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虾青素产生菌红法夫酵母中依赖烟酰胺腺嘌呤二核苷酸磷酸的谷氨酸脱氢酶基因:利用其启动子进行基因的可控表达。

The NADP-dependent glutamate dehydrogenase gene from the astaxanthin producer Xanthophyllomyces dendrorhous: use of Its promoter for controlled gene expression.

作者信息

Rodríguez-Sáiz Marta, Godio Ramiro P, Alvarez Vanessa, de la Fuente Juan Luis, Martín Juan F, Barredo José Luis

机构信息

R&D Biology, Antibióticos S.A, Avenida de Antibióticos 59-61, 24009, León, Spain.

出版信息

Mol Biotechnol. 2009 Feb;41(2):165-72. doi: 10.1007/s12033-008-9123-y. Epub 2008 Nov 18.

Abstract

The gdhA gene encoding the NADP-dependent glutamate dehydrogenase (GDH) activity from Xanthophyllomyces dendrorhous has been cloned and characterized, and its promoter used for controlled gene expression in this red-pigmented heterobasidiomycetous yeast. We determined the nucleotide sequence of a 4701 bp DNA genomic fragment, showing an open reading frame of 1871 bp interrupted by five introns with fungal consensus splice-site junctions. The predicted protein (455 amino acids; 49 kDa) revealed high identity to GDHs, especially to those from the fungi Cryptococcus neoformans (70%), Sclerotinia sclerotiorum (66%), and several species of Aspergillus (66-67%). Gene phylogenies support the grouping of X. dendrorhous GDH close to those from the majority of the filamentous fungi. The promoter region of the gdhA gene (PgdhA) contains a TATA-like box and two large pyrimidine stretches. The use of PgdhA for gene expression was validated by electrotransformation of X. dendrorhous using an in-frame fusion with the hygromycin resistance gene (hygR) as a reporter. X. dendrorhous transformants were able to grow in YEME complex medium and in Czapek minimal medium supplemented with 50 microg/ml hygromycin, but gene expression in Czapek medium was repressed when using ammonium acetate as a nitrogen source. PgdhA is a valuable tool for controlled gene expression in Basidiomycetes.

摘要

已克隆并鉴定了来自红酵母(Xanthophyllomyces dendrorhous)的编码依赖于NADP的谷氨酸脱氢酶(GDH)活性的gdhA基因,其启动子用于在这种产红色色素的异担子菌酵母中进行基因的可控表达。我们测定了一个4701 bp DNA基因组片段的核苷酸序列,该序列显示一个1871 bp的开放阅读框,被5个具有真菌共有剪接位点连接的内含子打断。预测的蛋白质(455个氨基酸;49 kDa)与GDH具有高度同源性,尤其是与新型隐球菌(Cryptococcus neoformans)(70%)、核盘菌(Sclerotinia sclerotiorum)(66%)以及几种曲霉属(Aspergillus)物种(66 - 67%)的GDH同源。基因系统发育分析支持红酵母GDH与大多数丝状真菌的GDH归为一组。gdhA基因的启动子区域(PgdhA)包含一个类似TATA的框和两个大的嘧啶延伸序列。通过将与潮霉素抗性基因(hygR)的框内融合作为报告基因对红酵母进行电转化,验证了PgdhA用于基因表达的功能。红酵母转化体能够在YEME复合培养基以及添加了50 μg/ml潮霉素的察氏基本培养基中生长,但是当使用乙酸铵作为氮源时,察氏培养基中的基因表达受到抑制。PgdhA是担子菌中用于可控基因表达的一种有价值的工具。

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