ArticleMicroorganisms2022
Transcriptome Profiling Analysis of Phosphate-Solubilizing Mechanism of
Article in Microorganisms, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 14 citations in OpenAlex.
- Mechanisms of Pseudomonas spp. as plant growth promoting rhizobacteria: plant nutrition and biocontrol.Antonie van Leeuwenhoek · 2026Review
- Transcriptome analysis ofMicrobiology spectrum · 2026Article
- Omics-driven research progress on phosphate activation mechanisms and stress adaptability regulation of Phosphate-Solubilizing Microorganisms (PSMs).Frontiers in microbiology · 2026Review
- Phosphate availability modulates the weathering effectiveness and molecular response of Caballeronia mineralivorans PML1(12).BMC microbiology · 2025Article
- Manure-Amended One-Year-Reclamation Promoted Soil Bacterial Phylotypic and Phenotypic Shifts in a Typical Coal-Mining Area.Microorganisms · 2025Article
- Transcriptomic and metabolomic analysis of recalcitrant phosphorus solubilization mechanisms inFrontiers in microbiology · 2025Article
- Enhancing carrot (Frontiers in microbiology · 2024Article
- Effect of ammonium stress on phosphorus solubilization of a novel marine mangrove microorganism Bacillus aryabhattai NM1-A2 as revealed by integrated omics analysis.BMC genomics · 2023Article
- Moderate organic fertilizer substitution for partial chemical fertilizer improved soil microbial carbon source utilization and bacterial community composition in rain-fed wheat fields: current year.Frontiers in microbiology · 2023Article
Corrections and comments
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
Abstract
Phosphate-solubilizing bacteria (PSB) can alleviate available phosphorus deficiency without causing environmental pollution, unlike chemical phosphate fertilizers. However, the phosphate solubilization mechanisms of PSB are still unclear. Transcriptome sequencing was used to analyze the expression patterns of differential expressed genes (DEGs) of the phosphate-solubilizing bacterium W134 under the conditions of soluble phosphorus (group A), insoluble phosphorus (group B), and lacking phosphorus (group C). Nine DEGs in three different groups were detected by quantitative real-time polymerase chain reaction (qRT-PCR). Then, high performance liquid chromatography (HPLC) was applied to detect the concentrations and composition of organic acids. Compared with group A, Gene Ontology (GO) annotation showed that the cluster of W134 DEGs in groups B and C were basically the same. Besides, the results of enrichment Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway indicated that genes in the Citrate cycle (TCA cycle) pathway closely related to organic acid production were significantly upregulated. The qRT-PCR results were almost consistent with the expression trends of the transcriptome data. The HPLC results showed that the formic acid, ascorbic acid, acetic acid, citric acid, and succinic acid concentrations were significantly increased in group B and C (p < 0.05), while the contents of lactic acid and malic acid were significantly increased in group B (p < 0.05). The above results provided further validation that the upregulated genes should be related to W134 secretion of organic acids. Our study revealed several potential candidate genes and tried to explain phosphate solubilization mechanisms. This provides a new insight for calcareous reclaimed soil, and it will reduce the need of chemical phosphate fertilizers to promote environmentally friendly agriculture.
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Registered trials
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