<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12</volume><submitter>Martinez J</submitter><pubmed_abstract>The aim of this work was to study the value of the main allergen Asp n 3 of &lt;i>Aspergillus niger&lt;/i> as a molecular marker of allergenicity and pathogenicity with the potential to be used in the identification of &lt;i>A. niger&lt;/i> as a contaminant and cause of spoilage of &lt;i>Mangifera indica.&lt;/i> Real-time polymerase chain reaction (RT-PCR) was used for the amplification of Asp n 3 gene. Two pairs of primers were designed: one for the amplification of the entire sequence and another one for the amplification of the most conserved region of this peroxisomal protein. The presence of &lt;i>A. niger&lt;/i> was demonstrated by the early detection of the allergenic protein Asp n 3 coding gene, which could be considered a species-specific marker. The use of primers designed based on the conserved region </pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>663323</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8273346</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The &lt;i>Aspergillus niger&lt;/i> Major Allergen (Asp n 3) DNA-Specific Sequence Is a Reliable Marker to Identify Early Fungal Contamination and Postharvest Damage in &lt;i>Mangifera indica&lt;/i> Fruit.</pubmed_title><pmcid>PMC8273346</pmcid><pubmed_authors>Martinez J</pubmed_authors><pubmed_authors>Sanchez P</pubmed_authors><pubmed_authors>Sunen E</pubmed_authors><pubmed_authors>Velez-Del-Burgo A</pubmed_authors><pubmed_authors>Postigo I</pubmed_authors><pubmed_authors>Nevado A</pubmed_authors><pubmed_authors>Gabriel M</pubmed_authors></additional><is_claimable>false</is_claimable><name>The &lt;i>Aspergillus niger&lt;/i> Major Allergen (Asp n 3) DNA-Specific Sequence Is a Reliable Marker to Identify Early Fungal Contamination and Postharvest Damage in &lt;i>Mangifera indica&lt;/i> Fruit.</name><description>The aim of this work was to study the value of the main allergen Asp n 3 of &lt;i>Aspergillus niger&lt;/i> as a molecular marker of allergenicity and pathogenicity with the potential to be used in the identification of &lt;i>A. niger&lt;/i> as a contaminant and cause of spoilage of &lt;i>Mangifera indica.&lt;/i> Real-time polymerase chain reaction (RT-PCR) was used for the amplification of Asp n 3 gene. Two pairs of primers were designed: one for the amplification of the entire sequence and another one for the amplification of the most conserved region of this peroxisomal protein. The presence of &lt;i>A. niger&lt;/i> was demonstrated by the early detection of the allergenic protein Asp n 3 coding gene, which could be considered a species-specific marker. The use of primers designed based on the conserved region </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2025-05-31T23:47:03.64Z</modification><creation>2025-05-31T23:47:03.64Z</creation></dates><accession>S-EPMC8273346</accession><cross_references><pubmed>34262539</pubmed><doi>10.3389/fmicb.2021.663323</doi></cross_references></HashMap>