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首页> 外文期刊>Journal of bacteriology >Expression and Mutational Analysis of the glnB Genomic Region in the Heterocyst-Forming Cyanobacterium Anabaena sp. Strain PCC 7120
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Expression and Mutational Analysis of the glnB Genomic Region in the Heterocyst-Forming Cyanobacterium Anabaena sp. Strain PCC 7120

机译:glnB基因组区域在形成异囊的蓝藻蓝藻中的表达和突变分析。应变PCC 7120

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In the filamentous, heterocyst-forming cyanobacterium Anabaena sp. strain PCC 7120, the glnB gene is expressed at considerable levels both in the presence and in the absence of combined nitrogen, although induction, influenced by NtcA, takes place upon combined-nitrogen deprivation likely localized to vegetative cells. In spite of extensive efforts, a derivative of PCC 7120 lacking a functional glnB gene could be obtained only with constructs that lead to overexpression of a downstream open reading frames (ORF), particularly all2318. Strain CSP10 [glnB all2318(Con)] exhibited growth rates similar to those of the wild type when it was using nitrate or ammonium, but its diazotrophic growth was impaired. However, it differentiated heterocysts with a time course and distribution pattern similar to those of the wild type, although with no cyanophycin-containing polar granules, and exhibited impaired nitrogenase activity under oxic conditions, but not under microoxic conditions. In the mutant, NtcA-dependent inducion of the hetC and nifH genes was unaltered, but induction of the urtA gene and urea transport activity were increased. Active uptake of nitrite was also increased and insensitive to the ammonium-promoted inhibition observed for the wild type. Thus, regulation of the nitrite transport activity requires the glnB gene product. In the presence of a wild-type glnB gene, neither inactivation nor overexpression of all2318 produced an apparent phenotype. Thus, in an otherwise wild-type background, the glnB gene appears to be essential for growth of strain PCC 7120. For growth with combined nitrogen but not for diazotrophic growth, the requirement for glnB can be overridden by increasing the expression of all2318 (and/or ORFs downstream of it).
机译:在丝状,形成异囊的蓝细菌 Anabaena sp。中。在存在和不存在联合氮的情况下,PCC 7120菌株, glnB 基因均以相当高的水平表达,尽管诱导是受NtcA的影响,而联合氮的剥夺可能发生在营养细胞上。尽管付出了巨大的努力,但只有通过导致下游开放阅读框(ORF),特别是all2318过度表达的构建体,才能获得缺乏功能性 glnB 基因的PCC 7120衍生物。菌株CSP10 [ glnB all2318(Con)]的生长速率与使用硝酸盐或铵盐的野生型相似,但重氮营养的生长受到了损害。然而,尽管没有含氰霉素的极性颗粒,它以与野生型相似的时间过程和分布模式区分了异质囊,并且在有氧条件下而不是在微氧条件下显示出受损的固氮酶活性。在该突变体中, hetC nifH 基因的NtcA依赖性诱导没有改变,但是 urtA 基因的诱导和尿素转运活性增加。 。亚硝酸盐的主动摄取也增加了,并且对野生型观察到的氨促进的抑制不敏感。因此,调节亚硝酸盐转运活性需要 glnB 基因产物。在野生型 glnB 基因的存在下,all2318的失活和过表达均不会产生明显的表型。因此,在其他野生型背景下, glnB 基因对于PCC 7120菌株的生长似乎必不可少。对于结合氮的生长而不是对重氮营养的生长, glnB < / em>可以通过增加all2318(和/或其下游的ORF)的表达来覆盖。

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