Improved Imprinting Technique for Study of Plant Tissues

The exposed surface of plant tissues is coated with nail varnish. When peeled off, the transparent coating film bean a replica imprint of the tissue. Transparent adhesive tape is used for lifting the film imprint and mounting is on a microslide without curling. By a similar method, an opaque sealant replica with an aluminum foil support may be prepared which can serve as a mold for obtaining a transparent secondary imprint useful for light microscopic studies. The replicas can be stored like herbarium specimens for future use.     

Differentiation of Gram Positive and Gram Negative Bacteria in Transparent Acrylic Resin Emulsion Replicas of Surfaces of Plants

When acrylic resin emulsion (Rohm & Haas Primal AC-33) is allowed to dry on a leaf surface, it can be peeled off to give a transparent replica of the surface with bacteria and fungi embedded in it. The distribution of micro-organisms in the replica appears to reflect the patterns in which they occur naturally on the surface. The resin replicas may be stained by a variety of microscopical stains, the best of which is phenol-acetic-aniline blue, and are suitable for high power light microscopy.
Acrylic resin emulsion differs from widely used cellulose-based materials in that permanent differentiated preparations of Gram positive and Gram negative stained bacteria may be produced from a wide variety of types of surface.     

Fluid dynamic study in a femoral artery branch casting of man with upstream main lumen curvature for steady flow

An in-vitro, steady flow investigation was conducted in a hollow, transparent vascular replica of the profunda femoris branch of man for a range of physiological flow conditions. The replica casting tested was obtained from a human cadaver and indicated some plaque formation along the main lumen and branch. The flow visualization observations and measured pressure distributions indicated the highly three-dimensional flow characteristics with arterial curvature and branching, and the important role of centrifugal effects in fluid transport mechanisms.     

Electrophoretic separation of plasma lipoproteins in agarose gel

A method has been developed for the separation of serum or plasma lipoproteins by electrophoresis in an agarose-agar gel mixture. The gel is applied to the surface of a thin polyester photographic film strip. With minor alterations in technique either single samples on individual strips or many samples on one large sheet may be processed. After fixation and dehydration the transparent film is stained with Sudan Black B and washed with water. The finished electrophoretogram can be obtained in 5 hr and consists of widely separated bands of lipoprotein fractions on a colorless transparent background, ideally suited for scanning with a densitometer. Plasma samples from different subjects show pre-beta lipoproteins of different mobilities. An effect of gel concentration on the extent of lipoprotein migration is demonstrated. The clearcut separation of lipoproteins by this method will facilitate the classification of hyperlipoproteinemias and improve quantitative estimates of lipoprotein distribution.     

Single-Stage Carbon Replicas of Microspores

Single-stage surface replicas of treated or fresh pollen grains can be made ready for the electron microscope in 1.5 hr. The microspores are discharged into a drop of 50% acetone on a 1 cm square of cleaved mica and air dried. Carbon is evaporated to a film thickness of 35 mμ during rotation of the mica support. The carbon film and microspores are parted from the mica with water and heated in 2-aminoethanol at 145-155 C for 10 min to 3 hr. The replicas are then washed 5 min or longer on water at 90 C and picked up on electron microscope grids. The resulting self-shadowed surface replica can be immediately observed by electron microscopy.     

A Disrupting Factor in Silver Staining Techniques

Single-stage surface replicas of treated or fresh pollen grains can be made ready for the electron microscope in 1.5 hr. The microspores are discharged into a drop of 50% acetone on a 1 cm square of cleaved mica and air dried. Carbon is evaporated to a film thickness of 35 mμ during rotation of the mica support. The carbon film and microspores are parted from the mica with water and heated in 2-aminoethanol at 145-155 C for 10 min to 3 hr. The replicas are then washed 5 min or longer on water at 90 C and picked up on electron microscope grids. The resulting self-shadowed surface replica can be immediately observed by electron microscopy.     

Quorum-based synchronization protocols for multimedia replicas

Multiple replicas of multimedia objects are distributed to peers in overlay networks. In quorum-based (QB) protocols, every replica may not be up-to-date and the up-to-date replica can be found in the version counter. Multimedia objects are characterized in terms of not only data structure but also quality of service (QoS) parameters like frame rate. A transaction reads a parameter of a replica while there is a type of read operation to read a whole state of a replica. Each parameter of a replica is changed through a write operation. Thus, the data structure and QoS parameters of a replica are independently manipulated. In the multimedia quorum-based (MQB) protocol, multiple replicas of a multimedia object are synchronized based on the newness precedent relation. An object is an encapsulation of data and abstract operations for manipulating the data. There are enriching and impoverishing types of write operations. Some data is added to a replica in an enriching operation. On the other hand, some data in a replica is removed in an impoverishing operation. In order to reduce the overhead to write every replica in a quorum, we take an approach that the state of each replica is not always updated. If a transaction issues an enriching write operation, every replica in the write quorum is updated in the same way as the QB protocol. On the other hand, if an impoverishing write operation is issued, every replica is not updated in the quorum. Impoverishing operations are just recorded in replicas. On receipt of a read operation to read a whole state, impoverishing operations recorded are performed on a replica. The MQB protocol is evaluated in terms of the processing overhead of replicas. We show that the processing overhead of each replica can be reduced in the MQB protocol.     

Improved antigen retrieval in freeze-fracture cytochemistry by evaporation of carbon as first replication layer

The recently developed freeze-fracture replica immunolabeling technique uses sodium dodecyl sulfate to clean replicas obtained from chemically unfixed, rapidly frozen cells by evaporation of platinum as first and carbon as second replication layer. The detergent dissolves remains of cellular material with the exception of components which are in direct contact to the replica film. Membrane lipids and membrane protein complexes of the protoplasmic and the exoplasmic membrane halves remain attached to the replica film and are accessible for cytochemical localization. We immunolabeled the membrane proteins caveolin-1 and connexin 43 in mouse cell lines as well as the membrane attached protein tetrachloroethene reductive dehalogenase (PceA) in bacterial cells at freeze-fracture replicas generated by different evaporation parameters. The labeling experiments for caveolin-1 and the PceA showed that freeze-fracture replication of cellular membranes accomplished with thin platinum layers as well as replication with carbon as first evaporation layer lead in these cases to an improved antigen retrieval, whereas the labeling efficiency of connexin 43 was not affected by different evaporation conditions.     

A modified procedure for replica plating of mammalian cells allowing selection of clones based on gene expression.

The polyester cloth replica-plating technique for selection of mammalian cell clones was modified by growing cells in colonies on a flexible polytetrafluoroethylene membrane and then transferring them completely to polyester cloth (27-microns mesh), from which a replica was made by allowing cells to transfer to a cloth of smaller pore size (17-microns mesh). Using this technique, two phenotype selection methods are demonstrated here: in situ hybridization for detection of a specific mRNA and a photographic film assay for detection of luciferase expression. Cells were transfected with pSV2AL-A delta 5' in which firefly luciferase cDNA is under the control of the simian virus 40 promoter. The luciferase assay was adapted for colonies on polyester cloth; cells were permeabilized with digitonin to allow access of ATP and luciferin to the cell without disruption of colonies. Clones selected for expression or nonexpression of luciferase by the photographic film assay were positive or negative for expression after isolation from the cloth replica and subsequent growth under conventional culture conditions. The replica-plating procedure described here should be generally applicable to most mammalian cell types. The ability to produce replicas of colonies, combined with in situ hybridization or assays that can be adapted to in situ detection, provides phenotype selection for clones based on gene expression independent of growth characteristics.     

Simple preparation of novel photochromic polyvinyl alcohol/carboxymethyl cellulose security barcode incorporated with lanthanide-doped aluminate for anticounterfeiting applications

Forgery and low-quality products pose a danger to society. Therefore, there are increasing demands for the production of easy-to-recognize and difficult-to-copy anticounterfeiting materials. Products with smart photochromic and fluorescence properties can change colour and emission spectra responding to a light source. In this context, we devised a straightforward preparation of a luminescent polyvinyl alcohol/carboxymethyl cellulose (PVA/CMC) nanocomposite to function as a transparent labelling film. The lanthanide-doped aluminate (LdA) was prepared in the nanoparticle form to indicate diameters of 35–115 nm. Different ratios of the LdA were physically dispersed in the PVA/CMC nanocomposite label film to provide photochromic, ultraviolet protection, antimicrobial activity, and hydrophobic properties. Fluorescence peaks were detected at 365 and 519 nm to indicate a colour change to green. As a result of increasing the phosphor ratio, improved superhydrophobic activity was achieved as the contact angle was increased from 126.1° to 146.0° without affecting the film's original physical and mechanical properties. Both ultraviolet (UV) light protection and antibacterial activity were also investigated. The films showed a quick and reversible photochromic response without fatigue. The current strategy reported the development of a photochromic smart label that is transparent, cost effective, and flexible. As a result, numerous anticounterfeiting products can benefit from the current label for a better market. LdA-loaded PVA/CMC films demonstrated antibacterial activity between poor, good, very good, and outstanding as the percentage of LdA in the film matrix increased. The current film can be applied as a transparent photochromic security barcode for anticounterfeiting applications and smart packaging.     

Film mulch with irrigation and rainfed cultivations improves maize production and water use efficiency in Ethiopia

Improving productivity of maize (Zea mays L.) and water use efficiency is of great significance for agriculture in Ethiopia. In this study, the effects of ridge‐furrow with film mulch cultivation were tested on maize yields in Melkassa, Ethiopia. Three field experiments (drip irrigation, furrow irrigation and rainfed) were conducted each with randomised complete block design with three replicates. The drip irrigation experiment was conducted in the dry season and constituted three film mulch methods (non‐mulch, transparent film mulch and black film mulch) with three irrigation levels (357, 435 and 515 mm). The furrow irrigation experiment was also conducted in the dry season and constituted two film mulches (non‐mulch and transparent film mulch) with three irrigation levels (484, 674 and 865 mm). The rainfed experiment was conducted in the rainy season and constituted three mulches (non‐mulch, transparent film mulch and black film mulch) with two farming methods (ridge‐furrow farming and flat farming). In the drip irrigation experiment, the highest maize yields (5.9 ± 0.6 t ha^?1) and irrigation water use efficiency (9.6 ± 1 kg ha^?1 mm^?1) were recorded in the treatment using black film mulch with high irrigation, with increases of 68% and 68.4% compared to using non‐mulch treatment at that irrigation level. In the furrow irrigation experiment, maize yields and irrigation water use efficiency reached 7 (± 0.8) t ha^?1 and 9.1 (± 1.9) kg ha^?1 mm^?1 in the treatment using transparent film mulch with medium irrigation (674 mm), with increases of 46% and 46.8% compared to that with non‐mulch treatment. In the rainfed experiment, the film mulch rather than farming method had positive effects on the maize yields and rainwater use efficiency. The average maize yield reached 8.5 (± 0.7) t ha^?1 in the film mulch treatments, with an increase of 39% than using the non‐mulch treatment. Compared with that of non‐mulch treatment, the net income in the film mulch treatments increased by 94% in the furrow experiment and 31% in the rainfed experiment. Our results indicate that the ridge‐furrow with film mulch system can be recommended for water‐saving irrigation with low cost in dry seasons, and film mulch with flat farming can be recommended in rainy seasons for maize production in Ethiopia. This study provides strong evidence that maize productivity can be effectively improved in Ethiopia and other similar areas of the world using this simple and cost‐effective technology.     

High‐Performance Ta2O5/Al‐Doped Ag Electrode for Resonant Light Harvesting in Efficient Organic Solar Cells

A efficient indium tin oxide (ITO)‐free transparent electrode based on an improved Ag film is designed by introducing small amount of Al during co‐deposition, producing ultrathin and smooth Ag film with low loss. A transparent electrode as thin as 4 nm is achieved by depositing the film on top of Ta₂O₅ layer, and organic solar cells based on such ultrathin electrode are built, producing power conversion efficiency over 7%. The device efficiency can be optimized by simply tuning Ta₂O₅ layer thickness external to the organic photovoltaic (OPV) structure to create an optical cavity resonance inside the photoactive layer. Therefore Ta₂O₅/Al‐doped Ag films function as a high‐performance electrode with high transparency, low resistance, improved photon management capability and mechanical flexibility.     

Agarose bioplastic‐based drug delivery system for surgical and wound dressings

We have developed an agarose‐based biocompatible drug delivery vehicle. The vehicle is in the form of thin, transparent, strong and flexible films. The biocompatibility and haemocompatibility of the films is confirmed using direct and indirect contact biological assay. Contact angle measurement exhibits hydrophilic nature of the films, and protein adsorption test shows low protein adsorption on the film surface. Drugs, antibiotics and antiseptics, retain their potency after their incorporation into the films. Our bioplastic films can be a versatile medium for drug delivery applications, especially as wound and surgical dressings where a fast drug release rate is desired.     

Carbon nanotube array: A new MIP platform

Here we demonstrate that a free-standing carbon nanotube (CNT) array can be used as a large surface area and high porosity 3D platform for molecular imprinted polymer (MIP), especially for surface imprinting. The thickness of polymer grafted around each CNT can be fine-tuned to imprint different sizes of target molecules, and yet it can be thin enough to expose every imprint site to the target molecules in solution without sacrificing the capacity of binding sites. The performance of this new CNT–MIP architecture was first assessed with a caffeine-imprinted polypyrrole (PPy) coating on two types of CNT arrays: sparse and dense CNTs. Real-time pulsed amperometric detection was used to study the rebinding of the caffeine molecules onto these CNT-MIPPy sensors. The dense CNT-MIPPy sensor presented the highest sensitivity, about 15 times better when compared to the conventional thin film, whereas an improvement of 3.6 times was recorded on the sparse CNT. However, due to the small tube-to-tube spacing in the dense CNT array, electrode fouling was observed during the detection of concentrated caffeine in phosphate buffer solution. A new I–V characterization method using pulsed amperometry was introduced to investigate the electrical characterization of these new devices. The resistance value derived from the I–V plot provides insight into the electrical conductivity of the CNT transducer and also the effective surface area for caffeine imprinting.     

The influence of ultraviolet radiation on growth,photosynthesis and phenolic levels of green and red lettuce: potential for exploiting effects of ultraviolet radiation in a production system

Studies have shown that natural ultraviolet (UV) radiation increases secondary products such as phenolics but can significantly inhibit biomass accumulation in lettuce plants. In the work presented here, the effect of UV radiation on phenolic concentration and biomass accumulation was assessed in relation to photosynthetic performance in red and green lettuce types. Lettuce plants in polythene clad tunnels were exposed to either ambient (UV transparent film) or UV-free conditions (UV blocking film). The study tested whether growth reduction in lettuce plants exposed to natural UV radiation is because of inhibition of photosynthesis by direct damage to the photosynthetic apparatus or by internal shading by anthocyanins. Ambient levels of UV radiation did not limit the efficiency of photosynthesis suggesting that phenolic compounds may effectively protect the photosynthetic apparatus. Growth inhibition does, however, occur in red lettuce and could be explained by the high metabolic cost of phenolic compounds for UV protection. From a commercial perspective, UV transparent and UV blocking films offer opportunities because, in combination, they could increase plant quality as well as productivity. Growing plants continuously under a UV blocking film, and then 6 days before the final harvest transferring them to a UV transparent film, showed that high yields and high phytochemical content can be achieved complementarily.     

Promotive effects of a silk film on epidermal recovery from full-thickness skin wounds

We examined the effects of the transparent fibroin film (silk film) on full-thickness skin wounds. Full-thickness dermatotomies (15 mm x 9 mm) were prepared on the dorsal wall of CRJ:CD-1 nu/nu (ICR nu/nu) mice. The area of the wounds dressed with silk film was reduced to 10% of that made by the dermatotomy 14 days after the dermatotomy and were covered with regenerated epidermis 21 days after the dermatotomy. In contrast, less recovery and epidermal regeneration were found 14 days after dermatotomy in the wounds dressed with a conventional hydrocolloid dressing (Duro Active). Furthermore, only partial incomplete epidemal growth was obtained 21 days after dermatotomy. Most importantly, the healing time of wounds dressed with silk film was 7 days shorter than those dressed with DuoActive dressing. The silk film showed an almost similar or slightly better promotive effect as the lyophilized porcine dermis (Alloask D), which is used as a dressing for burns, ulcers, and decubitis. Histologic findings revealed that there was greater collagen regeneration and less inflammation and neutrophil-lymphocyte infiltration of the wounds dressed with silk film than with DuoActive dressing. It is clear that regeneration of the epidermis and dermis of the wound beds covered with silk film was faster than with DuoActive dressing. Finally, silk film is easily obtainable, sterilizable, and transparent, and it allows easy observation of tissue recovery. Therefore, silk film offers advantages over other dressings and may be clinically useful for wound treatment.     

On-chip cell culture on a microarray of extracellular matrix with surface modification of poly(dimethylsiloxane)

Microfluidic cell culture chips allow to perform assays of small-volume samples rapidly and reproducibly. Most of these chips are made of poly(dimethylsiloxane) (PDMS), which is a flexible, durable, transparent and inexpensive polymer that can be easily applied to fabrication of microstructures by photolithography and replica molding. However, not many cells are able to grow on unmodified PDMS because the cells need appropriate scaffolds on the surface. Here we report surface modification of a PDMS substrate with a microarray of extracellular matrix (ECM) for on-chip cell culture. The ECM proteins collagen and fibronectin were covalently immobilized on an 8 x 8 microarray format by micropatterned UV-induced graft polymerization through a photomask and dehydration-condensation reaction through a microfabricated stencil. Identical spots of ECMs were successfully formed and the geometry of the spots accurately corresponded to the micropattern of the photomask and stencil. We demonstrate the culture of CHO-K1 cells on the ECM microarray chip. Cells proliferated on the fibronectin spots during the 2-day culture.     

遮荫和红膜处理对高山红景天根生物量及红景天甙含量季节变化的影响

采用纱布遮荫(覆以透明膜)和红色滤光膜处理人工种植生长3年和4年的高山红景天,观察了根生物量和红景天甙含量的季节变化结果表明,纱布遮荫处理(相对光强为全光照的51．8％)下根的生物量显著下降;红景天甙含量略有增加,红景天甙产量(红景天甙含量与根生物量乘积)则有所降低,但差异均不显著,红色滤光膜处理(相对光强为全光照的51．8％)与纱布遮荫处理相比,根生物量减少但不显著,红景天甙的含量和产量则显著增加,生长季末前者的红景天甙含量为后者的1．63倍(生长3年)和1．55倍(生长4年),红景天甙产量为后者的1．44倍(生长3年)和1．45倍(生长4年)。     

A composite agarose–polyacrylamide matrix as two-dimensional hard support for solid-phase protein assays

The solid-phase protein assays using blotting membranes as hard support do not allow achieving the low background and sensitivity of protein staining in clear gels. The membrane opacity complicates imaging of results on standard lab documentation systems. We describe a low-cost transparent matrix that can be used as an alternative to polymeric membranes for solid-phase assays. Protein samples are spotted onto a dry film of composite agarose–polyacrylamide matrix covering standard glass microscopic slides. After rehydration in protein-fixing solution, matrix with protein samples can be detached from glass support and stained as conventional protein polyacrylamide gels.     

A simple and sensitive method for detection of pullulanase and isoamylase activities in polyacrylamide gels

Summary Pullulanase and isoamylase activities in PAGE bands have been detected and distinguished by using a two-step, replica-gel revealing assay. The de-branching activity is first revealed as a bluish-purple band by incubating an amylopectin-agar replica gel and then exposing this to iodine vapour. In the second step, pullulanase can be distinguished from isoamylase by a similar procedure using pullulan-agar replica gel and revealing hydrolysis by flooding the plate with ethanol; pullulanase activity shows a colorless band. The procedure exclude other amylases activities. The sensitivity is such that 0.0015 unit of pullulanase and 0.0004 unit of isoamylase activities can be detected easily.