<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Abada A</submitter><funding>Simons Foundation</funding><funding>The Angel Faivovich Foundation for Ecological Research The Weizmann SABRA - Yeda-Sela - WRC Program The Estate of Emile Mimran, and the Maurice and Vivienne Wohl Biology Endowment</funding><funding>European Research Council</funding><funding>The Dean of Faculty fellowship The Sir Charles Clore Postdoctoral Fellowship</funding><funding>Minerva Foundation</funding><funding>The Weizmann SAERI program</funding><pagination>1167-1183</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10356946</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(8)</volume><pubmed_abstract>Microbial interactions govern marine biogeochemistry. These interactions are generally considered to rely on exchange of organic molecules. Here we report on a novel inorganic route of microbial communication, showing that algal-bacterial interactions between Phaeobacter inhibens bacteria and Gephyrocapsa huxleyi algae are mediated through inorganic nitrogen exchange. Under oxygen-rich conditions, aerobic bacteria reduce algal-secreted nitrite to nitric oxide (NO) through denitrification, a well-studied anaerobic respiratory mechanism. The bacterial NO is involved in triggering a cascade in algae akin to programmed cell death. During death, algae further generate NO, thereby propagating the signal in the algal population. Eventually, the algal population collapses, similar to the sudden de</pubmed_abstract><journal>The ISME journal</journal><pubmed_title>Aerobic bacteria produce nitric oxide via denitrification and promote algal population collapse.</pubmed_title><pmcid>PMC10356946</pmcid><funding_grant_id>622065</funding_grant_id><funding_grant_id>101075514</funding_grant_id><pubmed_authors>Huang Zhang I</pubmed_authors><pubmed_authors>Lipsman V</pubmed_authors><pubmed_authors>Sperfeld M</pubmed_authors><pubmed_authors>Babbin AR</pubmed_authors><pubmed_authors>Rocha J</pubmed_authors><pubmed_authors>Carmieli R</pubmed_authors><pubmed_authors>Abada A</pubmed_authors><pubmed_authors>Beiralas R</pubmed_authors><pubmed_authors>Segev E</pubmed_authors><pubmed_authors>Duchin-Rapp Y</pubmed_authors><pubmed_authors>Cohen B</pubmed_authors><pubmed_authors>Narvaez D</pubmed_authors><pubmed_authors>Yuda L</pubmed_authors><pubmed_authors>Ben-Dor S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Aerobic bacteria produce nitric oxide via denitrification and promote algal population collapse.</name><description>Microbial interactions govern marine biogeochemistry. These interactions are generally considered to rely on exchange of organic molecules. Here we report on a novel inorganic route of microbial communication, showing that algal-bacterial interactions between Phaeobacter inhibens bacteria and Gephyrocapsa huxleyi algae are mediated through inorganic nitrogen exchange. Under oxygen-rich conditions, aerobic bacteria reduce algal-secreted nitrite to nitric oxide (NO) through denitrification, a well-studied anaerobic respiratory mechanism. The bacterial NO is involved in triggering a cascade in algae akin to programmed cell death. During death, algae further generate NO, thereby propagating the signal in the algal population. Eventually, the algal population collapses, similar to the sudden de</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Aug</publication><modification>2026-03-18T14:07:07.475Z</modification><creation>2025-08-23T03:08:58.251Z</creation></dates><accession>S-EPMC10356946</accession><cross_references><pubmed>37173383</pubmed><doi>10.1038/s41396-023-01427-8</doi></cross_references></HashMap>