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排序方式: 共有345条查询结果,搜索用时 15 毫秒
21.
Renata Plocinska Luis Martinez Purushotham Gorla Emmanuel Pandeeti Krishna Sarva Ewelina Blaszczyk Jaroslaw Dziadek Murty V. Madiraju Malini Rajagopalan 《Journal of bacteriology》2014,196(23):4120-4129
The septal association of Mycobacterium tuberculosis MtrB, the kinase partner of the MtrAB two-component signal transduction system, is necessary for the optimal expression of the MtrA regulon targets, including ripA, fbpB, and ftsI, which are involved in cell division and cell wall synthesis. Here, we show that MtrB, irrespective of its phosphorylation status, interacts with Wag31, whereas only phosphorylation-competent MtrB interacts with FtsI. We provide evidence that FtsI depletion compromises the MtrB septal assembly and MtrA regulon expression; likewise, the absence of MtrB compromises FtsI localization and, possibly, FtsI activity. We conclude from these results that FtsI and MtrB are codependent for their activities and that FtsI functions as a positive modulator of MtrB activation and MtrA regulon expression. In contrast to FtsI, Wag31 depletion does not affect MtrB septal assembly and MtrA regulon expression, whereas the loss of MtrB increased Wag31 localization and the levels of PknA/PknB (PknA/B) serine-threonine protein kinase-mediated Wag31 phosphorylation. Interestingly, we found that FtsI decreased levels of phosphorylated Wag31 (Wag31∼P) and that MtrB interacted with PknA/B. Overall, our results indicate that MtrB interactions with FtsI, Wag31, and PknA/B are required for its optimal localization, MtrA regulon expression, and phosphorylation of Wag31. Our results emphasize a new role for MtrB in cell division and cell wall synthesis distinct from that regulating the MtrA phosphorylation activities. 相似文献
22.
Mette Kristensen Francesco Savorani Gitte Ravn-Haren Morten Poulsen Jaroslaw Markowski Flemming H. Larsen Lars O. Dragsted Søren B. Engelsen 《Metabolomics : Official journal of the Metabolomic Society》2010,6(1):129-136
Risk of cardiovascular disease is related to cholesterol distribution in different lipoprotein fractions. Lipoproteins in
rodent model studies can only reliably be measured by time- and plasma-consuming fractionation. An alternative method to measure
cholesterol distribution in the lipoprotein fractions in rat plasma is presented in this paper. Plasma from two rat studies
(n = 68) was used in determining the lipoprotein profile by an established ultracentrifugation method and proton nuclear magnetic
resonance (NMR) spectra of replicate samples was obtained. From the ultracentrifugation reference data and the NMR spectra,
an interval partial least-square (iPLS) regression model to predict the amount of cholesterol in the different lipoprotein
fractions was developed. The relative errors of the prediction models were between 12 and 33% and had correlation coefficients
(r) between 0.96 and 0.84. The models were tested with an independent test set giving prediction errors between 19 and 46%
and r between 0.96 and 0.76. Prediction of High, Low and Very Low Density Lipoprotein (HDL, LDL and VLDL) and total cholesterol
was conducted in a study where rats had been supplemented with two doses of air-dried apple-powder. No significant difference
in LDL, VLDL and total cholesterol was observed between the groups. The high apple-powder (20%) group had significantly lower
HDL cholesterol (11%, P = 0.0452) than the control group. It is concluded that the iPLS approach yielded excellent regression models and thus univocal
established chemometric analysis of NMR spectra of rat plasma as a strong and efficient way to quantify lipoprotein fractions
in rat studies. 相似文献
23.
Pawel Mazur Tomasz Magdziarz Andrzej Bak Zdzislaw Chilmonczyk Teresa Kasprzycka-Guttman Irena Misiewicz-Krzemińska Katarzyna Skupińska Jaroslaw Polanski 《Journal of molecular modeling》2010,16(7):1205-1212
Isothiocyanates (ITC) are well-known chemopreventive agents extracted from vegetables. This activity results from the activation
of human oxidoreductase. In this letter, the uncompetitive activatory mechanism of ITC was investigated using docking and
molecular dynamics simulations. This indicates that NAD(P)H:quinone oxidoreductase can efficiently improve enzyme-substrate
recognition within the catalytic site if the ITC activator supports the interaction in the uncompetitive binding site. 相似文献
24.
25.
Dihydroneopterin aldolase (DHNA) catalyzes the conversion of 7,8-dihydroneopterin (DHNP) to 6-hydroxymethyl-7,8-dihydropterin (HP) and the epimerization of DHNP to 7,8-dihydromonopterin (DHMP). Although crystal structures of the enzyme from several microorganisms have been reported, no structural information is available about the critical interactions between DHNA and the trihydroxypropyl moiety of the substrate, which undergoes bond cleavage and formation. Here, we present the structures of Staphylococcus aureus DHNA (SaDHNA) in complex with neopterin (NP, an analog of DHNP) and with monapterin (MP, an analog of DHMP), filling the gap in the structural analysis of the enzyme. In combination with previously reported SaDHNA structures in its ligand-free form (PDB entry 1DHN) and in complex with HP (PDB entry 2DHN), four snapshots for the catalytic center assembly along the reaction pathway can be derived, advancing our knowledge about the molecular mechanism of SaDHNA-catalyzed reactions. An additional step appears to be necessary for the epimerization of DHMP to DHNP. Three active site residues (E22, K100, and Y54) function coordinately during catalysis: together, they organize the catalytic center assembly, and individually, each plays a central role at different stages of the catalytic cycle. 相似文献
26.
Brzostek A Dziadek B Rumijowska-Galewicz A Pawelczyk J Dziadek J 《FEMS microbiology letters》2007,275(1):106-112
Recent reports have indicated that cholesterol plays a crucial role during the uptake of mycobacteria by macrophages. However, the significance of cholesterol modification enzymes encoded by Mycobacterium tuberculosis for bacterial pathogenicity remains unknown. Here, the authors explored whether the well-known cholesterol modification enzyme, cholesterol oxidase (ChoD), is important for virulence of the tubercle bacillus. Homologous recombination was used to replace the choD gene from the M. tuberculosis genome with a nonfunctional copy. The resultant mutant (delta choD) was attenuated in peritoneal macrophages. No attenuation in macrophages was observed when the same strain was complemented with an intact choD gene controlled by a heat shock promoter (delta choDP(hsp)choD). The mice infection experiments confirm the significance of ChoD in the pathogenesis of M. tuberculosis. 相似文献
27.
Staszkiewicz J Skowronski MT Kaminski T Siawrys G Krazinski BE Kusmider M Przala J Okrasa S 《Animal reproduction science》2007,101(1-2):97-112
Previous studies have demonstrated the presence of endogenous opioid peptides (EOP) in the ovary and suggested their implication in local interactions within ovarian structures. Nevertheless, data pertaining to the expression of genes, coding for the opioid precursors, in ovarian cells are still rudimentary and not available for the pig. The study was undertaken to test whether genes of the opioid precursors - proopiomelanocortin (POMC), proenkephalin (PENK) and prodynorphin (PDYN) - are expressed in non-treated and gonadotropin-treated theca and granulosa cells isolated from ovarian follicles of the pig. The cells were isolated from small (days 15-16 of the estrous cycle) and large (days 19-20) porcine follicles. Dispersed cells were cultured in Eagle's medium under the water saturated atmosphere of 95% air and 5% CO(2), in the presence or absence of respective gonadotropin; theca cells with LH (100 ng/ml) and granulosa cells with FSH (100 ng/ml). Following 24h-incubation, the cells were harvested and the total RNA was isolated. The expression of genes coding for opioid precursors was estimated by the semi-quantitative RT-PCR technique involving co-amplification of the target cDNA (POMC, PENK or PDYN) and control cDNA (beta-actin or 18S rRNA). Specificities of PCR products were confirmed by Southern analysis and sequencing. In theca cells the expression of opioid precursors appeared to be gonadotropin-dependent except for PENK in the cells isolated from large follicles. In turn, granulosa cells exhibited the expression of POMC and PENK genes independently on treatment with FSH. This gonadotropin induced the expression of PDYN gene in granulosa cells isolated from small and large follicles and significantly increased POMC mRNA content in the cells from the large ones. The present studies indicate that porcine follicular cells (especially granulosa cells) may produce opioid peptides and that gonadotropins may modulate gene expression of their precursors in these cells. Moreover, our results support a participation of opioid peptides in the local regulations within ovarian follicle. 相似文献
28.
Ter Halle A Wiszniowski J Richard C 《Communications in agricultural and applied biological sciences》2007,72(2):45-52
Photochemistry is one of the main ways of pollutants degradation in the environment. There is an obvious lack of data concerning the photostability of agrochemicals on plant foliage. We report here the first photodegradation study of a triketonic herbicide (sulcotrione) used as a substitute of atrazine. To mimic surface Leaves, we used films made of carnauba grey wax or of cuticular wax extracted from maize Leaves. Under simulated solar light, sulcotrione was rapidly phototyzed. The phototysis was much faster on cuticular wax films than in aqueous phase. Moreover, the formulated sulcotrione (Mikado) disappeared even more quickly than the pure active ingredient. Sulcotrione mainly underwent an intramolecular cyclization. To validate these observations, sulcotrione and its main photoproduct were monitored after maize field treatment. The day after the treatment the main photoproduct was detected on the maize leaves and suLcotrione had already significantly disappeared. This experiment demonstrates that phototysis can be a relevant process in real conditions after field treatment. 相似文献
29.
Protein evolution is governed by processes that alter primary sequence but also the length of proteins. Protein length may change in different ways, but insertions, deletions and duplications are the most common. An optimal protein size is a trade‐off between sequence extension, which may change protein stability or lead to acquisition of a new function, and shrinkage that decreases metabolic cost of protein synthesis. Despite the general tendency for length conservation across orthologous proteins, the propensity to accept insertions and deletions is heterogeneous along the sequence. For example, protein regions rich in repetitive peptide motifs are well known to extensively vary their length across species. Here, we analyze length conservation of coiled‐coils, domains formed by an ubiquitous, repetitive peptide motif present in all domains of life, that frequently plays a structural role in the cell. We observed that, despite the repetitive nature, the length of coiled‐coil domains is generally highly conserved throughout the tree of life, even when the remaining parts of the protein change, including globular domains. Length conservation is independent of primary amino acid sequence variation, and represents a conservation of domain physical size. This suggests that the conservation of domain size is due to functional constraints. Proteins 2015; 83:2162–2169. © 2015 Wiley Periodicals, Inc. 相似文献