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从木质素降解担子菌朱红密孔菌中克隆并鉴定第二个漆酶基因

Cloning and characterization of a second laccase gene from the lignin-degrading basidiomycete Pycnoporus cinnabarinus.

作者信息

Temp U, Zierold U, Eggert C

机构信息

Institute of General Microbiology and Microbial Genetics, Friedrich-Schiller University Jena, Neugasse 24, D-07743, Jena, Germany.

出版信息

Gene. 1999 Aug 5;236(1):169-77. doi: 10.1016/s0378-1119(99)00239-5.

Abstract

The gene lcc3-2 encoding a second laccase of the white-rot fungus Pycnoporus cinnabarinus has been cloned, sequenced, and characterized. The isolated gene consists of 2840bp, with the coding region interrupted by ten introns and flanked by an upstream region in which putative CAAT and TATA boxes were identified. The cDNA of lcc3-2 contains an open reading frame of 1563bp. The deduced mature laccase protein consisted of 498 amino acids and was preceded by a signal peptide of 23 amino acids. The sequence of lcc3-2 reveals 73% similarity on the protein level to the previously characterized lcc3-1. The new laccase gene shares highest similarity to lcc1 from Trametes villosa (75%), and lcc2 from the unidentified basidiomycete CECT 20197 (75%). The calculated isoelectric point (pI) of 6.1 for the gene product LCC3-2 was in good agreement with the experimentally determined pI of a laccase secreted by P. cinnabarinus grown on cellulose. Transcription analysis using competitive reverse transcription (RT)-PCR showed that lcc3-2 was expressed in glucose and cellulose containing cultures. However, in contrast to lcc3-1, lcc3-2 transcription was not increased in response to 2,5-xylidine.

摘要

编码朱红密孔菌(Pycnoporus cinnabarinus)第二种漆酶的基因lcc3-2已被克隆、测序和表征。分离出的基因由2840bp组成,编码区被10个内含子中断,两侧是一个上游区域,在该区域中鉴定出了推定的CAAT盒和TATA盒。lcc3-2的cDNA包含一个1563bp的开放阅读框。推导的成熟漆酶蛋白由498个氨基酸组成,前面有一个23个氨基酸的信号肽。lcc3-2的序列在蛋白质水平上与先前表征的lcc3-1有73%的相似性。新的漆酶基因与绒毛栓菌(Trametes villosa)的lcc1(75%)和未鉴定的担子菌CECT 20197的lcc2(75%)具有最高的相似性。基因产物LCC3-2计算出的等电点(pI)为6.1,与在纤维素上生长的朱红密孔菌分泌的漆酶的实验测定pI高度一致。使用竞争性逆转录(RT)-PCR进行的转录分析表明,lcc3-2在含有葡萄糖和纤维素的培养物中表达。然而,与lcc3-1不同,lcc3-2的转录不会因2,5-二甲基苯胺而增加反应。

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