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Substrate Metabolism-Driven Assembly of High-Quality CdS xSe1- x Quantum Dots in Escherichia coli: Molecular Mechanisms and Bioimaging Application.

Identifieur interne : 000120 ( Main/Exploration ); précédent : 000119; suivant : 000121

Substrate Metabolism-Driven Assembly of High-Quality CdS xSe1- x Quantum Dots in Escherichia coli: Molecular Mechanisms and Bioimaging Application.

Auteurs : Li-Jiao Tian [République populaire de Chine] ; Yuan Min [République populaire de Chine] ; Wen-Wei Li [République populaire de Chine] ; Jie-Jie Chen [République populaire de Chine] ; Nan-Qing Zhou [République populaire de Chine] ; Ting-Ting Zhu [République populaire de Chine] ; Dao-Bo Li [République populaire de Chine] ; Jing-Yuan Ma [République populaire de Chine] ; Peng-Fei An [République populaire de Chine] ; Li-Rong Zheng [République populaire de Chine] ; Hai Huang [République populaire de Chine] ; Yang-Zhong Liu [République populaire de Chine] ; Han-Qing Yu [République populaire de Chine]

Source :

RBID : pubmed:30969107

Descripteurs français

English descriptors

Abstract

Biosynthesis offers opportunities for cost-effective and sustainable production of semiconductor quantum dots (QDs), but is currently restricted by poor controllability on the synthesis process, resulting from limited knowledge on the assembly mechanisms and the lack of effective control strategies. In this work, we provide molecular-level insights into the formation mechanism of biogenic QDs (Bio-QDs) and its connection with the cellular substrate metabolism in Escherichia coli. Strengthening the substrate metabolism for producing more reducing power was found to stimulate the production of several reduced thiol-containing proteins (including glutaredoxin and thioredoxin) that play key roles in Bio-QDs assembly. This effectively diverted the transformation route of the selenium (Se) and cadmium (Cd) metabolic from Cd3(PO4)2 formation to CdS xSe1- x QDs assembly, yielding fine-sized (2.0 ± 0.4 nm), high-quality Bio-QDs with quantum yield (5.2%) and fluorescence lifetime (99.19 ns) far exceeding the existing counterparts. The underlying mechanisms of Bio-QDs crystallization and development were elucidated by density functional theory calculations and molecular dynamics simulation. The resulting Bio-QDs were successfully used for bioimaging of cancer cells and tumor tissue of mice without extra modification. Our work provides fundamental knowledge on the Bio-QDs assembly mechanisms and proposes an effective, facile regulation strategy, which may inspire advances in controlled synthesis and practical applications of Bio-QDs as well as other bionanomaterials.

DOI: 10.1021/acsnano.9b01581
PubMed: 30969107


Affiliations:


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Le document en format XML

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Se
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<term>Animals (MeSH)</term>
<term>Cadmium (chemistry)</term>
<term>Cadmium (pharmacology)</term>
<term>Cell Survival (drug effects)</term>
<term>Escherichia coli (drug effects)</term>
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<div type="abstract" xml:lang="en">Biosynthesis offers opportunities for cost-effective and sustainable production of semiconductor quantum dots (QDs), but is currently restricted by poor controllability on the synthesis process, resulting from limited knowledge on the assembly mechanisms and the lack of effective control strategies. In this work, we provide molecular-level insights into the formation mechanism of biogenic QDs (Bio-QDs) and its connection with the cellular substrate metabolism in Escherichia coli. Strengthening the substrate metabolism for producing more reducing power was found to stimulate the production of several reduced thiol-containing proteins (including glutaredoxin and thioredoxin) that play key roles in Bio-QDs assembly. This effectively diverted the transformation route of the selenium (Se) and cadmium (Cd) metabolic from Cd
<sub>3</sub>
(PO
<sub>4</sub>
)
<sub>2</sub>
formation to CdS
<sub>x</sub>
Se
<sub>1- x</sub>
QDs assembly, yielding fine-sized (2.0 ± 0.4 nm), high-quality Bio-QDs with quantum yield (5.2%) and fluorescence lifetime (99.19 ns) far exceeding the existing counterparts. The underlying mechanisms of Bio-QDs crystallization and development were elucidated by density functional theory calculations and molecular dynamics simulation. The resulting Bio-QDs were successfully used for bioimaging of cancer cells and tumor tissue of mice without extra modification. Our work provides fundamental knowledge on the Bio-QDs assembly mechanisms and proposes an effective, facile regulation strategy, which may inspire advances in controlled synthesis and practical applications of Bio-QDs as well as other bionanomaterials.</div>
</front>
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<Year>2020</Year>
<Month>08</Month>
<Day>19</Day>
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<Year>2020</Year>
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<Day>19</Day>
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<Volume>13</Volume>
<Issue>5</Issue>
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<ArticleTitle>Substrate Metabolism-Driven Assembly of High-Quality CdS
<sub>x</sub>
Se
<sub>1- x</sub>
Quantum Dots in Escherichia coli: Molecular Mechanisms and Bioimaging Application.</ArticleTitle>
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<AbstractText>Biosynthesis offers opportunities for cost-effective and sustainable production of semiconductor quantum dots (QDs), but is currently restricted by poor controllability on the synthesis process, resulting from limited knowledge on the assembly mechanisms and the lack of effective control strategies. In this work, we provide molecular-level insights into the formation mechanism of biogenic QDs (Bio-QDs) and its connection with the cellular substrate metabolism in Escherichia coli. Strengthening the substrate metabolism for producing more reducing power was found to stimulate the production of several reduced thiol-containing proteins (including glutaredoxin and thioredoxin) that play key roles in Bio-QDs assembly. This effectively diverted the transformation route of the selenium (Se) and cadmium (Cd) metabolic from Cd
<sub>3</sub>
(PO
<sub>4</sub>
)
<sub>2</sub>
formation to CdS
<sub>x</sub>
Se
<sub>1- x</sub>
QDs assembly, yielding fine-sized (2.0 ± 0.4 nm), high-quality Bio-QDs with quantum yield (5.2%) and fluorescence lifetime (99.19 ns) far exceeding the existing counterparts. The underlying mechanisms of Bio-QDs crystallization and development were elucidated by density functional theory calculations and molecular dynamics simulation. The resulting Bio-QDs were successfully used for bioimaging of cancer cells and tumor tissue of mice without extra modification. Our work provides fundamental knowledge on the Bio-QDs assembly mechanisms and proposes an effective, facile regulation strategy, which may inspire advances in controlled synthesis and practical applications of Bio-QDs as well as other bionanomaterials.</AbstractText>
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<LastName>Tian</LastName>
<ForeName>Li-Jiao</ForeName>
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<Affiliation>CAS Key Laboratory of Urban Pollutant Conversion, Department of Applied Chemistry , University of Science and Technology of China , Hefei 230026 , China.</Affiliation>
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<LastName>Chen</LastName>
<ForeName>Jie-Jie</ForeName>
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<Identifier Source="ORCID">0000-0002-2539-8305</Identifier>
<AffiliationInfo>
<Affiliation>CAS Key Laboratory of Urban Pollutant Conversion, Department of Applied Chemistry , University of Science and Technology of China , Hefei 230026 , China.</Affiliation>
</AffiliationInfo>
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<ForeName>Nan-Qing</ForeName>
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<ForeName>Ting-Ting</ForeName>
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<LastName>Ma</LastName>
<ForeName>Jing-Yuan</ForeName>
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<ForeName>Peng-Fei</ForeName>
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<LastName>Zheng</LastName>
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<LastName>Huang</LastName>
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</AffiliationInfo>
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<ForeName>Yang-Zhong</ForeName>
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<Affiliation>CAS Key Laboratory of Urban Pollutant Conversion, Department of Applied Chemistry , University of Science and Technology of China , Hefei 230026 , China.</Affiliation>
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<Affiliation>CAS Key Laboratory of Urban Pollutant Conversion, Department of Applied Chemistry , University of Science and Technology of China , Hefei 230026 , China.</Affiliation>
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<Year>2019</Year>
<Month>04</Month>
<Day>15</Day>
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</Article>
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<Country>United States</Country>
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<RegistryNumber>0</RegistryNumber>
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<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
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<MeshHeading>
<DescriptorName UI="D012643" MajorTopicYN="N">Selenium</DescriptorName>
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<QualifierName UI="Q000494" MajorTopicYN="N">pharmacology</QualifierName>
</MeshHeading>
<MeshHeading>
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<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
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<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="Y">assembly mechanism</Keyword>
<Keyword MajorTopicYN="Y">bioimaging</Keyword>
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<name sortKey="Chen, Jie Jie" sort="Chen, Jie Jie" uniqKey="Chen J" first="Jie-Jie" last="Chen">Jie-Jie Chen</name>
<name sortKey="Huang, Hai" sort="Huang, Hai" uniqKey="Huang H" first="Hai" last="Huang">Hai Huang</name>
<name sortKey="Li, Dao Bo" sort="Li, Dao Bo" uniqKey="Li D" first="Dao-Bo" last="Li">Dao-Bo Li</name>
<name sortKey="Li, Wen Wei" sort="Li, Wen Wei" uniqKey="Li W" first="Wen-Wei" last="Li">Wen-Wei Li</name>
<name sortKey="Liu, Yang Zhong" sort="Liu, Yang Zhong" uniqKey="Liu Y" first="Yang-Zhong" last="Liu">Yang-Zhong Liu</name>
<name sortKey="Ma, Jing Yuan" sort="Ma, Jing Yuan" uniqKey="Ma J" first="Jing-Yuan" last="Ma">Jing-Yuan Ma</name>
<name sortKey="Min, Yuan" sort="Min, Yuan" uniqKey="Min Y" first="Yuan" last="Min">Yuan Min</name>
<name sortKey="Yu, Han Qing" sort="Yu, Han Qing" uniqKey="Yu H" first="Han-Qing" last="Yu">Han-Qing Yu</name>
<name sortKey="Zheng, Li Rong" sort="Zheng, Li Rong" uniqKey="Zheng L" first="Li-Rong" last="Zheng">Li-Rong Zheng</name>
<name sortKey="Zhou, Nan Qing" sort="Zhou, Nan Qing" uniqKey="Zhou N" first="Nan-Qing" last="Zhou">Nan-Qing Zhou</name>
<name sortKey="Zhu, Ting Ting" sort="Zhu, Ting Ting" uniqKey="Zhu T" first="Ting-Ting" last="Zhu">Ting-Ting Zhu</name>
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