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    假尿苷合成酶RsuA介导近岸聚球藻PCC 7002对盐胁迫的适应性

    PSEUDOURIDINE SYNTHASE RSUA MEDIATES SALT STRESS ADAPTATION IN COASTAL SYNECHOCOCCUS sp. PCC 7002

    • 摘要: 为了探究近岸浮游植物的盐适应机制, 本研究选取近岸广盐性蓝藻——聚球藻PCC 7002开展盐胁迫机制研究。利用实验室前期构建的以5000 bp为单位逐段缺失的聚球藻突变株文库, 进行盐胁迫筛选, 获得了一株响应盐胁迫的突变株Δ480。随后通过对缺失片段所含基因进行逐个敲除, 确定假尿苷合成酶编码基因rsuA是导致突变株盐胁迫敏感的关键基因。进一步测定突变株(ΔrsuA)、回补株(ΔrsuA::rsuA)及超表达株(OE-rsuA)在标准盐浓度(0.3 mol/L NaCl)和高盐浓度(1.2 mol/L NaCl)条件下的生理参数, 发现ΔrsuA在高盐胁迫下生长速率、叶绿素a含量及光系统II最大光化学效率(Fv/Fm)均较野生型显著降低; 回补株表型可恢复至野生型水平, 确认表型是由于该基因失活所致。通过转录组分析发现, 正常条件下细胞通过上调核糖体相关基因表达来代偿因rsuA缺失导致的核糖体组装不稳定的功能缺陷, 而在盐胁迫条件下细胞对应激蛋白的需求被急剧放大, ΔrsuA突变株由于功能核糖体不足而无法及时表达大量的相关蛋白, 导致突变株无法适应高盐条件。综上, 本研究发现rsuA基因是聚球藻PCC 7002适应高盐环境的关键基因, 其缺失导致藻株在盐胁迫下光合性能和生长受抑, 其作用机制可能与影响核糖体功能及翻译稳态有关。本研究首次揭示了RsuA蛋白在蓝藻盐胁迫适应中的功能, 为深入理解蓝藻环境适应性机制提供了新线索。

       

      Abstract: To investigate the salt adaptation mechanisms of coastal phytoplankton, this study selected the euryhaline cyanobacterium Synechococcus sp. PCC 7002, which inhabits coastal waters, for salt stress research. Using a whole-genome mutant library of Synechococcus constructed in our laboratory by sequential deletions in 5000 bp increments, we performed a salt-stress screen and obtained a mutant strain Δ480 that exhibited a response to salt stress. Subsequently, by individually knocking out the genes contained in the deleted fragment, the pseudouridine synthase-encoding gene rsuA was identified as the key gene responsible for the salt-sensitive phenotype of the mutant. Physiological parameters of the knockout mutant (ΔrsuA), complementation strain (ΔrsuA::rsuA), and overexpression strain (OE-rsuA) were measured under standard salt concentration (0.3 mol/L NaCl) and high-salt concentration (1.2 mol/L NaCl). The results showed that under high salt stress, ΔrsuA exhibited significantly reduced growth rate, chlorophyll a content, and maximum photochemical efficiency of photosystem II (Fv/Fm) compared to the wild type. The phenotype of the complementation strain was restored to wild-type levels, confirming that the phenotype was caused by inactivation of this gene. Transcriptomic analysis revealed that under normal conditions, cells compensate for the functional defect in ribosome assembly resulting from rsuA deletion through upregulating the expression of ribosome-related genes. However, under salt stress conditions, the cellular demand for stress proteins is dramatically amplified. The ΔrsuA mutant, due to insufficient functional ribosomes, fails to express sufficient stress-related proteins promptly, rendering it unable to adapt to high-salt conditions. In conclusion, this study identifies rsuA as a crucial gene for the adaptation of Synechococcus sp. PCC 7002 to high-salt environments. Its deletion leads to impaired photosynthetic performance and growth inhibition under salt stress, potentially by affecting ribosome function and translational homeostasis. This research reveals, for the first time, the function of RsuA in the salt stress adaptation of cyanobacteria, providing new insights into the environmental adaptation mechanisms of cyanobacteria.

       

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