广东省橘园黄龙病发生与危害的影响因素研究

【目的】柑橘黄龙病是世界柑橘生产上的毁灭性病害。探明广东省橘园黄龙病发生与危害的影响因素,可为该病的科学防控提供依据。【方法】在广东省惠州、肇庆、云浮、江门、阳江、清远、韶关等柑橘产区,调查了不同柑橘品种、不同气候和地理条件、不同种植模式和不同管理水平果园的黄龙病发病率,并以常规PCR和实时荧光定量PCR对样品进行了分子检测。【结果】不同柑橘栽培品种发病率:红江橙为78.05%,马水橘为76.04%,砂糖橘为73.20%,贡柑为69.30%,年橘为63.00%,沙田柚为58.68%,柠檬为56.96%;砧木品种发病率:酸橘为15.30%,枳壳为6.57%,柠檬为4.43%;低纬、高温、多台风地区果园的黄龙病发病率较高;山地果园的黄龙病发病率低于平地果园;连片种植果园的黄龙病发病率高于零散种植果园;管理不善的果园中黄龙病发病率高于管理较好的果园。【结论】除了自然因素(低纬、高温、多台风、平原地形)外,聚集种植和管理不善等因素也有利于黄龙病的发生与流行。因此,有针对性地安排果园布局和加强果园管理可以减轻黄龙病的危害。     

噬菌体抗体库技术

噬菌体抗体库技术是指从人外周血、脾或骨髓淋巴细胞提取总RNA,利用逆转录-多聚酶链反应（RT-PCR）方法扩增抗体的全套可变区基因,通过噬菌体表面展示技术,把抗体Fab段或单链抗体表达在噬菌体表面,构建人源抗体库.噬菌体抗体将基因型（genotype）和表型（phenotype）统一于一体,将选择能力和扩增能力偶联起来,具有强大的筛选能力,能够在体外模拟体内的抗体生成过程,使抗体工程技术进入了一个新的时代.     

中国北方草原对气候干旱的响应

草原生长动态受气候条件的影响和制约,在很大程度上取决于水分条件.为了较好阐明草原生长与干旱气候关系,利用表征草原生长变化的NDVI(Normalized Difference Vegetation Index)指数和表征干旱的SPI(Standardized Precipitation Index)指数研究了荒漠草原、典型草原、草甸草原与干旱气候的线性关系,表明荒漠草原的生长动态受季节性干旱影响很大,短期、中长期和长期干旱对荒漠草原影响较小.典型草原对季节性干旱响应较强,而对短期、中长期和长期的干旱响应较弱.草甸草原对季节性和长期干旱响应较强.并且草原对降雨量的响应具有时滞效应,水分盈亏对草原的影响是累积效应.利用基于虚拟变量的回归模型和简单回归模型模拟了草原NDVI对SPI指数的响应关系,基于虚拟变量的回归模型显示出对草原NDVI与SPI关系的较优拟合度.表明了草原生长动态对干旱气候响应具有季节性效应.     

Characteristics of an endophytic pyrene-degrading bacterium of Enterobacter sp. 12J1 from Allium macrostemon Bunge

One pyrene-degrading endophytic bacterium was isolated from plants grown in polycyclic aromatic hydrocarbon-contaminated soils and identified as Enterobacter sp. 12J1 based on the 16S rDNA gene sequence analysis. Heavy metal and antibiotic resistance, degradation of pyrene, solubilization of inorganic phosphate and cell surface hydrophobicity characteristics of the isolate were further characterized. The isolate was also evaluated for promoting plant growth of wheat and maize and pyrene removal from pyrene-amended soil in pot experiments. High-performance liquid chromatograph (HPLC) analysis showed that the degradation rate of pyrene (5 mg l⁻¹) by the endophytic bacterial strain 12J1 was 83.8% under 28 °C for 7 days. The Enterobacter sp. 12J1 could produce indole acetic acid (IAA), siderophore and solubilize inorganic phosphate. The Enterobacter sp. 12J1 also has a cell surface hydrophobicity. In the live bacterial inoculation experiment, an increase in pyrene removal varying from 60% to 107% was observed in the planted soils treated with 100 mg kg⁻¹ of pyrene compared with the unplanted soils. The rate of pyrene removal increased by 43–65% in the live bacterium-inoculated planted soils compared with the dead bacterium-inoculated planted soils. Although there were no significant differences in the total culturable bacterial numbers between live and dead bacterial inoculation, the numbers of pyrene-degrading bacteria were significantly greater in the live bacterium-inoculated planted or unplanted soils. The isolate could colonize the tissue (root and stem) interiors and rhizosphere soils of wheat and maize after root inoculation.     

Complete DNA sequence and gene analysis of the virulence plasmid pCP301 of Shigella flexneri 2a

The complete nucleotide sequence and organization of the large virulence plasmid pCP301 (termed by us) of Shigella flexneri 2a strain 301 were determined and analyzed. The result showed that the entire DNA sequence of pCP301 is composed of 221618 bp which form a circular plasmid. Sequence analysis identified 272 open reading frames (ORFs), among which, 194 correspond to the proteins described previously, 61 have low identity (<60%) to known proteins and the rest 17 have no regions of significant homology with proteins in database. The genes of pCP301 mainly include the genes associated with bacterial virulence, the genes associated with regulation and the genes relating to plasmid maintenance, stability and DNA metabolism. Insertion sequence (IS) elements are 68 kb in length and account for 30 percent of complete sequence of the plasmid which indicates that gene multiple rearrangements of the pCP301 have taken place in Shigella flexneri evolution history. The research result is helpful for interpreting the pathogenesis of Shigella, as well as the genetics and evolution of the plasmid.     

Complete DNA sequence and gene analysis of the virulence plasmid pCP301 of Shigella flexneri 2a

Bacteria Shigella spp. are highly contagious, severely harmful and gram-negative facultative intracellular pathogens. They may cause shigellosis characterized by fever, dehydration and hematochezia in clinic, and shigellosis has been remaining a leading cause of infant mortality in the world. Shigella belongs to the family Enterobacteriaceae and the group Escherichiaeae, which are divided into four species and at least 47 serotypes: Shigella dysenteriae (13 serotypes), Shigella flexneri (15 …     

Fusion Step-Specific Influence of Cholesterol on SNARE-Mediated Membrane Fusion

Cholesterol is a major component of biological membranes and is known to affect vesicle fusion. However, the mechanism by which cholesterol modulates SNARE-dependent intracellular fusion is not well understood. Using the fluorescence assay and dye-labeled SNAREs and the fluorescent lipids, we dissected cholesterol effects on individual fusion steps including SNARE complex formation, hemifusion, pore formation, and pore dilation. At physiological high concentrations, cholesterol stimulated hemifusion as much as 30-fold, but its stimulatory effect diminished to 10-fold and three-fold for subsequent pore formation and pore expansion at 40 mol %, respectively. The results show that cholesterol serves as a strong stimulator for hemifusion but acts as mild stimulators for pore opening and expansion. Strong stimulation of hemifusion and mild stimulation of pore formation are consistent with the fusion model based on the intrinsic negative curvature of cholesterol. However, even a milder effect of cholesterol on pore expansion is contradictory to such a simple curvature-based prediction. Thus, we speculate that cholesterol also affects the conformation of the transmembrane domains of SNAREs, which modulates the fusion kinetics.     

单克隆抗体与多克隆抗体配对ELISA方法比较

以人绒毛膜促性腺激素(HCG)为抗原,制备出对HCG的多克隆抗体和特异性单克隆抗体,并进行抗体纯化和特性分析,利用辣根过氧化物酶(HRP)分别对其进行了标记.采用双抗夹心ELISA试验,探讨了多克隆抗体与单克隆抗体配对的若干事项.结果表明,利用单克隆抗体和酶标多克隆抗体配对,并用含动物血清的稀释液稀释酶标抗体,可实现对检测原的高特异性和高灵敏度检测.