生物技术通报 ›› 2026, Vol. 42 ›› Issue (8): 276-286.doi: 10.13560/j.cnki.biotech.bull.1985.2025-1174

• 研究报告 • 上一篇    

番茄根际放线菌GNLJ-7菌株的生物功能及全基因组分析

迪丽拜尔·吐尔逊1, 祖丽胡玛尔·亚库普2, 包慧芳2, 詹发强2, 杨蓉2, 史应武2, 杨红梅2, 楚敏2, 房世杰1, 王宁2()   

  1. 1.新疆维吾尔自治区农业科学院农产品加工研究所,乌鲁木齐 830000
    2.新疆维吾尔自治区农业科学院微生物研究所,乌鲁木齐 830000
  • 收稿日期:2025-10-30 出版日期:2026-08-26 发布日期:2026-08-17
  • 通讯作者: 王宁wangning@xaas.ac.cn
  • 基金资助:
    新疆维吾尔自治区重点研发计划课题(2022B02019-3);新疆维吾尔自治区厅地联动课题(2025B04034-002)

Biological Function and Whole-genome Analysis of Actinobacteria Strain GNLJ-7 Isolated from Tomato Rhizosphere

TUERXUN Di-li-bai-er1, YAKUPU Zu-li-hu-ma-er2, BAO Hui-fang2, ZHAN Fa-qiang2, YANG Rong2, SHI Ying-wu2, YANG Hong-mei2, CHU Min2, FANG Shi-jie1, WANG Ning2()   

  1. 1.Institute of Agro-product Processing, Xinjiang Academy of Agricultural Sciences, Urumqi 830000
    2.Institute of Microbiology, Xinjiang Academy of Agricultural Sciences, Urumqi 830000
  • Received:2025-10-30 Published:2026-08-26 Online:2026-08-17

摘要:

目的 从番茄根际分离出菌株GNLJ-7,通过全基因组测序技术解析其功能,为开发绿色促生生防菌剂提供优良菌种与理论支撑。 方法 通过皿内种子萌发及盆栽实验验证GNLJ-7对番茄生长及杂草分枝列当寄生的影响;检测平板测定其溶磷、固氮和产铁载体能力;采用16S rRNA和全基因组学测序,明确菌株GNLJ-7的分类学地位,利用PacBio和Illumina双平台测序技术完成全基因组测序,并通过COG、KEGG、GO等数据库进行基因功能注释与次级代谢产物合成基因簇和主要代谢通路的预测。 结果 经鉴定菌株GNLJ-7为海鞘戈登氏菌(Gordonia didemni)。盆栽实验表明,该菌株能显著促进番茄根系发育,使根长和根重分别增加26%和47%,并有效抑制分枝列当种子的萌发与寄生,在菌剂浓度为1.0×102 CFU/mL时,对列当种子萌发的抑制率达到86.47%。功能验证显示其具有固氮、溶磷和产铁载体的能力。基因组中鉴定到与吲哚-3-乙酸(IAA)合成(trpA/B/C/D/E/F/S)、溶磷(phoA、phoD)、铁载体合成(pksD/E/F)及固氮(nifH、nifA)相关的关键基因,并预测到10个次级代谢产物生物合成基因簇和与促生生防功能相关的代谢通路。 结论 菌株G. didemni GNLJ-7能够显著促进番茄根系生长并抑制分枝列当寄生。其基因组中存在的固氮(nifH、nifA)、溶磷(phoA、phoD)、铁载体合成(pksD/E/F)及IAA合成(trpA/B/C/D/E/F/S)相关基因,共同构成了其发挥促生和生物防治作用的分子基础。

关键词: Gordonia didemni, 全基因组测序, 分枝列当, 生物防治, 促生机制, 根际促生菌, 功能基因

Abstract:

Objective Strain GNLJ-7 was isolated from tomato rhizosphere. Its functional mechanisms were elucidated through whole-genome sequencing, aiming to provide an excellent microbial strain and theoretical support for developing green plant-growth-promoting and biocontrol agents. Method The effects of GNLJ-7 on tomato growth and Phelipanche aegyptiaca parasitism were evaluated via in-plate seed germination and pot experiments. Its phosphate-solubilizing, nitrogen-fixing, and siderophore-producing abilities were assessed using plate-based assays. Taxonomic identification of strain GNLJ-7 was performed by 16S rRNA and whole-genome sequencing. The genome was sequenced using both PacBio and Illumina platforms, followed by functional annotation via COG, KEGG, and GO databases. Secondary metabolite biosynthetic gene clusters and key metabolic pathways were predicted. Result Strain GNLJ‑7 was identified as Gordonia didemni. Pot experiments showed that the strain significantly promoted tomato root development, increasing root length and root weight by 26% and 47%, respectively, and effectively inhibited the germination and parasitism of P. aegyptiaca seeds. At a concentration of 1.0×102 CFU/mL, the inhibition rate on Orobanche seed germination reached 86.47%. Functional tests confirmed its abilities in nitrogen fixation, phosphate solubilization, and siderophore production. Key genes involved in indole‑3‑acetic acid (IAA) biosynthesis (trpA/B/C/D/E/F/S), phosphate solubilization (phoA, phoD), siderophore synthesis (pksD/E/F), and nitrogen fixation (nifH/A) were identified in the genome. Ten secondary metabolite biosynthetic gene clusters and metabolic pathways associated with plant‑growth‑promoting and biocontrol functions were predicted. Conclusion The strain Gordonia didemni GNLJ-7 significantly promotes tomato root growth and inhibits the parasitism of Phelipanche aegyptiaca. Genes associated with nitrogen fixation (nifH, nifA), phosphorus solubilization (phoA, phoD), siderophore synthesis (pksD/E/F), and IAA biosynthesis (trpA/B/C/D/E/F/S) identified in its genome collectively form the molecular basis for its plant growth-promoting and biocontrol activities.

Key words: Gordonia didemni, whole-genome sequencing, Phelipanche aegyptiaca, biocontrol, growth-promoting mechanism, plant growth-promoting rhizobacteria, functional genes