杂交构树UDP-葡萄糖脱氢酶基因编码蛋白的亚细胞定位及其启动子5'端缺失片段的功能分析

为了研究杂交构树UDP-葡萄糖脱氢酶基因（DDBJ，BpUGDH基因登录号为LC457701）启动子不同区域的表达活性，利用5'端缺失及同源重组实验技术，将5个不同长度的BpUGDH启动子5'端缺失片段与GUS基因连接，并通过农杆菌介导法瞬时转化烟草；同时，为了定位BpUGDH基因编码的蛋白在细胞中表达的具体位置，利用GFP报告基因融合目的基因进行蛋白质的亚细胞定位。结果显示：BpUGDH基因启动子-244 bp以内的序列均能介导GUS基因的诱导表达，并且-973、-465、-355、-281和-244 bp之间的区域可能对BpUGDH基因启动子的活性发挥着至关重要的作用。另外，BpUGDH基因编码蛋白的亚细胞定位结果显示：BpUGDH位于叶绿体中。     

A compartmental model for the study of diurnal rhythms in cell proliferation

A mathematical model taking into account the observed diurnal variations in cell kinetics is presented. Its principle is to divide each phase of the cell cycle into a definite number of compartments and to assume time-dependent probabilities of transition from one compartment to the following; general properties of the model are derived.The particular case where the only time-dependent transition probabilities are those corresponding to the G₁ phase is studied. A characterization of the joint percentages of S and M cells variations is given. The application of the model to interpretation of published experimental data obtained in hamster cheek pouch epithelium is given.     

Partial purification and characterization of exoinulinase produced from Bacillus sp.

Inulinase are industrial food enzymes which have gained much attention in recent scenario. In this study, Inulinase producing eight bacterial colonies were isolated and screened from three different plant root tubers soil sample. Among 8 inulinase producing colonies, the higher yielding colony was selected with 25.10?U/mL for further studies. The best inulinase producing colony was identified by partial 16S rRNA gene sequence as Bacillus sp. The crude inulinase was purified by using ammonium sulphate precipitation, dialysis and ion exchange chromatography on DEAE – sephacel and obtained 1.9 purification fold with total activity 293 U. The purified enzyme was subjected to characterization studies and it was found to be stable at 30–60?°C and optimum temperature was at 55?°C. The enzyme was stable at pH 3.0–7.0 and optimum pH was at 6.5. The K_m and V_max value for inulinase was found to be 0.117?mg/mL and 4.45?μmol?min?mg^?1 respectively, demonstrate its greater affinity. Hence, this enzyme can be widely used for the production of fructose, and fructooligosaccharides, which are important ingredients in food and pharmaceutical industry.     

Seaweeds,then and now

An historical overview of meetings of the International Seaweed Symposium is presented. A summary of attempts since 1952 to establish a seaweed industry in British Columbia is given. A brief review of recent developments in the area in relation to a seaweed industry is outlined.     

The influence of temperature on nest site choice and reproductive strategy in a temperate zone Polistes wasp

Abstract. 1. Field experiments with Polistes fuscutus showed that more nests were initiated, co-foundress groups were larger, broods developed faster, and workers eclosed earlier in sun-warmed sites than in cool ones.
2. These results suggest that colonies nesting in sun-warmed shelters gained a fitness advantage over those in cooler shelters. More rapid brood development means that such colonies reach the ergonomic stage more quickly, which in turn means a higher expectancy of survival and greater productivity at the end of the season.
3. We argue that thermal properties constitute an important component of Polistes nest site quality in temperate regions and that these properties influence joining and usurping strategies as well as nest site choice in spring Polistes females. Other factors being equal, a joining or usurping female should opt for a colony in a warm site over one in a cool site, leading to the larger foundress groups we found in warm shelters.
4. We hypothesize that the selective advantage of philopatry in temperate zone Polistes populations is that it brings spring females to nest sites of proven quality.     

Research experience modifies how participants profit from journal clubs in academia

Because Journal Clubs (JClubs) represent valued educational tools, we often assume optimality of Journal Club practices. We analyze here JClubs records from a research group to identify factors that modify how much attendants benefit from discussing a paper. We demonstrate that attendants benefit most from papers focusing on systems similar to those they work on and that their ability to profit from different contribution types changes with research experience. Common JClubs practices such as the assignment of the paper selection to a single individual could thus compromise participant experience. Our conclusions may also be generalizable to situations outside academia.     

Application of bioluminescence ATP measurement for evaluation of fungal viability of foxing spots on old documents

An adenosine triphosphate (ATP) bioluminescence‐based protocol was tested to assess the viability of fungal species in old documents damaged by foxing. Foxing appears as scattered yellow brownish‐red stains, damaging the aesthetics of documents and their long‐term readability. In the field of cultural heritage conservation, the debate over the mechanism of foxing is ongoing. Previous studies found evidence of mold‐like structures in some coloured areas; however, many species have not yet been identified and their role in the phenomenon is not understood. To better understand their involvement in this type of paper decay, we focused our attention first on their viability. We demonstrated the reliability and sensitivity of the ATP bioluminescence assay compared with conventional methods based on cultivation, which has rarely given rise to in vitro growth from foxed papers. From nine books dating back from the 19th and 20th centuries, the mean ATP amount of foxed spots ranged from 0.29 to 3.63 ng/cm², suggesting the presence of strains inside the brownish spots and providing evidence of their viability. Outside the spots, ATP content was considered negligible, with a mean ATP amount of 0 to 0.03 ng/cm². ATP assay appears to be a useful and robust method for the detection and quantification of viable elements in foxing spots. Copyright © 2012 John Wiley & Sons, Ltd.     

Industrial Requirements of Materials for Electrical Double Layer Capacitors: Impact on Current and Future Applications

Electrical double layer capacitors (EDLCs) are nowadays considered one of the most important energy storage technologies. In recent years, great efforts have been made toward the development of novel materials, active and inactive, suitable for the realization of advanced EDLCs displaying higher performance, especially in terms of energy, compared to the state‐of‐the‐art devices. Nevertheless, the applicability of these materials in real devices and the industrial requirements related to the development of innovative EDLCs are not always properly addressed by the scientific community. This short review addresses these two fundamental aspects, with the aim to supply an updated set of information about the industrial requirements for the materials usable in commercial EDLCs. Additionally, the review also provides an updated overview about the present and estimated future market size of EDLCs as well as present and future applications of this technology addressing the market‐specific needs. This “application‐oriented” information is pivotal for a successful development and large‐scale production of advanced EDLCs.     

Simultaneous secretion of seven lignocellulolytic enzymes by an industrial second-generation yeast strain enables efficient ethanol production from multiple polymeric substrates

A major hurdle in the production of bioethanol with second-generation feedstocks is the high cost of the enzymes for saccharification of the lignocellulosic biomass into fermentable sugars. Simultaneous saccharification and fermentation with Saccharomyces cerevisiae yeast that secretes a range of lignocellulolytic enzymes might address this problem, ideally leading to consolidated bioprocessing. However, it has been unclear how many enzymes can be secreted simultaneously and what the consequences would be on the C6 and C5 sugar fermentation performance and robustness of the second-generation yeast strain. We have successfully expressed seven secreted lignocellulolytic enzymes, namely endoglucanase, β-glucosidase, cellobiohydrolase I and II, xylanase, β-xylosidase and acetylxylan esterase, in a single second-generation industrial S. cerevisiae strain, reaching 94.5 FPU/g CDW and enabling direct conversion of lignocellulosic substrates into ethanol without preceding enzyme treatment. Neither glucose nor the engineered xylose fermentation were significantly affected by the heterologous enzyme secretion. This strain can therefore serve as a promising industrial platform strain for development of yeast cell factories that can significantly reduce the enzyme cost for saccharification of lignocellulosic feedstocks.