15 research outputs found

    Flux-sum analysis: a metabolite-centric approach for understanding the metabolic network

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    <p>Abstract</p> <p>Background</p> <p>Constraint-based flux analysis of metabolic network model quantifies the reaction flux distribution to characterize the state of cellular metabolism. However, metabolites are key players in the metabolic network and the current reaction-centric approach may not account for the effect of metabolite perturbation on the cellular physiology due to the inherent limitation in model formulation. Thus, it would be practical to incorporate the metabolite states into the model for the analysis of the network.</p> <p>Results</p> <p>Presented herein is a metabolite-centric approach of analyzing the metabolic network by including the turnover rate of metabolite, known as flux-sum, as key descriptive variable within the model formulation. By doing so, the effect of varying metabolite flux-sum on physiological change can be simulated by resorting to mixed integer linear programming. From the results, we could classify various metabolite types based on the flux-sum profile. Using the <it>i</it>AF1260 <it>in silico </it>metabolic model of <it>Escherichia coli</it>, we demonstrated that this novel concept complements the conventional reaction-centric analysis.</p> <p>Conclusions</p> <p>Metabolite flux-sum analysis elucidates the roles of metabolites in the network. In addition, this metabolite perturbation analysis identifies the key metabolites, implicating practical application which is achievable through metabolite flux-sum manipulation in the areas of biotechnology and biomedical research.</p

    Treatment of complicated skin and soft-tissue infections caused by resistant bacteria: value of linezolid, tigecycline, daptomycin and vancomycin

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    Antibiotic-resistant organisms causing both hospital-and community-acquired complicated skin and soft-tissue infections (cSSTI) are increasingly reported. A substantial medical and economical burden associated with MRSA colonisation or infection has been documented. The number of currently available appropriate antimicrobial agents is limited. Good quality randomised, controlled clinical trial data on antibiotic efficacy and safety is available for cSSTI caused by MRSA. Linezolid, tigecycline, daptomycin and vancomycin showed efficacy and safety in MRSA-caused cSSTI. None of these drugs showed significant superiority in terms of clinical cure and eradication rates. To date, linezolid offers by far the greatest number of patients included in controlled trials with a strong tendency of superiority over vancomycin in terms of eradication and clinical success

    Multi-Tree Decomposition Methods for Large-Scale Mixed Integer Nonlinear Optimization

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    Most industrial optimization problems are sparse and can be formulated as block-separable mixed-integer nonlinear programming (MINLP) problems, defined by linking low-dimensional sub-problems by (linear) coupling constraints. Decomposition methods solve a block-separable MINLP by alternately solving master problems and sub-problems. In practice, decomposition methods are sometimes the only possibility to compute high-quality solutions of large-scale optimization problems. However, efficient implementations may require expert knowledge and problem-specific features. Recently, there is renewed interest in making these methods accessible to general users by developing generic decomposition frameworks and modelling support. The focus of this chapter is on so-called multi-tree decomposition methods, which iteratively approximate the feasible area without using a single (global) branch-and-bound tree, i.e. branch-and-bound is only used for solving sub-problems. After an introduction, we describe first outer approximation (OA) decomposition methods, including the adaptive, multivariate partitioning (AMP) and the novel decomposition-based outer approximation (DECOA) algorithm . This is followed by a description of multi-tree methods using a reduced master problem for solving large-scale industrial optimization problems. The first method to be described applies parallel column generation (CG) and iterative fixing for solving nonconvex transport optimization problems with several hundred millions of variables and constraints. The second method is based on a novel approach combining CG and compact outer approximation. The last methodology to be discussed is the general Benders decomposition method for globally solving large nonconvex stochastic programs using a reduced mixed-integer programming (MIP) master problem
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