40 research outputs found
Soil Respiration in Relation to Photosynthesis of Quercus mongolica Trees at Elevated CO2
Knowledge of soil respiration and photosynthesis under elevated CO2 is crucial for exactly understanding and predicting the carbon balance in forest ecosystems in a rapid CO2-enriched world. Quercus mongolica Fischer ex Ledebour seedlings were planted in open-top chambers exposed to elevated CO2 (EC = 500 µmol mol−1) and ambient CO2 (AC = 370 µmol mol−1) from 2005 to 2008. Daily, seasonal and inter-annual variations in soil respiration and photosynthetic assimilation were measured during 2007 and 2008 growing seasons. EC significantly stimulated the daytime soil respiration by 24.5% (322.4 at EC vs. 259.0 mg CO2 m−2 hr−1 at AC) in 2007 and 21.0% (281.2 at EC vs. 232.6 mg CO2 m−2 hr−1 at AC) in 2008, and increased the daytime CO2 assimilation by 28.8% (624.1 at EC vs. 484.6 mg CO2 m−2 hr−1 at AC) across the two growing seasons. The temporal variation in soil respiration was positively correlated with the aboveground photosynthesis, soil temperature, and soil water content at both EC and AC. EC did not affect the temperature sensitivity of soil respiration. The increased daytime soil respiration at EC resulted mainly from the increased aboveground photosynthesis. The present study indicates that increases in CO2 fixation of plants in a CO2-rich world will rapidly return to the atmosphere by increased soil respiration
AAV-mediated human PEDF inhibits tumor growth and metastasis in murine colorectal peritoneal carcinomatosis model
<p>Abstract</p> <p>Background</p> <p>Angiogenesis plays an important role in tumor growth and metastasis, therefore antiangiogenic therapy was widely investigated as a promising approach for cancer therapy. Recently, pigment epithelium-derived factor (PEDF) has been shown to be the most potent inhibitor of angiogenesis. Adeno-associated virus (AAV) vectors have been intensively studied due to their wide tropisms, nonpathogenicity, and long-term transgene expression <it>in vivo</it>. The objective of this work was to evaluate the ability of AAV-mediated human PEDF (hPEDF) as a potent tumor suppressor and a potential candidate for cancer gene therapy.</p> <p>Methods</p> <p>Recombinant AAV<sub>2 </sub>encoding hPEDF (rAAV<sub>2</sub>-hPEDF) was constructed and produced, and then was assigned for <it>in vitro </it>and <it>in vivo </it>experiments. Conditioned medium from cells infected with rAAV<sub>2</sub>-hPEDF was used for cell proliferation and tube formation tests of human umbilical vein endothelial cells (HUVECs). Subsequently, colorectal peritoneal carcinomatosis (CRPC) mouse model was established and treated with rAAV<sub>2</sub>-hPEDF. Therapeutic efficacy of rAAV<sub>2</sub>-hPEDF were investigated, including tumor growth and metastasis, survival time, microvessel density (MVD) and apoptosis index of tumor tissues, and hPEDF levels in serum and ascites.</p> <p>Results</p> <p>rAAV<sub>2</sub>-hPEDF was successfully constructed, and transmission electron microscope (TEM) showed that rAAV<sub>2</sub>-hPEDF particles were non-enveloped icosahedral shape with a diameter of approximately 20 nm. rAAV<sub>2</sub>-hPEDF-infected cells expressed hPEDF protein, and the conditioned medium from infected cells inhibited proliferation and tube-formation of HUVECs <it>in vitro</it>. Furthermore, in CRPC mouse model, rAAV<sub>2</sub>-hPEDF significantly suppressed tumor growth and metastasis, and prolonged survival time of treated mice. Immunofluorescence studies indicated that rAAV<sub>2</sub>-hPEDF could inhibit angiogenesis and induce apoptosis in tumor tissues. Besides, hPEDF levels in serum and ascites of rAAV<sub>2</sub>-hPEDF-treated mice were significant higher than those in rAAV<sub>2</sub>-null or normal saline (NS) groups.</p> <p>Conclusions</p> <p>Thus, our results suggest that rAAV<sub>2</sub>-hPEDF may be a potential candidate as an antiangiogenic therapy agent.</p
The Application of PRF Variation to Squint Spotlight SAR
This paper focuses on a novel squint spotlight SAR mode, where the PRI variation is employed to increase the range swath width, especially for high-resolution imaging. The spotlight SAR is developed to increase the azimuth resolution via steering the antenna beam to always illuminate the same area on the ground during the whole data acquisition interval. However, requirement of high resolution and large squint angle leads to large Range Cell Migration (RCM). Therefore, to ensure the scattered echoes along the azimuth to be completely received within the fixed reception window, the range swath has to be much narrower than the reception window. In order to increase the range swath, we can change the PRI along the azimuth to shift the reception window according to the variation of instantaneous slant range. This paper first derives the PRI variation scheme. Afterward, a modified time-domain Back-Projection Algorithm (BPA) is presented to implement the focusing. Finally, simulation results are given to validate the presented SAR mode and corresponding imaging processor
Efficient Degradation of Malathion in the Presence of Detergents Using an Engineered Organophosphorus Hydrolase Highly Expressed by <i>Pichia pastoris</i> without Methanol Induction
The biodegradation of pesticides
by organophosphorus hydrolases
(OPHs) requires an efficient enzyme production technology in industry.
Herein, a <i>Pichia pastoris</i> strain was constructed
for the extracellular expression of <i>Po</i>OPH<sub>M9</sub>, an engineered malathion-degrading enzyme. After optimization, the
maximum titer and yield of fermentation reached 50.8 kU/L and 4.1
g<sub>protein</sub>/L after 3 days, with the highest space-time yield
(STY) reported so far, 640 U L<sup>–1</sup> h<sup>–1</sup>. <i>Po</i>OPH<sub>M9</sub> displayed its high activity
and stability in the presence of 0.1% (w/w) plant-derived detergent.
Only 0.04 mg/mL enzyme could completely remove 0.15 mM malathion in
aqueous solution within 20 min. Furthermore, 12 μmol malathion
on apples and cucumbers surfaces was completely removed by 0.05 mg/mL <i>Po</i>OPH<sub>M9</sub> in tap water after 35 min washing. The
efficient production of the highly active <i>Po</i>OPH<sub>M9</sub> has cleared a major barrier to biodegradation of pesticide
residues in food industry
Weakening Ligand–Liquid Affinity to Suppress the Desorption of Surface-Passivated Ligands from Perovskite Nanocrystals
The interfacial migration of surface-bound
ligands highly affects
the colloidal stability and optical quality of semiconductor nanocrystals,
of which the underlying mechanism is not fully understood. Herein,
colloidal CsPbBr3 perovskite nanocrystals (PNCs) with fragile
dynamic equilibrium of ligands are taken as the examples to reveal
the important role of balancing ligand-solid/solvent affinity in suppressing
the desorption of ligands. As a micellar surfactant, glycyrrhizic
acid (GA) with bulky hydrophobic and hydrophilic groups exhibits a
relatively smaller diffusion coefficient (∼440 μm2/s in methanol) and weaker ligand–liquid affinity than
that of conventional alkyl amine and carboxy ligands. Consequently,
hydrophilic GA-passivated PNCs (PNCs-GA) show excellent colloidal
stability in various polar solvents with dielectric constant ranging
from 2.2 to 32.6 and efficient photoluminescence with a quantum yield
of 85.3%. Due to the suppressed desorption of GA, the morphological
and optical properties of PNCs-GA are well maintained after five rounds
purification and two months long-term storage. At last, hydrophilic
PNCs-GA are successfully patterned through inkjet- and screen-printing
technology. These findings offer deep insights into the interfacial
chemistry of colloidal NCs and provide a universal strategy for preparing
high-quality hydrophilic PNCs
Establishment and evaluation of the primary cultured tibial osteoblast model of broiler chicks
Osteoblasts are considered as a major factor contributing to bone development and mineralization, however, few studies have been done to establish and evaluate the primary cultured tibial osteoblast model of broiler chicks. Therefore, in the present study, two experiments were conducted to establish and evaluate the primary cultured tibial osteoblast model of broiler chicks. In experiment 1, osteoblasts were isolated from the tibia of one-day-old Arbor Acre male broiler chicks using the explant method and identified through the cell morphology, alkaline phosphatase (ALP) and alizarin red staining. Experiment 2 was carried out to evaluate the vitality and mineralization of primary cultured tibial osteoblasts of broilers on days 4, 8, 12, 16, 20, 24, 28 and 32 after incubation, respectively. The results from experiment 1 demonstrated that primary cultured tibial osteoblasts of broilers showed a spindle-shaped, triangular or polygonal morphology. More than 95% of the cells were stained blue-black after ALP staining, and mineralized nodules were formed after 4 days of continuous incubation. In experiment 2, lactate dehydrogenase (LDH) activity stayed at a relatively stabilized level although incubation time affected (P=0.0012) it during the whole culture period. Additionally, incubation time affected (P≤0.0001) the number and proportion of the area of mineralized nodules. They increased linearly and quadratically (P<0.04) with the increase of incubation time, and remained at a stabilized level from 24 to 32 days of incubation. The estimates of the optimal incubation time were 17 and 26 days based on the best fitted broken-line or quadratic models (P<0.0001) of the number and proportion of the area of mineralized nodules, respectively. These results indicate that the primary cultured tibial osteoblast model of broilers has been established successfully by the explant method, and it showed typical osteoblast morphology and characteristics of ALP activity and mineralization, and could maintain a relatively stabilized vitality from 4 to 32 days of incubation; and the optimal incubation time of primary tibial osteoblasts was 17 to 26 days. Therefore, it could be used to further study the underlying mechanisms of bone development and mineralization of broiler chicks
Kinetically and thermodynamically controlled one-pot growth of gold nanoshells with NIR-II absorption for multimodal imaging-guided photothermal therapy
Abstract Since the successful clinical trial of AuroShell for photothermal therapy, there is currently intense interest in developing gold-based core-shell structures with near-infrared (NIR) absorption ranging from NIR-I (650–900 nm) to NIR-II (900–1700 nm). Here, we propose a seed-mediated successive growth approach to produce gold nanoshells on the surface of the nanoscale metal–organic framework (NMOF) of UiO-66-NH2 (UiO = the University of Oslo) in one pot. The key to this strategy is to modulate the proportion of the formaldehyde (reductant) and its regulator / oxidative product of formic acid to harness the particle nucleation and growth rate within the same system. The gold nanoshells propagate through a well-oriented and controllable diffusion growth pattern (points → facets → octahedron), which has not been identified. Most strikingly, the gold nanoshells prepared hereby exhibit an exceedingly broad and strong absorption in NIR-II with a peak beyond 1300 nm and outstanding photothermal conversion efficiency of 74.0%. Owing to such superior performance, these gold nanoshells show promising outcomes in photoacoustic (PA), computed tomography (CT), and photothermal imaging-guided photothermal therapy (PTT) for breast cancer, as demonstrated both in vitro and in vivo