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利用直接表达载体通过在酿酒酵母中进行遗传互补对哈茨木霉的咪唑甘油磷酸脱水酶基因进行分子克隆。

Molecular cloning of the imidazoleglycerolphosphate dehydratase gene of Trichoderma harzianum by genetic complementation in Saccharomyces cerevisiae using a direct expression vector.

作者信息

Goldman G H, Demolder J, Dewaele S, Herrera-Estrella A, Geremia R A, Van Montagu M, Contreras R

机构信息

Laboratorium voor Genetica, Universiteit Gent, Belgium.

出版信息

Mol Gen Genet. 1992 Sep;234(3):481-8. doi: 10.1007/BF00538709.

Abstract

The Trichoderma harzianum imidazoleglycerolphosphate dehydratase gene (igh) has been isolated by complementation of a Saccharomyces cerevisiae his3 mutant using a direct expression vector. This Escherichia coli-yeast shuttle vector was developed to allow efficient cloning and expression of cDNA libraries. The cDNA is 627 nucleotides long and codes for a protein of 209 amino acids with an apparent molecular mass of 22,466 daltons. The predicted protein sequence showed 63.6%, 58.7%, and 38.4% identity respectively to the corresponding enzymes from S. cerevisiae, Pichia pastoris and E. coli. Northern analysis showed that the expression of the igh gene in T. harzianum is not inhibited by external histidine and the level of igh mRNA was about threefold higher in cells starved of histidine.

摘要

通过使用直接表达载体对酿酒酵母his3突变体进行互补,分离出了哈茨木霉咪唑甘油磷酸脱水酶基因(igh)。开发这种大肠杆菌-酵母穿梭载体是为了实现cDNA文库的高效克隆和表达。该cDNA长627个核苷酸,编码一种209个氨基酸的蛋白质,表观分子量为22,466道尔顿。预测的蛋白质序列与酿酒酵母、巴斯德毕赤酵母和大肠杆菌的相应酶分别具有63.6%、58.7%和38.4%的同一性。Northern分析表明,哈茨木霉中igh基因的表达不受外源组氨酸的抑制,并且在缺乏组氨酸的细胞中igh mRNA水平大约高3倍。

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