Algicidal Molecular Mechanism and Toxicological Degradation of Microcystis aeruginosa by White-Rot Fungi.
Identifieur interne : 000013 ( Main/Corpus ); précédent : 000012; suivant : 000014Algicidal Molecular Mechanism and Toxicological Degradation of Microcystis aeruginosa by White-Rot Fungi.
Auteurs : Guoming Zeng ; Pei Gao ; Jiale Wang ; Jinxi Zhang ; Maolan Zhang ; Da SunSource :
- Toxins [ 2072-6651 ] ; 2020.
Abstract
Current research on the inhibition of Microcystis aeruginosa growth is primarily focused on algae-lysing bacteria, and few studies have investigated the inhibitory mechanisms by which fungi affect it at the molecular level. A comparative analysis of the effects of Phanerochaete chrysosporium on the expression of the algal cell antioxidant protease synthesis gene prx, the biological macromolecule damage and repair genes recA, grpE, and fabZ, and the photosynthesis system-related genes psaB, psbD1 and rbcL, as well as genes for algal toxin synthesis mcyB, were performed to elucidate the molecular mechanism of Phanerochaete chrysosporium against Microcystis aeruginosa cells. RT-qPCR technology was used to study the molecular mechanism of algal cell inhibition by Phanerochaete chrysosporium liquid containing metabolites of Phanerochaete chrysosporium, Phanerochaete chrysosporium supernatant and Phanerochaete chrysosporium inactivated via high temperature sterilization at the gene expression level. Compared with the control, the chlorophyll-a contents dropped, and the recA, grpE, fabZ, and prx increased, but the psaB, psbD1, rbcL and mcyB showed that they were significantly reduced, which indicated that Phanerochaete chrysosporium can not only effectively destroy algal cells, but they may also reduce the expression of the Microcystis aeruginosa toxin gene and significantly block the metabolic system underlying the growth of algal cells and the synthesis of microcystins.
DOI: 10.3390/toxins12060406
PubMed: 32575534
PubMed Central: PMC7354498
Links to Exploration step
pubmed:32575534Le document en format XML
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<front><div type="abstract" xml:lang="en">Current research on the inhibition of <i>Microcystis aeruginosa</i>
growth is primarily focused on algae-lysing bacteria, and few studies have investigated the inhibitory mechanisms by which fungi affect it at the molecular level. A comparative analysis of the effects of <i>Phanerochaete chrysosporium</i>
on the expression of the algal cell antioxidant protease synthesis gene <i>prx</i>
, the biological macromolecule damage and repair genes <i>recA</i>
, <i>grpE</i>
, and <i>fabZ</i>
, and the photosynthesis system-related genes <i>psaB</i>
, <i>psbD1</i>
and <i>rbcL</i>
, as well as genes for algal toxin synthesis <i>mcyB</i>
, were performed to elucidate the molecular mechanism of <i>Phanerochaete chrysosporium</i>
against <i>Microcystis aeruginosa</i>
cells. RT-qPCR technology was used to study the molecular mechanism of algal cell inhibition by <i>Phanerochaete chrysosporium</i>
liquid containing metabolites of <i>Phanerochaete chrysosporium</i>
, <i>Phanerochaete chrysosporium</i>
supernatant and <i>Phanerochaete chrysosporium</i>
inactivated via high temperature sterilization at the gene expression level. Compared with the control, the chlorophyll-a contents dropped, and the <i>recA</i>
, <i>grpE</i>
, <i>fabZ</i>
, and <i>prx</i>
increased, but the <i>psaB</i>
, <i>psbD1</i>
, <i>rbcL</i>
and <i>mcyB</i>
showed that they were significantly reduced, which indicated that <i>Phanerochaete chrysosporium</i>
can not only effectively destroy algal cells, but they may also reduce the expression of the <i>Microcystis aeruginosa</i>
toxin gene and significantly block the metabolic system underlying the growth of algal cells and the synthesis of microcystins.</div>
</front>
</TEI>
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<Month>08</Month>
<Day>13</Day>
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<Title>Toxins</Title>
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<ArticleTitle>Algicidal Molecular Mechanism and Toxicological Degradation of <i>Microcystis aeruginosa</i>
by White-Rot Fungi.</ArticleTitle>
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<Abstract><AbstractText>Current research on the inhibition of <i>Microcystis aeruginosa</i>
growth is primarily focused on algae-lysing bacteria, and few studies have investigated the inhibitory mechanisms by which fungi affect it at the molecular level. A comparative analysis of the effects of <i>Phanerochaete chrysosporium</i>
on the expression of the algal cell antioxidant protease synthesis gene <i>prx</i>
, the biological macromolecule damage and repair genes <i>recA</i>
, <i>grpE</i>
, and <i>fabZ</i>
, and the photosynthesis system-related genes <i>psaB</i>
, <i>psbD1</i>
and <i>rbcL</i>
, as well as genes for algal toxin synthesis <i>mcyB</i>
, were performed to elucidate the molecular mechanism of <i>Phanerochaete chrysosporium</i>
against <i>Microcystis aeruginosa</i>
cells. RT-qPCR technology was used to study the molecular mechanism of algal cell inhibition by <i>Phanerochaete chrysosporium</i>
liquid containing metabolites of <i>Phanerochaete chrysosporium</i>
, <i>Phanerochaete chrysosporium</i>
supernatant and <i>Phanerochaete chrysosporium</i>
inactivated via high temperature sterilization at the gene expression level. Compared with the control, the chlorophyll-a contents dropped, and the <i>recA</i>
, <i>grpE</i>
, <i>fabZ</i>
, and <i>prx</i>
increased, but the <i>psaB</i>
, <i>psbD1</i>
, <i>rbcL</i>
and <i>mcyB</i>
showed that they were significantly reduced, which indicated that <i>Phanerochaete chrysosporium</i>
can not only effectively destroy algal cells, but they may also reduce the expression of the <i>Microcystis aeruginosa</i>
toxin gene and significantly block the metabolic system underlying the growth of algal cells and the synthesis of microcystins.</AbstractText>
</Abstract>
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<AffiliationInfo><Affiliation>Institute of Life Sciences & Biomedicine Collaborative Innovation Center, Wenzhou University, Wenzhou 325035, China.</Affiliation>
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<Language>eng</Language>
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<Agency>National Natural Science Foundation of China</Agency>
<Country>International</Country>
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<Agency>Chongqing Science and Technology Commission Project of China</Agency>
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