151 research outputs found
Analysis of Cd44-Containing Lipid Rafts: Recruitment of Annexin II and Stabilization by the Actin Cytoskeleton
CD44, the major cell surface receptor for hyaluronic acid (HA), was shown to localize to detergent-resistant cholesterol-rich microdomains, called lipid rafts, in fibroblasts and blood cells. Here, we have investigated the molecular environment of CD44 within the plane of the basolateral membrane of polarized mammary epithelial cells. We show that CD44 partitions into lipid rafts that contain annexin II at their cytoplasmic face. Both CD44 and annexin II were released from these lipid rafts by sequestration of plasma membrane cholesterol. Partition of annexin II and CD44 to the same type of lipid rafts was demonstrated by cross-linking experiments in living cells. First, when CD44 was clustered at the cell surface by anti-CD44 antibodies, annexin II was recruited into the cytoplasmic leaflet of CD44 clusters. Second, the formation of intracellular, submembranous annexin IIâp11 aggregates caused by expression of a trans-dominant mutant of annexin II resulted in coclustering of CD44. Moreover, a frequent redirection of actin bundles to these clusters was observed. These basolateral CD44/annexin IIâlipid raft complexes were stabilized by addition of GTPÎłS or phalloidin in a semipermeabilized and cholesterol-depleted cell system. The low lateral mobility of CD44 in the plasma membrane, as assessed with fluorescent recovery after photobleaching (FRAP), was dependent on the presence of plasma membrane cholesterol and an intact actin cytoskeleton. Disruption of the actin cytoskeleton dramatically increased the fraction of CD44 which could be recovered from the light detergent-insoluble membrane fraction. Taken together, our data indicate that in mammary epithelial cells the vast majority of CD44 interacts with annexin II in lipid rafts in a cholesterol-dependent manner. These CD44-containing lipid microdomains interact with the underlying actin cytoskeleton
Schizosaccharomyces versatilis represents a distinct evolutionary lineage of fission yeast
The fission yeast species Schizosaccharomyces japonicus is currently divided into two varietiesâS. japonicus var. japonicus and S. japonicus var. versatilis. Here we examine the var. versatilis isolate CBS5679. The CBS5679 genome shows 88% identity to the reference genome of S. japonicus var. japonicus at the coding sequence level, with phylogenetic analyses suggesting that it has split from the S. japonicus lineage 25 million years ago. The CBS5679 genome contains a reciprocal translocation between chromosomes 1 and 2, together with several large inversions. The products of genes linked to the major translocation are associated with âmetabolismâ and âcellular assemblyâ ontology terms. We further show that CBS5679 does not generate viable progeny with the reference strain of S. japonicus. Although CBS5679 shares closer similarity to the âtypeâ strain of var. versatilis as compared to S. japonicus, it is not identical to the type strain, suggesting population structure within var. versatilis. We recommend that the taxonomic status of S. japonicus var. versatilis is raised, with it being treated as a separate species, Schizosaccharomyces versatilis
Telomere-to-telomere Schizosaccharomyces japonicus genome assembly reveals hitherto unknown genome features
Schizosaccharomyces japonicus belongs to the single-genus class Schizosaccharomycetes, otherwise known as âfission yeasts.â As part of a composite model system with its widely studied S. pombe sister species, S. japonicus has provided critical insights into the workings and the evolution of cell biological mechanisms. Furthermore, its divergent biology makes S. japonicus a valuable model organism in its own right. However, the currently available genome assembly contains gaps and has been unable to resolve centromeres and other repeat-rich chromosomal regions. Here we present a telomere-to-telomere long-read genome assembly of the S. japonicus genome. This includes the three megabase-length chromosomes, with centromeres hundreds of kilobases long, rich in 5S ribosomal RNA genes, transfer RNA genes, long terminal repeats, and short repeats. We identify a gene-sparse region on chromosome 2 that resembles a 331 kb centromeric duplication. We revise the genome size of S. japonicus to at least 16.6 Mb and possibly up to 18.12 Mb, at least 30% larger than previous estimates. Our whole genome assembly will support the growing S. japonicus research community and facilitate research in new directions, including centromere and DNA repeat evolution, and yeast comparative genomics
Curvature-induced expulsion of actomyosin bundles during cytokinetic ring contraction
Many eukaryotes assemble a ring-shaped actomyosin network that contracts to drive cytokinesis. Unlike actomyosin in sarcomeres, which cycles through contraction and relaxation, the cytokinetic ring disassembles during contraction through an unknown mechanism. Here we find in Schizosaccharomyces japonicus and Schizosaccharomyces pombe that, during actomyosin ring contraction, actin filaments associated with actomyosin rings are expelled as micron-scale bundles containing multiple actomyosin ring proteins. Using functional isolated actomyosin rings we show that expulsion of actin bundles does not require continuous presence of cytoplasm. Strikingly, mechanical compression of actomyosin rings results in expulsion of bundles predominantly at regions of high curvature. Our work unprecedentedly reveals that the increased curvature of the ring itself promotes its disassembly. It is likely that such a curvature-induced mechanism may operate in disassembly of other contractile networks
Correction: Carbon dioxide uptake from natural gas by binary ionic liquidâwater mixtures
Correction for âCarbon dioxide uptake from natural gas by binary ionic liquidâwater mixturesâ by Kris Anderson et al., Green Chem., 2015, DOI: 10.1039/c5gc00720h
Carbon dioxide uptake from natural gas by binary ionic liquid water mixtures
[EN] Carbon dioxide solubility in a set of carboxylate ionic liquids formulated with stoicheiometric amounts of water is found to be significantly higher than for other ionic liquids previously reported. This is due to synergistic chemical and physical absorption. The formulated ionic liquid/water mixtures show greatly enhanced carbon dioxide solubility relative to both anhydrous ionic liquids and aqueous ionic liquid solutions, and are competitive with commercial chemical absorbers, such as activated N-methyldiethanolamine or monoethanolamine.The authors would like to acknowledge PETRONAS for financial support of this research, and Cytec (especially Dr Al Robertson) for supplying some of the phosphonium ionic liquids used.Anderson, K.; Atkins, MP.; Estager, J.; Kuah, Y.; Ng, S.; Oliferenko, AA.; Plechkova, NV.... (2015). Carbon dioxide uptake from natural gas by binary ionic liquid water mixtures. Green Chemistry. 17(8):4340-4354. https://doi.org/10.1039/c5gc00720hS43404354178Cenovus, http://www.cenovus.com/operations/technology/co2-enhanced-oil-recovery.htmlV. Alvarado and E.Manrique, Enhanced Oil Recovery: Field Planning and Development Strategies, Gulf Professional Publishing, Amsterdam, 2010British Petroleum , In Salah Gas, http://www.insalahco2.com/index.php?option=com_content&view=frontpage&Itemid=1&lang=enN. Stern , The Economics of Climate Change: The Stern Review, Cambridge University Press, Cambridge, 2007Alvarado, V., & Manrique, E. (2010). Enhanced Oil Recovery: An Update Review. Energies, 3(9), 1529-1575. doi:10.3390/en3091529S. Rackley , Carbon Capture and Storage, Elsevier Science, Oxford, 2009H. Huppert , Carbon Capture and Storage in Europe EASAC Policy Report 20, German National Academy of Sciences, Leopoldina, 2013Organisation for the Prohibition of Chemical Weapons (OPCW) , The Chemical Weapons Convention, http://www.opcw.org/html/db/cwc/eng/cwc_frameset.htmlRubin, E. S., Mantripragada, H., Marks, A., Versteeg, P., & Kitchin, J. (2012). The outlook for improved carbon capture technology. Progress in Energy and Combustion Science, 38(5), 630-671. doi:10.1016/j.pecs.2012.03.003G. H. Koch , M. P. H.Brongers, N. G.Thompson, Y. P.Virmani and J. H.Payer, Corrosion Costs and Preventive Strategies in the United States FHWA-RD-01-156, CC Technologies Laboratories, Inc, NACE International, 2001Law Offices of Casper Meadows Schwartz & Cook, â$80 Million Recovery in Toxic Exposure Suitâ, http://www.cmslaw.com/Verdicts-Settlements/80-Million-Recovery-in-Toxic-Exposure-Suit.shtmlL. Grunwald , U.S. EPA Cites UNOCAL for Spill Violations, Press Release, United States Environmental Protection Agency, 1995Lee, K. B., Beaver, M. G., Caram, H. S., & Sircar, S. (2008). Reversible Chemisorbents for Carbon Dioxide and Their Potential Applications. Industrial & Engineering Chemistry Research, 47(21), 8048-8062. doi:10.1021/ie800795yDu, N., Park, H. B., Dal-Cin, M. M., & Guiver, M. D. (2012). Advances in high permeability polymeric membrane materials for CO2separations. Energy Environ. Sci., 5(6), 7306-7322. doi:10.1039/c1ee02668bM. Freemantle , An Introduction to Ionic Liquids, RSC Publications, Cambridge, UK, 2010Earle, M. J., Esperança, J. M. S. S., Gilea, M. A., Canongia Lopes, J. N., Rebelo, L. P. N., Magee, J. W., ⌠Widegren, J. A. (2006). The distillation and volatility of ionic liquids. Nature, 439(7078), 831-834. doi:10.1038/nature04451Forsyth, M., Howlett, P. C., Tan, S. K., MacFarlane, D. R., & Birbilis, N. (2006). An Ionic Liquid Surface Treatment for Corrosion Protection of Magnesium Alloy AZ31. Electrochemical and Solid-State Letters, 9(11), B52. doi:10.1149/1.2344826Fraser, K. J., & MacFarlane, D. R. (2009). Phosphonium-Based Ionic Liquids: An Overview. Australian Journal of Chemistry, 62(4), 309. doi:10.1071/ch08558K. R. Seddon , Ionic liquids: Designer solvents?, in The International George Papatheodorou Symposium: Proceedings, ed. S. Boghosian, V. Dracopoulos, C. G. Kontoyannis and G. A. Voyiatzis, Institute of Chemical Engineering and High Temperature Chemical Processes, Patras, 1999, pp. 131â135M. Deetlefs , M.Fanselow and K. R.Seddon, RSC Adv.W. Freyland , Coulombic Fluids: Bulk and Interfaces, Springer, Heidelberg, 2011Electrodeposition from Ionic Liquids, ed. F. Endres, D. MacFarlane and A. Abbott, Wiley-VCH, Weinheim, 2008Electrochemical Aspects of Ionic Liquids, ed. H. Ohno, Wiley-Interscience, Hoboken, New Jersey, 2005Ionic Liquids: From Knowledge to Application, ed. N. V. Plechkova, R. D. Rogers and K. R. Seddon, American Chemical Society, Washington D.C., 2009Ionic Liquids in Synthesis, ed. P. Wasserscheid and T. Welton, Wiley-VCH, Weinheim, 2nd edn, 2008Plechkova, N. V., & Seddon, K. R. (2008). Applications of ionic liquids in the chemical industry. Chem. Soc. Rev., 37(1), 123-150. doi:10.1039/b006677jIonic Liquids UnCOILed: Critical Expert Overviews, ed. N. V. Plechkova and K. R. Seddon, Wiley, Hoboken, New Jersey, 2013Ionic Liquids Further UnCOILed: Critical Expert Overviews, ed. N. V. Plechkova and K. R. Seddon, Wiley, Hoboken, New Jersey, 2014Ionic Liquids Completely UnCOILed: Critical Expert Overviews, ed. N. V. Plechkova and K. R. Seddon, Wiley, Hoboken, New Jersey, 2015Blanchard, L. A., Hancu, D., Beckman, E. J., & Brennecke, J. F. (1999). Green processing using ionic liquids and CO2. Nature, 399(6731), 28-29. doi:10.1038/19887C. VillagrĂĄn , C. E.Banks, M.Deetlefs, G.Driver, W. R.Pitner, R. G.Compton and C.Hardacre, Chloride Determination in Ionic Liquids, in Ionic Liquids IIIB: Fundamentals, Progress, Challenges, and Opportunities - Transformations and Processes, ed. R. D. Rogers and K. R. Seddon, ACS Symp. Ser., Vol. 902, American Chemical Society, Washington D.C., 2005, vol. 902, pp. 244â258J. L. Anthony , E. J.Maginn and J. F.Brennecke, Gas Solubilities in 1-n-Butyl-3-methylimidazolium Hexafluorophosphate, in Ionic Liquids: Industrial Applications to Green Chemistry, ed. R. D. Rogers and K. R. Seddon, ACS Symp. Ser, Vol. 818, American Chemical Society, Washington D.C., 2002, vol. 818, pp. 260â269J. H. Davis Jr. , Working Salts: Syntheses and Uses of Ionic Liquids Containing Functionalized Ions, in Ionic Liquids: Industrial Applications to Green Chemistry, ed. R. D. Rogers and K. R. Seddon, ACS Symp. Ser, Vol. 818, American Chemical Society, Washington D.C., 2002, vol. 818, pp. 247â259Bates, E. D., Mayton, R. D., Ntai, I., & Davis, J. H. (2002). CO2Capture by a Task-Specific Ionic Liquid. Journal of the American Chemical Society, 124(6), 926-927. doi:10.1021/ja017593dWang, C., Luo, X., Zhu, X., Cui, G., Jiang, D., Deng, D., ⌠Dai, S. (2013). The strategies for improving carbon dioxide chemisorption by functionalized ionic liquids. RSC Advances, 3(36), 15518. doi:10.1039/c3ra42366bRamdin, M., de Loos, T. W., & Vlugt, T. J. H. (2012). State-of-the-Art of CO2Capture with Ionic Liquids. Industrial & Engineering Chemistry Research, 51(24), 8149-8177. doi:10.1021/ie3003705Zhang, X., Zhang, X., Dong, H., Zhao, Z., Zhang, S., & Huang, Y. (2012). Carbon capture with ionic liquids: overview and progress. Energy & Environmental Science, 5(5), 6668. doi:10.1039/c2ee21152aYokozeki, A., & Shiflett, M. B. (2009). Separation of Carbon Dioxide and Sulfur Dioxide Gases Using Room-Temperature Ionic Liquid [hmim][Tf2N]. Energy & Fuels, 23(9), 4701-4708. doi:10.1021/ef900649cCabaço, M. I., Besnard, M., Danten, Y., & Coutinho, J. A. P. (2012). Carbon Dioxide in 1-Butyl-3-methylimidazolium Acetate. I. Unusual Solubility Investigated by Raman Spectroscopy and DFT Calculations. The Journal of Physical Chemistry A, 116(6), 1605-1620. doi:10.1021/jp211211nCarvalho, P. J., AĚlvarez, V. H., SchroĚder, B., Gil, A. M., Marrucho, I. M., Aznar, M., ⌠Coutinho, J. A. P. (2009). Specific Solvation Interactions of CO2on Acetate and Trifluoroacetate Imidazolium Based Ionic Liquids at High Pressures. The Journal of Physical Chemistry B, 113(19), 6803-6812. doi:10.1021/jp901275bGoodrich, B. F., de la Fuente, J. C., Gurkan, B. E., Zadigian, D. J., Price, E. A., Huang, Y., & Brennecke, J. F. (2011). Experimental Measurements of Amine-Functionalized Anion-Tethered Ionic Liquids with Carbon Dioxide. Industrial & Engineering Chemistry Research, 50(1), 111-118. doi:10.1021/ie101688aGoodrich, B. F., de la Fuente, J. C., Gurkan, B. E., Lopez, Z. K., Price, E. A., Huang, Y., & Brennecke, J. F. (2011). Effect of Water and Temperature on Absorption of CO2by Amine-Functionalized Anion-Tethered Ionic Liquids. The Journal of Physical Chemistry B, 115(29), 9140-9150. doi:10.1021/jp2015534Ferguson, J. L., Holbrey, J. D., Ng, S., Plechkova, N. V., Seddon, K. R., Tomaszowska, A. A., & Wassell, D. F. (2011). A greener, halide-free approach to ionic liquid synthesis. Pure and Applied Chemistry, 84(3), 723-744. doi:10.1351/pac-con-11-07-21Shiflett, M. B., Kasprzak, D. J., Junk, C. P., & Yokozeki, A. (2008). Phase behavior of {carbon dioxide+[bmim][Ac]} mixtures. The Journal of Chemical Thermodynamics, 40(1), 25-31. doi:10.1016/j.jct.2007.06.003Shiflett, M. B., & Yokozeki, A. (2009). Phase Behavior of Carbon Dioxide in Ionic Liquids: [emim][Acetate], [emim][Trifluoroacetate], and [emim][Acetate] + [emim][Trifluoroacetate] Mixtures. Journal of Chemical & Engineering Data, 54(1), 108-114. doi:10.1021/je800701jShiflett, M. B., Drew, D. W., Cantini, R. A., & Yokozeki, A. (2010). Carbon Dioxide Capture Using Ionic Liquid 1-Butyl-3-methylimidazolium Acetate. Energy & Fuels, 24(10), 5781-5789. doi:10.1021/ef100868aCabaço, M. I., Besnard, M., Danten, Y., & Coutinho, J. A. P. (2011). Solubility of CO2in 1-Butyl-3-methyl-imidazolium-trifluoro Acetate Ionic Liquid Studied by Raman Spectroscopy and DFT Investigations. The Journal of Physical Chemistry B, 115(13), 3538-3550. doi:10.1021/jp111453aGurau, G., RodrĂguez, H., Kelley, S. P., Janiczek, P., Kalb, R. S., & Rogers, R. D. (2011). Demonstration of Chemisorption of Carbon Dioxide in 1,3-Dialkylimidazolium Acetate Ionic Liquids. Angewandte Chemie International Edition, 50(50), 12024-12026. doi:10.1002/anie.201105198Besnard, M., Cabaço, M. I., Vaca ChĂĄvez, F., Pinaud, N., SebastiĂŁo, P. J., Coutinho, J. A. P., ⌠Danten, Y. (2012). CO2 in 1-Butyl-3-methylimidazolium Acetate. 2. NMR Investigation of Chemical Reactions. The Journal of Physical Chemistry A, 116(20), 4890-4901. doi:10.1021/jp211689zJaniczek, P., Kalb, R. S., Thonhauser, G., & Gamse, T. (2012). Carbon dioxide absorption in a technical-scale-plant utilizing an imidazolium based ionic liquid. Separation and Purification Technology, 97, 20-25. doi:10.1016/j.seppur.2012.03.003Ober, C. A., & Gupta, R. B. (2012). pH Control of Ionic Liquids with Carbon Dioxide and Water: 1-Ethyl-3-methylimidazolium Acetate. Industrial & Engineering Chemistry Research, 51(6), 2524-2530. doi:10.1021/ie201529dStevanovic, S., PodgorĹĄek, A., PĂĄdua, A. A. H., & Costa Gomes, M. F. (2012). Effect of Water on the Carbon Dioxide Absorption by 1-Alkyl-3-methylimidazolium Acetate Ionic Liquids. The Journal of Physical Chemistry B, 116(49), 14416-14425. doi:10.1021/jp3100377Stevanovic, S., Podgorsek, A., Moura, L., Santini, C. C., Padua, A. A. H., & Costa Gomes, M. F. (2013). Absorption of carbon dioxide by ionic liquids with carboxylate anions. International Journal of Greenhouse Gas Control, 17, 78-88. doi:10.1016/j.ijggc.2013.04.017Wang, G., Hou, W., Xiao, F., Geng, J., Wu, Y., & Zhang, Z. (2011). Low-Viscosity Triethylbutylammonium Acetate as a Task-Specific Ionic Liquid for Reversible CO2Absorption. Journal of Chemical & Engineering Data, 56(4), 1125-1133. doi:10.1021/je101014qWilhelm, E., Battino, R., & Wilcock, R. J. (1977). Low-pressure solubility of gases in liquid water. Chemical Reviews, 77(2), 219-262. doi:10.1021/cr60306a003Miyano, Y., & Fujihara, I. (2004). Henryâs constants of carbon dioxide in methanol at 250â500 K. Fluid Phase Equilibria, 221(1-2), 57-62. doi:10.1016/j.fluid.2004.04.017Fernandez, E. S., & Goetheer, E. L. V. (2011). DECAB: Process development of a phase change absorption process. Energy Procedia, 4, 868-875. doi:10.1016/j.egypro.2011.01.131Zhang, J., Zhang, S., Dong, K., Zhang, Y., Shen, Y., & Lv, X. (2006). Supported Absorption of CO2 by Tetrabutylphosphonium Amino Acid Ionic Liquids. Chemistry - A European Journal, 12(15), 4021-4026. doi:10.1002/chem.200501015Saravanamurugan, S., Kunov-Kruse, A. J., Fehrmann, R., & Riisager, A. (2014). Amine-Functionalized Amino Acid-based Ionic Liquids as Efficient and High-Capacity Absorbents for CO2. ChemSusChem, 7(3), 897-902. doi:10.1002/cssc.201300691J. Speight , Lange's Handbook of Chemistry, McGraw-Hill, New York, 16th edn, 2005, Section 1.18, pp. 1.310â1.314Cammarata, L., Kazarian, S. G., Salter, P. A., & Welton, T. (2001). Molecular states of water in room temperature ionic liquidsElectronic Supplementary Information available. See http://www.rsc.org/suppdata/cp/b1/b106900d/. Physical Chemistry Chemical Physics, 3(23), 5192-5200. doi:10.1039/b106900dNitta, I., Tomiie, Y., & Koo, C. H. (1952). The crystal structure of potassium bicarbonate, KHCO3. Acta Crystallographica, 5(2), 292-292. doi:10.1107/s0365110x52000848Sass, R. L., & Scheuerman, R. F. (1962). The crystal structure of sodium bicarbonate. Acta Crystallographica, 15(1), 77-81. doi:10.1107/s0365110x62000158AdamovĂĄ, G., Gardas, R. L., Nieuwenhuyzen, M., Puga, A. V., Rebelo, L. P. N., Robertson, A. J., & Seddon, K. R. (2012). Alkyltributylphosphonium chloride ionic liquids: synthesis, physicochemical properties and crystal structure. Dalton Transactions, 41(27), 8316. doi:10.1039/c1dt10466gGottlieb, H. E., Kotlyar, V., & Nudelman, A. (1997). NMR Chemical Shifts of Common Laboratory Solvents as Trace Impurities. The Journal of Organic Chemistry, 62(21), 7512-7515. doi:10.1021/jo971176vSheldrick, G. M. (2007). A short history ofSHELX. Acta Crystallographica Section A Foundations of Crystallography, 64(1), 112-122. doi:10.1107/s0108767307043930Allen, F. H., & Motherwell, W. D. S. (2002). Applications of the Cambridge Structural Database in organic chemistry and crystal chemistry. Acta Crystallographica Section B Structural Science, 58(3), 407-422. doi:10.1107/s0108768102004895Ramnial, T., Taylor, S. A., Bender, M. L., Gorodetsky, B., Lee, P. T. K., Dickie, D. A., ⌠Clyburne, J. A. C. (2008). Carbon-Centered Strong Bases in Phosphonium Ionic Liquids. The Journal of Organic Chemistry, 73(3), 801-812. doi:10.1021/jo701289dDietzel, P. D. C., & Jansen, M. (2002). Tetramethylphosphonium hydrogen carbonate. Acta Crystallographica Section E Structure Reports Online, 58(9), o1003-o1004. doi:10.1107/s1600536802013168Li, H., Hou, Y., & Yang, Y. (2011). Tetraethylammonium bicarbonate trihydrate. Acta Crystallographica Section E Structure Reports Online, 67(8), o1991-o1991. doi:10.1107/s1600536811026080McMullan, R., & Jeffrey, G. A. (1959). Hydrates of the Tetranâbutyl and Tetraiâamyl Quaternary Ammonium Salts. The Journal of Chemical Physics, 31(5), 1231-1234. doi:10.1063/1.1730574Smiglak, M., Hines, C. C., & Rogers, R. D. (2010). New hydrogen carbonate precursors for efficient and byproduct-free syntheses of ionic liquids based on 1,2,3-trimethylimidazolium and N,N-dimethylpyrrolidinium cores. Green Chemistry, 12(3), 491. doi:10.1039/b920003gMaton, C., Van Hecke, K., & Stevens, C. V. (2015). Peralkylated imidazolium carbonate ionic liquids: synthesis using dimethyl carbonate, reactivity and structure. New Journal of Chemistry, 39(1), 461-468. doi:10.1039/c4nj01301hBondi, A. (1964). van der Waals Volumes and Radii. The Journal of Physical Chemistry, 68(3), 441-451. doi:10.1021/j100785a001Van den Berg, J.-A., & Seddon, K. R. (2003). Critical Evaluation of CâH¡¡¡X Hydrogen Bonding in the Crystalline State. Crystal Growth & Design, 3(5), 643-661. doi:10.1021/cg034083hAdamovĂĄ, G., Canongia Lopes, J. N., Rebelo, L. P. N., Santos, L. M. N. B., Seddon, K. R., & Shimizu, K. (2014). The alternation effect in ionic liquid homologous series. Phys. Chem. Chem. Phys., 16(9), 4033-4038. doi:10.1039/c3cp54584aAdamovĂĄ, G., Gardas, R. L., Nieuwenhuyzen, M., Puga, A. V., Rebelo, L. P. N., Robertson, A. J., & Seddon, K. R. (2012). Alkyltributylphosphonium chloride ionic liquids: synthesis, physicochemical properties and crystal structure. Dalton Transactions, 41(27), 8316. doi:10.1039/c1dt10466gM. B. Shiflett and A.Yokozeki, Phase Behaviour of Gases in Ionic Liquids, in Ionic Liquids UnCOILed: Critical Expert Overviews, ed. N. V. Plechkova and K. R. Seddon, Wiley, Hoboken, New Jersey, 2013, pp. 349â398Ibrahim, A. Y., Ashour, F. H., Ghallab, A. O., & Ali, M. (2014). Effects of piperazine on carbon dioxide removal from natural gas using aqueous methyl diethanol amine. Journal of Natural Gas Science and Engineering, 21, 894-899. doi:10.1016/j.jngse.2014.10.011Anonymous , Piperazine â Why It's Used And How It Works, The Contractor (Optimized Gas Treating, Inc.), Houston, 2008, 2 [4], http://www.ogtrt.com/files/contactors/vol_2_issue_4.pd
Revised fission yeast gene and allele nomenclature guidelines for machine readability
Standardized nomenclature for genes, gene products, and isoforms is crucial to prevent ambiguity and enable clear communication of scientific data, facilitating efficient biocuration and data sharing. Standardized genotype nomenclature, which describes alleles present in a specific strain that differ from those in the wild-type reference strain, is equally essential to maximize research impact and ensure that results linking genotypes to phenotypes are Findable, Accessible, Interoperable, and Reusable (FAIR). In this publication, we extend the fission yeast clade gene nomenclature guidelines to support the curation efforts at PomBase (www.pombase.org), the Schizosaccharomyces pombe Model Organism Database. This update introduces nomenclature guidelines for noncoding RNA genes, following those set forth by the Human Genome Organisation Gene Nomenclature Committee. Additionally, we provide a significant update to the allele and genotype nomenclature guidelines originally published in 1987, to standardize the diverse range of genetic modifications enabled by the fission yeast genetic toolbox. These updated guidelines reflect a community consensus between numerous fission yeast researchers. Adoption of these rules will improve consistency in gene and genotype nomenclature, and facilitate machine-readability and automated entity recognition of fission yeast genes and alleles in publications or datasets. In conclusion, our updated guidelines provide a valuable resource for the fission yeast research community, promoting consistency, clarity, and FAIRness in genetic data sharing and interpretation
THE CHANGES OF FUNCTIONAL ACTIVITY OF A THYROID AND METABOLISM OF THYROID HORMONES IN TEENAGED GIRLS IN DIFFERENT ETHNIC GROUPS OF EASTERN SIBERIA AS AN IMPORTANT COMPONENT OF LONG-TERM ADAPTATION TO EXTREME CLIMATIC AND GEOGRAPHICAL CONDITIONS OF LIVING
Girls and teenaged girls of different ethnic groups living in Tofalaria during different age period were examined. The aim of this research was to establish the peculiarities of functioning of pituitary-thyroid system and metabolism of thyroid hormones in healthy girls and teenagers living under adverse climatic and geographical conditions depending on their ethnicity. It was set that in ethnic Tofs girls and in Europoids girls in age group of 7-11 there were differences in the content of the active fractions of thyroid hormones testifying different mechanisms of maintenance of thyroid homeostasis. These differences remain in age group of 12-14, when changes in pituitary section of the system are added to them. The functioning of pituitary-thyroid system-level of neuro-endocrine regulation in native girls of Tofalaria of 15-18 goes in more economical way. This is actually the result of genetically determined long-term adaptation of natives' organism to extreme climatic and geographical environmental factors
Biochemical and Molecular Mechanisms of Folate Transport in Rat Pancreas; Interference with Ethanol Ingestion
Folic acid is an essential nutrient that is required for one-carbon biosynthetic processes and for methylation of biomolecules. Deficiency of this micronutrient leads to disturbances in normal physiology of cell. Chronic alcoholism is well known to be associated with folate deficiency which is due, in part to folate malabsorption. The present study deals with the mechanistic insights of reduced folate absorption in pancreas during chronic alcoholism. Male Wistar rats were fed 1 g/kg body weight/day ethanol (20% solution) orally for 3 months and the mechanisms of alcohol associated reduced folate uptake was studied in pancreas. The folate transport system in the pancreatic plasma membrane (PPM) was found to be acidic pH dependent one. The transporters proton coupled folate transporter (PCFT) and reduced folate carrier (RFC) are involved in folate uptake across PPM. The folate transporters were found to be associated with lipid raft microdomain of the PPM. Ethanol ingestion decreased the folate transport by reducing the levels of folate transporter molecules in lipid rafts at the PPM. The decreased transport efficiency of the PPM was reflected as reduced folate levels in pancreas. The chronic ethanol ingestion led to decreased pancreatic folate uptake. The decreased levels of PCFT and RFC expression in rat PPM were due to decreased association of these proteins with lipid rafts (LR) at the PPM
- âŚ