Cloning and functional characterization of the cis-aconitic acid decarboxylase (CAD) gene from Aspergillus terreus

被引:94
|
作者
Kanamasa, Shin [2 ]
Dwiarti, Lies [3 ]
Okabe, Mitsuyasu [3 ]
Park, Enoch Y. [1 ,3 ]
机构
[1] Shizuoka Univ, Grad Sch Sci & Technol, Biotechnol Lab, Integrated Biosci Sect,Suruga Ku, Shizuoka 4228529, Japan
[2] Japan Sci & Technol Agcy, JST Innovat Satellite Shizuoka, Naka Ku, Hamamatsu, Shizuoka 4328561, Japan
[3] Shizuoka Univ, Fac Agr, Biotechnol Lab, Dept Appl Biol Chem,Suruga Ku, Shizuoka 4228529, Japan
关键词
cis-aconitic acid decarboxylase; Aspergillus terreus; itaconic acid; gene cloning; gene expression;
D O I
10.1007/s00253-008-1523-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A filamentous fungus Aspergillus terreus produces itaconic acid, which is predicted to be derived from cis-aconitic acid via catalysis by cis-aconitic acid decarboxylase (CAD) in the carbon metabolism of the fungus. To clarify the enzyme's function and a pathway for itaconic acid biosynthesis, we cloned a novel gene encoding the enzyme. The open reading frame of this gene (CAD1) consists of 1,529 bp encoding 490 amino acids and is interrupted by a single intron. Among the identified proteins in the database, the primary structure of the protein encoded by CAD1 shared high identity with the MmgE/PrpD family of proteins, including a number of 2-methylcitrate dehydratases of bacteria. The cloned gene excluding an intron was introduced into the expression plasmid pAUR-CAD1 controlled by the ADH1 promoter. The CAD activity in Saccharomyces cerevisiae was confirmed by directly detecting itaconic acid as a product from cis-aconitic acid as a substrate. This result reveals for the first time that this gene encodes CAD, which is essential for itaconic acid production in A. terreus.
引用
收藏
页码:223 / 229
页数:7
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