170 research outputs found

    Chemical Characteristics of Electron Shuttles Affect Extracellular Electron Transfer: Shewanella decolorationis NTOU1 Simultaneously Exploiting Acetate and Mediators

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    In the present study, we found that our isolate Shewanella decolorationis NTOU1 is able to degrade acetate under anaerobic condition with concomitant implementation of extracellular electron transfer (EET). With +0.63 V (vs. SHE) poised on the anode, in a 72-h experiment digesting acetate, only 2 mM acetate was consumed, which provides 6% of the electron equivalents derived from the initial substrate mass to support biomass (5%) and current generation (1%). To clarify the effects on EET of the addition of electron-shuttles, riboflavin, anthraquinone-2,6-disulfonate (AQDS), hexaammineruthenium, and hexacyanoferrate were selected to be spiked into the electrochemical cell in four individual experiments. It was found that the mediators with proton-associated characteristics (i.e., riboflavin and AQDS) would not enhance current generation, but the metal-complex mediators (i.e., hexaammineruthenium, and hexacyanoferrate) significantly enhanced current generation as the concentration increased. According to the results of electrochemical analyses, the i-V graphs represent that the catalytic current induced by the primitive electron shuttles started at the onset potential of −0.27 V and continued increasing until +0.73 V. In the riboflavin-addition experiment, the catalytic current initiated at the same potential but rapid saturated beyond −0.07 V; this indicated that the addition of riboflavin affects mediator secretion by S. decolorationis NTOU1. It was also found that the current was eliminated after adding 48 mM N-acetyl-L-methionine (i.e., the cytochrome inhibitor) when using acetate as a substrate, indicating the importance of outer-membrane cytochrome

    Search for an Invisibly Decaying Z\u27 Boson at Belle II in e⁺e⁻ → μ⁺μ⁻(e±^{\pm}μ^{\mp}) Plus Missing Energy Final States

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    Measurements of the branching fractions for BKγB \to K^{*}\gamma decays at Belle II

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    This paper reports a study of BKγB \to K^{*}\gamma decays using 62.8±0.662.8\pm 0.6 fb1^{-1} of data collected during 2019--2020 by the Belle II experiment at the SuperKEKB e+ee^{+}e^{-} asymmetric-energy collider, corresponding to (68.2±0.8)×106(68.2 \pm 0.8) \times 10^6 BBB\overline{B} events. We find 454±28454 \pm 28, 50±1050 \pm 10, 169±18169 \pm 18, and 160±17160 \pm 17 signal events in the decay modes B0K0[K+π]γB^{0} \to K^{*0}[K^{+}\pi^{-}]\gamma, B0K0[KS0π0]γB^{0} \to K^{*0}[K^0_{\rm S}\pi^{0}]\gamma, B+K+[K+π0]γB^{+} \to K^{*+}[K^{+}\pi^{0}]\gamma, and B+K+[K+π0]γB^{+} \to K^{*+}[K^{+}\pi^{0}]\gamma, respectively. The uncertainties quoted for the signal yield are statistical only. We report the branching fractions of these decays: B[B0K0[K+π]γ]=(4.5±0.3±0.2)×105,\mathcal{B} [B^{0} \to K^{*0}[K^{+}\pi^{-}]\gamma] = (4.5 \pm 0.3 \pm 0.2) \times 10^{-5}, B[B0K0[KS0π0]γ]=(4.4±0.9±0.6)×105,\mathcal{B} [B^{0} \to K^{*0}[K^0_{\rm S}\pi^{0}]\gamma] = (4.4 \pm 0.9 \pm 0.6) \times 10^{-5}, B[B+K+[K+π0]γ]=(5.0±0.5±0.4)×105, and\mathcal{B} [B^{+} \to K^{*+}[K^{+}\pi^{0}]\gamma] = (5.0 \pm 0.5 \pm 0.4)\times 10^{-5},\text{ and} B[B+K+[KS0π+]γ]=(5.4±0.6±0.4)×105,\mathcal{B} [B^{+} \to K^{*+}[K^0_{\rm S}\pi^{+}]\gamma] = (5.4 \pm 0.6 \pm 0.4) \times 10^{-5}, where the first uncertainty is statistical, and the second is systematic. The results are consistent with world-average values

    Measurement of the integrated luminosity of the Phase 2 data of the Belle II experiment

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    From April to July 2018, a data sample at the peak energy of the γ(4S) resonance was collected with the Belle II detector at the SuperKEKB electron-positron collider. This is the first data sample of the Belle II experiment. Using Bhabha and digamma events, we measure the integrated luminosity of the data sample to be (496.3 ± 0.3 ± 3.0) pb-1, where the first uncertainty is statistical and the second is systematic. This work provides a basis for future luminosity measurements at Belle II

    Anaerobic biotransformation of pyridine in estuarine sediments

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