首页> 外文期刊>Biological Control: Theory and Application in Pest Management >Biological control of Pythium aphanidermatum in cucumber with a combined application of Lysobacter enzymogenes strain 3.1T8 and chitosan
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Biological control of Pythium aphanidermatum in cucumber with a combined application of Lysobacter enzymogenes strain 3.1T8 and chitosan

机译:溶菌酶基因菌株3.1T8和壳聚糖联合应用对黄瓜瓜果腐霉的生物防治

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摘要

Pythium aphanidermatum (Edson) Fitzp., causing root and crown rot in cucumber, was successfully managed by Lysobacter enzymogenes strain 3.1T8. Greenhouse experiments were performed with cucumber plants grown in rockwool blocks up to 5 weeks with a recirculated nutrient solution. Application of L. enzymogenes 3.1T8 in combination with chitosan (the deacetylated derivative of chitin) reduced the number of diseased plants by 50-100% in four independent experiments relative to the Pythium control. Application of chitosan or the bacterial inoculant alone was not effective. Washed bacterial cells plus chitosan inhibited Pythium-induced disease, but the supernatant without bacterial cells combined with chitosan was not effective. The most effective and convenient type of commercially available chitosan was selected. Chitosan disappeared from the hydroponic system within 24 h after application, which we attribute to enzyme expression of L. enzymogenes 3.1T8 induced by the exposure to chitosan. Plate counts of the nutrient solution on a general bacterial medium showed the dominance of the inoculated strain, and an increased bacterial population growing on chitin and chitosan as single carbon source. The population density of L. enzymogenes 3.1T8 on the cucumber roots was investigated with a strain specific real-time TaqMan PCR. Highest chitosan concentrations applied (0.1 and 0.03 g/plant) resulted in the highest numbers of L. enzymogenes 3.1T8 present on roots; i.e. 108-109 cells/g root. Substantially higher numbers of bacterial cells were observed by scanning electron microscopy after application of chitosan; no morphological or other qualitative differences were found. The results indicate that addition of chitosan enhanced the biocontrol efficacy of L. enzymogenes 3.1T8; either chitosan serves as C- and N-source for the antagonist, induces antagonistic gene expression, or both.
机译:造成黄瓜根冠腐烂的腐霉腐霉(Pythium aphanidermatum(Edson)Fitzp。)已成功地通过溶菌酶酶基因菌株3.1T8处理。用循环营养液对生长在岩棉块中的黄瓜植株进行长达5周的温室试验。相对于腐霉菌对照,在四个独立的实验中,将酶促产乳杆菌3.1T8与壳聚糖(几丁质的脱乙酰化衍生物)组合使用可使患病植物的数量减少50-100%。单独使用壳聚糖或细菌接种剂无效。洗涤过的细菌细胞加壳聚糖可抑制腐霉病诱导的疾病,但没有细菌细胞与壳聚糖结合的上清液无效。选择了最有效和方便的市售壳聚糖类型。壳聚糖在施用后24小时内从水培系统中消失,这归因于暴露于壳聚糖诱导的L.酶基因3.1T8的酶表达。在普通细菌培养基上对营养液进行平板计数表明,接种菌株占优势,并且在几丁质和壳聚糖作为单一碳源的情况下,细菌种群增加。用菌株特异性实时TaqMan PCR研究黄瓜根上的L.酶基因3.1T8的种群密度。施用最高的壳聚糖浓度(每株植物0.1和0.03 g)导致根部存在的L.酶基因3.1T8数量最多。即108-109个细胞/克根。应用壳聚糖后,通过扫描电子显微镜观察到的细菌细胞数量明显增加;没有发现形态或其他定性差异。结果表明,壳聚糖的添加增强了L.酶基因3.1T8的生物防治功效。壳聚糖既可以用作拮抗剂的C源和N源,也可以诱导拮抗基因的表达,或两者兼而有之。

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