Biotechnology Bulletin ›› 2026, Vol. 42 ›› Issue (7): 304-314.doi: 10.13560/j.cnki.biotech.bull.1985.2025-0949

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Whole-genome Analysis and Functional Verification of a Phosphate-solubilizing Bacterium Isolated from Traditional Chinese Medicine Residues

DING Hong-xia, GAO Gui-wen, HUANG Yu-lan(), ZHAO Rui(), HUANG Yi-bo, FENG He-xin, LONG Sha   

  1. Heilongjiang Bayi Agricultural University, College of Life Science and Technology, Daqing 163319
  • Received:2025-09-03 Online:2026-07-26 Published:2026-07-20
  • Contact: HUANG Yu-lan, ZHAO Rui E-mail:691369440@qq.com;178415197@qq.com

Abstract:

Objective To clarify the phosphate-solubilizing mechanism of Acinetobacter sp. DF1 isolated from traditional Chinese medicine residues, and provide a theoretical basis and technical support for the construction of high-efficiency phosphate-solubilizing engineered strains and the development of biological bacterial fertilizers. Method The DF1 strain was cultured, and its genomic DNA was extracted for sequencing, assembly and functional annotation against multiple databases. The phosphate-solubilizing genes pqqB and pqqC were cloned, recombinant vectors were constructed and transformed into Escherichia coli. After screening and identification, the phosphate-solubilizing capacity of the recombinant strains was determined. Result The results showed that the genome of DF1 was 3 831 735 bp in full length with a GC content of 38.9%, which was predicted to contain 3 482 protein-coding genes and 91 non-coding RNAs, and was enriched in various functional genes related to phosphate-solubilizing metabolism. The key phosphate-solubilizing genes pqqB and pqqC were cloned, and recombinant expression vectors were constructed and transformed into E. coli. Positive recombinant strains were obtained through resistance screening and PCR identification. The results of the phosphate-solubilizing capacity assay demonstrated that both recombinant strains exhibited significant ability to solubilize inorganic and organic phosphorus, and secreted five organic acids including oxalic acid, tartaric acid, malic acid, acetic acid and citric acid, among which the citric acid secretion levels reached as high as (1 753.10 ± 156.38) mg/L and (1 720.30 ± 206.35) mg/L, respectively. Conclusion This study first clarifies the genomic characteristics of Acinetobacter sp. DF1 isolated from traditional Chinese medicine residues, elucidates the molecular mechanism of phosphate solubilization, and confirms that the pqqB and pqqC genes play a core role in the phosphate-solubilizing process.

Key words: Acinetobacter, whole-genome sequencing, phosphorus-solubilizing bacteria, biological bacterial fertilizer