超高产杂交水稻皮秒分辨荧光特性

采用时间分辨荧光光谱测试系统，研究了超高产杂交水稻(Oryza sativa L.)两优培九(P9)和对照汕优63(SH 63)类囊体膜的荧光光谱特性和时间特性。以脉宽为120ps，重复率为4MHz，波长为514nm的Ar^-激光分别激发P9和SH 63水稻类囊体膜荧光。通过对其超快荧光的时间特性和光谱特性比较研究发现：无论是在灌浆期还是在扬花期，P9水稻类囊体膜中光系统I激发能传递的速度比光系统Ⅱ的快；P9和SH 63两种水稻类囊体膜在灌浆期的激发能传递速度都比扬花期的快；两种水稻类囊体膜的光谱特性还给出，在从扬花期到灌浆期这一生长发育过程中，SH63水稻类囊体膜的色素成分和结合状态发生了变化，而P9却没有出现这种变化。     

Enhanced-contrast two-photon optogenetic pH sensing and pH-resolved brain imaging

We present experiments on cell cultures and brain slices that demonstrate two-photon optogenetic pH sensing and pH-resolved brain imaging using a laser driver whose spectrum is carefully tailored to provide the maximum contrast of a ratiometric two-photon fluorescence readout from a high-brightness genetically encoded yellow-fluorescent-protein-based sensor, SypHer3s. Two spectrally isolated components of this laser field are set to induce two-photon-excited fluorescence (2PEF) by driving SypHer3s through one of two excitation pathways—via either the protonated or deprotonated states of its chromophore. With the spectrum of the laser field accurately adjusted for a maximum contrast of these two 2PEF signals, the ratio of their intensities is shown to provide a remarkably broad dynamic range for pH measurements, enabling high-contrast optogenetic deep-brain pH sensing and pH-resolved 2PEF imaging within a vast class of biological systems, ranging from cell cultures to the living brain.     

Shade adaptation in cyanobacteria

Growth of Anacystis in high light in the presence of sublethal concentrations of DCMU-type inhibitors leads to an increased synthesis of phycocyanin paralleled by a reduced rate of ³⁵S methionine incorporation into the D1 protein compared to the high light controls, as is characteristic for naturally-induced shade phenotype. On the contrary, sun phenotype is characterized by a low rate of antenna synthesis, but a high rate of ³⁵S methionine incorporation into the D1 protein.Room temperature excitation spectra of 684 nm fluorescence emission clearly demonstrate the participation of the extraordinarily high concentration of phycocyanin in artificially shade-adapted cells in excitation energy transfer to chlorophyll.It could be shown that the development of shade-type appearance is not simply the consequence of an imbalance in electron transport, since an addition of thiosulphate to cultures growing in high light in the presence of DCMU-type inhibitors can only partially prevent or revert the change from sun to artificial-herbicide-induced-shade phenotype. This is regarded as evidence that the dynamic herbicide-binding D1 protein itself may play a role as a light meter in the process of natural shade adaptation, the rate of its degradation and resynthesis possibly giving the signal for the adaptive reorganization of the photosynthetic apparatus. The chain of signal transduction remains to be established.Abbreviations atrazine 2-chloro-4-(ethylamino)-6-(isopropylamino)-s-triazine - chl chlorophyll - D1 reaction center polypeptide carrying the secondary plastoquinone electron acceptor of PS II - DCMU 3-(3,4-dichlorophenyl)-1,1-dimethylurea - PAGE polyacrylamide gel electrophoresis - PAR photosynthetically active radiation - PC phycocyanin - PCC Pasteur Culture Collection - PS photosystem - Q_B secondary plastoquinone electron acceptor of PS II - SAUG Sammlung von Algenkulturen am Pflanzenphysiologischen Institut der Universtität Göttingen - SDS sodium dodecyl sulphate Dedicated to Professor Wilhelm Menke on the occasion of his 80th birthday.     

Short term effect of ultraviolet-B radiation on photosystem 2 photochemistry in the cyanobacteriumSynechococcus 6301

Exposure of intact cells of theSynechococcus 6301 to UV-B radiation induced a loss in photosystem 2 (PS 2) electron transport activity prior to the alteration in pigment complexes. Thus the degradation of PS 2 was not directly related to pigment alteration. Supported by Young Scientist grant No. SRJSYIB-05192 from the Department of Science and Technology, Goverment of India to SDSM.     

A quantitative description of fluorescence excitation spectra in intact bean leaves greened under intermittent light

We present a simple approach for the calculation of in vivo fluorescence excitation spectra from measured absorbance spectra of the isolated pigments involved. Taking into account shading of the pigments by each other, energy transfer from carotene to chlorophyll a, and light scattering by the leaf tissue, we arrive at a model function with 6 free parameters. Fitting them to the measured fluorescence excitation spectrum yields good correspondence between theory and experiment, and parameter estimates which agree with independent measurements. The results are discussed with respect to the origin and the interpretation of in vivo excitation spectra in general.     

The relationship of intercompartmental excitation transfer rate constants to those of an underlying physical model

In studies on photosynthetic systems it is common practice to interpret the results of time-resolved fluorescence experiments on the basis of compartmental, or target, models. Each compartment represents a group of molecules with similar fluorescence characteristics. In cases of practical interest, the members of each compartment are spatially contiguous and make up part of an overall energy-transferring system. Since a rate constant describing the overall transfer between compartments is not that of any pair of molecules in the system, this question naturally rises: what do we learn about the microscopic structure from these data? In this note we introduce ‘compartment melting’, a smooth mathematical connection between the compartmental and microscopic levels. We then show, on the basis of model calculations on finite lattices in one, two, and three dimensions, that average microscopic rates at the interfaces between compartments may be estimated from observed intercompartmental rates. The estimate involves a modest number of structural assumptions about the system. As examples of the method, which is applicable mainly to systems containing homogeneous pigment pools, some recent chlorophyll-protein antenna studies are analyzed.