Schaap P J, Müller Y, Baars J J, Op den Camp H J, Sonnenberg A S, van Griensven L J, Visser J
Section Molecular Genetics of Industrial Microorganisms, Wageningen Agricultural University, The Netherlands.
Mol Gen Genet. 1996 Feb 25;250(3):339-47. doi: 10.1007/BF02174392.
The gene encoding NADP+-dependent glutamate dehydrogenase (gdhA) was isolated from an Agaricus bisporus recombinant phage lambda library. The deduced amino acid sequence would specify a 457-amino acid protein that is highly homologous in sequence to those derived from previously isolated and characterized genes coding for microbial NADP+-GDH. The open reading frame is interrupted by six introns. None of the introns is located at either one of the positions of the two introns conserved in the corresponding open reading frames of the ascomycete fungi Aspergillus nidulans and Neurospora crassa. Northern analysis suggests that the A. bisporus gdhA gene is transcriptionally regulated and that, unlike the case in ascomycetes, transcription of this gene is repressed upon the addition of ammonium to the culture.
编码依赖于NADP⁺的谷氨酸脱氢酶(gdhA)的基因是从双孢蘑菇重组噬菌体λ文库中分离得到的。推导的氨基酸序列将指定一个457个氨基酸的蛋白质,其序列与先前分离和表征的编码微生物NADP⁺-GDH的基因高度同源。开放阅读框被六个内含子打断。这些内含子均不在构巢曲霉和粗糙脉孢菌子囊菌相应开放阅读框中保守的两个内含子位置之一。Northern分析表明,双孢蘑菇gdhA基因受到转录调控,并且与子囊菌不同的是,向培养物中添加铵后该基因的转录受到抑制。