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991.
992.
Combination of 16S rRNA-targeted oligonucleotide probes with flow cytometry for analyzing mixed microbial populations. 总被引:51,自引:49,他引:51 下载免费PDF全文
R I Amann B J Binder R J Olson S W Chisholm R Devereux D A Stahl 《Applied microbiology》1990,56(6):1919-1925
Fluorescent oligonucleotide hybridization probes were used to label bacterial cells for analysis by flow cytometry. The probes, complementary to short sequence elements within the 16S rRNA common to phylogenetically coherent assemblages of microorganisms, were labeled with tetramethylrhodamine and hybridized to suspensions of fixed cells. Flow cytometry was used to resolve individual target and nontarget bacteria (1 to 5 microns) via probe-conferred fluorescence. Target cells were quantified in an excess of nontarget cells. The intensity of fluorescence was increased additively by the combined use of two or three fluorescent probes complementary to different regions of the same 16S rRNA. 相似文献
993.
Transformation of leukotriene A4 methyl ester to leukotriene C4 monomethyl ester by cytosolic rat glutathione transferases 总被引:6,自引:0,他引:6
Bengt Mannervik Helgi Jensson Per Ålin Lars Örning Sven Hammarström 《FEBS letters》1984,175(2):289-293
Six major basic cytosolic glutathione transferases from rat liver catalyzed the conversion of leukotriene A4 methyl ester to the corresponding leukotriene C4 monomethyl ester. Glutathione transferase 4-4, the most active among these enzymes, had a Vmax of 615 nmol X min-1 X mg protein-1 at 30 degrees C in the presence of 5 mM glutathione. It was followed in efficiency by transferase 3-4 which had a Vmax of 160 nmol X min-1 X mg-1 under the same conditions. Transferases 1-1, 1-2, 2-2 and 3-3 had at least 30 times lower Vmax values than transferase 4-4. 相似文献
994.
Phylogenetic probes for analyzing abundance and spatial organization of nitrifying bacteria 总被引:7,自引:0,他引:7
Mobarry BK Wagner M Urbain V Rittmann BE Stahl DA 《Applied and environmental microbiology》1997,63(2):815
Volume 62, no. 6, p. 2157, Table 1: the sequence for probe Nso1225, 5(prm1)-CGCGATTGTATTACGTGTGA-3(prm1), should read 5(prm1)-CGCCATTGTATTACGTGTGA-3(prm1). [This corrects the article on p. 2156 in vol. 62.]. 相似文献
995.
Two elongation responses to auxin respond differently to protein synthesis inhibition 总被引:3,自引:4,他引:3 下载免费PDF全文
The first and second responses to auxin react differently to the inhibition of protein synthesis by cycloheximide. It was determined that the protein with the shortest half-life, among the several necessary for the first response, is different from its counterpart among the several necessary for the second response. Specifically, the protein half-lives are 28 minutes and 11 minutes for the first and second responses, respectively. 相似文献
996.
997.
998.
Francois‐Pierre J Martin Yulan Wang Norbert Sprenger Ivan K S Yap Serge Rezzi Ziad Ramadan Emma Peré‐Trepat Florence Rochat Christine Cherbut Peter van Bladeren Laurent B Fay Sunil Kochhar John C Lindon Elaine Holmes Jeremy K Nicholson 《Molecular systems biology》2008,4(1)
Gut microbiome–host metabolic interactions affect human health and can be modified by probiotic and prebiotic supplementation. Here, we have assessed the effects of consumption of a combination of probiotics (Lactobacillus paracasei or L. rhamnosus) and two galactosyl‐oligosaccharide prebiotics on the symbiotic microbiome–mammalian supersystem using integrative metabolic profiling and modeling of multiple compartments in germ‐free mice inoculated with a model of human baby microbiota. We have shown specific impacts of two prebiotics on the microbial populations of HBM mice when co‐administered with two probiotics. We observed an increase in the populations of Bifidobacterium longum and B. breve, and a reduction in Clostridium perfringens, which were more marked when combining prebiotics with L. rhamnosus. In turn, these microbial effects were associated with modulation of a range of host metabolic pathways observed via changes in lipid profiles, gluconeogenesis, and amino‐acid and methylamine metabolism associated to fermentation of carbohydrates by different bacterial strains. These results provide evidence for the potential use of prebiotics for beneficially modifying the gut microbial balance as well as host energy and lipid homeostasis. 相似文献
999.
Chi CN Gianni S Calosci N Travaglini-Allocatelli C Engström K Jemth P 《FEBS letters》2007,581(6):1109-1113
An important question in protein folding is whether the folding mechanism is sequence dependent and conserved for homologous proteins. In this work we compared the kinetic folding mechanism of five postsynaptic density protein-95, disc-large tumor suppressor protein, zonula occludens-1 (PDZ) domains, sharing similar topology but having different primary structures. Investigation of the different proteins under various experimental conditions revealed that the folding kinetics of each member of the PDZ family can be described by a model with two transition states separated by an intermediate. Moreover, the positions of the two transition states along the reaction coordinate (as given by their beta(T)-values) are fairly constant for the five PDZ domains. 相似文献
1000.
Tova Rahn Martin Ridderstrle Hans Tornqvist Vincent Manganiello Gudrun Fredrikson Per Belfrage Eva Degerman 《FEBS letters》1994,350(2-3):314-318
Incubation of rat adipocytes with wortmannin, a potent and selective phosphatidylinositol 3-kinase (PI 3-kinase) inhibitor, completely blocked the antilipolytic action of insulin (IC50≈ 100 nM), the insulin-induced activation and phosphorylation of cGMP-inhibited cAMP phosphodiesterase (cGI-PDE) as well as the activation of the insulin-stimulated cGI-PDE kinase (IC50≈ 10–30 nM). No direct effects of the inhibitor on the insulin-stimulated cGI-PDE kinase, the cGI-PDE and the hormone-sensitive lipase were observed. These data suggest that activation of PI 3-kinase upstream of the insulin-stimulated cGI-PDE kinase in the antilipolytic insulin signalchain has an essential role for insulin-induced cGI-PDE activation/ phosphorylation and anti-lipolysis. 相似文献