排序方式: 共有64条查询结果,搜索用时 15 毫秒
31.
32.
Karen L Stirrett Julian A Ferreras Sebastian M Rossi Richard L Moy Fabio V Fonseca Luis EN Quadri 《BMC microbiology》2008,8(1):122
Background
Yersinia pestis is the causative agent of plague and a potential agent of bioterrorism and biowarfare. The plague biothreat and the emergence of multidrug-resistant plague underscore the need to increase our understanding of the intrinsic potential of Y. pestis for developing antimicrobial resistance and to anticipate the mechanisms of resistance that may emerge in Y. pestis. Identification of Y. pestis genes that, when overexpressed, are capable of reducing antibiotic susceptibility is a useful strategy to expose genes that this pathogen may rely upon to evolve antibiotic resistance via a vertical modality. In this study, we explored the use of a multicopy suppressor, Escherichia coli host-based screening approach as a means to expose antibiotic resistance determinant candidates in Y. pestis. 相似文献33.
34.
Molchanova IV Karavaeva EN Mikhaĭlovskaia LN Pozolotina VN Lobanova LV 《Radiatsionnaia biologiia, radioecologiia / Rossi?skaia akademiia nauk》2004,44(5):603-607
The Techa river was contaminated in 1949-1956 from the nuclear enterprise "Mayak". The investigations were carried out in flood plain of the Techa river in 1992-2001. 90Sr and 137Cs stores were calculated in the soil-vegetation cover. There is uneven character of the spatial radionuclides contamination of the investigated area. The store with 90Sr changes from 25 to 930 kBq/m2 (0.7-25.0 Ci/km2) and that with 137Cs--from 30 to 1700 kBq/m2 (0.8-46.0 Ci/km2). In the preriver-bed soils the ratio 90Sr/137Cs increases with further from discharge point. Individual effective dose was calculated for the Brodocalmak population. 90Sr was revealed in the flood plain soils of the Iset river. The contribution of the contaminated Techa river and its flood plains soils accounted for as by incorporated radionuclides as background gamma-radiation does not exceed 0.13-0.17 mSv/yr if the contaminated Techa river utilization is limited. In other case the contribution of the contaminated Techa river increases to 1.6-3.0 mSv/yr. These values exceed international safety norms. 相似文献
35.
Konovalova NV Karavaeva NA Gribkov AA Luzgina VN Evstigneeva RP 《Bioorganicheskaia khimiia》2000,26(2):112-117
Diporphyrin systems based on tetraphenylporphyrin derivatives bridged with dipeptide or tripeptide spacers containing Gly and Phe residues were synthesized, and their physicochemical properties were studied. 相似文献
36.
Boev S. F. Vagin A. I. Solomatin S. Yu. Savostyanov D. V. Siluyanov V. V. Shmakov A. S. Zaitsev B. D. Teplykh A. A. Borodina I. A. Karavaeva O. A. Guliy O. I. 《Biophysics》2019,64(3):416-423
Biophysics - Abstract—The effect of pulsed terahertz radiation at a wavelength of 66 μm, a pulse duration of 100 ns, and a pulse energy of 200 mJ on a suspension of microbial cells was... 相似文献
37.
Kristina EN Clark Henry Lopez Bahja Ahmed Abdi Sandra G Guerra Xu Shiwen Korsa Khan Oseme Etomi George R Martin David J Abraham Christopher P Denton Richard J Stratton 《Arthritis research & therapy》2015,17(1)
IntroductionClinical diversity in systemic sclerosis (SSc) reflects multifaceted pathogenesis and the effect of key growth factors or cytokines operating within a disease-specific microenvironment. Dermal interstitial fluid sampling offers the potential to examine local mechanisms and identify proteins expressed within lesional tissue. We used multiplex cytokine analysis to profile the inflammatory and immune activity in the lesions of SSc patients.MethodsDermal interstitial fluid sample from the involved forearm skin, and synchronous plasma samples were collected from SSc patients (n = 26, diffuse cutaneous SSc (DcSSc) n = 20, limited cutaneous SSc (LcSSc) n = 6), and healthy controls (HC) (n = 10) and profiled by Luminex® array for inflammatory cytokines, chemokines, and growth factors.ResultsLuminex® profiling of the dermal blister fluid showed increased inflammatory cytokines (median interleukin ( IL)-6 in SSc 39.78 pg/ml, HC 5.51 pg/ml, p = 0.01, median IL-15 in SSc 6.27 pg/ml, HC 4.38 pg/ml, p = 0.03), chemokines (monocyte chemotactic protein (MCP)-3 9.81 pg/ml in SSc, 7.18 pg/ml HC, p = 0.04), and profibrotic growth factors (platelet derived growth factor (PDGF)-AA 10.38 pg/ml versus 6.94 pg/ml in HC, p = 0.03). In general dermal fluid and plasma cytokine levels did not correlate, consistent with predominantly local production of these factors within the dermal lesions, rather than leakage from the serum. In hierarchical clustering and network analysis IL-6 emerged as a key central mediator.ConclusionsOur data confirm that an immuno-inflammatory environment and aberrant vascular repair are intimately linked to fibroblast activation in lesional skin in SSc. This non-invasive method could be used to profile disease activity in the clinic, and identifies key inflammatory or pro-fibrotic proteins that might be targeted therapeutically. Distinct subgroups of SSc may be defined that show innate or adaptive immune cytokine signatures. 相似文献
38.
JELENA MLINAREC DRAEN A. PAPE VINJA BESENDORFER 《Botanical journal of the Linnean Society. Linnean Society of London》2006,150(2):177-186
The karyotype of the Mediterranean species Anemone hortensis L. (Ranunculaceae) was characterized with emphasis on heterochromatin distribution and localization of ribosomal (18S−5.8S−26S and 5S rDNA) and telomeric repeats (TTTAGGG). Diploid chromosome complement, 2 n = 2 x = 16, common to all investigated populations, consisted of three acrocentric, one meta-submetacentric and four metacentric chromosomes ranging in size from 6.34 to 10.47 µm. Fluorescence in situ hybridization (FISH) with 18S and 5S rDNA probes revealed two 18S−5.8S−26S rDNA loci on a satellite and secondary constriction of acrocentric chromosome pair 2 and terminally on acrocentric chromosome pair 3, and two 5S rDNA loci in the pericentromeric region of meta-submetacentric chromosome pair 4 and in the proximity of the 18S−5.8S−26S rDNA locus on chromosome pair 2. The only GC-rich heterochromatin, as revealed by fluorochrome Chromomycin A3 staining, was that associated with nucleolar organizer regions, whereas AT-rich heterochromatin, stained with 4,6-diamino-2-phenylindole (DAPI), was distributed intercalarly and terminally on the long arm of all three acrocentric chromosomes, and terminally on chromosomes 4 and 5. FISH with Arabidopsis -type telomeric repeats (TTTAGGG) as a probe revealed two classes of signals, small dot-like and large bands, at chromosome termini exclusively, where they corresponded to terminal DAPI-stained heterochromatin. Heteromorphism of chromosome pair 4, which refers to terminal DAPI bands and FISH signals, was observed in populations of Anemone hortensis . Chromosome pairing during meiosis was regular with formation of localized chiasmata proximal to the centromere. © 2006 The Linnean Society of London, Botanical Journal of the Linnean Society , 2006, 150 , 177–186. 相似文献
39.
Background
Endosymbionts that manipulate the reproduction of their hosts have been reported widely in invertebrates. One such group of endosymbionts is the male-killers. To date all male-killers reported are bacterial in nature, but comprise a diverse group. Ladybirds have been described as a model system for the study of male-killing, which has been reported in multiple species from widespread geographic locations. Whilst criteria of low egg hatch-rate and female-biased progenic sex ratio have been used to identify female hosts of male-killers, variation in vertical transmission efficiency and host genetic factors may result in variation in these phenotypic indicators of male-killer presence. Molecular identification of bacteria and screening for bacterial presence provide us with a more accurate method than breeding data alone to link the presence of the bacteria to the male-killing phenotype. In addition, by identifying the bacteria responsible we may find evidence for horizontal transfer between endosymbiont hosts and can gain insight into the evolutionary origins of male-killing. Phylogenetic placement of male-killing bacteria will allow us to address the question of whether male-killing is a potential strategy for only some, or all, maternally inherited bacteria. Together, phenotypic and molecular characterisation of male-killers will allow a deeper insight into the interactions between host and endosymbiont, which ultimately may lead to an understanding of how male-killers identify and kill male-hosts. 相似文献40.
选择内蒙古28个样地采集的10种棘豆属植物56个单株,提取样品的基因组DNA,对其叶绿体psbA trnH序列进行扩增、测序,所得序列利用ClustalX软件进行对位排列,并用MEGA50软件采用最大似然法构建系统发育树。结果显示:(1)10种棘豆属psbA trnH序列的变异位点50个,信息位点36个,种间碱基差异百分率为34%,GC含量变化范围在2318%~2572%之间。(2)棘豆属与黄芪属各为一支,自展支持率达99%,这10种棘豆属植物可能为单系起源。(3)系统树中小叶小花棘豆与小花棘豆的样本独立成一支,支持将小叶小花棘豆作为小花棘豆的变种来处理。(4)多叶棘豆、砂珍棘豆和黄毛棘豆的样本相互混杂,表明亲缘关系很近,支持《内蒙古植物志》将三者归入真棘豆亚属轮叶棘豆组的观点。(5)缘毛棘豆与薄叶棘豆的样本聚成一支,支持将二者归入矮生棘豆组。研究表明,psbA trnH序列可为棘豆属下种间系统发育关系研究提供分子证据。 相似文献