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通过共表达意大利青霉羊毛甾醇14α-脱甲基酶(cyp51)和黑曲霉细胞色素P450还原酶(cprA)基因提高黑曲霉对14α-脱甲基酶抑制剂(DMIs)的抗性。

Increased resistance to 14 alpha-demethylase inhibitors (DMIs) in Aspergillus niger by coexpression of the Penicillium italicum eburicol 14 alpha-demethylase (cyp51) and the A. niger cytochrome P450 reductase (cprA) genes.

作者信息

van den Brink H J, van Nistelrooy H J, de Waard M A, van den Hondel C A, van Gorcom R F

机构信息

TNO Nutrition and Food Research Institute, Department of Molecular Genetics and Gene Technology, Rijswijk, The Netherlands.

出版信息

J Biotechnol. 1996 Aug 20;49(1-3):13-8. doi: 10.1016/0168-1656(96)01403-4.

Abstract

In this paper we describe the effects of over-expression of the Penicillium italicum gene encoding eburicol 14 alpha-demethylase (cyp51), in Aspergillus niger strains with one or multiple copies of the gene encoding cytochrome P450 reductase (cprA), on the eburicol 14 alpha-demethylase activity. Eburicol 14 alpha-demethylase activity was determined by measuring the resistance of transformants against some eburicol 14 alpha-demethylase inhibitors (DMIs). DMIs are widely used as fungicides in crop protection and human and veterinarian health care. DMI resistance in a transformant overexpressing both CPR and CYP51 was increased 5-30-fold compared to DMI resistance in the wild type strain, depending on the test compound used. Resistance in this strain was approximately 2-5-fold increased compared to DMI resistance in a transformant that was overexpressing the cyp51 gene but had only the wild type copy of the cprA gene and approximately 3-12-fold increased compared to a strain overexpressing the cprA gene (and having only the wild type copy of the cyp51 gene). These results show the importance of CPR overexpression for increasing cytochrome P450 activities in filamentous fungi.

摘要

在本文中,我们描述了在具有一个或多个细胞色素P450还原酶(cprA)编码基因拷贝的黑曲霉菌株中,意大利青霉编码羊毛甾醇14α-脱甲基酶(cyp51)的基因过表达对羊毛甾醇14α-脱甲基酶活性的影响。通过测量转化体对一些羊毛甾醇14α-脱甲基酶抑制剂(DMIs)的抗性来测定羊毛甾醇14α-脱甲基酶活性。DMIs在作物保护以及人类和兽医医疗保健中被广泛用作杀菌剂。与野生型菌株相比,同时过表达CPR和CYP51的转化体对DMIs的抗性提高了5至30倍,这取决于所使用的测试化合物。与只过表达cyp51基因但只有cprA基因野生型拷贝的转化体相比,该菌株的抗性提高了约2至5倍;与过表达cprA基因(且只有cyp51基因野生型拷贝)的菌株相比,抗性提高了约3至12倍。这些结果表明了CPR过表达对于增加丝状真菌中细胞色素P450活性的重要性。

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