Surface Display of a Redox Enzyme and its Site-Specific Wiring to Gold Electrodes
The generation of a current through interaction between bacteria and electrodes has been explored by various methods. We demonstrate the attachment of living bacteria through a surface displayed redox enzyme, alcohol dehydrogenase II. The unnatural amino acid para-azido-l-phenylalanine was incorpora...
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Veröffentlicht in: | Journal of the American Chemical Society 2013-01, Vol.135 (1), p.70-73 |
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container_title | Journal of the American Chemical Society |
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creator | Amir, Liron Carnally, Stewart A Rayo, Josep Rosenne, Shaked Melamed Yerushalmi, Sarit Schlesinger, Orr Meijler, Michael M Alfonta, Lital |
description | The generation of a current through interaction between bacteria and electrodes has been explored by various methods. We demonstrate the attachment of living bacteria through a surface displayed redox enzyme, alcohol dehydrogenase II. The unnatural amino acid para-azido-l-phenylalanine was incorporated into a specific site of the displayed enzyme, facilitating electron transfer between the enzyme and an electrode. In order to attach the bacteria carrying the surface displayed enzyme to a surface, a linker containing an alkyne and a thiol moiety on opposite ends was synthesized and attached to the dehydrogenase site specifically through a copper(I)-catalyzed azide–alkyne cycloaddition reaction. Using this approach we were able to covalently link bacteria to gold-coated surfaces and to gold nanoparticles, while maintaining viability and catalytic activity. We show the performance of a biofuel cell using these modified bacteria at the anode, which resulted in site-specific dependent fuel cell performance for at least a week. This is the first example of site-specific attachment of a true living biohybrid to inorganic material. |
doi_str_mv | 10.1021/ja310556n |
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We demonstrate the attachment of living bacteria through a surface displayed redox enzyme, alcohol dehydrogenase II. The unnatural amino acid para-azido-l-phenylalanine was incorporated into a specific site of the displayed enzyme, facilitating electron transfer between the enzyme and an electrode. In order to attach the bacteria carrying the surface displayed enzyme to a surface, a linker containing an alkyne and a thiol moiety on opposite ends was synthesized and attached to the dehydrogenase site specifically through a copper(I)-catalyzed azide–alkyne cycloaddition reaction. Using this approach we were able to covalently link bacteria to gold-coated surfaces and to gold nanoparticles, while maintaining viability and catalytic activity. We show the performance of a biofuel cell using these modified bacteria at the anode, which resulted in site-specific dependent fuel cell performance for at least a week. This is the first example of site-specific attachment of a true living biohybrid to inorganic material.</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/ja310556n</identifier><identifier>PMID: 23231821</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Alcohol Dehydrogenase - chemistry ; Alcohol Dehydrogenase - metabolism ; Alkynes - chemistry ; Azides - chemistry ; Azides - metabolism ; Catalysis ; Copper - chemistry ; Cyclization ; Electrodes ; Escherichia coli - chemistry ; Escherichia coli - metabolism ; Gold - chemistry ; Gold - metabolism ; Oxidation-Reduction ; Phenylalanine - analogs & derivatives ; Phenylalanine - chemistry ; Phenylalanine - metabolism ; Surface Properties ; Zymomonas - enzymology ; Zymomonas - metabolism</subject><ispartof>Journal of the American Chemical Society, 2013-01, Vol.135 (1), p.70-73</ispartof><rights>Copyright © 2012 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a315t-770582b0d4141c16bae68c2424902ff2a1f9c57d1bd713848703727807da84fe3</citedby><cites>FETCH-LOGICAL-a315t-770582b0d4141c16bae68c2424902ff2a1f9c57d1bd713848703727807da84fe3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ja310556n$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ja310556n$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2763,27075,27923,27924,56737,56787</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23231821$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Amir, Liron</creatorcontrib><creatorcontrib>Carnally, Stewart A</creatorcontrib><creatorcontrib>Rayo, Josep</creatorcontrib><creatorcontrib>Rosenne, Shaked</creatorcontrib><creatorcontrib>Melamed Yerushalmi, Sarit</creatorcontrib><creatorcontrib>Schlesinger, Orr</creatorcontrib><creatorcontrib>Meijler, Michael M</creatorcontrib><creatorcontrib>Alfonta, Lital</creatorcontrib><title>Surface Display of a Redox Enzyme and its Site-Specific Wiring to Gold Electrodes</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>The generation of a current through interaction between bacteria and electrodes has been explored by various methods. We demonstrate the attachment of living bacteria through a surface displayed redox enzyme, alcohol dehydrogenase II. The unnatural amino acid para-azido-l-phenylalanine was incorporated into a specific site of the displayed enzyme, facilitating electron transfer between the enzyme and an electrode. In order to attach the bacteria carrying the surface displayed enzyme to a surface, a linker containing an alkyne and a thiol moiety on opposite ends was synthesized and attached to the dehydrogenase site specifically through a copper(I)-catalyzed azide–alkyne cycloaddition reaction. Using this approach we were able to covalently link bacteria to gold-coated surfaces and to gold nanoparticles, while maintaining viability and catalytic activity. We show the performance of a biofuel cell using these modified bacteria at the anode, which resulted in site-specific dependent fuel cell performance for at least a week. 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subjects | Alcohol Dehydrogenase - chemistry Alcohol Dehydrogenase - metabolism Alkynes - chemistry Azides - chemistry Azides - metabolism Catalysis Copper - chemistry Cyclization Electrodes Escherichia coli - chemistry Escherichia coli - metabolism Gold - chemistry Gold - metabolism Oxidation-Reduction Phenylalanine - analogs & derivatives Phenylalanine - chemistry Phenylalanine - metabolism Surface Properties Zymomonas - enzymology Zymomonas - metabolism |
title | Surface Display of a Redox Enzyme and its Site-Specific Wiring to Gold Electrodes |
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