<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(38)</volume><submitter>Thanapaul NB</submitter><pubmed_abstract>Rhizobium bacteria convert atmospheric nitrogen into ammonia that leguminous plants can use as a nitrogen source, reducing the need for synthetic nitrogen fertilizers. &lt;i>Bradyrhizobium&lt;/i> sp. SUTN9-2 is an effective biofertilizer suitable for legume-rice rotational cropping systems that promotes growth and stress resistance. Deploying this biofertilizer for sustainable agriculture requires a rapid and cost-effective method for monitoring bacterial concentrations in the soil. In this work, we developed and optimized an antibody-based biosensor for the detection of &lt;i>Bradyrhizobium&lt;/i> sp. SUTN9-2 via electrochemical impedance spectroscopy (EIS). The immunosensor was fabricated by covalently immobilizing a recombinant antibody specific to SUTN9-2 onto a dithiobis-succinimidyl propionate (DSP) self-assembled monolayer on a gold electrode. The resulting immunosensor effectively captures &lt;i>Bradyrhizobium&lt;/i> sp. SUTN9-2 cells are present in samples, leading to changes in electrode impedance. The immunosensor demonstrated excellent specificity, a wide linear detection range of 1 × 10&lt;sup>3&lt;/sup> to 1 × 10&lt;sup>7&lt;/sup> CFU/mL (&lt;i>R&lt;/i> &lt;sup>2&lt;/sup> = 0.992), and a limit of detection approaching the single-cell detection limit. The compatibility of the sensor with a soil sample was also demonstrated. The platform holds great promise for the portable monitoring of soil biofertilizer levels and could also be adapted to other strains of interest.</pubmed_abstract><journal>ACS omega</journal><pagination>44489-44498</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12489705</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Sensitive Detection of Nitrogen-Fixing Soil Bacteria by Impedimetric Immunosensing.</pubmed_title><pmcid>PMC12489705</pmcid><pubmed_authors>Yamabhai M</pubmed_authors><pubmed_authors>Pinyou P</pubmed_authors><pubmed_authors>Blay V</pubmed_authors><pubmed_authors>Thanapaul NB</pubmed_authors><pubmed_authors>Bista S</pubmed_authors><pubmed_authors>Tittabutr P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sensitive Detection of Nitrogen-Fixing Soil Bacteria by Impedimetric Immunosensing.</name><description>Rhizobium bacteria convert atmospheric nitrogen into ammonia that leguminous plants can use as a nitrogen source, reducing the need for synthetic nitrogen fertilizers. &lt;i>Bradyrhizobium&lt;/i> sp. SUTN9-2 is an effective biofertilizer suitable for legume-rice rotational cropping systems that promotes growth and stress resistance. Deploying this biofertilizer for sustainable agriculture requires a rapid and cost-effective method for monitoring bacterial concentrations in the soil. In this work, we developed and optimized an antibody-based biosensor for the detection of &lt;i>Bradyrhizobium&lt;/i> sp. SUTN9-2 via electrochemical impedance spectroscopy (EIS). The immunosensor was fabricated by covalently immobilizing a recombinant antibody specific to SUTN9-2 onto a dithiobis-succinimidyl propionate (DSP) self-assembled monolayer on a gold electrode. The resulting immunosensor effectively captures &lt;i>Bradyrhizobium&lt;/i> sp. SUTN9-2 cells are present in samples, leading to changes in electrode impedance. The immunosensor demonstrated excellent specificity, a wide linear detection range of 1 × 10&lt;sup>3&lt;/sup> to 1 × 10&lt;sup>7&lt;/sup> CFU/mL (&lt;i>R&lt;/i> &lt;sup>2&lt;/sup> = 0.992), and a limit of detection approaching the single-cell detection limit. The compatibility of the sensor with a soil sample was also demonstrated. The platform holds great promise for the portable monitoring of soil biofertilizer levels and could also be adapted to other strains of interest.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-06-04T05:07:49.319Z</modification><creation>2026-05-05T03:12:33.903Z</creation></dates><accession>S-EPMC12489705</accession><cross_references><pubmed>41048798</pubmed><doi>10.1021/acsomega.5c06583</doi></cross_references></HashMap>