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ArticleCurrent microbiology2026

Glutamine-hydrolyzing GMP Synthase Gene (guaA) Regulates Siderophore Synthesis in the Nitrogen-fixing Bacterium (NFB) Kosakonia radicincitans GXGL-4A.

Er-Xing Wang, Bao-Yun Feng, Ya-Ting Zhang, Meng-Ting Zhang, Lu-Rong Xu, Yan-Wen Xue, Yun-Peng Chen

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Article in Current microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Er-Xing WangDepartment of Resources and Environment, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, 200240, China.
Bao-Yun FengDepartment of Resources and Environment, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, 200240, China.
Ya-Ting ZhangDepartment of Resources and Environment, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, 200240, China.
Meng-Ting ZhangDepartment of Resources and Environment, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, 200240, China.
Lu-Rong XuAsset Management and Shared Equipment's Office, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, 200240, China.
Yan-Wen XueAsset Management and Shared Equipment's Office, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, 200240, China.
Yun-Peng ChenDepartment of Resources and Environment, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai, 200240, China. ypchen7274@sjtu.edu.cn.

Funding

the National Natural Science Foundation of China 31870496
6 · The paper itself

Abstract

The nitrogen-fixing bacterium Kosakonia radicincitans GXGL-4A can produce siderophore to sequester iron, which is essential for survival and bacteriostasis. In this investigation, a mutant, M246-2, resulting from Tn5 insertion mutagenesis of the strain GXGL-4A, was found to have lost the ability to synthesize siderophores. Whole-genome sequencing of the mutant M246-2 revealed that the insertion site is within the nucleotide sequence of the guaA gene encoding glutamine-hydrolyzing guanosine monophosphate (GMP) synthase. The deletion of the guaA gene (∆guaA) resulted in the loss of the ability to produce siderophores in the strain GXGL-4A and a significant slowdown in the bacterial growth curve. Moreover, the intracellular GMP contents in the strains M246-2 and ∆guaA were statistically significantly reduced compared to the wild-type strain GXGL-4A. The bacterial functional complementation and guaA gene deletion experiments revealed that the guaA gene modulated the siderophore synthesis in the strain GXGL-4A. The results of differential transcriptome analysis showed that the transcription levels of genes related to the siderophore synthesis in the mutant M246-2 had no significant changes compared to the wild-type strain GXGL-4A, suggesting that the guaA gene may modulate the siderophore synthesis of the strain GXGL-4A through a complex mechanism at the non-transcriptional level.

Indexed as

Bacterial ProteinsGlutamineRhizobiaceaeSiderophoresGene DeletionGene Expression ProfilingGene Expression Regulation, BacterialGenetic Complementation TestIronMutagenesis, InsertionalNitrogen FixationBacterial ProteinsGlutamineIronSiderophores

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.