Evidence map›Paper›PMID 40841905›Full record

ArticleMicrobial cell factories2025

Regulation of the Ald gene encoding alanine dehydrogenase and its induction of ammonium-tolerant nitrogen fixation in Paenibacillus polymyxa WLY78.

Haowei Zhang, Yuxing Han, Hui Tan, Qin Li, Sanfeng Chen

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Article in Microbial cell factories, 2025. 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

5 authors.

Haowei ZhangCollege of Biological Sciences, China Agricultural University, Beijing, 100193, China.
Yuxing HanCollege of Biological Sciences, China Agricultural University, Beijing, 100193, China.
Hui TanCollege of Biological Sciences, China Agricultural University, Beijing, 100193, China.
Qin LiCollege of Biological Sciences, China Agricultural University, Beijing, 100193, China. liqin@cau.edu.cn.
Sanfeng ChenCollege of Biological Sciences, China Agricultural University, Beijing, 100193, China. chensf@cau.edu.cn.

Funding

Biological Breeding-National Science and Technology Major Project 2024ZD0407903
6 · The paper itself

Abstract

backgroundPaenibacillus polymyxa WLY78, a Gram-positive diazotroph with plant growth promotion and phytopathogen suppression, represents a promising candidate for agricultural biofertilizers. However, its nitrogen fixation capacity is inherently limited by ammonium-mediated repression. Recent studies revealed that ammonium-tolerant nitrogen fixation in certain Paenibacillus species correlates with alanine overproduction mediated by alanine dehydrogenase (ADH) encoded by the ald gene.

resultsThis study establishes a dual regulatory mechanism governing ald expression in P. polymyxa WLY78. The transcription activator AdeR positively regulates ald expression, while the global nitrogen regulator GlnR exerts repression on both ald and its activator gene adeR. Under high ammonium conditions, GlnR-mediated suppression maintains basal ald expression levels, preventing alanine biosynthesis. Upregulation of ald expression through high-copy plasmid or mutagenesis of GlnR-binding sites in the adeR-ald regulatory region significantly enhanced alanine concentration. Both endogenous overproduction and exogenous supplementation of alanine suppressed glutamine synthetase (GS) activity, thereby reducing intracellular glutamine levels. This prevents the formation of glutamine-feedback-inhibited GS complexes (FBI-GS), disrupting the GlnR-FBI-GS interaction required for nif gene repression. Consequently, GlnR transitions to its activated state, enabling nif gene expression even under elevated ammonium concentrations.

conclusionsOur findings elucidate a conserved regulatory paradigm in Paenibacillus species where alanine metabolism modulates nitrogen fixation through GS-mediated metabolic signaling. The ald overexpression or exogenous alanine supplementation can bypass ammonium inhibition provides practical strategies for enhancing biofertilizer performance in nitrogen-rich agricultural soils.

Indexed as

Alanine DehydrogenaseAmmonium CompoundsGene Expression Regulation, BacterialNitrogen FixationPaenibacillus polymyxaAlanineBacterial ProteinsGlutamate-Ammonia LigaseAlanineAlanine DehydrogenaseAmmonium CompoundsBacterial ProteinsGlutamate-Ammonia LigaseAdeRald geneAmmonium-tolerant nitrogen fixationGlnRPaenibacillus polymyxa

Identifiers

PMID40841905
PMCPMC12369066

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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 OpenQuestion graph.