Growth densities regulate the response to elevated CO2 in a farmed seaweed Pyropia haitanensis (Bangiales,Rhodophyta)

Journal of Applied Phycology - Atmospheric CO2 concentration is predicted to nearly double by the end of this century. There are a large number of reports on the effects of elevated atmospheric CO2...     

海南尖峰岭国家级自然保护区森林动态监测样地鸟类和兽类多样性

2016年8月至2019年2月, 我们利用红外相机对海南尖峰岭60 ha森林动态监测样地的鸟类和兽类进行了调查。共在79个位点上布设了红外相机, 累积27,848个相机日, 获得可鉴定到物种的独立有效照片15,320张。经鉴定, 共拍摄到46种野生动物, 包括16种兽类(隶属于6目11科)和30种鸟类(隶属于8目16科)。其中, 属于国家I级重点保护的野生动物有3种, 即海南孔雀雉(Polyplectron katsumatae)、海南山鹧鸪(Arborophila ardens)和中华穿山甲(Manis pentadactyla), 属于国家II级重点保护的野生动物有6种, 分别是猕猴(Macaca mulatta)、巨松鼠(Ratufa bicolor)、红原鸡(Gallus gallus)、白鹇(Lophura nycthemera)、松雀鹰(Accipiter virgatus)和蓝背八色鸫(Pitta soror)。拍摄率最高的前5种兽类依次是帚尾豪猪(Atherurus macrourus)、红腿长吻松鼠(Dremomys pyrrhomerus)、白腹巨鼠(Leopoldamys edwardsi)、赤腹松鼠(Callosciurus erythraeus)和赤麂(Muntiacus vaginalis);前5种鸟类依次是白鹇、海南孔雀雉、蓝背八色鸫、海南山鹧鸪和栗颊噪鹛(Garrulax castanotis)。本研究补充调查了海南尖峰岭国家级自然保护区兽类和鸟类的多样性, 与之前的基线调查对比分析了大样地内野生动物物种及其相对多度的动态变化, 可为保护区生物多样性监测方案设计和保护对策的制定提供科学依据。     

基于CRISPR/Cas9基因编辑技术的本科教学实验体系的创建与实践

CRISPR/Cas9是新兴的基因编辑技术,在生命科学研究中发挥着重要的作用。将它引入本科生的实验教学,使本科生了解这项前沿科研技术很有意义。我们创建了一个基于CRISPR/ Cas9技术的本科教学实验体系。该实验体系侧重CRISPR/Cas9技术在哺乳动物细胞中的应用,选用一株基因组上被插入mCherry基因的小鼠胚胎成纤维细胞为实验材料,命名为STO-82。首先设计靶向mCherry的sgRNA,构建CRISPR-Cas9/sgRNA共表达质粒。经测序验证无误后,转染到STO-82细胞。采用流式细胞仪分析检测mCherry阴性和阳性两群细胞,分选出阴性单细胞并扩大培养。最后用测序检验单克隆细胞中靶标DNA序列的编辑情况。结果显示,靶位点有插入或缺失突变,说明体系创建成功。该实验体系将sgRNA设计、CRISPR-Cas9/sgRNA共表达质粒的构建、细胞转染、单细胞分选、单克隆细胞培养、测序序列分析等内容融合为一个综合实验,用于高年级本科生的实验教学。根据实际情况,将教学实践内容分解分块教学,也可以做完整性项目教学。本教学实践采用10人左右的小班分块教学,2人一组,经过3个班（共13组）的实践,绝大部分学生都能完成实验,得到预期结果。通过这个实验,学生加深了对CRISPR/Cas9技术的原理和实验流程的理解,锻炼了实验操作能力和严谨的科研思维,也使学生对该技术的医疗应用风险有了一些认识。     

Heterogeneous preparation of cellulose–polyaniline conductive composites with cellulose activated by acids and its electrical properties

A series of conductive composites cellulose–polyaniline (PANI) were heterogeneously synthesized by chemical oxidative polymerization of aniline with native cellulose activated by various acids. The chemical structure and morphology of the composites were examined by FT-IR analysis and TEM. TGA was used to study their thermal properties. The composites prepared using the di-basic acids exhibited more favorable conductivity than the composites prepared using the monobasic acids. The content of PANI increased with increasing of activation time, and while the conductivity decreased because of the aggregation of PANI particles at the activation time range from 50 to 120 min. Both the PANI content and the electrical conductivity increased with an increase of the amount of aniline, and reached the maximum values at the 0.5 g aniline, respectively. The acids were able to successfully activate cellulose and lead to the improvement of the accessibility and reactivity of the O–H groups. The composites were highly stable compared to pure cellulose due to the safeguard from PANI slices. This work provided a facile method for the synthesis of cellulose–polyaniline conductive composites with excellent conductivity.     

Structure of the F‐spondin domain of mindin,an integrin ligand and pattern recognition molecule

Mindin (spondin‐2) is an extracellular matrix protein of unknown structure that is required for efficient T‐cell priming by dendritic cells. Additionally, mindin functions as a pattern recognition molecule for initiating innate immune responses. These dual functions are mediated by interactions with integrins and microbial pathogens, respectively. Mindin comprises an N‐terminal F‐spondin (FS) domain and C‐terminal thrombospondin type 1 repeat (TSR). We determined the structure of the FS domain at 1.8‐Å resolution. The structure revealed an eight‐stranded antiparallel β‐sandwich motif resembling that of membrane‐targeting C2 domains, including a bound calcium ion. We demonstrated that the FS domain mediates integrin binding and identified the binding site by mutagenesis. The mindin FS domain therefore represents a new integrin ligand. We further showed that mindin recognizes lipopolysaccharide (LPS) through its TSR domain, and obtained evidence that C‐mannosylation of the TSR influences LPS binding. Through these dual interactions, the FS and TSR domains of mindin promote activation of both adaptive and innate immune responses.     

Nonenzymatic glucose sensor based on ultrasonic-electrodeposition of bimetallic PtM (M = Ru, Pd and Au) nanoparticles on carbon nanotubes–ionic liquid composite film

We report here for the first time on the fabrication of highly dispersed PtM (M = Ru, Pd and Au) nanoparticles on composite film of multi-walled carbon nanotubes (MWNTs)–ionic liquid (IL, i.e., trihexyltetradecylphosphonium bis(trifluoromethylsulfonyl)imide) by using ultrasonic-electrodeposition method. The PtM nanoparticles are characterized by scanning electron microscopy, X-ray photoelectron spectroscopy and X-ray diffraction, and we find that they are well-dispersed and exhibit alloy properties. Electrochemical experiments show that the PtRu(1:1, i.e., ratio of c(H₂PtCl₆)/c(RuCl₃))–MWNT–IL nanocomposite modified glassy carbon electrode (PtRu(1:1)–MWNT–IL/GCE) has smaller electron transfer resistance and larger active surface area than PtRu(1:1)/GCE, PtRu(1:1)–MWNT/GCE, PtPd(1:1)–MWNT–IL/GCE and PtAu(1:1)–MWNT–IL/GCE. The PtRu(1:1)–MWNT–IL/GCE also presents stronger electrocatalytic activity toward the glucose oxidation than other electrodes. At −0.1 V, the electrode responds linearly to glucose up to 15 mM in neutral media, with a detection limit of 0.05 mM (S/N = 3) and detection sensitivity of 10.7 μA cm⁻² mM⁻¹. Meanwhile, the interference of ascorbic acid, uric acid, acetamidophenol and fructose is effectively avoided. The as-made sensor was applied to the determination of glucose in serum and urine samples. The results agreed closely with the results obtained by a hospital. This novel nonenzyme sensor thus has potential application in glucose detection.     

Estrogenic activities of extracts of Chinese licorice (Glycyrrhiza uralensis) root in MCF-7 breast cancer cells

Despite the wide use of Chinese licorice root (Glycyrrhiza uralensis) for the treatment of menopausal complaints, little is known on its potential estrogenic properties, and available information relative to its effects on cell proliferation is contradictory. In this study, the estrogenic properties of licorice root were evaluated in vitro by use of several assays. The effects of increasing concentrations of a DMSO extract of licorice root on the growth of MCF-7 breast cancer cells were biphasic. The extract showed an ER-dependent growth-promoting effect at low concentrations and an ER-independent anti-proliferative activity at high concentrations. In further experiments, licorice root was sequentially extracted to yield four fractions: hexane, EtOAc, methanol and H₂O. Only the EtOAc extract had effects on cell proliferation similar to the DMSO extract. The hexane extract had no effect on cell growth. In contrast, the methanol and water extracts showed an ER-independent, growth-promoting effect. Similar to its effects on cell proliferation, the EtOAc extract had a biphasic effect on S phase cell cycle distribution and the level of PCNA protein. This extract-induced transactivation of endogenous ERα in MCF-7 cells, supported by inducing down-regulation of ERα protein and mRNA levels, and up-regulation of ERα target genes pS2 and GREB1. These results suggest that the activity of licorice root and the balance between increased risk for cancer and prevention of estrogen-dependent breast cancer may depend on the amount of dietary intake.     

Sudden failure of biological nitrogen and carbon removal in the full-scale pre-denitrification process treating cokes wastewater

A full-scale pre-denitrification process treating cokes wastewater containing toxic compounds such as phenols, cyanides and thiocyanate has shown good performance in carbon and nitrogen removal. However, field operators have been having trouble with its instability without being able to identify the causes. To clarify the main cause of these sudden failures of the process, comprehensive studies were conducted on the pre-denitrification process using a lab-scale reactor system with real cokes wastewater. First, the shock loading effects of three major pollutants were investigated individually. As the loading amount of phenol increased to 600 mg/L, more COD, TOC and phenol itself were flowed into the aerobic reactor, but phenol itself did not inhibit nitrification and denitrification, owing to the effect of dilution and its rapid biodegradation. Higher loading of ammonia or thiocyanate slightly enhanced the removal efficiency of organic matter, but caused the final discharge concentration of total nitrogen to be above its legal limit of 60 mg-N/L. Meanwhile, continuous inflow of abnormal wastewater collected during unstable operation of the full-scale pre-denitrification process, caused a sudden failure of nitrogen removal in the lab-scale process, like the removal pattern of the full-scale one. This was discovered to be due to the lack of inorganic carbon in the aerobic reactor where autotrophic nitrification occurs.     

A TGF‐β‐induced gene, βig‐h3, is crucial for the apoptotic disappearance of the medial edge epithelium in palate fusion

TGF‐β3, TβR‐I, and TGF‐β‐activated Smad2 has been suggested to be a series of signaling molecules for secondary palate fusion. In this article, we show that a gene induced by TGF‐β, βig‐h3, is coincidentally expressed with TGF‐β3 in medial edge epithelial (MEE) cells undergoing apoptosis during normal palatal fusion. βig‐h3 was also highly expressed in the areas of post‐weaning mammary gland cells and developing phalangeal joints in which TGF‐β3 or BMP‐4‐induced apoptosis occurs, respectively. Blocking of βig‐h3 expression in E12.5 embryos with antisense oligodeoxynucleotides (ODN) resulted in cleft of the secondary palate in 84% of the treated mice that were born. Moreover, the antisense ODN treatment resulted in a failure of apoptosis in the MEE between palatal shelves in physical contact in organ culture. We conclude that βig‐h3 expression in the MEE is stimulated by TGF‐β3, causes cell death, and consequently results in complete fusion of the apposed palatal shelves. J. Cell. Biochem. 107: 818–825, 2009. © 2009 Wiley‐Liss, Inc.