Algicidal Molecular Mechanism and Toxicological Degradation of Microcystis aeruginosa by White-Rot Fungi.
Identifieur interne : 000042 ( Main/Exploration ); précédent : 000041; suivant : 000043Algicidal Molecular Mechanism and Toxicological Degradation of Microcystis aeruginosa by White-Rot Fungi.
Auteurs : Guoming Zeng [République populaire de Chine] ; Pei Gao [République populaire de Chine] ; Jiale Wang [République populaire de Chine] ; Jinxi Zhang [République populaire de Chine] ; Maolan Zhang [République populaire de Chine] ; Da Sun [République populaire de Chine]Source :
- 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
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Chine</country><wicri:regionArea>Chongqing Engineering Laboratory of Nano/Micro Biological Medicine Detection Technology, School of Architecture and Engineering, Chongqing University of Science and Technology, Chongqing 401331</wicri:regionArea><wicri:noRegion>Chongqing 401331</wicri:noRegion></affiliation><affiliation wicri:level="1"><nlm:affiliation>China Metallurgical Construction Engineering Group Co., Ltd., Chongqing 643000, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>China Metallurgical Construction Engineering Group Co., Ltd., Chongqing 643000</wicri:regionArea><wicri:noRegion>Chongqing 643000</wicri:noRegion></affiliation></author><author><name sortKey="Zhang, Jinxi" sort="Zhang, Jinxi" uniqKey="Zhang J" first="Jinxi" last="Zhang">Jinxi Zhang</name><affiliation wicri:level="1"><nlm:affiliation>Chongqing Engineering Laboratory of Nano/Micro Biological Medicine Detection Technology, School of Architecture and Engineering, Chongqing University of Science and Technology, Chongqing 401331, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Chongqing Engineering Laboratory of Nano/Micro Biological Medicine Detection Technology, School of Architecture and Engineering, Chongqing University of Science and Technology, Chongqing 401331</wicri:regionArea><wicri:noRegion>Chongqing 401331</wicri:noRegion></affiliation><affiliation wicri:level="1"><nlm:affiliation>China Metallurgical Construction Engineering Group Co., Ltd., Chongqing 643000, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>China Metallurgical Construction Engineering Group Co., Ltd., Chongqing 643000</wicri:regionArea><wicri:noRegion>Chongqing 643000</wicri:noRegion></affiliation></author><author><name sortKey="Zhang, Maolan" sort="Zhang, Maolan" uniqKey="Zhang M" first="Maolan" last="Zhang">Maolan Zhang</name><affiliation wicri:level="1"><nlm:affiliation>Chongqing Engineering Laboratory of Nano/Micro Biological Medicine Detection Technology, School of Architecture and Engineering, Chongqing University of Science and Technology, Chongqing 401331, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Chongqing Engineering Laboratory of Nano/Micro Biological Medicine Detection Technology, School of Architecture and Engineering, Chongqing University of Science and Technology, Chongqing 401331</wicri:regionArea><wicri:noRegion>Chongqing 401331</wicri:noRegion></affiliation><affiliation wicri:level="1"><nlm:affiliation>China Metallurgical Construction Engineering Group Co., Ltd., Chongqing 643000, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>China Metallurgical Construction Engineering Group Co., Ltd., Chongqing 643000</wicri:regionArea><wicri:noRegion>Chongqing 643000</wicri:noRegion></affiliation></author><author><name sortKey="Sun, Da" sort="Sun, Da" uniqKey="Sun D" first="Da" last="Sun">Da Sun</name><affiliation wicri:level="1"><nlm:affiliation>Institute of Life Sciences & Biomedicine Collaborative Innovation Center, Wenzhou University, Wenzhou 325035, China.</nlm:affiliation><country xml:lang="fr">République populaire de Chine</country><wicri:regionArea>Institute of Life Sciences & Biomedicine Collaborative Innovation Center, Wenzhou University, Wenzhou 325035</wicri:regionArea><wicri:noRegion>Wenzhou 325035</wicri:noRegion></affiliation></author></analytic><series><title level="j">Toxins</title><idno type="eISSN">2072-6651</idno><imprint><date when="2020" type="published">2020</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><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><pubmed><MedlineCitation Status="In-Process" Owner="NLM"><PMID Version="1">32575534</PMID><DateRevised><Year>2020</Year><Month>08</Month><Day>13</Day></DateRevised><Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">2072-6651</ISSN><JournalIssue CitedMedium="Internet"><Volume>12</Volume><Issue>6</Issue><PubDate><Year>2020</Year><Month>06</Month><Day>19</Day></PubDate></JournalIssue><Title>Toxins</Title><ISOAbbreviation>Toxins (Basel)</ISOAbbreviation></Journal><ArticleTitle>Algicidal Molecular Mechanism and Toxicological Degradation of <i>Microcystis aeruginosa</i> by White-Rot Fungi.</ArticleTitle><ELocationID EIdType="pii" ValidYN="Y">E406</ELocationID><ELocationID EIdType="doi" ValidYN="Y">10.3390/toxins12060406</ELocationID><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><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Zeng</LastName><ForeName>Guoming</ForeName><Initials>G</Initials><AffiliationInfo><Affiliation>Chongqing Engineering Laboratory of Nano/Micro Biological Medicine Detection Technology, School of Architecture and Engineering, Chongqing University of Science and Technology, Chongqing 401331, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>China Metallurgical Construction Engineering Group Co., Ltd., Chongqing 643000, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Gao</LastName><ForeName>Pei</ForeName><Initials>P</Initials><AffiliationInfo><Affiliation>Chongqing Engineering Laboratory of Nano/Micro Biological Medicine Detection Technology, School of Architecture and Engineering, Chongqing University of Science and Technology, Chongqing 401331, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>China Metallurgical Construction Engineering Group Co., Ltd., Chongqing 643000, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Wang</LastName><ForeName>Jiale</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Chongqing Engineering Laboratory of Nano/Micro Biological Medicine Detection Technology, School of Architecture and Engineering, Chongqing University of Science and Technology, Chongqing 401331, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>China Metallurgical Construction Engineering Group Co., Ltd., Chongqing 643000, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Zhang</LastName><ForeName>Jinxi</ForeName><Initials>J</Initials><AffiliationInfo><Affiliation>Chongqing Engineering Laboratory of Nano/Micro Biological Medicine Detection Technology, School of Architecture and Engineering, Chongqing University of Science and Technology, Chongqing 401331, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>China Metallurgical Construction Engineering Group Co., Ltd., Chongqing 643000, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Zhang</LastName><ForeName>Maolan</ForeName><Initials>M</Initials><Identifier Source="ORCID">0000-0002-9662-8323</Identifier><AffiliationInfo><Affiliation>Chongqing Engineering Laboratory of Nano/Micro Biological Medicine Detection Technology, School of Architecture and Engineering, Chongqing University of Science and Technology, Chongqing 401331, China.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>China Metallurgical Construction Engineering Group Co., Ltd., Chongqing 643000, China.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sun</LastName><ForeName>Da</ForeName><Initials>D</Initials><Identifier Source="ORCID">0000-0001-7747-9951</Identifier><AffiliationInfo><Affiliation>Institute of Life Sciences & Biomedicine Collaborative Innovation Center, Wenzhou University, Wenzhou 325035, China.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>51808086</GrantID><Agency>National Natural Science Foundation of China</Agency><Country>International</Country></Grant><Grant><GrantID>cstc2018jcyjAX0078,cstc2019jcyj-msxmX0562</GrantID><Agency>Chongqing Science and Technology Commission Project of China</Agency><Country>International</Country></Grant><Grant><GrantID>ckrc2019015,ckrc2019047</GrantID><Agency>Scientific Research Funding Project of Chongqing University of Science and Technology</Agency><Country>International</Country></Grant><Grant><GrantID>W20170010</GrantID><Agency>Water pollution control and management technology innovation project in Wenzhou</Agency><Country>International</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2020</Year><Month>06</Month><Day>19</Day></ArticleDate></Article><MedlineJournalInfo><Country>Switzerland</Country><MedlineTA>Toxins (Basel)</MedlineTA><NlmUniqueID>101530765</NlmUniqueID><ISSNLinking>2072-6651</ISSNLinking></MedlineJournalInfo><CitationSubset>IM</CitationSubset><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="Y">Microcystis aeruginosa</Keyword><Keyword MajorTopicYN="Y">microcystins</Keyword><Keyword MajorTopicYN="Y">molecular mechanism</Keyword><Keyword MajorTopicYN="Y">white-rot fungi</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2020</Year><Month>05</Month><Day>04</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2020</Year><Month>06</Month><Day>09</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2020</Year><Month>06</Month><Day>18</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2020</Year><Month>6</Month><Day>25</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2020</Year><Month>6</Month><Day>25</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2020</Year><Month>6</Month><Day>25</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>epublish</PublicationStatus><ArticleIdList><ArticleId 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first="Jiale" last="Wang">Jiale Wang</name><name sortKey="Zeng, Guoming" sort="Zeng, Guoming" uniqKey="Zeng G" first="Guoming" last="Zeng">Guoming Zeng</name><name sortKey="Zhang, Jinxi" sort="Zhang, Jinxi" uniqKey="Zhang J" first="Jinxi" last="Zhang">Jinxi Zhang</name><name sortKey="Zhang, Jinxi" sort="Zhang, Jinxi" uniqKey="Zhang J" first="Jinxi" last="Zhang">Jinxi Zhang</name><name sortKey="Zhang, Maolan" sort="Zhang, Maolan" uniqKey="Zhang M" first="Maolan" last="Zhang">Maolan Zhang</name><name sortKey="Zhang, Maolan" sort="Zhang, Maolan" uniqKey="Zhang M" first="Maolan" last="Zhang">Maolan Zhang</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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