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51.
C.-T. Lai J. R. Ehleringer A. J. Schauer P. P. Tans† D. Y. Hollinger‡ K. T. Paw U§ J. W. Munger¶ S. C. Wofsy¶ 《Global Change Biology》2005,11(4):633-643
The δ13C values of atmospheric carbon dioxide (CO2) can be used to partition global patterns of CO2 source/sink relationships among terrestrial and oceanic ecosystems using the inversion technique. This approach is very sensitive to estimates of photosynthetic 13C discrimination by terrestrial vegetation (ΔA), and depends on δ13C values of respired CO2 fluxes (δ13CR). Here we show that by combining two independent data streams – the stable isotope ratios of atmospheric CO2 and eddy‐covariance CO2 flux measurements – canopy scale estimates of ΔA can be successfully derived in terrestrial ecosystems. We also present the first weekly dataset of seasonal variations in δ13CR from dominant forest ecosystems in the United States between 2001 and 2003. Our observations indicate considerable summer‐time variation in the weekly value of δ13CR within coniferous forests (4.0‰ and 5.4‰ at Wind River Canopy Crane Research Facility and Howland Forest, respectively, between May and September). The monthly mean values of δ13CR showed a smaller range (2–3‰), which appeared to significantly correlate with soil water availability. Values of δ13CR were less variable during the growing season at the deciduous forest (Harvard Forest). We suggest that the negative correlation between δ13CR and soil moisture content observed in the two coniferous forests should represent a general ecosystem response to the changes in the distribution of water resources because of climate change. Shifts in δ13CR and ΔA could be of sufficient magnitude globally to impact partitioning calculations of CO2 sinks between oceanic and terrestrial compartments. 相似文献
52.
Pearce LR Huang X Boudeau J Pawłowski R Wullschleger S Deak M Ibrahim AF Gourlay R Magnuson MA Alessi DR 《The Biochemical journal》2007,405(3):513-522
The mTOR (mammalian target of rapamycin) protein kinase is an important regulator of cell growth. Two complexes of mTOR have been identified: complex 1, consisting of mTOR-Raptor (regulatory associated protein of mTOR)-mLST8 (termed mTORC1), and complex 2, comprising mTOR-Rictor (rapamycininsensitive companion of mTOR)-mLST8-Sin1 (termed mTORC2). mTORC1 phosphorylates the p70 ribosomal S6K (S6 kinase) at its hydrophobic motif (Thr389), whereas mTORC2 phosphorylates PKB (protein kinase B) at its hydrophobic motif (Ser473). In the present study, we report that widely expressed isoforms of unstudied proteins termed Protor-1 (protein observed with Rictor-1) and Protor-2 interact with Rictor and are components of mTORC2. We demonstrate that immunoprecipitation of Protor-1 or Protor-2 results in the co-immunoprecipitation of other mTORC2 subunits, but not Raptor, a specific component of mTORC1. We show that detergents such as Triton X-100 or n-octylglucoside dissociate mTOR and mLST8 from a complex of Protor-1, Sin1 and Rictor. We also provide evidence that Rictor regulates the expression of Protor-1, and that Protor-1 is not required for the assembly of other mTORC2 subunits into a complex. Protor-1 is a novel Rictor-binding subunit of mTORC2, but further work is required to establish its role. 相似文献
53.
U Kyaw Tha Paw 《International journal of biometeorology》1988,32(2):73-77
Clustering of organisms under cold air temperature conditions is modelled with a finite-difference method. Metabolic functions of temperature are used to simulate completely ectothermic, completely endothermic, and other organisms. To adequately match real conditions, the core temperature is kept constant at a high level, while the periphery of the organism cluster is assigned a lower temperature representing the cold conditions under which clustering is observed for organisms. The numerical model reasonably predicts the observed temperature distribution in honeybee clusters. The results do not support suggestions that organisms could overheat in the core of a cluster if they do not use thermoregulatory mechanisms to cool down. Endothermic organisms are not as efficient as ectothermic ones in heating a cluster core temperature to a given level. The general ectothermic metabolic rate function exhibited one of the highest efficiencies for heating the cluster. 相似文献
54.
E. Jagiełło-Wójtowicz A. Niewiadomy A. Chodkowska K. Pawłowski K. Sarna 《Russian Journal of Bioorganic Chemistry》2014,40(3):352-357
4-(1,3,4-Thiadiazol-2-yl)benzene-1,3-diols 5-substituted in the heterocyclic ring were obtained by the reaction of the commercially available hydrazides or thiosemicarbazides with sulfinylbis[(2,4-dihydroxyphenyl)methanethione]. The synthesized compounds were screened for their influence on CNS in an in vivo model. Computer aided prediction tools were used for the evaluation of toxicological properties. Additionally, based on the Lipinski filters, the drug-likeness of compounds was assessed. They revealed that the compounds possess properties which can suggest favorable pharmacokinetics in the body after oral admission. 相似文献
55.
Prasad N. Paradkar Kimberley B. Zumbrennen Barry H. Paw Diane M. Ward Jerry Kaplan 《Molecular and cellular biology》2009,29(4):1007-1016
Mitoferrin 1 and mitoferrin 2 are homologous members of the mitochondrial solute carrier family. Mitoferrin 1 is required for mitochondrial iron delivery in developing erythrocytes. Here we show that mitoferrin 1 and mitoferrin 2 contribute to mitochondrial iron delivery in a variety of cells. Reductions in mitoferrin 1 and/or mitoferrin 2 levels by RNA interference result in decreased mitochondrial iron accumulation, heme synthesis, and iron-sulfur cluster synthesis. The ectopic expression of mitoferrin 1 in nonerythroid cells silenced for mitoferrin 2 or the expression of mitoferrin 2 in cells silenced for mitoferrin 1 restored heme synthesis to “baseline” levels. The ectopic expression of mitoferrin 2, however, did not support hemoglobinization in erythroid cells deficient in mitoferrin 1. Mitoferrin 2 could not restore heme synthesis in developing erythroid cells because of an inability of the protein to accumulate in mitochondria. The half-life of mitoferrin 1 was increased in developing erythroid cells, while the half-life of mitoferrin 2 did not change. These results suggest that mitochondrial iron accumulation is tightly regulated and that controlling mitoferrin levels within the mitochondrial membrane provides a mechanism to regulate mitochondrial iron levels.Iron is a required element for all eukaryotes, but iron can be toxic at high concentrations. Consequently, the cellular acquisition of iron is highly regulated, as is the concentration of free iron in biological fluids. The regulation of iron concentration is extended to cellular organelles that either store or utilize iron. Mitochondria utilize iron for the synthesis of heme and iron-sulfur (Fe-S) clusters. These prosthetic groups are used within the mitochondria and are exported for use by cytosolic and nuclear proteins. The mechanisms that regulate mitochondrial iron levels are not known, although it is clear that mitochondrial iron levels must be regulated. For example, the loss of function mutations in genes that encode enzymes required for Fe-S cluster synthesis or the Atm1 transporter that exports Fe-S clusters, results in excessive mitochondrial iron accumulation in yeast and humans (for a review, see reference 11).The mechanisms that regulate mitochondrial iron pools are not well defined. Mitochondrial iron pools might be regulated at the level of import. Mitoferrin 1 (Mfrn1) has been shown to be required for mitochondrial iron import in developing erythroid cells. A mutation in zebrafish Mfrn1 (frascati) or the deletion of mouse Mfrn1 leads to defects in hemoglobinization due to a deficit in mitochondrial iron uptake (17). The phenotype of frascati zebrafish is restricted to developing red blood cells; other cell types showed no evidence of a mitochondrial iron phenotype. Mfrn1 has a paralogue, Mfrn2, and both genes have homologues MRS3 and MRS4 in Saccharomyces cerevisiae. Yeast with deletions of MRS3 and MRS4 grows poorly under low iron conditions due to impaired mitochondrial iron acquisition (5, 10, 13, 23). In yeast, the expression of Mfrn1 or Mfrn2 in Δmrs3 Δmrs4 cells can correct the poor growth under low iron conditions. The expression of either mouse or zebrafish Mfrn1 as a transgene in frascati zebrafish corrected the hemoglobin deficiency in cells, but the expression of Mfrn2 did not (17). These observations raise three questions. (i) What is the role of Mfrn2 in mitochondrial iron metabolism? (ii) Is iron transport into mitochondria regulated? (iii) If Mfrn2 transports iron into the mitochondria of vertebrate cells, why doesn''t Mfrn2 rescue the mitochondrial defect in Mfrn1-deficient zebrafish?Here, we show that Mfrn1 and Mfrn2 can transport iron into the mammalian mitochondria of nonerythroid cells. The ectopic expression of either Mfrn1 or Mfrn2 can restore mitochondrial iron transport in cells silenced for Mfrn2 and -1, respectively, but ectopic expression has little effect on increasing mitochondrial iron levels above the baseline values. Mitochondrial iron levels do not increase over the baseline because the levels of Mfrns are regulated posttranslationally. Mfrn1 accumulates in the mitochondria of developing red blood cells as a result of an increased protein half-life. In contrast, Mfrn2 does not accumulate in developing red blood cells or other cells, as the half-life of Mfrn2 protein remains constant. 相似文献
56.
Agnieszka?K.?KowalkowskaEmail authorView authors OrcID profile
return OK on get Michalina?Paw?owicz Patrycja?Guzanek Agnieszka?T.?Krawczyńska 《Protoplasma》2018,255(6):1811-1825
The analysis of flowers collected at different stages of anthesis provides strong evidence to conclude that the shell-shaped hypochile and the knobs of epichile form a nectary. The scent comes from the aromatic constituents of nectar and the epichile tissue and the apices of all tepals (osmophores). The comparison between pollinated and unpollinated flowers revealed that the anthesis of unpollinated flowers lasted up to the 16th day. The nectariferous secretory cells formed single-layered epidermis and several layers of underlying parenchyma built by small, isodiametric cells with thin walls and dense cytoplasm, relatively large nuclei, supplied by collateral vascular bundles. During the floral lifespan, the residues of secreted material were higher on the hypochile cells. The lipoid-carbohydrate material and lipid globules in the cell walls and in the cytoplasm were localised. The abundance of starch grains was observed at the beginning of anthesis and their gradual reduction during the flower lifespan. At the end of anthesis in unpollinated flowers, the lipoid-carbohydrate-phenolic materials have been demonstrated. The phenolic material was the same as in plastoglobuli. The features such as irregular plasmalemma, the secretory vesicles that fuse with it, fully developed dictyosomes, numerous profiles of ER indicate vesicle-mediated process of secretion. The substances could be transported by vesicles to the periplasmic space via granulocrine secretion and then to the external surface. Both micro-channels and slightly developed periplasmic space were visible in the hypochile epidermis. This is the first time for anatomical survey of secretory tissue in pollinated and unpollinated flowers of E. helleborine. 相似文献
57.
Using simulated data, we compared five methods of phylogenetic tree
estimation: parsimony, compatibility, maximum likelihood, Fitch-
Margoliash, and neighbor joining. For each combination of substitution
rates and sequence length, 100 data sets were generated for each of 50
trees, for a total of 5,000 replications per condition. Accuracy was
measured by two measures of the distance between the true tree and the
estimate of the tree, one measure sensitive to accuracy of branch lengths
and the other not. The distance-matrix methods (Fitch- Margoliash and
neighbor joining) performed best when they were constrained from estimating
negative branch lengths; all comparisons with other methods used this
constraint. Parsimony and compatibility had similar results, with
compatibility generally inferior; Fitch- Margoliash and neighbor joining
had similar results, with neighbor joining generally slightly inferior.
Maximum likelihood was the most successful method overall, although for
short sequences Fitch- Margoliash and neighbor joining were sometimes
better. Bias of the estimates was inferred by measuring whether the
independent estimates of a tree for different data sets were closer to the
true tree than to each other. Parsimony and compatibility had particular
difficulty with inaccuracy and bias when substitution rates varied among
different branches. When rates of evolution varied among different sites,
all methods showed signs of inaccuracy and bias.
相似文献
58.
Zajdel P Marciniec K Maślankiewicz A Satała G Duszyńska B Bojarski AJ Partyka A Jastrzębska-Więsek M Wróbel D Wesołowska A Pawłowski M 《Bioorganic & medicinal chemistry》2012,20(4):1545-1556
Two series of arylpiperazinyl-alkyl quinoline-, isoquinoline-, naphthalene-sulfonamides with flexible (13-26) and semi-rigid (33-36) alkylene spacer were synthesized and evaluated for 5-HT(1A), 5-HT(2A), 5-HT(6), 5-HT(7) and selected compounds for D(2), D(3), D(4) receptors. The compounds with a mixed 5-HT and D receptors profile 16 (N-{4-[4-(3-chlorophenyl)-piperazin-1-yl]-butyl}-3-quinolinesulfonamide) and 36 (4-(4-{2-[4-(4-chloro-phenyl)-piperazin-1-yl]-ethyl}-piperidine-1-sulfonyl)-isoquinoline), displaying antagonistic activity at 5-HT(7), 5-HT(2A), D(2) postsynaptic sites, produced antidepressant-like effects in the forced swim test in mice and showed significant anxiolytic activity in the plus-maze test in rats. The lead compound 36, a multi-receptor 5-HT(2A)/5-HT(7)/D(2)/D(3)/D(4) agent, also displayed significant antipsychotic properties in the MK-801-induced hyperlocomotor activity in mice. 相似文献
59.
Gordon J. Hildick-Smith Jeffrey D. Cooney Caterina Garone Laura S. Kremer Tobias B. Haack Jonathan N. Thon Non Miyata Daniel S. Lieber Sarah E. Calvo H. Orhan Akman Yvette Y. Yien Nicholas C. Huston Diana S. Branco Dhvanit I. Shah Matthew L. Freedman Carla M. Koehler Joseph E. Italiano Jr. Andreas Merkenschlager Skadi Beblo Tim M. Strom Thomas Meitinger Peter Freisinger M. Alice Donati Holger Prokisch Vamsi K. Mootha Salvatore DiMauro Barry H. Paw 《American journal of human genetics》2013
60.