Serveur d'exploration sur le phanerochaete

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Simultaneous removal of ciprofloxacin, norfloxacin, sulfamethoxazole by co-producing oxidative enzymes system of Phanerochaete chrysosporium and Pycnoporus sanguineus.

Identifieur interne : 000102 ( Main/Exploration ); précédent : 000101; suivant : 000103

Simultaneous removal of ciprofloxacin, norfloxacin, sulfamethoxazole by co-producing oxidative enzymes system of Phanerochaete chrysosporium and Pycnoporus sanguineus.

Auteurs : Nan Gao [République populaire de Chine] ; Chun-Xiao Liu [République populaire de Chine] ; Qiu-Man Xu [République populaire de Chine] ; Jing-Sheng Cheng [République populaire de Chine] ; Ying-Jin Yuan [République populaire de Chine]

Source :

RBID : pubmed:29268173

Descripteurs français

English descriptors

Abstract

Pycnoporus sanguineus could remove 98.5% ciprofloxacin (CIP), 96.4% norfloxacin (NOR), 100% sulfamethoxazole (SMX), and 100% their mixture through biotransformation within 2 d, while Phanerochaete chrysosporium could only remove 64.5% CIP, 73.2% NOR, and 63.3% SMX through biosorption and biotransformation within 8 d, respectively. The efficiencies of antibiotic bioremoval under co-culture were more than that under the pure culture of P. chrysosporium but less than that under the pure culture of P. sanguineus. However, only 2% CIP and 3% NOR under co-culture were detected in the mycelia. In vitro enzymatic degradation and in vivo cytochrome P450 inhibition experiments revealed that laccase and cytochrome P450 could play roles in the removal of above all antibiotics, while manganese peroxidase could only play role in SMX removal. Transformation products of CIP and NOR under the pure culture of P. chrysosporium could be assigned to three different reaction pathways: (i) defluorination or dehydration, (ii) decarboxylation, and (iii) oxidation of the piperazinyl substituent. Additionally, other pathways, (iv) monohydroxylation, and (v) demethylation or deethylation at position N1 also occurred under the co-culture and pure culture of P. sanguineus. Antibacterial activity of antibiotics could be eliminated after treatments with pure and co-culture of P. chrysosporium and P. sanguineus. The cytotoxicity of the metabolites of SMX and NOR under co-culture was lower than that under the pure culture of P. sanguineus, indicating co-culture is a more environmentally friendly strategy to eliminate SMX and NOR.

DOI: 10.1016/j.chemosphere.2017.12.062
PubMed: 29268173


Affiliations:


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Le document en format XML

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<term>Ciprofloxacin (isolation & purification)</term>
<term>Coculture Techniques (MeSH)</term>
<term>Norfloxacin (isolation & purification)</term>
<term>Oxidation-Reduction (MeSH)</term>
<term>Oxidative Stress (MeSH)</term>
<term>Phanerochaete (enzymology)</term>
<term>Phanerochaete (metabolism)</term>
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<term>Norfloxacine (isolement et purification)</term>
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<term>Phanerochaete (enzymologie)</term>
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<term>Pycnoporus (métabolisme)</term>
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<div type="abstract" xml:lang="en">Pycnoporus sanguineus could remove 98.5% ciprofloxacin (CIP), 96.4% norfloxacin (NOR), 100% sulfamethoxazole (SMX), and 100% their mixture through biotransformation within 2 d, while Phanerochaete chrysosporium could only remove 64.5% CIP, 73.2% NOR, and 63.3% SMX through biosorption and biotransformation within 8 d, respectively. The efficiencies of antibiotic bioremoval under co-culture were more than that under the pure culture of P. chrysosporium but less than that under the pure culture of P. sanguineus. However, only 2% CIP and 3% NOR under co-culture were detected in the mycelia. In vitro enzymatic degradation and in vivo cytochrome P450 inhibition experiments revealed that laccase and cytochrome P450 could play roles in the removal of above all antibiotics, while manganese peroxidase could only play role in SMX removal. Transformation products of CIP and NOR under the pure culture of P. chrysosporium could be assigned to three different reaction pathways: (i) defluorination or dehydration, (ii) decarboxylation, and (iii) oxidation of the piperazinyl substituent. Additionally, other pathways, (iv) monohydroxylation, and (v) demethylation or deethylation at position N
<sub>1</sub>
also occurred under the co-culture and pure culture of P. sanguineus. Antibacterial activity of antibiotics could be eliminated after treatments with pure and co-culture of P. chrysosporium and P. sanguineus. The cytotoxicity of the metabolites of SMX and NOR under co-culture was lower than that under the pure culture of P. sanguineus, indicating co-culture is a more environmentally friendly strategy to eliminate SMX and NOR.</div>
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<DescriptorName UI="D001711" MajorTopicYN="N">Biotransformation</DescriptorName>
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<DescriptorName UI="D002939" MajorTopicYN="N">Ciprofloxacin</DescriptorName>
<QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018920" MajorTopicYN="N">Coculture Techniques</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D009643" MajorTopicYN="N">Norfloxacin</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D010084" MajorTopicYN="Y">Oxidation-Reduction</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D018384" MajorTopicYN="N">Oxidative Stress</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D020075" MajorTopicYN="N">Phanerochaete</DescriptorName>
<QualifierName UI="Q000201" MajorTopicYN="Y">enzymology</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D055494" MajorTopicYN="N">Pycnoporus</DescriptorName>
<QualifierName UI="Q000201" MajorTopicYN="Y">enzymology</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
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<DescriptorName UI="D013420" MajorTopicYN="N">Sulfamethoxazole</DescriptorName>
<QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName>
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<Keyword MajorTopicYN="N">Biotransformation products</Keyword>
<Keyword MajorTopicYN="N">Co-culture</Keyword>
<Keyword MajorTopicYN="N">Fluoroquinolones</Keyword>
<Keyword MajorTopicYN="N">Oxidative enzymes</Keyword>
<Keyword MajorTopicYN="N">Sulfamethoxazole</Keyword>
<Keyword MajorTopicYN="N">White rot fungi</Keyword>
</KeywordList>
</MedlineCitation>
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<PubMedPubDate PubStatus="received">
<Year>2017</Year>
<Month>07</Month>
<Day>05</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="revised">
<Year>2017</Year>
<Month>11</Month>
<Day>18</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="accepted">
<Year>2017</Year>
<Month>12</Month>
<Day>10</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2017</Year>
<Month>12</Month>
<Day>22</Day>
<Hour>6</Hour>
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<PubMedPubDate PubStatus="medline">
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<PubMedPubDate PubStatus="entrez">
<Year>2017</Year>
<Month>12</Month>
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<Hour>6</Hour>
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<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">29268173</ArticleId>
<ArticleId IdType="pii">S0045-6535(17)32032-5</ArticleId>
<ArticleId IdType="doi">10.1016/j.chemosphere.2017.12.062</ArticleId>
</ArticleIdList>
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<list>
<country>
<li>République populaire de Chine</li>
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<country name="République populaire de Chine">
<noRegion>
<name sortKey="Gao, Nan" sort="Gao, Nan" uniqKey="Gao N" first="Nan" last="Gao">Nan Gao</name>
</noRegion>
<name sortKey="Cheng, Jing Sheng" sort="Cheng, Jing Sheng" uniqKey="Cheng J" first="Jing-Sheng" last="Cheng">Jing-Sheng Cheng</name>
<name sortKey="Liu, Chun Xiao" sort="Liu, Chun Xiao" uniqKey="Liu C" first="Chun-Xiao" last="Liu">Chun-Xiao Liu</name>
<name sortKey="Xu, Qiu Man" sort="Xu, Qiu Man" uniqKey="Xu Q" first="Qiu-Man" last="Xu">Qiu-Man Xu</name>
<name sortKey="Yuan, Ying Jin" sort="Yuan, Ying Jin" uniqKey="Yuan Y" first="Ying-Jin" last="Yuan">Ying-Jin Yuan</name>
</country>
</tree>
</affiliations>
</record>

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