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从香菇(Grifola frondosa)中克隆编码纤维二糖脱氢酶的cDNA并进行特性分析

Molecular cloning and characterization of a cDNA encoding cellobiose dehydrogenase from the wood-rotting fungus Grifola frondosa.

作者信息

Yoshida Makoto, Ohira Tsuyoshi, Igarashi Kiyohiko, Nagasawa Hiromichi, Samejima Masahiro

机构信息

Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan.

出版信息

FEMS Microbiol Lett. 2002 Dec 17;217(2):225-30. doi: 10.1111/j.1574-6968.2002.tb11479.x.

Abstract

Cloning of a cDNA encoding cellobiose dehydrogenase (CDH) from the wood-rotting fungus Grifola frondosa, which produces the edible maitake mushroom, was performed using reverse transcription-polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends. The CDH cDNA consisted of 2469 bp, including an open reading frame encoding the 18-amino acid signal peptide at the N-terminal region and the 750-amino acid mature protein with a predicted molecular mass of 79.6 kDa and a pI value of 4.32. Analysis of the amino acid sequence revealed that it contains a flavin-binding motif, two glucose-methanol-choline oxidoreductase motifs, and two possible residues for heme ligand binding (Met61 and His58). The amino acid sequence of G. frondosa CDH (GfrCDH) has a high degree of identity with three known CDHs from basidiomycetes, but not with two CDHs from ascomycetes. In addition, transcription of the CDH gene in G. frondosa grown on several carbon sources was analyzed by RT-PCR. mRNA of GfrCDH was detected from mycelia grown on cellobiose and cellulose, but not on glucose. Consequently, transcription of the GfrCDH gene seems to be promoted under conditions favoring cellulose degradation, and to be regulated by carbon catabolite repression.

摘要

利用逆转录-聚合酶链反应(RT-PCR)和cDNA末端快速扩增技术,从可食用舞茸的木腐真菌灰树花中克隆了编码纤维二糖脱氢酶(CDH)的cDNA。该CDH cDNA由2469个碱基对组成,包括一个在N端区域编码18个氨基酸信号肽的开放阅读框和一个750个氨基酸的成熟蛋白,预测分子量为79.6 kDa,pI值为4.32。氨基酸序列分析表明,它含有一个黄素结合基序、两个葡萄糖-甲醇-胆碱氧化还原酶基序以及两个可能的血红素配体结合残基(Met61和His58)。灰树花CDH(GfrCDH)的氨基酸序列与来自担子菌的三种已知CDH具有高度同源性,但与来自子囊菌的两种CDH不同源。此外,通过RT-PCR分析了灰树花在几种碳源上生长时CDH基因的转录情况。在以纤维二糖和纤维素为碳源生长的菌丝体中检测到了GfrCDH的mRNA,但在以葡萄糖为碳源生长的菌丝体中未检测到。因此,GfrCDH基因的转录似乎在有利于纤维素降解的条件下被促进,并受碳分解代谢物阻遏调控。

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