首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Mechanism by which contact with plant cuticle triggers cutinase gene expression in the spores of Fusarium solani f. sp. pisi
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Mechanism by which contact with plant cuticle triggers cutinase gene expression in the spores of Fusarium solani f. sp. pisi

机译:与植物角质层接触触发枯萎镰刀菌孢子中角质酶基因表达的机制。 sp。皮斯

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摘要

Spores of the phytopathogenic fungus Fusarium solani f. sp. pisi were shown to produce the extracellular enzyme, cutinase, only when cutin or cutin hydrolysate was added to the spore suspension. Dihydroxy-C16 acid and trihydroxy-C18 acid, which are unique cutin monomers, showed the greatest cutinase-inducing activity. Experiments with several compounds structurally related to these fatty acids suggested that both a ω-hydroxyl and a midchain hydroxyl are required for cutinase-inducing activity. Cutinase appeared in the medium 30-45 min after the addition of the inducers to the spore suspension, and the activity level increased for 6 hr. Addition of cycloheximide (5 μg/ml) completely inhibited cutinase production, suggesting that protein synthesis was involved in the increase of cutinase activity. Immunoblot analysis with rabbit antibodies prepared against cutinase showed that cutinase protein increased in parallel with the increase in enzyme activity. Measurement of cutinase-specific RNA levels by dot-blot hybridization with 32P-labeled cutinase cDNA showed that the cutinase gene transcripts could be detected within 15 min after addition of the inducers. Addition of exogenous cutinase greatly enhanced the level of cutinase gene transcripts induced by cutin. These results strongly suggest that the fungal spore senses that it is in contact with the plant by the production of small amounts of cutin monomers catalyzed by the low level of cutinase carried by the spore and that these monomers induce the synthesis of cutinase needed for penetration of the fungus into the plant.
机译:植物病原真菌Fusarium solani的孢子。 sp。仅当将角质或角质水解产物添加到孢子悬浮液中时,pis才产生胞外酶角质酶。二羟基-C16酸和三羟基-C18酸是独特的角质素单体,表现出最大的角质酶诱导活性。在结构上与这些脂肪酸相关的几种化合物的实验表明,角质酶诱导活性既需要ω-羟基,又需要中链羟基。向孢子悬浮液中添加诱导剂后30-45分钟,角质酶出现在培养基中,并且活性水平提高了6小时。添加环己酰亚胺(5μg/ ml)完全抑制了角质酶的产生,表明蛋白质合成与角质酶活性的增加有关。用针对角质酶制备的兔抗体进行的免疫印迹分析表明,角质酶蛋白与酶活性的增加同时增加。通过与 32 P标记的角质酶cDNA斑点杂交检测角质酶特异性RNA水平,结果表明,加入诱导剂后15分钟内即可检测到角质酶基因转录本。外源角质酶的加入大大提高了角质诱导的角质酶基因转录水平。这些结果强烈表明,真菌孢子通过孢子携带的低水平角质酶的催化产生少量角质单体而感觉到它与植物接触,并且这些单体诱导了角质酶渗透所需的角质酶的合成。真菌进入植物。

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