1,672 research outputs found

    Asymptotic Optimality Theory For Decentralized Sequential Multihypothesis Testing Problems

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    The Bayesian formulation of sequentially testing M3M \ge 3 hypotheses is studied in the context of a decentralized sensor network system. In such a system, local sensors observe raw observations and send quantized sensor messages to a fusion center which makes a final decision when stopping taking observations. Asymptotically optimal decentralized sequential tests are developed from a class of "two-stage" tests that allows the sensor network system to make a preliminary decision in the first stage and then optimize each local sensor quantizer accordingly in the second stage. It is shown that the optimal local quantizer at each local sensor in the second stage can be defined as a maximin quantizer which turns out to be a randomization of at most M1M-1 unambiguous likelihood quantizers (ULQ). We first present in detail our results for the system with a single sensor and binary sensor messages, and then extend to more general cases involving any finite alphabet sensor messages, multiple sensors, or composite hypotheses.Comment: 14 pages, 1 figure, submitted to IEEE Trans. Inf. Theor

    Decentralized Two-Sided Sequential Tests for A Normal Mean

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    This article is concerned with decentralized sequential testing of a normal mean μ\mu with two-sided alternatives. It is assumed that in a single-sensor network system with limited local memory, i.i.d. normal raw observations are observed at the local sensor, and quantized into binary messages that are sent to the fusion center, which makes a final decision between the null hypothesis H0:μ=0H_0: \mu = 0 and the alternative hypothesis H1:μ=±1.H_1: \mu = \pm 1. We propose a decentralized sequential test using the idea of tandem quantizers (or equivalently, a one-shot feedback). Surprisingly, our proposed test only uses the quantizers of the form I(Xnλ),I(X_{n} \ge \lambda), but it is shown to be asymptotically Bayes. Moreover, by adopting the principle of invariance, we also investigate decentralized invariant tests with the stationary quantizers of the form I(Xn>λ),I(|X_{n}| > \lambda), and show that λ=0.5\lambda = 0.5 only leads to a suboptimal decentralized invariant sequential test. Numerical simulations are conducted to support our arguments.Comment: 5 pages, conferenc

    Biosynthesis of caffeic acid in Escherichia coli using its endogenous hydroxylase complex

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    <p>Abstract</p> <p>Background</p> <p>Caffeic acid (3,4-dihydroxycinnamic acid) is a natural phenolic compound derived from the plant phenylpropanoid pathway. Caffeic acid and its phenethyl ester (CAPE) have attracted increasing attention for their various pharmaceutical properties and health-promoting effects. Nowadays, large-scale production of drugs or drug precursors via microbial approaches provides a promising alternative to chemical synthesis and extraction from plant sources.</p> <p>Results</p> <p>We first identified that an <it>Escherichia coli </it>native hydroxylase complex previously characterized as the 4-hydroxyphenylacetate 3-hydroxylase (4HPA3H) was able to convert <it>p</it>-coumaric acid to caffeic acid efficiently. This critical enzymatic step catalyzed in plants by a membrane-associated cytochrome P450 enzyme, <it>p</it>-coumarate 3-hydroxylase (C3H), is difficult to be functionally expressed in prokaryotic systems. Moreover, the performances of two tyrosine ammonia lyases (TALs) from <it>Rhodobacter </it>species were compared after overexpression in <it>E. coli</it>. The results indicated that the TAL from <it>R. capsulatus </it>(<it>Rc</it>) possesses higher activity towards both tyrosine and <it>L</it>-dopa. Based on these findings, we further designed a dual pathway leading from tyrosine to caffeic acid consisting of the enzymes 4HPA3H and <it>Rc</it>TAL. This heterologous pathway extended <it>E. coli </it>native tyrosine biosynthesis machinery and was able to produce caffeic acid (12.1 mg/L) in minimal salt medium. Further improvement in production was accomplished by boosting tyrosine biosynthesis in <it>E. coli</it>, which involved the alleviation of tyrosine-induced feedback inhibition and carbon flux redirection. Finally, the titer of caffeic acid reached 50.2 mg/L in shake flasks after 48-hour cultivation.</p> <p>Conclusion</p> <p>We have successfully established a novel pathway and constructed an <it>E. coli </it>strain for the production of caffeic acid. This work forms a basis for further improvement in production, as well as opens the possibility of microbial synthesis of more complex plant secondary metabolites derived from caffeic acid. In addition, we have identified that TAL is the rate-limiting enzyme in this pathway. Thus, exploration for more active TALs via bio-prospecting and protein engineering approaches is necessary for further improvement of caffeic acid production.</p

    Dehydratase mediated 1-propanol production in metabolically engineered Escherichia coli

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    Abstract Background With the increasing consumption of fossil fuels, the question of meeting the global energy demand is of great importance in the near future. As an effective solution, production of higher alcohols from renewable sources by microorganisms has been proposed to address both energy crisis and environmental concerns. Higher alcohols contain more than two carbon atoms and have better physiochemical properties than ethanol as fuel substitutes. Results We designed a novel 1-propanol metabolic pathway by expanding the well-known 1,2-propanediol pathway with two more enzymatic steps catalyzed by a 1,2-propanediol dehydratase and an alcohol dehydrogenase. In order to engineer the pathway into E. coli, we evaluated the activities of eight different methylglyoxal synthases which play crucial roles in shunting carbon flux from glycolysis towards 1-propanol biosynthesis, as well as two secondary alcohol dehydrogenases of different origins that reduce both methylglyoxal and hydroxyacetone. It is evident from our results that the most active enzymes are the methylglyoxal synthase from Bacillus subtilis and the secondary alcohol dehydrogenase from Klebsiella pneumoniae, encoded by mgsA and budC respectively. With the expression of these two genes and the E. coli ydjG encoding methylglyoxal reductase, we achieved the production of 1,2-propanediol at 0.8 g/L in shake flask experiments. We then characterized the catalytic efficiency of three different diol dehydratases on 1,2-propanediol and identified the optimal one as the 1,2-propanediol dehydratase from Klebsiella oxytoca, encoded by the operon ppdABC. Co-expressing this enzyme with the above 1,2-propanediol pathway in wild type E. coli resulted in the production of 1-propanol at a titer of 0.25 g/L. Conclusions We have successfully established a new pathway for 1-propanol production by shunting the carbon flux from glycolysis. To our knowledge, it is the first time that this pathway has been utilized to produce 1-propanol in E. coli. The work presented here forms a basis for further improvement in production. We speculate that dragging more carbon flux towards methylglyoxal by manipulating glycolytic pathway and eliminating competing pathways such as lactate generation can further enhance the production of 1-propanol.</p

    Probing Triple-W Production and Anomalous WWWW Coupling at the CERN LHC and future 100TeV proton-proton collider

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    Triple gauge boson production at the LHC can be used to test the robustness of the Standard Model and provide useful information for VBF di-boson scattering measurement. Especially, any derivations from SM prediction will indicate possible new physics. In this paper we present a detailed Monte Carlo study on measuring WWW production in pure leptonic and semileptonic decays, and probing anomalous quartic gauge WWWW couplings at the CERN LHC and future hadron collider, with parton shower and detector simulation effects taken into account. Apart from cut-based method, multivariate boosted decision tree method has been exploited for possible improvement. For the leptonic decay channel, our results show that at the sqrt{s}=8(14)[100] TeV pp collider with integrated luminosity of 20(100)[3000] fb-1, one can reach a significance of 0.4(1.2)[10]sigma to observe the SM WWW production. For the semileptonic decay channel, one can have 0.5(2)[14]sigma to observe the SM WWW production. We also give constraints on relevant Dim-8 anomalous WWWW coupling parameters.Comment: Accepted version by JHE

    Biosynthesis of isoprenoids, polyunsaturated fatty acids and flavonoids in Saccharomyces cerevisiae

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    Industrial biotechnology employs the controlled use of microorganisms for the production of synthetic chemicals or simple biomass that can further be used in a diverse array of applications that span the pharmaceutical, chemical and nutraceutical industries. Recent advances in metagenomics and in the incorporation of entire biosynthetic pathways into Saccharomyces cerevisiae have greatly expanded both the fitness and the repertoire of biochemicals that can be synthesized from this popular microorganism. Further, the availability of the S. cerevisiae entire genome sequence allows the application of systems biology approaches for improving its enormous biosynthetic potential. In this review, we will describe some of the efforts on using S. cerevisiae as a cell factory for the biosynthesis of high-value natural products that belong to the families of isoprenoids, flavonoids and long chain polyunsaturated fatty acids. As natural products are increasingly becoming the center of attention of the pharmaceutical and nutraceutical industries, the use of S. cerevisiae for their production is only expected to expand in the future, further allowing the biosynthesis of novel molecular structures with unique properties
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