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Dye induced quenching of firefly luciferase–luciferin bioluminescence
The quenching of firefly bioluminescence (BL) in presence of xanthene dyes and tetratolylporphyrin was investigated. The BL intensity was quenched with an altered decay pattern in presence of xanthene dyes and tetratolylporphyrin. The electronic absorption spectra indicate that there is no significa...
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Published in: | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Molecular and biomolecular spectroscopy, 2007-11, Vol.68 (3), p.851-859 |
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description | The quenching of firefly bioluminescence (BL) in presence of xanthene dyes and tetratolylporphyrin was investigated. The BL intensity was quenched with an altered decay pattern in presence of xanthene dyes and tetratolylporphyrin. The electronic absorption spectra indicate that there is no significant interaction occurring between the dyes and the BL components in the ground state. The BL quenching decay rate and fluorescence quenching studies of luciferin by the dyes suggest an energy transfer through an exciplex, involving oxyluciferin, in the excited state and the dyes, in the ground state. The bimolecular quenching rate constant (
K
q) values obtained from fluorescence studies varied between 7.7
×
10
12 and 19.8
×
10
12
M
−1
s
−1. The magnitude of the bimolecular quenching rate constants confirmed the complex formation between dye and excited oxyluciferin. The exciplex subsequently undergoes a non-radiative decay to the ground state via a combination of heavy atom induced and Förster-type energy transfer. The decay rate constants in presence and in absence of dyes vary between 7.47
×
10
−4 and 7.6
×
10
−2
s
−1. In the presence of dyes the effective decay rate constants (
k
eff) increased while the lifetime of light emitting species decreased. The kinetic studies in presence of singlet oxygen scavengers, like β-carotene and NaN
3, prove that there is no significant quenching of the firefly BL due to the formation of singlet oxygen. |
doi_str_mv | 10.1016/j.saa.2007.01.003 |
format | article |
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K
q) values obtained from fluorescence studies varied between 7.7
×
10
12 and 19.8
×
10
12
M
−1
s
−1. The magnitude of the bimolecular quenching rate constants confirmed the complex formation between dye and excited oxyluciferin. The exciplex subsequently undergoes a non-radiative decay to the ground state via a combination of heavy atom induced and Förster-type energy transfer. The decay rate constants in presence and in absence of dyes vary between 7.47
×
10
−4 and 7.6
×
10
−2
s
−1. In the presence of dyes the effective decay rate constants (
k
eff) increased while the lifetime of light emitting species decreased. The kinetic studies in presence of singlet oxygen scavengers, like β-carotene and NaN
3, prove that there is no significant quenching of the firefly BL due to the formation of singlet oxygen.</description><identifier>ISSN: 1386-1425</identifier><identifier>DOI: 10.1016/j.saa.2007.01.003</identifier><identifier>PMID: 17317285</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Animals ; Bioluminescence ; Coloring Agents - metabolism ; Electrons ; Energy transfer ; Eosine Yellowish-(YS) - metabolism ; Erythrosine - metabolism ; Exciplex ; Firefly Luciferin - metabolism ; Fluorescein - metabolism ; Free Radical Scavengers - metabolism ; Kinetics ; Luciferases, Firefly - metabolism ; Luminescence ; Rose Bengal - metabolism ; Singlet Oxygen - metabolism ; Spectrometry, Fluorescence ; Time Factors ; Xanthene dyes</subject><ispartof>Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2007-11, Vol.68 (3), p.851-859</ispartof><rights>2007 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c351t-ca26424b3a96c15e81e6696a6c1ffd8dce9ae745f8bae1895c1a9e0d6c1778893</citedby><cites>FETCH-LOGICAL-c351t-ca26424b3a96c15e81e6696a6c1ffd8dce9ae745f8bae1895c1a9e0d6c1778893</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17317285$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KrishnaMurthy, N.V.</creatorcontrib><creatorcontrib>Sudhaharan, T.</creatorcontrib><creatorcontrib>Ram Reddy, A.</creatorcontrib><title>Dye induced quenching of firefly luciferase–luciferin bioluminescence</title><title>Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy</title><addtitle>Spectrochim Acta A Mol Biomol Spectrosc</addtitle><description>The quenching of firefly bioluminescence (BL) in presence of xanthene dyes and tetratolylporphyrin was investigated. The BL intensity was quenched with an altered decay pattern in presence of xanthene dyes and tetratolylporphyrin. The electronic absorption spectra indicate that there is no significant interaction occurring between the dyes and the BL components in the ground state. The BL quenching decay rate and fluorescence quenching studies of luciferin by the dyes suggest an energy transfer through an exciplex, involving oxyluciferin, in the excited state and the dyes, in the ground state. The bimolecular quenching rate constant (
K
q) values obtained from fluorescence studies varied between 7.7
×
10
12 and 19.8
×
10
12
M
−1
s
−1. The magnitude of the bimolecular quenching rate constants confirmed the complex formation between dye and excited oxyluciferin. The exciplex subsequently undergoes a non-radiative decay to the ground state via a combination of heavy atom induced and Förster-type energy transfer. The decay rate constants in presence and in absence of dyes vary between 7.47
×
10
−4 and 7.6
×
10
−2
s
−1. In the presence of dyes the effective decay rate constants (
k
eff) increased while the lifetime of light emitting species decreased. The kinetic studies in presence of singlet oxygen scavengers, like β-carotene and NaN
3, prove that there is no significant quenching of the firefly BL due to the formation of singlet oxygen.</description><subject>Animals</subject><subject>Bioluminescence</subject><subject>Coloring Agents - metabolism</subject><subject>Electrons</subject><subject>Energy transfer</subject><subject>Eosine Yellowish-(YS) - metabolism</subject><subject>Erythrosine - metabolism</subject><subject>Exciplex</subject><subject>Firefly Luciferin - metabolism</subject><subject>Fluorescein - metabolism</subject><subject>Free Radical Scavengers - metabolism</subject><subject>Kinetics</subject><subject>Luciferases, Firefly - metabolism</subject><subject>Luminescence</subject><subject>Rose Bengal - metabolism</subject><subject>Singlet Oxygen - metabolism</subject><subject>Spectrometry, Fluorescence</subject><subject>Time Factors</subject><subject>Xanthene dyes</subject><issn>1386-1425</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp9kE1OwzAQhb0A0VI4ABuUFbsET5w4jlihAgWpEhtYW449Blf5KXGD1B134IacBEeNxI7VaDTvPc37CLkAmgAFfr1JvFJJSmmRUEgoZUdkDkzwGLI0n5FT7zeUUhApPSEzKBgUqcjnZHW3x8i1ZtBooo8BW_3u2reos5F1Pdp6H9WDdhZ75fHn63taXBtVrquHxrXodTDhGTm2qvZ4Ps0FeX24f1k-xuvn1dPydh1rlsMu1irlWZpVTJVcQ44CkPOSq7BYa4TRWCosstyKSiGIMtegSqQm3ItCiJItyNUhd9t34V2_k40LH9S1arEbvOSCcUazUQgHoe4770MVue1do_q9BCpHYnIjAzE5EpMUZCAWPJdT-FA1aP4cE64guDkIMFT8dNhLr91Y3wRYeidN5_6J_wWLf3_A</recordid><startdate>20071101</startdate><enddate>20071101</enddate><creator>KrishnaMurthy, N.V.</creator><creator>Sudhaharan, T.</creator><creator>Ram Reddy, A.</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20071101</creationdate><title>Dye induced quenching of firefly luciferase–luciferin bioluminescence</title><author>KrishnaMurthy, N.V. ; Sudhaharan, T. ; Ram Reddy, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c351t-ca26424b3a96c15e81e6696a6c1ffd8dce9ae745f8bae1895c1a9e0d6c1778893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Bioluminescence</topic><topic>Coloring Agents - metabolism</topic><topic>Electrons</topic><topic>Energy transfer</topic><topic>Eosine Yellowish-(YS) - metabolism</topic><topic>Erythrosine - metabolism</topic><topic>Exciplex</topic><topic>Firefly Luciferin - metabolism</topic><topic>Fluorescein - metabolism</topic><topic>Free Radical Scavengers - metabolism</topic><topic>Kinetics</topic><topic>Luciferases, Firefly - metabolism</topic><topic>Luminescence</topic><topic>Rose Bengal - metabolism</topic><topic>Singlet Oxygen - metabolism</topic><topic>Spectrometry, Fluorescence</topic><topic>Time Factors</topic><topic>Xanthene dyes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KrishnaMurthy, N.V.</creatorcontrib><creatorcontrib>Sudhaharan, T.</creatorcontrib><creatorcontrib>Ram Reddy, A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KrishnaMurthy, N.V.</au><au>Sudhaharan, T.</au><au>Ram Reddy, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dye induced quenching of firefly luciferase–luciferin bioluminescence</atitle><jtitle>Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy</jtitle><addtitle>Spectrochim Acta A Mol Biomol Spectrosc</addtitle><date>2007-11-01</date><risdate>2007</risdate><volume>68</volume><issue>3</issue><spage>851</spage><epage>859</epage><pages>851-859</pages><issn>1386-1425</issn><abstract>The quenching of firefly bioluminescence (BL) in presence of xanthene dyes and tetratolylporphyrin was investigated. The BL intensity was quenched with an altered decay pattern in presence of xanthene dyes and tetratolylporphyrin. The electronic absorption spectra indicate that there is no significant interaction occurring between the dyes and the BL components in the ground state. The BL quenching decay rate and fluorescence quenching studies of luciferin by the dyes suggest an energy transfer through an exciplex, involving oxyluciferin, in the excited state and the dyes, in the ground state. The bimolecular quenching rate constant (
K
q) values obtained from fluorescence studies varied between 7.7
×
10
12 and 19.8
×
10
12
M
−1
s
−1. The magnitude of the bimolecular quenching rate constants confirmed the complex formation between dye and excited oxyluciferin. The exciplex subsequently undergoes a non-radiative decay to the ground state via a combination of heavy atom induced and Förster-type energy transfer. The decay rate constants in presence and in absence of dyes vary between 7.47
×
10
−4 and 7.6
×
10
−2
s
−1. In the presence of dyes the effective decay rate constants (
k
eff) increased while the lifetime of light emitting species decreased. The kinetic studies in presence of singlet oxygen scavengers, like β-carotene and NaN
3, prove that there is no significant quenching of the firefly BL due to the formation of singlet oxygen.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>17317285</pmid><doi>10.1016/j.saa.2007.01.003</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Bioluminescence Coloring Agents - metabolism Electrons Energy transfer Eosine Yellowish-(YS) - metabolism Erythrosine - metabolism Exciplex Firefly Luciferin - metabolism Fluorescein - metabolism Free Radical Scavengers - metabolism Kinetics Luciferases, Firefly - metabolism Luminescence Rose Bengal - metabolism Singlet Oxygen - metabolism Spectrometry, Fluorescence Time Factors Xanthene dyes |
title | Dye induced quenching of firefly luciferase–luciferin bioluminescence |
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