Studies on Nitrogen Fixation and Photosynthesis in Azolla imbricata Roxb and Azolla fiticuloides Lam.

Azolla imbricata and Azolla filieuloides were studied in regard to the nitrogenase- catalyzed reactions of C2H2 reduction and H2 production, employing gas chromatography; and photosynthetic CO2 uptake as well as simultaneous determinations of C2H2 reduction, photosynthesis and respiration in a closed system. Photosynthetic CO2 uptake and respiratory C02 production were determined using an infrared gas analyzer. These studies have indicated the following 1. Nitrogenase-catalyzed C2H2 reduction is largely light dependent. About 10,000 lux were required for saturation in A imbricata. A concentration of 10% C2H2 in the gas phase is saturating for C2H2 reduction and 1% CO inhibits C2H2 reduction with concomitant H2 production. 2. A determination of C2H2 reduction activity as a function of leaf age established a develop mental gradient in both A. imbricata and A. fgliculaides. In both species activity is negligible in the apex, increases markedly in progressively older leaves, plateaus, and decreases as leaves senesce. The developmental gradient of activity is much steeper in A. imbricate than in A. filiculoieds due to differences in their gross morphology. 3. Nitrogenase-eatalyzed H2 production in A. imbricata was not detectable under Ar but was appreciable under Ar containing 15% C2H2 and 2% CO. H2 production was also determined under the latter gas phase as a function of leaf. These studies implicate the occurrence of an uptake hydrogenase. 4. The photosynthetic compensation points in air are approximately 30 ppm CO2 for A. imbricata and A. filiculoides. 5. Simultaneous measurements of photosynthesis, respiration and C2H2 reduction in A. imbricata demonstrated the immediate dependence of nitrogenase on photosynthetically captured radiation for energy but an indirect dependence on CO2 fixation.     

Neural differentiation of human embryonic stem cells as an in vitro tool for the study of the expression patterns of the neuronal cytoskeleton during neurogenesis

The neural differentiation of human embryonic stem cells (ESCs) is a potential tool for elucidating the key mechanisms involved in human neurogenesis. Nestin and β-III-tubulin, which are cytoskeleton proteins, are marker proteins of neural stem cells (NSCs) and neurons, respectively. However, the expression patterns of nestin and β-III-tubulin in neural derivatives from human ESCs remain unclear. In this study, we found that neural progenitor cells (NPCs) derived from H9 cells express high levels of nestin and musashi-1. In contrast, β-III-tubulin was weakly expressed in a few NPCs. Moreover, in these cells, nestin formed filament networks, whereas β-III-tubulin was distributed randomly as small particles. As the differentiation proceeded, the nestin filament networks and the β-III-tubulin particles were found in both the cell soma and the cellular processes. Moreover, the colocalization of nestin and β-III-tubulin was found mainly in the cell processes and neurite-like structures and not in the cell soma. These results may aid our understanding of the expression patterns of nestin and β-III-tubulin during the neural differentiation of H9 cells.     

甲壳动物的生殖量与环境关系：Ⅰ.枝角类

生殖量是生殖潜力(reproductivepotential)的一个主要标志,也是生态系统(含生产力)和种群生态学(含数量变动)的一个主要内容。它在很大程度上是由遗传因子(基因)决定的,表现在各类动物的生殖量有很     

红三叶人工草地营养元素的生物循环

 本文研究了我国北亚热带高海拔地区红三叶人工草地11种营养元素的生物循环特征。结果表明:1.营养元素的存留量、归还量和吸收量均可分为5个水平;(1)高量级：氮、钾、钙;(2)中量级：磷、镁;(3)低量级：铁;(4)少量级：锰、锌、铜、硼;(5)微量级：钼。2．红三叶群落地上部的净生产量、自然归还量和元素的存留量均显著高于地下部。3．红三叶人工草地的元素输出量以氮、钾、钙较大。此外,对草用和种用红三叶群落营养元素生物循环特征的差异进行了比较。为维持本区红三叶人工草地营养元素的平衡,目前必须施用磷肥,施用量不能小于250kg·hm-2过磷酸钙。     

Activation characteristics of transient receptor potential ankyrin 1 and its role in nociception

Transient receptor potential (TRP) ankyrin 1 (TRPA1) is a Ca(2+)-permeant, nonselective cationic channel. It is predominantly expressed in the C afferent sensory nerve fibers of trigeminal and dorsal root ganglion neurons and is highly coexpressed with the nociceptive ion channel transient receptor potential vanilloid 1 (TRPV1). Several physical and chemical stimuli have been shown to activate the channel. In this study, we have used electrophysiological techniques and behavioral models to characterize the properties of TRPA1. Whole cell TRPA1 currents induced by brief application of lower concentrations of N-methyl maleimide (NMM) or allyl isothiocyanate (AITC) can be reversed readily by washout, whereas continuous application of higher concentrations of NMM or AITC completely desensitized the currents. The deactivation and desensitization kinetics differed between NMM and AITC. TRPA1 current amplitude increased with repeated application of lower concentrations of AITC, whereas saturating concentrations of AITC induced tachyphylaxis, which was more pronounced in the presence of extracellular Ca(2+). The outward rectification exhibited by native TRPA1-mediated whole cell and single-channel currents was minimal as compared with other TRP channels. TRPA1 currents were negatively modulated by protons and polyamines, both of which activate the heat-sensitive channel, TRPV1. Interestingly, neither protein kinase C nor protein kinase A activation sensitized AITC-induced currents, but each profoundly sensitized capsaicin-induced currents. Current-clamp experiments revealed that AITC produced a slow and sustained depolarization as compared with capsaicin. TRPA1 is also expressed at the central terminals of nociceptors at the caudal spinal trigeminal nucleus. Activation of TRPA1 in this area increases the frequency and amplitude of miniature excitatory or inhibitory postsynaptic currents. In behavioral studies, intraplantar and intrathecal administration of AITC induced more pronounced and prolonged changes in nociceptive behavior than those induced by capsaicin. In conclusion, the characteristics of TRPA1 we have delineated suggest that it might play a unique role in nociception.     

Insufficient peroxiredoxin-2 expression in uterine NK cells obtained from a murine model of abortion

The CBA/J × DBA/2 mouse mating combination is prone to spontaneous embryo loss, in contrast to the MHC-identical CBA/J × BALB/c mating combination, which yields successful pregnancies. The underlying mechanisms for these observations are unclear. In this study, multi-vision immunohistochemical staining (IHC), flow cytometry and Western blot analysis were used to detect peroxiredoxin-2 (PRX-2) expression in the uterine natural killer (uNK) cells from CBA/J × DBA/2 and CBA/J × BALB/c mice. In IHC analysis, co-localization of PRX-2 and lectin from Dolichos biflorus agglutinin (DBA-lectin) was confirmed and the frequency of PRX-2(+) DBA-lectin(+) cells was significantly lower in CBA/J × DBA/2 than CBA/J × BALB/c. In flow cytometry and Western blotting, PRX-2 was found expressed at a significantly lower level in CBA/J × DBA/2 mice. PRX-2 inhibition with a neutralizing antibody significantly decreased PRX-2 expression, increased the cytotoxicity of uNK cells, and increased the percentage of embryo loss in CBA/J × DBA/2J mice. Our data suggest that PRX-2 may be involved in the modulation of maternal-fetal tolerance and that insufficient expression of this protein may correlate with increased embryo loss in CBA/J × DBA/2J mice.     

Secretory expression of a heterologous nattokinase in <Emphasis Type="Italic">Lactococcus lactis</Emphasis>

Nattokinase has been reported as an oral health product for the prevention of atherosclerosis. We developed a novel strategy to express a nattokinase from Bacillus subtilis in a live delivery vehicle, Lactococcus lactis. Promoter P _nisZ and signal peptide SP_Usp were used for inducible and secretory expression of nattokinase in L. lactis. Western blotting analysis demonstrated that nattokinase was successfully expressed, and about 94% of the enzyme was secreted to the culture. The recombinant nattokinase showed potent fibrinolytic activity, equivalent to 41.7 urokinase units per milliliter culture. Expression and delivery of such a fibrinolytic enzyme in the food-grade vehicle L. lactis would facilitate the widespread application of nattokinase in the control and prevention of thrombosis diseases.