水稻白叶枯病菌及其毒素引起烟草叶片组织坏死机制的研究

 水稻白叶枯病菌JXO Ⅲ细胞悬浮液及其分泌的毒素溶液接种到烟草叶片中,都能在烟草叶片上产生快速的坏死反应。引起坏死反应所需的最短时间分别为接种后8 h和0.5 h。低浓度的JXOⅢ(< 107 cfu/ml)接种后36~48 h内形成褪绿斑,而低浓度的毒素(< 2.5 mg/ml)接种后随时间延长在接点无任何可见变化。依文斯蓝(Evans blue)染色发现,毒素和JXOⅢ分别在接种后0.5 h和6 h内细胞大量死亡。叶圆片法测定表明,接种毒素后2 h内烟草细胞膜透性迅速上升,接种JXOⅢ后9 h细胞膜透性开始明显上升。毒素处理的烟草叶片中LOX、POX、SOD、CAT活性水平较对照降低,而JXOⅢ处理中上述酶活性较对照有不同程度的增加。蛋白质合成抑制剂环己酰亚胺,RNA合成抑制剂放线菌素D和钙离子通道阻断剂氯化镧分别以7.1×10^-5 M、1×10^-4 M和1×10^-3 M浓度有效地抑制JXOⅢ在烟草上形成坏死反应,这些抑制剂对毒素在烟草上的坏死反应则没有影响。     

水稻白叶枯病菌转录调控因子OxyRxoo对细菌抗氧化系统的调控作用

病原细菌对活性氧的降解是抗氧化和侵染中的重要毒性机制之一。阐述了水稻白叶枯病菌（Xanthomonas oryzaepv.oryzae）的转录调控因子OxyRxoo在病菌抗氧化系统中的调控作用,以及目前对OxyRxoo的研究进展。     

Stability of bacterial leaf spot resistance in peach regenerants under in vitro,greenhouse and field conditions

Summary Phenotypic stability of bacterial leaf spot resistance in peach (Prunus persica (L.) Batsch) regenerants, either selected at the cellular level for insensitivity to a toxic culture filtrate of Xanthomonas campestris pv. pruni or screened at the whole plant level for resistance to X. campestris pv. pruni, was investigated. A detached-leaf bioassay was used to evaluate the original regenerants again after three years in the greenhouse and also after a two to three year cycle of tissue culture propagation. Peach trees derived through micropropagation from the original regenerants were also evaluated after one to three years growth in the field. Although leaf spot resistance was retained in some regenerants over time in the greenhouse, following in vitro propagation, and under field conditions, resistance was either lost or not expressed in others. Regenerants # 19-1 and #156-6, derived from embryo callus of bacterial spot susceptible Sunhigh, were significantly more resistant than Sunhigh. High levels of resistance were exhibited in greenhouse plants and field-grown trees of regenerant #122-1, derived from embryo callus of moderately resistant Redhaven. This research provides additional evidence that selecting or screening for somaclonal variants with disease resistance is a feasible approach to obtaining peach trees with increased levels of bacterial spot resistance.Abbreviations TC Tissue-Cultured - TF Toxic culture Filtrate     

Comparison of leaf and pod disease reactions of beans (Phaseolus vulgaris L.) inoculated by different methods with strains of Xanthomonas campestris pv. Phaseoli (Smith) dye

Summary Common blight disease in beans (Phaseolus vulgaris), caused by the bacterium Xanthomonas campestris pv. phaseoli, reduces crop yield and seed quality. Information is needed on the variation of leaves and pods disease reaction to strains of the bacterium after different inoculation methods. Phaseolus vulgaris cultivars Red Kidney Charlevoix, GN Harris, GN 1140, and GN Emerson were inoculated with three different strains of Xanthomonas campestris pv. phaseoli at two inoculum concentrations (10⁸ and 10⁶ bacterial cells/ml) using water soaking, multiple needle, and razor blade inoculation on leaves, and razor blade scratch, dissecting needle, and razor blade cut inoculation on pods. Differential cultivar disease reactions of leaves, pods, or both to the bacterial strains were observed in some cases. Significant interactions among cultivars, inoculation methods, strains, and inoculum concentrations (leaves) were found. A rapid leaf chlorosis developed 6 to 7 days after inoculation. Strains of bacteria did not show specificity in inducing this reaction, but rapid leaf chlorosis was associated with high inoculum concentration and with the water soaking and multiple needle methods. Another experiment was conducted to count the number of living bacterial cells deposited in the leaf tissue after inoculation by different methods. The number of bacteria deposited by water soaking or multiple needle was higher than that deposited by razor blade.Published as Paper No. 8584, Journal Series, Nebraska Agricultural Experiment Station. Research was conducted under Project No. 20–36.     

杂交稻野败胞质对稻瘟病菌、白叶枯病菌感病性的研究

选用3个水稻野败胞质不育系及相应的保持系,3个恢复系及它们相应的野败胞质代换系,这些不育系、保持系同恢复系配组的18个 F_1,分别在秧苗期接种属我国7个稻瘟病生理小种群的21个菌株;在成株期接种15个白叶枯病菌株。结果表明,野败胞质较之正常胞质表现对这两种病菌感病稍轻;这种差异在多数保持系的基因型背景下达到显著水准,     

Genetic Analysis of Resistance to Xanthomonas campestris pv. oryzae (Ishiyama) Dye in a Rice Breeding Line ARC 10464

The genetics of resistance to three Indian pathotypes of Xanthomonas campestris pv. oryzae, namely, IX01, IX08 and IX09, was studied in a landrace of Indica rice ‘ARC 10464’. Resistance to each of the two pathotypes IX01 and IX09 was governed by two independently-inherited dominant genes while a single dominant gene was operative against patho-type 1X08. The joint segregation tests conducted on F₂ plant progenies (F₃ families) using pathotypes IX01, IX08 and IX09 suggested that the gene/(s) effective against each of the pathotypes are different.     

Inheritance of resistance to Xanthomonas campestris pv phaseoli in tetary bean (Phaseolus acutifolius)

Summary The F1, F2 and F3 from two crosses within Phaseolus acutifolius were exposed to Xanthomonas campestris pv phaseoli to analyse the inheritance of resistance. The resistant parent, PI 319.443, gave a hypersensitive reaction in leaves and pods with small necrotic lesions. Based on the resistance of F1, the segregation in F2 and the reaction of F3 plants and lines, it is concluded that resistance in leaves and pods is governed by one dominant gene. Comparisons are made with the resistance to X. campetris in P. vulgaris.     

抗福美双假单胞菌株的NTG化学诱变及分子探针鉴定

利用微生物的抗药性筛选抗福美双的假单胞菌株Ｔ４６，然后通过亚硝基胍（ＮＴＧ）化学诱变获得了对福美双敏感的三株突变株Ｔ４６Ｎ１０、Ｔ４６Ｎ７和Ｔ４６Ｎ１７。利用这三个突变株作受体，通过基因克隆的方法筛选到了可使三个突变株恢复抗性的克隆，抗性基因分别被定位在７ｋｂ、２．５ｋｂ和２０ｋｂ的ＥｃｏＲⅠ片段上。将这三个克隆分别用（３２）Ｐ标记后制成分子探针，然后分别与三个突变菌株的总ＤＮＡ进行ＤＮＡ－ＤＮＡ分子杂交，结果表明，各突变株均存在与菌株Ｔ４６的抗福美双基因克隆的高度同源性，经结合形态、生理生化等分析后证实这三株突变株均源自于出发菌株Ｔ４６。     

Influence of soil properties on the vertical movement of genetically-marked Pseudomonas fluorescens through large soil microcosms

Summary Vertical translocation of the introduced transposon Tn5-tagged Pseudomonas fluorescens cells was studies after irrigation of 50-cm long soil columns of loamy sand. The soil in the columns was slowly brought to saturation using groundwater, and enough water was then slowly added to permit collection of the percolated water. Introduced bacteria were transported to lower soil layers to a significantly higher degree in undisturbed soil cores than in repacked cores; water transport was hampered in both core types due to high soil bulk densities. Soil bulk density affected the degree of transport of the introduced cells; progressively more cells were translocated to deeper soil layers and into the percolation water at decreasing soil bulk densities. Repeated percolation of soil at a bulk density of 1.25 caused an increase in Tn5-tagged cell numbers in the lower soil layers and in the percolated water. Further, cells initially introduced into a dry (5.3% moisture) soil were translocated to a lesser extent than cells introduced into a wetter (13% moisture) soil. Finally, wheat roots enhanced the water-induced transport of introduced cells to the 40- and 50-cm deep soil layers and into the effluent, but not to the remaining soil layers. Large soil columns such as those used in the present study are useful in assessing the transport and survival of introduced bacterial cells in soils under a variety of simulated environmental conditions.     

竹炭固定化紫外诱变假单胞菌处理间甲酚废水的研究

用紫外光对假单胞菌株进行诱变,以竹炭为载体,将紫外诱变假单胞菌固定在竹炭上,用竹炭固定化紫外诱变假单胞菌处理间甲酚水样。考察竹炭固定化紫外诱变假单胞菌投加量和水样pH值对间甲酚去除的影响以及进水浓度随反应时间的变化关系,研究竹炭固定化紫外诱变假单胞菌去除间甲酚的反应动力学。结果表明:相对于原菌株,菌株经紫外诱变后,生长周期缩短了6h。经紫外照射120s的假单胞菌可以在竹炭表面及内部孔隙形成明显菌胶团,诱变菌在竹炭上所成的生物量明显较未经诱变菌增加。竹炭固定化紫外诱变假单胞菌能有效地去除水样中间甲酚。竹炭固定化紫外诱变假单胞菌投加量和水样pH值影响到间甲酚的去除效果,pH值在4～6时,间甲酚的去除效果较好。20g竹炭固定化紫外诱变假单胞菌处理100mL初始浓度50,100,120,150,180mg·L-1间甲酚模拟水样42h,去除率依次为90.9%,76.4%,72.9%,64.6%和49.7%。竹炭固定化紫外诱变假单胞菌对间甲酚的去除能较好地符合零级反应方程。