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1.
2.
Ronald B. Walter Julie Harless Rita T. Svensson Klaus D. Kallman Donald C. Morizot Rodney S. Nairn 《Genomics》1991,10(4)
Fish gene mapping studies have identified several syntenic groups showing conservation over more than 400 million years of vertebrate evolution. In particular, Xiphophorus linkage group IV has been identified as a homolog of human chromosomes 15 and 19. During mammalian evolution, loci coding for glucosephosphate isomerase, peptidase D, muscle creatine kinase, and several DNA repair genes (ERCC1, ERCC2, and XRCC1) appear as a conserved syntenic group on human chromosome 19. When X. clemenciae and X. milleri PstI endonuclease-digested genomic DNA was used in Southern analysis with a human ERCC2 DNA repair gene probe, a strongly cross-hybridizing restriction fragment length polymorphism was observed. Backcrosses to X. clemenciae from X. milleri × X. clemenciae F1 hybrids allowed tests for linkage of the ERCC2-like polymorphism to markers covering a large proportion of the genome. Statistically significant evidence for linkage was found only for ERCC2L1 and CKM (muscle creatine kinase), with a total of 41 parents and 2 recombinants (4.7% recombination, χ2 = 35.37, P < 0.001); no evidence for linkage to GPI and PEPD in linkage group IV was detected. The human chromosome 19 synteny of ERCC2 and CKM thus appears to be conserved in Xiphophorus, while other genes located nearby on human chromosome 19 are in a separate linkage group in this fish. If Xiphophorus gene arrangements prove to be primitive, human chromosome 19 may have arisen from chromosome fusion or translocation events at some point since divergence of mammals and fishes from a common ancestor. 相似文献
3.
Simulated climate change impacts on fluxes of carbon in Norway spruce ecosystems along a climatic transect in Sweden 总被引:2,自引:0,他引:2
Per-Erik Jansson Magnus Svensson Dan Berggren Kleja David Gustafsson 《Biogeochemistry》2008,89(1):81-94
A simulation study based on recent regional climate scenarios for Sweden investigated possible changes in carbon (C) dynamics
and net ecosystem exchange (NEE) of Swedish Norway spruce forest ecosystems. Four sites, representative of well-drained soils
in four regions, were included. Stand development was simulated for a 100-year rotation period using a coupled model describing
abiotic and biotic processes in the soil-plant-atmosphere system. Two IPCC climate change scenarios, corresponding to a mean
annual temperature increase of about 2°C (A2) or 3°C (B2) from the reference period 1961–1990 to a new period 2061–2090, were
considered. Annual maximum snow depth decreased with the increase in air temperature, whereas maximum soil frost depth and
mean annual soil temperature showed only small changes, especially for the sites in northern Sweden. Simulations suggested
that in the warmer climate, gross primary production (GPP) increased by 24–32% in northern Sweden and by 32–43% in the south.
In the north, the increase was related to the combined effect of air and soil temperature extending the growing season, whereas
in the south it was mainly governed by increased N availability due to increased soil temperature. NEE increased by about
20% (A2) or 25% (B2) at all sites, more or less solely due to increased accumulation of C in the tree biomass (including harvest
residues), since changes in soil C were small compared with the current climate. Both light use efficiency and water use efficiency
were improved in the future climate scenarios, despite increases in atmospheric CO2 not being considered. 相似文献
4.
S E Sedelnikova S Ch Agalarov I A Eliseikina N P Fomenkova S V Nikonov M B Garber L A Svensson A Liljas 《Journal of molecular biology》1991,220(3):549-550
Crystals of protein S6 from the small ribosomal subunit of an extreme thermophile, Thermus thermophilus, have been obtained by the hanging-drop/vapor diffusion technique using methane pentanediol as a precipitant in the presence of potassium fluoride. The crystals belong to the space group C222 with cell parameters a = 106.7, b = 52.8, c = 41.0 A. They diffract to 2.0 A resolution. 相似文献
5.
Tasso Miliotis Per-Olof Ericsson Gyrgy Marko-Varga Robert Svensson Johan Nilsson Thomas Laurell Rainer Bischoff 《Journal of chromatography. B, Analytical technologies in the biomedical and life sciences》2001,752(2)
A methodology for the rapid and quantitative analysis of phosphorylation sites in proteins is presented. The coupling of capillary high-performance liquid chromatography (HPLC) to electrospray ionization mass spectrometry (ESI-MS) allowed one to distinguish phosphorylation sites based on retention time and mass difference from complex peptide mixtures. The methodology was first evaluated and validated for a mixture of non-, mono-, and dityrosine-phosphorylated synthetic peptides, corresponding to the tryptic fragment 485–496 (ALGADDSYYTAR) of the human protein tyrosine kinase ZAP-70. The limits of detection for the non-, mono- and diphosphorylated peptides were about 15, 40 and 100 fmol, respectively, when using a 300 μm I.D. column. Application of the method was extended to identify phosphopeptides generated from a trypsin digest of recombinant autophosphorylated ZAP-70, in particular with respect to quantifying the status at the regulatory phosphorylation sites Tyr-492 and Tyr-493. Combination of chromatographic and on-line tandem mass spectrometry data allowed one to ascertain the identity of the detected peptides, a prerequisite to analyses in more complex biological samples. As an extension to the methodology described above, we evaluated the feasibility of interfacing capillary HPLC to matrix assisted laser desorption ionisation time-of-flight mass spectrometry (MALDI-TOF-MS), using a micromachined piezoelectric flow-through dispenser as the interface. This enabled direct arraying of chromatographically separated components onto a target plate that was precoated with matrix for subsequent analysis by MALDI-TOF-MS without further sample handling. 相似文献
6.
The starch‐binding domain family CBM41—An in silico analysis of evolutionary relationships 下载免费PDF全文
Within the CAZy database, there are 81 carbohydrate‐binding module (CBM) families. A CBM represents a non‐catalytic domain in a modular arrangement of glycoside hydrolases (GHs). The present in silico study has been focused on starch‐binding domains from the family CBM41 that are usually part of pullulanases from the α‐amylase family GH13. Currently there are more than 1,600 sequences classified in the family CBM41, almost exclusively from Bacteria, and so a study was undertaken in an effort to divide the members into relevant groups (subfamilies) and also to contribute to the evolutionary picture of family CBM41. The CBM41 members adopt a β‐sandwich fold (~100 residues) with one carbohydrate‐binding site formed by the side‐chains of three aromatic residues that interact with carbohydrate. The family CBM41 can be divided into two basic subdivisions, distinguished from each other by a characteristic sequence pattern or motif of the three essential aromatics as follows: (i) “W‐W‐~10aa‐W” (the so‐called Streptococcus/Klebsiella‐type); and (ii) “W‐W‐~30aa‐W” (Thermotoga‐type). Based on our bioinformatics analysis it is clear that the first and second positions of the motif can be occupied by aromatic residues (Phe, Tyr, His) other than tryptophan, resulting in the existence of six different carbohydrate‐binding CBM41 groups, that reflect mostly differences in taxonomy, but which should retain the ability to bind an α‐glucan. In addition, three more groups have been proposed that, although lacking the crucial aromatic motif, could possibly employ other residues from remaining parts of their sequence for binding carbohydrate. Proteins 2017; 85:1480–1492. © 2017 Wiley Periodicals, Inc. 相似文献
7.
Srikanth Mairpady Shambat Axana Haggar Francois Vandenesch Gerard Lina Willem J. B. van Wamel Gayathri Arakere Mattias Svensson Anna Norrby-Teglund 《PloS one》2014,9(8)
Epidemiological studies of Staphylococcus aureus have shown a relation between certain clones and the presence of specific virulence genes, but how this translates into virulence-associated functional responses is not fully elucidated. Here we addressed this issue by analyses of community-acquired S. aureus strains characterized with respect to antibiotic resistance, ST types, agr types, and virulence gene profiles. Supernatants containing exotoxins were prepared from overnight bacterial cultures, and tested in proliferation assays using human peripheral blood mononuclear cells (PBMC). The strains displayed stable phenotypic response profiles, defined by either a proliferative or cytotoxic response. Although, virtually all strains elicited superantigen-mediated proliferative responses, the strains with a cytotoxic profile induced proliferation only in cultures with the most diluted supernatants. This indicated that the superantigen-response was masked by a cytotoxic effect which was also confirmed by flow cytometry analysis. The cytotoxic supernatants contained significantly higher levels of α-toxin than did the proliferative supernatants. Addition of α-toxin to supernatants characterized as proliferative switched the response into cytotoxic profiles. In contrast, no effect of Panton Valentine Leukocidin, δ-toxin or phenol soluble modulin α-3 was noted in the proliferative assay. Furthermore, a significant association between agr type and phenotypic profile was found, where agrII and agrIII strains had predominantly a proliferative profile whereas agrI and IV strains had a predominantly cytotoxic profile. The differential response profiles associated with specific S. aureus strains with varying toxin production could possibly have an impact on disease manifestations, and as such may reflect specific pathotypes. 相似文献
8.
Studies on methionyl-tRNA synthetase. 3. Enzyme dependence for maximum methionyl-tRNA formation 总被引:1,自引:0,他引:1
I Svensson 《Biochimica et biophysica acta》1968,167(1):179-183
9.
Edward E. Nishizawa William L. Miller Robert R. Gorman Gordon L. Bundy Jan Svensson Mats Hamberg 《Prostaglandins & other lipid mediators》1975,9(1)
Prostaglandin D2 was found to be a potent inhibitor of platelet aggregation. Aggregation of human platelets by ADP, collagen and prostaglandin G2 was inhibited more strongly by PGD2 than by PGE1. Although ADP-induced aggregation of rabbit platelets was inhibited more strongly by PGE1 than by PGD2 the latter prostaglandin gave a more long-lasting inhibitory effect on platelet aggregation following intravenous or oral administration. These results coupled with the finding that PGD2 has less hypotensive effects on the cardiovascular system than PGE1 suggest the possible use of PGD2 as an antithrombotic agent. 相似文献
10.