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首页> 外文期刊>Journal of bacteriology >Regulation by cyanate of the genes involved in carbon and nitrogen assimilation in the cyanobacterium Synechococcus sp. strain PCC 7942.
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Regulation by cyanate of the genes involved in carbon and nitrogen assimilation in the cyanobacterium Synechococcus sp. strain PCC 7942.

机译:氰酸盐调控的蓝藻Syechococcus sp。中涉及碳和氮同化的基因。株PCC 7942。

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A mutant (M45) of the cyanobacterium Synechococcus sp. strain PCC 7942, which is defective in active transport of nitrate, was used for the studies of the nitrogen regulation of the genes involved in nitrate and CO2 assimilation. In a medium containing 30 mM nitrate as the nitrogen source, M45 grew under constant stress of nitrogen deficiency and accumulated a five-times-larger amount of the transcript of nirA, the gene for nitrite reductase, compared with nitrate-grown wild-type cells. By contrast, the level of the transcript of rbcL, the gene for the large subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase, was 40% of the wild-type level. Addition of ammonium to the culture of M45 abolished the accumulation of the nirA transcript and stimulated the accumulation of the rbcL transcript, showing that ammonium repressed and activated the transcription of nirA and rbcL, respectively. Glutamine, the initial product of ammonium fixation, also showed negative and positive effects on nirA and rbcL, respectively. One of the metabolites of glutamine, carbamoylphosphate, and its decomposition product, cyanate, were found to repress nirA and also to markedly activate rbcL. Cyanate negatively regulated another ammonium-repressible gene, glnA, but had no effect on the psbAI and rps1 genes. The effects of cyanate were not ascribable to the ammonium and CO, resulting from its decomposition. These findings suggested that cyanate may act as a regulator of the ammonium-responsive genes involved in carbon and nitrogen assimilation in the cyanobacterium.
机译:蓝藻Syechococcus sp。的突变体(M45)。在硝酸盐主动转运方面存在缺陷的PCC 7942菌株用于研究硝酸盐和CO2同化相关基因的氮调节。在含有30 mM硝酸盐作为氮源的培养基中,M45在氮缺乏的恒定压力下生长,并且与硝酸盐生长的野生型细胞相比,积累了5倍数量的亚硝酸还原酶基因nirA转录本。 。相比之下,rbcL的转录水平是野生型水平的40%,该基因是核糖-1,5-双磷酸羧化酶/加氧酶大亚基的基因。向M45培养物中添加铵消除了nirA转录物的积累并刺激了rbcL转录物的积累,表明铵分别抑制和激活了nirA和rbcL的转录。铵固定的初始产物谷氨酰胺也分别对nirA和rbcL表现出负面和正面影响。谷氨酰胺的一种代谢产物氨基甲酰基磷酸酯及其分解产物氰酸盐被发现抑制nirA并显着激活rbcL。氰酸盐对另一个可抑制铵离子的基因glnA负调节,但对psbAI和rps1基因没有影响。氰酸盐的影响不是由于铵和CO的分解而引起的。这些发现表明,氰酸盐可能充当了与蓝细菌中碳和氮同化有关的铵响应基因的调节剂。

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