Montesinos M L, Muro-Pastor A M, Herrero A, Flores E
Instituto de Bioquímica Vegetal y Fotosíntesis, Consejo Superior de Investigaciones Científicas-Universidad de Sevilla, E-41092 Sevilla, Spain.
J Biol Chem. 1998 Nov 20;273(47):31463-70. doi: 10.1074/jbc.273.47.31463.
Ammonium is an important nitrogen source for many microorganisms and plants. Ammonium transporters whose activity can be probed with [14C]methylammonium have been described in several organisms including some cyanobacteria, and amt genes encoding ammonium/methylammonium permeases have been recently identified in yeast, Arabidopsis thaliana, and some bacteria. The unicellular cyanobacterium Synechocystis sp. PCC 6803 exhibited a [14C]methylammonium uptake activity that was inhibited by externally added ammonium. Three putative amt genes that are found in the recently published complete sequence of the chromosome of strain PCC 6803 were inactivated by insertion of antibiotic resistance-encoding gene-cassettes. The corresponding mutant strains were impaired in uptake of [14C]methylammonium. Open reading frame sll0108 (amt1) was responsible for a high affinity uptake activity (Ks for methylammonium, 2.7 microM), whereas open reading frames sll1017 (amt2) and sll0537 (amt3) made minor contributions to uptake at low substrate concentrations. Expression of the three amt genes was higher in nitrogen-starved cells than in cells incubated in the presence of a source of nitrogen (either ammonium or nitrate), but amt1 was expressed at higher levels than the other two amt genes. Transcription of amt1 was found to take place from a promoter bearing the structure of the cyanobacterial promoters activated by the nitrogen control transcription factor, NtcA.
铵是许多微生物和植物的重要氮源。在包括一些蓝细菌在内的几种生物体中,已描述了可用[14C]甲基铵探测其活性的铵转运蛋白,并且最近在酵母、拟南芥和一些细菌中鉴定出了编码铵/甲基铵通透酶的amt基因。单细胞蓝细菌聚球藻属PCC 6803表现出[14C]甲基铵摄取活性,该活性受到外部添加铵的抑制。在最近公布的菌株PCC 6803染色体完整序列中发现的三个假定的amt基因通过插入抗生素抗性编码基因盒而失活。相应的突变菌株在[14C]甲基铵摄取方面受损。开放阅读框sll0108(amt1)负责高亲和力摄取活性(甲基铵的Ks为2.7 microM),而开放阅读框sll1017(amt2)和sll0537(amt3)在低底物浓度下对摄取的贡献较小。这三个amt基因在氮饥饿细胞中的表达高于在存在氮源(铵或硝酸盐)的情况下培养的细胞,但amt1的表达水平高于其他两个amt基因。发现amt1的转录发生在一个具有由氮控制转录因子NtcA激活的蓝细菌启动子结构的启动子上。