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从白腐真菌黄孢原毛平革菌中鉴定出一个新的细胞色素P-450基因。

Identification of a novel cytochrome P-450 gene from the white rot fungus Phanerochaete chrysosporium.

作者信息

Kullman S W, Matsumura F

机构信息

Department of Environmental Toxicology, University of California, Davis 95616, USA.

出版信息

Appl Environ Microbiol. 1997 Jul;63(7):2741-6. doi: 10.1128/aem.63.7.2741-2746.1997.

Abstract

A gene fragment belonging to the cytochrome P-450 superfamily has been cloned and identified from stationary cultures of the filamentous fungus Phanerochaete chrysosporium by reverse transcriptase (RT)-PCR. A set of degenerate primers homologous to highly conserved regions of known cytochrome P-450 sequences were used for initial RT-PCRs. Individual PCR products were cloned, sequenced, and identified as those belonging to the cytochrome P-450 superfamily based on amino acid sequence homologies and the presence of the highly conserved heme binding region. The nucleotide sequence of a single cDNA clone indicated the presence of an open reading frame encoding a partial cytochrome P-450 protein of 208 amino acids. Comparisons of the deduced amino acid sequence of the partial protein to other known cytochrome P-450 sequences indicate that it is the first member of a new family of cytochrome P-450s, designated CYP63-1A. Northern blot analysis suggests that CYP63-1A is expressed under both nitrogen-rich and nitrogen-deficient culture conditions and thus not under the same regulatory constraints as the well-studied lignin and manganese peroxidases. Western blot analyses using antibodies raised to the heme binding region of CYP63-1A indicate that the protein has a molecular mass of approximately 44,000 Da.

摘要

通过逆转录酶(RT)-PCR技术,从丝状真菌黄孢原毛平革菌的静止培养物中克隆并鉴定出一个属于细胞色素P-450超家族的基因片段。使用一组与已知细胞色素P-450序列的高度保守区域同源的简并引物进行初始RT-PCR。将各个PCR产物进行克隆、测序,并根据氨基酸序列同源性和高度保守的血红素结合区域的存在,鉴定其属于细胞色素P-450超家族。单个cDNA克隆的核苷酸序列表明存在一个开放阅读框,编码一个由208个氨基酸组成的部分细胞色素P-450蛋白。将该部分蛋白的推导氨基酸序列与其他已知细胞色素P-450序列进行比较,表明它是细胞色素P-450一个新家族的首个成员,命名为CYP63-1A。Northern印迹分析表明,CYP63-1A在富氮和缺氮培养条件下均有表达,因此不受与研究充分的木质素和锰过氧化物酶相同的调控限制。使用针对CYP63-1A血红素结合区域产生的抗体进行的Western印迹分析表明,该蛋白的分子量约为44,000 Da。

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