Purification and the Secondary Structure of Fucoidanase from Fusarium sp. LD8

The fucoidanase from Fusarium sp. (LD8) was obtained by solid-state fermentation. The fermented solid medium was extracted by citric acid buffer, and the extracts were precipitated by acetone and purified by Sephadex G-100 successively. The results showed that the specific fucoidanase activity of purified enzyme was 22.7-fold than that of the crude enzyme. The recovery of the enzyme was 23.9%. The purified enzyme gave a single band on SDS-PAGE gel, and the molecular weight of fucoidanase was about 64 kDa. The isoelectric point of the enzyme was 4.5. The enzyme properties were also studied. The results showed that the optimum temperature and pH were 60°C and 6.0, respectively; the temperature of half inactivation was 50°C, and the most stable pH for the enzyme was 6.0. KM, and the Vmax of the enzyme was 8.9 mg·L−1 and 2.02 mg·min−1·mL−1 by using fucoidan from Fucus vesiculosus as substrate. The compositions of the secondary structure of fucoidanase were estimated by FTIR, the second derivative spectra, and the curve-fitting analysis of the amide I bands in their spectra. The results showed that β-sheet was the dominant component (58.6%) and α-helix was the least (12%); the content of β-turn and random coil were 15.39% and 14.5%, respectively

An intrinsic link between long-term UV/optical variations and X-ray loudness in quasars

Observations have shown that UV/optical variation amplitude of quasars depend on several physi- cal parameters including luminosity, Eddington ratio, and likely also black hole mass. Identifying new factors which correlate with the variation is essential to probe the underlying physical processes. Combining ~ten years long quasar light curves from SDSS stripe 82 and X-ray data from Stripe 82X, we build a sample of X-ray detected quasars to investigate the relation between UV/optical variation amplitude ($\sigma_{rms}$) and X-ray loudness. We find that quasars with more intense X-ray radiation (com- pared to bolometric luminosity) are more variable in UV/optical. Such correlation remains highly significant after excluding the effect of other parameters including luminosity, black hole mass, Ed- dington ratio, redshift, rest-frame wavelength (i.e., through partial correlation analyses). We further find the intrinsic link between X-ray loudness and UV/optical variation is gradually more prominent on longer timescales (up to 10 years in the observed frame), but tends to disappear at timescales < 100 days. This suggests a slow and long-term underlying physical process. The X-ray reprocessing paradigm, in which UV/optical variation is produced by a variable central X-ray emission illuminating the accretion disk, is thus disfavored. The discovery points to an interesting scheme that both the X-ray corona heating and UV/optical variation is quasars are closely associated with magnetic disc turbulence, and the innermost disc turbulence (where corona heating occurs) correlates with the slow turbulence at larger radii (where UV/optical emission is produced).Comment: 9 pages, 4 figures, 1 table, accepted by Ap

Selection and reversal of Plasmodium berghei resistance in the mouse model following repeated high doses of artemether

Artemether, a derivative of artemisinin, is effectively used for the treatment of malaria without any clinically relevant resistance to date. Artemether has also been developed as an antischistosomal agent, exhibiting highest activity against immature parasites. Here, we employ a rodent model and investigate whether the proposed artemether treatment schedule to prevent schistosome-attributable morbidity might select for Plasmodium berghei resistance. Mice infected with an ANKA strain of P. berghei were treated with artemether at either 47mg/kg or 300mg/kg. Once every 7-10days, parasitized erythrocytes were passed to the next group of mice, receiving the same doses of artemether, for 50passages. Resistance development was slow but increased considerably over the final ten passages. At the higher dose of artemether, the indices of resistance were4.8 and8.8 after 40and 50passages, respectively. Importantly, resistance was unstable, since sensitivity reverted to near-normal after five passages without drug pressure. A moderate index of P. berghei resistance and no apparent reversibility was found in comparative experiments employing pyronaridine. In conclusion, the pace of resistance development in P. berghei to repeated high doses of artemether is slow and reversibl

Recombinant immunotoxin anti-c-Met/PE38KDEL inhibits proliferation and promotes apoptosis of gastric cancer cells

<p>Abstract</p> <p>Background</p> <p>Our study aims to evaluate the anti-growth effects of recombinant immunotoxin (IT) anti-c-Met/PE38KDEL on gastric cancer cells, and its mechnisms.</p> <p>Methods</p> <p>Gastric cancer cells were treated with increasing doses of IT and c-Met protein was quantified by Western blotting. Cell proliferation was determined by Cell Counting Kit-8 assay (CCK). [³H]-leucine incorporation assay was used to evaluate IT inhibition of protein synthesis. Cell apoptosis was quantified by flow cytometry. Caspase activities were measured using colorimetric protease assays.</p> <p>Results</p> <p>Cell growth and protein synthesis of the gastric cancer cell lines were suppressed by IT in a dose- and time-dependent manner. IT also induced apoptosis in a dose-dependent manner. The apoptosis rates of gastric cancer cell lines MKN-45 and SGC7901 were 19.19% and 27.37%, respectively when treated with 50 ng/ml of IT. There were significant increase ofcaspase-3 activity at 24 hr of IT treatment (100 ng/ml) (P < 0.01) in these gastric cancer cell lines.</p> <p>Conclusions</p> <p>IT anti-c-Met/PE38KDEL has anti-growth effects on the gastric cancer cell lines <it>in vitro</it>, and it provides an experimental basis for c-Met-targeted therapy towards <it>in vivo </it>testing.</p

Practical and stereoselective electrocatalytic 1,2-diamination of alkenes.

The 1,2-diamine motif is widely present in natural products, pharmaceutical compounds, and catalysts used in asymmetric synthesis. The simultaneous introduction of two amino groups across an alkene feedstock is an appealing yet challenging approach for the synthesis of 1,2-diamines, primarily due to the inhibitory effect of the diamine products to transition metal catalysts and the difficulty in controlling reaction diastereoselectivity and regioselectivity. Herein we report a scalable electrocatalytic 1,2-diamination reaction that can be used to convert stable, easily available aryl alkenes and sulfamides to 1,2-diamines with excellent diastereoselectivity. Monosubstituted sulfamides react in a regioselective manner to afford 1,2-diamines bearing different substituents on the two amino groups. The combination of an organic redox catalyst and electricity not only obviates the use of any transition metal catalyst and oxidizing reagent, but also ensures broad reaction compatibility with a variety of electronically and sterically diverse substrates