外源绿原酸对苹果抗病相关酶的影响

采用离体培养方法对富士、红星和八棱海棠进行绿原酸处理,研究苹果在外源绿原酸处理下POD、PPO、PAL活性的动态变化以及绿原酸含量的变化。结果表明,富士以0.0001%绿原酸、红星以0.0008%绿原酸、八棱海棠以0.0004%绿原酸处理后,其PAL活性均显著提高,苹果体内也因此而提高了绿原酸水平。     

大豆品种的抗病性与叶片内苯丙氨酸解氨酶活性关系的研究

在抗病品种东农9674，东农1572和感病品种黑农39，东农95-165上接种大豆灰斑病菌的1号，2号，4号，6号，7号等5个生理小种，测定从接种到显症前与抗性有关的苯丙氨酸解氨酶活性的变化。研究结果表明，抗病的大豆品种接种不同生理小种的灰斑病菌后，PAL的活性分别从第6-7天起吴上升趋势且明显高于对照；相反感病品种从8-9天起PAL活性明显低于对照，因此说明PAL的活性与大豆抗灰斑病性呈正相关关系。     

稻瘟菌细胞壁热解物诱导水稻抗稻瘟病的研究

以水稻近等基因系和广东省稻瘟病菌优势小种ZC13的细胞壁热解物(HDS)为材料进行诱导抗病性的研究。HDS通过细胞壁121°C 20 m in热解获得。HDS中葡萄糖质量浓度为176.83 m g/mL。HDS在体外对稻瘟病菌的孢子萌发和菌丝生长均无抑制作用,但处理水稻后可以显著提高水稻对稻瘟病菌的抗病性。在亲和性品系中,诱导抗病效果最高可达82.47%,且浓度与活性间存在正相关趋势;在非亲和品系中,热解物处理引起HR反应。HDS处理后,水稻过氧化物酶(POD)和苯丙氨酸解氨酶(PAL)活力明显升高。     

拮抗菌与病原菌处理对采后桃果实多酚氧化酶、过氧化物酶及苯丙氨酸解氨酶的诱导

 Pichiamembranefaciens能有效抑制桃果实采后软腐病。笔者观测和比较接种拮抗酵母菌P .mem branefaciens和软腐病菌Rhizopusstolonifer对采后桃果实多酚氧化酶 (PPO)、过氧化物酶 (POD)和苯丙氨酸解氨酶(PAL)活性的诱导情况。试验结果表明 ,桃果实接种P .membranefaciens +R .stolonifer 2 4h后 ,PPO和PAL活性开始升高 ,并在整个试验过程中一直保持较高的水平。只接种R .stolonifer也能诱导桃果实PPO和PAL活性的增加 ,但效果不如接种拮抗菌 +病原菌的好。然而 ,接种拮抗菌 +病原菌和只接种病原菌对诱导POD活性都没有明显的作用。可以认为 ,拮抗菌诱导抗性相关酶活性的提高是发挥抑病作用的一种重要方式     

无机铜试剂对棉花苯丙氨酸解氨酶活性的影响

利用无机铜试剂（CIE）在新陆早17和新陆中26两棉花品种的3叶期和蕾期进行叶面喷施,检测棉株叶片内的苯丙氨酸解氨酶（PAL）的活性变化。结果表明,两品种在3叶期和蕾期均表现为PAL活性显著增高,第2天后即开始产生对PAL活性诱导作用,第10天后PAL的活性开始回落至对照组水平;两品种蕾期PAL的诱导活性均明显高于3叶期,且PAL高活性水平持续天数较3叶期长;棉花不同生育期使用CIE,均可增强棉叶PAL的活性;两品种在不同生育期的PAL活性出现峰值的时间、强度不一,显示出品种抗性的差异性。试验表明,CIE可诱导增强棉叶中PAL的活性。     

玉米叶片中次生代谢物丁布含量和苯丙氨酸解氨酶活性的关系研究

[目的]分析比较不同玉米品种在不同生育时期丁布含量和苯丙氨酸解氨酶活性变化。[方法]采用高效液相色谱法对各个生育时期倒1叶、倒3叶丁布含量进行检测及PAL含量的测定。[结果]结果表明:不同玉米品种倒1叶、倒3叶丁布含量随着生育期的增加而减少,并且倒1叶减少的速度大于倒3叶;而苯丙氨酸解氨酶活性随着生育时期的增加而升高。[结论]玉米叶片随着生育时期增加苯丙氨酸解氨酶活性与丁布含量之间存在负相关关系。     

Response dynamics of three defense related enzymes in cotton leaves to the interactive stress of Helicoverpa armigera (Hübner) herbivory and omethoate application

In order to explore the response dynamics of the activities of defense related enzymes in cotton leaves towards the interactive stress of Helicoverpa armigera herbivory and omethoate application, the activities of phenylalanine ammonia-lyase(PAL), lipoxygenase(LOX), and polyphenol oxidase(PPO) were examined from 6 to 126 h after cotton leaves were treated 12 h of H. armigera herbivory, and then sprayed with 800 mg L–1 omethoate. The results showed that the changes in the activities of PAL, LOX and PPO that occured under the interactive stress of H. armigera herbivory and omethoate application reflected the interactive effects of the two stresses on cotton defense. The similarity between the response dynamics of PAL, LOX, and PPO activities in cotton leaves under the interactive stress and that under H. armigera herbivory treatment alone showed that the induction of H. armigera herbivory on the activities of PAL, LOX and PPO in cotton leaves played a leading role in the interactive effects, and the effect of omethoate application played only a minor role. A joint factor analysis was performed according to a method which has been used to analyze the joint toxicity of pesticides; this analysis sought to clarify if there was a synergistic, antagonistic, or additive effect on PAL, LOX, and PPO activity in cotton leaves resulting from the interactive H. armigera herbivory and omethoate treatment. In the interactive effect on the response of PAL activity in cotton leaves, antagonistic effects of the omethoate application towards H. armigera herbivory were observed at 6 and 12 h. Synergistic effects were then observed at 18 and 30 h. Antagonistic effects were observed from 54 to 78 h and synergistic effects were finally observed at 126 h. The correlation between H. armigera herbivory and omethoate application in the interactive effect on cotton defense responses of LOX activity also fluctuated from synergism to antagonism during the time course. In the interactive effect on PPO activity, only antagonism was observed between H. armigera herbivory and omethoate application. In the interactive stress of H. armigera herbivory and omethoate application on cotton defense responses, omethoate affected the defense responses of cotton to H. armigera herbivory by producing antagonistic and synergistic effects. These results will be useful to understand the relationship between host plant and herbivorous pest.     

薇甘菊萎蔫病毒感染对薇甘菊光合特性和4种酶活性的影响

为明确薇甘菊萎蔫病毒(Mikania micrantha wilt virus,MMWV)对薇甘菊(Mikania micrantha)叶片生理生化的影响,探讨了MMWV侵染对薇甘菊叶片超氧化物岐化酶(superoxide dismutase,SOD)、过氧化物酶(peroxidase,POD)、多酚氧化酶(polyphenol oxidase,PPO)和苯丙氨酸解氨酶(phenylalanine ammonia-lyase,PAL)活性及叶绿素总含量和光合特性的影响.结果表明:MMWV感染薇甘菊16d内叶片的SOD活性均比对照组高,其中第16天达最大值,但接种后第24和32天SOD活性分别比对照低了13.28％和25.37％;POD活性在接种后16-32d均显著高于对照.PPO和PAL变化趋势相似,在接种后第8天这两个酶的活性分别比对照高了77.75％和23.58％,而在第32天分别比对照减少了14.27％和20.53％.随着侵染时间的增加,感病薇甘菊叶片中叶绿素含量减少,叶绿素a/b值逐步降低;同时最大净光合速率(Pmax)和光饱和点(LSP)分别比健康对照减少了32.34％和12.52％,而对暗呼吸速率(Rd),光补偿点(LCP)和表观量子效率(AQY)无显著影响.表明MMWV侵染可减低薇甘菊叶片光合作用的效率.     

井冈霉素A对水稻纹枯病菌的毒力和作用机理研究

根据水稻纹枯病菌 Rhizoctonia solani AG- 1IA在含系列浓度井冈霉素 A马铃薯葡萄糖琼脂培养基 (PDA)上的菌丝生长速率 ,计算出药剂的毒力回归方程为:Y=3.2 30 9+0 .872 0 X,r=0 .9910 ,药剂的 EC50 =10 6 .9μg/ m L,EC75=6 34.5 μg/ m L。在含 5 0 0 μg/ m L井冈霉素 A的 PDA上水稻纹枯病菌的菌丝生长抑制率为 74 .1% ,而田间水稻植株上人工接菌的药效试验结果表明 ,5 0 μg/ m L药液喷洒后 7d和 14 d的防效即可分别达到 77.4 %和 76 .7% ,即药剂在 PDA平板上的理论抑制作用仅是田间活体植株上对病菌实际作用效果的 1/ 10。比较室内毒力和田间药效试验的结果可以看出 ,井冈霉素 A具有对病原菌和寄主植物双重作用的特性。研究首次发现 ,在室内培养基上不能有效抑制病菌生长的 1μg/ m L的井冈霉素 A可以在水稻植株未喷药部位产生防御水稻纹枯病的作用 ,且能够持续诱导植物防御反应相关酶——过氧化物酶 (PO)和苯丙氨酸解氨酶 (PAL)的活性增高,表明该药剂可以激发水稻抗性防卫反应的表达。     

Chitosan Stimulates Defense Reactions in Grapevine Leaves and Inhibits Development of Botrytis Cinerea

Chitosan (β-1,4-linked glucosamine oligomer) derived from crab shells conferred a high protection of grapevine leaves against grey mould caused by Botrytis cinerea. Under controlled conditions, it was shown to be an efficient elicitor of some defense reactions in grapevine leaves and to inhibit directly the in vitro development of B. cinerea. Treatment of grapevine leaves by chitosan led to marked induction of lipoxygenase (LOX), phenylalanine ammonia-lyase (PAL) and chitinase activities, three markers of plant defense responses. Dose-response curves show that maximum defense reactions (PAL and chitinase activities) and strong reduction of B. cinerea infection were achieved with 75–150 mg l⁻¹ chitosan. However, greater concentrations of chitosan did not protect grapevine leaves with the same efficiency, but inhibited mycelial growth in vitro. Present results underlined the potency of chitosan in inducing some defense responses in grapevine leaves which in turn might improve resistance to grey mould.