<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chow YY</submitter><funding>Malaysian Ministry of Higher Education</funding><pagination>13-21</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5121152</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>This study aimed to establish the colonization behavior and proliferation potential of three endophytes and one pathogen &lt;i>Ganoderma boninense&lt;/i> (Gb) introduced into oil palm ramets (host model). The endophytes selected were &lt;i>Diaporthe phaseolorum&lt;/i> (WAA02), &lt;i>Trichoderma asperellum&lt;/i> (T2), and &lt;i>Penicillium citrinum&lt;/i> (BTF08). Ramets were first inoculated with 100 mL of fungal cells (10&lt;sup>6&lt;/sup> cfu mL&lt;sup>-&lt;/sup>&lt;sup>1&lt;/sup>) via soil drenching. For the next 7 days, ramets were sampled and subjected to three different assays to detect and identify fungal colonization, and establish their proliferation potential &lt;i>in planta&lt;/i>. Plate assay revealed the presence of endophytes in root, stem and leaf tissues within 7 days after inoculation. Polymerase Chain Reaction (PCR) d</pubmed_abstract><journal>Journal of advanced research</journal><pubmed_title>Understanding colonization and proliferation potential of endophytes and pathogen &lt;i>in planta&lt;/i> via plating, polymerase chain reaction and ergosterol assay.</pubmed_title><pmcid>PMC5121152</pmcid><funding_grant_id>ERGS/1/2013/STWN03/MUSM/02/1</funding_grant_id><pubmed_authors>Ting AS</pubmed_authors><pubmed_authors>Rahman S</pubmed_authors><pubmed_authors>Chow YY</pubmed_authors></additional><is_claimable>false</is_claimable><name>Understanding colonization and proliferation potential of endophytes and pathogen &lt;i>in planta&lt;/i> via plating, polymerase chain reaction and ergosterol assay.</name><description>This study aimed to establish the colonization behavior and proliferation potential of three endophytes and one pathogen &lt;i>Ganoderma boninense&lt;/i> (Gb) introduced into oil palm ramets (host model). The endophytes selected were &lt;i>Diaporthe phaseolorum&lt;/i> (WAA02), &lt;i>Trichoderma asperellum&lt;/i> (T2), and &lt;i>Penicillium citrinum&lt;/i> (BTF08). Ramets were first inoculated with 100 mL of fungal cells (10&lt;sup>6&lt;/sup> cfu mL&lt;sup>-&lt;/sup>&lt;sup>1&lt;/sup>) via soil drenching. For the next 7 days, ramets were sampled and subjected to three different assays to detect and identify fungal colonization, and establish their proliferation potential &lt;i>in planta&lt;/i>. Plate assay revealed the presence of endophytes in root, stem and leaf tissues within 7 days after inoculation. Polymerase Chain Reaction (PCR) d</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jan</publication><modification>2025-04-18T12:03:30.819Z</modification><creation>2019-06-06T16:38:51Z</creation></dates><accession>S-EPMC5121152</accession><cross_references><pubmed>27895938</pubmed><doi>10.1016/j.jare.2016.10.008</doi></cross_references></HashMap>