Search

The preparation of biodiesel from Styrax Tonkinensis catalyzed by solid acid S2O82-/ZrO2-TiO2-Fe3O4 at an autoclave was studied in this paper. The magnetic catalysts were characterized by XRD, which explained the high catalytic effect. At the same time, the recovery rate and usage count of catalysts were also studied. And the results showed that a high yield of transesterification can be obtained in a closed autoclave at the condition of catalyst amount 5 %, reaction time 1.5 h, reaction temperature 373K and methanol and oil molar ratio 10:1. The results also showed that the catalysts were still with a higher catalytic efficiency when the catalysts were calcinated after the forth usage.

The occurrence of volatile arsenic in natural gas, could lead to the poisoning of catalyst in processing equipment, and pose a serious threat to human health. In order to detect the total volatile arsenic in natural gas, this paper analyzed the characteristic and original mechanism of the volatile arsenic first, then a novel method was carried out by using silver nitrate solution, saturated potassium persulfate solution and concentrated nitric acid solution as sorption solution, followed by volatile arsenic determination with ICP-MS .The result showed that 2% silver nitrate solution had a good adsorption effect to volatile arsenic, and the recoveries of arsenic ranged from 87%~103%, which basically met the demand for the rapid detection of volatile arsenic in natural gas.

Styrax confusus Hemsl., a promising energy plant, was used as raw material for biodiesel preparation in this paper. The transesterification was catalyzed by magnetic catalyst S2O82--ZrO2/Fe3O4, prepared by chemical co-precipitation method. TEM images indicat that the average particle diameter of magnetic core Fe3O4 and catalyst carrier ZrO2/Fe3O4 are 5-20 nm and 30-50 nm respectively. Because of its unique porous structure the BET surface area could up to 140.75 m2/g. The results show that a best catalytic activity is obtained when the solid catalyst impregnated in 2.5 mol·L-1 (NH4)2S2O8, calcined at 400 °C for 3 h, and a high methyl ester yield could be obtained under the optimal reaction conditions of catalyst amount 4.5 % (wt/wt oil), molar ratio of methanol/oil 6:1, reaction temperature 65 °C and time 2.0 h.

Progesterone is an important steroid hormone in the regulation of the bovine estrous cycle. The steroidogenic acute regulatory protein (StAR) is an indispensable component for transporting cholesterol to the inner mitochondrial membrane, which is one of the rate-limiting steps for progesterone synthesis. Low-density lipoprotein (LDL) supplies cholesterol precursors for progesterone formation, and the lysosomal degradation pathway of LDL is essential for progesterone biosynthesis in granulosa cells after ovulation. However, it is currently unknown how LDL and lysosomes coordinate the expression of the StAR gene and progesterone production in bovine granulosa cells. Here, we investigated the role of lysosomes in LDL-treated bovine granulosa cells. Our results reported that LDL induced expression of StAR messenger RNA and protein as well as expression of cholesterol side-chain cleavage cytochrome P-450 (CYP11A1) messenger RNA and progesterone production in cultured bovine granulosa cells. The number of lysosomes in the granulosa cells was also significantly increased by LDL; whereas the lysosomal inhibitor, chloroquine, strikingly abolished these LDL-induced effects. Our results indicate that LDL promotes StAR expression, synthesis of progesterone, and formation of lysosomes in bovine granulosa cells, and lysosomes participate in the process by releasing free cholesterol from hydrolyzed LDL.

Oocyte aging due to delayed fertilization is associated with declining quality and developmental potential. Intracellular calcium (Ca(2+)) concentration ([Ca(2+)]i) regulates oocyte growth, maturation, and fertilization and has also been implicated in aging. Using bovine oocytes, we tested the hypothesis that oocyte aging could be delayed by reducing [Ca(2+)]ivia blocking the influx of extracellular Ca(2+) or chelating ooplasmic free Ca(2+). After IVM, cumulus-oocyte complexes or denuded oocytes were cultured in medium supplemented with 1-octanol, phorbol 12-myristate 13-acetate, or 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetrakis-acetoxymethyl ester (BAPTA-AM) to manipulate [Ca(2+)]i. Addition of 1-mM 1-octanol increased blastocyst development rates in the cumulus-oocyte complexes aged for 6 hours by IVF and for 6, 12, and 24 hours by parthenoactivation, and this effect was independent of the presence of cumulus cells. The intracellular levels of ATP, Glutathione, and Glutathione disulfide were not affected by 1-octanol, but [Ca(2+)]i was significantly decreased. When oocytes were cultured in Ca(2+)-free medium for 12 hours, the blastocyst development rate was greater and the beneficial effects of 1-octanol on oocyte aging were abolished. However, when the medium was supplemented with phorbol 12-myristate 13-acetate, [Ca(2+)]i increased and the blastocyst development rate decreased. Moreover, BAPTA-AM reduced [Ca(2+)]i and increased blastocyst development rates after IVF or parthenoactivation. We conclude that the age-associated developmental potency decline was delayed by blocking the influx of extracellular Ca(2+) or reducing ooplasmic free Ca(2+). 1-Octanol, BAPTA-AM, or Ca(2+)-free medium could be used to lengthen the fertilization windows of aged bovine oocytes.

Lysosomotropic amines cause serious side effects such as cytoplasmic vacuolation and cell death. TRPML1 (also known as mucolipin1), a member of the transient receptor potential (TRP) protein family, may regulate fusion/fission of vesicles along the endocytic pathway and some aspects of lysosomal ion homeostasis. Nevertheless, it is still unknown whether TRPML1 is involved in death of mammalian cells induced by lysosomotropic agents. In this study, imidazole was used as a model to investigate the role of TRPML1 in the cytotoxicity of lysosomotropic agents. Overexpression of wild-type TRPML1 inhibited imidazole-induced vacuole formation and cell death in human endometrial adenocarcinoma (HEC-1B) cells. In contrast, siRNA-mediated TRPML1 knockdown increased the cell death induced by imidazole. Bafilomycin A1 raises the pH of acidic organelles and therefore suppresses accumulation of weak bases in them. Similarly, lysosomal pH was raised in TRPML1-overexpressing cells; therefore, we inferred that TRPML1 protected against imidazole toxicity by regulating the pH of acidic organelles. We concluded that TRPML1 had a novel role in protecting against lysosomotropic amine toxicity.

Ultrafiltration (UF) membranes of six selected poly(amidesulfonamide)s (PASAs) were prepared and studied. The pure water flux and the retention of albumin (bovine serum) were used to evaluate the quality of the UF performance of the fabricated membrane. Membranes with good mechanical strength were obtained by using the phase inversion method. A comparison of the UF performance of the PASA membranes fabricated from a casting solution containing 12% w/w PASAs and 4% w/w lithium bromide in dimethylacetamide was made. The best retention of albumin ( bovine serum) by membranes prepared under the conditions studied from the selected homopolymers of PASAs, and their corresponding pure water flux at 0.207 MPa, ranged from 84.6 to 100% and 120 to 396 L m -2 h -1 , respectively.

Accumulating evidence indicates that cellular and molecular abnormalities occur during oocyte aging, including fragmentation, increases in intracellular reactive oxygen species (ROS), and abnormal Ca(2+) oscillations. The objective of the present study was to characterize the relationships between intracellular ROS, Ca(2+) homeostasis of endoplasmic reticulum (ER), and fragmentation in aged porcine MII oocytes. Prolonged culture (36 h) of porcine oocytes resulted in elevated intracellular ROS level, impaired ER Ca(2+) homeostasis (i.e., Ca(2+) storage, Ca(2+) rising patterns after electroactivation, and the cluster distribution of ER), and increased fragmentation rates. However, when the porcine oocytes were treated with 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetrakis(acetoxymethyl ester), an intracellular Ca(2+) chelator, the fragmentation was significantly inhibited during in vitro aging. In order to pursue the underlying mechanisms, H2O2 and cycloheximide (CHX) were used to artificially increase or inhibit, respectively, the intracellular ROS levels in aged porcine oocytes during in vitro culture. The results demonstrated that incubation of porcine MII oocytes with H2O2 damaged the ER clusters and the Ca(2+) regulation of ER, leading to a high proportion of fragmented oocytes. In contrast, CHX, an intracellular inhibitor of ROS generation, prevented both increase of ROS level and damage of the ER Ca(2+) homeostasis in porcine oocytes during aging, resulting in low fragmentation rate. We conclude that the increased intracellular ROS damaged the ER clusters and ER Ca(2+) homeostasis, resulting in a disorder in ooplasmic free Ca(2+), which caused the fragmentations seen in porcine MII oocytes during aging.

Cyclic sulphonium cations (1)–(3) form 1 : 2 salts with TCNQ which are organic conductors at room temperature (σr.t. 1 × 10–3–2.0 S cm–1); the X-ray crystal structure of 1-methyl-1,4-dithianium TCNQ salt (MDT)1+(TCNQ)2–(1) has been determined.