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来自食用草菇(Volvariella volvacea)的漆酶的生化与分子特性

Biochemical and molecular characterization of a laccase from the edible straw mushroom, Volvariella volvacea.

作者信息

Chen Shicheng, Ge Wei, Buswell John A

机构信息

Department of Biology and the Centre for International Services to Mushroom Biotechnology, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong SAR, China.

出版信息

Eur J Biochem. 2004 Jan;271(2):318-28. doi: 10.1046/j.1432-1033.2003.03930.x.

Abstract

We have isolated a laccase (lac1) from culture fluid of Volvariella volvacea, grown in a defined medium containing 150 micro m CuSO4, by ion-exchange and gel filtration chromatography. Lac1 has a molecular mass of 58 kDa as determined by SDS/PAGE and an isoelectric point of 3.7. Degenerate primers based on the N-terminal sequence of purified lac1 and a conserved copper-binding domain were used to generate cDNA fragments encoding a portion of the lac1 protein and RACE was used to obtain full-length cDNA clones. The cDNA of lac1 contained an ORF of 1557 bp encoding 519 amino acids. The amino acid sequence from Ala25 to Asp41 corresponded to the N-terminal sequence of the purified protein. The first 24 amino acids are presumed to be a signal peptide. The expression of lac1 is regulated at the transcription level by copper and various aromatic compounds. RT-PCR analysis of gene transcription in fungal mycelia grown on rice-straw revealed that, apart from during the early stages of substrate colonization, lac1 was expressed at every stage of the mushroom developmental cycle defined in this study, although the levels of transcription varied considerably depending upon the developmental phase. Transcription of lac1 increased sharply during the latter phase of substrate colonization and reached maximum levels during the very early stages (primordium formation, pinhead stage) of fruit body morphogenesis. Gene expression then declined to approximately 20-30% of peak levels throughout the subsequent stages of sporophore development.

摘要

我们通过离子交换和凝胶过滤色谱法,从在含有150微摩尔硫酸铜的限定培养基中生长的草菇培养液中分离出一种漆酶(lac1)。通过SDS/PAGE测定,Lac1的分子量为58 kDa,等电点为3.7。基于纯化的lac1的N端序列和保守的铜结合结构域设计的简并引物,用于生成编码lac1蛋白一部分的cDNA片段,并使用RACE获得全长cDNA克隆。lac1的cDNA包含一个1557 bp的开放阅读框,编码519个氨基酸。从Ala25到Asp41的氨基酸序列与纯化蛋白的N端序列相对应。前24个氨基酸被认为是信号肽。Lac1的表达在转录水平上受到铜和各种芳香化合物的调控。对在稻草上生长的真菌菌丝体中的基因转录进行RT-PCR分析表明,除了在底物定殖的早期阶段外,在本研究定义的蘑菇发育周期的每个阶段,lac1都有表达,尽管转录水平因发育阶段而异。在底物定殖的后期阶段,lac1的转录急剧增加,并在子实体形态发生的非常早期阶段(原基形成、针头期)达到最高水平。然后,在随后的子实体发育阶段,基因表达下降至峰值水平的约20-30%。

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