<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yu L</submitter><funding>National Water Pollution Control and Treatment Science and Technology Major Project</funding><pagination>e7188</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6599450</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7</volume><pubmed_abstract>In this study, a SYBR Green quantitative real-time PCR method was established and applied. Relative expression of the synthetic genes from &lt;i>Microcystis&lt;/i> gas vesicles (&lt;i>gvpC&lt;/i>), algal toxin genes (&lt;i>mcyA&lt;/i>), and polysaccharides (&lt;i>espL&lt;/i>) from water and sediments of Meiliang Bay and from the center of Lake Taihu were tested from January to June, 2017. Indoor &lt;i>Microcystis aeruginosa&lt;/i> was used as the control group. The kit for total RNA extraction in &lt;i>Microcystis&lt;/i> was optimized. Results showed that the optimized kit extracted high-concentrations and high-quality total RNA from &lt;i>Microcystis&lt;/i>. The extraction purity and concentration were significantly higher than those extracted by the original kit. The transcription level of &lt;i>gvpC&lt;/i> increased gradually until a</pubmed_abstract><journal>PeerJ</journal><pubmed_title>Recruitment of cyanobacteria by reverse transcription quantitative real-time PCR based on expression of &lt;i>Microcystis&lt;/i> gene.</pubmed_title><pmcid>PMC6599450</pmcid><funding_grant_id>2018ZX07208-004, 2017ZX07204-5</funding_grant_id><pubmed_authors>Yu L</pubmed_authors><pubmed_authors>Shi L</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Wu X</pubmed_authors><pubmed_authors>Yu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Recruitment of cyanobacteria by reverse transcription quantitative real-time PCR based on expression of &lt;i>Microcystis&lt;/i> gene.</name><description>In this study, a SYBR Green quantitative real-time PCR method was established and applied. Relative expression of the synthetic genes from &lt;i>Microcystis&lt;/i> gas vesicles (&lt;i>gvpC&lt;/i>), algal toxin genes (&lt;i>mcyA&lt;/i>), and polysaccharides (&lt;i>espL&lt;/i>) from water and sediments of Meiliang Bay and from the center of Lake Taihu were tested from January to June, 2017. Indoor &lt;i>Microcystis aeruginosa&lt;/i> was used as the control group. The kit for total RNA extraction in &lt;i>Microcystis&lt;/i> was optimized. Results showed that the optimized kit extracted high-concentrations and high-quality total RNA from &lt;i>Microcystis&lt;/i>. The extraction purity and concentration were significantly higher than those extracted by the original kit. The transcription level of &lt;i>gvpC&lt;/i> increased gradually until a</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2026-04-29T03:22:58.606Z</modification><creation>2019-07-25T07:00:25Z</creation></dates><accession>S-EPMC6599450</accession><cross_references><pubmed>31289701</pubmed><doi>10.7717/peerj.7188</doi></cross_references></HashMap>