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综述了植物病原微生物产生的降解酶的种类、作用方式、在致病中的地位及研究进展,阐明了细胞壁降解酶的双重作用即作为病原物侵染的致病因子及作为植物防卫反应的激发子,为寄主一病原物分子互作提供一定的参考. 相似文献
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综述了植物病原微生物产生的降解酶的种类、作用方式、在致病中的地位及研究进展,阐明了细胞壁降解酶的双重作用:即作为病原物侵染的致病因子及作为植物防卫反应的激发子,为寄主一病原物分子互作提供一定的参考。 相似文献
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综述了植物病原微生物产生的降解酶的种类、作用方式、在致病中的地位及研究进展,阐明了细胞壁降解酶的双重作用:即作为病原物侵染的致病因子及作为植物防卫反应的激发子,为寄主一病原物分子互作提供一定的参考。 相似文献
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昆虫病原微生物对其寄主行为的调控作用研究进展 总被引:2,自引:0,他引:2
昆虫病原微生物是调控昆虫种群数量动态的重要因子,其作为生物防治害虫的重要手段被广泛应用。昆虫病原物往往通过调控其寄主行为来提高自身的适应性,而有些寄主行为的改变却是其应对病原物侵染的免疫反应。发烧行为被证明可抑制病原增殖并延长寄主死亡;取食行为变化影响病原物或寄主的适应性;繁殖行为主要表现在产卵力、交配行为和性信息素等方面的变化;社会性行为改变对整个社会群体的适应性或病原物传播有影响;病原物所引起的寄主防卫和群集能力下降被认为对病原传播不利;病虫趋光和趋地行为、顶峰行为和活体寄主传病行为等被认为是病原物操纵的有利于病原微生物扩散和传播的行为。明确昆虫病原物调控其寄主行为的策略和机制对于寻找到新的害虫防治方法有指导意义。 相似文献
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植物防卫反应基因的类型、表达、调控和应用何晨阳,王金生(南京农业大学,210014)防卫反应基因是寄生植物中被诱导表达抗病反应的一类基因。早在70年代人们就发现寄主植物抗病性表达需要RNA和蛋白质的合成,也需要新合成的特殊酶类[1],同时也注意到植物防卫反应常常受到病原物及其激发子的诱导。从此,在研究植物对病原物防卫反应的生化和分子生物学机制方面取得了很大的进展[2]。 相似文献
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植物与病原微生物互作分子基础的研究进展 总被引:4,自引:0,他引:4
植物在与病原微生物共同进化过程中形成了复杂的免疫防卫体系。植物的先天免疫系统可大致分为两个层面。第一个层面的免疫基于细胞表面的模式识别受体对病原物相关分子模式的识别,该免疫过程被称为病原物相关分子模式触发的免疫(PAMP-triggered immunity,PTI),能帮助植物抵抗大部分病原微生物;第二个层面的免疫起始于细胞内部,主要依靠抗病基因编码的蛋白产物直接或间接识别病原微生物分泌的效应子并且激发防卫反应,来抵抗那些能够利用效应子抑制第一层面免疫的病原微生物,这一过程被称为效应子触发的免疫(Effector-triggered immunity,ETI)。这两个层面的免疫都是基于植物对"自我"及"非我"的识别,依靠MAPK级联等信号网络,将识别结果传递到细胞核内,调控相应基因的表达,做出适当的免疫应答。本文着重阐述了植物与病原微生物互作过程中不同层面的免疫反应所发生主要事件的分子基础及研究进展。 相似文献
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微生物与植物之间存在错综复杂的双向交流和串扰,植物与病原微生物互作直接影响寄主植物的生存状况,而植物和益生微生物互作则有利于宿主的生长和健康,共生微生物也会从中受益。不管是病原微生物还是有益微生物进入植物体内,植物miRNA都会迅速做出响应,同时微生物也可以产生miRNA样RNA(miRNA-likeRNA,milRNA)影响植物健康,可见miRNA(或milRNA)是植物与微生物互作过程中迅速响应的重要媒介分子,其内在机制研究近年来取得了许多进展。文中概述了植物-病原微生物、植物-益生微生物互作中miRNA的调控作用,重点阐述了植物miRNA在植物-病原微生物互作过程中对寄主植物抗病性的调控作用和植物-益生微生物互作过程中对宿主植物生长发育及代谢的调控,以及真菌milRNA对寄主植物的跨界调控作用。 相似文献
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Soon RL Li J Boyce JD Harper M Adler B Larson I Nation RL 《Journal of applied microbiology》2012,113(4):940-951
Contact angle analysis of cell surface hydrophobicity (CSH) describes the tendency of a water droplet to spread across a lawn of filtered bacterial cells. Colistin‐induced disruption of the Gram‐negative outer membrane necessitates hydrophobic contacts with lipopolysaccharide (LPS). We aimed to characterize the CSH of Acinetobacter baumannii using contact angles, to provide insight into the mechanism of colistin resistance. Contact angles were analysed for five paired colistin‐susceptible and resistant Ac. baumannii strains. Drainage of the water droplet through bacterial layers was demonstrated to influence results. Consequently, measurements were performed 0·66 s after droplet deposition. Colistin‐resistant cells exhibited lower contact angles (38·8±2·8–46·8±1·3°) compared with their paired colistin‐susceptible strains (40·7±3·0–48·0±1·4°; anova ; P < 0·05). Contact angles increased at stationary phase (50·3±2·9–61·5±2·5° and 47·4±2·0–50·8±3·2°, susceptible and resistant, respectively, anova ; P < 0·05) and in response to colistin 32 mg l?1 exposure (44·5±1·5–50·6±2·8° and 43·5±2·2–48·0±2·2°, susceptible and resistant, respectively; anova ; P < 0·05). Analysis of complemented strains constructed with an intact lpxA gene, or empty vector, highlighted the contribution of LPS to CSH. Compositional outer‐membrane variations likely account for CSH differences between Ac. baumannii phenotypes, which influence the hydrophobic colistin–bacterium interaction. Important insight into the mechanism of colistin resistance has been provided. Greater consideration of contact angle methodology is necessary to ensure accurate analyses are performed. 相似文献
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Leskovac V Trivić S Pericin D Kandrac J 《Journal of industrial microbiology & biotechnology》2004,31(4):155-160
In the present communication, a general method for the kinetic analysis of random bisubstrate mechanisms is described. The method comprises a stepwise application of the following kinetic and ligand-binding experiments: determination of steady-state kinetic constants, product inhibition patterns, maximum rate relationships, application of alternate substrates, application of dead-end inhibitors, direct binding of substrates, kinetic isotope effects, and isotope exchange studies. This general method was applied to a practical example: a yeast alcohol dehydrogenase-catalyzed oxidation of 2-propanol by NAD+ at pH 7.0, 25°C. It was found that this fully reversible reaction proceeds by a steady-state random Bi-Bi mechanism, whereby both dead-end complexes are formed. 相似文献
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According to the currently accepted model, enzymes searching for specific recognition sequences or structural elements (modified nucleotides, breaks, single-stranded DNA fragments, etc.) slide at a high rate along DNA. Such sliding is possible only if the enzymes possess sufficiently high affinity for all DNA, sequence notwithstanding. Therefore, significant differences in their affinity for specific and nonspecific DNA sequences are unlikely, and the formation of a complex between an enzyme and its target DNA is not a basic factor of enzyme specificity. To elucidate such factors, we have analyzed many DNA replication, DNA repair, topoisomerization, integration, and recombination enzymes using a number of physicochemical methods, including the method of stepwise increase in ligand complexity developed in our laboratory. It has been shown that high affinity of all studied enzymes for long DNAs is provided by the formation of many weak contacts of the enzyme with all nucleotide units covered by the protein globule. The main role lies in the contact between positively charged amino acid residues and internucleoside phosphate groups; however, the contribution of each contact is very small, and the full contact interface usually resembles that characteristic of interactions between oppositely charged biopolymer surfaces. In some cases, a significant contribution to the affinity is made through hydrophobic and/or van der Waals interactions of the enzymes with nucleotide bases. On the whole, such nonspecific interactions provide for five to eight orders of enzyme affinity for DNA, depending on the enzyme. Specific interactions of enzymes with long DNAs, in contrast to their contacts with small ligands, are usually weak and comparable in efficiency with weak nonspecific contacts. The sum of specific interactions most often provides for approximately one or, rarely, two orders of affinity. According to structural data, DNA binding to any of the investigated enzymes is followed by a stage of DNA conformation adjustment, which includes partial or complete DNA melting, deformation of its backbone, stretching, compression, bending or kinking, eversion of nucleotides from the DNA helix, etc. The full set of such changes is specific for each individual enzyme. The fact that all enzyme-dependent changes in DNA are effected through weak specific (rather than strong) interactions is very important. Enzyme-specific changes in DNA conformation are required for effective adjustment of reacting orbitals to an accuracy of 10°–15°, which is possible only in the case of specific DNAs. A transition from nonspecific to specific DNA leads to an increase in the reaction rate (k
cat) by four to eight orders of magnitude. Thus, the stages of DNA conformation adjustment and catalysis proper provide for the high specificity of enzyme action. 相似文献
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实验室条件下采用生长速率法测定化合物N-(4-甲基-2-氨基苯并噻唑)α-氨基-α-(3-三氟甲基苯基)-O,O-二(2-烷氧基乙基)亚膦酸酯对小麦赤霉病原菌(Fusarium graminearum)的离体抑制效果,并初步研究了其抑制小麦赤霉病原菌作用机制.实验结果表明,该化合物对小麦赤霉病原菌的EC_(50)为46.05 μg/mL,当化合物浓度为50 μg/mL时,对该病原菌的抑制率就达到了60.5 %.以浓度为250 μg/mL的该供试化合物处理小麦赤霉病原菌菌丝24 h后,其细胞膜通透性增强,菌体内还原糖、几丁糖和可溶性蛋白含量及几丁质酶活性在短时间内均出现先升高然后下降的趋势. 相似文献
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植物杀虫剂研究概况 总被引:3,自引:0,他引:3
付秀芹 《武汉生物工程学院学报》2006,(1)
简要综述不同资源类型的植物杀虫剂,通过其有效成份生物碱类、萜类、黄酮类、精油类、光活化毒素类等物质影响昆虫生长发育及消化系统、呼吸系统、代谢系统、神经肌肉系统等从而达到杀虫的目的。同时对其发展前景提出了展望。 相似文献