The STN8 kinase‐PBCP phosphatase system is responsible for high‐light‐induced reversible phosphorylation of the PSII inner antenna subunit CP29 in rice

Reversible phosphorylation of thylakoid light‐harvesting proteins is a mechanism to compensate for unbalanced excitation of photosystem I (PSI) versus photosystem II (PSII) under limiting light. In monocots, an additional phosphorylation event on the PSII antenna CP29 occurs upon exposure to excess light, enhancing resistance to light stress. Different from the case of the major LHCII antenna complex, the STN7 kinase and its related PPH1 phosphatase were proven not to be involved in CP29 phosphorylation, indicating that a different set of enzymes act in the high‐light (HL) response. Here, we analyze a rice stn8 mutant in which both PSII core proteins and CP29 phosphorylation are suppressed in HL, implying that STN8 is the kinase catalyzing this reaction. In order to identify the phosphatase involved, we produced a recombinant enzyme encoded by the rice ortholog of AtPBCP, antagonist of AtSTN8, which catalyzes the dephosphorylation of PSII core proteins. The recombinant protein was active in dephosphorylating P‐CP29. Based on these data, we propose that the activities of the OsSTN8 kinase and the antagonistic OsPBCP phosphatase, in addition to being involved in the repair of photo‐damaged PSII, are also responsible for the HL‐dependent reversible phosphorylation of the inner antenna CP29.     

夜间低温对番茄幼苗磷素吸收及转运的影响

以‘辽园多丽’番茄幼苗为试材,采用营养液栽培模式,以夜温15℃为对照,对夜间低温(6℃)影响番茄幼苗磷素吸收及转运过程的因素进行研究。结果显示:(1)夜间低温胁迫导致番茄幼苗根系活力受到显著抑制。(2)夜间低温条件下,番茄幼苗根系中酸性磷酸酶活性无明显变化,而其地上部酸性磷酸酶活性增强,且以叶片中活性增加较大。(3)夜间低温胁迫使根系中磷酸盐转运蛋白基因LePT1和LePT2的相对表达量较对照增加,地上部磷酸盐转运蛋白基因LePT1的表达受到抑制,且叶片中受到的抑制作用更显著。(4)夜间低温胁迫处理营养液中剩余磷素含量始终多于对照;其番茄幼苗地下部和地上部中磷素绝对含量均下降,且叶片比茎的下降幅度更大。(5)夜间低温胁迫使番茄幼苗伤流强度下降,伤流液中磷素含量随着处理天数的增加而增加,在处理第9天时极显著高于对照。研究表明,夜间低温导致番茄幼苗根系活力降低,诱导植株中磷酸盐转运蛋白基因LePT1的表达下调以及伤流强度降低,从而引起磷素由茎向叶片中的转运过程受到明显抑制。     

Modelling of temperature-controlled internode elongation applied to chrysanthemum

The DIF concept states that equal internode length can be achieved with the same difference between day and night temperature irrespective of the mean 24 h temperature. However, the physiological background of the DIF concept is unclear. An attempt to model internode elongation is presented based on three plausible processes, namely (1) the accumulation of elongation requirements during the day, (2) elongation during the night using elongation requirements and (3) the limitation of internode length due to low turgor pressure unable to counter cell wall elasticity. Each reaction rate constant, one per process, depends on temperature according to Arrhenius' Law. The resulting process-based model describes internode elongation in time and was calibrated on a chrysanthemum data set. Chrysanthemum plants were grown in growth chambers with rigorously defined day and night temperatures. In total, 16 temperature treatments were applied, resulting from the combination of four day and four night temperatures (16, 20, 24 and 28 degrees C). Internode elongation was measured for the tenth internode in ten plants per treatment. The percentage variance accounted for, R2adj, was almost 91%. Transferability of model parameters was shown to exist by cross validation. Simulation of the internode length in time as function of mean 24 h temperature and DIF showed that the DIF concept is not apparent after a growing period of 10 d, but is visible after 20 d. This model structure for describing internode elongation might also be applicable for other plants that show the DIF concept.     

A novel UV laser-induced visible blue radiation from protein crystals and aggregates: scattering artifacts or fluorescence transitions of peptide electrons delocalized through hydrogen bonding?

Proteins lacking prosthetic groups and/or cofactors are known to undergo electronic excitation transitions only upon exposure to UV-C (< 280 nm) and UV-B (280-320 nm), but not UV-A (320-400 nm) photons. Here, we report the discovery of a novel excitation that peaks at approximately 340 nm and yields visible violet-blue radiation with apparent band maxima at approximately 425, 445, 470, and 500 nm. All proteins and large polypeptides examined in solid form, and in solutions, display this quenchable and photobleachable radiation which can be established not owing to aromatic sidechains. As a note of caution, we wish to state that we have not been able to completely eliminate the possibility that the radiation may be an artifact owing to second order effects such as, e.g., Raman scattering of Raman-scattered photons; however, we assert that all our experiments indicate that the radiation actually owes to some form of fluorescence. We propose that peptide electrons that have been delocalized through intramolecular or intermolecular hydrogen bond formation display these long-wavelength electronic transitions. If confirmed by future studies, this preliminary discovery may turn out to have important implications for biomolecular spectroscopy, protein crystallography, and materials science.     

去果河套蜜瓜源叶碳水化合物及其相关酶昼夜变化特征

以河套蜜瓜为试材,在果实迅速膨大期通过去果处理改变库源关系,研究源叶净光合速率,蔗糖、还原糖和淀粉含量及其代谢相关酶活性的昼夜变化规律。结果表明:(1)源叶的净光合速率为单峰曲线,无明显的"光合午休"现象,去果处理对其无影响。(2)源叶中蔗糖和还原糖含量的昼夜变化为单峰曲线,蔗糖磷酸合成酶和蔗糖合成酶合成方向活性的昼夜变化为双峰曲线,蔗糖合成酶分解方向、酸性转化酶和中性转化酶活性的昼夜变化无明显规律,改变库源关系对这些指标均无显著影响;蔗糖含量升高受蔗糖磷酸合成酶和蔗糖合成酶合成方向正调控,而蔗糖含量降低则受多种酶的共同调节。(3)源叶中淀粉含量和腺苷二磷酸葡萄糖焦磷酸化酶活性的昼夜变化为单峰曲线,去果处理可以显著提高淀粉含量和腺苷二磷酸葡萄糖焦磷酸化酶活性,淀粉含量升高受腺苷二磷酸葡萄糖焦磷酸化酶正调控。     

暗期干扰对棉铃虫两个不同地理种群滞育抑制作用的比较

至今,所测试昆虫的光周期反应均表明,光周期反应对暗期干扰高度敏感,短暂的光脉冲都可在不同程度上逆转长夜效应,抑制滞育的发生。在研究了棉铃虫Helicoverpa armigera泰安种群(36.15°N,116.59°E)和喀佐种群(41.34°N,120.27°E)光周期反应的基础上,在滞育诱导的短光周期下(L12:D12和L9:D15),分别测试了暗期不同时段1h光脉冲对这两个不同地理种群滞育抑制的影响。25和22℃下的光周期反应显示了泰安种群在长暗期11—14 h的滞育率均显著低于喀佐种群;泰安种群的临界暗长分别为11.7 h和11.5 h,喀佐种群分别为10.5 h和10.3 h,泰安种群均比喀佐种群长1.2 h。在所测试的暗期干扰实验中,除了极少数光脉冲干扰点外,泰安种群蛹滞育率显著低于喀佐种群,但两者的滞育反应曲线基本相似。在短光周期L9:D15下,泰安种群和喀佐种群均显示了光脉冲落入暗期的第9—11小时最有效地抑制了滞育的发生。在短光周期L12∶D12下,泰安种群和喀佐种群在25℃时均显示了光脉冲落入暗期的第3—4小时和第10小时导致了最低的滞育发生;但在22℃时,喀佐种群只在暗期的第3—4小时显示了最高的滞育抑制。这些结果揭示了偏南的泰安种群对暗期干扰的敏感性强于偏北的喀佐种群,但这两个地理种群的最高光敏感位点基本相同。     

Quantitative phase microscopy with enhanced contrast and improved resolution through ultra‐oblique illumination (UO‐QPM)

Recent developments in phase contrast microscopy have enabled the label‐free visualization of certain organelles due to their distinct morphological features, making this method an attractive alternative in the study of cellular dynamics. However tubular structures such as endoplasmic reticulum (ER) networks and complex dynamics such as the fusion and fission of mitochondria, due to their low phase contrast, still need fluorescent labeling to be adequately imaged. In this article, we report a quantitative phase microscope with ultra‐oblique illumination that enables us to see those structures and their dynamics with high contrast for the first time without labeling. The imaging capability was validated through comparison to the fluorescence images with the same field‐of‐view. The high image resolution (~270 nm) was validated using both beads and cellular structures. Furthermore, we were able to record the vibration of ER networks at a frame rate of 250 Hz. We additionally show complex cellular processes such as remodeling of the mitochondria networks through fusion and fission and vesicle transportation along the ER without labels. Our high spatial and temporal resolution allowed us to observe mitochondria “spinning”, which has not been reported before, further demonstrating the advantages of the proposed method.      

Uniform light delivery in volumetric optoacoustic tomography

Accurate image reconstruction in volumetric optoacoustic tomography implies the efficient generation and collection of ultrasound signals around the imaged object. Non‐uniform delivery of the excitation light is a common problem in optoacoustic imaging often leading to a diminished field of view, limited dynamic range and penetration, as well as impaired quantification abilities. Presented here is an optimized illumination concept for volumetric tomography that utilizes additive manufacturing via 3D printing in combination with custom‐made optical fiber illumination. The custom‐designed sample chamber ensures convenient access to the imaged object along with accurate positioning of the sample and a matrix array ultrasound transducer used for collection of the volumetric image data. Ray tracing is employed to optimize the positioning of the individual fibers in the chamber. Homogeneity of the generated light excitation field was confirmed in tissue‐mimicking agar spheres. Applicability of the system to image entire mouse organs ex vivo has been showcased. The new approach showed a clear advantage over conventional, single‐sided illumination strategies by eliminating the need to correct for illumination variances and resulting in enhancement of the effective field of view, greater penetration depth and significant improvements in the overall image quality.      

异色瓢虫不同光环境下的交配行为

光照条件是影响昆虫生长发育及生理行为变化的重要环境因子之一。以重要的捕食性天敌异色瓢虫为研究对象,借助动物行为自动观察系统对其在不同光照强度、光周期和光波长下的交配行为及繁殖力进行了分析研究。结果显示:(1)异色瓢虫的各交配行为和繁殖能力在有光和黑暗处理间具有显著差异;(2)异色瓢虫的求偶行为不受光照强度变化的影响,而交配持续时间及交配间隔时间在高光照强度下均显著短于低光照强度。尽管异色瓢虫的累积产卵量在不同光照强度间未见显著性差异,但是其幼虫孵化率随光照强度的增强显著降低;(3)异色瓢虫在光照时间较长的条件下表现出较高的交配求偶欲望,交配持续时间及交配间隔时间随光照时间的延长而缩短,其累积产卵量和幼虫孵化率均随光照时间的延长而显著增加;(4)不同环境颜色对异色瓢虫的求偶行为没有显著影响,但是其交配持续时间及交配间隔时间随照射光波长的增加而显著降低,雌虫的累积产卵量和幼虫孵化率均在黄色(575 nm)和绿色(510 nm)条件下最高,且显著大于其它处理。结果表明异色瓢虫的交配受光照条件影响极为显著,为进一步深入研究异色瓢虫环境适应性及提升其在生物防治中大规模饲养中的扩繁效率提供了重要的理论依据。     

Photoperiodic regulation of receptacle induction in Sargassum horneri (Phaeophyceae) using clonal thalli

We developed a clonal culture of Sargassum horneri to investigate the effect of photoperiod on reproduction in this species. Regenerated vegetative thalli were obtained using lateral branches excised from a thallus grown from a single embryo under short‐day conditions (SD = 10:14 h light : dark cycle). Lateral branches excised from the SD‐regenerated thallus became vegetative thalli that remained in that phase as long as they were cultured under SD. When an excised lateral branch was cultured under long‐day conditions (LD = 14:10 h light : dark cycle), it began to enter the reproductive phase while still less than 50 mm long. Induction of the reproductive phase was accompanied by a distinctive morphological change – suppression of blade formation at the apical region of the branch; elongation of branches without blades was then followed by differentiation of receptacles bearing conceptacles on their surface. Apices of receptacles were able to interconvert between reproductive and vegetative phases, as blades resprouted upon transfer from LD to SD. The critical day length for induction of receptacle formation was between 13 and 14 h; receptacle formation was also induced under SD conditions with night breaks (NBs). These results strongly suggest that reproductive regulation of S. horneri is a photoperiodic long‐day response. NBs with blue and green light were effective for reproductive induction but not with red light. This suggests that blue‐ and/or green‐light photoreceptors are involved in the photoperiodic reproductive response of S. horneri.