Aichi M, Takatani N, Omata T
Laboratory of Molecular Plant Physiology, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, 464-8601 Japan.
J Bacteriol. 2001 Oct;183(20):5840-7. doi: 10.1128/JB.183.20.5840-5847.2001.
In Synechocystis sp. strain PCC 6803, the genes encoding the proteins involved in nitrate assimilation are organized into two transcription units, nrtABCD-narB and nirA, the expression of which was repressed by ammonium and induced by inhibition of ammonium assimilation, suggesting involvement of NtcA in the transcriptional regulation. Under inducing conditions, expression of the two transcription units was enhanced by nitrite, suggesting regulation by NtcB, the nitrite-responsive transcriptional enhancer we previously identified in Synechococcus sp. strain PCC 7942. The slr0395 gene, which encodes a protein 47% identical to Synechococcus NtcB, was identified as the Synechocystis ntcB gene, on the basis of the inability of an slr0395 mutant to rapidly accumulate the transcripts of the nitrate assimilation genes upon induction and to respond to nitrite. While Synechococcus NtcB strictly requires nitrite for its action, Synechocystis NtcB enhanced transcription significantly even in the absence of nitrite. Whereas the Synechococcus ntcB mutant expresses the nitrate assimilation genes to a significant level in an NtcA-dependent manner, the Synechocystis ntcB mutant showed only low-level expression of the nitrate assimilation genes, indicating that NtcA by itself cannot efficiently promote expression of these genes in Synechocystis. Activities of the nitrate assimilation enzymes in the Synechocystis ntcB mutant were consequently low, being 40 to 50% of the wild-type level, and the cells grew on nitrate at a rate approximately threefold lower than that of the wild-type strain. These results showed that the contribution of NtcB to the expression of nitrate assimilation capability varies considerably among different strains of cyanobacteria.
在聚球藻属(Synechocystis)PCC 6803菌株中,编码参与硝酸盐同化作用相关蛋白质的基因被组织成两个转录单元,即nrtABCD - narB和nirA,其表达受铵抑制,并在铵同化作用受抑制时被诱导,这表明NtcA参与转录调控。在诱导条件下,这两个转录单元的表达会因亚硝酸盐而增强,这表明由我们之前在聚球藻属(Synechococcus)PCC 7942菌株中鉴定出的亚硝酸盐响应性转录增强子NtcB进行调控。slr0395基因编码一种与聚球藻NtcB有47%同一性的蛋白质,基于slr0395突变体在诱导后无法快速积累硝酸盐同化基因的转录本以及对亚硝酸盐无反应,该基因被鉴定为聚球藻(Synechocystis)的ntcB基因。虽然聚球藻NtcB的作用严格需要亚硝酸盐,但即使在没有亚硝酸盐的情况下,聚球藻NtcB也能显著增强转录。聚球藻ntcB突变体以依赖NtcA的方式将硝酸盐同化基因表达至显著水平,而聚球藻ntcB突变体仅显示出硝酸盐同化基因的低水平表达,这表明NtcA自身无法在聚球藻中有效促进这些基因的表达。因此,聚球藻ntcB突变体中硝酸盐同化酶的活性较低,仅为野生型水平的40%至50%,并且细胞在硝酸盐上生长的速率比野生型菌株低约三倍。这些结果表明,NtcB对硝酸盐同化能力表达的贡献在不同蓝藻菌株中差异很大。