The Response of Bean Plants to UV-B Radiation Under Different Irradiances of Background Visible Light

Plants of Phaseolus vulgaris L. (cv. Stella) were grown in controlledconditions under three different irradiances of visible lightwith or without UV-B (280–320nm) radiation. The biologicallyeffective UV-B radiation (UV-B_BE) was 6.17 kJ m^–2 d^–1,and simulated a c. 5% decrease in stratospheric ozone at 55.7?N,13.4?E. The photon flux densities of the photosyntheticallyactive radiation (PAR, 400–700 nm) were either 700 µmolm^–2–1 (HL), 500, µmol m^–2 s^–1(ML) or 230 µmol m^–2 s^–1 PAR (LL). Under highlight (HL) conditions plus UV-B radiation, bean plants appearedmost resistant to the enhanced levels of UV-B radiation, andresponded only by increasing leaf thickness by c. 18%. A smallincrease in UV screening pigments was also observed. Both thelower irradiances (ML and LL) increased the sensitivity of theplants to UV-B radiation. Changes in leaf structure were alsoobserved. Photosystem II was inhibited under ML and LL togetherwith UV-B radiation, as determined by Chi fluorescence inductionand calculation of the fluorescence half-rise times. Leaf reflectivitymeasurements showed that the amount of PAR able to penetrateleaves of UV-B treated plants was reduced, and that a possiblecorrelation may exist between the reduced PAR levels, loss ofChi and lowered photosynthetic activity, especially for LL +UV-Bgrown plants, where surface reflection from leaves was highest.Changes in leaf chlorophyll content were mostly confined toplants grown under LL + UV-B, where a decrease of c. 20% wasfound. With regard to protective pigments (the carotenoids andUV screening pigments) plants subjected to different visiblelight conditions responded differently. Among the growth parametersmeasured, there was a substantial decrease in leaf area, particularlyunder LL + UV-B (c. 47% relative to controls), where leaf dryweight was also reduced by c. 25%. Key words: Chlorophyll fluorescence induction, bean, flavonoids, Phaseolus vulgaris, reflectance, UV-B radiation     

正交设计优化微波辅助测定延胡索叶总生物碱含量

通过微波辅助提取的方式,以延胡索叶总生物碱含量为考察指标,通过单因素试验和正交试验对总生物碱提取方法进行优化。重点考察了微波提取温度、时间、料液比、提取缓冲液pH值等因素对延胡索叶总生物碱得率的影响。各因素对延胡索叶总生物碱提取量的影响大小依次为:提取缓冲液pH值料液比提取温度。其最佳的提取方法为:提取缓冲液pH值为1. 0,料液比1∶100,提取温度60℃,提取时间20 min。在此条件下,叶总生物碱含量为25. 910 mg/g。利用微波辅助提取延胡索叶中总生物碱,不仅耗时短,效率高,而且操作简单、稳定,为延胡索叶总生物碱含量测定提供一定的技术支持。     

模拟氮沉降对长白山岳桦林下草本植物和土壤肥力的短期影响

选取长白山岳桦林中的岳桦-蟹甲草群落（Comm.Betula ermanii-Parasenecio forrestii）、岳桦-藜芦群落（Comm.Betula ermanii-Veratrum nigrum）和岳桦-小叶章群落（Comm.Betula ermanii-Deyeuxia purpurea）开展野外模拟氮沉降实验,采用野外原位模拟实验方法,设置对照（0 kg·hm^-2·a^-1）、低氮（30 kg·hm^-2·a^-1）、中氮（50 kg·hm^-2·a^-1）和高氮（100 kg·hm^-2·a^-1）4个氮处理水平,测定草本植物生长状况和土壤肥力,研究岳桦林下草本层植物和土壤肥力对氮沉降的短期响应。结果显示：（1）岳桦林下草本植物随氮沉降量的增加而加速生长,小叶章对氮沉降的响应较为敏感,藜芦次之,蟹甲草最弱;（2）氮添加造成林下土壤肥力发生变化,有机质含量下降,特别是岳桦-小叶章群落下的土壤有机质含量下降最明显;土壤总氮和速效氮含量增大,岳桦-蟹甲草群落下的土壤总氮和速效氮增加最多;土壤总磷和速效磷含量减小,岳桦-小叶章群落下的土壤总磷和速效磷含量的减少最多。本研究结果表明氮添加在短期内会促进长白山岳桦林下草本植物生长,尤其是小叶章的生长,加快土壤有机质的分解和磷的释放,逐步改变土壤肥力并反馈给植物,促使其进一步变化。     

模拟氮沉降对长白山苔原灌草混合群落中植物光合特性的影响

由于草本植物持续上侵长白山灌木苔原,形成了强烈的灌草群落种间竞争。本研究以牛皮杜鹃-小叶章群落（Comm.Rhododendron aureum-Deyeuxia purpurea）为对象,根据小叶章的入侵程度设置4种盖度差异显著的样方（无、轻度、中度、重度入侵）,并设3个施氮水平（自然状态、添加11.8 kgN·hm^-2·a^-1及添加23.6 kgN·hm^-2·a^-1）,进行原位氮沉降模拟实验,监测灌木牛皮杜鹃和草本植物小叶章光合特性的差异和变化趋势,研究小叶章入侵苔原带的内在生理机制。结果显示：（1）小叶章净光合速率大于牛皮杜鹃,小叶章盖度越高、其叶绿素含量越高,而牛皮杜鹃叶绿素含量降低,随着小叶章入侵程度的增加,其净光合速率增强;（2）施氮可以提高牛皮杜鹃和小叶章的叶绿素含量和净光合速率,促进植物生长,但小叶章的增幅更大,从而增强了小叶章的竞争优势;（3）施氮和小叶章入侵具有复合作用,小叶章盖度越大,对其施氮导致小叶章净光合速率与叶绿素含量的增幅越大,而牛皮杜鹃的增幅减小。所以小叶章的成功入侵可能与其具有较高的净光合速率有关,并且施氮有利于提高小叶章的净光合速率,随着氮沉降的继续增加,更有利于小叶章的生长并提高其竞争力。     

铜绿假单胞菌PAO1 ku基因缺失菌株的构建及其对生物被膜耐药性的影响

【背景】铜绿假单胞菌是常见的条件致病菌,易形成生物被膜,具有基因突变率高、耐药性强的特点。非同源末端连接是DNA双链断裂的主要修复途径之一,修复过程会导致DNA突变产生。【目的】研究非同源末端连接对生物被膜中的铜绿假单胞菌基因突变率和耐药性的影响。【方法】通过基因无痕敲除的方法构建PAO1菌株的ku基因缺失突变株Δku并构建其回补株。对比研究突变株和野生菌株生物被膜形成能力、生物被膜状态下各菌的基因突变率以及对抗生素的耐受性。通过荧光定量PCR检测生物被膜中PAO1菌株ku基因的表达水平。【结果】各突变株生物被膜形成能力无显著差异;与野生菌株相比,突变株Δku在生物被膜中的基因突变率以及对环丙沙星和庆大霉素的最低抑菌浓度(minimum inhibitory concentration,MIC)下降。荧光定量PCR结果表明,ku基因在生物被膜形成早期转录水平有明显上调。【结论】非同源末端连接修复途径对生物被膜中的铜绿假单胞菌基因突变率以及耐药性的提高有一定的作用。本研究将为后续进一步阐释铜绿假单胞菌耐药产生机制提供一定的理论依据。     

Inhibition of the Arp2/3 complex impairs early embryo development of porcine parthenotes

The Arp2/3 complex, which nucleates actin filaments, comprises a stable assembly of seven-protein subunits including two actin-related proteins (Arp2 and Arp3). Previous work showed that Arp2/3 binds to the sides of actin filaments and is concentrated at the leading edges of motile cells. In the present study, we show that the Arp2/3 complex is critical for cytokinesis during early embryonic development in porcine parthenotes. The Arp2/3 complex is concentrated at the cortex of each cell at the 1-, 2-, and 4-cell stages, and at the periphery at the morula stage. The amount of Arp2/3 significantly decreased at the blastocyst stage in parthenogenetically activated porcine embryos. Inhibition of the Arp2/3 complex in the pig embryos by the Arp2/3-specific inhibitor CK666 resulted in abnormal cell division, a decrease in developmental rate and total cell numbers, and an increase in the ratio of trophectoderm cell number to inner cell mass number in blastocyst-stage embryos. In addition, 4-cell stage embryos subjected to CK666 treatment exhibited significantly decreased expression of ZGA genes (Pou5f1, Sox2, and Nanog), suggesting that the Arp2/3 complex plays an important role in early porcine embryo development. Thus, our data demonstrate that the Arp2/3 complex is required for early embryonic development in pigs and appears to regulate the expression of pluripotency genes.     

不同施肥处理对柑橘粉虱和柑橘潜叶蛾发生的影响

柑橘粉虱Dialeurodes citri Ashmead和柑橘潜叶蛾Phyllocnistis citrella Stainton是柑橘的主要害虫,为了评估施肥对其发生的影响,本研究调查了施用有机肥、化肥、复混肥(有机肥与化肥混合)的砂糖橘苗木上这两种害虫的发生危害情况。结果表明,施用有机肥的苗木上柑橘粉虱的卵和若虫数量显著低于化肥,由柑橘粉虱诱发的煤污病发病程度也显著低于化肥处理。有机肥处理柑橘粉虱成虫数量也最少,但与化肥、复混肥差异未达显著水平。另外,柑橘潜叶蛾为害情况在3种肥料处理之间则没有显著差异。说明施有机肥的砂糖橘对柑桔粉虱的吸引作用最弱,其次为复混肥,化肥最吸引柑橘粉虱。3种施肥处理对柑橘潜叶蛾的吸引作用差异不明显。     

Expression and production of bioactive human interleukin-18 in transgenic tobacco plants

The cDNA of human interleukin-18 (hIL-18) was successfully inserted into the genome of tobacco plant, Nicotiana tabacum cv. NC-89, using Agrobacterium tumefaciens-mediated transformation. Insertion and translation of hIL-18 in transformants were confirmed by PCR, ELISA, and Western blot, respectively. The transformed extracts contained the recombinant hIL-18 protein up to 0.05% of total soluble protein. Activity of the recombinant hIL-18 in plant cells was confirmed by the induction of IFN- on IL-18-responsive J6-1 cells by the extracts obtained from the transformants. The expression level of hIL-18 (351 ng g^–1 tobacco tissue) obtained in the present study may be sufficient to induce responses/effects in vivo.     

Salvianolic Acid B Ameliorates Lipopolysaccharide-Induced Albumin Leakage from Rat Mesenteric Venules through Src-Regulated Transcelluar Pathway and Paracellular Pathway

Lipopolysaccharide (LPS) causes microvascular barrier disruption, leading to albumin leakage from microvessels resulting in a range of disastrous sequels. Salvianolic acid B (SalB) is a major water-soluble component derived from Salvia miltiorrhiza. Previous studies showed its potential to attenuate microvascular barrier dysfunction, but the underlying mechanism is not fully understood. The present study was intended to investigate the impact of SalB on endothelial cell barrier in vivo in rat mesenteric venules as well as in vitro in human umbilical vein endothelial cells (HUVECs), aiming at disclosing the mechanism thereof, particularly the role of Src in its action. Male Wistar rats were challenged by infusion of LPS (2 mg/kg/h) through left femoral vein for 90 min. SalB (5 mg/kg/h) was administrated either simultaneously with LPS or 30 min after LPS infusion through the left jugular vein. Vesicles in venular walls were observed by electron microscopy. HUVECs were incubated with LPS with or without SalB. The expression of Zonula occluden-1 (ZO-1), VE-cadherin, caveolin-1 and Src in HUVECs was assessed by Western blot and confocal microscopy, binding of SalB to Src was measured using Surface Plasmon Resonance and BioLayer Interferometry. Treatment with SalB inhibited albumin leakage from rat mesenteric venules and inhibited the increase of vesicle number in venular endothelial cells induced by LPS. In addition, SalB inhibited the degradation of ZO-1, the phosphorylation and redistribution of VE-cadherin, the expression and phosphorylation of caveolin-1, and phosphoirylation of Src in HUVECs exposed to LPS. Furthermore, SalB was found able to bind to Src. This study demonstrates that protection of SalB against microvascular barrier disruption is a process involving both para- and trans-endothelial cell pathway, and highly suggests Src as the key enzyme for SalB to work.     

水蕨(Ceratopteris thalictroides)查尔酮合成酶基因的克隆和表达

查尔酮合酶(chalcone synthase, CHS)是植物类黄酮化合物合成的关键酶,有关蕨类植物CHS基因的序列及功能信息尚不完善。本研究采用快速扩增cDNA末端(RACE)技术克隆获得了模式蕨类植物——水蕨(Ceratopteris thalictroides)CtCHS基因(GenBank登录号:JX027616.1),其cDNA序列全长为1616 bp,具有3个外显子和2个内含子,开放阅读框(ORF)为1215 bp,编码404个氨基酸。进化树分析表明,CtCHS与问荆(Equisetum arvense)、松叶蕨(Psilotum nudum)和3种薄囊蕨的查尔酮合成酶基因聚为一枝,说明这些蕨类植物亲缘关系较近且为单系起源。通过构建原核表达体系成功获得CtCHS蛋白的多克隆抗体并用于免疫印迹分析,结果表明CtCHS基因的表达明显受紫外光(UV)诱导。CtCHS基因的克隆与表达分析为进一步研究水蕨类黄酮化合物的合成及其调控机制提供了依据。