<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Qiu M</submitter><funding>Zhanjiang Competitive Allocation Project of Science and Technology Development Special Fund</funding><funding>Guangdong Provincial Special Fund for Modern Agricultural Industry Technology Innovation Team</funding><funding>Zhanjing Competitive Allocation Project of Science and Technology Development Special Fund</funding><funding>Guangdong Provincial Special Foundation for Modern Agriculture Industry Technology Innovation Team</funding><funding>Guangdong Provincial Key Research and Development Program</funding><funding>National Natural Science Foundation of China</funding><funding>Characteristic Innovation Project of Colleges and Universities in Guangdong Province</funding><pagination>e0368222</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9769839</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(6)</volume><pubmed_abstract>Fusarium oxysporum is ubiquitous and can easily contaminate food during processing and storage, potentially producing T-2 toxin, which can pose a severe health risk to public health. Previous research on the presence of T-2 has focused on starch-rich foods, while protein- and amino acid-rich foods have received relatively little attention. In this study, the effects of amino acids on the growth of F. oxysporum and its T-2 production were investigated by gene deletion and complementation experiments. The results showed that amino acids, including aspartic acid, methionine, isoleucine, serine, phenylalanine, and cysteine, significantly inhibited the growth of F. oxysporum, while promoting T-2 synthesis, with cysteine having the most pronounced effect. The target of rapamycin complex 1 (TORC1</pubmed_abstract><journal>Microbiology spectrum</journal><pubmed_title>Cysteine Inhibits the Growth of Fusarium oxysporum and Promotes T-2 Toxin Synthesis through the Gtr/Tap42 Pathway.</pubmed_title><pmcid>PMC9769839</pmcid><funding_grant_id>200915134541577</funding_grant_id><funding_grant_id>2021KJ149</funding_grant_id><funding_grant_id>32172215</funding_grant_id><funding_grant_id>2020KQNCX025</funding_grant_id><funding_grant_id>2021B020260001</funding_grant_id><funding_grant_id>31871898</funding_grant_id><funding_grant_id>2020A03009</funding_grant_id><funding_grant_id>2021KJ151</funding_grant_id><pubmed_authors>Sun L</pubmed_authors><pubmed_authors>Fang Z</pubmed_authors><pubmed_authors>Deng Q</pubmed_authors><pubmed_authors>Huang X</pubmed_authors><pubmed_authors>Qiu M</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors><pubmed_authors>Deng Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cysteine Inhibits the Growth of Fusarium oxysporum and Promotes T-2 Toxin Synthesis through the Gtr/Tap42 Pathway.</name><description>Fusarium oxysporum is ubiquitous and can easily contaminate food during processing and storage, potentially producing T-2 toxin, which can pose a severe health risk to public health. Previous research on the presence of T-2 has focused on starch-rich foods, while protein- and amino acid-rich foods have received relatively little attention. In this study, the effects of amino acids on the growth of F. oxysporum and its T-2 production were investigated by gene deletion and complementation experiments. The results showed that amino acids, including aspartic acid, methionine, isoleucine, serine, phenylalanine, and cysteine, significantly inhibited the growth of F. oxysporum, while promoting T-2 synthesis, with cysteine having the most pronounced effect. The target of rapamycin complex 1 (TORC1</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2026-06-12T09:58:40.275Z</modification><creation>2024-11-19T17:29:07.588Z</creation></dates><accession>S-EPMC9769839</accession><cross_references><pubmed>36314982</pubmed><doi>10.1128/spectrum.03682-22</doi></cross_references></HashMap>