稻瘟病菌激发子诱导非寄主植物的抗病效果

 Hyphal cell wall crude elicitor(CWE)of rice blast pathogen could induce hypersensitive response in tobacco and induce other nonhost plants to be resistant to other fungal pathogens.When corn was treated with CWE,they inhibited the infection of Exserohilum turcicum and Curvularia lunata,and when plants of capsicum and cucumber were treated with CWE,they inhibited the infection of Colletotrichum gloeospori-oides.CWE solution showed no bioactivity on spore germination and hyphal growth of the experiment fungi in vitro.Nonhost resistance induced by CWE to other fungal pathogens was not complete resistance.The induced resistant effect(IRE) increased as CWE concentration increased,however,IRE had somehow satura-ted concentration of CWE.Induced nonhost resistance by incompatible pathogen was quantitative to other compatible pathogens.The induced resistance was best at 2 or 3 d after CWE treatment,and then decreased.IRE was about 20 percent in 10 d after CWE treatment.     

生物土壤添加剂对连作黄瓜防御酶系及酚类物质含量的影响

 The changes of several defense enzyme activities and phenolic compound in cucumber roots were examined after biological soil amendment(BSA) was applied to the cucumber continuous cropping through pot trials.It could promote seedling growth and reduce disease incidence.The results showed that the activities of defense enzymes such as peroxidase(POD),polyphenol oxidase(PPO) and TTC in treated cucumber roots were measured significantly higher than that of control.The activities of POD and PPO in BSA-treated roots were significantly higher than that of control after inoculation with Fusarium oxysporum(Schl.)f.sp.Cucumerinum.Phenolic compound content of roots decreased in the initial period of inoculation,increased after di-sease incidence,but it was higher in BSA-treated than that of control.These indicated that BSA could induce the defense enzyme activities and increased phenolic compound in cucumber roots.     

黄瓜-酸黄瓜渐渗系霜霉病抗性及感病前后几种酶活性的变化

 Using resistant and susceptible cultivars as controls, the resistant evaluation to Pseudoperonospora cubensis was carried out in 12 introgression lines from wide cross between cucumber(Cucumis sativus L.) and sour cucumber(Cucumis hystrix Chakr.). Three enzyme activities including POD, SOD and PAL were analyzed before and 7 d after inoculation, and the POD isozyme was detected by polyacrylamide electrophoresis. The inoculation results showed that, of the 12 accessions, 3 were identified as high resistant, 5 were moderately resistant and 4 were moderately susceptible to downy mildew. The enzyme activities of POD, SOD and PAL were greatly increased in resistant accessions after inoculation. PAL enzyme activities showed close correlation with disease rating before or after inoculation, which implicated that PAL enzyme activity might be used to estimate the resistance to downy mildew. POD isozyme electrophoresis showed that the number and intensity for the bands of resistant lines were significantly increased more than those of susceptible lines after inoculation.     

一个二粒小麦LRR类受体蛋白激酶基因的克隆和鉴定

 Near the HMW-glutenin gene of wheat (Triticum aestivum), there is a locus (temporarily named TaXa) encoding LRR-receptor-like protein kinase, which is homologous to disease resistance protein Xa21 of rice (Oryza sativa). Through RT-PCR approach, a cDNA clone of ZS2002 was isolated from the orthologous locus of TaXa in Triticum turgidum. ZS2002 was 3 081 bp long and encoding a peptide composed of 1 026 amino acid. The protein included N-terminal conserved sequence, LRR domains, a transmembrane region and a serine/threonine protein kinase domain. ZS2002 was expressed in root, stem, leaf and spike. The transcribing in seedling leaves was significantly enhanced by Blumeria graminis f.sp. tritici. TaXa gene might play a role in powdery mildew resistance reaction in Triticum.     

壳寡糖诱导烟草防御酶系活性变化及PR-1a基因表达研究

 The activity change of defensive enzymes and PR-1a gene expression of tobacco (Nicotiana tabacum) seedling induced by chito-oligosaccharides were studied. The results showed that high level systemic acquired resistance (SAR) was expressed in tobacco plants treated with chito-oligosaccharides solution at the concentration of 50 μg/mL. PAL activity increased greatly with 2 peaks, the activity of SOD decreased initially followed by an increase with higher increment, and the activity of POD peaked early followed by a gentle fall in chito-oligosaccharide treated plants. The PR-1a gene was strongly expressed in tobacco due to systemic acquired resistance induced by chito-oligosaccharides. At 168 h after inoculation the expression quantity (co-pies/2 μL) of PR-1a gene was increased to 2 469.6 in treated tobacco leaf, reached 392.6% than that at 0 h after inoculation, it was increased 3.05 times of that in untreated control.     

基于小麦白粉病菌rDNA ITS序列的PCR分子检测

 Wheat powdery mildew(Blumeria graminis f.sp.tritici) is the one of main wheat diseases in China.Based on the internal transcribed spacer(ITS) sequences of ribosome of B.graminis f.sp.tritici,three molecular primer pairs(F1/R,F2/R and F3/R) were designed to detect the fungal pathogen of wheat powdery mildew.The species specificity of these primers was confirmed.F1/R was demonstrated a higher sensitivity than the other two primer pairs,and could detect as low as 1 pg DNA of B.graminis f.sp.tritici.Furthermore,F1/R primer pair was used to detect the pathogen DNA extracted from wheat leaves showing chlorosis and typical symptoms of powdery mildew caused by artificial inoculation with B.graminis f.sp.tritici.The preliminary results demonstrated the usefulness of this primer pair and its potential applications in efficient detection of wheat powdery mildew pathogen from leaves with latent infections at early growth stages of wheat.     

寄主诱导下的玉米弯孢叶斑病菌致病性分化相关蛋白的动态变化研究

 Reinoculation and two-dimensional electrophoresis were performed to analyze the pathogenicity differentiation of Curvularia lunata.Resistant host inbred lines Shen135,Mo17,and 78599-1 were reinoculated(six generations) with low virulent isolate WS18.Results showed that the disease index had no significant change for the first 2 generations of inoculation.At the third generation,the incidence of disease was increased and the number of differential expressed proteins of mycelia were more than that in the first 2 generations.More than 100 differential expressed proteins were found in the mycelia of fifth generation when compared with the original one.In the experiment,10 differentially expressed proteins were identified by MALDI-TOF-MS analysis.Three proteins were related directly to the differentiation of virulence,2 were related to allergen,4 were related to the metabolism of carbon or signaling pathway and 1 was unkonwn to Curvularia lunata.     

外源茉莉酸和真菌激发子诱导白菜CaMBP10的表达

 Recently,CaMBP10 was identified as a plant lipid transfer protein(LTP).In the study,four leaves old cabbages were treated with exogenous jasmonic acid(JA),JA plus LTP,fungal elicitor,200 mmol/L NaCl and 20% PEG respectively for understanding the functions of CaMBP10 in vivo.The expression of CaMBP10 was determined by using semi-quantitative RT-PCR.The results showed that the expressions of CaMBP10 were dramatically up-regulated in different levels under indicated conditions.It demonstrated that CaMBP10 was involved in biotic and abiotic stress response.     

低钾逆境下根结线虫感染所诱导的番茄根巨型细胞的组织病理学反应

 Comparison of histopathological response and quantitative measurement of giant cell(GC) induced by Meloidogyne javanica in tomato root were studied under potassium-deficient(0.2 mmol/L K⁺) and replete conditions(control,6.0 mmol/L K⁺).K⁺-deficient stress did not impede the formation and maintenance of GC.The mean number of GC per feeding site as well as the mean diameter of GC did not differ between the treatments.However,the thickness of cell wall including components resulted from the accumulated polysaccharide and the length of cell-wall ingrowth increased 5-25 d after inoculation in K⁺-deficient as compared with K⁺-replete conditions.An increase of cell-wall ingrowth suggested a kind of compensational response to the potassium stress.     

苏云金芽孢杆菌晶体蛋白对北方根结线虫生物测定方法的建立和杀虫效果评价

 A bioassay procedure was developed to assess the toxicity of Bacillus thuringiensis crystal protein against Meloidogyne hapla,a root-knot nematode,under laboratory conditions.Reproducibility and precision of the bioassay results were optimal when forty 2nd stage juveniles were incubated in the dissolved crystal protein solution at 25℃,pH9.0 for 7 days.The juveniles were stained with 1% KMnO₄ for 2 hours or methylene blue solution for 1 hour to distinguish living and dead ones.By the bioassay procedure,the LC₅₀ value of strain YBT-1532 crystal protein against M.hapla was determined as 0.304±0.086 mg/mL(LC₅₀±1.96SE).Moreover,the strain YBT-1532 showed toxicity to Caenorhabditis elegans,a free-living nematode.All results indicated that YBT-1532 is a toxic strain to plant-parasitic nematode,and has the potential to control plant-parasitic nematode.     

外源茉莉酸甲酯诱导的水稻叶片蛋白质差异表达分析

 以抗稻瘟病水稻近等基因系C101LAC及CO39为材料,应用差异蛋白组学技术对外源茉莉酸甲酯（MeJA）诱导8 h和12 h后的水稻叶片蛋白质差异表达变化进行了分析。采用PEG 4000预沉淀法提取水稻叶片总蛋白,经双向电泳、凝胶染色和图像分析,结果表明：与对照相比MeJA处理后的2个水稻品系中共有21个蛋白质表现为2倍以上的表达差异。其中,MeJA处理8 h后,CO39中的差异表达蛋白质点有5个,C101LAC中有8个,U5为2个品系中均新增的蛋白质点。MeJA处理12 h后,CO39中有6个差异表达蛋白质点,C101LAC中则有5个。经胶内酶解、MALDI TOF/TOF质谱分析及数据库检索,成功对21个差异表达蛋白质进行了鉴定,其中新增的蛋白质点U5被鉴定为内切β 1,3 1,4 葡聚糖酶。依据GO数据库和UniProtKB数据库提供的蛋白质注释信息,按照功能可将21个差异表达蛋白质分为8类,分别在植物抗性、氨基酸代谢、信号转导、光合作用、光呼吸、糖代谢、蛋白质合成与分解及细胞代谢等方面发挥作用。     

玫瑰黄链霉菌Men-myco-93-63诱抗粗蛋白对黄瓜的诱抗作用

玫瑰黄链霉菌Strempomyces roseoflavus Men-myco-93-63是分离自马铃薯疮痂病自然衰退土壤中的一株拮抗链霉菌,该菌株及其代谢产物对多种重要的植物病原菌都具有较强的抑制作用,为了探明该生防菌产生的诱抗粗蛋白对黄瓜抗病性的诱导作用,采用离体叶片接种的方法,发现诱抗粗蛋白诱导黄瓜叶片灰霉病发病直径显著小于对照;经组织染色法和紫外分光光度计法测定,发现诱抗粗蛋白可以诱导黄瓜叶片中活性氧（ROS）的积累和超氧化物歧化酶（SOD）、过氧化物酶（POD）和多酚氧化酶（PPO）等抗病相关酶活性的显著提高;通过实时荧光定量PCR（qRT-PCR）测定,发现诱抗粗蛋白还可以诱导黄瓜叶片中PR-1a、PR-3、PR-9和NPR1等抗病相关基因表达的上调,试验结果表明Men-myco-93-63产生的诱抗粗蛋白能够诱导黄瓜抗病性的提升。     

生防菌株LB-1培养液对黄瓜的抑病促生作用

 LB-1为新筛选的生防近缘毛壳(Chaetomium subaffine)菌株。为明确LB-1培养液的抑病促生效果,本研究以黄瓜为供试植物,分别采用灌根和叶面喷施的方式,测定了LB-1培养液对黄瓜枯萎病和黄瓜白粉病的抑制效果;通过种子萌发、盆栽苗和生化检测试验,分析了LB-1培养液对黄瓜的促生作用。结果发现,LB-1培养液对黄瓜枯萎病抑制作用效果甚微,但对黄瓜白粉病生防效果明显,黄瓜叶片接菌24 h后叶面喷施LB-1培养液对白粉病的防效高达48.86%。LB-1培养液浸润催芽处理24 h的黄瓜种子萌发率和根长均显著高于对照(P=0.05),且LB-1培养液浸种、灌根、叶面喷施处理均能促进黄瓜幼苗的生长发育。LB-1没有产嗜铁素、产氢氰酸、固氮和溶磷能力,但能够产生吲哚乙酸(Indoleacetic acid,IAA)。表明生防菌株LB-1培养液能有效抑制黄瓜白粉病的发生,促进黄瓜种子萌发和植株生长,而且其促生作用可能通过产生IAA来实现。     

生防菌株LB-1培养液对黄瓜的抑病促生作用

 LB-1为新筛选的生防近缘毛壳(Chaetomium subaffine)菌株。为明确LB-1培养液的抑病促生效果,本研究以黄瓜为供试植物,分别采用灌根和叶面喷施的方式,测定了LB-1培养液对黄瓜枯萎病和黄瓜白粉病的抑制效果;通过种子萌发、盆栽苗和生化检测试验,分析了LB-1培养液对黄瓜的促生作用。结果发现,LB-1培养液对黄瓜枯萎病抑制作用效果甚微,但对黄瓜白粉病生防效果明显,黄瓜叶片接菌24 h后叶面喷施LB-1培养液对白粉病的防效高达48.86%。LB-1培养液浸润催芽处理24 h的黄瓜种子萌发率和根长均显著高于对照(P=0.05),且LB-1培养液浸种、灌根、叶面喷施处理均能促进黄瓜幼苗的生长发育。LB-1没有产嗜铁素、产氢氰酸、固氮和溶磷能力,但能够产生吲哚乙酸(Indoleacetic acid,IAA)。表明生防菌株LB-1培养液能有效抑制黄瓜白粉病的发生,促进黄瓜种子萌发和植株生长,而且其促生作用可能通过产生IAA来实现。     

外源NO对NaCl胁迫下玉米幼苗生长和渗透调节能力的影响

采用水培法,研究了50、100、200μmol·L~(-1)外源一氧化氮(NO)供体硝普钠(SNP)对盐胁迫下玉米幼苗生长和渗透调节能力的影响。结果表明,外施NO可明显缓解Na Cl胁迫对玉米幼苗生长的抑制作用,与不施SNP的处理相比,100μmol·L~(-1)SNP处理全株干重的增加幅度达到19%。外施NO降低盐胁迫下玉米幼苗叶片及根系中可溶性糖和可溶性蛋白的含量,其中叶片中可溶性糖和可溶性蛋白分别降低19.9%和7.9%,根系中可溶性糖和可溶性蛋白含量分别降低9.6%和9%。外源一氧化氮(NO)使盐胁迫下玉米幼苗根系、生长叶和成熟叶叶鞘的Na~+含量分别降低38.4%、5.1%和17.2%;同时,增加根系和成熟叶叶鞘中K~+、Ca~(2+)、Mg~(2+)含量,降低玉米幼苗各器官内的Na~+/K~+、Na~+/Ca~(2+)比值,维持盐胁迫下玉米幼苗中的离子平衡,但对成熟叶片中离子含量的影响不大。研究认为,外源NO可维持盐胁迫下玉米幼苗的碳氮代谢平衡,改善玉米幼苗离子的吸收与分配,缓解Na Cl胁迫对玉米幼苗带来的伤害,其中以100μmol·L~(-1)的SNP处理效果最明显。     

真菌Sr18代谢产物对根结线虫胁迫下黄瓜叶片保护酶的影响

为探究根结线虫胁迫下丝状真菌Sr18代谢产物对黄瓜的作用机理,采用温室盆栽及人工接种试验,研究了不同浓度的Sr18代谢产物对南方根结线虫胁迫下黄瓜叶片保护酶的影响。结果表明,线虫侵染黄瓜根部以后,黄瓜叶片SOD、POD和CAT活性减弱,PPO和PAL浓度降低。施加不同浓度的Sr18代谢产物,能够使线虫胁迫下的黄瓜叶片SOD、POD和CAT活性增强,使PPO和PAL的含量增加,说明Sr18代谢产物能够提高黄瓜的保护酶活性与含量,增强黄瓜对南方根结线虫的抗性。     

Searching by Differential Display for New Genes Implicated in Induced Disease Resistance of Cucumber Treated with Acibenzolar-S-methyl

Acibenzolar-S-methyl (ASM) is a chemical activator of systemic disease resistance in plants. In this study, we used differential display to identify ASM-inducible defense response genes involved in induced disease resistance. As a result, we cloned three ASM-inducible genes from cucumber, encoding a chitinase, a putative protein disulfide isomerase and a putative mitochondrial-protein-like protein. Expression of these genes was induced within 24 hr after treatment of cucumber leaves with ASM. These results suggest that differential display is a useful tool for understanding the mode of action of ASM and defense responses. Received 6 September 2000/ Accepted in revised form 11 April 2001     

一个小麦茉莉酮酸酯诱导蛋白基因的克隆和鉴定

 用基因芯片技术结合分池法(bulked segregating analysis,BSA)对参与小麦(Triticum aestivum L.)"兰考90(6)"抗白粉病反应或与抗病基因连锁的EST进行了分析。从"中国春"中克隆了一个与Ta-JA1高度相似的新的小麦茉莉酮酸酯诱导蛋白基因(GenBank登录号:EU035635),命名为Ta-JA2。Ta-JA2和Ta-JA1的cDNA序列有99%相同,编码304个氨基酸组成的多肽。Ta-JA2具有植物病原应答诱导蛋白-dirigent-类蛋白的典型保守功能域和jacalin-类植物血球凝集素的典型保守功能域。Ta-JA2主要在叶片和茎中表达,在根和幼穗中几乎不表达;在幼叶、壮叶和旗叶中的表达水平依次增强;在"中国春"和一个二粒小麦(Triticum dicoccoides)品系幼叶中的表达受白粉菌(Blumeria graminis f.sp.tritici)的诱导而增强;在"兰考90(6)21-12"叶片中的表达保持稳定而较高的水平。根据氨基酸序列的相似性建立了Ta-JA2类似蛋白的树形图,提供了植物中此类基因的进化信息。     

Resistance responses of albino leaves of Triticum timopheevii mutants inoculated with Erysiphe graminis f.sp. tritici

Albino chlorophyll mutants induced in Triticum timopheevii by γ-irradiation were used to study the influence of photosynthetic activity on the development of two isolates of Erysiphe graminis f.sp. tritici , and host resistance responses, 72 h after inoculation. The results showed that the percentage of pathogenic units inhibited by papilla response and epidermal cell hypersensitivity was lower on albino primary seedling leaves than on normal green seedling leaves. On albino leaves, the development of pathogenic units which established a successful penetration was either decreased or retarded, depending on the isolate used. This effect could be attributed to the limited supply of assimilates from the albino host due to the lack of photosynthetic activity.     

Proteomic analysis of a compatible interaction between Pisum sativum (pea) and the downy mildew pathogen Peronospora viciae

A proteomic approach was used to identify host proteins altering in abundance during Peronospora viciae infection of a susceptible cultivar of pea (Pisum sativum cv. Livioletta). Proteins were extracted from fully developed pea leaflets at 4 days post-inoculation, before visible symptoms were apparent. Cytoplasmic proteins and membrane- and nucleic acid-associated proteins from infected and control leaves were examined using two-dimensional difference gel electrophoresis. The majority of proteins had a similar abundance in control and infected leaves; however, several proteins were altered in abundance and twelve were found to have increased significantly in the latter. These proteins were selected for either matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry or electro-spray ionisation quadrupole time-of-flight tandem mass spectrometry analysis following trypsin digestion, with sequence identity being assigned to eight of the proteins. These included the ABR17 stress-response protein, the pathogen-induced PI176 protein, three photosynthetic proteins, a glycine-rich RNA binding protein and two glyceraldehyde 3-phosphate dehydrogenases (cytosolic and chloroplastic) which can be induced by a range of abiotic and biotic stresses in many plant species. The possible roles of these proteins in the response of the pea plant during P. viciae infection are discussed. This study represents the first proteomic analysis of downy mildew infection of pea leaves, and provides the basis for further work to elucidate molecular mechanisms of compatibility in P. viciae infections.