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111.
112.
Yaghoob Hamedi Khojasteh Sharifi-Sarasiabi Farzaneh Dehghan Reza Safari Sheren To Irene Handayuni Hidayat Trimarsanto Ric N. Price Sarah Auburn 《PloS one》2016,11(11)
BackgroundMalaria remains endemic at low levels in the south-eastern provinces of Iran bordering Afghanistan and Pakistan, with the majority of cases attributable to P. vivax. The national guidelines recommend chloroquine (CQ) as blood-stage treatment for uncomplicated P. vivax, but the large influx of imported cases enhances the risk of introducing CQ resistance (CQR).ConclusionsThe contrasting low versus high diversity in the two sub-populations (K1 and K2) infers that a combination of local transmission and cross-border malaria from higher transmission regions shape the genetic make-up of the P. vivax population in south-eastern Iran. There was no molecular evidence of CQR amongst the local or imported cases, but ongoing clinical surveillance is warranted. 相似文献
113.
Temperature-activity relationships of cation activation and ouabain inhibition of (Na+ + K+)-ATPase.
The nonlinear temperature-activity relationship of membrane preparations of (Na+ + K+)-ATPase gives rise to discontinuities in Arrhenius plots of this enzyme. The different apparent energies of activation of (Na+ + K+) — ATPase which are observed above and below the critical temperature of the system have been considered to result from different conformational forms of the enzyme protein. Because both activation of (Na+ + K+)-ATPase by cations, and its specific inhibition by cardiac glycosides may be influenced by the conformational form of the enzyme protein, we have reexamined the effect of temperature upon the activation energy of the system under the different experimental conditions of cation activation and ouabain inhibition.Our results indicate that the activation of (Na+ + K+)-ATPase by cations, is less influenced by change in temperature than is inhibition of the enzyme by ouabain. In addition, mild lipolysis by phospholipase-A had a marked effect upon the ouabain-dependent response of the enzyme to temperature, but not upon the cation-dependent response. The effect of phospholipase-A can be overcome by reincubation of the treated preparation with phosphatidyl serine.We conclude that the ouabain-dependent temperature effects of (Na+ + K+)-ATPase are more dependent upon the integrity and nature of the membrane lipids than are the cation-dependent responses. It is possible that phosphatidyl serine plays a unique role in this regard. 相似文献
114.
Activation energy and phospholipid requirements of membrane-bound adenosine triphosphatases 总被引:1,自引:0,他引:1
In order to evaluate the role of lipids in the function of membrane ATPase reactions, the apparent activation energies of membrane-bound (Na+ + K+)-ATPase and membrane-bound Mg2+-ATPase have been measured under conditions frequently supposed to alter the membrane lipids in vitro.In the case of (Na+ + K+)-ATPase, the untreated enzyme was shown to have two different activation energies as shown by an Arrhenius plot comprising two straight lines which intersect at the “critical temperature.” Treatment of the preparation with detergents or with phospholipase C causes some alteration in the spécifie activity of the enzyme but did not significantly alter the activation energies or the critical temperature. After treatment with phospholipase A, however, the Arrhenius plot appeared linear over the entire temperature range studied. Subsequent treatment of phospholipase A-treated preparations with phosphatidylserine restored the control response.Conversely, untreated preparations of Mg2+-ATPase give an Arrhenius plot which is neither linear nor composed of two intersecting straight lines. This plot, which we regard as curvilinear, does not permit a unique value of the activation energy to be determined. The shape of this plot is unaltered by detergent or by treatment with phospholipase C. In contrast to (Na+ + K+)-ATPase, it is also unaffected by treat-with phospholipase A or phospholipase A followed by phosphatidylserine.We conclude that although (Na+ + K+)-ATPase and Mg2+-ATPase are frequently closely associated in many membranes, their functions involve the presence of different membrane lipids. 相似文献
115.
Monica To
a Csaba Paizs Cornelia Majdik Paula Moldovan Lajos Novk Pl Kolonits va Szab Lszl Poppe Florin-Dan Irimie 《Journal of Molecular Catalysis .B, Enzymatic》2002,17(6):241-248
A series of 10-alkyl-10H-phenothiazine-3-carbaldehydes (2a–h) were obtained by Vilsmeier–Haack formylation from the corresponding 10-alkyl-10H-phenothiazines (1a–h) and reduced to (10-alkyl-10H-phenothiazine-3-yl)methanols (3a–h) by two alternative methods. The baker’s yeast catalyzed reaction proved to be superior over the NaBH4 reduction and yielded the desired 3-hydroxymethylphenothiazines (3a–h) almost quantitatively. 相似文献
116.
117.
To TT Witten PE Renn J Bhattacharya D Huysseune A Winkler C 《Development (Cambridge, England)》2012,139(1):141-150
Osteoclasts are macrophage-related bone resorbing cells of hematopoietic origin. Factors that regulate osteoclastogenesis are of great interest for investigating the pathology and treatment of bone diseases such as osteoporosis. In mammals, receptor activator of NF-κB ligand (Rankl) is a regulator of osteoclast formation and activation: its misexpression causes osteoclast stimulation and osteoporotic bone loss. Here, we report an osteoporotic phenotype that is induced by overexpression of Rankl in the medaka model. We generated transgenic medaka lines that express GFP under control of the cathepsin K promoter in osteoclasts starting at 12 days post-fertilization (dpf), or Rankl together with CFP under control of a bi-directional heat-shock promoter. Using long-term confocal time-lapse imaging of double and triple transgenic larvae, we monitored in vivo formation and activation of osteoclasts, as well as their interaction with osteoblasts. Upon Rankl induction, GFP-positive osteoclasts are first observed in the intervertebral regions and then quickly migrate to the surface of mineralized neural and haemal arches, as well as to the centra of the vertebral bodies. These osteoclasts are TRAP (tartrate-resistant acid phosphatase) and cathepsin K positive, mononuclear and highly mobile with dynamically extending protrusions. They are exclusively found in tight contact with mineralized matrix. Rankl-induced osteoclast formation resulted in severe degradation of the mineralized matrix in vertebral bodies and arches. In conclusion, our in vivo imaging approach confirms a conserved role of Rankl in osteoclastogenesis in teleost fish and provides new insight into the cellular interactions during bone resorption in an animal model that is useful for genetic and chemical screening. 相似文献
118.
119.
Nguyen To Uyen Suk-Youl Park Ji-Woo Choi Hyun-Ju Lee Kosuke Nishi Jeong-Sun Kim 《Nucleic acids research》2009,37(20):6960-6969
Among four types of bacterial restriction enzymes that cleave a foreign DNA depending on its methylation status, type I enzymes composed of three subunits are interesting because of their unique DNA cleavage and translocation mechanisms performed by the restriction subunit (HsdR). The elucidated N-terminal fragment structure of a putative HsdR subunit from Vibrio vulnificus YJ016 reveals three globular domains. The nucleolytic core within an N-terminal nuclease domain (NTD) is composed of one basic and three acidic residues, which include a metal-binding site. An ATP hydrolase (ATPase) site at the interface of two RecA-like domains (RDs) is located close to the probable DNA-binding site for translocation, which is far from the NTD nucleolytic core. Comparison of relative domain arrangements with other functionally related ATP and/or DNA complex structures suggests a possible translocation and restriction mechanism of the HsdR subunit. Furthermore, careful analysis of its sequence and structure implies that a linker helix connecting two RDs and an extended region within the nuclease domain may play a central role in switching the DNA translocation into the restriction activity. 相似文献
120.
Modified internucleotide linkage featuring the C3′‐O‐P‐CH2‐O‐C4″ phosphonate grouping as an isosteric alternative to the phosphodiester C3′‐O‐P‐O‐CH2‐C4″ bond was studied in order to learn more on its stereochemical arrangement, which we showed earlier to be of prime importance for the properties of the respective oligonucleotide analogues. Two approaches were pursued: First, the attempt to prepare the model dinucleoside phosphonate with 13C‐labeled CH2 group present in the modified internucleotide linkage that would allow for a more detailed evaluation of the linkage conformation by NMR spectroscopy. Second, the use of ab initio calculations along with molecular dynamics (MD) simulations in order to observe the most populated conformations and specify main structural elements governing the conformational preferences. To deal with the former aim, a novel synthesis of key labeled reagent (CH3O)2P(O)13CH2OH for dimer preparation had to be elaborated using aqueous 13C‐formaldehyde. The results from both approaches were compared and found consistent. © 2009 Wiley Periodicals, Inc. Biopolymers 91: 514–529, 2009. This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at biopolymers@wiley.com 相似文献