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21.
Microbial metabolomics: past,present and future methodologies 总被引:1,自引:0,他引:1
Mashego MR Rumbold K De Mey M Vandamme E Soetaert W Heijnen JJ 《Biotechnology letters》2007,29(1):1-16
Microbial metabolomics has received much attention in recent years mainly because it supports and complements a wide range
of microbial research areas from new drug discovery efforts to metabolic engineering. Broadly, the term metabolomics refers
to the comprehensive (qualitative and quantitative) analysis of the complete set of all low molecular weight metabolites present
in and around growing cells at a given time during their growth or production cycle. This review focuses on the past, current
and future development of various experimental protocols in the rapid developing area of metabolomics in the ongoing quest
to reliably quantify microbial metabolites formed under defined physiological conditions. These developments range from rapid
sample collection, instant quenching of microbial metabolic activity, extraction of the relevant intracellular metabolites
as well as quantification of these metabolites using enzyme based and or modern high tech hyphenated analytical protocols,
mainly chromatographic techniques coupled to mass spectrometry (LC-MSn, GC-MSn, CE-MSn), where n indicates the number of tandem mass spectrometry, and nuclear magnetic resonance spectroscopy (NMR). 相似文献
22.
Quorum sensing is a bacterial mechanism used to synchronize the coordinated response of a microbial population. Because quorum sensing in Gram-negative bacteria depends on release and detection of a diffusible signaling molecule (autoinducer) among a multicellular group, it is considered a simple form of cell-cell communication for the purposes of mathematical analysis. Stochastic equation systems have provided a common approach to model biochemical or biophysical processes. Recently, the effect of noise to synchronize a specific homogeneous quorum sensing network was successfully modeled using a stochastic equation system with fixed parameters. The question remains of how to model quorum sensing networks in a general setting. To address this question, we first set a stochastic equation system as a general model for a heterogeneous quorum sensing network. Then, using two relevant biophysical characteristics of Gram-negative bacteria (the permeability of the cell membrane to the autoinducer and the symmetry of autoinducer diffusion) we construct the solution of the stochastic equation system at an abstract level. The solution indicates that stable synchronization of a quorum sensing network is robustly induced by an environment with a heterogenous distribution of extracellular and intracellular noise. The synchronization is independent of the initial state of the system and is solely the result of the connectivity of the cell network established through the effects of extracellular noise. 相似文献
23.
我国马铃薯软腐病防治的研究进展 总被引:1,自引:0,他引:1
马铃薯软腐病是马铃薯细菌性病害中最严重的一种,简要介绍了我国马铃薯软腐病的病原菌、病害性状以及对病害的防治方法。利用现代生物技术手段人为地操纵细菌群体感应系统,将会成为提高植物抗病性的新方法、新途径。 相似文献
24.
目的观察LuxS基因缺失后变形链球菌生物膜成熟初期的变化情况。方法通过扫描电镜观察标准菌和缺陷菌在不同营养环境中生物膜成熟初期的形成情况。结果对不同营养环境中形成的生物膜观察,发现在富含蔗糖的环境中,缺陷菌成熟初期的生物膜形成能力较标准菌弱。结论 LuxS基因缺失后变形链球菌在蔗糖环境中生物膜形成的能力减弱。 相似文献
25.
群体感应信号分子及其抑制剂快速检测方法的建立 总被引:2,自引:0,他引:2
细菌能自发产生、释放一些特定的信号分子,并能感知其浓度变化,调节微生物的群体行为,这一调控系统称为群体感应。细菌群体感应参与包括人类、动植物病原菌致病力在内的多种生物学功能的调节,群体感应抑制剂成为抗感染药物开发的靶点。利用紫色色杆菌(Chromobacterium violaceum)和根癌农杆菌(Agrobacterium tumefaciens)作为指示菌,建立检测高丝氨酸内酯(AHLs)及其抑制剂的简便方法。结果表明,通过平板交叉划线接种,使用指示菌能够有效地检测AHLs,并且通过薄层层析(TLC)与细菌生物感应器相结合的方法可以快速、方便地鉴定AHLs的种类;通过双层平板法观察指示菌色素产生情况,能够有效地检测群体感应信号分子AHLs抑制剂,且该方法简单易行。 相似文献
26.
The bacterial cell to cell signalling system known as quorum sensing (QS) is essential for the regulation of virulence in
many pathogens and offers a specific biochemical target for novel antibacterial therapies. Expanding on earlier work, in which
consideration was given to the primary QS system (lasR system) in a homogeneous population of the common human pathogen Pseudomonas aeruginosa, we build a simple spatial model of an early-stage P. aeruginosa biofilm subject to treatment with topically applied anti-QS drugs (of two specific kinds) and conventional antibiotics. In
the case of a slowly growing biofilm we show that both kinds of anti-quorum sensing drug are effective in reducing the level
of the relevant signal molecule (3-oxo-C12-homoserine lactone; henceforth AHL), in each case obtaining an explicit bound on
the steady-state AHL profile in terms of a prescribed surface drug concentration. Using numerical methods, we are also able
to reproduce the hysteretic phenomena exhibited by the homogeneous model, in particular showing that for each kind of anti-QS
drug there is a parameter regime in which a catastrophic collapse occurs in the steady-state AHL concentration as the surface
drug concentration passes some critical value; an alternative way of interpreting this result is to say that, for a prescribed
surface drug concentration, there is a critical biofilm depth such that treatment is successful until this depth is reached,
but fails thereafter. In the thick-biofilm limit we show that the critical concentration of each drug increases exponentially
with the biofilm thickness (or, conversely, that the critical depth increases logarithmically with surface drug concentration);
this is dramatically different to the behaviour observed in the corresponding homogeneous model, where the critical concentrations
grow linearly with bacterial carrying capacity, and thus highlights the relative difficulty of treating a large, spatially-structured
population with diffusing antibacterials. 相似文献
27.
Pseudomonas aeruginosa and species of the Burkholderia cepacia complex are the primary bacterial pathogens contributing to lung disease in patients with cystic fibrosis. Quorum sensing systems using N-acyl homoserine lactone (AHL) signal molecules are involved in the regulation of a number of virulence factors in these species. Extracts of mucopurulent respiratory secretions from 13 cystic fibrosis patients infected with P. aeruginosa and/or strains of the B. cepacia complex were fractionated using reverse-phase fast pressure liquid chromatography and analyzed for the presence of AHLs using a traI-luxCDABE-based reporter that responds to AHLs with acyl chains ranging between 4 and 12 carbons. Using this assay system, a broad range of AHLs were detected and identified despite being present at low concentrations in limited sample volumes. N-(3-oxo-dodecanoyl)-l-homoserine lactone, N-(3-oxo-decanoyl)-l-homoserine lactone and N-octanoyl-l-homoserine lactone (OHL) were the AHLs most frequently identified. OHL and N-decanoyl-l-homoserine lactone were detected in nanomolar concentrations compared to picomolar amounts of the 3-oxo-derivatives of the AHLs identified. 相似文献
28.
Adjele Wilson James N. Kinney Petrus H. Zwart Claire Punginelli Sandrine D'Haene Fran?ois Perreau Michael G. Klein Diana Kirilovsky Cheryl A. Kerfeld 《The Journal of biological chemistry》2010,285(24):18364-18375
The photoprotective processes of photosynthetic organisms involve the dissipation of excess absorbed light energy as heat. Photoprotection in cyanobacteria is mechanistically distinct from that in plants; it involves the orange carotenoid protein (OCP), a water-soluble protein containing a single carotenoid. The OCP is a new member of the family of blue light-photoactive proteins; blue-green light triggers the OCP-mediated photoprotective response. Here we report structural and functional characterization of the wild type and two mutant forms of the OCP, from the model organism Synechocystis PCC6803. The structural analysis provides high resolution detail of the carotenoid-protein interactions that underlie the optical properties of the OCP, unique among carotenoid-proteins in binding a single pigment per polypeptide chain. Collectively, these data implicate several key amino acids in the function of the OCP and reveal that the photoconversion and photoprotective responses of the OCP to blue-green light can be decoupled. 相似文献
29.
30.
Acyl-homoserine lactone (HSL) quorum sensing molecules play an important role in regulation of virulence gene expression in Pseudomonas aeruginosa. Here, we show that 3O-C(12)-HSL can disrupt barrier integrity in human epithelial Caco-2 cells as evidenced by decreased transepithelial electrical resistance (TER), increased paracellular flux, reduction in the expression and distribution of ZO-1 and occludin, and reorganization of F-actin. P. aeruginosa 3O-C(12)-HSL activate p38 and p42/44 kinases, and inhibition of these kinases partly prevented 3O-C(12)-HSL-induced changes in TER, paracellular flux and expression of occludin and ZO-1. These findings demonstrate that P. aeruginosa 3O-C(12)-HSL can modulate tight junction integrity of Caco-2 cells. 相似文献