Frías José E, Herrero Antonia, Flores Enrique
Instituto de Bioquímica Vegetal y Fotosíntesis, Consejo Superior de Investigaciones Científicas-Universidad de Sevilla, Centro de Investigaciones Científicas Isla de la Cartuja, E-41092 Seville, Spain.
J Bacteriol. 2003 Sep;185(17):5037-44. doi: 10.1128/JB.185.17.5037-5044.2003.
Expression of the nitrate assimilation nir operon in the filamentous, heterocyst-forming cyanobacterium Anabaena sp. strain PCC 7120 requires the action of both the global nitrogen control transcription factor NtcA and the pathway-specific transcriptional regulator NtcB. In the genome of this cyanobacterium, the ntcB gene is found in a cluster of genes located in the complementary strand, upstream from the nir operon. Just downstream of ntcB, there is an open reading frame, all0601 (previously designated orf356 and now designated the cnaT gene), that putatively encodes a protein similar to proteins with glycosyl transferase activity and that is also present clustered together with ntcB homologues or nitrate assimilation structural genes in other cyanobacterial genomes. An insertional mutant of cnaT was generated and found to be unable to assimilate nitrate, although it could use ammonium or dinitrogen as a source of nitrogen for growth. In the mutant, under derepression conditions, nir operon mRNA (as determined by RNA-DNA hybridization and primer extension analysis) and enzymes of the nitrate reduction system (i.e., nitrate reductase and nitrite reductase) were expressed at low or undetectable levels. Inactivation of cnaT did not impair expression of ntcB, and expression of cnaT itself was constitutive and regulated by neither NtcA nor NtcB. Regulation of expression of the nir operon in Anabaena sp. strain PCC 7120 by CnaT and the previously described regulatory elements, NtcA and NtcB, is discussed.
在丝状、形成异形胞的蓝细菌鱼腥藻Anabaena sp.菌株PCC 7120中,硝酸盐同化nir操纵子的表达需要全局氮控制转录因子NtcA和途径特异性转录调节因子NtcB的共同作用。在这种蓝细菌的基因组中,ntcB基因位于互补链上nir操纵子上游的一组基因中。在ntcB的紧邻下游,有一个开放阅读框all0601(以前称为orf356,现在称为cnaT基因),其推测编码一种与具有糖基转移酶活性的蛋白质相似的蛋白质,并且在其他蓝细菌基因组中也与ntcB同源物或硝酸盐同化结构基因聚集在一起。构建了cnaT的插入突变体,发现其无法同化硝酸盐,尽管它可以利用铵或二氮作为生长的氮源。在该突变体中,在去阻遏条件下,nir操纵子mRNA(通过RNA-DNA杂交和引物延伸分析确定)和硝酸盐还原系统的酶(即硝酸盐还原酶和亚硝酸还原酶)以低水平或无法检测到的水平表达。cnaT的失活并不损害ntcB的表达,并且cnaT自身的表达是组成型的,不受NtcA或NtcB的调节。本文讨论了鱼腥藻Anabaena sp.菌株PCC 7120中CnaT以及先前描述的调节元件NtcA和NtcB对nir操纵子表达的调节。