intervals of 5 nm. The emission spectrum was measured for each excitation wavelength between 310 and 700 nm. Crystals were excited in the range of 260 to 400 nm and emitted energy in the range of 350 to 600 nm. The maximum excitation and emission wavelengths were 369.6 nm and 446.9 nm, respectively (Fig. ​(Fig.22 A). Figure ​Figure2B2B shows an example of a fluorescence spectrum for crystals excited at a wavelength of 350 nm, which were emitted at a wavelength of 375 to 550 nm with the maximum emission at 439 nm.Open in a separate windowFIG. 2.(A) Photoluminescence spectrum of a single crystal prepared using the gel method. (B) Emission fluorescence spectrum of a single crystal excited at 350 nm. cps, counts per second.Energy-dispersive X-ray (EDX) elemental analyses of single purified crystals were performed using an EMAX-5770 electron microscope equipped with a microanalysis system (Horiba, Tokyo, Japan). The analyses were carried out at 20 kV of accelerating voltage and 0.26 nA of probe current. As shown in Fig. ​Fig.33 A, crystals contained large amounts of carbon, oxygen, and calcium, with smaller amounts of magnesium, sodium, silica, sulfur, phosphorus, and chlorine. When the number of calcium atoms was converted to 100, the composition with respect to magnesium, sodium, silicon, sulfur, phosphorus, and chlorine was 19.1, 12.2, 5.10, 2.35, 1.22, and 1.83, respectively. We confirmed that the crystals react with hydrochloric acid using the Meingen reaction (4) and that they emit gas (CO₂) upon melting. The crystal is possibly a calcium carbonate species, because its spectrum was similar to that of standard calcium carbonate (Fig. ​(Fig.3B).3B). The inability of Geobacillus to catalyze crystal formation under anaerobic conditions suggests that the oxygen incorporated into the crystals may be derived from atmospheric oxygen.Open in a separate windowFIG. 3.EDX spectrum of crystals. (A) Crystal formed through catalysis by G. thermoglucosidasius. (B) Purified calcium carbonate.The structure of purified crystals was analyzed by the Bragg-Brentano method by using a RINT-2000 powder X-ray diffractometer (Rigaku, Tokyo, Japan) with a graphite monochromator, a scintillation counter scanning rate of 4°/min, and a rotary stage. The X-ray generator was operated at 40 kV and 100 to 200 mA. The divergence and receiving slits for the diffracted beam were set at 0.01° and 0.15 mm, respectively. The scanning regions of the diffraction angle (2 theta) were 20° to 90° at a step interval of 0.02° and a scan rate of 2.0°/min. Spectra were collected by using a diffractometer with a graphite monochromator and Cu Kα radiation (Fig. ​(Fig.4).4). The peak pattern of crystals was consistent with that of CaCO₃ as a reference at up to 60° in 2 theta degrees, but the peak intensity of crystals was not consistent with that of the CaCO₃ reference at over 40° in 2 theta degrees. A comparison of the X-ray diffraction pattern with the powder diffraction file (PDF-2) provided by the International Centre for Diffraction Data suggested that the crystals are magnesian calcite [(Ca, Mg)CO₃] (PDF identification number 00-043-0697). Therefore, the data indicate that the crystals formed by Geobacillus nucleation are calcite-type calcium carbonate, in which some of the calcium in the crystal structure has been replaced by magnesium, sodium, sulfur, chlorine, and phosphorus.Open in a separate windowFIG. 4.Powder X-ray diffraction patterns of the CaCO₃ reference (bottom) and the unidentified crystal formed by G. thermoglucosidasius catalysis (top).We observed that visible calcite crystals formed within 4 h in the area around colonies of G. thermoglucosidasius cultured on crystal formation gel. This observation supports the contention that G. thermoglucosidasius secretes nano-sized nucleus-like factors that are associated with extracellular crystal formation. Addadi et al. (1) reported that acidic matrix macromolecules of polystyrene film, which are involved in regulating calcite growth, often contain aspartic acid-rich domains and covalently bound sulfated polysaccharides. They proposed that sulfates and beta-sheet-structured carboxylates cooperate in oriented calcite crystal nucleation (1). In our study, the rate of crystal formation may have been enhanced due to the gel matrices that regulated the dispersion of calcium ions.G. thermoglucosidasius was unable to catalyze calcite formation under anaerobic conditions, indicating that oxygen is required for the formation of calcite crystals. Accordingly, we proposed that the following two reactions are involved in G. thermoglucosidasius-catalyzed calcite formation when either formate, 2Ca²⁺ + 2HCOO⁻ + O₂ → 2CaCO₃ + 2H⁺, or acetate, 2Ca²⁺ + 2CH₃COO⁻ + 3O₂ → 2CaCO₃ + 2CO₂ + 2H⁺, is involved.The precise role G. thermoglucosidasius-catalyzed calcite formation plays in the environment has not been elucidated. Reports demonstrating that bacteria adsorbed onto inorganic minerals are resistant to various chemical and physical stressors suggest a possible role for bacterially catalyzed calcite formation (7, 13, 26). We found endospore-like substances adsorbed on the surface of purified calcite. Purified calcite formed by G. thermoglucosidasius nucleation and exposed to extreme conditions (i.e., washing with 70% ethyl alcohol, treatment with protease and DNase, UV irradiation at 254 nm, boiling for 15 min, freezing at −80°C for 48 h) was incubated on the surface of SCD nutrient agar at 60°C for 14 to 18 h, resulting in the formation of a bacterial colony around the calcite. Though the calcite crystals are inorganic substances and were completely dehydrated, G. thermoglucosidasius cells and/or endospores could have been adsorbed to the surface and protected from the extreme conditions in a cryptobiotic state (6, 10). We confirmed that the colony was growing concentrically around the calcite that had been exposed to the extreme environment. These results indicated that calcite-bound cells were more resistant to physicochemical stressors.The calcite formation was initiated under oligotrophic conditions in which formate or acetate was present, as were trace amounts of calcium. If G. thermoglucosidasius cells were exposed to conditions unsuitable for their growth in the natural environment, they would be expected to catalyze the formation of calcite and adsorb onto it, living in a cryptobiotic state until conditions improved. It is assumed that G. thermoglucosidasius cells adsorb onto calcite as a means of surviving unfavorable conditions but remain there and continue to grow under favorable oligotrophic conditions. Calcite formation may therefore be one of the means these organisms use to survive in extreme environments.G. thermoglucosidasius-catalyzed calcite crystals may have a number of applications that can be exploited. Metal oxide-type phosphors, which are conventionally used in fluorescent lamps and cathode ray tubes, are generally prepared by doping high-purity and precious rare earth with an activator (31). Different CaCO₃ modifications doped with Eu³⁺, Tb³⁺, or Ce³⁺ have been synthesized as phosphor hosts, and their luminescent properties have been determined (8). The maximum excitation and emission wavelengths for Eu³⁺-doped calcite-type red phosphor are 393 nm and 611 nm, respectively (18). Vaterite-type CaCO₃ doped with Ce³⁺ and Tb³⁺ emits green light, and its maximum excitation and emission wavelengths are 275 nm and 545 nm, respectively (11). However, the drastic loss of fluorescence intensity these phosphors display at room temperature is disadvantageous. In addition, these phosphors have a very narrow emission wavelength interval of 50 nm. The calcite crystals formed by G. thermoglucosidasius nucleation, on the other hand, are excited by a wavelength interval of 260 to 400 nm, and their emission wavelengths are from 350 to 600 nm. The wide emission wavelength interval is a novel fluorescence property of G. thermoglucosidasius-catalyzed calcite crystals. Unlike conventional phosphors, calcite crystals formed by G. thermoglucosidasius nucleation can be prepared without rare earth, and they accommodate magnesium, sodium, sulfur, and phosphorus atoms in the carbonate host lattice. We may expect new industrial applications for G. thermoglucosidasius-catalyzed calcite phosphor, owing to its fluorescence stability without loss of intensity.G. thermoglucosidasius calcite phosphor could have potential advantages as a filler in rubber and plastics, fluorescent particles in stationery ink, and a fluorescent marker for biochemistry applications (15) and also with uses in other biodevices (24). Our study may provide novel inorganic materials with a range of photoluminescent properties that can be fabricated from calcite doped with various heavy-metal ions (e.g., Cu²⁺, Ni²⁺, Cd²⁺). In materials engineering, environmentally friendly systems with minimal energy consumption and resource depletion are required for producing materials and composites. Biological processes serve as impressive archetypes of sustainable materials technologies. Because of its potential benefits in this regard, the study of biominerals has gained recognition as an important area of biomimetic materials science (27).     

Sphingomyelin Activates Hepatitis C Virus RNA Polymerase in a Genotype-Specific Manner

Hepatitis C virus (HCV) replication and infection depend on the lipid components of the cell, and replication is inhibited by inhibitors of sphingomyelin biosynthesis. We found that sphingomyelin bound to and activated genotype 1b RNA-dependent RNA polymerase (RdRp) by enhancing its template binding activity. Sphingomyelin also bound to 1a and JFH1 (genotype 2a) RdRps but did not activate them. Sphingomyelin did not bind to or activate J6CF (2a) RdRp. The sphingomyelin binding domain (SBD) of HCV RdRp was mapped to the helix-turn-helix structure (residues 231 to 260), which was essential for sphingomyelin binding and activation. Helix structures (residues 231 to 241 and 247 to 260) are important for RdRp activation, and 238S and 248E are important for maintaining the helix structures for template binding and RdRp activation by sphingomyelin. 241Q in helix 1 and the negatively charged 244D at the apex of the turn are important for sphingomyelin binding. Both amino acids are on the surface of the RdRp molecule. The polarity of the phosphocholine of sphingomyelin is important for HCV RdRp activation. However, phosphocholine did not activate RdRp. Twenty sphingomyelin molecules activated one RdRp molecule. The biochemical effect of sphingomyelin on HCV RdRp activity was virologically confirmed by the HCV replicon system. We also found that the SBD was the lipid raft membrane localization domain of HCV NS5B because JFH1 (2a) replicon cells harboring NS5B with the mutation A242C/S244D moved to the lipid raft while the wild type did not localize there. This agreed with the myriocin sensitivity of the mutant replicon. This sphingomyelin interaction is a target for HCV infection because most HCV RdRps have 241Q.Hepatitis C virus (HCV) has a positive-stranded RNA genome and belongs to the family Flaviviridae (21). HCV chronically infects more than 130 million people worldwide (34), and HCV infection often induces liver cirrhosis and hepatocellular carcinoma (19, 28). To date, pegylated interferon (PEG-IFN) and ribavirin are the standard treatments for HCV infection. However, many patients cannot tolerate their serious side effects. Therefore, the development of new and safer therapeutic methods with better efficacy is urgently needed.Lipids play important roles in HCV infection and replication. For example, the HCV core associates with lipid droplets and recruits nonstructural proteins and replication complexes to lipid droplet-associated membranes which are involved in the production of infectious virus particles (24). HCV RNA replication depends on viral protein association with raft membranes (2, 30). The association of cholesterol and sphingolipid with HCV particles is also important for virion maturation and infectivity (3). The inhibitors of the sphingolipid biosynthetic pathway, ISP-1 and HPA-12, which specifically inhibit serine palmitoyltransferase (SPT) (23) and ceramide trafficking from the endoplasmic reticulum (ER) to the Golgi apparatus (37), suppress HCV virus production in cell culture but not viral RNA replication by the JFH1 replicon (3). Other serine SPT inhibitors (myriocin and NA255) inhibit genotype 1b replication (4, 29, 33). Very-low-density lipoprotein (VLDL) also interacts with the HCV virion (15).Sakamoto et al. reported that sphingomyelin bound to HCV RNA-dependent polymerase (RdRp) at the sphingomyelin binding domain (SBD; amino acids 230 to 263 of RdRp) to recruit HCV RdRp on the lipid rafts, where the HCV complex assembles, and that NA255 suppressed HCV replication by releasing HCV RdRp from the lipid rafts (29). In the present study, we analyzed the effect of sphingomyelin on HCV RdRp activity in vitro and found that sphingomyelin activated HCV RdRp activity in a genotype-specific manner. We also determined the sphingomyelin activation domain and the activation mechanism. Finally, we confirmed our biochemical data by a HCV replicon system.     

Photooxidation pathway of chlorophyll Z in photosystem II as Studied by Fourier transform infrared spectroscopy

The oxidation pathway of chlorophyll Z (ChlZ) in photosystem II (PSII) at cryogenic temperatures was studied by means of light-induced Fourier transform infrared (FTIR) difference spectroscopy. To examine the involvement of redox-active beta-carotene (Car) in the pathway, two Car molecules in Mn-depleted PSII membranes of spinach were selectively bleached by illumination at 250 K in the presence of ferricyanide and silicomolybdate. Successful bleaching of Car was demonstrated by disappearance of the light-induced FTIR signals of Car+ at 1465, 1440, and 1147 cm(-1) at 80 K under an oxidative condition. Even in the Car-bleached PSII, the ChlZ+/ChlZ signal at 1713/1687 cm(-1), which is attributed to the upshift of the 9-keto C=O band of ChlZ upon its oxidation, was induced by illumination at 80 K retaining about 80% of the intensity of the control PSII sample. The concomitant appearance of shoulders at 1727/1699 cm(-1) may indicate that both of the two ChlZ molecules on the D1 and D2 sides are photooxidized. The multiphasic kinetics of formation of the ChlZ+/ChlZ signal by continuous illumination at 80 K were mostly unchanged by Car depletion, while the formation rates at 210 K were appreciably reduced in Car-bleached PSII. These results indicate that there are electron-transfer pathways from ChlZ to P680+ that do not involve Car, and they are indeed dominant at 80 K. Although the pathways via Car are mostly blocked at this temperature, the contribution of such pathways to ChlZ oxidation becomes significant at higher temperatures.     

Dll4-selective Notch signaling induces ephrinB2 gene expression in endothelial cells

The Notch pathway is involved in multiple aspects of vascular development, including arterial-venous differentiation. Here, we show that Notch stimulation instructively induces arterial characteristics in endothelial cells (EC). Forced expression of Notch intracellular domain (NICD, activated form of Notch) induced mRNA expression for a subset of arterial-specific markers such as ephrinB2, connexin40, and HERP1 only in EC but not other cell lines. In co-culture experiments using EC and either Dll4- or Jagged1-expressing cells, we found that Dll4 stimulation but not Jagged1 markedly induced ephrinB2 expression. An inducible expression of HERP1 and HERP2 by NICD has no measurable effects on expression of ephrinB2 and venous marker EphB4 although either HERP1 or HERP2 overexpression exerts potent inhibitory effects on EphB4 expression without ephrinB2 induction. We also found no functional interaction between Notch and TGF-beta-ALK1 signalings in an induction of ephrinB2 expression. These results suggest that Dll4-stimulated Notch signaling induces a part of arterial characteristics only in EC via HERP-independent mechanism. Our data provide new insight into the molecular mechanism of ligand-selective Notch activation during differentiation of arterial EC.     

Intestinal and peri-tumoral lymphatic endothelial cells are resistant to radiation-induced apoptosis

Radiation therapy is a widely used cancer treatment, but it is unable to completely block cancer metastasis. The lymphatic vasculature serves as the primary route for metastatic spread, but little is known about how lymphatic endothelial cells respond to radiation. Here, we show that lymphatic endothelial cells in the small intestine and peri-tumor areas are highly resistant to radiation injury, while blood vessel endothelial cells in the small intestine are relatively sensitive. Our results suggest the need for alternative therapeutic modalities that can block lymphatic endothelial cell survival, and thus disrupt the integrity of lymphatic vessels in peri-tumor areas.