东海原甲藻对羊栖菜合子生长及光合活性的化感作用研究

为评估东海原甲藻(Prorocentrum donghaiense)赤潮发生对羊栖菜(Sargassum fusiformis)幼苗产量的影响并探讨其化感机理,在实验室条件下分别利用浓度为1.00×10⁵cells/mL东海原甲藻活细胞悬浮液(LC)、细胞破碎液(RC)和无细胞滤液(FC)培养羊栖菜合子,并对其生长发育及光合活性进行测定。结果显示,LC、RC和FC均会抑制羊栖菜合子的生长、叶绿素a合成和光合活性,其中FC及LC对合子的抑制程度相似且均大于RC。JIP-test分析表明,FC及LC对合子的最大量子产率(φP_o)、性能指数(PI)及PSⅡ反应中心密度(RCs/ABS)的抑制作用显著大于RC。表明东海原甲藻主要通过向细胞外释放化感物质产生抑制作用,这些化感物质抑制了羊栖菜合子PSⅡ的电子传递,使PSⅡ部分光化学反应中心(RCs)失活,进而使大量激发能转化为热能被耗散掉。而RC中可能含有某些能够刺激羊栖菜合子生长的物质,从而在一定程度上抵消了化感物质的抑制作用。结果表明东海原甲藻对羊栖菜合子的抑制作用主要是由化感物质引起的,东海原甲藻赤潮可以抑制羊栖菜合子的发育和光合活性,减少羊栖菜种苗产量,并最终阻碍了羊栖菜产业的发展。     

Chemical Composition and Anti‐Alzheimer's Disease‐Related Activities of a Functional Oil from the Edible Seaweed Hizikia fusiforme

Cholinergic disorder, oxidative stress, and neuroinflammation play important roles in the pathology of Alzheimer's disease. To explore the healthy potential of the edible seaweed Hizikia fusiforme on this aspect, a functional oil (HFFO) was extracted from this alga and investigated on its constituents by gas chromatography‐mass spectrometry (GC/MS) in this study. Its anti‐Alzheimer's related bioactivities including acetylcholinesterase (AChE) inhibition, antioxidation, and anti‐neuroinflammation were evaluated, traced, and simulated by in vitro and in silico methods. GC/MS analysis indicated that HFFO mainly contained arachidonic acid (ARA), 11,14,17‐eicosatrienoic acid (ETrA), palmitic acid, phytol, etc. HFFO showed moderate AChE inhibition and antioxidant activity. Bioactivity tracing using commercial standards verified that AChE inhibition of HFFO mainly originated from ARA and ETrA, whereas antioxidant activity mainly from ARA. Lineweaver?Burk plots showed that both ARA and ETrA are noncompetitive AChE inhibitors. A molecular docking study demonstrated low CDOCKER interaction energy of ?26.33 kcal/mol for ARA and ?43.70 kcal/mol for ETrA when interacting with AChE and multiple interactions in the ARA (or ETrA)?AChE complex. In the anti‐neuroinflammatory evaluation, HFFO showed no toxicity toward BV‐2 cells at 20 μg/mL and effectively inhibited the production of nitroxide and reduced the level of reactive oxygen species in lipopolysaccharide‐induced BV‐2 cells. The results indicated that HFFO could be used in functional foods for its anti‐Alzheimer's disease‐related activities.     

Highly luminescent and biocompatible,l‐citrulline‐capped ZnS:Mn nanocrystals for rapid screening of metal accumulating Lysinibacillus fusiformis bacteria

Biocompatible and highly luminescent manganese doped zinc sulfide (ZnS:Mn) nanocrystals of average particle size 10 nm have been synthesized by capping with a novel amino acid ligand, l ‐citrulline. Though there are many reports on the bioimaging applications of nanostructured semiconductors, the present study focused on the detection of a special type of metal accumulating bacteria, Lysinibacillus fusiformis. This bacterium has significant applications in the disposal of metal components from industrial effluents. In this context, the detection of this bacterium is quite important and the present work demonstrates a novel technique for this bacterial detection. The synthesized nanocrystals were attached to Lysinibacillus fusiformis and characteristics of the bioconjugated system were studied. The blue shift observed in the ultraviolet‐visible absorption and photoluminescence spectra of the bioconjugated system, confirms conjugation of the Lysinibacillus fusiformis with l ‐citrulline‐capped ZnS:Mn. When the bioconjugated system (capped ZnS:Mn + bacteria) was observed using a fluorescent microscope under excitation wavelengths 365.4 nm (ultraviolet), 435.8 nm (blue) and 546.1 nm (green), fluorescence emissions were obtained in yellow, green and red regions respectively. The study of relative growth of Lysinibacillus fusiformis in the presence of l ‐citrulline‐capped ZnS:Mn proves biocompatible property of these nanocrystals and their tunable color properties under different excitation wavelengths make them ideal for biolabeling applications. Copyright © 2013 John Wiley & Sons, Ltd.     

Histochemical evidence of β‐chitin in parapodial glandular organs and tubes of Spiophanes (Annelida,Sedentaria: Spionidae), and first studies on selected Annelida

A generic character of the genus Spiophanes (Annelida, Sedentaria: Spionidae) is the presence of parapodial glandular organs. Parapodial glandular organs in Spiophanes species include secretory cells with cup‐shaped microvilli, similar to those present in deep‐sea inhabiting vestimentiferans and frenulate Siboglinidae. These cells are supposed to secrete β‐chitin for tube‐building. In this study, transverse histological and/or ultrathin sections of parapodial glandular organs and tubes of Spiophanes spp. as well as of Glandulospio orestes (Spionidae) and Owenia fusiformis (Oweniidae) were examined. Fluorescent markers together with confocal laser scanning microscopy, and Raman spectroscopy were used to detect chitin in the parapodial glandular organs of Spiophanes and/or in the glands of Owenia and Glandulospio. Tubes of these taxa were tested for chitin to elucidate the use of it for tube‐building. The examinations revealed a distinct labelling of the gland contents. Raman spectroscopy documented the presence of β‐chitin in both gland types of Spiophanes. The tubes of Spiophanes were found to have a grid‐like structure that seems to be built with this β‐chitin. Tests of tubes of Dipolydora quadrilobata (Spionidae) for chitin were negative. However, the results of our study provide strong evidence that Spiophanes species, O. fusiformis and probably also G. orestes produce chitin and supposedly use it for tube‐building. This implies that the production of chitin and its use as a constituent part of tube‐building is more widespread among polychaetes as yet known. The histochemical data presented in this study support previous assumptions inferring homology of parapodial glandular organs of Spionidae and Siboglinidae based on ultrastructure. Furthermore, transmission electron microscopy‐based evidence of secretory cells with nail‐headed microvilli in O. fusiformis suggests homology of parapodial grandular organs across annelids including Sipuncula. J. Morphol. 276:1433–1447, 2015. © 2015 Wiley Periodicals, Inc.     

Hizikia fusiforme extract enhances dendritic cell maturation in vitro and in vivo

ABSTRACT

Dendritic cells (DCs) are play critical roles in the priming and regulation of immune responses. DCs rapidly process and convey these antigens to prime antigen-specific T cells. Therefore, regulation of DCs functions is important for immunity and immunotherapies. Immune adjuvants for DCs activation are needed to improve the efficacy of vaccines against tumors and many infectious diseases. Therefore, we demonstrate that H. fusiformis extract can regulate DCs maturation and activation. H. fusiformis extract induced costimulatory molecules (CD 80 and CD86), antigen-presenting molecules (major histocompatibility complex (MHC) I and II), CCR7 expression, and interleukin (IL)-12 production in DCs. These effects are associated with upregulation of mitogen-activated protein kinase (MAPK) signaling pathway. In addition, H. fusiformis extract induces costimulatory molecules on splenic DCs and activated CD8⁺ T cells in vivo. Taken together, these findings suggest that H. fusiformis extract may be a potential efficient immune therapeutic compound in DCs-mediated immunotherapies.     

Gelling agents for tissue culture of the seaweed Hizikia fusiformis

Callus and blade formation of the seaweed Hizikia fusiformis depended on the gelling agents used under axenic culture conditions. Excised cylindrical pieces (5 mm) of the hold fast were cultured on seven different gelling agents in seawater with added Provasoli's enrichment (PESI), at 40 μmol m⁻² s⁻¹ light intensity, 18 −C for 1 month. The highest percent of callus formation (47%), from holdfast pieces, was produced on solid medium composed of 2.0% high gel strength agar. No callus was formed in liquid medium. Blades, from holdfast pieces, were formed in PESI liquid medium at the rate of 45%, while the high level of axenic blade formation (30%) on solid support was observed on 0.5% high gel strength agar. Callus and blade were identified with the original strain, at the DNA level, using random amplified polymorphic DNAs. This revised version was published online in August 2006 with corrections to the Cover Date.