Theoretical Study on Storage and Release of Firefly Luciferin

Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin (SLH2) may serve as a storage form of luciferin (LH2). In the present article, we employed density functional theory calculation to uncover the mechanism and detailed process of t...

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Published inPhotochemistry and photobiology Vol. 98; no. 1; pp. 184 - 192
Main Authors Guo, Ya‐Jie, Cui, Cheng‐Xing, Liu, Ya‐Jun
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.01.2022
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Abstract Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin (SLH2) may serve as a storage form of luciferin (LH2). In the present article, we employed density functional theory calculation to uncover the mechanism and detailed process of the storage and release reactions. Due to lack of available crystallographic structure of the related enzyme, the calculation was performed on a model system. For the storage reaction, possible amino acid residues were used for imitating the protein environment. For the release reaction, the dielectric constant of 3.0 was employed to simulate the polarity of the protein cavity. The computational results indicated that the reactions from LH2 to SLH2 and from SLH2 to LH2 are both exergonic, which favor the storage and release processes and coincide with the experimental observation. Basing on experimental and current theoretical study, we supplemented the stages of LH2 storage and release in the entire bioluminescent cycle of firefly. The current theoretical calculation could inspire the study on LH2 storage and release of other bioluminescent organisms. This figure shows an entire bioluminescent cycle of firefly by supplementing the stages of LH2 storage and release in the present paper.
AbstractList Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin (SLH2 ) may serve as a storage form of luciferin (LH2 ). In the present article, we employed density functional theory calculation to uncover the mechanism and detailed process of the storage and release reactions. Due to lack of available crystallographic structure of the related enzyme, the calculation was performed on a model system. For the storage reaction, possible amino acid residues were used for imitating the protein environment. For the release reaction, the dielectric constant of 3.0 was employed to simulate the polarity of the protein cavity. The computational results indicated that the reactions from LH2 to SLH2 and from SLH2 to LH2 are both exergonic, which favor the storage and release processes and coincide with the experimental observation. Basing on experimental and current theoretical study, we supplemented the stages of LH2 storage and release in the entire bioluminescent cycle of firefly. The current theoretical calculation could inspire the study on LH2 storage and release of other bioluminescent organisms.Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin (SLH2 ) may serve as a storage form of luciferin (LH2 ). In the present article, we employed density functional theory calculation to uncover the mechanism and detailed process of the storage and release reactions. Due to lack of available crystallographic structure of the related enzyme, the calculation was performed on a model system. For the storage reaction, possible amino acid residues were used for imitating the protein environment. For the release reaction, the dielectric constant of 3.0 was employed to simulate the polarity of the protein cavity. The computational results indicated that the reactions from LH2 to SLH2 and from SLH2 to LH2 are both exergonic, which favor the storage and release processes and coincide with the experimental observation. Basing on experimental and current theoretical study, we supplemented the stages of LH2 storage and release in the entire bioluminescent cycle of firefly. The current theoretical calculation could inspire the study on LH2 storage and release of other bioluminescent organisms.
Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin (SLH2) may serve as a storage form of luciferin (LH2). In the present article, we employed density functional theory calculation to uncover the mechanism and detailed process of the storage and release reactions. Due to lack of available crystallographic structure of the related enzyme, the calculation was performed on a model system. For the storage reaction, possible amino acid residues were used for imitating the protein environment. For the release reaction, the dielectric constant of 3.0 was employed to simulate the polarity of the protein cavity. The computational results indicated that the reactions from LH2 to SLH2 and from SLH2 to LH2 are both exergonic, which favor the storage and release processes and coincide with the experimental observation. Basing on experimental and current theoretical study, we supplemented the stages of LH2 storage and release in the entire bioluminescent cycle of firefly. The current theoretical calculation could inspire the study on LH2 storage and release of other bioluminescent organisms. This figure shows an entire bioluminescent cycle of firefly by supplementing the stages of LH2 storage and release in the present paper.
Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin (SLH2) may serve as a storage form of luciferin (LH2). In the present article, we employed density functional theory calculation to uncover the mechanism and detailed process of the storage and release reactions. Due to lack of available crystallographic structure of the related enzyme, the calculation was performed on a model system. For the storage reaction, possible amino acid residues were used for imitating the protein environment. For the release reaction, the dielectric constant of 3.0 was employed to simulate the polarity of the protein cavity. The computational results indicated that the reactions from LH2 to SLH2 and from SLH2 to LH2 are both exergonic, which favor the storage and release processes and coincide with the experimental observation. Basing on experimental and current theoretical study, we supplemented the stages of LH2 storage and release in the entire bioluminescent cycle of firefly. The current theoretical calculation could inspire the study on LH2 storage and release of other bioluminescent organisms.
Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin ( SLH 2 ) may serve as a storage form of luciferin ( LH 2 ). In the present article, we employed density functional theory calculation to uncover the mechanism and detailed process of the storage and release reactions. Due to lack of available crystallographic structure of the related enzyme, the calculation was performed on a model system. For the storage reaction, possible amino acid residues were used for imitating the protein environment. For the release reaction, the dielectric constant of 3.0 was employed to simulate the polarity of the protein cavity. The computational results indicated that the reactions from LH 2 to SLH 2 and from SLH 2 to LH 2 are both exergonic, which favor the storage and release processes and coincide with the experimental observation. Basing on experimental and current theoretical study, we supplemented the stages of LH 2 storage and release in the entire bioluminescent cycle of firefly. The current theoretical calculation could inspire the study on LH 2 storage and release of other bioluminescent organisms.
Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin (SLH ) may serve as a storage form of luciferin (LH ). In the present article, we employed density functional theory calculation to uncover the mechanism and detailed process of the storage and release reactions. Due to lack of available crystallographic structure of the related enzyme, the calculation was performed on a model system. For the storage reaction, possible amino acid residues were used for imitating the protein environment. For the release reaction, the dielectric constant of 3.0 was employed to simulate the polarity of the protein cavity. The computational results indicated that the reactions from LH to SLH and from SLH to LH are both exergonic, which favor the storage and release processes and coincide with the experimental observation. Basing on experimental and current theoretical study, we supplemented the stages of LH storage and release in the entire bioluminescent cycle of firefly. The current theoretical calculation could inspire the study on LH storage and release of other bioluminescent organisms.
Author Cui, Cheng‐Xing
Guo, Ya‐Jie
Liu, Ya‐Jun
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CitedBy_id crossref_primary_10_1016_j_jphotochemrev_2022_100537
crossref_primary_10_1016_j_jcat_2024_115590
crossref_primary_10_1098_rsbl_2023_0585
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Snippet Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin (SLH2) may serve as a storage form of...
Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin ( SLH 2 ) may serve as a storage form...
Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin (SLH ) may serve as a storage form of...
Among numerous bioluminescent organisms, firefly is the most studied one. Recent experiment proposed that sulfoluciferin (SLH2 ) may serve as a storage form of...
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SubjectTerms Amino Acids
Animals
Bioluminescence
Computer applications
Crystal structure
Crystallography
Density functional theory
Dielectric constant
Fireflies
Firefly Luciferin - chemistry
Luciferases, Firefly - metabolism
Luciferin
Luciferins
Luminescent Measurements - methods
Models, Theoretical
Polarity
Proteins
Title Theoretical Study on Storage and Release of Firefly Luciferin
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fphp.13496
https://www.ncbi.nlm.nih.gov/pubmed/34333799
https://www.proquest.com/docview/2623496034
https://www.proquest.com/docview/2557536829
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