2,114 research outputs found

    Picosecond time-resolved fluorescence spectra of photosystem I and II in Chlorella pyrenoidosa

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    AbstractPicosecond time-resolved fluorescence spectra emitted from intact cells of the green alga Chlorella pyrenoidosa have been measured by means of a new detection technique using a microchannel-plate photomultiplier. A fluorescence band (F700) was observed at 690–730 nm in the initial time region (0–180 ps), in addition to the well-known spectrum (F685) of photosystem II (PS II)-chlorophyll a (Chla) with a peak at 685 nm. F700 decays rapidly with lifetime of 104 ps, while F685 decays much more slowly in bi-exponential form with lifetimes of 0.64 and 1.7 ns. Appearance of F700 is independent of closure of the reaction center II (RC II). F700 is thus assigned to the fluorescence from PS I-Chl a, whose decay is governed by a fast energy transfer process from the antenna Chl aof PS I to P700 of RC I

    Model for the hydration of non-polar compounds and polymers

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    We introduce an exactly solvable statistical-mechanical model of the hydration of non-polar compounds, based on grouping water molecules in clusters where hydrogen bonds and isotropic interactions occur; interactions between clusters are neglected. Analytical results show that an effective strengthening of hydrogen bonds in the presence of the solute, together with a geometric reorganization of water molecules, are enough to yield hydrophobic behavior. We extend our model to describe a non-polar homopolymer in aqueous solution, obtaining a clear evidence of both ``cold'' and ``warm'' swelling transitions. This suggests that our model could be relevant to describe some features of protein folding.Comment: REVTeX, 6 pages, 3 figure

    Circadian Clock Synchronization of the Cell Cycle in Zebrafish Occurs through a Gating Mechanism Rather Than a Period-phase Locking Process

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    Studies from a number of model systems have shown that the circadian clock controls expression of key cell cycle checkpoints, thus providing permissive or inhibitory windows in which specific cell cycle events can occur. However, a major question remains: Is the clock actually regulating the cell cycle through such a gating mechanism or, alternatively, is there a coupling process that controls the speed of cell cycle progression? Using our light-responsive zebrafish cell lines, we address this issue directly by synchronizing the cell cycle in culture simply by changing the entraining light-dark (LD) cycle in the incubator without the need for pharmacological intervention. Our results show that the cell cycle rapidly reentrains to a shifted LD cycle within 36 h, with changes in p21 expression and subsequent S phase timing occurring within the first few hours of resetting. Reentrainment of mitosis appears to lag S phase resetting by 1 circadian cycle. The range of entrainment of the zebrafish clock to differing LD cycles is large, from 16 to 32 hour periods. We exploited this feature to explore cell cycle entrainment at both the population and single cell levels. At the population level, cell cycle length is shortened or lengthened under corresponding T-cycles, suggesting that a 1:1 coupling mechanism is capable of either speeding up or slowing down the cell cycle. However, analysis at the single cell level reveals that this, in fact, is not true and that a gating mechanism is the fundamental method of timed cell cycle regulation in zebrafish. Cell cycle length at the single cell level is virtually unaltered with varying T-cycles

    Effect of Kanji and Kana Reading on Cerebral Blood Flow

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    開始ページ、終了ページ: 冊子体のページ付

    Why is TeV-scale a geometric mean of neutrino mass and GUT-scale?

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    Among three typical energy scales, a neutrino mass scale (mνm_\nu\sim 0.1 eV), a GUT scale (MGUT1016M_{GUT}\sim 10^{16} GeV), and a TeV-scale (MNP1M_{NP}\sim 1 TeV), there is a fascinating relation of MNPmνMGUTM_{NP}\simeq \sqrt{m_\nu\cdot M_{GUT}}. The TeV-scale, MNPM_{NP}, is a new physics scale beyond the standard model which is regarded as supersymmetry in this letter. We suggest a simple supersymmetric neutrinophilic Higgs doublet model, which realizes the above relation dynamically as well as the suitable mνm_\nu through a tiny vacuum expectation value of neutrinophilic Higgs without additional scales other than MNPM_{NP} and MGUTM_{GUT}. A gauge coupling unification, which is an excellent feature in the supersymmetric standard model, is preserved automatically in this setup.Comment: 7 page
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