Brito N, Avila J, Perez M D, Gonzalez C, Siverio J M
Departmento de Bioquímica y Biología Molecular, Universidad de La Laguna, Tenerife, Canarias, Spain.
Biochem J. 1996 Jul 1;317 ( Pt 1)(Pt 1):89-95. doi: 10.1042/bj3170089.
The nitrite reductase-encoding gene (YNI1) from the yeast Hansenula polymorpha was isolated from a lambda EMBL3 H. polymorpha genomic DNA library, using as a probe a 481 bp DNA fragment from the gene of Aspergillus nidulans encoding nitrite reductase (niiA). An open reading frame of 3132 bp, encoding a putative protein of 1044 amino acids with high similarity with nitrite reductases from fungi, was located by DNA sequencing in the phages lambdaNB5 and lambdaJA13. Genes YNI1 and YNR1 (encoding nitrate reductase) are clustered, separated by 1700 bp. Northern blot analysis showed that expression of YNI1 and YNR1 is co-ordinately regulated; induced by nitrate and nitrite and repressed by sources of reduced nitrogen, even in the presence of nitrate. A mutant lacking nitrite reductase activity was obtained by deletion of the chromosomal copy of YNI1. The mutant does not grow in nitrate or in nitrite; it exhibits a similar level of transcription of YNR1 to the wild type, but the nitrate reductase enzymic activity is only about 50% of the wild type. In the presence of nitrate the delta ynil::URA3 mutant extrudes approx. 24 nmol of nitrite/h per mg of yeast (wet weight), about five times more than the wild type.
从多形汉逊酵母的λEMBL3基因组DNA文库中分离出编码亚硝酸还原酶的基因(YNI1),使用来自构巢曲霉亚硝酸还原酶(niiA)基因的481 bp DNA片段作为探针。通过对噬菌体λNB5和λJA13进行DNA测序,定位到一个3132 bp的开放阅读框,其编码一个1044个氨基酸的假定蛋白质,与真菌的亚硝酸还原酶具有高度相似性。基因YNI1和YNR1(编码硝酸还原酶)成簇,相隔1700 bp。Northern印迹分析表明,YNI1和YNR1的表达受到协同调控;由硝酸盐和亚硝酸盐诱导,并被还原态氮源抑制,即使存在硝酸盐也是如此。通过缺失YNI1的染色体拷贝获得了一个缺乏亚硝酸还原酶活性的突变体。该突变体在硝酸盐或亚硝酸盐中均不能生长;它的YNR1转录水平与野生型相似,但硝酸还原酶的酶活性仅为野生型的约50%。在硝酸盐存在的情况下,δynil::URA3突变体每毫克酵母(湿重)每小时挤出约24 nmol的亚硝酸盐,约为野生型的五倍。