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Cuticle-degrading proteases produced by the entomopathogenic fungus Beauveria bassiana in the presence of coffee berry borer cuticle

机译:在咖啡bore虫角质层存在下由昆虫病原真菌球孢白僵菌产生的表皮降解蛋白酶

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摘要

A Brazilian isolate of Beauveria bassiana (CG425) that shows high virulence against the coffee berry borer (CBB) was examined for the production of subtilisin-like (Pr1) and trypsin-like (Pr2) cuticle-degrading proteases. Fungal growth was either in nitrate-medium or in CBB cuticle-containing medium under both buffered and unbuffered conditions. In unbuffered medium supplemented with cuticle, the pH of cultures dropped and Pr1 and Pr2 activities were detected in high amounts only at a pH of 5.5 or higher. In buffered cultures, Pr1 and Pr2 activities were higher in medium supplemented with cuticle compared to activities with nitrate-medium. The Pr1 and Pr2 activities detected were mostly in the culture supernatant. These data suggest that Pr1 and Pr2 proteases produced by strain CG425 are induced by components of CBB cuticle, and that the culture pH influences the expression of these proteases, indicating the occurrence of an efficient mechanism of protein secretion in this fungus. The results obtained in this study extend the knowledge about protease production in B. bassiana CG425, opening new avenues for studying the role of secreted proteases in virulence against the coffee berry borer during the infection process.
机译:检查了巴西对虾球孢白僵菌(CG425)的抗咖啡果蝇(CBB)的高毒力,研究了枯草杆菌蛋白酶样(Pr1)和胰蛋白酶样(Pr2)角质层降解蛋白酶的产生。在缓冲和非缓冲条件下,真菌均在硝酸盐培养基或含CBB表皮的培养基中生长。在补充了表皮的非缓冲培养基中,培养液的pH下降,仅在5.5或更高的pH下才大量检测到Pr1和Pr2活性。在缓冲培养中,补充了表皮的培养基中的Pr1和Pr2活性高于硝酸盐培​​养基。检测到的Pr1和Pr2活性主要在培养上清液中。这些数据表明,由菌株CG425产生的Pr1和Pr2蛋白酶是由CBB表皮的成分诱导的,并且培养pH影响这些蛋白酶的表达,表明在这种真菌中蛋白分泌的有效机制的出现。这项研究中获得的结果扩展了球孢杆菌CG425中蛋白酶生产的知识,为研究分泌的蛋白酶在感染过程中对咖啡against的毒力中的作用开辟了新途径。

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