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黑曲霉葡萄糖-6-磷酸脱氢酶编码基因(gsdA)的分离与鉴定

Isolation and characterization of the glucose-6-phosphate dehydrogenase encoding gene (gsdA) from Aspergillus niger.

作者信息

van den Broek P, Goosen T, Wennekes B, van den Broek H

机构信息

Department of Genetics, Agricultural University Wageningen, The Netherlands.

出版信息

Mol Gen Genet. 1995 Apr 20;247(2):229-39. doi: 10.1007/BF00705654.

Abstract

Genomic and cDNA clones encoding glucose-6-phosphate dehydrogenase (G6PD) were isolated from the fungus Aspergillus niger. Sequence analysis of the glucose-6-phosphate dehydrogenase gene (gsdA) revealed an open reading frame of 1530 bp, encoding a protein of 58,951 kDa. The gsdA gene is interrupted by nine introns the most proximal of which is exceptionally large (348 bp). The region upstream of the ATG contains several C+T-rich stretches. The two major and one minor transcription start points are all located within these regions. In the upstream region several direct and inverted repeats, but no clear TATA or CCAAT boxes can be found. A. niger strains overproducing G6PD were constructed by cotransformation of gsdA subclones. Overexpression of G6PD was shown to be deleterious for the fungus, especially when cotransformants were grown on media containing ammonia. Attempts to construct a gsdA null mutant by gene disruption were unsuccessful.

摘要

从黑曲霉中分离出编码葡萄糖-6-磷酸脱氢酶(G6PD)的基因组和cDNA克隆。对葡萄糖-6-磷酸脱氢酶基因(gsdA)的序列分析显示,其开放阅读框为1530 bp,编码一种58,951 kDa的蛋白质。gsdA基因被9个内含子打断,其中最靠近上游的内含子特别大(348 bp)。ATG上游区域包含几个富含C+T的片段。两个主要转录起始点和一个次要转录起始点均位于这些区域内。在上游区域可发现几个正向和反向重复序列,但未发现明确的TATA或CCAAT框。通过共转化gsdA亚克隆构建了过量产生G6PD的黑曲霉菌株。结果表明,G6PD的过表达对真菌有害,尤其是当共转化子在含有氨的培养基上生长时。通过基因破坏构建gsdA缺失突变体的尝试未成功。

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