一株耐盐碱促生细菌的分离鉴定及其全基因组测序分析

Identification of A Saline-alkali Tolerant Plant Growth-promoting Bacterium and Its Whole Genome Analysis

  • 摘要:
    目的 筛选分离出高效的耐盐碱促生菌,分析其耐盐碱、促生特性及机理,为开发盐碱地微生物肥料提供候选菌种。
    方法 从盐地碱蓬根际土壤中分离筛选出耐盐碱菌株,基于形态学及16S rDNA基因序列分析对其进行分类鉴定,并对菌株的固氮、溶磷、解钾、产铁载体和产IAA等促生长特性进行定性检测,同时结合菌株的全基因组信息,从基因角度分析菌株的耐盐碱和促生分子机制。
    结果 筛选出一株耐盐碱菌株NMGSB13,该菌株能在5% ~ 15%盐度和pH 7.0 ~ 9.0的条件下生长,并具有固氮、溶磷、解钾、产铁载体和产吲哚乙酸(IAA)等性能。基于16S rDNA基因片段测序分析鉴定出该菌株为克锡勒氏菌(Kushneria sp.)。全基因组测序分析的结果表明,该菌株具有合成四氢嘧啶和脯氨酸的完整通路以及一系列编码Na + /H + 逆向转运蛋白的基因,它们可以调节细胞内外渗透压平衡帮助菌株抵御盐胁迫。此外,基因组中还发现了一系列参与固氮、溶磷、解钾、产铁载体和产IAA的代谢通路或调控基因。
    结论 得到一株耐盐碱的促生细菌(Kushneria sp. NMGSB13),基于全基因组数据解析了该菌株耐盐碱及促生长的分子机制,为今后开发可用于盐碱地修复的微生物肥料提供了理论依据及菌种资源。

     

    Abstract:
    Objective This study aimed to isolate and screen highly efficient saline-alkali tolerant, plant growth-promoting bacteria, to analyze their saline and alkali tolerances, growth-promoting traits, action mechanisms, and to identify candidate strains for developing microbial fertilizers to restore saline-alkali soil.
    Method Salt-tolerant, plant growth-promoting bacterial strains were isolated from the rhizosphere soil of Suaeda salsa, a kind of halophyte. Morphological analysis and 16S rDNA gene sequencing were used for bacterial strain classification. Then, the ability of bacterial strains in nitrogen fixation, phosphate solubilization, potassium release, iron chelation, and IAA production were qualitatively assessed. Finally, the whole genome of bacterial strain was sequenced and then annotated in different database to elucidate its salt tolerance and plant growth promotion mechanisms.
    Result A saline-alkali tolerant strain, NMGSB13, was identified as a bacterium of Kushneria sp. based on 16S rDNA gene sequencing. The NMGSB13 strain could grow at 5% - 15% of salinity and pH 7.0 - 9.0, and exhibit the plant growth-promoting abilities with nitrogen fixation, phosphorus and potassium solubilization, siderophore production, and IAA production. Whole genome sequencing indicated that NMGSB13 possessed the complete pathways to ectoine and proline biosynthesis and a series of genes encoding Na + /H + exchangers, which regulated the balance of intracellular and extracellular osmotic pressure, helping bacterium to resist salt stress. In addition, several biosynthesis pathways or regulating genes were also identified for involving in nitrogen fixation, phosphate solubilization, potassium release, siderophore production, and IAA production.
    Conclusion A saline-alkali tolerant, plant growth-promoting Kushneria sp. NMGSB13 was obtained, which exhibited abilities of nitrogen fixation, phosphorus and potassium solubilization, siderophore production, and IAA production. The salt tolerance and plant growth-promoting mechanisms for this strain were elucidated at the genomic level. This study provided a theoretical insight as well as an elite strain resource for further developing microbial fertilizers to restore saline-alkali soil.

     

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